CMTM4 CKLF like MARVEL transmembrane domain containing 4
Information
- Symbol
- CMTM4
- Type
- protein-coding
- Description
- CKLF like MARVEL transmembrane domain containing 4
- Entrez Gene ID
- 146223
- Genome
- hg19
- Position
- chr16:66,648,653-66,730,610
- Genome
- hg38
- Position
- chr16:66,614,750-66,696,707
- MIM
- 607887 OMIM
- HGNC
- HGNC:19175 HGNC
- Ensembl
- ENSG00000183723 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
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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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| 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 | CKLFSF4 |
| MIM | 607887 OMIM |
| HGNC | HGNC:19175 HGNC |
| Ensembl | ENSG00000183723 Ensembl |
| AllianceGenome | HGNC:19175 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000394106.7 | hg38 | chr16 | 66,614,750 | 66,696,743 | 81,994 |
| ENST00000330687.8 | hg38 | chr16 | 66,614,750 | 66,696,707 | 81,958 |
| ENST00000563952.1 | hg38 | chr16 | 66,621,757 | 66,696,707 | 74,951 |
| ENST00000330687.8 | hg19 | chr16 | 66,648,653 | 66,730,610 | 81,958 |
| ENST00000394106.7 | hg19 | chr16 | 66,648,653 | 66,730,646 | 81,994 |
| ENST00000563952.1 | hg19 | chr16 | 66,655,660 | 66,730,610 | 74,951 |
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