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Gene : FBXO38 Homo sapiens

Name  ? F-box protein 38 Cytological Location  5q32
Brief Description  F-box protein 38
Description  This gene encodes a large protein that contains an F-box domain and may participate in protein ubiquitination. The encoded protein is a transcriptional co-activator of Krueppel-like factor 7 (Klf7). A heterozygous mutation in this gene was found in individuals with autosomal dominant distal hereditary motor neuronopathy type IID. There is a pseudogene for this gene on chromosome 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]
  • synonyms:
  • FBXO38,
  • OTTHUMG00000129929,
  • uc031slt.2,
  • SP329,
  • MOKA,
  • SP329,
  • MOKA,
  • HGNC:28844,
  • Fbx38,
  • BC005873,
  • NM_030793,
  • Fbx38,
  • HMN2D,
  • FLJ13962
  • identifiers:
  • 81545,
  • ENSG00000145868,
  • FBXO38

Genome feature

Region: gene ? Length: 58902  
Location: 5:148383935-148442836 Cyto location: 5q32

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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


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]


Homologue Displayer


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 Pathways

3753 SN Ps

5 Cross References

19 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results