Genomic Map
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Target Gene Details
Entrez Gene ID: | 11322 |
Gene Name: | transmembrane channel like 6 |
Gene Aliases: |
EV1, EVER1, EVIN1, LAK-4P |
Location: |
Chr.17:78108775-78132427 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TMC6 | NM_007267.7 | NP_009198.4 | ||
| BC023597.2 | AAH23597.1 | |||
| HY057592.1 |
Target Gene Details
Entrez Gene ID: | 147138 |
Gene Name: | transmembrane channel like 8 |
Gene Aliases: |
EV2, EVER2, EVIN2 |
Location: |
Chr.17:78129296-78142968 on Build GRCh38 |
Assay Gene Location: | Within Exon 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TMC8 | NM_152468.4 | 4 | 718 | NP_689681.2 |
| XM_011524402.2 | 4 | 2196 | XP_011522704.1 | |
| XM_011524403.2 | 4 | 2195 | XP_011522705.1 | |
| XM_011524404.2 | 4 | 2195 | XP_011522706.1 | |
| XM_011524406.2 | 4 | 2198 | XP_011522708.1 | |
| XM_011524409.2 | 4 | 2200 | XP_011522711.1 | |
| XM_011524410.2 | 4 | 2198 | XP_011522712.1 | |
| XM_011524411.2 | 4 | 2198 | XP_011522713.1 | |
| XM_017024238.1 | 4 | 2197 | XP_016879727.1 | |
| XM_017024239.1 | 4 | 2197 | XP_016879728.1 | |
| XM_017024240.1 | 4 | 2197 | XP_016879729.1 | |
| XM_017024241.1 | 4 | 2196 | XP_016879730.1 | |
| XM_017024244.1 | 4 | 2198 | XP_016879733.1 | |
| AK090478.1 | 4 | 678 | ||
| AK303499.1 | 4 | 717 | ||
| AK310623.1 | 4 | 904 | ||
| AY057380.1 | 3 | 336 | AAL25837.1 | |
| AY099358.1 | 4 | 708 | AAM44454.1 | |
| AY099359.1 | 3 | 227 | AAM44455.1 | |
| AY236500.1 | 3 | 405 | AAP69878.1 | |
| BC110296.1 | 4 | 710 | AAI10297.1 | |
| BC141865.1 | 3 | 562 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833554 | Chr.17:77977426 - 78151914 on Build GRCh38 | Gain+Loss |
 TNRC6C-AS1
TMC6
C17orf99
TMC8
TNRC6C
|
| nsv470607 | Chr.17:78121280 - 78177341 on Build GRCh38 | Loss |
TMC6
TK1
C17orf99
SYNGR2
TMC8
|
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Set Membership: |
Intragenic
Exonic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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