Genomic Map
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Target Gene Details
Entrez Gene ID: | 28990 |
Gene Name: | asteroid homolog 1 (Drosophila) |
Gene Aliases: |
HT001 |
Location: |
Chr.3:131013873-131026854 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ASTE1 | NM_001288950.1 | NP_001275879.1 | ||
| NM_014065.3 | NP_054784.2 | |||
| NR_110229.1 | ||||
| XM_017006266.1 | XP_016861755.1 | |||
| XM_017006267.1 | XP_016861756.1 | |||
| XM_017006268.1 | XP_016861757.1 | |||
| XM_017006269.1 | XP_016861758.1 | |||
| AF113539.1 | AAF14876.1 | |||
| AK027258.1 | ||||
| AK027806.1 | BAB55383.1 | |||
| AK294156.1 | ||||
| AK301388.1 | ||||
| BC030274.1 | ||||
| BC103709.1 | AAI03710.1 | |||
| BC110616.2 | AAI10617.1 |
Target Gene Details
Entrez Gene ID: | 27032 |
Gene Name: | ATPase secretory pathway Ca2+ transporting 1 |
Gene Aliases: |
ATP2C1A, BCPM, HHD, PMR1, SPCA1, hSPCA1 |
Location: |
Chr.3:130850500-131016712 on Build GRCh38 |
Assay Gene Location: | Within Exon 31 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ATP2C1 | NM_001001485.2 | 28 | 3468 | NP_001001485.1 |
| NM_001001486.1 | 28 | 3270 | NP_001001486.1 | |
| NM_001001487.1 | 28 | 3240 | NP_001001487.1 | |
| NM_001199180.1 | 28 | 3458 | NP_001186109.1 | |
| NM_001199182.1 | 27 | 3371 | NP_001186111.1 | |
| NM_001199183.1 | 28 | 3331 | NP_001186112.1 | |
| NM_001199185.1 | 27 | 3287 | NP_001186114.1 | |
| XM_005247354.2 | 28 | 3513 | XP_005247411.1 | |
| XM_005247355.2 | 29 | 3640 | XP_005247412.1 | |
| XM_005247356.2 | 29 | 3393 | XP_005247413.1 | |
| XM_005247358.2 | 28 | 3217 | XP_005247415.1 | |
| XM_011512686.2 | 19 | 2322 | XP_011510988.1 | |
| XM_017006164.1 | 29 | 3271 | XP_016861653.1 | |
| AF225981.1 | 28 | 3214 | AAF35375.1 | |
| AK074692.1 | 26 | 2951 | BAC11142.1 | |
| AK296470.1 | 28 | 3385 | ||
| AK299945.1 | 27 | 3127 | ||
| AL833453.1 | 1 | 3516 | ||
| BC028139.1 | 27 | 3157 | AAH28139.1 |
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Set Membership: |
Intragenic
Exonic
Intronic
Non-exonic
non-DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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