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Entrez Gene ID: | 116984 |
Gene Name: | ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2 |
Gene Aliases: |
CENTD1, PARX |
Location: |
Chr.4:36005404-36244784 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 2 - Exon 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ARAP2 | NM_015230.4 | NP_056045.2 | ||
| NR_146894.2 | ||||
| XM_047449571.1 | XP_047305527.1 | |||
| XM_047449572.1 | XP_047305528.1 | |||
| XM_047449573.1 | XP_047305529.1 | |||
| XM_047449574.1 | XP_047305530.1 | |||
| XM_047449575.1 | XP_047305531.1 | |||
| XM_047449576.1 | XP_047305532.1 | |||
| AW274408.1 | ||||
| AY049733.1 | AAL12170.1 | |||
| CB992251.1 |
Entrez Gene ID: | 439933 |
Gene Name: | uncharacterized LOC439933 |
Gene Aliases: |
- |
Location: |
Chr.4:36244116-36274215 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 1 - Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LOC439933 | NR_122079.1 |
DGV Version: |
Release date: 2025-12-01, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3600217 | Chr.4:36111290 - 36503831 on Build GRCh38 | Loss |
|
| nsv5459508 | Chr.4:36111339 - 36503870 on Build GRCh38 | Deletion |
|
| nsv829907 | Chr.4:36158672 - 36317960 on Build GRCh38 | Gain |
|
| nsv4108087 | Chr.4:34556437 - 36507744 on Build GRCh38 | Deletion |
|
| esv3569373 | Chr.4:35669991 - 36407345 on Build GRCh38 | Loss |
|
Set Membership: |
|