Hs03357919_cn

• Gene Symbol: TMEM51
• Assay Reference Genome Location: Chr.1:15178967 on build GRCh38
• Cytoband: 1p36.21

Target Gene Details

• Entrez Gene ID: 55092
• Gene Name: transmembrane protein 51
• Gene Aliases: C1orf72
• Location: Chr.1:15152418-15220480 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
TMEM51	NM_001136216.1			NP_001129688.1
	NM_001136217.1			NP_001129689.1
	NM_001136218.1			NP_001129690.1
	NM_001319665.1			NP_001306594.1
	NM_018022.2			NP_060492.1
	NR_135082.1
	XM_011541676.1			XP_011539978.1
	XM_017001590.1			XP_016857079.1
	AK001061.1			BAA91486.1
	AK098467.1
	AK129922.1
	AK292184.1
	AL525184.3
	BC000593.2			AAH00593.1
	BC005177.2			AAH05177.1
	BP275401.1
	BQ416935.1
	DC295166.1
	DC345032.1
	HY053313.1
	HY144080.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv833425	Chr.1:15083330 - 15291728 on Build GRCh38	Gain	TMEM51-AS1 C1orf195 KAZN FHAD1 TMEM51
nsv159446	Chr.1:15174383 - 15184166 on Build GRCh38	Deletion	TMEM51

More Information

Additional Information:

For this assay, SNP(s) [rs114857745] 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

Gene Ontology Categories:

Process(es)

biological_process

Function(s)

molecular_function
protein binding