Cluster composition

Functions

Category	Name	IntersectionWithQuery	PValue	GenesInTerm	GenesInQuery	GenesInTermInQuery	ID
GeneOntologyMolecularFunction	ubiquitin-like ligase-substrate adaptor activity	PRAMEF9 PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27 PRAME	1.09e-06	82	82	6	GO:1990756
GeneOntologyMolecularFunction	enzyme-substrate adaptor activity	PRAMEF9 PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27 PRAME	2.59e-06	95	82	6	GO:0140767
GeneOntologyMolecularFunction	nuclear retinoic acid receptor binding	PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27 PRAME	3.06e-06	55	82	5	GO:0042974
GeneOntologyMolecularFunction	acetylcholine receptor activity	CHRNA1 CHRNB2 HRH3	1.11e-04	23	82	3	GO:0015464
GeneOntologyMolecularFunction	nuclear receptor binding	PRAMEF19 PRAMEF15 PRAMEF4 SLC30A9 PRAMEF27 PRAME	1.21e-04	187	82	6	GO:0016922
GeneOntologyMolecularFunction	microfilament motor activity	MYH8 MYO1A MYH15	5.08e-04	38	82	3	GO:0000146
GeneOntologyMolecularFunction	transmembrane transporter activity	SLC7A9 CNNM4 NALF1 TRPC1 SCN10A SLC30A9 KCNT1 CHRNA1 SLC38A6 CHRNB2 RHCE RHD SLC30A6	9.93e-04	1180	82	13	GO:0022857
GeneOntologyMolecularFunction	inorganic cation transmembrane transporter activity	CNNM4 NALF1 TRPC1 SCN10A SLC30A9 KCNT1 RHCE RHD SLC30A6	1.07e-03	627	82	9	GO:0022890
GeneOntologyMolecularFunction	ammonium channel activity	RHCE RHD	1.07e-03	12	82	2	GO:0008519
GeneOntologyMolecularFunction	acetylcholine binding	CHRNA1 CHRNB2	1.26e-03	13	82	2	GO:0042166
GeneOntologyMolecularFunction	channel activity	NALF1 TRPC1 SCN10A KCNT1 CHRNA1 CHRNB2 RHCE RHD	1.40e-03	525	82	8	GO:0015267
GeneOntologyMolecularFunction	passive transmembrane transporter activity	NALF1 TRPC1 SCN10A KCNT1 CHRNA1 CHRNB2 RHCE RHD	1.42e-03	526	82	8	GO:0022803
GeneOntologyMolecularFunction	cytoskeletal motor activity	KIF21B MYH8 MYO1A MYH15	1.42e-03	118	82	4	GO:0003774
GeneOntologyMolecularFunction	monoatomic cation transmembrane transporter activity	CNNM4 NALF1 TRPC1 SCN10A SLC30A9 KCNT1 CHRNA1 CHRNB2 SLC30A6	1.59e-03	664	82	9	GO:0008324
GeneOntologyMolecularFunction	RNA polymerase II-specific DNA-binding transcription factor binding	PRAMEF19 PRAMEF15 PITX1 PRAMEF4 SLC30A9 PRAMEF27 PRAME	1.63e-03	417	82	7	GO:0061629
GeneOntologyMolecularFunction	phosphatidylinositol-3,5-bisphosphate phosphatase activity	MTMR3 OCRL	1.93e-03	16	82	2	GO:0106018
GeneOntologyMolecularFunction	acetylcholine-gated monoatomic cation-selective channel activity	CHRNA1 CHRNB2	2.18e-03	17	82	2	GO:0022848
GeneOntologyMolecularFunction	transporter activity	SLC7A9 CNNM4 NALF1 TRPC1 SCN10A SLC30A9 KCNT1 CHRNA1 SLC38A6 CHRNB2 RHCE RHD SLC30A6	2.19e-03	1289	82	13	GO:0005215
GeneOntologyMolecularFunction	monoatomic cation channel activity	NALF1 TRPC1 SCN10A KCNT1 CHRNA1 CHRNB2	2.88e-03	343	82	6	GO:0005261
GeneOntologyMolecularFunction	metal ion transmembrane transporter activity	CNNM4 NALF1 TRPC1 SCN10A SLC30A9 KCNT1 SLC30A6	3.00e-03	465	82	7	GO:0046873
GeneOntologyMolecularFunction	amino acid binding	IDO1 ASS1 NOS2	3.38e-03	73	82	3	GO:0016597
GeneOntologyMolecularFunction	postsynaptic neurotransmitter receptor activity	CHRNA1 CHRNB2 HRH3	3.64e-03	75	82	3	GO:0098960
GeneOntologyMolecularFunction	inorganic molecular entity transmembrane transporter activity	CNNM4 NALF1 TRPC1 SCN10A SLC30A9 KCNT1 RHCE RHD SLC30A6	3.86e-03	758	82	9	GO:0015318
GeneOntologyBiologicalProcess	oocyte development	TDRD5 PRAMEF19 PRAMEF15 PRAMEF4 ZP3	4.69e-05	99	82	5	GO:0048599
GeneOntologyBiologicalProcess	acetylcholine receptor signaling pathway	TRPC1 CHRNA1 CHRNB2 HRH3	5.03e-05	51	82	4	GO:0095500
GeneOntologyBiologicalProcess	oocyte differentiation	TDRD5 PRAMEF19 PRAMEF15 PRAMEF4 ZP3	5.66e-05	103	82	5	GO:0009994
GeneOntologyBiologicalProcess	cellular response to acetylcholine	TRPC1 CHRNA1 CHRNB2 HRH3	5.86e-05	53	82	4	GO:1905145
GeneOntologyBiologicalProcess	positive regulation of cell population proliferation	PRAMEF25 PRAMEF9 PRAMEF19 TIRAP PRAMEF15 CLEC7A PELI1 S1PR2 PRAMEF4 RPA1 ZP3 PRAMEF27 PRAME CHRNB2 HRH3	6.20e-05	1190	82	15	GO:0008284
GeneOntologyBiologicalProcess	response to acetylcholine	TRPC1 CHRNA1 CHRNB2 HRH3	7.28e-05	56	82	4	GO:1905144
GeneOntologyBiologicalProcess	postsynaptic signal transduction	TRPC1 CHRNA1 CHRNB2 HRH3	1.65e-04	69	82	4	GO:0098926
