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Gene : KIFBP Homo sapiens

Name  ? kinesin family binding protein Cytological Location  10q22.1
Brief Description  kinesin family binding protein
Description  This gene encodes a kinesin family member 1 binding protein that is characterized by two tetratrico peptide repeats. The encoded protein localizes to the mitochondria and may be involved in regulating transport of the mitochondria. Mutations in this gene are associated with Goldberg-Shprintzen megacolon syndrome. [provided by RefSeq, Mar 2010]
  • synonyms:
  • OTTHUMG00000018363,
  • HGNC:23419,
  • NM_015634,
  • KBP,
  • KIF1 binding protein,
  • KBP,
  • KIAA1279,
  • DKFZP586B0923,
  • TTC20,
  • kinesin binding protein,
  • KIF1BP,
  • KIF1BP,
  • KIAA1279,
  • BC012180,
  • TTC20,
  • identifiers:
  • 26128,
  • ENSG00000198954,

Genome feature

Region: gene ? Length: 28180  
Location: 10:68988803-69016982 Cyto location: 10q22.1

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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]


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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

4 Homologues

0 Located Features

97 Rna Seq Results