TBC1D12

TBC1D12
Identifiers
Aliases	TBC1D12, Tbc1 domain family, member 12, TBC1 domain family member 12
External IDs	MGI: 2384803 HomoloGene: 50835 GeneCards: TBC1D12
Gene location (Human)
Chr.	Chromosome 10 (human)[1]
End	94,536,332 bp[1]
Gene location (Mouse)
Chr.	Chromosome 19 (mouse)[2]
End	38,908,367 bp[2]
RNA expression pattern
	Top expressed in
	corpus callosum; ; inferior olivary nucleus; ; subthalamic nucleus; ; substantia nigra; ; Brodmann area 46; ; spinal cord; ; globus pallidus; ; inferior ganglion of vagus nerve; ; internal globus pallidus;
	More reference expression data
	n/a
Gene ontology
Molecular function	GO:0005097, GO:0005099, GO:0005100 GTPase activator activity;
Cellular component	autophagosome; recycling endosome; intracellular anatomical structure;
Biological process	regulation of vesicle fusion; regulation of autophagosome assembly; intracellular protein transport; GO:0032861, GO:0032862, GO:0032856 activation of GTPase activity;
	Sources:Amigo / QuickGO
Orthologs
	23232
	209478
	ENSG00000108239
	ENSMUSG00000048720
	O60347
	Q6A039
	NM_015188
	NM_145952; NM_001362424
	NP_056003
	NP_666064; NP_001349353
	Wikidata
View/Edit Human	View/Edit Mouse

TBC1D12 is a protein with a conserved TBC domain that in humans is encoded by the TBC1D12 gene.[5]

References

GRCh38: Ensembl release 89: ENSG00000108239 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000048720 - Ensembl, May 2017
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: TBC1 domain family, member 12".