CMTM3 CKLF like MARVEL transmembrane domain containing 3
Information
- Symbol
- CMTM3
- Type
- protein-coding
- Description
- CKLF like MARVEL transmembrane domain containing 3
- Entrez Gene ID
- 123920
- Genome
- hg19
- Position
- chr16:66,637,935-66,647,795
- Genome
- hg38
- Position
- chr16:66,604,032-66,613,892
- MIM
- 607886 OMIM
- HGNC
- HGNC:19174 HGNC
- Ensembl
- ENSG00000140931 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 14 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
14 |
 |
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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| Category | : |
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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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| Category | : |
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| 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 | BNAS2 |
| SYNONYM | CKLFSF3 |
| MIM | 607886 OMIM |
| HGNC | HGNC:19174 HGNC |
| Ensembl | ENSG00000140931 Ensembl |
| AllianceGenome | HGNC:19174 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000361909.8 | hg38 | chr16 | 66,604,276 | 66,613,892 | 9,617 |
| ENST00000424011.6 | hg38 | chr16 | 66,604,032 | 66,613,892 | 9,861 |
| ENST00000564060.5 | hg38 | chr16 | 66,604,732 | 66,612,934 | 8,203 |
| ENST00000568477.5 | hg38 | chr16 | 66,605,273 | 66,612,768 | 7,496 |
| ENST00000460097.5 | hg38 | chr16 | 66,604,310 | 66,613,892 | 9,583 |
| ENST00000565666.5 | hg38 | chr16 | 66,604,341 | 66,610,060 | 5,720 |
| ENST00000567572.6 | hg38 | chr16 | 66,604,704 | 66,613,887 | 9,184 |
| ENST00000565922.1 | hg38 | chr16 | 66,604,732 | 66,613,478 | 8,747 |
| ENST00000566121.1 | hg38 | chr16 | 66,605,521 | 66,612,760 | 7,240 |
| ENST00000565003.5 | hg38 | chr16 | 66,604,895 | 66,611,061 | 6,167 |
| ENST00000562707.5 | hg38 | chr16 | 66,604,157 | 66,612,701 | 8,545 |
| ENST00000424011.6 | hg19 | chr16 | 66,637,935 | 66,647,795 | 9,861 |
| ENST00000562707.5 | hg19 | chr16 | 66,638,060 | 66,646,604 | 8,545 |
| ENST00000361909.8 | hg19 | chr16 | 66,638,179 | 66,647,795 | 9,617 |
| ENST00000460097.5 | hg19 | chr16 | 66,638,213 | 66,647,795 | 9,583 |
| ENST00000565666.5 | hg19 | chr16 | 66,638,244 | 66,643,963 | 5,720 |
| ENST00000567572.6 | hg19 | chr16 | 66,638,607 | 66,647,790 | 9,184 |
| ENST00000564060.5 | hg19 | chr16 | 66,638,635 | 66,646,837 | 8,203 |
| ENST00000565922.1 | hg19 | chr16 | 66,638,635 | 66,647,381 | 8,747 |
| ENST00000565003.5 | hg19 | chr16 | 66,638,798 | 66,644,964 | 6,167 |
| ENST00000568477.5 | hg19 | chr16 | 66,639,176 | 66,646,671 | 7,496 |
| ENST00000566121.1 | hg19 | chr16 | 66,639,424 | 66,646,663 | 7,240 |
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