Autonomic neuropathy
Gene: NTRK1EnsemblGeneIds (GRCh38): ENSG00000198400
EnsemblGeneIds (GRCh37): ENSG00000198400
OMIM: 191315, Gene2Phenotype
NTRK1 is in 11 panels
1 review
Alison Yeung (Victorian Clinical Genetics Services)
Sources: LiteratureCreated: 11 Nov 2020, 5:02 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
OMIM# 191315 NEUROTROPHIC TYROSINE KINASE, RECEPTOR, TYPE 1; NTRK1
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Literature
- Phenotypes
-
- OMIM# 191315 NEUROTROPHIC TYROSINE KINASE, RECEPTOR, TYPE 1
- NTRK1
- OMIM
- 191315
- Clinvar variants
- Variants in NTRK1
- Penetrance
- None
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Alison Yeung (Victorian Clinical Genetics Services)Gene: ntrk1 has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Alison Yeung (Victorian Clinical Genetics Services)Gene: ntrk1 has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Alison Yeung (Victorian Clinical Genetics Services)gene: NTRK1 was added gene: NTRK1 was added to Autonomic neuropathy. Sources: Literature Mode of inheritance for gene: NTRK1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: NTRK1 were set to OMIM# 191315 NEUROTROPHIC TYROSINE KINASE, RECEPTOR, TYPE 1; NTRK1 Review for gene: NTRK1 was set to GREEN