Assay Details
Target Gene Details
Entrez Gene ID: | 4753 |
Gene Name: | neural EGFL like 2 |
Gene Aliases: |
NRP2 |
Location: |
Chr.12:44508275-44921848 on Build GRCh38 |
Assay Gene Location: | Within Intron 20 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NELL2 | NM_001145107.1 | NP_001138579.1 | ||
NM_001145108.1 | NP_001138580.1 | |||
NM_001145109.1 | NP_001138581.1 | |||
NM_001145110.1 | NP_001138582.1 | |||
NM_006159.2 | NP_006150.1 | |||
XM_005268905.3 | XP_005268962.1 | |||
XM_011538396.1 | XP_011536698.1 | |||
XM_017019341.1 | XP_016874830.1 | |||
XM_017019342.1 | XP_016874831.1 | |||
XM_017019343.1 | XP_016874832.1 | |||
XM_017019344.1 | XP_016874833.1 | |||
AK095637.1 | ||||
AK295125.1 | ||||
AK297521.1 | ||||
AK299277.1 | ||||
AK299733.1 | ||||
AK309825.1 | ||||
AK315960.1 | ||||
AK316058.1 | ||||
BC020544.1 | AAH20544.1 | |||
D83018.1 | BAA11681.1 | |||
D89629.1 | BAB46925.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1049818 | Chr.12:44092509 - 44740000 on Build GRCh38 | Gain | TMEM117 NELL2 |
nsv1051285 | Chr.12:44054046 - 45582132 on Build GRCh38 | Loss | RACGAP1P PLEKHA8P1 DBX2 ANO6 TMEM117 NELL2 |
More Information
Additional Information:
For this assay, SNP(s) [rs74085095] 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 |