Wingless-Type MMTV Integration Site Family, Member 7B

Alternative Names

  • WNT7B

Associated Diseases

Microphthalmia, Syndromic 9
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OMIM Number

601967

NCBI Gene ID

7477

Uniprot ID

P56706

Length

56,797 bases

No. of Exons

5

No. of isoforms

1

Protein Name

Protein Wnt-7b

Molecular Mass

39327 Da

Amino Acid Count

349

Genomic Location

chr22:45,920,366-45,977,162

Gene Map Locus
22q13.31

Description

This gene is a member of the WNT gene family, which 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. Among members of the human WNT family, this gene product is most similar to WNT7A protein. [From RefSeq]

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_058238.3:c.739C>TSaudi ArabiaNC_000022.11:g.45923167G>ALikely PathogenicPathogenicMicrophthalmia, Syndromic 9NM_058238.3:c.739C>T; NP_478679.1:p.Arg247Trp1475762618437886
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