BBS4

BBS4
Identifiers
AliasesBBS4, Bardet-Biedl syndrome 4
External IDsOMIM: 600374; MGI: 2143311; HomoloGene: 13197; GeneCards: BBS4; OMA:BBS4 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

585

102774

Ensembl

ENSG00000140463

ENSMUSG00000025235

UniProt

Q96RK4

Q8C1Z7

RefSeq (mRNA)

NM_001252678
NM_033028
NM_001320665

NM_175325
NM_001359558

RefSeq (protein)

NP_001239607
NP_001307594
NP_149017

NP_780534
NP_001346487

Location (UCSC)Chr 15: 72.69 – 72.74 MbChr 9: 59.23 – 59.26 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Bardet–Biedl syndrome 4 is a protein that in humans is encoded by the BBS4 gene.

This gene encodes a protein which contains tetratricopeptide repeats (TPR), similar to O-linked N-acetylglucosamine transferase. Mutations in this gene have been observed in patients with Bardet–Biedl syndrome type 4. The encoded protein may play a role in pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation.