Genomic Map
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Target Gene Details
Entrez Gene ID: | 942 |
Gene Name: | CD86 molecule |
Gene Aliases: |
B7-2, B7.2, B70, CD28LG2, LAB72 |
Location: |
Chr.3:122055362-122121143 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CD86 | NM_001206924.1 | NP_001193853.1 | ||
| NM_001206925.1 | NP_001193854.1 | |||
| NM_175862.4 | NP_787058.4 | |||
| AK291497.1 | ||||
| AK294663.1 | ||||
| AK301237.1 | ||||
| AK313103.1 | ||||
| AK316203.1 | ||||
| BC040261.1 | AAH40261.1 | |||
| DA619360.1 | ||||
| L25259.1 | AAA58389.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv528646 | Chr.3:122048207 - 122062539 on Build GRCh38 | Loss |
 CD86
ILDR1
|
| esv33139 | Chr.3:121781553 - 122372984 on Build GRCh38 | Loss |
CD86
SLC15A2
CSTA
ILDR1
IQCB1
CCDC58
EAF2
CASR
|
| nsv3972 | Chr.3:122030645 - 122062809 on Build GRCh38 | Insertion |
CD86
ILDR1
|
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Additional Information:
For this assay, SNP(s) [rs115869255] 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
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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