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Gene : WASF5P Homo sapiens

Name  ? WASP family member 5, pseudogene Cytological Location  6p21.33
description  This gene is a pseudogene belonging to the family of genes encoding Wiskott-Aldrich syndrome (WAS) proteins, which are involved in the transmission of signals to the actin cytoskeleton. Wiskott-Aldrich syndrome is a disease of the immune system. This pseudogene, which is apparently not transcribed, resembles the gene encoding the WAS protein family member 3, which is located on chromosome 13. [provided by RefSeq, Jul 2008]
  • synonyms:
  • Em:D84394.5,
  • WAS protein family member 5, pseudogene,
  • OTTHUMG00000031266,
  • WAS protein family, member 5, pseudogene,
  • HGNC:21665,
  • NG_007617
  • identifiers:
  • 387122,
  • ENSG00000231402,
  • WASF5P

Genome feature

Region: gene ?
Location: No location information in HumanMine Cyto location: 6p21.33


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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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Gene --> Orthologues

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

2011 SN Ps

3 Cross References

7 Data Sets

0 Homologues

0 Located Features

53 Rna Seq Results