Gene
HM13
histocompatibility minor 13
- HGNC 16435↗(opens in a new tab)
- Ensembl gene ENSG00000101294↗(opens in a new tab)
- NCBI Gene 81502↗(opens in a new tab)
Summary
- Cytogenetic location
- 20q11.21
- Coordinates
- Chromosome 20: 31,514,442–31,569,543 (GRCh38)
- Exons
- 13 exons across 55.1 kb
- Protein
- 426 amino acids
- Also known as
- H13, dJ324O17.1, SPP, PSL3, IMP1, IMPAS, PSENL3, SPPL1
- Previous symbols
- HM13-IT1
- MANE Select transcript
- ENST00000398174.9NM_178581.3
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
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How HM13 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 1.7 kb of the gene's 55.1 kb; 1,281 of those bases code for the protein.
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.
Cite this page
Dante Labs. (n.d.). HM13 gene: histocompatibility minor 13. Retrieved 17 October 2026, from https://dantelabs.com/genes/hm13
Dante Labs. HM13 gene: histocompatibility minor 13 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/hm13
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