GeneOntologyCellularComponent	Cul2-RING ubiquitin ligase complex	PRAMEF9 PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27 PRAME	3.07e-08	47	83	6	GO:0031462
GeneOntologyCellularComponent	cullin-RING ubiquitin ligase complex	PRAMEF9 PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27 PRAME USP47	2.16e-05	212	83	7	GO:0031461
GeneOntologyCellularComponent	ubiquitin ligase complex	PRAMEF9 PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27 PRAME USP47	5.02e-04	352	83	7	GO:0000151
GeneOntologyCellularComponent	ankyrin-1 complex	RHCE RHD	6.87e-04	10	83	2	GO:0170014
HumanPheno	Positive direct antiglobulin test	RHCE RHD	6.36e-05	3	24	2	HP:0032366
HumanPheno	Anti-erythrocyte autoantibody positivity	RHCE RHD	6.36e-05	3	24	2	HP:6000388
MousePheno	abnormal spermatogonia proliferation	PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27 PRAME	2.85e-06	47	67	5	MP:0002685
MousePheno	enlarged urinary bladder	MYH8 PRAMEF19 PRAMEF15 HGSNAT ZFYVE26 PRAMEF4	1.89e-05	116	67	6	MP:0011874
Domain	PRAME_family	PRAMEF25 PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27 PRAME	1.66e-10	19	83	6	IPR026271
Domain	-	CMIP PRAMEF25 PRAMEF19 PRAMEF15 LRRC61 LRTM2 PRAMEF4 PRAMEF27 PRAME	1.26e-05	321	83	9	3.80.10.10
Domain	L_dom-like	CMIP PRAMEF25 PRAMEF19 PRAMEF15 LRRC61 LRTM2 PRAMEF4 PRAMEF27 PRAME	1.50e-05	328	83	9	IPR032675
Domain	Ammonium_transpt	RHCE RHD	1.93e-04	5	83	2	IPR001905
Domain	Ammonium_transp	RHCE RHD	1.93e-04	5	83	2	PF00909
Domain	NH4_transpt_AmtB-like_dom	RHCE RHD	1.93e-04	5	83	2	IPR024041
Domain	RhesusRHD	RHCE RHD	1.93e-04	5	83	2	IPR002229
Domain	-	RHCE RHD	4.04e-04	7	83	2	1.10.3430.10
Domain	Ammonium/urea_transptr	RHCE RHD	4.04e-04	7	83	2	IPR029020
Domain	Myosin_head_motor_dom	MYH8 MYO1A MYH15	6.38e-04	38	83	3	IPR001609
Domain	MYOSIN_MOTOR	MYH8 MYO1A MYH15	6.38e-04	38	83	3	PS51456
Domain	Myosin_head	MYH8 MYO1A MYH15	6.38e-04	38	83	3	PF00063
Domain	MYSc	MYH8 MYO1A MYH15	6.38e-04	38	83	3	SM00242
Domain	IQ	MYH8 MYO1A SCN10A MYH15	7.84e-04	93	83	4	PS50096
Domain	Cation_efflux	SLC30A9 SLC30A6	8.58e-04	10	83	2	IPR002524
Domain	Cation_efflux	SLC30A9 SLC30A6	8.58e-04	10	83	2	PF01545
Domain	-	SLC30A9 SLC30A6	1.05e-03	11	83	2	1.20.1510.10
Domain	Cation_efflux_TMD	SLC30A9 SLC30A6	1.05e-03	11	83	2	IPR027469
Domain	TUDOR	TDRD5 TDRD15	1.72e-03	14	83	2	PF00567
Domain	Myosin_N	MYH8 MYH15	1.97e-03	15	83	2	PF02736
Domain	Myosin_N	MYH8 MYH15	1.97e-03	15	83	2	IPR004009
Domain	Nicotinic_acetylcholine_rcpt	CHRNA1 CHRNB2	2.25e-03	16	83	2	IPR002394
Domain	Myosin_tail_1	MYH8 MYH15	2.85e-03	18	83	2	PF01576
Domain	Myosin_tail	MYH8 MYH15	2.85e-03	18	83	2	IPR002928
Domain	Myosin-like_IQ_dom	MYH8 MYH15	3.18e-03	19	83	2	IPR027401
Domain	-	MYH8 MYH15	3.18e-03	19	83	2	4.10.270.10
Domain	IQ	MYH8 MYO1A SCN10A	3.89e-03	71	83	3	PF00612
Domain	-	CHRNA1 CHRNB2	4.65e-03	23	83	2	1.20.120.370
Domain	Acetylcholine_rcpt_TM	CHRNA1 CHRNB2	4.65e-03	23	83	2	IPR027361
Domain	TUDOR	TDRD5 TDRD15	4.65e-03	23	83	2	PS50304
Domain	TUDOR	TDRD5 TDRD15	6.37e-03	27	83	2	SM00333
Domain	IPT	MET PKHD1L1	6.37e-03	27	83	2	SM00429
Domain	FYVE	MTMR3 ZFYVE26	7.33e-03	29	83	2	PF01363
Domain	FYVE	MTMR3 ZFYVE26	7.33e-03	29	83	2	SM00064
Domain	IQ_motif_EF-hand-BS	MYH8 MYO1A SCN10A	7.53e-03	90	83	3	IPR000048
Domain	Tudor	TDRD5 TDRD15	7.83e-03	30	83	2	IPR002999
Domain	TIG	MET PKHD1L1	8.35e-03	31	83	2	PF01833
Pubmed	Sertoli cell-only phenotype and scRNA-seq define PRAMEF12 as a factor essential for spermatogenesis in mice.	PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27 PRAME	2.49e-09	22	89	5	31729367
Pubmed	MAGE-B4, a binding partner of PRAMEF12, is dispensable for spermatogenesis and male fertility in mice.	PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27 PRAME	5.00e-09	25	89	5	37451217
Pubmed	Differences in gene expression between mouse and human for dynamically regulated genes in early embryo.	PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27 PRAME	9.19e-09	28	89	5	25089626
Pubmed	Retinoic acid receptors are required for skeletal growth, matrix homeostasis and growth plate function in postnatal mouse.	PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27 PRAME	2.99e-08	35	89	5	19389355
Pubmed	Preferentially Expressed Antigen in Melanoma (PRAME) and the PRAME Family of Leucine-Rich Repeat Proteins.	PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27	1.88e-07	20	89	4	26694250
