Reference for GDAP1. Search for GDAP1

AI searches containing GDAP1

GDAP1

GDAP1

Protein-coding gene in the species Homo sapiens

differentiation-associated protein 1 is a type of protein that in humans is encoded by the GDAP1 gene. This gene encodes a member of the ganglioside-induced differentiation-associated

GDAP1

Charcot–Marie–Tooth disease

Neuromuscular disease

dynamin 2 (DNM2), ganglioside-induced differentiation-associated protein 1 (GDAP1), and mitofusin 2 (MFN2), can cause axonal forms of CMT. Due to the close

Charcot–Marie–Tooth disease

Charcot–Marie–Tooth_disease

Charcot–Marie–Tooth disease classifications

Peripheral nervous system disorders

Autosomal dominant CMT2F 606595 HSPB1 7q11.23 Autosomal dominant CMT2H 607731 GDAP1 8q21.11 Autosomal dominant Allelic with subtype CMT2K CMT2I 607677 MPZ 1q23

Charcot–Marie–Tooth disease classifications

Charcot–Marie–Tooth_disease_classifications

Chromosome 8

Human chromosome

(fms-related tyrosine kinase 2, Pfeiffer syndrome) FGL1: Fibrinogen-like protein 1 GDAP1: ganglioside-induced differentiation-associated protein 1 GDF6: growth differentiation

Chromosome 8

Chromosome_8

Glutathione S-transferase, C-terminal domain

Protein domain

all-helical sub-domain. This entry is the C-terminal domain. EEF1E1; EEF1G; GDAP1; GSTA1; GSTA2; GSTA3; GSTA4; GSTA5; GSTM1; GSTM2; GSTM3; GSTM4; GSTM5; GSTO1;

Glutathione S-transferase, C-terminal domain

Glutathione_S-transferase,_C-terminal_domain

List of human protein-coding genes 3

HGNC:29583; Q5JQS6 6145 GCSH HGNC:4208; P23434 6146 GDA HGNC:4212; Q9Y2T3 6147 GDAP1 HGNC:15968; Q8TB36 6148 GDAP1L1 HGNC:4213; Q96MZ0 6149 GDAP2 HGNC:18010;

List of human protein-coding genes 3

List_of_human_protein-coding_genes_3

PLEKHM3

phosphate binding. PLEKHM3 is thought to interact with a protein called GDAP1, which is responsible for differentiation in neuronal cell types and plays

PLEKHM3

List of OMIM disorder codes

2F; 606595; HSPB1 Charcot–Marie–Tooth disease, axonal, type 2K; 607831; GDAP1 Charcot–Marie–Tooth disease, axonal, type 2L; 608673; HSPB8 Charcot–Marie–Tooth

List of OMIM disorder codes

List_of_OMIM_disorder_codes