Cluster composition

Functions

Category	Name	IntersectionWithQuery	PValue	GenesInTerm	GenesInQuery	GenesInTermInQuery	ID
GeneOntologyMolecularFunction	chemokine receptor activity	CCR2 GPR17	7.41e-04	26	31	2	GO:0004950
GeneOntologyMolecularFunction	G protein-coupled chemoattractant receptor activity	CCR2 GPR17	7.41e-04	26	31	2	GO:0001637
GeneOntologyMolecularFunction	aminoacyl-tRNA ligase activity	EPRS1 DALRD3	1.93e-03	42	31	2	GO:0004812
GeneOntologyMolecularFunction	ligase activity, forming carbon-oxygen bonds	EPRS1 DALRD3	1.93e-03	42	31	2	GO:0016875
GeneOntologyMolecularFunction	catalytic activity, acting on RNA	EPRS1 EXOSC10 DALRD3 POLR3F	3.78e-03	417	31	4	GO:0140098
Domain	NUT	NUTM2B NUTM2A	2.49e-05	5	30	2	IPR024310
Domain	NUT_N	NUTM2B NUTM2A	2.49e-05	5	30	2	IPR024309
Domain	NUT	NUTM2B NUTM2A	2.49e-05	5	30	2	PF12881
Domain	EGF-like_dom	ADGRE4P MASP1 FRAS1 HYAL3	6.43e-04	249	30	4	IPR000742
Domain	EGF_3	ADGRE4P MASP1 HYAL3	6.21e-03	235	30	3	PS50026
Domain	EGF	ADGRE4P FRAS1 HYAL3	6.21e-03	235	30	3	SM00181
Domain	EGF_CA	ADGRE4P MASP1	8.38e-03	86	30	2	PF07645
Domain	EGF_CA	ADGRE4P MASP1	1.10e-02	99	30	2	PS01187
Domain	ASX_HYDROXYL	ADGRE4P MASP1	1.12e-02	100	30	2	PS00010
Domain	EGF-type_Asp/Asn_hydroxyl_site	ADGRE4P MASP1	1.25e-02	106	30	2	IPR000152
Pubmed	The clinicopathologic features of YWHAE-FAM22 endometrial stromal sarcomas: a histologically high-grade and clinically aggressive tumor.	NUTM2B NUTM2A	2.46e-06	3	32	2	22456610
Pubmed	The clinical phenotype of YWHAE-NUTM2B/E positive pediatric clear cell sarcoma of the kidney.	NUTM2E NUTM2B	2.46e-06	3	32	2	26542179
Pubmed	Assisted reproductive technologies induce temporally specific placental defects and the preeclampsia risk marker sFLT1 in mouse.	SLC16A1 PRL	1.23e-05	6	32	2	32471820
Pubmed	Atypical protein kinase C iota (PKCλ/ι) ensures mammalian development by establishing the maternal-fetal exchange interface.	SLC16A1 PRL	6.36e-05	13	32	2	32513715
Pubmed	Differential requirements for Tousled-like kinases 1 and 2 in mammalian development.	ASF1B PRL	1.11e-04	17	32	2	28708136
Pubmed	Genome-wide expression analysis of Ptf1a- and Ascl1-deficient mice reveals new markers for distinct dorsal horn interneuron populations contributing to nociceptive reflex plasticity.	KCNIP2 PDYN	1.24e-04	18	32	2	23616538
Pubmed	ARHGEF18/p114RhoGEF Coordinates PKA/CREB Signaling and Actomyosin Remodeling to Promote Trophoblast Cell-Cell Fusion During Placenta Morphogenesis.	SLC16A1 PRL	1.24e-04	18	32	2	33842485
Pubmed	Lipid signatures reflect the function of the murine primary placentation†.	SLC16A1 PRL	1.87e-04	22	32	2	34850819
Pubmed	Loss of function of the maternal membrane oestrogen receptor ERα alters expansion of trophoblast cells and impacts mouse fertility.	SLC16A1 PRL	2.05e-04	23	32	2	36239412
Pubmed	Proteome analysis of the HIV-1 Gag interactome.	EPRS1 EXOSC10	7.57e-04	44	32	2	25010285
Cytoband	10q23.2	NUTM2D NUTM2A	6.36e-05	17	32	2	10q23.2
Cytoband	10q22.3	NUTM2E NUTM2B	4.18e-04	43	32	2	10q22.3
Cytoband	Ensembl 112 genes in cytogenetic band chr3p21	CCR2 DALRD3 HYAL3	1.38e-03	316	32	3	chr3p21
Cytoband	3p21.31	CCR2 DALRD3	2.23e-03	100	32	2	3p21.31
Cytoband	Ensembl 112 genes in cytogenetic band chr7q36	FASTK ABCB8	5.52e-03	159	32	2	chr7q36
Cytoband	Ensembl 112 genes in cytogenetic band chr2q14	GPR17 PSD4	5.93e-03	165	32	2	chr2q14
Cytoband	Ensembl 112 genes in cytogenetic band chr10q23	NUTM2D NUTM2A	8.19e-03	195	32	2	chr10q23
Cytoband	Ensembl 112 genes in cytogenetic band chr10q22	NUTM2E NUTM2B	9.27e-03	208	32	2	chr10q22
Drug	spiradoline	EXOSC10 PRL PDYN ABCB8	4.41e-07	46	31	4	CID000005620
Drug	Neuropeptide Ff	GPR17 PRL PDYN ABCB8	2.28e-06	69	31	4	CID000123797
Drug	beta-Casomorphin I	PRL PDYN	1.07e-05	4	31	2	CID000126671
Drug	AC1L4HYX	PRL PDYN	1.07e-05	4	31	2	CID000157408
Disease	Endometrial Stromal Sarcoma	NUTM2B NUTM2A	9.97e-06	5	30	2	C0206630
Disease	Clear cell sarcoma of kidney	NUTM2E NUTM2B	1.50e-05	6	30	2	C0334488
Disease	Cocaine Abuse	PRL RECK PDYN	2.90e-04	127	30	3	C0009171
Disease	Bradycardia	PRL PDYN	3.20e-04	26	30	2	C0428977
Disease	Autosomal Dominant Parkinsonism	PRL PDYN	3.72e-04	28	30	2	C0752098
Disease	Autosomal Dominant Juvenile Parkinson Disease	PRL PDYN	3.72e-04	28	30	2	C0752097
Disease	PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE	PRL PDYN	3.72e-04	28	30	2	C1868675
Disease	Parkinsonism, Experimental	PRL PDYN	3.72e-04	28	30	2	C0752101
Disease	Autosomal Recessive Parkinsonism	PRL PDYN	3.72e-04	28	30	2	C0752100
Disease	Familial Juvenile Parkinsonism	PRL PDYN	3.72e-04	28	30	2	C0752104
Disease	Ramsay Hunt Paralysis Syndrome	PRL PDYN	3.72e-04	28	30	2	C0242423
Disease	Parkinsonism, Juvenile	PRL PDYN	4.27e-04	30	30	2	C0752105
Disease	Parkinsonian Disorders	PRL PDYN	4.27e-04	30	30	2	C0242422
Disease	Hypotension	PRL PDYN	1.33e-03	53	30	2	C0020649

