Gene
SH2D7
SH2 domain containing 7
- HGNC 34549↗(opens in a new tab)
- Ensembl gene ENSG00000183476↗(opens in a new tab)
- NCBI Gene 646892↗(opens in a new tab)
Summary
- Cytogenetic location
- 15q25.1
- Coordinates
- Chromosome 15: 78,092,561–78,104,362 (GRCh38)
- Exons
- 6 exons across 11.8 kb
- Protein
- 451 amino acids
- Also known as
- LOC646892
- MANE Select transcript
- ENST00000328828.6NM_001101404.2
- Locus type
- gene with protein product
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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No Genome Test report reads SH2D7 yet. The test sequences your whole genome, so your data includes it all the same.
How SH2D7 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
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 2.2 kb of the gene's 11.8 kb; 1,356 of those bases code for the protein.
How a genome test reads SH2D7
1
position in SH2D7 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 11.8 kb of SH2D7, introns included, not only the 2.2 kb of exons.
External links
Gene records
Transcript
Protein
Clinical
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.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). SH2D7 gene: SH2 domain containing 7. Retrieved 16 October 2026, from https://dantelabs.com/genes/sh2d7
Dante Labs. SH2D7 gene: SH2 domain containing 7 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/sh2d7
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