TMEM238

TMEM238
Identifiers
Aliases	TMEM238, transmembrane protein 238
External IDs	MGI: 1922935; HomoloGene: 47692; GeneCards: TMEM238; OMA:TMEM238 - orthologs
Gene location (Human)
Chr.	Chromosome 19 (human)
End	55,384,292 bp
Gene location (Mouse)
Chr.	Chromosome 7 (mouse)
End	4,792,655 bp
RNA expression pattern
	Top expressed in
	mucosa of transverse colon; ; olfactory zone of nasal mucosa; ; body of pancreas; ; duodenum; ; right lobe of liver; ; minor salivary glands; ; skin of abdomen; ; human kidney; ; left lobe of thyroid gland; ; right lobe of thyroid gland;
	Top expressed in
	epithelium of stomach; ; parotid gland; ; lacrimal gland; ; right kidney; ; ileum; ; left lobe of liver; ; jejunum; ; embryo; ; vestibular membrane of cochlear duct; ; transitional epithelium of urinary bladder;
	More reference expression data
	n/a
Orthologs
	388564
	664968
	ENSG00000233493
	ENSMUSG00000030431
	C9JI98
	A9JSM3
	NM_001190764
	NM_029384
	NP_001177693
	NP_083660
	Wikidata
View/Edit Human	View/Edit Mouse

Transmembrane protein 238 is a transmembrane protein that in humans is encoded by the TMEM238 gene. The Homo sapiens TMEM238 gene is related to Bardet-Biedl Syndrome 2 and may play a role in amino acid transport, primarily showing expression in stomach and colon tissues.