Assay Details
Target Gene Details
Entrez Gene ID: | 83692 |
Gene Name: | CD99 molecule like 2 |
Gene Aliases: |
CD99B, MIC2L1 |
Location: |
Chr.X:150766336-150898816 on Build GRCh38 |
Assay Gene Location: | Within Exon 13 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CD99L2 | NM_001184808.1 | 8 | 1313 | NP_001171737.1 |
| NM_001242614.1 | 12 | 1562 | NP_001229543.1 | |
| NM_031462.3 | 11 | 1532 | NP_113650.2 | |
| NM_134445.3 | 8 | 1316 | NP_604394.1 | |
| NM_134446.3 | 9 | 1385 | NP_604395.1 | |
| AK023776.1 | 10 | 1218 | ||
| AK024278.1 | 7 | 1039 | ||
| AK125020.1 | 12 | 1373 | ||
| AK126859.1 | 2 | 1931 | ||
| AK293244.1 | ||||
| AK295217.1 | 7 | 989 | ||
| AL136580.1 | 11 | 1421 | CAB66515.1 | |
| AY358837.1 | 11 | 1405 | AAQ89196.1 | |
| BC025729.1 | 12 | 2753 | AAH25729.1 | |
| BC030536.1 | 11 | 1392 | AAH30536.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv508813 | Chr.X:150735078 - 150811481 on Build GRCh38 | Insertion |
|
| nsv525661 | Chr.X:150731781 - 150792646 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs112296727] 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: |
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Genomic Map