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Gene : HMSD Homo sapiens

Name  ? histocompatibility minor serpin domain containing Cytological Location  18q22.1
Brief Description  histocompatibility minor serpin domain containing
Description  This gene encodes a serpin-domain containing protein that may function as a serine protease inhibitor. This gene is primarily expressed in cells of myeloid lineage. A polymorphism in this gene may result in the expression a splice variant that encodes a minor histocompatibility antigen. [provided by RefSeq, Oct 2010]
  • synonyms:
  • AC009802,
  • C18orf53,
  • uc010dqj.4,
  • histocompatibility (minor) serpin domain containing,
  • C18orf53,
  • ACC-6,
  • HSMD-v,
  • HMSD,
  • ACC-6,
  • NM_001123366,
  • ACC6,
  • ACC6,
  • OTTHUMG00000060593,
  • HGNC:23037
  • identifiers:
  • 284293,
  • ENSG00000221887,
  • HMSD

Genome feature

Region: gene ? Length: 20071  
Location: 18:63949259-63969329 Cyto location: 18q22.1

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

3753 SN Ps

4 Cross References

10 Data Sets

0 Homologues

0 Located Features

97 Rna Seq Results