Genomic Map
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Target Gene Details
Entrez Gene ID: | 9382 |
Gene Name: | component of oligomeric golgi complex 1 |
Gene Aliases: |
CDG2G, LDLB |
Location: |
Chr.17:73193034-73208507 on Build GRCh38 |
Assay Gene Location: | Within Intron 13 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| COG1 | NM_018714.2 | NP_061184.1 | ||
| AB037802.1 | 13 | 3627 | BAA92619.1 | |
| AK025633.1 | ||||
| AK098224.1 | ||||
| AL359611.1 | CAB94881.1 | |||
| BC021985.2 | AAH21985.1 | |||
| BC047465.1 | AAH47465.1 |
Target Gene Details
Entrez Gene ID: | 84923 |
Gene Name: | family with sequence similarity 104 member A |
Gene Aliases: |
- |
Location: |
Chr.17:73207353-73232394 on Build GRCh38 |
Assay Gene Location: | Within Exon 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FAM104A | NM_001098832.1 | 4 | 2161 | NP_001092302.1 |
| NM_001289410.1 | 2 | 1998 | NP_001276339.1 | |
| NM_001289411.1 | 3 | 2016 | NP_001276340.1 | |
| NM_001289412.1 | 4 | 1934 | NP_001276341.1 | |
| NM_032837.2 | 3 | 2098 | NP_116226.2 | |
| AK027681.1 | 3 | 1983 | BAB55292.1 | |
| AK074755.1 | 3 | 1984 | BAC11183.1 | |
| BC011054.1 | 3 | 1823 | AAH11054.1 | |
| BC025238.1 | 3 | 1861 | AAH25238.1 | |
| BX537858.1 | 4 | 2065 | ||
| BX648968.1 | 5 | 2077 |
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 |
 CPSF4L
SSTR2
SDK2
C17orf80
FAM104A
CDC42EP4
COG1
|
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Additional Information:
For this assay, SNP(s) [rs76058650] 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
Intronic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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