DNAJC19 DnaJ heat shock protein family (Hsp40) member C19
Information
- Symbol
- DNAJC19
- Type
- protein-coding
- Description
- DnaJ heat shock protein family (Hsp40) member C19
- Entrez Gene ID
- 131118
- Genome
- hg19
- Position
- chr3:180,701,497-180,707,524
- Genome
- hg38
- Position
- chr3:180,983,709-180,989,736
- MIM
- 608977 OMIM
- HGNC
- HGNC:30528 HGNC
- Ensembl
- ENSG00000205981 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 18 |
Likely pathogenic | 1 | 18 |
Benign | 0 | 24 |
Likely benign | 0 | 104 |
Conflicting classifications of pathogenicity | 0 | 10 |
not provided | 0 | 2 |
Uncertain significance | 0 | 96 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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34 |
![]() |
212 |
![]() |
4 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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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
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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 | PAM18 |
SYNONYM | TIM14 |
SYNONYM | TIMM14 |
MIM | 608977 OMIM |
HGNC | HGNC:30528 HGNC |
Ensembl | ENSG00000205981 Ensembl |
AllianceGenome | HGNC:30528 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000382564.8 | hg38 | chr3 | 180,983,709 | 180,989,736 | 6,028 |
ENST00000486355.1 | hg38 | chr3 | 180,984,275 | 180,989,769 | 5,495 |
ENST00000491873.5 | hg38 | chr3 | 180,984,278 | 180,989,710 | 5,433 |
ENST00000688055.1 | hg38 | chr3 | 180,983,922 | 180,989,741 | 5,820 |
ENST00000646965.1 | hg38 | chr3 | 180,984,526 | 180,989,667 | 5,142 |
ENST00000479269.5 | hg38 | chr3 | 180,984,565 | 180,989,518 | 4,954 |
ENST00000382564.8 | hg19 | chr3 | 180,701,497 | 180,707,524 | 6,028 |
ENST00000688055.1 | hg19 | chr3 | 180,701,710 | 180,707,529 | 5,820 |
ENST00000486355.1 | hg19 | chr3 | 180,702,063 | 180,707,557 | 5,495 |
ENST00000491873.5 | hg19 | chr3 | 180,702,066 | 180,707,498 | 5,433 |
ENST00000646965.1 | hg19 | chr3 | 180,702,314 | 180,707,455 | 5,142 |
ENST00000479269.5 | hg19 | chr3 | 180,702,353 | 180,707,306 | 4,954 |
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