Genomic Map
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Target Gene Details
Entrez Gene ID: | 10138 |
Gene Name: | YY1 associated factor 2 |
Gene Aliases: |
- |
Location: |
Chr.12:42157104-42238368 on Build GRCh38 |
Assay Gene Location: | Within Intron 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| YAF2 | NM_001190977.2 | NP_001177906.1 | ||
| NM_001190979.2 | NP_001177908.1 | |||
| NM_001320080.1 | NP_001307009.1 | |||
| NM_005748.5 | NP_005739.2 | |||
| NR_135139.1 | ||||
| NR_135140.1 | ||||
| XM_006719184.3 | XP_006719247.1 | |||
| XM_006719185.3 | XP_006719248.1 | |||
| XM_011537728.2 | XP_011536030.1 | |||
| XM_011537729.2 | XP_011536031.1 | |||
| XM_017018669.1 | XP_016874158.1 | |||
| AI654632.1 | ||||
| AK291355.1 | ||||
| AK294260.1 | ||||
| AK296191.1 | ||||
| BC037777.2 | AAH37777.1 | |||
| CB963485.1 | ||||
| CB993159.1 | ||||
| DA011078.1 | ||||
| DA491895.1 | ||||
| HY111766.1 |
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Additional Information:
For this assay, SNP(s) [rs74341899] 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
|
Panther Classification:
Gene Ontology Categories:
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