KCNH6 potassium voltage-gated channel subfamily H member 6
Information
- Symbol
- KCNH6
- Type
- protein-coding
- Description
- potassium voltage-gated channel subfamily H member 6
- Entrez Gene ID
- 81033
- Genome
- hg19
- Position
- chr17:61,600,764-61,624,088
- Genome
- hg38
- Position
- chr17:63,523,403-63,546,727
- MIM
- 608168 OMIM
- HGNC
- HGNC:18862 HGNC
- Ensembl
- ENSG00000173826 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 144 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
154 |
![]() |
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 | ERG-2 |
SYNONYM | ERG2 |
SYNONYM | HERG2 |
SYNONYM | Kv11.2 |
SYNONYM | hERG-2 |
MIM | 608168 OMIM |
HGNC | HGNC:18862 HGNC |
Ensembl | ENSG00000173826 Ensembl |
AllianceGenome | HGNC:18862 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000456941.6 | hg38 | chr17 | 63,523,334 | 63,546,032 | 22,699 |
ENST00000580652.5 | hg38 | chr17 | 63,523,357 | 63,536,213 | 12,857 |
ENST00000314672.10 | hg38 | chr17 | 63,523,358 | 63,546,727 | 23,370 |
ENST00000581784.5 | hg38 | chr17 | 63,523,334 | 63,548,977 | 25,644 |
ENST00000583023.1 | hg38 | chr17 | 63,523,403 | 63,546,727 | 23,325 |
ENST00000456941.6 | hg19 | chr17 | 61,600,695 | 61,623,393 | 22,699 |
ENST00000581784.5 | hg19 | chr17 | 61,600,695 | 61,626,338 | 25,644 |
ENST00000580652.5 | hg19 | chr17 | 61,600,718 | 61,613,574 | 12,857 |
ENST00000314672.10 | hg19 | chr17 | 61,600,719 | 61,624,088 | 23,370 |
ENST00000583023.1 | hg19 | chr17 | 61,600,764 | 61,624,088 | 23,325 |
Genome browser