GDAP1 Products

Antibodies
GDAP1 Antibody
GDAP1 Antibody
NBP1-84430
Species: Hu, Mu, Rt
Applications: WB, ICC/IF, IHC, IHC-P
Host: Rabbit Polyclonal
GDAP1 Antibody
GDAP1 Antibody
NBP1-84429
Species: Hu, Mu, Rt
Applications: IHC, IHC-P
Host: Rabbit Polyclonal
Proteins
Recombinant Human GDAP1 Prote ...
Recombinant Human GDAP1 Protein
H00054332-P02
Species: Hu
Applications: WB, ELISA, PA
Recombinant Human GDAP1 Prote ...
Recombinant Human GDAP1 Protein
H00054332-P01
Species: Hu
Applications: WB, ELISA, PA
Recombinant Human GDAP1 Prote ...
Recombinant Human GDAP1 Protein
H00054332-Q01
Species: Hu
Applications: WB, ELISA, PA
RNAi
GDAP1 RNAi
GDAP1 RNAi
H00054332-R01
Species: Hu
Applications: RNAi, RNAi SP
GDAP1 RNAi
GDAP1 RNAi
H00054332-R02
Species: Hu
Applications: RNAi, RNAi SP

Description

The GDAP1 gene encodes for a member of the ganglioside-induced differentiation-associated protein family that is active in signal transduction pathways during neuronal development. These proteins also monitor the mitochondrial network by endorsing mitochondrial fission. Isoform 1 is 358 amino acids long at 41 kDA while isoform 2 is 290 amino acids long at approximately 33 kDA. Neuropathy, muscular dystrophy, and multiple forms of Charcot-Marie-Tooth Disease have been linked to mutations in the GDAP1 gene. The GDAP1 gene is involved in NgR-p75(NTR)-Mediated signaling and interacts with genes such as FIS1, ATP6V1D, TUBB, UBC, and YWHAB.

Bioinformatics

Entrez Human
Uniprot Human
Human
Human
Product By Gene ID 54332
Alternate Names
  • CMT4A
  • Charcot-Marie-Tooth neuropathy 4A
  • CMT2K
  • CMT4
  • truncated ganglioside differentiation associated protein 1
  • CMTRIA
  • ganglioside differentiation associated protein 1
  • ganglioside-induced differentiation-associated protein 1

PTMs for GDAP1

Learn more about PTMs related to GDAP1.

Phosphorylation
Ribosylation

Bioinformatics Tool for GDAP1

Discover related pathways, diseases and genes to GDAP1. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.
 
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