KCNJ14 potassium inwardly rectifying channel subfamily J member 14
Information
- Symbol
- KCNJ14
- Type
- protein-coding
- Description
- potassium inwardly rectifying channel subfamily J member 14
- Entrez Gene ID
- 3770
- Genome
- hg19
- Position
- chr19:48,964,506-48,970,237
- Genome
- hg38
- Position
- chr19:48,461,249-48,466,980
- MIM
- 603953 OMIM
- HGNC
- HGNC:6260 HGNC
- Ensembl
- ENSG00000182324 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
0 |
 |
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 | IRK4 |
| SYNONYM | KIR2.4 |
| MIM | 603953 OMIM |
| HGNC | HGNC:6260 HGNC |
| Ensembl | ENSG00000182324 Ensembl |
| AllianceGenome | HGNC:6260 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000391884.2 | hg38 | chr19 | 48,461,249 | 48,466,980 | 5,732 |
| ENST00000342291.3 | hg38 | chr19 | 48,455,574 | 48,466,980 | 11,407 |
| ENST00000342291.3 | hg19 | chr19 | 48,958,831 | 48,970,237 | 11,407 |
| ENST00000391884.2 | hg19 | chr19 | 48,964,506 | 48,970,237 | 5,732 |
Genome browser