Genomic Map
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Target Gene Details
Entrez Gene ID: | 535 |
Gene Name: | ATPase H+ transporting V0 subunit a1 |
Gene Aliases: |
ATP6N1, ATP6N1A, Stv1, VPP1, Vph1, a1 |
Location: |
Chr.17:42458844-42522579 on Build GRCh38 |
Assay Gene Location: | Within Exon 21 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ATP6V0A1 | NM_001130020.1 | 20 | 2472 | NP_001123492.1 |
| NM_001130021.1 | 21 | 2469 | NP_001123493.1 | |
| NM_005177.3 | 20 | 2451 | NP_005168.2 | |
| XM_005257459.1 | 21 | 2472 | XP_005257516.1 | |
| XM_005257461.1 | XP_005257518.1 | |||
| XM_005257463.2 | XP_005257520.1 | |||
| XM_011524908.1 | 19 | 2346 | XP_011523210.1 | |
| XM_017024766.1 | 21 | 2472 | XP_016880255.1 | |
| XM_017024767.1 | 21 | 2435 | XP_016880256.1 | |
| XM_017024768.1 | 20 | 2417 | XP_016880257.1 | |
| XM_017024769.1 | 19 | 2309 | XP_016880258.1 | |
| XM_017024770.1 | XP_016880259.1 | |||
| XM_017024771.1 | XP_016880260.1 | |||
| XM_017024772.1 | 20 | 2282 | XP_016880261.1 | |
| XM_017024773.1 | 20 | 2863 | XP_016880262.1 | |
| XM_017024774.1 | 20 | 2445 | XP_016880263.1 | |
| AK223554.1 | 20 | 2418 | BAD97274.1 | |
| AK294512.1 | 20 | 2296 | ||
| AK294789.1 | 17 | 1950 | ||
| AK295682.1 | 20 | 2375 | ||
| AK299784.1 | 19 | 2290 | ||
| AK316305.1 | 20 | 2442 | ||
| AL137683.1 | 3 | 465 | CAB70874.1 | |
| BC032398.1 | 21 | 2401 | AAH32398.1 | |
| BX648978.1 | 20 | 2434 | CAI56709.1 | |
| CR627443.1 | 14 | 1377 | CAH10528.1 | |
| L78933.1 | 20 | 2453 | AAL77442.1 | |
| Z71460.1 | 20 | 2453 | CAA96077.1 |
Target Gene Details
Entrez Gene ID: | 100847046 |
Gene Name: | microRNA 5010 |
Gene Aliases: |
mir-5010 |
Location: |
Chr.17:42514188-42514307 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MIR5010 | NR_049808.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1064012 | Chr.17:42427786 - 42606703 on Build GRCh38 | Gain |
 HSD17B1
PSMC3IP
NAGLU
COASY
ATP6V0A1
MIR5010
MIR548AT
FAM134C
MLX
|
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Set Membership: |
Intragenic
Exonic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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