KCNG3 potassium voltage-gated channel modifier subfamily G member 3
Information
- Symbol
- KCNG3
- Type
- protein-coding
- Description
- potassium voltage-gated channel modifier subfamily G member 3
- Entrez Gene ID
- 170850
- Genome
- hg19
- Position
- chr2:42,669,157-42,721,122
- Genome
- hg38
- Position
- chr2:42,442,017-42,493,982
- MIM
- 606767 OMIM
- HGNC
- HGNC:18306 HGNC
- Ensembl
- ENSG00000171126 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
22 |
![]() |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | KV10.1 |
SYNONYM | KV6.3 |
MIM | 606767 OMIM |
HGNC | HGNC:18306 HGNC |
Ensembl | ENSG00000171126 Ensembl |
AllianceGenome | HGNC:18306 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000306078.2 | hg38 | chr2 | 42,442,017 | 42,493,982 | 51,966 |
ENST00000394973.4 | hg38 | chr2 | 42,442,032 | 42,493,977 | 51,946 |
ENST00000306078.2 | hg19 | chr2 | 42,669,157 | 42,721,122 | 51,966 |
ENST00000394973.4 | hg19 | chr2 | 42,669,172 | 42,721,117 | 51,946 |
Genome browser