Cluster composition

Functions

Category	Name	IntersectionWithQuery	PValue	GenesInTerm	GenesInQuery	GenesInTermInQuery	ID
GeneOntologyMolecularFunction	ATP:phosphate antiporter activity	SLC25A25 SLC25A23	3.32e-05	3	67	2	GO:0140987
GeneOntologyMolecularFunction	organophosphate:phosphate antiporter activity	SLC25A25 SLC25A23	2.30e-04	7	67	2	GO:0015315
Domain	Envoplakin	EVPLL EVPL	1.16e-05	2	64	2	IPR030460
Pubmed	Differential localization of Mox-1 and Mox-2 proteins indicates distinct roles during development.	MEOX1 MEOX2	3.88e-06	2	69	2	9032023
Pubmed	APP involvement in retinogenesis of mice.	PTF1A APP	3.88e-06	2	69	2	20978902
Pubmed	The single amphioxus Mox gene: insights into the functional evolution of Mox genes, somites, and the asymmetry of amphioxus somitogenesis.	MEOX1 MEOX2	3.88e-06	2	69	2	12051829
Pubmed	Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport.	TTC8 BBS7	3.88e-06	2	69	2	15231740
Pubmed	Interaction between the scaffold proteins CBP by IQGAP1 provides an interface between gene expression and cytoskeletal activity.	EXOC5 EIF4G2 APP SNRNP200	1.11e-05	69	69	4	32238831
Pubmed	Reelin protects against amyloid β toxicity in vivo.	APP MEOX2	1.16e-05	3	69	2	26152694
Pubmed	Characterization of the human B cell RAG-associated gene, hBRAG, as a B cell receptor signal-enhancing glycoprotein dimer that associates with phosphorylated proteins in resting B cells.	CHST15 HCK	1.16e-05	3	69	2	10749872
Pubmed	Identification of the mitochondrial ATP-Mg/Pi transporter. Bacterial expression, reconstitution, functional characterization, and tissue distribution.	SLC25A25 SLC25A23	1.16e-05	3	69	2	15123600
Pubmed	Identification of a novel human subfamily of mitochondrial carriers with calcium-binding domains.	SLC25A25 SLC25A23	1.16e-05	3	69	2	15054102
Pubmed	Glucagon regulation of oxidative phosphorylation requires an increase in matrix adenine nucleotide content through Ca2+ activation of the mitochondrial ATP-Mg/Pi carrier SCaMC-3.	SLC25A25 SLC25A23	1.16e-05	3	69	2	23344948
Pubmed	Homeodomain proteins Mox1 and Mox2 associate with Pax1 and Pax3 transcription factors.	MEOX1 MEOX2	2.32e-05	4	69	2	11423130
Pubmed	BBS7 and TTC8 (BBS8) mutations play a minor role in the mutational load of Bardet-Biedl syndrome in a multiethnic population.	TTC8 BBS7	2.32e-05	4	69	2	19402160
Pubmed	Mechanisms of MEOX1 and MEOX2 regulation of the cyclin dependent kinase inhibitors p21 and p16 in vascular endothelial cells.	MEOX1 MEOX2	2.32e-05	4	69	2	22206000
Pubmed	Lifting the lid on Pandora's box: the Bardet-Biedl syndrome.	TTC8 BBS7	2.32e-05	4	69	2	15917208
Pubmed	Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous families.	TTC8 BBS7	2.32e-05	4	69	2	28761321
Pubmed	Transient activation of meox1 is an early component of the gene regulatory network downstream of hoxa2.	MEOX1 MEOX2	2.32e-05	4	69	2	21245383
