BBS10

BBS10
Identifiers
Aliases	BBS10, C12orf58, Bardet-Biedl syndrome 10
External IDs	OMIM: 610148; MGI: 1919019; HomoloGene: 49781; GeneCards: BBS10; OMA:BBS10 - orthologs
Gene location (Human)
Chr.	Chromosome 12 (human)
End	76,348,415 bp
Gene location (Mouse)
Chr.	Chromosome 10 (mouse)
End	111,137,588 bp
RNA expression pattern
	Top expressed in
	Achilles tendon; ; endothelial cell; ; ventricular zone; ; ganglionic eminence; ; Epithelium of choroid plexus; ; retinal pigment epithelium; ; Brodmann area 23; ; germinal epithelium; ; islet of Langerhans; ; bronchial epithelial cell;
	Top expressed in
	spermatocyte; ; otolith organ; ; spermatid; ; utricle; ; genital tubercle; ; lumbar spinal ganglion; ; seminiferous tubule; ; zygote; ; tail of embryo; ; oocyte;
	More reference expression data
	n/a
Gene ontology
Molecular function	nucleotide binding; protein binding; ATP binding;
Cellular component	cell projection; cilium;
Biological process	photoreceptor cell maintenance; retina homeostasis; regulation of protein-containing complex assembly; chaperone-mediated protein complex assembly; response to stimulus; visual perception; non-motile cilium assembly;
	Sources:Amigo / QuickGO
Orthologs
	79738
	71769
	ENSG00000179941
	ENSMUSG00000035759
	Q8TAM1
	Q9DBI2
	NM_024685
	NM_027914
	NP_078961
	NP_082190
	Wikidata
View/Edit Human	View/Edit Mouse

Bardet–Biedl syndrome 10, also known as BBS10 is a human gene.