1. Panels
  2. Pain syndromes
  3. NGF
STRs in panel
Prev Next
Regions in panel
Prev Next

Pain syndromes

Gene: NGF

Green List (high evidence)
NGF (nerve growth factor)
EnsemblGeneIds (GRCh38): ENSG00000134259
EnsemblGeneIds (GRCh37): ENSG00000134259
OMIM: 162030, Gene2Phenotype
NGF is in 7 panels

0 reviews

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Neuropathy, hereditary sensory and autonomic, type V, 608654
  • HSAN 5
  • Congenital sensory neuropathy with selective loss of small myelinated fibers
  • Hereditary sensory neuropathy type V
OMIM
162030
Clinvar variants
Variants in NGF
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 Neuropathy, hereditary sensory and autonomic, type V, 608654; HSAN 5; Congenital sensory neuropathy with selective loss of small myelinated fibers; Hereditary sensory neuropathy type V for gene: NGF

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: NGF was added gene: NGF was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green Mode of inheritance for gene: NGF was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: NGF were set to 26562335; 20978020; 14976160; 15131306 Phenotypes for gene: NGF were set to Neuropathy, hereditary sensory and autonomic, type V, 608654; HSAN 5; Congenital sensory neuropathy with selective loss of small myelinated fibers; Hereditary sensory neuropathy type V