FKTN (Gene)

Organism:

Homo sapiens

Synonyms:CMD1X, ENTREZ:2218, FCMD, FKTN, HGNC:3622, LGMD2M, LGMDR13, MDDGA4, MDDGB4, MDDGC4, MIM:607440, NM_001079802, NM_001198963, NM_001351496, NM_001351497, NM_001351498, NM_001351499, NM_001351500, NM_001351501, NM_001351502, NM_006731, NP_001073270, NP_001185892, NP_001338425, NP_001338426, NP_001338427, NP_001338428, NP_001338429, NP_001338430, NP_001338431, NP_006722, NR_147213, NR_147214, XM_006717014, XM_011518368, XM_011518369, XM_011518370, XM_011518371, XM_011518373, XM_011518374, XM_011518375, XM_011518376, XM_011518378, XM_011518379, XM_011518381, XM_011518387, XM_011518390, XM_011518391, XM_017014462, XM_017014463, XM_017014464, XM_017014465, XM_017014467, XM_017014468, XM_017014469, XM_017014470, XM_017014472, XM_017014473, XM_017014475, XP_006717077, XP_011516670, XP_011516671, XP_011516672, XP_011516673, XP_011516675, XP_011516676, XP_011516677, XP_011516678, XP_011516680, XP_011516681, XP_011516683, XP_011516689, XP_011516692, XP_011516693, XP_016869951, XP_016869952, XP_016869953, XP_016869954, XP_016869956, XP_016869957, XP_016869958, XP_016869959, XP_016869961, XP_016869962, XP_016869964, XR_001746242, XR_001746243, XR_001746244, XR_001746245, XR_001746248, XR_002956770, fukutin

Omim:OMIM:607440

Id:ENSG00000106692

Hgnc:HGNC:3622

Entrez:2218

Ensembl:ENSG00000106692

Description:fukutin

The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2010]

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CFDE DD-Knowledge Graph

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

CFDE Gene-Centric Appyter

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

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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 FKTN.

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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 FKTN.

Results found

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	GSE168473 0 V 1 ISONIAZID HUMAN UP Gene Set (Entity type)	A Gene Set from LINCS
	GSE138789 metformin 0 v 1 human up Gene Set (Entity type)	A Gene Set from LINCS
	GSE199107 tryptophan 6 v 7 human up Gene Set (Entity type)	A Gene Set from LINCS
	GSE169356 ivermectin prostate gland 0 v 1 human up Gene Set (Entity type)	A Gene Set from LINCS
	GSE169356 FOXA1 inhibition prostate gland Ivermectin 0 v 1 human up Gene Set (Entity type)	A Gene Set from LINCS
	GSE220097 4 V 1 ENZALUTAMIDE HUMAN UP Gene Set (Entity type)	A Gene Set from LINCS
	GSE93156 idelalisib B cell 1 v 0 human dn Gene Set (Entity type)	A Gene Set from LINCS
	GSE76425 0 V 12 LENALIDOMIDE HUMAN UP Gene Set (Entity type)	A Gene Set from LINCS
	GSE143782 calcitriol 7 v 11 human dn Gene Set (Entity type)	A Gene Set from LINCS