GSN (Gene)

Organism:

Homo sapiens

Synonyms:ADF, AGEL, ENTREZ:2934, GSN, HGNC:4620, MIM:137350, NM_000177, NM_001127662, NM_001127663, NM_001127664, NM_001127665, NM_001127666, NM_001127667, NM_001258029, NM_001258030, NM_001353053, NM_001353054, NM_001353055, NM_001353056, NM_001353057, NM_001353058, NM_001353059, NM_001353060, NM_001353061, NM_001353062, NM_001353063, NM_001353064, NM_001353065, NM_001353066, NM_001353067, NM_001353068, NM_001353069, NM_001353070, NM_001353071, NM_001353072, NM_001353073, NM_001353074, NM_001353075, NM_001353076, NM_001353077, NM_001353078, NM_198252, NP_000168, NP_001121134, NP_001121135, NP_001121136, NP_001121137, NP_001121138, NP_001121139, NP_001244958, NP_001244959, NP_001339982, NP_001339983, NP_001339984, NP_001339985, NP_001339986, NP_001339987, NP_001339988, NP_001339989, NP_001339990, NP_001339991, NP_001339992, NP_001339993, NP_001339994, NP_001339995, NP_001339996, NP_001339997, NP_001339998, NP_001339999, NP_001340000, NP_001340001, NP_001340002, NP_001340003, NP_001340004, NP_001340005, NP_001340006, NP_001340007, NP_937895, XM_005251944, XM_011518584, XM_011518585, XM_011518593, XM_011518594, XM_017014645, XM_017014648, XM_024447522, XM_024447523, XM_024447524, XP_005252001, XP_011516886, XP_011516887, XP_011516895, XP_011516896, XP_016870134, XP_016870137, XP_024303290, XP_024303291, XP_024303292, XR_001746283, gelsolin

Omim:OMIM:137350

Id:ENSG00000148180

Hgnc:HGNC:4620

Entrez:2934

Ensembl:ENSG00000148180

Description:gelsolin

The protein encoded by this gene binds to the "plus" ends of actin monomers and filaments to prevent monomer exchange. The encoded calcium-regulated protein functions in both assembly and disassembly of actin filaments. Defects in this gene are a cause of familial amyloidosis Finnish type (FAF). Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

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CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View GSN'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 GSN.

CFDE Gene-Centric Appyter

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

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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 GSN.

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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 GSN.

Results found

Linked to

	Label	Description
	T60-Adrenal Consensus Gene Set (Entity type)	A Gene Set from MoTrPAC
	T61-Colon Consensus Gene Set (Entity type)	A Gene Set from MoTrPAC
	GSE179112 GSE179113 hydroxyl Hutt45 4 v 3 human dn Gene Set (Entity type)	A Gene Set from LINCS
	GSE158834 ADIPOR2 knockout HEK293 7 v 3 human up Gene Set (Entity type)	A Gene Set from LINCS
	GSE118548 trametinib T84 1 v 2 human up Gene Set (Entity type)	A Gene Set from LINCS
	GSE218097 SOX10 overexpression glial cell 2 v 1 human up Gene Set (Entity type)	A Gene Set from LINCS
	GSE151412 sorafenib 2 v 1 human up Gene Set (Entity type)	A Gene Set from LINCS
	GSE158834 7 V 3 PALMITIC ACID HUMAN UP Gene Set (Entity type)	A Gene Set from LINCS
	GSE179667 NVP-BEZ235 U-87MG Uppsala 0 v 1 human dn Gene Set (Entity type)	A Gene Set from LINCS
	Ataxia Phenotype (Entity type)	Cerebellar ataxia refers to ataxia due to dysfunction of the cerebellum. This causes a variety of el...