Hs00252428_cn

• Gene Symbol: MROH7
• Assay Reference Genome Location: Chr.1:54673111 on build GRCh38
• Cytoband: 1p32.3

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 7 - Exon 8

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 8 - Exon 9

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 MROH7 TTC4 PARS2
nsv546299	Chr.1:54653842 - 54684791 on Build GRCh38	Gain	MROH7-TTC4 MROH7
nsv1000673	Chr.1:54630765 - 54818045 on Build GRCh38	Gain	MROH7-TTC4 LEXM MROH7 TTC4 TTC22 ACOT11 PARS2
nsv546266	Chr.1:54404143 - 54887697 on Build GRCh38	Gain	MROH7-TTC4 LEXM MROH7 TTC4 TTC22 FAM151A SSBP3 ACOT11 DHCR24 PARS2
nsv461594	Chr.1:54593622 - 54757517 on Build GRCh38	Gain	MROH7-TTC4 MROH7 TTC4 FAM151A ACOT11 PARS2
dgv38e212	Chr.1:54627539 - 54817638 on Build GRCh38	Gain	MROH7-TTC4 LEXM MROH7 TTC4 TTC22 ACOT11 PARS2
nsv817614	Chr.1:54580862 - 55735351 on Build GRCh38	Gain	LOC100507634 TMEM61 MROH7 TTC4 FAM151A BSND PCSK9 MIR4422 PARS2 MROH7-TTC4 LEXM USP24 TTC22 ACOT11 DHCR24
nsv829904	Chr.1:54548613 - 54721384 on Build GRCh38	Loss	MROH7-TTC4 MROH7 TTC4 FAM151A ACOT11

More Information

• Set Membership: Intragenic, Non-exonic, DGV Variation