Genomic Map
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Target Gene Details
Entrez Gene ID: | 9577 |
Gene Name: | brain and reproductive organ-expressed (TNFRSF1A modulator) |
Gene Aliases: |
BRCC4, BRCC45 |
Location: |
Chr.2:27890615-28338901 on Build GRCh38 |
Assay Gene Location: | Within Intron 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BRE | NM_001261840.1 | NP_001248769.1 | ||
| NM_004899.4 | NP_004890.2 | |||
| NM_199191.2 | NP_954661.1 | |||
| NM_199192.2 | NP_954662.1 | |||
| NM_199193.2 | NP_954663.1 | |||
| NM_199194.2 | NP_954664.1 | |||
| AF015767.1 | AAB69387.1 | |||
| AF420602.1 | AAL17814.1 | |||
| AF420603.1 | AAL17816.1 | |||
| AF420604.1 | AAL17817.1 | |||
| AF420605.1 | AAL17818.1 | |||
| AK000097.1 | BAA90943.1 | |||
| AK123076.1 | BAC85532.1 | |||
| AK291086.1 | ||||
| AY438031.1 | AAR30499.1 | |||
| BC001251.1 | AAH01251.1 | |||
| L38616.1 | AAA64231.1 |
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Additional Information:
For this assay, SNP(s) [rs140362867] 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
Intronic
Non-exonic
non-DGV Variation
|
Gene Ontology Categories:
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