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Gene : GCOM1 Homo sapiens

Name  ? GRINL1A complex locus 1 Cytological Location  15q21.3
Brief Description  GRINL1A complex locus 1
Description  This locus represents naturally occurring readthrough transcription between the neighboring MYZAP (myocardial zonula adherens protein) and POLR2M (polymerase (RNA) II (DNA directed) polypeptide M) genes on chromosome 15. Alternative splicing results in multiple readthrough transcript variants. Readthrough variants may encode proteins that share sequence identity with the upstream gene product or with both the upstream and downstream gene products. Some readthrough transcript variants are also expected to be candidates for nonsense-mediated decay (NMD). [provided by RefSeq, Oct 2013]
  • synonyms:
  • uc002aem.4,
  • OTTHUMG00000176411,
  • MYZAP-POLR2M readthrough,
  • Gcom2,
  • FLJ30973,
  • GCOM1,
  • HGNC:26424,
  • GRINL1A,
  • MYZAP,
  • GRINL1A,
  • gcom,
  • NM_001018090
  • identifiers:
  • 145781,
  • ENSG00000137878,
  • GCOM1

Genome feature

Region: gene ? Length: 125654  
Location: 15:57591904-57717557 Cyto location: 15q21.3

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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

0 SN Ps

4 Cross References

12 Data Sets

0 Homologues

0 Located Features

43 Rna Seq Results