Gene
WNT7B
Wnt family member 7B
- HGNC 12787↗(opens in a new tab)
- Ensembl gene ENSG00000188064↗(opens in a new tab)
- NCBI Gene 7477↗(opens in a new tab)
Summary
- Cytogenetic location
- 22q13.31
- Coordinates
- Chromosome 22: 45,920,366–45,977,162 (GRCh38)
- Exons
- 4 exons across 56.8 kb
- Protein
- 349 amino acids
- MANE Select transcript
- ENST00000339464.9NM_058238.3
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
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How WNT7B is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 3.9 kb of the gene's 56.8 kb; 1,050 of those bases code for the protein.
Traits linked to WNT7B
The Human Phenotype Ontology lists these as features of the rare conditions WNT7B can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
Cite this page
Dante Labs. (n.d.). WNT7B gene: Wnt family member 7B. Retrieved 17 October 2026, from https://dantelabs.com/genes/wnt7b
Dante Labs. WNT7B gene: Wnt family member 7B [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/wnt7b
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