Genomic Map
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Target Gene Details
Entrez Gene ID: | 55028 |
Gene Name: | chromosome 17 open reading frame 80 |
Gene Aliases: |
HLC-8, MIG3, SPEP1 |
Location: |
Chr.17:73232233-73248959 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 3 - Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| C17orf80 | NM_001100621.2 | NP_001094091.1 | ||
| NM_001100622.2 | NP_001094092.1 | |||
| NM_001288770.1 | NP_001275699.1 | |||
| NM_001288771.1 | NP_001275700.1 | |||
| NM_017941.5 | NP_060411.2 | |||
| NR_110105.1 | ||||
| XM_005257487.3 | XP_005257544.1 | |||
| XM_006721966.3 | XP_006722029.1 | |||
| XM_011524961.1 | XP_011523263.1 | |||
| XM_017024806.1 | XP_016880295.1 | |||
| AK000728.1 | BAA91344.1 | |||
| AK292838.1 | ||||
| AK301905.1 | ||||
| AL136740.1 | CAB66674.1 | |||
| AY163812.1 | AAO25513.1 | |||
| BC005005.2 | AAH05005.1 | |||
| BG754800.1 | ||||
| DC372573.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833534 | Chr.17:73155642 - 73349355 on Build GRCh38 | Loss |
 C17orf80
COG1
FAM104A
CDC42EP4
SSTR2
CPSF4L
SDK2
|
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Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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