ALX4

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ALX4
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases ALX4, CRS5, FND2, ALX homeobox 4
External IDs MGI: 108359 HomoloGene: 7229 GeneCards: ALX4
RNA expression pattern
PBB GE ALX4 208330 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_021926

NM_007442

RefSeq (protein)

NP_068745

NP_031468.1
NP_031468

Location (UCSC) Chr 11: 44.26 – 44.31 Mb Chr 2: 93.64 – 93.68 Mb
PubMed search [1] [2]
Wikidata
View/Edit Human View/Edit Mouse

Homeobox protein aristaless-like 4 is a protein that in humans is encoded by the ALX4 gene.[3][4][5]


Interactions[edit]

ALX4 has been shown to interact with Lymphoid enhancer-binding factor 1.[6]

References[edit]

  1. ^ "Human PubMed Reference:". 
  2. ^ "Mouse PubMed Reference:". 
  3. ^ Wu YQ, Badano JL, McCaskill C, Vogel H, Potocki L, Shaffer LG (Nov 2000). "Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome". Am J Hum Genet. 67 (5): 1327–32. doi:10.1016/S0002-9297(07)62963-2. PMC 1288575Freely accessible. PMID 11017806. 
  4. ^ Bartsch O, Wuyts W, Van Hul W, Hecht JT, Meinecke P, Hogue D, Werner W, Zabel B, Hinkel GK, Powell CM, Shaffer LG, Willems PJ (Jul 1996). "Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11". Am J Hum Genet. 58 (4): 734–42. PMC 1914683Freely accessible. PMID 8644736. 
  5. ^ "Entrez Gene: ALX4 aristaless-like homeobox 4". 
  6. ^ Boras, Kata; Hamel Paul A (Jan 2002). "Alx4 binding to LEF-1 regulates N-CAM promoter activity". J. Biol. Chem. United States. 277 (2): 1120–7. doi:10.1074/jbc.M109912200. ISSN 0021-9258. PMID 11696550. 

Further reading[edit]

External links[edit]