Genomic Map
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Target Gene Details
Entrez Gene ID: | 1410 |
Gene Name: | crystallin alpha B |
Gene Aliases: |
CMD1II, CRYA2, CTPP2, CTRCT16, HEL-S-101, HSPB5, MFM2 |
Location: |
Chr.11:111908620-111913213 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 5 - Exon 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CRYAB | NM_001289807.1 | NP_001276736.1 | ||
| NM_001289808.1 | NP_001276737.1 | |||
| NM_001885.2 | NP_001876.1 | |||
| XM_011542608.1 | XP_011540910.1 | |||
| XM_011542609.2 | XP_011540911.1 | |||
| AF007162.1 | AAC19161.1 | |||
| AK314029.1 | ||||
| BC007008.1 | AAH07008.1 | |||
| BI759672.1 | ||||
| BM721803.1 | ||||
| BT006770.1 | AAP35416.1 | |||
| FJ224314.1 | ||||
| FJ876064.1 | ||||
| KM220603.1 | ||||
| KM220604.1 | ||||
| KM220605.1 | ||||
| KM220606.1 | ||||
| KM220607.1 | ||||
| M24906.1 | AAA60267.1 | |||
| S45630.1 | AAB23453.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv482162 | Chr.11:111908626 - 111911749 on Build GRCh38 | Loss |
 CRYAB
|
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Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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