CTTNBP2

Last updated
CTTNBP2
Identifiers
Aliases CTTNBP2 , C7orf8, CORTBP2, Orf4, cortactin binding protein 2
External IDs OMIM: 609772 MGI: 1353467 HomoloGene: 14125 GeneCards: CTTNBP2
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_033427
NM_001363349
NM_001363350
NM_001363351

NM_080285

RefSeq (protein)

NP_219499
NP_001350278
NP_001350279
NP_001350280

NP_525024

Location (UCSC) Chr 7: 117.71 – 117.87 Mb Chr 6: 18.37 – 18.51 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Cortactin-binding protein 2 is a protein that in humans is encoded by the CTTNBP2 gene. [5] [6]

Contents

Function

This gene encodes a protein with six ankyrin repeats and several proline-rich regions. A similar gene in rat interacts with a central regulator of the actin cytoskeleton. [6]

Interactions

CTTNBP2 has been shown to interact with:

Related Research Articles

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<span class="mw-page-title-main">CTTNBP2NL</span> Protein-coding gene in the species Homo sapiens

CTTNBP2 N-terminal-like protein is a protein that in humans is encoded by the CTTNBP2NL gene. It is a substrate for phosphorylation.

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References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000077063 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000000416 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Cheung J, Petek E, Nakabayashi K, Tsui LC, Vincent JB, Scherer SW (Nov 2001). "Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31". Genomics. 78 (1–2): 7–11. doi:10.1006/geno.2001.6651. PMID   11707066.
  6. 1 2 "Entrez Gene: CTTNBP2 cortactin binding protein 2".
  7. 1 2 3 4 5 Goudreault M, D'Ambrosio LM, Kean MJ, Mullin MJ, Larsen BG, Sanchez A, Chaudhry S, Chen GI, Sicheri F, Nesvizhskii AI, Aebersold R, Raught B, Gingras AC (Jan 2009). "A PP2A phosphatase high density interaction network identifies a novel striatin-interacting phosphatase and kinase complex linked to the cerebral cavernous malformation 3 (CCM3) protein". Mol. Cell. Proteomics. 8 (1): 157–71. doi:10.1074/mcp.M800266-MCP200. PMC   2621004 . PMID   18782753.

Further reading