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Gene : FAM9A Homo sapiens

Name  ? family with sequence similarity 9 member A Cytological Location  Xp22.31
Brief Description  family with sequence similarity 9 member A
Description  This gene is a member of a gene family which arose through duplication on the X chromosome. The encoded protein may be a nuclear protein that is localized to the nucleolus, and has some similarity to a synaptonemal complex protein. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Aug 2011]
  • synonyms:
  • uc004csg.4,
  • NM_174951,
  • OTTHUMG00000021110,
  • testis expressed 39A,
  • TEX39A,
  • family with sequence similarity 9, member A,
  • HGNC:18403,
  • FAM9A,
  • TEX39A
  • identifiers:
  • 171482,
  • ENSG00000183304,
  • FAM9A

Genome feature

Region: gene ? Length: 10589  
Location: X:8790795-8801383 reverse strand Cyto location: Xp22.31


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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

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]

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

0 SN Ps

5 Cross References

14 Data Sets

62 Homologues

0 Located Features

97 Rna Seq Results