Genomic Map
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Target Gene Details
Entrez Gene ID: | 25829 |
Gene Name: | transmembrane protein 184B |
Gene Aliases: |
C22orf5, FM08, HS5O6A, HSPC256 |
Location: |
Chr.22:38216045-38273034 on Build GRCh38 |
Assay Gene Location: | Within Exon 13 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TMEM184B | NM_001195071.1 | 9 | 2771 | NP_001182000.1 |
| NM_001195072.1 | 10 | 2857 | NP_001182001.1 | |
| NM_012264.4 | 9 | 2756 | NP_036396.2 | |
| XM_011530112.2 | 10 | 2826 | XP_011528414.2 | |
| XM_011530113.1 | 9 | 2771 | XP_011528415.1 | |
| XM_011530114.1 | 9 | 2803 | XP_011528416.1 | |
| XM_011530115.2 | 8 | 2562 | XP_011528417.1 | |
| XM_011530116.2 | XP_011528418.2 | |||
| XM_011530117.1 | 10 | 2869 | XP_011528419.1 | |
| XM_011530118.1 | 10 | 2843 | XP_011528420.1 | |
| XM_011530119.1 | 8 | 2597 | XP_011528421.1 | |
| XM_017028754.1 | 9 | 2842 | XP_016884243.1 | |
| XM_017028755.1 | 9 | 2799 | XP_016884244.1 | |
| XM_017028756.1 | 10 | 2756 | XP_016884245.1 | |
| XM_017028757.1 | 9 | 2544 | XP_016884246.1 | |
| XM_017028758.1 | XP_016884247.1 | |||
| XM_017028759.1 | 8 | 2561 | XP_016884248.1 | |
| AB097053.1 | 9 | 2727 | BAC77406.1 | |
| AF161374.1 | 1 | 970 | AAF28934.1 | |
| AK075417.1 | 7 | 2244 | BAC11607.1 | |
| AK095109.1 | 1 | 3076 | ||
| AL096879.1 | 8 | 2449 | CAB51403.1 | |
| AL117649.1 | 1 | 1332 | ||
| BC015489.1 | 9 | 2712 | AAH15489.2 | |
| BX648345.1 | 9 | 2807 | CAH56159.1 | |
| CR627445.1 | 1 | 3958 | CAH10529.1 | |
| CR749859.1 | 10 | 2763 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv834194 | Chr.22:38063495 - 38240504 on Build GRCh38 | Loss |
 BAIAP2L2
MAFF
PLA2G6
PICK1
TMEM184B
SLC16A8
SNORA92
|
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Additional Information:
For this assay, SNP(s) [rs75292970] 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
|
Panther Classification:
Gene Ontology Categories:
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