Pubmed	Organization of the gene (RHCE) encoding the human blood group RhCcEe antigens and characterization of the promoter region.	RHCE RHD	6.48e-06	2	89	2	8188244
Pubmed	E variants found in Japanese and c antigenicity alteration without substitution in the second extracellular loop.	RHCE RHD	6.48e-06	2	89	2	11724987
Pubmed	Tryptophan availability selectively limits NO-synthase induction in macrophages.	IDO1 NOS2	6.48e-06	2	89	2	12525575
Pubmed	DCS-1, DCS-2, and DFV share amino acid substitutions at the extracellular RhD protein vestibule.	RHCE RHD	6.48e-06	2	89	2	17900276
Pubmed	RHD and RHCE molecular analysis in weak D blood donors and in patients with Rh antibodies against their own corresponding Rh antigen.	RHCE RHD	6.48e-06	2	89	2	32697929
Pubmed	The Rh blood group system: a review.	RHCE RHD	6.48e-06	2	89	2	10627438
Pubmed	Polymorphisms in the promoter regions of RHD and RHCE genes in the Chinese Han population.	RHCE RHD	6.48e-06	2	89	2	37823181
Pubmed	Sequence diversity of the Rh blood group system in Basques.	RHCE RHD	6.48e-06	2	89	2	30089826
Pubmed	Review: the molecular basis of the Rh blood group phenotypes.	RHCE RHD	6.48e-06	2	89	2	15373666
Pubmed	Interplay between IDO1 and iNOS in human retinal pigment epithelial cells.	IDO1 NOS2	6.48e-06	2	89	2	31267172
Pubmed	Intron 4 of the RH Gene in Han Chinese, Tibetan, and Mongol Populations.	RHCE RHD	6.48e-06	2	89	2	26579938
Pubmed	Accurate long-read sequencing allows assembly of the duplicated RHD and RHCE genes harboring variants relevant to blood transfusion.	RHCE RHD	6.48e-06	2	89	2	34968422
Pubmed	Transfusion strategy for weak D Type 4.0 based on RHD alleles and RH haplotypes in Tunisia.	RHCE RHD	6.48e-06	2	89	2	29193104
Pubmed	Regarding the size of Rh proteins.	RHCE RHD	6.48e-06	2	89	2	1898705
Pubmed	PCR screening for common weak D types shows different distributions in three Central European populations.	RHCE RHD	6.48e-06	2	89	2	11161244
Pubmed	RH diversity in Mali: characterization of a new haplotype RHDDIVa/RHCEceTI(D2).	RHCE RHD	6.48e-06	2	89	2	25857637
Pubmed	The low-prevalence Rh antigen STEM (RH49) is encoded by two different RHCEce818T alleles that are often in cis to RHDDOL.	RHCE RHD	6.48e-06	2	89	2	22738288
Pubmed	Multiple Rh messenger RNA isoforms are produced by alternative splicing.	RHCE RHD	6.48e-06	2	89	2	1379850
Pubmed	RHCE variants inherited with altered RHD alleles in Brazilian blood donors.	RHCE RHD	6.48e-06	2	89	2	27111588
Pubmed	Characterization of the mouse Rh blood group gene.	RHCE RHD	6.48e-06	2	89	2	10329015
Pubmed	Alteration of RH gene structure and expression in human dCCee and DCW-red blood cells: phenotypic homozygosity versus genotypic heterozygosity.	RHCE RHD	6.48e-06	2	89	2	8822955
Pubmed	Kynurenine is an endothelium-derived relaxing factor produced during inflammation.	IDO1 NOS2	6.48e-06	2	89	2	20190767
Pubmed	Genetic recombination at the human RH locus: a family study of the red-cell Evans phenotype reveals a transfer of exons 2-6 from the RHD to the RHCE gene.	RHCE RHD	6.48e-06	2	89	2	8808597
Pubmed	Molecular background of Rh D-positive, D-negative, D(el) and weak D phenotypes in Chinese.	RHCE RHD	6.48e-06	2	89	2	12201845
Pubmed	Variant RH alleles and Rh immunisation in patients with sickle cell disease.	RHCE RHD	6.48e-06	2	89	2	24960646
Pubmed	RHCEceMO is frequently in cis to RHDDAU0 and encodes a hr(S) -, hr(B) -, RH:-61 phenotype in black persons: clinical significance.	RHCE RHD	6.48e-06	2	89	2	23772606
Pubmed	Comprehensive phenotypic and molecular investigation of RhD and RhCE variants in Moroccan blood donors.	RHCE RHD	6.48e-06	2	89	2	30418133
Pubmed	A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genes.	RHCE RHD	6.48e-06	2	89	2	23550903
Pubmed	Molecular cloning and primary structure of the human blood group RhD polypeptide.	RHCE RHD	6.48e-06	2	89	2	1438298
Pubmed	Determination of the N-terminal sequence of human red cell Rh(D) polypeptide and demonstration that the Rh(D), (c), and (E) antigens are carried by distinct polypeptide chains.	RHCE RHD	6.48e-06	2	89	2	3135863
Pubmed	Molecular background of D(C)(e) haplotypes within the white population.	RHCE RHD	6.48e-06	2	89	2	12084172
Pubmed	The analysis of nucleotide substitutions, gaps, and recombination events between RHD and RHCE genes through complete sequencing.	RHCE RHD	6.48e-06	2	89	2	10924335
Pubmed	Sequences and evolution of mammalian RH gene transcripts and proteins.	RHCE RHD	6.48e-06	2	89	2	9811965
