Assay Details
Target Gene Details
Entrez Gene ID: | 23295 |
Gene Name: | mahogunin ring finger 1 |
Gene Aliases: |
RNF156 |
Location: |
Chr.16:4616493-4690974 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MGRN1 | NM_001142289.2 | NP_001135761.2 | ||
NM_001142290.2 | NP_001135762.1 | |||
NM_001142291.2 | NP_001135763.2 | |||
NM_015246.3 | NP_056061.1 | |||
NR_102267.1 | ||||
XM_005255217.1 | XP_005255274.1 | |||
XM_005255218.1 | XP_005255275.1 | |||
XM_005255219.3 | XP_005255276.1 | |||
XM_005255220.3 | XP_005255277.1 | |||
XM_005255221.3 | XP_005255278.1 | |||
XM_011522441.1 | XP_011520743.1 | |||
XM_017023091.1 | XP_016878580.1 | |||
XM_017023092.1 | XP_016878581.1 | |||
XM_017023093.1 | XP_016878582.1 | |||
AB011116.1 | ||||
AK299052.1 | ||||
BC050389.1 | AAH50389.1 | |||
CN314787.1 | ||||
DA118421.1 | ||||
DA590130.1 | ||||
EF471397.2 | ||||
EF471398.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1160333 | Chr.16:4570296 - 4709737 on Build GRCh38 | Deletion | MGRN1 ANKS3 MIR6769A UBALD1 NUDT16L1 C16orf96 |
nsv1046986 | Chr.16:4049000 - 5555721 on Build GRCh38 | Gain | RBFOX1 SMIM22 NMRAL1 LINC01569 C16orf89 TFAP4 CORO7-PAM16 ALG1 C16orf96 LOC105371063 PAM16 MIR6769A SEPT12 UBALD1 CDIP1 ADCY9 GLYR1 EEF2KMT NAGPA VASN ZNF500 MGRN1 GLIS2-AS1 SRL ANKS3 GLIS2 ROGDI C16orf71 NAGPA-AS1 NUDT16L1 UBN1 HMOX2 DNAJA3 PPL CORO7 SEC14L5 |
nsv1050237 | Chr.16:4641028 - 4744872 on Build GRCh38 | Loss | MGRN1 ANKS3 C16orf71 MIR6769A NUDT16L1 |
More Information
Additional Information:
For this assay, SNP(s) [rs72770332] 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 |