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Gene

WNT7A

Wnt family member 7A

Summary

Cytogenetic location
3p25.1
Coordinates
Chromosome 3: 13,816,258–13,880,071 (GRCh38)
Exons
4 exons across 63.8 kb
Protein
349 amino acids
Also known as
Wnt-7a
MANE Select transcript
ENST00000285018.5NM_004625.4
Locus type
gene with protein product
  • Very high
  • Confident
  • Low
  • Very low

Reference genomeGRCh38

Positions on gene and variant pages follow this choice, in this browser.

Curated reports relevant to this gene

No Genome Test report reads WNT7A yet. The test sequences your whole genome, so your data includes it all the same.

How WNT7A is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 3, with a bracket where WNT7A sits. WNT7A and 8 genes near it on chromosome 3, from 13,348,165 to 14,348,164.Chromosome 33p25.1p26.3p26.2p26.1p25.3p25.2p25.1p24.3p24.2p24.1p23p22.3p22.2p22.1p21.33p21.32p21.31p21.2p21.1p14.3p14.2p14.1p13p12.3p12.2p12.1p11.2p11.1q11.1q11.2q12.1q12.2q12.3q13.11q13.12q13.13q13.2q13.31q13.32q13.33q21.1q21.2q21.3q22.1q22.2q22.3q23q24q25.1q25.2q25.31q25.32q25.33q26.1q26.2q26.31q26.32q26.33q27.1q27.2q27.3q28q2913.4 Mb13.6 Mb13.8 Mb14 Mb14.2 MbNUP210: 13,316,231–13,420,395, reverse strandNUP210HDAC11: 13,479,724–13,506,424, forward strandHDAC11FBLN2: 13,549,073–13,638,504, forward strandFBLN2WNT7A: 13,816,258–13,880,071, reverse strandWNT7ACHCHD4: 14,112,077–14,124,876, reverse strandCHCHD4TMEM43: 14,124,998–14,143,681, forward strandTMEM43: 14,135,217–14,148,252, forward strandXPC: 14,145,145–14,178,767, reverse strandXPCLSM3: 14,178,749–14,216,186, forward strandLSM3Diagram of WNT7A: 4 exons on the reverse strand of chromosome 3Exon 4: 2 known disease-causing sitesExon 3: 1 known disease-causing siteExon 4: 13,816,258–13,819,423, 3,166 basesExon 3: 13,854,532–13,854,803, 272 basesExon 2: 13,874,947–13,875,173, 227 basesExon 1: 13,879,746–13,880,071, 326 bases43215′3′

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 4 kb of the gene's 63.8 kb; 1,050 of those bases code for the protein.

How a genome test reads WNT7A

4

positions in WNT7A where ClinVar classes a change as pathogenic or likely pathogenic

None of them falls in a region short reads find hard.

A whole genome covers all 63.8 kb of WNT7A, introns included, not only the 4 kb of exons.

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.
  • ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
  • The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
  • Data release 2026.10.16-c6eea6bf.

Cite this page

APA

Dante Labs. (n.d.). WNT7A gene: Wnt family member 7A. Retrieved 17 October 2026, from https://dantelabs.com/genes/wnt7a

Vancouver

Dante Labs. WNT7A gene: Wnt family member 7A [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/wnt7a

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