Pubmed	A two-locus gene conversion model with selection and its application to the human RHCE and RHD genes.	RHCE RHD	6.48e-06	2	89	2	12857961
Pubmed	Specific amino acid substitutions cause distinct expression of JAL (RH48) and JAHK (RH53) antigens in RhCE and not in RhD.	RHCE RHD	6.48e-06	2	89	2	20233350
Pubmed	Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety.	RHCE RHD	6.48e-06	2	89	2	12393640
Pubmed	Molecular genetic basis of the human Rhesus blood group system.	RHCE RHD	6.48e-06	2	89	2	8220426
Pubmed	A recombination hot spot in the Rh genes revealed by analysis of unrelated donors with the rare D-- phenotype.	RHCE RHD	6.48e-06	2	89	2	8900235
Pubmed	RHDweak partial 4.0 is associated with an altered RHCEce(48C, 105T, 733G, 744C, 1025T) allele in the Tunisian population.	RHCE RHD	6.48e-06	2	89	2	23742316
Pubmed	Isolation of a new cDNA clone encoding an Rh polypeptide associated with the Rh blood group system.	RHCE RHD	6.48e-06	2	89	2	7916743
Pubmed	A comprehensive survey of both RHD and RHCE allele frequencies in sub-Saharan Africa.	RHCE RHD	6.48e-06	2	89	2	24033223
Pubmed	RHDDOL1 and RHDDOL2 encode a partial D antigen and are in cis with the rare RHCE*ceBI allele in people of African descent.	RHCE RHD	6.48e-06	2	89	2	22690701
Pubmed	No Distinction of Orthology/Paralogy between Human and Chimpanzee Rh Blood Group Genes.	RHCE RHD	6.48e-06	2	89	2	26872772
Pubmed	RHCEceTI encodes partial c and partial e and is often in cis to RHDDIVa.	RHCE RHD	6.48e-06	2	89	2	22804620
Pubmed	Intricate combinatorial patterns of exon splicing generate multiple Rh-related isoforms in human erythroid cells.	RHCE RHD	6.48e-06	2	89	2	7789951
Pubmed	Differential expression of PRAMEL1, a cancer/testis antigen, during spermatogenesis in the mouse.	PRAMEF19 PRAMEF15 PRAMEF4	1.07e-05	17	89	3	23565261
Pubmed	Mouse Pramel1 regulates spermatogonial development by inhibiting retinoic acid signaling during spermatogenesis.	PRAMEF19 PRAMEF15 PRAMEF4	1.07e-05	17	89	3	37781892
Pubmed	The promoter of the oocyte-specific gene, Oog1, functions in both male and female meiotic germ cells in transgenic mice.	PRAMEF19 PRAMEF15 PRAMEF4	1.29e-05	18	89	3	23894331
Pubmed	Oogenesin is a novel mouse protein expressed in oocytes and early cleavage-stage embryos.	PRAMEF19 PRAMEF15 PRAMEF4	1.29e-05	18	89	3	12890732
Pubmed	Oocyte-specific gene Oog1 suppresses the expression of spermatogenesis-specific genes in oocytes.	PRAMEF19 PRAMEF15 PRAMEF4	1.29e-05	18	89	3	29731491
Pubmed	Identification of a new expanding family of genes characterized by atypical LRR domains. Localization of a cluster preferentially expressed in oocyte.	PRAMEF19 PRAMEF15 PRAMEF4	1.29e-05	18	89	3	14675769
Pubmed	Pramel15 facilitates zygotic nuclear DNMT1 degradation and DNA demethylation.	PRAMEF19 PRAMEF15 PRAMEF4	1.29e-05	18	89	3	39181896
Pubmed	Pramel7 mediates ground-state pluripotency through proteasomal-epigenetic combined pathways.	PRAMEF19 PRAMEF15 PRAMEF4	1.52e-05	19	89	3	28604677
Pubmed	ZAR1 and ZAR2 are required for oocyte meiotic maturation by regulating the maternal transcriptome and mRNA translational activation.	PRAMEF19 PRAMEF15 PRAMEF4 CPEB1	1.53e-05	58	89	4	31598710
Pubmed	Oog1, an oocyte-specific protein, interacts with Ras and Ras-signaling proteins during early embryogenesis.	PRAMEF19 PRAMEF15 PRAMEF4	1.79e-05	20	89	3	16580637
Pubmed	Pramel7 mediates LIF/STAT3-dependent self-renewal in embryonic stem cells.	PRAMEF19 PRAMEF15 PRAMEF4	1.79e-05	20	89	3	21425410
Pubmed	Reactive Neutrophil Responses Dependent on the Receptor Tyrosine Kinase c-MET Limit Cancer Immunotherapy.	MET NOS2	1.94e-05	3	89	2	29045907
Pubmed	Therapeutic targeting of argininosuccinate synthase 1 (ASS1)-deficient pulmonary fibrosis.	MET ASS1	1.94e-05	3	89	2	33508432
Pubmed	Generation and characterisation of Rhd and Rhag null mice.	RHCE RHD	1.94e-05	3	89	2	19807729
Pubmed	Identification of four classes of brain nicotinic receptors using beta2 mutant mice.	CHRNA1 CHRNB2	1.94e-05	3	89	2	9614223
Pubmed	Hydrophobic cluster analysis and modeling of the human Rh protein three-dimensional structures.	RHCE RHD	1.94e-05	3	89	2	16584906
Pubmed	Evolutionary history of the Rh blood group-related genes in vertebrates.	RHCE RHD	1.94e-05	3	89	2	10970100
