Pain syndromes
Gene: NTRK1
NTRK1 (neurotrophic receptor tyrosine kinase 1)
EnsemblGeneIds (GRCh38): ENSG00000198400
EnsemblGeneIds (GRCh37): ENSG00000198400
OMIM: 191315, Gene2Phenotype
NTRK1 is in 11 panels
EnsemblGeneIds (GRCh38): ENSG00000198400
EnsemblGeneIds (GRCh37): ENSG00000198400
OMIM: 191315, Gene2Phenotype
NTRK1 is in 11 panels
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Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Genomics England PanelApp
- Phenotypes
-
- HSAN 4
- Insensitivity to pain, congenital, with anhidrosis, 256800
- Hereditary sensory neuropathy type IV
- OMIM
- 191315
- Clinvar variants
- Variants in NTRK1
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
1 Apr 2020, Gel status: 3
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Added phenotypes HSAN 4; Insensitivity to pain, congenital, with anhidrosis, 256800; Hereditary sensory neuropathy type IV for gene: NTRK1
1 Apr 2020, Gel status: 3
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: NTRK1 was added gene: NTRK1 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green Mode of inheritance for gene: NTRK1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: NTRK1 were set to 11668614; 8696348; 18077166 Phenotypes for gene: NTRK1 were set to HSAN 4; Insensitivity to pain, congenital, with anhidrosis, 256800; Hereditary sensory neuropathy type IV