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Gene : HFM1 Homo sapiens

Name  ? helicase for meiosis 1 Cytological Location  1p22.2
Brief Description  helicase for meiosis 1
Description  The protein encoded by this gene is thought to be an ATP-dependent DNA helicase and is expressed mainly in germ-line cells. Defects in this gene are a cause of premature ovarian failure 9 (POF9). [provided by RefSeq, Apr 2014]
  • synonyms:
  • NM_001017975,
  • Si-11,
  • AB204867,
  • SEC63D1,
  • FLJ39011,
  • FLJ36760,
  • OTTHUMG00000010093,
  • HFM1, ATP dependent DNA helicase homolog,
  • HFM1, ATP-dependent DNA helicase homolog (S. cerevisiae),
  • Si-11-6,
  • MER3,
  • SEC63 domain containing 1,
  • uc001doa.4,
  • SEC63D1,
  • POF9,
  • helicase,
  • HGNC:20193,
  • HFM1,
  • MER3
  • identifiers:
  • 164045,
  • ENSG00000162669,
  • HFM1

Genome feature

Region: gene ? Length: 147243  
Location: 1:91260766-91408008 reverse strand Cyto location: 1p22.2


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

3753 SN Ps

5 Cross References

16 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results