Pubmed	Mox-1 and Mox-2 define a novel homeobox gene subfamily and are differentially expressed during early mesodermal patterning in mouse embryos.	MEOX1 MEOX2	2.32e-05	4	69	2	1363541
Pubmed	Single-domain antibody-SH3 fusions for efficient neutralization of HIV-1 Nef functions.	AP1G2 HCK	2.32e-05	4	69	2	22345475
Pubmed	VRK3-mediated nuclear localization of HSP70 prevents glutamate excitotoxicity-induced apoptosis and Aβ accumulation via enhancement of ERK phosphatase VHR activity.	VRK3 APP	2.32e-05	4	69	2	27941812
Pubmed	USP21 negatively regulates antiviral response by acting as a RIG-I deubiquitinase.	DHX58 MEOX2	3.86e-05	5	69	2	24493797
Pubmed	Mammalian COPII coat component SEC24C is required for embryonic development in mice.	PTF1A MEOX2	3.86e-05	5	69	2	24876386
Pubmed	The absence of BBSome function decreases synaptogenesis and causes ectopic synapse formation in the retina.	TTC8 BBS7	3.86e-05	5	69	2	32433491
Pubmed	Meox homeodomain proteins are required for Bapx1 expression in the sclerotome and activate its transcription by direct binding to its promoter.	MEOX1 MEOX2	3.86e-05	5	69	2	15024065
Pubmed	A dual fate of the hindlimb muscle mass: cloacal/perineal musculature develops from leg muscle cells.	MEOX1 MEOX2	5.79e-05	6	69	2	15653949
Pubmed	Pax1 and Pax9 activate Bapx1 to induce chondrogenic differentiation in the sclerotome.	MEOX1 MEOX2	5.79e-05	6	69	2	12490554
Pubmed	Interleukins 19, 20, and 24 signal through two distinct receptor complexes. Differences in receptor-ligand interactions mediate unique biological functions.	IL22RA1 IL19	5.79e-05	6	69	2	12351624
Pubmed	Protein kinase R and the integrated stress response drive immunopathology caused by mutations in the RNA deaminase ADAR1.	DHX58 MEOX2	8.09e-05	7	69	2	34343497
Pubmed	Mox2 is a component of the genetic hierarchy controlling limb muscle development.	MEOX1 MEOX2	8.09e-05	7	69	2	10403250
Pubmed	Quantitative analysis of HSP90-client interactions reveals principles of substrate recognition.	TRIM49 SF3B3 RHOBTB1 CLK2 MAP4K2 HCK	9.77e-05	372	69	6	22939624
Pubmed	Dissection of epistasis in oligogenic Bardet-Biedl syndrome.	TTC8 BBS7	1.08e-04	8	69	2	16327777
Pubmed	NHE6 depletion corrects ApoE4-mediated synaptic impairments and reduces amyloid plaque load.	APP MEOX2	1.08e-04	8	69	2	34617884
Pubmed	Direct role of Bardet-Biedl syndrome proteins in transcriptional regulation.	TTC8 BBS7	1.38e-04	9	69	2	22302990
Pubmed	Recruitment of PCM1 to the centrosome by the cooperative action of DISC1 and BBS4: a candidate for psychiatric illnesses.	TTC8 BBS7	1.38e-04	9	69	2	18762586
Pubmed	Ubiquitylation of BBSome is required for ciliary assembly and signaling.	TTC8 BBS7	1.38e-04	9	69	2	36744302
Pubmed	Congenital Hepatic Fibrosis Overview ─ RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY	TTC8 BBS7 GLIS2	1.54e-04	52	69	3	20301743
Pubmed	A novel protein LZTFL1 regulates ciliary trafficking of the BBSome and Smoothened.	TTC8 BBS7	1.73e-04	10	69	2	22072986
