Genomic Map
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Target Gene Details
Entrez Gene ID: | 388341 |
Gene Name: | leucine rich repeat containing 75A |
Gene Aliases: |
C17orf76, FAM211A |
Location: |
Chr.17:16442005-16492191 on Build GRCh38 |
Assay Gene Location: | Within Exon 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LRRC75A | NM_001113567.2 | NP_001107039.1 | ||
| NM_207387.3 | NP_997270.2 | |||
| XM_011523845.2 | 4 | 676 | XP_011522147.1 | |
| XM_017024619.1 | XP_016880108.1 | |||
| XM_017024620.1 | XP_016880109.1 | |||
| AK093015.1 | BAC04020.1 | |||
| AL833245.1 | 2 | 513 | ||
| AL833260.1 | 2 | 513 | ||
| BC144381.1 | ||||
| BF966204.1 |
Target Gene Details
Entrez Gene ID: | 125144 |
Gene Name: | LRRC75A antisense RNA 1 |
Gene Aliases: |
C17orf45, C17orf76-AS1, FAM211A-AS1, NCRNA00188, TSAP19 |
Location: |
Chr.17:16438987-16470648 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LRRC75A-AS1 | NR_027171.1 | |||
| NR_027172.2 | ||||
| NR_027173.1 | ||||
| NR_027174.1 | ||||
| NR_027175.1 | ||||
| NR_027176.1 | ||||
| NR_027177.1 | ||||
| NR_027178.1 | ||||
| NR_045023.1 | ||||
| NR_045025.1 | ||||
| AK308482.1 | ||||
| BP377665.1 | ||||
| DA131201.1 | ||||
| DA193585.1 | ||||
| DA383448.1 | ||||
| DA485648.1 | ||||
| DA494627.1 | ||||
| DA769571.1 | ||||
| DA793334.1 | ||||
| DA802938.1 | ||||
| DA857697.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1063764 | Chr.17:16268335 - 16759600 on Build GRCh38 | Loss |
 SNORD49A
PIGL
TRPV2
CCDC144A
LRRC75A-AS1
LRRC75A
CENPV
SNORD49B
ZNF287
MIR1288
SNORD65
UBB
ZNF624
|
| esv2715702 | Chr.17:15750514 - 16668268 on Build GRCh38 | Deletion |
SNORD49A
PIGL
ADORA2B
TRPV2
CCDC144A
MEIS3P1
ZSWIM7
LRRC75A-AS1
LRRC75A
LOC101928567
CENPV
SNORD49B
CDRT15P2
NCOR1
ZNF287
TTC19
MIR1288
SNORD65
UBB
ZNF624
|
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Additional Information:
For this assay, SNP(s) [rs73287095] 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
Exonic
Intronic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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