KCNV2 |
- 30
Haplo
Score - -5
Triplo
Score
Gene Facts External Data Attribution
- HGNC Symbol
- KCNV2 (HGNC:19698) HGNC Entrez Ensembl OMIM UCSC Uniprot GeneReviews LOVD LSDB ClinVar
- HGNC Name
- potassium voltage-gated channel modifier subfamily V member 2
- Gene type
- protein-coding gene
- Locus type
- gene with protein product
- Previous symbols
- No previous names found
- Alias symbols
- Kv8.2
- %HI
- 44.67(Read more about the DECIPHER Haploinsufficiency Index)
- pLI
- 0(Read more about gnomAD pLI score)
- LOEUF
- 1.96(Read more about gnomAD LOEUF score)
- Cytoband
- 9p24.2
- Genomic Coordinates
-
GRCh37/hg19: chr9:2717510-2730037 NCBI Ensembl UCSC GRCh38/hg38: chr9:2717510-2730037 NCBI Ensembl UCSC - MANE Select Transcript
- NM_133497.4 ENST00000382082.4 (Read more about MANE Select)
- Function
- Potassium channel subunit. Modulates channel activity by shifting the threshold and the half-maximal activation to more negative values. (Source: Uniprot)
Dosage Sensitivity Summary (Gene)
Dosage ID:
ISCA-26136
ClinGen Curation ID:
CCID:007357
Curation Status:
Complete
Issue Type:
Dosage Curation -
Gene
Haploinsufficiency:
Gene Associated with Autosomal Recessive Phenotype
(30)
Triplosensitivity:
Not Yet Evaluated
Last Evaluated:
08/22/2016
Haploinsufficiency (HI) Score Details
HI Score:
30
HI Evidence Strength:
Gene Associated with Autosomal Recessive Phenotype
(Disclaimer)
HI Disease:
- cone dystrophy with supernormal rod response Monarch
Triplosensitivity (TS) Score Details
TS Evidence Strength:
Not Yet Evaluated (Disclaimer)
Genomic View
Select assembly:
(NC_000009.11)
(NC_000009.12)