Genomic Map
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Target Gene Details
Entrez Gene ID: | 83857 |
Gene Name: | transmembrane and tetratricopeptide repeat containing 1 |
Gene Aliases: |
ARG99, OLF, TMTC1A |
Location: |
Chr.12:29500813-29784759 on Build GRCh38 |
Assay Gene Location: | Within Exon 23 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TMTC1 | NM_001193451.1 | 18 | 8630 | NP_001180380.1 |
| NM_175861.3 | 18 | 8721 | NP_787057.2 | |
| XM_005253499.4 | 20 | 8882 | XP_005253556.1 | |
| XM_017020003.1 | 19 | 8715 | XP_016875492.1 | |
| XM_017020004.1 | 19 | 8675 | XP_016875493.1 | |
| XM_017020005.1 | 17 | 8488 | XP_016875494.1 | |
| XM_017020007.1 | 16 | 7908 | XP_016875496.1 | |
| AF433169.1 | 1 | 1654 | AAQ04260.1 | |
| BG413338.1 | 1 | 121 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv469190 | Chr.12:29459492 - 29658538 on Build GRCh38 | Gain |
 OVCH1
OVCH1-AS1
TMTC1
|
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Additional Information:
For this assay, SNP(s) [rs68017043] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Gene Ontology Categories:
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