1. Panels
  2. Genomic imprinting
  3. SEPT4
Genes in panel
Prev Next
STRs in panel
Prev Next
Regions in panel
Prev Next

Genomic imprinting

Gene: SEPT4

Red List (low evidence)
SEPT4 (septin 4)
EnsemblGeneIds (GRCh38): ENSG00000108387
EnsemblGeneIds (GRCh37): ENSG00000108387
OMIM: 603696, Gene2Phenotype
SEPT4 is in 0 panels

1 review

Sarah Leigh (Genomics England Curator)

I don't know

Circadian expression reported in CircaDB (http://circadb.hogeneschlab.org/human)
Created: 22 Dec 2020, 6:10 p.m. | Last Modified: 22 Dec 2020, 6:10 p.m.
Panel Version: 0.26
SEPT4 is the previous gene name, the current HGNC approved name is SEPTIN4
Created: 22 Dec 2020, 12:22 p.m. | Last Modified: 22 Dec 2020, 12:22 p.m.
Panel Version: 0.24
Created: 22 Dec 2020, 12:22 p.m.
Last Modified: 22 Dec 2020, 12:22 p.m.
Panel version: 0.26

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
Sources
  • Literature
Tags
new-gene-name
OMIM
603696
Clinvar variants
Variants in SEPT4
Penetrance
None
Publications
Panels with this gene

History Filter Activity

22 Dec 2020, Gel status: 1

Added Tag

Sarah Leigh (Genomics England Curator)

Tag new-gene-name tag was added to gene: SEPT4.

22 Dec 2020, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications

Sarah Leigh (Genomics England Curator)

gene: SEPT4 was added gene: SEPT4 was added to Imprinted Genes. Sources: Literature Mode of inheritance for gene: SEPT4 was set to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed) Publications for gene: SEPT4 were set to 30794780; 26769960