Genomic Map
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Target Gene Details
Entrez Gene ID: | 79962 |
Gene Name: | DnaJ heat shock protein family (Hsp40) member C22 |
Gene Aliases: |
wus |
Location: |
Chr.12:49346917-49353684 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| DNAJC22 | NM_001304944.1 | 3 | 1191 | NP_001291873.1 |
| NM_024902.3 | 2 | 729 | NP_079178.2 | |
| XM_005269155.2 | 2 | 240 | XP_005269212.1 | |
| XM_005269156.2 | 2 | 240 | XP_005269213.1 | |
| XM_005269157.2 | 2 | 240 | XP_005269214.1 | |
| AK055747.1 | 3 | 1191 | ||
| BC033236.1 | 2 | 388 | AAH33236.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv832405 | Chr.12:49326496 - 49517079 on Build GRCh38 | Gain |
 TROAP
C1QL4
LOC100335030
DNAJC22
SPATS2
|
| dgv1497n100 | Chr.12:49284746 - 49438835 on Build GRCh38 | Gain |
PRPH
TROAP
C1QL4
LOC100335030
LOC101927267
DNAJC22
SPATS2
|
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Additional Information:
For this assay, SNP(s) [rs76011041] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
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