Pubmed	Promotion of Anti-Tuberculosis Macrophage Activity by L-Arginine in the Absence of Nitric Oxide.	ASS1 NOS2	1.94e-05	3	89	2	34054815
Pubmed	Conserved evolution of the Rh50 gene compared to its homologous Rh blood group gene.	RHCE RHD	1.94e-05	3	89	2	9705835
Pubmed	The expansion of the PRAME gene family in Eutheria.	PRAMEF19 PRAME	1.94e-05	3	89	2	21347312
Pubmed	Binding of HIV-1 gp120 to the nicotinic receptor.	CHRNA1 CHRNB2	1.94e-05	3	89	2	1397297
Pubmed	The members of the RH gene family (RH50 and RH30) followed different evolutionary pathways.	RHCE RHD	1.94e-05	3	89	2	9929383
Pubmed	Protein-sequence studies on Rh-related polypeptides suggest the presence of at least two groups of proteins which associate in the human red-cell membrane.	RHCE RHD	1.94e-05	3	89	2	3146980
Pubmed	Oogenesis specific genes (Nobox, Oct4, Bmp15, Gdf9, Oogenesin1 and Oogenesin2) are differentially expressed during natural and gonadotropin-induced mouse follicular development.	PRAMEF19 PRAMEF15 PRAMEF4	2.76e-05	23	89	3	19480014
Pubmed	Incomplete reactivation of Oct4-related genes in mouse embryos cloned from somatic nuclei.	PRAMEF19 PRAMEF15 PRAMEF4	3.58e-05	25	89	3	12620990
Pubmed	Entire sequence of a mouse chromosomal segment containing the gene Rhced and a comparative analysis of the homologous human sequence.	RHCE RHD	3.87e-05	4	89	2	12459264
Pubmed	HLA-DRB1 molecules and the presentation of anchor peptides from RhD, RhCE, and KEL proteins.	RHCE RHD	3.87e-05	4	89	2	33675036
Pubmed	Association between ABO, Rhesus blood group systems and haemoglobin genotype among confirmed HIV/AIDS-TB co-infected patients in Enugu Urban, Nigeria.	RHCE RHD	3.87e-05	4	89	2	16722361
Pubmed	Expression profiling in transgenic FVB/N embryonic stem cells overexpressing STAT3.	PRAMEF19 PRAMEF15 PRAMEF4	4.04e-05	26	89	3	18500982
Pubmed	Thirteen Ovary-Enriched Genes Are Individually Not Essential for Female Fertility in Mice.	PRAMEF19 PRAMEF15 PRAMEF4	6.26e-05	30	89	3	38786026
Pubmed	RHCE represents the ancestral RH position, while RHD is the duplicated gene.	RHCE RHD	6.44e-05	5	89	2	11902138
Pubmed	Evolutionary conservation and diversification of Rh family genes and proteins.	RHCE RHD	6.44e-05	5	89	2	16227429
Pubmed	Genetic variation of innate immune genes in HIV-infected african patients with or without oropharyngeal candidiasis.	TIRAP CLEC7A	6.44e-05	5	89	2	20577092
Pubmed	LSM14B is essential for oocyte meiotic maturation by regulating maternal mRNA storage and clearance.	PRAMEF19 PRAMEF15 PRAMEF4	7.61e-05	32	89	3	37889087
Pubmed	Intralesional expression of mRNA of interferon- gamma , tumor necrosis factor- alpha , interleukin-10, nitric oxide synthase, indoleamine-2,3-dioxygenase, and RANTES is a major immune effector in Mediterranean spotted fever rickettsiosis.	IDO1 NOS2	9.65e-05	6	89	2	17674321
Pubmed	Conservation of dishevelled structure and function between flies and mice: isolation and characterization of Dvl2.	DVL2 NOS2	9.65e-05	6	89	2	8887313
Pubmed	SELENOPROTEINS. CRL2 aids elimination of truncated selenoproteins produced by failed UGA/Sec decoding.	PRAMEF9 PRAME	1.35e-04	7	89	2	26138980
Pubmed	Distinct roles for Dectin-1 and TLR4 in the pathogenesis of Aspergillus fumigatus keratitis.	TIRAP CLEC7A	1.79e-04	8	89	2	20617171
Pubmed	Mbd3, a component of the NuRD co-repressor complex, is required for development of pluripotent cells.	PRAMEF19 PRAMEF15 PRAMEF4	2.27e-04	46	89	3	17287250
Pubmed	Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.	MALRD1 PSMG1	2.30e-04	9	89	2	20062062
Pubmed	Nociceptors Boost the Resolution of Fungal Osteoinflammation via the TRP Channel-CGRP-Jdp2 Axis.	SCN10A CLEC7A	2.30e-04	9	89	2	28658621
Pubmed	Intracellular zinc homeostasis in leukocyte subsets is regulated by different expression of zinc exporters ZnT-1 to ZnT-9.	SLC30A9 SLC30A6	2.30e-04	9	89	2	17971500
Pubmed	Autosomal Dominant Sleep-Related Hypermotor (Hyperkinetic) Epilepsy	KCNT1 CHRNB2	2.88e-04	10	89	2	20301348
Pubmed	Zinc transporter 2 (SLC30A2) can suppress the vesicular zinc defect of adaptor protein 3-depleted fibroblasts by promoting zinc accumulation in lysosomes.	SLC30A9 SLC30A6	2.88e-04	10	89	2	17349999
Pubmed	DUX is a non-essential synchronizer of zygotic genome activation.	PRAMEF19 PRAMEF15 PRAMEF4	2.91e-04	50	89	3	31806660
Pubmed	[Genetic predisposition to development of toxic liver cirrhosis caused by alcohol].	RHCE RHD	3.51e-04	11	89	2	11436564
