Genomic Map
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Target Gene Details
Entrez Gene ID: | 57096 |
Gene Name: | retinitis pigmentosa GTPase regulator interacting protein 1 |
Gene Aliases: |
CORD13, LCA6, RGI1, RGRIP, RPGRIP, RPGRIP1d |
Location: |
Chr.14:21287977-21351316 on Build GRCh38 |
Assay Gene Location: | Within Exon 10 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RPGRIP1 | NM_020366.3 | 10 | 1269 | NP_065099.3 |
| XM_005267879.2 | 1 | 261 | XP_005267936.1 | |
| XM_005267880.2 | 1 | 261 | XP_005267937.1 | |
| XM_011536978.1 | 1 | 261 | XP_011535280.1 | |
| XM_011536979.1 | 1 | 261 | XP_011535281.1 | |
| XM_011536980.1 | 1 | 261 | XP_011535282.1 | |
| XM_011536981.1 | 1 | 261 | XP_011535283.1 | |
| XM_011536982.1 | 1 | 261 | XP_011535284.1 | |
| XM_017021473.1 | 1 | 261 | XP_016876962.1 | |
| AF260257.1 | 1 | 222 | AAF91371.1 | |
| AJ417067.1 | 10 | 1269 | CAD01135.1 | |
| AK301780.1 | 1 | 275 | ||
| BC039089.1 | 1 | 260 | AAH39089.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1054778 | Chr.14:21294781 - 21334420 on Build GRCh38 | Gain |
 RPGRIP1
|
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Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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