Assay Details
Target Gene Details
Entrez Gene ID: | 374977 |
Gene Name: | maestro heat like repeat family member 7 |
Gene Aliases: |
C1orf175, HEATR8 |
Location: |
Chr.1:54641740-54710267 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 5 - Exon 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MROH7 | NM_001039464.3 | NP_001034553.2 | ||
NM_001291332.1 | NP_001278261.1 | |||
NR_026782.2 | ||||
NR_111931.1 | ||||
AK130047.1 | BAC85285.1 | |||
AK301894.1 | ||||
AK302446.1 | ||||
AK302703.1 | ||||
AL096749.1 | ||||
AL832492.1 | ||||
BC126126.1 | ||||
BC143891.1 |
Target Gene Details
Entrez Gene ID: | 100527960 |
Gene Name: | MROH7-TTC4 readthrough (NMD candidate) |
Gene Aliases: |
HEATR8-TTC4 |
Location: |
Chr.1:54641740-54742657 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 6 - Exon 7 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MROH7-TTC4 | NR_037639.2 | |||
NR_037640.2 | ||||
NR_037641.2 | ||||
BX648088.1 | ||||
CR749830.1 | CAH18687.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1004778 | Chr.1:54635180 - 54764639 on Build GRCh38 | Gain | MROH7-TTC4 PARS2 TTC4 MROH7 |
nsv546299 | Chr.1:54653842 - 54684791 on Build GRCh38 | Gain | MROH7-TTC4 MROH7 |
nsv1000673 | Chr.1:54630765 - 54818045 on Build GRCh38 | Gain | MROH7-TTC4 PARS2 LEXM ACOT11 TTC4 MROH7 TTC22 |
nsv546266 | Chr.1:54404143 - 54887697 on Build GRCh38 | Gain | SSBP3 MROH7-TTC4 FAM151A PARS2 LEXM DHCR24 ACOT11 TTC4 MROH7 TTC22 |
nsv461594 | Chr.1:54593622 - 54757517 on Build GRCh38 | Gain | MROH7-TTC4 FAM151A PARS2 ACOT11 TTC4 MROH7 |
dgv38e212 | Chr.1:54627539 - 54817638 on Build GRCh38 | Gain | MROH7-TTC4 PARS2 LEXM ACOT11 TTC4 MROH7 TTC22 |
nsv817614 | Chr.1:54580862 - 55735351 on Build GRCh38 | Gain | PARS2 LEXM TTC4 BSND MROH7 TTC22 USP24 MROH7-TTC4 LOC100507634 FAM151A DHCR24 MIR4422 PCSK9 ACOT11 TMEM61 |
nsv829904 | Chr.1:54548613 - 54721384 on Build GRCh38 | Loss | MROH7-TTC4 FAM151A ACOT11 TTC4 MROH7 |
More Information
Additional Information:
For this assay, SNP(s) [rs550028680] 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 |