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Gene : GDAP1 Homo sapiens

Name  ? ganglioside induced differentiation associated protein 1 Cytological Location  8q21.11
Brief Description  ganglioside induced differentiation associated protein 1
Description  This gene encodes a member of the ganglioside-induced differentiation-associated protein family, which may play a role in a signal transduction pathway during neuronal development. Mutations in this gene have been associated with various forms of Charcot-Marie-Tooth Disease and neuropathy. Two transcript variants encoding different isoforms and a noncoding variant have been identified for this gene. [provided by RefSeq, Feb 2012]
  • synonyms:
  • CMT4A,
  • CMT4,
  • Charcot-Marie-Tooth neuropathy 4A,
  • GDAP1,
  • CMT4,
  • OTTHUMG00000164509,
  • CMT4A,
  • CMTRIA,
  • HGNC:15968,
  • uc003yah.4,
  • NM_018972,
  • CMT2K
  • identifiers:
  • 54332,
  • ENSG00000104381,
  • GDAP1

Genome feature

Region: gene ? Length: 138490  
Location: 8:74350383-74488872 Cyto location: 8q21.11


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

4 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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Expression

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

Gene Ontology

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Other

915 SN Ps

5 Cross References

19 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results