Assay Details
Target Gene Details
Entrez Gene ID: | 10457 |
Gene Name: | glycoprotein nmb |
Gene Aliases: |
HGFIN, NMB |
Location: |
Chr.7:23246206-23275110 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
GPNMB | NM_001005340.1 | NP_001005340.1 | ||
NM_002510.2 | NP_002501.1 | |||
XM_005249578.2 | XP_005249635.1 | |||
XM_017011676.1 | XP_016867165.1 | |||
XM_017011677.1 | XP_016867166.1 | |||
XM_017011678.1 | XP_016867167.1 | |||
AF322909.1 | AAG42839.1 | |||
AJ505015.1 | CAD43718.1 | |||
AK292078.1 | ||||
AK296779.1 | ||||
AK297031.1 | ||||
AK297051.1 | ||||
AK297055.1 | ||||
AK297803.1 | ||||
AK303071.1 | ||||
AK304671.1 | ||||
AK312279.1 | ||||
AY359124.1 | AAQ89481.1 | |||
BC011595.1 | AAH11595.1 | |||
BC032783.1 | AAH32783.1 | |||
BM750843.1 | ||||
BT007074.1 | AAP35737.1 | |||
CD105306.1 | ||||
X76534.1 | CAA54044.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1027363 | Chr.7:22817000 - 23271413 on Build GRCh38 | Gain | KLHL7-AS1 TOMM7 LOC101927890 FAM126A KLHL7 NUPL2 SNORD93 GPNMB |
nsv520600 | Chr.7:23245342 - 23253189 on Build GRCh38 | Loss | GPNMB |
nsv1016316 | Chr.7:23221900 - 23318018 on Build GRCh38 | Gain | IGF2BP3 LOC101927890 MALSU1 GPNMB |
More Information
Additional Information:
For this assay, SNP(s) [rs113194611,rs73686584] 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 |