Pubmed	A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome.	FANCG RPA1	4.20e-04	12	89	2	12724401
Pubmed	A novel ubiquitin ligase is deficient in Fanconi anemia.	FANCG RPA1	4.20e-04	12	89	2	12973351
Pubmed	The mouse Rhl1 and Rhag genes: sequence, organization, expression, and chromosomal mapping.	RHCE RHD	4.20e-04	12	89	2	10495887
Pubmed	Homologs of genes expressed in Caenorhabditis elegans GABAergic neurons are also found in the developing mouse forebrain.	MYH8 PITX1 FOXI2	4.29e-04	57	89	3	21122108
Cytoband	1p36.21	PRAMEF25 PRAMEF9 PRAMEF19 PRAMEF15 PRAMEF4	1.66e-07	63	90	5	1p36.21
Cytoband	Ensembl 112 genes in cytogenetic band chr1p36	PRAMEF25 PRAMEF9 PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27 RHCE RHD	5.99e-05	681	90	8	chr1p36
Cytoband	22q11.22	RAB36 PRAME	9.36e-04	23	90	2	22q11.22
GeneFamily	PRAME family	PRAMEF25 PRAMEF9 PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27 PRAME	1.30e-12	24	62	7	686
GeneFamily	Myosin heavy chains	MYH8 MYH15	1.18e-03	15	62	2	1098
GeneFamily	Cholinergic receptors nicotinic subunits	CHRNA1 CHRNB2	1.35e-03	16	62	2	173
GeneFamily	Zinc fingers FYVE-type\|Pleckstrin homology domain containing\|Rho guanine nucleotide exchange factors	MTMR3 ZFYVE26	5.05e-03	31	62	2	81
GeneFamily	Phosphoinositide phosphatases	MTMR3 OCRL	5.37e-03	32	62	2	1079
GeneFamily	Glycosyltransferase family 6\|Blood group antigens	RHCE RHD	7.13e-03	37	62	2	454
GeneFamily	Tudor domain containing	TDRD5 TDRD15	7.13e-03	37	62	2	780
Coexpression	GSE46242_TH1_VS_ANERGIC_TH1_CD4_TCELL_WITH_EGR2_DELETED_UP	CNNM4 GANC IDO1 UGGT2 S1PR2 RMC1 CPEB1	4.58e-06	199	87	7	M9716
Coexpression	KOHOUTEK_CCNT2_TARGETS	PRAMEF19 PRAMEF15 PRAMEF4 PRAMEF27 PRAME	7.54e-06	81	87	5	MM938
Coexpression	BYSTRYKH_HEMATOPOIESIS_STEM_CELL_AND_BRAIN_QTL_TRANS	PRAMEF19 PRAMEF15 PRAMEF4 RMC1 PCK2 ZMYM4	3.07e-05	180	87	6	MM612
ToppCell	facs-Marrow-B-cells-18m-Hematologic-megakaryocyte-erythroid_progenitor_cell\|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation	IDO1 PLA2G4F CTSE PKHD1L1 CHRNB2 RHD	1.19e-06	168	90	6	17fb9426eeea407b26fb895b8397faca95b7552d
ToppCell	facs-Marrow-B-cells-18m-Hematologic-megakaryocyte-erythroid_progenitor_cell\|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation	IDO1 PLA2G4F CTSE PKHD1L1 CHRNB2 RHD	1.19e-06	168	90	6	a61b39884851384cffd430079040546d125b2b40
ToppCell	COVID-19-Heart-EC_2\|Heart / Disease (COVID-19 only), tissue and cell type	MET CFAP54 CMIP NALF1 MMRN2 PELI1	2.22e-06	187	90	6	40ffc06a3e3251d9b12da390210d3e045af7537a
ToppCell	390C-Myeloid-Macrophage-SPP1+_Macrophage\|Macrophage / Donor, Lineage, Cell class and subclass (all cells)	FANCG PDE7A GANC PITX1 ZFYVE26	2.33e-05	168	90	5	8459d0a1bf6d4b5c83001097331f8b78fceb9305
ToppCell	Endothelial-B-IPF_04\|World / lung cells shred on cell class, cell subclass, sample id	NALF1 TRPC1 MMRN2 PKHD1L1 FAM87A	2.60e-05	172	90	5	d4e98ff9c7cbc95457e1d71fa60f151a2f178dae
ToppCell	5'-Parenchyma_lung-Immune_Myeloid-Myeloid_monocytic-classical_monocyte-Classical_monocytes-Classical_monocytes_L.1.2.4.0\|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5	KIF21B CD22 MTMR3 CLEC7A RHCE	2.75e-05	174	90	5	b6e3fa995def40a8fbdfc249fe108c303931a171
ToppCell	TCGA-Bone_and_Soft_Tissue-Primary_Tumor-Sarcoma-Monophasic_Synovial_Sarcoma-5\|TCGA-Bone_and_Soft_Tissue / Sample_Type by Project: Shred V9	PRAMEF9 PRAMEF15 PRAMEF4 HRH3	3.82e-05	93	90	4	3e05ea0f8f4a7cdb78a596f47d563dc3c94d4d8e
ToppCell	PCW_05-06-Hematologic_ErythroMegGranulo-Hem_ErythroMeg\|PCW_05-06 / Celltypes from embryonic and fetal-stage human lung	PITX1 CTSE PKHD1L1 RHCE RHD	3.98e-05	188	90	5	5d6faf45a9c0794b0c30b0a0601c10afbb8aa9ed
ToppCell	PCW_05-06-Hematologic_ErythroMegGranulo\|PCW_05-06 / Celltypes from embryonic and fetal-stage human lung	PITX1 CTSE PKHD1L1 RHCE RHD	3.98e-05	188	90	5	a0873783f0a2cd852563c05a275dddc72905ced2
ToppCell	PCW_05-06-Hematologic_ErythroMegGranulo-Hem_ErythroMeg-erythro\|PCW_05-06 / Celltypes from embryonic and fetal-stage human lung	PITX1 CTSE PKHD1L1 RHCE RHD	3.98e-05	188	90	5	29d804232d974a8c0029300345b287005b09bade
ToppCell	Control-Endothelial-VE_Venous\|Endothelial / Disease state, Lineage and Cell class	MET CMIP NALF1 ASS1 MMRN2	4.19e-05	190	90	5	4e30155203b4a8c5e496fcbe9348b67b98ebc625
