Assay Details
Target Gene Details
Entrez Gene ID: | 84225 |
Gene Name: | zinc finger MYND-type containing 15 |
Gene Aliases: |
SPGF14 |
Location: |
Chr.17:4740015-4746119 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 5 - Exon 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ZMYND15 | NM_001136046.2 | NP_001129518.1 | ||
NM_001267822.1 | NP_001254751.1 | |||
NM_032265.2 | NP_115641.1 | |||
XM_017025218.1 | XP_016880707.1 | |||
AK302181.1 | ||||
AK310469.1 | ||||
AL136893.1 | CAB66827.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv574273 | Chr.17:4585589 - 5460332 on Build GRCh38 | Gain | MINK1 LOC102724009 LOC101559451 KIF1C SPAG7 RPAIN ENO3 C1QBP MED11 LOC101927979 GP1BA LOC101928000 SMTNL2 NUP88 MIR6865 LOC100130950 INCA1 PSMB6 CHRNE TM4SF5 PLD2 ARRB2 SCIMP RABEP1 LOC400568 ZNF232 CXCL16 SLC25A11 ZMYND15 RNF167 USP6 ALOX15 VMO1 MIR6864 PFN1 C17orf107 SLC52A1 GLTPD2 ZFP3 DHX33 PELP1 CAMTA2 ZNF594 LOC107984973 |
nsv833346 | Chr.17:4646256 - 4860871 on Build GRCh38 | Loss | MINK1 LOC101559451 CXCL16 ZMYND15 VMO1 MED11 GLTPD2 PELP1 PSMB6 TM4SF5 PLD2 LOC107984973 ARRB2 |
nsv1952 | Chr.17:4726245 - 4748889 on Build GRCh38 | Insertion | MED11 CXCL16 ZMYND15 |
More Information
Additional Information:
For this assay, SNP(s) [rs200092260] 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 Non-exonic DGV Variation |