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Gene : FAM9B Homo sapiens

Name  ? family with sequence similarity 9 member B Cytological Location  Xp22.31
Brief Description  family with sequence similarity 9 member B
Description  This gene is a member of a gene family which arose through duplication on the X chromosome. The encoded protein may be localized to the nucleus as the protein contains several nuclear localization signals, and has similarity to a synaptonemal complex protein. [provided by RefSeq, Aug 2011]
  • synonyms:
  • family with sequence similarity 9, member B,
  • testis expressed 39B,
  • TEX39B,
  • HGNC:18404,
  • FAM9B,
  • NM_205849,
  • TEX39B,
  • OTTHUMG00000021114,
  • uc064xxo.1
  • identifiers:
  • 171483,
  • ENSG00000177138,
  • FAM9B

Genome feature

Region: gene ? Length: 9896  
Location: X:9024232-9034127 reverse strand Cyto location: Xp22.31

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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]


Homologue Displayer


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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

5 Cross References

15 Data Sets

62 Homologues

0 Located Features

97 Rna Seq Results