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Details on Person UniProt:Q9BPU9 B9D2
| Class:Id | ReferenceGeneProduct:219831 |
|---|---|
| _chainChangeLog | chain:1-175 added on Sat February 7 2015 |
| _displayName | UniProt:Q9BPU9 B9D2 |
| _timestamp | 2024-11-03 19:55:16 |
| chain | chain:1-175 |
| checksum | A8B8D1A637C3EF5D |
| comment | FUNCTION Component of the tectonic-like complex, a complex localized at the transition zone of primary cilia and acting as a barrier that prevents diffusion of transmembrane proteins between the cilia and plasma membranes.SUBUNIT Part of the tectonic-like complex (also named B9 complex). Interacts with TUBG1 (By similarity).INTERACTION The disease is caused by variants affecting the gene represented in this entry.DISEASE The disease is caused by variants affecting the gene represented in this entry.SIMILARITY Belongs to the B9D family. |
| created | [InstanceEdit:217385] Schmidt, EE, 2008-03-27 06:23:53 |
| description | recommendedName: B9 domain-containing protein 2 alternativeName: MKS1-related protein 2 |
| geneName | B9D2 MKSR2 |
| identifier | Q9BPU9 |
| isSequenceChanged | FALSE |
| keyword | Cell projection Ciliopathy Cilium Cilium biogenesis/degradation Cytoplasm Cytoskeleton Disease variant Joubert syndrome Meckel syndrome Nucleus Proteomics identification Reference proteome |
| modified | [InstanceEdit:9836292] Weiser, Joel, 2023-05-25 [InstanceEdit:9852000] Weiser, Joel, 2023-11-03 [InstanceEdit:9926675] Weiser, Joel, 2024-11-03 |
| name | B9D2 |
| referenceDatabase | [ReferenceDatabase:2] UniProt |
| referenceGene | [ReferenceDNASequence:8995860] ENSEMBL:ENSG00000123810 B9D2 [Homo sapiens] |
| secondaryIdentifier | B9D2_HUMAN |
| sequenceLength | 175 |
| species | [Species:48887] Homo sapiens |
| (referenceEntity) | [EntityWithAccessionedSequence:377736] B9D2 [cytosol] [Homo sapiens] |
| [Change default viewing format] | |
No pathways have been reviewed or authored by UniProt:Q9BPU9 B9D2 (219831)