Protein segments in the cluster

Peptide	Gene	Start	Entry
LCNLLCGKRLKGPPP	GPR17	336	Q13304
LLVLLSGASCPPCPK	ADGRE4P	6	Q86SQ3
GPPTLCCLKLAFLDP	BRWD3	996	Q6RI45
KCPSLLAAGCKPIIP	RECK	806	O95980
PILCVEIKPKCGFIP	IPPK	131	Q9H8X2
GLLLIPPVQPCCLGP	FASTK	51	Q14296
IVECCPVLLGPPLLG	SLC16A1	396	P53985
CPPCPVGTLALEVKG	FRAS1	396	Q86XX4
GPKPINPLICSLQCQ	PDYN	36	P01213
KLLPCCGPQALPSVS	KCNIP2	41	Q9NS61
EPVLGLCPLLPLFCC	PDZD3	86	Q86UT5
PGTLGCPLCPKAFPL	OVOL3	91	O00110
KEPQGIIACCNPVPP	EXOSC10	546	Q01780
LNCTPIKGLGLPGCI	ASF1B	176	Q9NVP2
LGVALCLGCGQPLPQ	HYAL3	11	O43820
GCRIAPLQKPVCGGP	CCR2	321	P41597
GRSLPTCLPVCGLPK	MASP1	426	P48740
CLQGPGVAPVLRCAP	DALRD3	66	Q5D0E6
KLQCCPGPTSPLIPA	EPB41L4B	836	Q9H329
LNPCIPLSGGCCVPK	ABCB8	451	Q9NUT2
ALCGGVVCPPPLLLA	NUTM2A	236	Q8IVF1
ALCGGVVCPPPLLLA	NUTM2B	236	A6NNL0
CGGVVCPPPLLLAAA	NUTM2D	166	Q5VT03
ALCGGVVCPPPLLLA	NUTM2E	236	B1AL46
LLCQSVAPLPICPGG	PRL	21	P01236
VGGAILCQLCKPPPL	TRIM46	166	Q7Z4K8
LCQLCKPPPLEATKG	TRIM46	171	Q7Z4K8
AGCTVPLPPRLGICL	TRIM46	681	Q7Z4K8
IPFKPLCELQPGAKC	EPRS1	1481	P07814
KAGLKCCLPTPPVDL	PSD4	181	Q8NDX1
IIPPTGLVRAPCGLC	POLR3F	276	Q9H1D9
LVVCGCLALPPLAEP	TRIL	11	Q7L0X0
PILGPSLLFCGKPAC	MYCBPAP	401	Q8TBZ2
KEQVPRGCPDGLCPL	ACP6	381	Q9NPH0
CVLCAGPEPLPPKGL	ZNF692	66	Q9BU19