DNAJC2 DnaJ heat shock protein family (Hsp40) member C2
Information
- Symbol
- DNAJC2
- Type
- protein-coding
- Description
- DnaJ heat shock protein family (Hsp40) member C2
- Entrez Gene ID
- 27000
- Genome
- hg19
- Position
- chr7:102,952,736-102,985,214
- Genome
- hg38
- Position
- chr7:103,312,289-103,344,767
- MIM
- 605502 OMIM
- HGNC
- HGNC:13192 HGNC
- Ensembl
- ENSG00000105821 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Uncertain significance | 0 | 62 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
64 |
 |
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 | MPHOSPH11 |
| SYNONYM | MPP11 |
| SYNONYM | ZRF1 |
| SYNONYM | ZUO1 |
| MIM | 605502 OMIM |
| HGNC | HGNC:13192 HGNC |
| Ensembl | ENSG00000105821 Ensembl |
| AllianceGenome | HGNC:13192 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000412522.1 | hg38 | chr7 | 103,335,242 | 103,344,830 | 9,589 |
| ENST00000379263.8 | hg38 | chr7 | 103,312,289 | 103,344,767 | 32,479 |
| ENST00000249270.11 | hg38 | chr7 | 103,312,474 | 103,344,666 | 32,193 |
| ENST00000379263.8 | hg19 | chr7 | 102,952,736 | 102,985,214 | 32,479 |
| ENST00000249270.11 | hg19 | chr7 | 102,952,921 | 102,985,113 | 32,193 |
| ENST00000412522.1 | hg19 | chr7 | 102,975,689 | 102,985,277 | 9,589 |
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