KIAA1279

From Wikipedia, the free encyclopedia
Jump to: navigation, search
KIF1BP
Identifiers
Aliases KIF1BP, KBP, KIAA1279, TTC20, KIF1 binding protein
External IDs MGI: 1919570 HomoloGene: 9223 GeneCards: KIF1BP
RNA expression pattern
PBB GE KIAA1279 212453 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_015634

NM_028197

RefSeq (protein)

NP_056449

NP_082473.2
NP_082473

Location (UCSC) Chr 10: 68.99 – 69.04 Mb Chr 10: 62.54 – 62.58 Mb
PubMed search [1] [2]
Wikidata
View/Edit Human View/Edit Mouse

KIF1-binding protein is a protein that in humans is encoded by the KIAA1279 gene.[3]

Clinical significance[edit]

Defects may be associated with Goldberg–Shprintzen syndrome (OMIM 609460).

Interactions[edit]

KIAA1279 has been shown to interact with Retinal G protein coupled receptor[4] and Dipeptidase 1.[4]

References[edit]

  1. ^ "Human PubMed Reference:". 
  2. ^ "Mouse PubMed Reference:". 
  3. ^ "Entrez Gene: KIAA1279 KIAA1279". 
  4. ^ a b Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (Oct 2005). "Towards a proteome-scale map of the human protein–protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514. 

Further reading[edit]

External links[edit]