Pubmed	Temporal expression pattern of Bardet-Biedl syndrome genes in adipogenesis.	TTC8 BBS7	1.73e-04	10	69	2	17379567
Pubmed	A BBSome subunit links ciliogenesis, microtubule stability, and acetylation.	TTC8 BBS7	1.73e-04	10	69	2	19081074
Pubmed	A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis.	TTC8 BBS7	1.73e-04	10	69	2	17574030
Pubmed	Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes.	TTC8 BBS7	1.73e-04	10	69	2	22139371
Pubmed	High-resolution gene expression analysis of the developing mouse kidney defines novel cellular compartments within the nephron progenitor population.	ZNF462 MEOX1 MEOX2	1.92e-04	56	69	3	19591821
Pubmed	Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations.	PDE4D HECTD4	2.11e-04	11	69	2	21642993
Pubmed	The centriolar satellite protein AZI1 interacts with BBS4 and regulates ciliary trafficking of the BBSome.	TTC8 BBS7	2.11e-04	11	69	2	24550735
Pubmed	A noncanonical PWI domain in the N-terminal helicase-associated region of the spliceosomal Brr2 protein.	SF3B3 SNRNP200	2.11e-04	11	69	2	25849387
Pubmed	Nephrocystin proteins NPHP5 and Cep290 regulate BBSome integrity, ciliary trafficking and cargo delivery.	TTC8 BBS7	2.11e-04	11	69	2	25552655
Pubmed	The SOX2-interactome in brain cancer cells identifies the requirement of MSI2 and USP9X for the growth of brain tumor cells.	PWP1 ZNF462 PPP2R5C IPO7 SCFD1	2.49e-04	282	69	5	23667531
Pubmed	Fgfr1 regulates development through the combinatorial use of signaling proteins.	MEOX1 MEOX2	2.53e-04	12	69	2	26341559
Pubmed	WW domains provide a platform for the assembly of multiprotein networks.	SF3B3 TBC1D4 SNRNP200 CPSF7	2.56e-04	154	69	4	16055720
Pubmed	The Hsp70-Hsp90 co-chaperone Hop/Stip1 shifts the proteostatic balance from folding towards degradation.	SF3B3 TBC1D4 IPO7 EIF4G2 SCFD1 SNRNP200 CPSF7	2.73e-04	638	69	7	33239621
Pubmed	Anterior visceral endoderm SMAD4 signaling specifies anterior embryonic patterning and head induction in mice.	MEOX1 MEOX2	2.98e-04	13	69	2	20941375
Pubmed	Intrinsic protein-protein interaction-mediated and chaperonin-assisted sequential assembly of stable bardet-biedl syndrome protein complex, the BBSome.	TTC8 BBS7	2.98e-04	13	69	2	22500027
Pubmed	Cellular substrates and pro-apoptotic function of the human HtrA4 protease.	SF3B3 IPO7 EIF4G2 SNRNP200	3.97e-04	173	69	4	31470122
Pubmed	Trim43a, Trim43b, and Trim43c: Novel mouse genes expressed specifically in mouse preimplantation embryos.	TRIM49 TRIM49C	4.01e-04	15	69	2	19703589
Pubmed	The concerted action of Meox homeobox genes is required upstream of genetic pathways essential for the formation, patterning and differentiation of somites.	MEOX1 MEOX2	4.01e-04	15	69	2	12925591
Pubmed	The BBSome controls IFT assembly and turnaround in cilia.	TTC8 BBS7	4.01e-04	15	69	2	22922713
Pubmed	BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly.	TTC8 BBS7	4.01e-04	15	69	2	20080638
