Assay Details
Target Gene Details
Entrez Gene ID: | 9854 |
Gene Name: | C2CD2 like |
Gene Aliases: |
DLNB23, TMEM24 |
Location: |
Chr.11:119107061-119118543 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 7 - Exon 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| C2CD2L | NM_001290474.1 | NP_001277403.1 | ||
| NM_014807.4 | NP_055622.3 | |||
| XM_006718948.3 | XP_006719011.1 | |||
| XM_011543076.2 | XP_011541378.1 | |||
| XM_017018625.1 | XP_016874114.1 | |||
| XM_017018626.1 | XP_016874115.1 | |||
| XM_017018627.1 | XP_016874116.1 | |||
| XM_017018628.1 | XP_016874117.1 | |||
| AB006623.2 | BAA22954.2 | |||
| AB094094.1 | BAC76048.1 | |||
| AK025223.1 | ||||
| BC010071.2 | AAH10071.2 | |||
| BC021254.2 | AAH21254.2 | |||
| BC022219.1 | AAH22219.1 | |||
| BC033083.1 | AAH33083.1 | |||
| BC075832.1 | AAH75832.1 | |||
| BX537572.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv556466 | Chr.11:119106009 - 119188695 on Build GRCh38 | Loss |
|
More Information
Set Membership: |
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Genomic Map