Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 84632 |
Gene Name: | actin filament associated protein 1 like 2 |
Gene Aliases: |
CTB-1144G6.4, KIAA1914, XB130 |
Location: |
Chr.10:114280730-114405143 on Build GRCh38 |
Assay Gene Location: | Within Intron 24 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| AFAP1L2 | XM_005270233.4 | XP_005270290.1 | ||
| XM_005270237.4 | XP_005270294.1 | |||
| XM_005270241.4 | XP_005270298.1 | |||
| XM_005270242.4 | XP_005270299.1 | |||
| XM_011540286.2 | XP_011538588.1 | |||
| XM_017016792.1 | XP_016872281.1 | |||
| XM_017016793.1 | XP_016872282.1 | |||
| XM_017016794.1 | XP_016872283.1 | |||
| XM_017016795.1 | XP_016872284.1 | |||
| XM_017016796.1 | XP_016872285.1 | |||
| XM_017016797.1 | XP_016872286.1 | |||
| XM_017016798.1 | XP_016872287.1 | |||
| XM_017016804.1 | XP_016872293.1 | |||
| XM_017016814.1 | XP_016872303.1 | |||
| XM_017016815.1 | XP_016872304.1 | |||
| XM_017016818.1 | XP_016872307.1 | |||
| XM_017016829.1 | XP_016872318.1 | |||
| XM_017016832.1 | XP_016872321.1 |
Target Gene Details
Entrez Gene ID: | 340706 |
Gene Name: | von Willebrand factor A domain containing 2 |
Gene Aliases: |
AMACO, CCSP-2, NET42 |
Location: |
Chr.10:114239254-114294500 on Build GRCh38 |
Assay Gene Location: | Within Exon 16 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| VWA2 | NM_001272046.1 | 11 | 1707 | NP_001258975.1 |
| NM_001320804.1 | 11 | 1649 | NP_001307733.1 | |
| XM_011539754.2 | 12 | 1884 | XP_011538056.1 | |
| XM_011539757.2 | 11 | 1979 | XP_011538059.1 | |
| XM_017016177.1 | 11 | 1459 | XP_016871666.1 | |
| XM_017016178.1 | 11 | 1459 | XP_016871667.1 | |
| XM_017016179.1 | 11 | 1412 | XP_016871668.1 | |
| XM_017016180.1 | 3 | 555 | XP_016871669.1 | |
| AJ536328.2 | 11 | 1631 | CAD60276.1 | |
| AK122716.1 | 11 | 1702 | BAC85505.1 | |
| AK127756.1 | 11 | 1538 | BAC87116.1 | |
| AY572972.1 | 11 | 1469 | AAT77225.1 | |
| BC128588.1 | 10 | 1475 |
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs74943198] 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
non-DGV Variation
|
Panther Classification:
Gene Ontology Categories:
Back To Top