CLEC4F C-type lectin domain family 4 member F
Information
- Symbol
- CLEC4F
- Type
- protein-coding
- Description
- C-type lectin domain family 4 member F
- Entrez Gene ID
- 165530
- Genome
- hg19
- Position
- chr2:71,035,775-71,047,731
- Genome
- hg38
- Position
- chr2:70,808,643-70,820,599
- MIM
- 620105 OMIM
- HGNC
- HGNC:25357 HGNC
- Ensembl
- ENSG00000152672 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 58 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
74 |
![]() |
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 | CLECSF13 |
SYNONYM | KCLR |
SYNONYM | KCR |
MIM | 620105 OMIM |
HGNC | HGNC:25357 HGNC |
Ensembl | ENSG00000152672 Ensembl |
AllianceGenome | HGNC:25357 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000426626.1 | hg38 | chr2 | 70,808,813 | 70,820,547 | 11,735 |
ENST00000272367.7 | hg38 | chr2 | 70,808,643 | 70,820,599 | 11,957 |
ENST00000272367.7 | hg19 | chr2 | 71,035,775 | 71,047,731 | 11,957 |
ENST00000426626.1 | hg19 | chr2 | 71,035,945 | 71,047,679 | 11,735 |
Genome browser