FAM135B

FAM135B
Identifiers
Aliases	FAM135B, C8ORFK32, family with sequence similarity 135 member B
External IDs	MGI: 1917613; HomoloGene: 66605; GeneCards: FAM135B; OMA:FAM135B - orthologs
Gene location (Human)
Chr.	Chromosome 8 (human)
End	138,497,261 bp
Gene location (Mouse)
Chr.	Chromosome 15 (mouse)
End	71,599,687 bp
RNA expression pattern
	Top expressed in
	left testis; ; sperm; ; right testis; ; testicle; ; cerebellar hemisphere; ; right hemisphere of cerebellum; ; gonad; ; sural nerve; ; pancreatic ductal cell; ; islet of Langerhans;
	Top expressed in
	spermatid; ; seminiferous tubule; ; spermatocyte; ; dentate gyrus of hippocampal formation granule cell; ; primary visual cortex; ; superior frontal gyrus; ; neural layer of retina; ; cerebellar cortex; ; supraoptic nucleus; ; neural tube;
	More reference expression data
	n/a
Orthologs
	51059
	70363
	ENSG00000147724
	ENSMUSG00000036800
	Q49AJ0
	Q9DAI6
	NM_015912; NM_001362965
	NM_177819
	NP_056996; NP_001349894
	NP_808487
	Wikidata
View/Edit Human	View/Edit Mouse

FAM135B is a human gene coding for a protein of unknown function. It is well conserved in primates, rodents, zebra fish. It has one paralog, FAM135A.