ToppCell	PBMC-Severe-Myeloid-Neutrophil-Neutrophil-Neu_4\|Severe / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.09)	CNNM4 UGGT2 OCRL USP47 SLC30A6	4.19e-05	190	90	5	3f0c7d130f66faea778fe567604edf1b4cdf85b3
ToppCell	PBMC-Severe-Myeloid-Neutrophil-Neutrophil-Neu_4\|Severe / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)	CNNM4 UGGT2 OCRL USP47 SLC30A6	4.40e-05	192	90	5	c09dcc73ff9c3855a0f3d7bfa0d5c99c09a117f2
ToppCell	normal_Lung-Epithelial_cells-Club\|normal_Lung / Location, Cell class and cell subclass	MET SUSD4 KRTAP3-1 ASS1 CTSE	4.74e-05	195	90	5	b46544ad5af04f4dbc2643637caa3d2d50d922ae
ToppCell	5'-Adult-SmallIntestine-Epithelial\|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract	SLC7A9 MALRD1 MYO1A CTSE PCK2	5.09e-05	198	90	5	8d629492d2199de8e036c19e9dacceb9c9e721a0
ToppCell	5'-Adult-SmallIntestine-Epithelial-mature_enterocytic-Enterocyte\|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract	SLC7A9 MALRD1 MYO1A CTSE PCK2	5.09e-05	198	90	5	6e6af8fad09f8e48b3f2ce463d5773b6a69864d1
ToppCell	5'-Adult-SmallIntestine\|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract	SLC7A9 MALRD1 MYO1A CTSE PCK2	5.22e-05	199	90	5	a5fffe381be1ba7d192b68d1d3937ce47663658e
ToppCell	Lung_Parenchyma-Control-Epithelial-Epithelial-Club\|Control / Location, Disease Group, Cell group, Cell class (2021.03.09)	MET SUSD4 KRTAP3-1 ASS1 CTSE	5.22e-05	199	90	5	2b17694cffbec28a2c8f165dfcff6bab94aa0f4c
ToppCell	Parenchyma_Control_(B.)-Epithelial-TX-Club\|Parenchyma_Control_(B.) / Sample group, Lineage and Cell type	MET SUSD4 KRTAP3-1 ASS1 CTSE	5.22e-05	199	90	5	111cfd589ec6795075d8d88d7664bfb23eba5bf6
ToppCell	Lung_Parenchyma-Control-Epithelial-Epithelial-Club-\|Control / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)	MET SUSD4 KRTAP3-1 ASS1 CTSE	5.22e-05	199	90	5	d583290a1d288b749ad17bc501c1487268c6551c
ToppCell	5'-Adult-SmallIntestine-Epithelial-mature_enterocytic\|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract	SLC7A9 MALRD1 MYO1A CTSE PCK2	5.22e-05	199	90	5	01c2721bc82cd672e9477029b4a7ecc77e2f1b00
ToppCell	(53)_Lymphoid_DC\|World / shred on Cell_type and subtype	CD300LD-AS1 IDO1 MMRN2 PRAME NSUN7	6.43e-05	208	90	5	30212cfacad94a7cc562a69efa73a31259851515
Disease	Anemia, Hemolytic, Congenital	RHCE RHD	7.44e-06	2	81	2	C0002881
Disease	Rh Deficiency Syndrome	RHCE RHD	2.23e-05	3	81	2	C0272052
Disease	Rh-Null, Regulator Type	RHCE RHD	2.23e-05	3	81	2	C1849387
Disease	Frontal Epilepsy, Benign, Childhood	KCNT1 CHRNB2	4.45e-05	4	81	2	C0393671
Disease	Epilepsy, Cingulate	KCNT1 CHRNB2	4.45e-05	4	81	2	C0393684
Disease	Epilepsy, Supplementary Motor	KCNT1 CHRNB2	4.45e-05	4	81	2	C0393683
Disease	Epilepsy, Opercular	KCNT1 CHRNB2	4.45e-05	4	81	2	C0393688
Disease	Epilepsy, Orbito-Frontal	KCNT1 CHRNB2	4.45e-05	4	81	2	C0751643
Disease	Epilepsy, Anterior Fronto-Polar	KCNT1 CHRNB2	4.45e-05	4	81	2	C0751642
Disease	Epilepsy, Frontal Lobe	KCNT1 CHRNB2	4.45e-05	4	81	2	C0085541
Disease	Autosomal dominant nocturnal frontal lobe epilepsy	KCNT1 CHRNB2	4.45e-05	4	81	2	cv:C3696898
Disease	unipolar depression, bipolar disorder	CNNM4 MMRN2 MYH15 TMPRSS5 SLC30A9	7.18e-05	156	81	5	EFO_0003761, MONDO_0004985
Disease	Autosomal Dominant Nocturnal Frontal Lobe Epilepsy	KCNT1 CHRNB2	1.55e-04	7	81	2	C3696898
Disease	autosomal dominant hyaline body myopathy (implicated_via_orthology)	MYH8 MYH15	3.30e-04	10	81	2	DOID:0111269 (implicated_via_orthology)
Disease	distal arthrogryposis type 2B3 (implicated_via_orthology)	MYH8 MYH15	3.30e-04	10	81	2	DOID:0111602 (implicated_via_orthology)
Disease	distal arthrogryposis type 1 (implicated_via_orthology)	MYH8 MYH15	3.30e-04	10	81	2	DOID:0111596 (implicated_via_orthology)
Disease	dilated cardiomyopathy 1S (implicated_via_orthology)	MYH8 MYH15	3.30e-04	10	81	2	DOID:0110454 (implicated_via_orthology)
Disease	congenital myopathy 6 (implicated_via_orthology)	MYH8 MYH15	3.30e-04	10	81	2	DOID:0080719 (implicated_via_orthology)
Disease	inclusion body myositis (implicated_via_orthology)	MYH8 MYH15	3.30e-04	10	81	2	DOID:3429 (implicated_via_orthology)
Disease	distal arthrogryposis type 2A (implicated_via_orthology)	MYH8 MYH15	3.30e-04	10	81	2	DOID:0111605 (implicated_via_orthology)
Disease	familial hypertrophic cardiomyopathy (implicated_via_orthology)	MYH8 MYH15	3.30e-04	10	81	2	DOID:0080326 (implicated_via_orthology)
Disease	distal myopathy (implicated_via_orthology)	MYH8 MYH15	4.83e-04	12	81	2	DOID:11720 (implicated_via_orthology)
