ATG13 (Gene)

Organism:

Homo sapiens

Synonyms:ATG13, ENTREZ:9776, HGNC:29091, KIAA0652, MIM:615088, NM_001142673, NM_001205119, NM_001205120, NM_001205121, NM_001205122, NM_001346311, NM_001346312, NM_001346313, NM_001346314, NM_001346315, NM_001346316, NM_001346317, NM_001346318, NM_001346319, NM_001346320, NM_001346321, NM_001346322, NM_001346323, NM_001346324, NM_001346325, NM_001346326, NM_001346327, NM_001346328, NM_001346329, NM_001346330, NM_001346331, NM_001346332, NM_001346333, NM_001346334, NM_001346335, NM_001346336, NM_001346337, NM_001346338, NM_001346340, NM_001346342, NM_001346344, NM_001346346, NM_001346348, NM_001346349, NM_001346350, NM_001346351, NM_001346352, NM_001346353, NM_001346354, NM_001346355, NM_001346356, NM_001346357, NM_001346358, NM_001346359, NM_001346360, NM_014741, NP_001136145, NP_001192048, NP_001192049, NP_001192050, NP_001192051, NP_001333240, NP_001333241, NP_001333242, NP_001333243, NP_001333244, NP_001333245, NP_001333246, NP_001333247, NP_001333248, NP_001333249, NP_001333250, NP_001333251, NP_001333252, NP_001333253, NP_001333254, NP_001333255, NP_001333256, NP_001333257, NP_001333258, NP_001333259, NP_001333260, NP_001333261, NP_001333262, NP_001333263, NP_001333264, NP_001333265, NP_001333266, NP_001333267, NP_001333269, NP_001333271, NP_001333273, NP_001333275, NP_001333277, NP_001333278, NP_001333279, NP_001333280, NP_001333281, NP_001333282, NP_001333283, NP_001333284, NP_001333285, NP_001333286, NP_001333287, NP_001333288, NP_001333289, NP_055556, NR_144422, NR_144423, NR_144424, PARATARG8, XM_005253265, XM_005253266, XM_005253268, XM_006718396, XM_011520493, XM_011520496, XM_011520499, XM_011520500, XM_011520502, XM_017018599, XM_017018603, XM_017018607, XM_017018618, XM_024448781, XP_005253322, XP_005253323, XP_005253325, XP_006718459, XP_011518795, XP_011518798, XP_011518801, XP_011518802, XP_011518804, XP_016874088, XP_016874092, XP_016874096, XP_016874107, XP_024304549, autophagy related 13

Omim:OMIM:615088

Id:0ae523f6-f179-581f-9cb4-18743e20ed8c

Hgnc:HGNC:29091

Entrez:9776

Ensembl:ENSG00000175224

Description:autophagy related 13

The protein encoded by this gene is an autophagy factor and a target of the TOR kinase signaling pathway. The encoded protein is essential for autophagosome formation and mitophagy. [provided by RefSeq, Oct 2016]

Analyze

CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View ATG13'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 ATG13.

CFDE Gene-Centric Appyter

The CFDE Gene Centric Appyter Resolves and Displays Gene-Centric information from CFDE APIs. Execute the Appyter using ATG13.

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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 ATG13.

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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 ATG13.

Results found

Linked to

	Label	Description
	GSE150244 TRIM8 knockout 3 v 0 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
	GSE220806 progesterone fibroblast 1 v 3 human dn Gene Set (Entity type)	A Gene Set from LINCS
	GSE242555 1 V 0 NICOTINAMIDE HUMAN DN Gene Set (Entity type)	A Gene Set from LINCS
	GSE203362 0 V 1 ENZALUTAMIDE HUMAN DN Gene Set (Entity type)	A Gene Set from LINCS
	GSE102757 1 V 0 PANOBINOSTAT MOUSE UP Gene Set (Entity type)	A Gene Set from LINCS
	GSE229973 3 V 2 CISPLATIN HUMAN DN Gene Set (Entity type)	A Gene Set from LINCS
	GSE197555 0 V 3 TRAMETINIB HUMAN UP 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
	GSE200982 PLAC8 knockout 0 v 2 human dn Gene Set (Entity type)	A Gene Set from LINCS