Pubmed	Maturation of postnatally generated olfactory bulb granule cells depends on functional γ-protocadherin expression.	PCDHGB5 PCDHGB4	4.01e-04	15	69	2	23515096
Pubmed	Lack of the mesodermal homeodomain protein MEOX1 disrupts sclerotome polarity and leads to a remodeling of the cranio-cervical joints of the axial skeleton.	MEOX1 MEOX2	4.01e-04	15	69	2	19520072
Pubmed	Fat4-Dchs1 signalling controls cell proliferation in developing vertebrae.	MEOX1 MEOX2	4.57e-04	16	69	2	27381226
Pubmed	New interaction partners for Nek4.1 and Nek4.2 isoforms: from the DNA damage response to RNA splicing.	ZNF462 CCDC88C SF3B3 PARPBP SNRNP200 MEOX1	5.47e-04	513	69	6	25798074
Pubmed	LCP1 preferentially binds clasped αMβ2 integrin and attenuates leukocyte adhesion under flow.	DHX58 IPO7 MTM1 EIF4G2 SNRNP200	6.15e-04	344	69	5	30333137
Pubmed	FGF signaling regulates development by processes beyond canonical pathways.	MEOX1 MEOX2	6.49e-04	19	69	2	33184218
Pubmed	Identification of a genomic reservoir for new TRIM genes in primate genomes.	TRIM49 TRIM49C	6.49e-04	19	69	2	22144910
Pubmed	A Human Tyrosine Phosphatase Interactome Mapped by Proteomic Profiling.	PWP1 TBCCD1 THOP1 IPO7 PTPRO MTM1 EVPL SNRNP200	6.79e-04	974	69	8	28675297
Pubmed	BMP signaling in the epiblast is required for proper recruitment of the prospective paraxial mesoderm and development of the somites.	MEOX1 MEOX2	7.20e-04	20	69	2	16943278
Pubmed	Immunomic analysis of human sarcoma.	TBC1D4 ACTR5	7.95e-04	21	69	2	12601173
Pubmed	Genomic analysis of mouse retinal development.	PWP1 PPP2R5C CLK2 BBS7 ESRRB GLIS2 TONSL CPSF7	8.38e-04	1006	69	8	15226823
Pubmed	CRISPR/Cas9-mediated Genomic Editing of Cluap1/IFT38 Reveals a New Role in Actin Arrangement.	CCDC88C TTC8 BBS7 SCFD1	8.66e-04	213	69	4	29615496
Pubmed	Large-scale mapping of human protein-protein interactions by mass spectrometry.	SF3B3 TBC1D4 VRK3 HUS1 CLK2 TONSL EIF4G2 SNRNP200 KPTN	9.59e-04	1284	69	9	17353931
Pubmed	Systematic Analysis of Human Protein Phosphatase Interactions and Dynamics.	TBCCD1 PPP2R5C SF3B3 IPO7 PTPRO SNRNP200	9.70e-04	573	69	6	28330616
Pubmed	TRIM33 drives prostate tumor growth by stabilizing androgen receptor from Skp2-mediated degradation.	ZNF462 SF3B3 SNRNP200 CPSF7	9.76e-04	220	69	4	35785414
Pubmed	The splicing factor FUBP1 is required for the efficient splicing of oncogene MDM2 pre-mRNA.	SF3B3 IPO7	1.04e-03	24	69	2	24798327
Pubmed	Diverse Fgfr1 signaling pathways and endocytic trafficking regulate mesoderm development.	MEOX1 MEOX2	1.13e-03	25	69	2	38834239
Pubmed	Identification of novel SH3 domain ligands for the Src family kinase Hck. Wiskott-Aldrich syndrome protein (WASP), WASP-interacting protein (WIP), and ELMO1.	SF3B3 HCK	1.13e-03	25	69	2	12029088
Pubmed	An organelle-specific protein landscape identifies novel diseases and molecular mechanisms.	TBC1D32 TTC8 EXOC5 PPP2R5C SF3B3 TBC1D4 BBS7 PTPRQ SNRNP200	1.17e-03	1321	69	9	27173435