Disease	myotonia congenita (implicated_via_orthology)	MYH8 MYH15	4.83e-04	12	81	2	DOID:2106 (implicated_via_orthology)
Disease	restrictive cardiomyopathy (implicated_via_orthology)	MYH8 MYH15	5.69e-04	13	81	2	DOID:397 (implicated_via_orthology)
Disease	Hypothermia, natural	NOS2 CHRNB2	6.63e-04	14	81	2	C0020672
Disease	distal arthrogryposis (implicated_via_orthology)	MYH8 MYH15	7.64e-04	15	81	2	DOID:0050646 (implicated_via_orthology)
Disease	Malaria, susceptibility to	TIRAP NOS2	8.71e-04	16	81	2	cv:C1970028
Disease	congenital myasthenic syndrome (implicated_via_orthology)	CHRNA1 CHRNB2	8.71e-04	16	81	2	DOID:3635 (implicated_via_orthology)
Disease	–	TIRAP NOS2	8.71e-04	16	81	2	611162
Disease	Malaria	TIRAP NOS2	1.37e-03	20	81	2	C0024530
Disease	sciatic neuropathy (implicated_via_orthology)	SCN10A HRH3	1.81e-03	23	81	2	DOID:11446 (implicated_via_orthology)
Disease	malaria (is_implicated_in)	TIRAP NOS2	1.98e-03	24	81	2	DOID:12365 (is_implicated_in)
Disease	ankylosing spondylitis	KIF21B MALRD1 NOS2	2.03e-03	91	81	3	EFO_0003898
Disease	primary biliary cholangitis (biomarker_via_orthology)	NOS2 CPEB1	2.69e-03	28	81	2	DOID:12236 (biomarker_via_orthology)

Protein segments in the cluster

Peptide	Gene	Start	Entry
YTKLPAQAIPCSLAW	TDRD5	581	Q8NAT2
APCIYWLPLTDSQIV	ACIN1	1221	Q9UKV3
ASNKELCFQWYIPPL	CFAP54	2926	Q96N23
SWENAPKYCLQLTIP	CMIP	121	Q8IY22
PLSFQCLKAPATLTW	CD300LD-AS1	26	Q96MU5
VAKCWDPSPQAYFTL	DVL2	351	O14641
SCYSLAPQIKVIAPW	ASS1	131	P00966
KALYLAGPNCLSPWK	NBEAL1	801	Q6ZS30
SFPKWYTPEACLQLR	RAB36	86	O95755
NANLLAWTCLPLFPK	PIK3C2G	571	O75747
ITWTPPAIFKSYCEI	CHRNA1	136	P02708
SYWVSDKRLPPCSLS	NOS2	811	P35228
PPILVYADCVLANWK	IDO1	121	P14902
YPLLKADPSLWCVSA	MGAT1	226	P26572
LSNPLCANPSYWAAV	LRRC61	136	Q9BV99
LDKTWPAAPYKCLST	MYO1A	801	Q9UBC5
NWCPYPMSKLVTLLA	MMRN2	56	Q9H8L6
VNKCWFLSYIKPSEP	SPINK8	46	P0C7L1
AWAVKDFAPNCPLYV	KCNT1	456	Q5JUK3
NLWVPSVYCTSPACK	CTSE	101	P14091
LWVNAPALSPKSYAS	FOXI2	41	Q6ZQN5
WCYSATLLLAPLPAS	LINC02901	186	Q4VX62
SGLFCVTVNPYKWLP	MYH8	121	P13535
LPKYNNCWLARTDPK	PCK2	86	Q16822
CKPDTYVPTCWLLNN	KRTAP3-1	56	Q9BYR8
PKLPIWLCNINGNYS	MINDY4B	361	A8MYZ0
CYLKEPKLANSVTPW	PDE7A	226	Q13946
DCRVKLWNYVPGLTP	KIF21B	1606	O75037
CWPGLSSYLDFTNPK	GANC	471	Q8TET4
CKWVLPILTQFTPYL	PRAMEF15	216	P0DUQ1
GTKELPYCPLWVSAT	FANCG	441	O15287
LLSKADCYVQLWLPT	PLA2G4F	61	Q68DD2
KSAFKLTWTAQPPCL	RBM12B-AS1	56	Q9P1G2
SGLPCWPYLTAEALK	NPIPB15	226	A6NHN6
PAAVLSYCQVWKIPA	PSMG1	216	O95456
SFEKRSLCKWYQPIP	MALRD1	1091	Q5VYJ5
PIASLTPYQSKWTIC	RPA1	186	P27694
SYPGCQPLKDTRAWA	ATP11AUN	16	Q6ZP68
LAPIISKPTWEYLYC	SLC7A9	426	P82251
IRSPYIDGCSPIKNW	BORA	316	Q6PGQ7
LWANSAVNPVLYPLC	HRH3	401	Q9Y5N1
IVNPNYCLGPLSWDK	HGSNAT	356	Q68CP4
ATCTWSGQLPPRNYK	CPEB1	291	Q9BZB8
ILFIWYCTCKSLPSP	CLDN12	191	P56749
WLPAFSILLLDYACP	S1PR2	246	O95136
AVAPAKFCLWYVVPS	FAM87A	46	P0C7U9
CSWASPVALNVQYAP	CD22	491	P20273
KLCGSYPQELIVPAW	MTMR3	186	Q13615
VRNLMLWSAVYLPCP	MTMR3	566	Q13615
CSEKTTAYWSQIPLP	PELI1	371	Q96FA3
WTQQICLPAIYKVFP	MET	556	P08581
YNNWAAKSLAPAPLS	PITX1	181	P78337
TCTWKLPTLAKFSPY	PRAME	241	P78395
LSPSKFYCQLIKWTP	TDRD15	251	B5MCY1
CWIALYAVEALPTCP	LRTM2	26	Q8N967
SGLFCVTINPYKWLP	MYH15	136	Q9Y2K3
KCLPWYPSLSQLKQL	PRAMEF19	311	Q5SWL8
TLPLYAWINTCKISP	NSUN7	201	Q8NE18
YCRWVAPKALVPTCL	NSUN7	676	Q8NE18
CKWVLPILTQFTPYL	PRAMEF25	216	A6NGN4
IKKWSIPCPLTLNYV	SLC38A6	211	Q8IZM9
SYSSKPPLWAAELCV	SELENOO	651	Q9BVL4
CKWVLPILTQFTPYL	PRAMEF27	216	A3QJZ7
SAAPKLPYDLWFKRC	TBC1D7	196	Q9P0N9
FIPKLNDSQYCKPWL	OCRL	601	Q01968
GSIFWLPPAIYKSAC	CHRNB2	141	P17787
LSSPCPPNWIIYEKS	CLEC7A	116	Q9BXN2
KLYALCTRAQPDGPW	CNNM4	146	Q6P4Q7
WPVLSLCYLIAPKSQ	TRPC1	361	P48995
CKWVLPILTQFTPYL	PRAMEF4	216	O60810
AAYFGLSVAWCLPKP	RHD	176	Q02161
AAYFGLTVAWCLPKP	RHCE	176	P18577
VPCKLYSSSWIVFQP	RMC1	331	Q96DM3
LLPTLWFCSPSAKYF	AGPAT1	21	Q99943
CPPCLTSLSQKYLIW	SCN10A	631	Q9Y5Y9
CKWVLPILTQFTPYL	PRAMEF9	216	P0DUQ2
YLECLQNLIWSSSPP	SUSD4	221	Q5VX71
PKVSTLNVWPLYICD	USP47	1296	Q96K76
WLLVLYLCPAASQPI	TMPRSS5	66	Q9H3S3
KNGYPWVLENPSCSL	TTC41P	146	Q6P2S7
PTKNPFTWLFLLVSC	TECR	231	Q9NZ01
FYINSLTGCKSWKPP	ARHGAP9	231	Q9BRR9
NLPWANKVTIGSYPC	PKHD1L1	1591	Q86WI1
LITPGFLQDPWCKYQ	TIRAP	146	P58753
TCLISYWVTLRKPSP	SLC30A6	76	Q6NXT4
CQVSGAYPPAKILWL	VSIG10	331	Q8N0Z9
PQPIESLLWAYCILA	SLC30A9	336	Q6PML9
YITWPTSCQKLLKPV	UGGT2	456	Q9NYU1
LLLWGSTELCYPQPL	ZP3	11	P21754
STELCYPQPLWLLQG	ZP3	16	P21754
YQKILGLQSPPVWCD	ZFYVE26	1521	Q68DK2
WECKQLGAYSPIVLL	ZMYM4	1366	Q5VZL5
SAKPVWRLETCYPQG	NALF1	161	B1AL88