GNPTG

GNPTG
Identifiers
Aliases	GNPTG, C16orf27, GNPTAG, LP2537, RJD9, N-acetylglucosamine-1-phosphate transferase gamma subunit, N-acetylglucosamine-1-phosphate transferase subunit gamma
External IDs	OMIM: 607838; MGI: 2147006; HomoloGene: 13047; GeneCards: GNPTG; OMA:GNPTG - orthologs
Gene location (Human)
Chr.	Chromosome 16 (human)
End	1,365,737 bp
Gene location (Mouse)
Chr.	Chromosome 17 (mouse)
End	25,459,098 bp
RNA expression pattern
	Top expressed in
	right adrenal cortex; ; left adrenal gland; ; left adrenal cortex; ; C1 segment; ; Brodmann area 9; ; cingulate gyrus; ; anterior cingulate cortex; ; prefrontal cortex; ; Amygdala; ; Hypothalamus;
	Top expressed in
	right kidney; ; neural layer of retina; ; superior frontal gyrus; ; primary visual cortex; ; parotid gland; ; cerebellar cortex; ; dentate gyrus of hippocampal formation granule cell; ; yolk sac; ; neural tube; ; lateral septal nucleus;
	More reference expression data
	n/a
Gene ontology
Molecular function	UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase activity; protein homodimerization activity;
Cellular component	extracellular region; Golgi membrane; Golgi apparatus; extracellular exosome; membrane; intracellular membrane-bounded organelle;
Biological process	N-glycan processing to lysosome; carbohydrate phosphorylation;
	Sources:Amigo / QuickGO
Orthologs
	84572
	214505
	ENSG00000090581
	ENSMUSG00000035521
	Q9UJJ9
	Q6S5C2
	NM_032520
	NM_172529; NM_001346737
	NP_115909
	NP_001333666; NP_766117
	Wikidata
View/Edit Human	View/Edit Mouse

GNPTG (“N-acetylglucosamine-1-phosphate transferase, gamma subunit.”) is a gene in the human body. It is one of three genes that were found to correlate with stuttering.