Pubmed	Prediction of the coding sequences of unidentified human genes. IX. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro.	TBC1D4 CHST15 PIP5K1C	1.21e-03	105	69	3	9628581
Pubmed	Structure--function relationships in HIV-1 Nef.	AP1G2 HCK	1.32e-03	27	69	2	11463741
Pubmed	Bardet-Biedl Syndrome Overview	TTC8 BBS7	1.32e-03	27	69	2	20301537
Pubmed	MECP2 directly interacts with RNA polymerase II to modulate transcription in human neurons.	PWP1 ZNF462 SF3B3 PTPRO HECTD4 SNRNP200 CPSF7 IL19	1.33e-03	1082	69	8	38697112
Pubmed	Comprehensive proteomic analysis of the human spliceosome.	SF3B3 SNRNP200 CPSF7	1.35e-03	109	69	3	12226669
Pubmed	Characterization of staufen1 ribonucleoproteins by mass spectrometry and biochemical analyses reveal the presence of diverse host proteins associated with human immunodeficiency virus type 1.	IPO7 SCFD1 SNRNP200 CPSF7	1.37e-03	241	69	4	23125841
Pubmed	Interaction with protocadherin-gamma regulates the cell surface expression of protocadherin-alpha.	PCDHGB5 PCDHGB4	1.42e-03	28	69	2	15347688
Pubmed	Intersectin (ITSN) family of scaffolds function as molecular hubs in protein interaction networks.	CCDC88C PDE4D FCHSD1	1.42e-03	111	69	3	22558309
Pubmed	Inherited genetic variant predisposes to aggressive but not indolent prostate cancer.	ZNF462 ESRRB	1.63e-03	30	69	2	20080650
Pubmed	Analysis of 30 genes (355 SNPS) related to energy homeostasis for association with adiposity in European-American and Yup'ik Eskimo populations.	TTC8 BBS7	1.63e-03	30	69	2	19077438
Pubmed	Muscle developmental defects in heterogeneous nuclear Ribonucleoprotein A1 knockout mice.	MEOX1 MEOX2	1.63e-03	30	69	2	28077597
Pubmed	Proteomic, functional, and domain-based analysis of in vivo 14-3-3 binding proteins involved in cytoskeletal regulation and cellular organization.	SF3B3 TBC1D4 CLK2 SNRNP200	1.68e-03	255	69	4	15324660
Pubmed	Proteomic analysis of complexes formed by human topoisomerase I.	SF3B3 SNRNP200	1.85e-03	32	69	2	15848144
Pubmed	Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides.	IPO7 EIF4G2 SCFD1 APP	1.88e-03	263	69	4	12665801
Pubmed	Histone methyltransferase DOT1L coordinates AR and MYC stability in prostate cancer.	TONSL HECTD4 SNRNP200 CPSF7	1.91e-03	264	69	4	32814769
Cytoband	Ensembl 112 genes in cytogenetic band chr11q14	TRIM49 CCDC83 TRIM49C	1.71e-03	156	69	3	chr11q14
GeneFamily	EF-hand domain containing\|Plakins	EVPLL EVPL	1.91e-04	8	48	2	939
GeneFamily	Bardet-Biedl syndrome associated\|BBSome	TTC8 BBS7	1.91e-04	8	48	2	1122
GeneFamily	Protein tyrosine phosphatases, receptor type	PTPRO PTPRQ	1.40e-03	21	48	2	813
GeneFamily	Bardet-Biedl syndrome associated\|BBSome	TTC8 BBS7	1.40e-03	21	48	2	980
Disease	Bardet-Biedl syndrome (implicated_via_orthology)	TBC1D32 TTC8 BBS7	1.91e-06	11	68	3	DOID:1935 (implicated_via_orthology)
Disease	Bardet-Biedl syndrome (is_implicated_in)	TTC8 BBS7	4.68e-04	14	68	2	DOID:1935 (is_implicated_in)
Disease	Bardet-Biedl syndrome 1 (disorder)	TTC8 BBS7	6.96e-04	17	68	2	C2936862
