Genomic Map
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Target Gene Details
Entrez Gene ID: | 124401 |
Gene Name: | ankyrin repeat and sterile alpha motif domain containing 3 |
Gene Aliases: |
- |
Location: |
Chr.16:4696510-4734377 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 5 - Exon 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ANKS3 | NM_001242929.1 | NP_001229858.1 | ||
| NM_001308089.1 | NP_001295018.1 | |||
| NM_001324129.1 | NP_001311058.1 | |||
| NM_001324130.1 | NP_001311059.1 | |||
| NM_133450.3 | NP_597707.1 | |||
| NR_040252.1 | ||||
| XM_005255119.3 | XP_005255176.1 | |||
| XM_005255121.3 | XP_005255178.1 | |||
| XM_011522372.1 | XP_011520674.1 | |||
| XM_011522373.1 | XP_011520675.1 | |||
| XM_011522374.1 | XP_011520676.1 | |||
| XM_011522378.1 | XP_011520680.1 | |||
| XM_017022935.1 | XP_016878424.1 | |||
| XM_017022936.1 | XP_016878425.1 | |||
| AB075857.1 | ||||
| AK057329.1 | ||||
| AK123371.1 | BAC85597.1 | |||
| AK123496.1 | BAC85629.1 | |||
| AK301683.1 | ||||
| BC050387.1 | AAH50387.1 | |||
| BM545219.1 | ||||
| BX333650.2 | ||||
| DR004376.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1046986 | Chr.16:4049000 - 5555721 on Build GRCh38 | Gain |
 DNAJA3
SEC14L5
MIR6769A
UBALD1
GLIS2
ZNF500
CORO7
C16orf96
MGRN1
LINC01569
SEPT12
RBFOX1
NAGPA-AS1
SRL
CORO7-PAM16
ANKS3
ROGDI
C16orf89
SMIM22
GLYR1
HMOX2
VASN
NAGPA
EEF2KMT
NUDT16L1
PPL
LOC105371063
TFAP4
C16orf71
ALG1
UBN1
GLIS2-AS1
NMRAL1
CDIP1
ADCY9
PAM16
|
| nsv571302 | Chr.16:4708464 - 4762815 on Build GRCh38 | Gain |
ANKS3
C16orf71
ZNF500
|
| nsv1050237 | Chr.16:4641028 - 4744872 on Build GRCh38 | Loss |
NUDT16L1
MGRN1
ANKS3
MIR6769A
C16orf71
|
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Additional Information:
For this assay, SNP(s) [rs73504498] 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
|
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