Assay Details
Target Gene Details
Entrez Gene ID: | 93627 |
Gene Name: | TBC1 domain containing kinase |
Gene Aliases: |
HSPC302, IHPRF3, TBCKL |
Location: |
Chr.4:106044317-106316704 on Build GRCh38 |
Assay Gene Location: | Within Intron 27 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TBCK | NM_001163435.2 | NP_001156907.1 | ||
NM_001163436.2 | NP_001156908.1 | |||
NM_001163437.2 | NP_001156909.1 | |||
NM_001290768.1 | NP_001277697.1 | |||
NM_033115.4 | NP_149106.2 | |||
XM_011532417.2 | XP_011530719.1 | |||
XM_017008846.1 | XP_016864335.1 | |||
XM_017008847.1 | XP_016864336.1 | |||
XM_017008848.1 | XP_016864337.1 | |||
XM_017008849.1 | XP_016864338.1 | |||
AB449876.1 | ||||
AF161420.1 | AAF28980.1 | |||
AK074305.1 | BAB85045.1 | |||
AK098157.1 | BAC05244.1 | |||
AK315571.1 | ||||
BC009208.2 | AAH09208.2 | |||
BC020853.2 | AAH20853.2 | |||
BC068496.1 | AAH68496.1 | |||
BX647851.1 | CAI46102.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv511247 | Chr.4:106101545 - 106144063 on Build GRCh38 | Gain | TBCK |
dgv9194n54 | Chr.4:106134539 - 106141514 on Build GRCh38 | Loss | TBCK |
nsv4450 | Chr.4:106116666 - 106161512 on Build GRCh38 | Deletion | TBCK |
nsv508301 | Chr.4:106127929 - 106171573 on Build GRCh38 | Deletion | TBCK |
nsv1000196 | Chr.4:103475625 - 106148054 on Build GRCh38 | Loss | TET2-AS1 INTS12 ARHGEF38-IT1 NPNT LOC101929577 TET2 CXXC4 GSTCD PPA2 LOC101929468 LOC101929529 TBCK TACR3 ARHGEF38 |
nsv437411 | Chr.4:106130950 - 106152940 on Build GRCh38 | Loss | TBCK |
More Information
Additional Information:
For this assay, SNP(s) [rs73836997] 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 |