1. Gene
  2. Bbs9 - Bardet-Biedl syndrome 9 Gene

Bbs9 - Bardet-Biedl syndrome 9 Gene

Rattus norvegicus

Also known as RGD1308472

Gene ID: 315484 | Gene type: protein coding

About Bbs9

Summary

Predicted to be involved in cilium assembly and protein localization to cilium. Predicted to act upstream of or within fat cell differentiation. Predicted to be located in centriolar satellite; ciliary transition zone; and pericentriolar material. Predicted to be part of BBSome. Predicted to be active in membrane. Human ortholog(s) of this gene implicated in Bardet-Biedl syndrome; Bardet-Biedl syndrome 9; craniosynostosis; and primary ovarian insufficiency. Orthologous to human BBS9 (Bardet-Biedl syndrome 9). [provided by Alliance of Genome Resources, Apr 2022]

Bbs9 Products(18)

mRNA Protein Name
XM_039082285.1 XP_038938213.1 protein PTHB1 isoform X5
XM_039082273.1 XP_038938201.1 protein PTHB1 isoform X1
XM_039082274.1 XP_038938202.1 protein PTHB1 isoform X1
XM_039082279.1 XP_038938207.1 protein PTHB1 isoform X1
XM_039082276.1 XP_038938204.1 protein PTHB1 isoform X1
XM_017595981.2 XP_017451470.1 protein PTHB1 isoform X1
XM_039082272.1 XP_038938200.1 protein PTHB1 isoform X1
XM_039082275.1 XP_038938203.1 protein PTHB1 isoform X1
XM_039082277.1 XP_038938205.1 protein PTHB1 isoform X1
XM_039082270.1 XP_038938198.1 protein PTHB1 isoform X1
XM_039082271.1 XP_038938199.1 protein PTHB1 isoform X1
XM_039082281.1 XP_038938209.1 protein PTHB1 isoform X2
XM_039082283.1 XP_038938211.1 protein PTHB1 isoform X3
XM_039082282.1 XP_038938210.1 protein PTHB1 isoform X3
XM_017595983.2 XP_017451472.1 protein PTHB1 isoform X3
XM_039082284.1 XP_038938212.1 protein PTHB1 isoform X4
XM_039082280.1 XP_038938208.1 protein PTHB1 isoform X1
XM_039082278.1 XP_038938206.1 protein PTHB1 isoform X1
Protein Preferred Names Protein Names

Bardet-Biedl syndrome 9

protein PTHB1

Orthologs Information

Species Symbol Source ID
Homo sapiens Bbs9 NCBI NCBI:27241