Assay Details
Target Gene Details
Entrez Gene ID: | 64072 |
Gene Name: | cadherin-related 23 |
Gene Aliases: |
CDHR23, USH1D |
Location: |
Chr.10:71396934-71815947 on Build GRCh38 |
Assay Gene Location: | Within Exon 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CDH23 | NM_001171930.1 | 4 | 593 | NP_001165401.1 |
NM_001171931.1 | 4 | 593 | NP_001165402.1 | |
NM_001171932.1 | 4 | 593 | NP_001165403.1 | |
NM_022124.5 | 4 | 593 | NP_071407.4 | |
NM_052836.3 | 4 | 593 | NP_443068.1 | |
XM_006717940.3 | 4 | 587 | XP_006718003.1 | |
XM_006717942.3 | 4 | 587 | XP_006718005.1 | |
XM_011540039.2 | 4 | 587 | XP_011538341.1 | |
XM_011540042.2 | 4 | 587 | XP_011538344.1 | |
XM_011540043.2 | 4 | 587 | XP_011538345.1 | |
XM_011540044.2 | 4 | 228 | XP_011538346.1 | |
XM_011540045.2 | 4 | 587 | XP_011538347.1 | |
XM_011540048.2 | 4 | 587 | XP_011538350.1 | |
XM_011540049.2 | 4 | 587 | XP_011538351.1 | |
XM_011540051.2 | 4 | 587 | XP_011538353.1 | |
XM_017016499.1 | 4 | 593 | XP_016871988.1 | |
XM_017016500.1 | 4 | 587 | XP_016871989.1 | |
AF312024.1 | 3 | 203 | AAG48303.1 | |
AY010111.2 | 3 | 203 | AAG27034.2 | |
AY358617.1 | 4 | 243 | AAQ88980.1 | |
BC011570.1 | 4 | 598 | AAH11570.1 | |
BC032581.1 | 4 | 599 | AAH32581.1 | |
BC065284.1 | 4 | 570 | AAH65284.1 | |
BC108254.1 | 2 | 433 | AAI08255.1 | |
BC136976.1 | 4 | 463 | ||
BC136977.1 | 4 | 462 | ||
BC139903.1 | 4 | 585 |
Target Gene Details
Entrez Gene ID: | 102723377 |
Gene Name: | uncharacterized LOC102723377 |
Gene Aliases: |
- |
Location: |
Chr.10:71508153-71511920 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC102723377 | NR_120672.1 | |||
BX103495.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2759766 | Chr.10:71478146 - 71526398 on Build GRCh38 | Loss |
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nsv1044971 | Chr.10:71272698 - 71673682 on Build GRCh38 | Gain |
![]() ![]() ![]() ![]() |
nsv523021 | Chr.10:71480316 - 71585307 on Build GRCh38 | Gain |
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nsv551502 | Chr.10:71402480 - 71687524 on Build GRCh38 | Gain |
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More Information
Additional Information:
For this assay, SNP(s) [rs116624130] 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: |
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Panther Classification:
Gene Ontology Categories:
