PRMT7 (Gene)

Organism:

Homo sapiens

Synonyms:ENTREZ:54496, HGNC:25557, MIM:610087, NM_001184824, NM_001290018, NM_001351143, NM_001351144, NM_001378018, NM_001378020, NM_001378021, NM_001378022, NM_001378023, NM_019023, NP_001171753, NP_001276947, NP_001338072, NP_001338073, NP_001364947, NP_001364949, NP_001364950, NP_001364951, NP_001364952, NP_061896, NR_147056, NR_147057, NR_147058, NR_165365, NR_165366, NR_165367, NR_165368, NR_165369, NR_165370, NR_165371, NR_165372, NR_165373, PRMT7, SBIDDS, XM_011523112, XM_011523113, XM_011523115, XM_011523116, XM_011523121, XM_011523124, XM_011523125, XM_011523126, XM_011523128, XM_017023292, XM_017023296, XM_017023297, XM_017023298, XM_017023299, XM_017023300, XM_017023301, XM_017023302, XM_017023303, XM_017023304, XM_017023311, XM_017023312, XP_011521414, XP_011521415, XP_011521417, XP_011521418, XP_011521423, XP_011521426, XP_011521427, XP_011521428, XP_011521430, XP_016878781, XP_016878785, XP_016878786, XP_016878787, XP_016878788, XP_016878789, XP_016878790, XP_016878791, XP_016878792, XP_016878793, XP_016878800, XP_016878801, XR_001751915, XR_001751921, XR_001751923, XR_001751924, XR_002957814, XR_002957818, XR_002957819, XR_002957822, XR_002957824, protein arginine methyltransferase 7

Omim:OMIM:610087

Id:ENSG00000132600

Hgnc:HGNC:25557

Entrez:54496

Ensembl:ENSG00000132600

Description:protein arginine methyltransferase 7

This gene encodes a member of the protein arginine N-methyltransferase family of proteins. The encoded enzyme transfers single methyl groups to arginine residues to generate monomethylarginines on histone proteins as well as other protein substrates. This enzyme plays a role in a wide range of biological processes, including neuronal differentiation, male germ line imprinting, small nuclear ribonucleoprotein biogenesis, and regulation of the Wnt signaling pathway. Mutations in this gene underlie multiple related syndromes in human patients characterized by intellectual disability, short stature and other features. The encoded protein may promote breast cancer cell invasion and metastasis in human patients. [provided by RefSeq, May 2017]

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CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View PRMT7's neighborhood in the knowledge graph.

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Playbook Workflow Builder: Gene-Centric Workflow

View Gene-Centric information about the gene from a pre-built PWB workflow. View the workflow with PRMT7.

CFDE Gene-Centric Appyter

The CFDE Gene Centric Appyter Resolves and Displays Gene-Centric information from CFDE APIs. Execute the Appyter using PRMT7.

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GDLPA Landing Pages Links

The Gene and Drug Landing Page Aggregator (GDLPA) finds links to primary and secondary source information from CFDE and other resources. Discover landing pages for PRMT7.

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Playbook Workflow Builder

The Playbook Workflow Builder helps you interactively construct workflows leveraging CFDE APIs without code. Start a new workflow with PRMT7.

Results found

Linked to

	Label	Description
	GSE102505 5 V 0 TUNICAMYCIN HUMAN DN Gene Set (Entity type)	A Gene Set from LINCS
	GSE135350 2 V 4 DEXAMETHASONE HUMAN DN Gene Set (Entity type)	A Gene Set from LINCS
	GSE120612 etoposide leukocyte 6 v 1 human up Gene Set (Entity type)	A Gene Set from LINCS
	GSE131887 5 V 2 DOXYCYCLINE MOUSE UP Gene Set (Entity type)	A Gene Set from LINCS
	GSE96649 1 V 0 DEXAMETHASONE HUMAN DN Gene Set (Entity type)	A Gene Set from LINCS
	GSE135350 3 V 5 DEXAMETHASONE HUMAN UP Gene Set (Entity type)	A Gene Set from LINCS
	GSE142210 11 V 10 PANOBINOSTAT HUMAN DN Gene Set (Entity type)	A Gene Set from LINCS
	GSE77108 saha 0 v 9 human up Gene Set (Entity type)	A Gene Set from LINCS
	GSE165548 gemcitabine 2 v 5 human up Gene Set (Entity type)	A Gene Set from LINCS
	GSE77108 0 V 9 SAHA HUMAN UP Gene Set (Entity type)	A Gene Set from LINCS