Assay Details
Target Gene Details
Entrez Gene ID: | 57407 |
Gene Name: | NmrA-like family domain containing 1 |
Gene Aliases: |
HSCARG, SDR48A1 |
Location: |
Chr.16:4461677-4476320 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NMRAL1 | NM_001305141.1 | NP_001292070.1 | ||
NM_001305142.1 | NP_001292071.1 | |||
NM_020677.4 | NP_065728.1 | |||
XM_006720905.3 | XP_006720968.1 | |||
XM_006720906.2 | XP_006720969.1 | |||
XM_011522567.2 | XP_011520869.1 | |||
XM_017023485.1 | XP_016878974.1 | |||
XM_017023486.1 | XP_016878975.1 | |||
XM_017023487.1 | XP_016878976.1 | |||
XM_017023488.1 | XP_016878977.1 | |||
XM_017023489.1 | XP_016878978.1 | |||
XM_017023490.1 | XP_016878979.1 | |||
XM_017023491.1 | XP_016878980.1 | |||
XM_017023492.1 | XP_016878981.1 | |||
AF225419.1 | AAG09721.1 | |||
AK098784.1 | ||||
BC002927.2 | AAH02927.1 | |||
BC007364.2 | AAH07364.1 | |||
HY171572.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1160332 | Chr.16:4367643 - 4486554 on Build GRCh38 | Duplication | NMRAL1 DNAJA3 CORO7-PAM16 CORO7 VASN HMOX2 |
nsv1046986 | Chr.16:4049000 - 5555721 on Build GRCh38 | Gain | GLIS2-AS1 PPL NUDT16L1 C16orf96 SEPT12 UBN1 HMOX2 ADCY9 RBFOX1 LINC01569 UBALD1 MGRN1 CDIP1 GLIS2 SEC14L5 LOC105371063 PAM16 NMRAL1 TFAP4 EEF2KMT DNAJA3 CORO7-PAM16 CORO7 ZNF500 NAGPA C16orf71 SMIM22 C16orf89 MIR6769A ALG1 ROGDI SRL NAGPA-AS1 GLYR1 ANKS3 VASN |
esv23732 | Chr.16:4340813 - 4476244 on Build GRCh38 | Gain | PAM16 NMRAL1 DNAJA3 CORO7-PAM16 CORO7 VASN HMOX2 |
More Information
Additional Information:
For this assay, SNP(s) [rs75205270] 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 |