KLC4 kinesin light chain 4
Information
- Symbol
- KLC4
- Type
- protein-coding
- Description
- kinesin light chain 4
- Entrez Gene ID
- 89953
- Genome
- hg19
- Position
- chr6:43,027,595-43,042,831
- Genome
- hg38
- Position
- chr6:43,059,857-43,075,093
- HGNC
- HGNC:21624 HGNC
- Ensembl
- ENSG00000137171 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely pathogenic | 0 | 2 |
| Benign | 0 | 2 |
| Uncertain significance | 0 | 84 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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88 |
![]() |
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
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| 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
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| 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
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| Category | : |
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| 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 | KNSL8 |
| SYNONYM | bA387M24.3 |
| HGNC | HGNC:21624 HGNC |
| Ensembl | ENSG00000137171 Ensembl |
| AllianceGenome | HGNC:21624 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000259708.7 | hg38 | chr6 | 43,059,857 | 43,075,093 | 15,237 |
| ENST00000394056.6 | hg38 | chr6 | 43,059,895 | 43,075,087 | 15,193 |
| ENST00000458460.6 | hg38 | chr6 | 43,059,653 | 43,067,397 | 7,745 |
| ENST00000479388.5 | hg38 | chr6 | 43,059,883 | 43,075,089 | 15,207 |
| ENST00000347162.10 | hg38 | chr6 | 43,059,631 | 43,075,093 | 15,463 |
| ENST00000453940.6 | hg38 | chr6 | 43,059,631 | 43,074,908 | 15,278 |
| ENST00000453940.6 | hg19 | chr6 | 43,027,369 | 43,042,646 | 15,278 |
| ENST00000347162.10 | hg19 | chr6 | 43,027,369 | 43,042,831 | 15,463 |
| ENST00000394056.6 | hg19 | chr6 | 43,027,633 | 43,042,825 | 15,193 |
| ENST00000458460.6 | hg19 | chr6 | 43,027,391 | 43,035,135 | 7,745 |
| ENST00000259708.7 | hg19 | chr6 | 43,027,595 | 43,042,831 | 15,237 |
| ENST00000479388.5 | hg19 | chr6 | 43,027,621 | 43,042,827 | 15,207 |
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