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Proto-oncogene Wnt-1

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(Redirected from WNT1)
Protein-coding gene in the species Homo sapiens
WNT1
Identifiers
Aliases WNT1 , BMND16, INT1, OI15, Wnt family member 1
External IDsOMIM: 164820; MGI: 98953; HomoloGene: 3963; GeneCards: WNT1; OMA:WNT1 - orthologs
Gene location (Human)
Chromosome 12 (human)
Chr. Chromosome 12 (human) [1]
Band 12q13.12Start48,978,322 bp [1]
End48,982,620 bp [1]
Gene location (Mouse)
Chromosome 15 (mouse)
Chr. Chromosome 15 (mouse)[2]
Band 15 F1|15 54.65 cMStart98,687,738 bp [2]
End98,691,718 bp [2]
RNA expression pattern
Bgee
Human Mouse (ortholog)
  • granulocyte

  • nucleus accumbens

  • superior frontal gyrus

  • right frontal lobe

  • prefrontal cortex

  • putamen

  • blood

  • caudate nucleus

  • bone marrow

  • Brodmann area 9
  • muscle layer of urethra

  • pelvic part of vagina

  • rhombic lip

  • ejaculatory duct

  • perineal part of vagina

  • inner cell mass

  • epithelium of seminiferous tubule of testis

  • choroid plexus of fourth ventricle

  • female urethra

  • morula
More reference expression data
BioGPS
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

7471

22408

Ensembl

ENSG00000125084

ENSMUSG00000022997

UniProt

P04628

P04426

RefSeq (mRNA)

NM_005430

NM_021279

RefSeq (protein)

NP_005421

NP_067254

Location (UCSC)Chr 12: 48.98 – 48.98 Mb Chr 15: 98.69 – 98.69 Mb
PubMed search[3] [4]
Wikidata

Proto-oncogene Wnt-1, or Proto-oncogene Int-1 homolog is a protein that in humans is encoded by the WNT1 (INT1 ) gene.[5] [6]

The WNT gene family consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region.[7]

See also

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References

[edit ]
  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000125084Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000022997Ensembl, 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. ^ van Ooyen A, Kwee V, Nusse R (Jan 1986). "The nucleotide sequence of the human int-1 mammary oncogene; evolutionary conservation of coding and non-coding sequences". EMBO J. 4 (11): 2905–9. doi:10.1002/j.1460-2075.1985.tb04021.x. PMC 554596 . PMID 2998762.
  6. ^ Arheden K, Mandahl N, Strombeck B, Isaksson M, Mitelman F (May 1988). "Chromosome localization of the human oncogene INT1 to 12q13 by in situ hybridization". Cytogenet Cell Genet. 47 (1–2): 86–87. doi:10.1159/000132513. PMID 3281802.
  7. ^ "Entrez Gene: WNT1 wingless-type MMTV integration site family, member 1".

Further reading

[edit ]
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