Disease	Bardet-Biedl syndrome	TTC8 BBS7	7.82e-04	18	68	2	cv:C0752166
Disease	mental development measurement	PCDHGB5 PCDHGB4	1.52e-03	25	68	2	EFO_0008230
Disease	glucose tolerance test	TBC1D4 MAP4K2	1.77e-03	27	68	2	EFO_0004307
Disease	Ciliopathies	TTC8 BBS7 GLIS2	2.12e-03	110	68	3	C4277690
Disease	diastolic blood pressure, unipolar depression	EIF4G2 HECTD4	2.18e-03	30	68	2	EFO_0003761, EFO_0006336
Disease	esophageal carcinoma	PDE4D HECTD4	2.18e-03	30	68	2	EFO_0002916

Protein segments in the cluster

Peptide	Gene	Start	Entry
YHCILEEADHLQEEY	BBS7	646	Q8IWZ6
VLQVHEHLNFQDYDN	CPED1	376	A4D0V7
LHLEETDENFHNYEF	TBC1D32	41	Q96NH3
YEVHHQKLVFFAEDV	APP	681	P05067
YLTSEAEEHHQLFDL	CLK2	441	P49760
IDQHEKEIHYLQDIF	CCDC65	161	Q8IXS2
LTYDHFHQSVQEIFE	AP1G2	761	O75843
NKQDLEAAYHITDIH	ARL9	126	Q6T311
FIYETEHHNGIAELL	PPP2R5C	211	Q13362
LYEHIHDLSLFLFND	ECT2L	806	Q008S8
LHEHSYIAEDYVEEL	ACTR5	246	Q9H9F9
QKYEDLETHLLSEQH	DBF4	301	Q9UBU7
ILHLSHENSIEDLQY	CCDC83	316	Q8IWF9
YIDQRIHELQEHIDD	PAAT	396	Q9H8K7
LLHNEDRHDDYFQER	CPSF7	441	Q8N684
NKAELLYDEENTIHH	PARPBP	371	Q9NWS1
EQLRELEAEFAHHNY	MEOX1	181	P50221
FYHVNVEIEDINDHT	PCDHGB4	116	Q9UN71
EEGIYTLNLHELHED	MAP4K2	506	Q12851
HDNYDQLEVHAAAIK	IL19	141	Q9UHD0
VNFLHHQLKGEYEEL	CCDC88C	1261	Q9P219
QHVLEFYEEIFSLAH	IPO7	646	O95373
HLYKENEGLHQFEEQ	KPTN	171	Q9Y664
LEDHYHADVAYHNNI	PDE4D	451	Q08499
REYEHFKQHELLSQE	EVPLL	221	A8MZ36
REYEHFKQHELLSQE	EVPL	266	Q92817
ELEAEFAHHNYLTRL	MEOX2	201	P50222
LLQDLVDHVNDYHVK	GLIS2	181	Q9BZE0
FYHVNVEIEDINDHT	PCDHGB5	116	Q9Y5G0
EDDHYRLNDELLHYI	HECTD4	396	Q9Y4D8
HDHVDLQVSALYALQ	EIF4G2	821	P78344
FHIHIEREENFTEYL	PTPRO	361	Q16827
QHINDHDFVDIYGLV	PTPRQ	2251	Q9UMZ3
EQAEVEFLSHQLHEY	PTF1A	46	Q7RTS3
VATNAHLDHYYQEEL	FCHSD1	216	Q86WN1
VAFQHFQELDEHISY	EXOC5	91	O00471
LYDYEAIHHEDLSFQ	HCK	86	P08631
YEDLHLEVHQTFQEL	CYP11B1	61	P15538
DALAALQDFYHREHV	DHX58	301	Q96C10
AYHSLRELFLDHNDL	ECM2	606	O94769
LEDIFHDLFYHLELQ	IL22RA1	156	Q8N6P7
EYQDEISLLLHNEGH	nan	61	Q6ZN92
HEALQDYELSQRHEE	ESRRB	371	O95718
EHQLKEHYQALQEES	CNTROB	366	Q8N137
LYQHFAEVSLHEEIL	KBTBD12	156	Q3ZCT8
LHHEEANNDIFLYEI	TRIM49	291	P0CI25
DYSLLLGVHNIDQHE	PIP5K1C	316	O60331
VHFDLLHEDVSLQYF	HUS1	261	O60921
EVLSYLELAQFHNAH	RHOBTB1	596	O94844
EDYLDLFDLAAHQIH	CHST15	311	Q7LFX5
QLDFEEFVHYLQDHE	SLC25A25	66	Q6KCM7
QEEDSFYVHHDILLS	PWP1	171	Q13610
EDHITQLHEYNDIKD	SWI5	191	Q1ZZU3
SHHFEDADNIYIFLE	PLK3	126	Q9H4B4
LAKALFEYIFHHEND	TTC8	191	Q8TAM2
LHENYHRETNENDIA	TMPRSS11F	281	Q6ZWK6
YHNAELFFLDIHNIH	MTM1	301	Q13496
EDYPAALQHQHQYLE	TONSL	81	Q96HA7
LHHEEANSDIFLYEI	TRIM49C	291	P0CI26
TDHYHAQPLEDNLFE	UBE2J1	26	Q9Y385
TYQALVHDVLDFHLN	SCFD1	276	Q8WVM8
LDALEFLHENEYVHG	VRK3	291	Q8IV63
HYLYQIAHLGDDDEE	SF3B3	356	Q15393
QLHAYEVEYHVLQDE	TBC1D4	1171	O60343
EDVDSEVILHHEYFL	SNRNP200	1226	O75643
YEDLKAHIQDVHTAF	ZNF462	16	Q96JM2
HFLLHSLENVEDVLY	SLC25A23	141	Q9BV35
HQAFVYDHLSDLLEL	TBCCD1	171	Q9NVR7
DGHIDFHEYLLLVFQ	RPTN	66	Q6XPR3
SLLQHDEVETYFHEF	THOP1	461	P52888
FQQLQLERHEYAEHL	GOLGA8IP	231	A6NC78