Hs00767937_cn

• Gene Symbol: TM4SF19
• Assay Reference Genome Location: Chr.3:196327530 on build GRCh38
• Cytoband: 3q29

Target Gene Details

• Entrez Gene ID: 116211
• Gene Name: transmembrane 4 L six family member 19
• Gene Aliases: OCTM4
• Location: Chr.3:196323546-196338420 on Build GRCh38
• Assay Gene Location: Within Exon 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
TM4SF19	NM_001204897.1	2	219	NP_001191826.1
	NM_001204898.1	2	219	NP_001191827.1
	NM_138461.3	2	219	NP_612470.2
	AF192910.1	2	175	AAQ13824.1
	AK310209.1	2	189
	BC146985.1	2	120
	BC146993.1	2	120
	BC147021.1	2	120
	BC171870.1	2	120
	BQ678650.1	2	185
	CA489370.1	2	219
	DB015357.1	2	189

Target Gene Details

• Entrez Gene ID: 100534611
• Gene Name: TM4SF19-TCTEX1D2 readthrough (NMD candidate)
• Gene Aliases: -
• Location: Chr.3:196316085-196338420 on Build GRCh38
• Assay Gene Location: Within Exon 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
TM4SF19-TCTEX1D2	NR_037950.1	2	219

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv997797	Chr.3:195931489 - 196486087 on Build GRCh38	Gain	TM4SF19-TCTEX1D2 ZDHHC19 SDHAP1 LOC105374301 TCTEX1D2 SLC51A TM4SF19-AS1 TM4SF19 UBXN7 TFRC UBXN7-AS1 RNF168 PCYT1A LINC00885
nsv1009811	Chr.3:196124925 - 196411200 on Build GRCh38	Gain	TM4SF19-AS1 TM4SF19-TCTEX1D2 TM4SF19 UBXN7 ZDHHC19 PCYT1A TCTEX1D2 LINC00885 SLC51A
nsv593071	Chr.3:196132016 - 196345571 on Build GRCh38	Gain	TM4SF19-AS1 TM4SF19-TCTEX1D2 TM4SF19 ZDHHC19 PCYT1A TCTEX1D2 LINC00885 SLC51A
nsv4183	Chr.3:196307196 - 196352238 on Build GRCh38	Deletion	TM4SF19-AS1 TM4SF19-TCTEX1D2 TM4SF19 UBXN7 TCTEX1D2
esv2759213	Chr.3:195382058 - 196344722 on Build GRCh38	Gain+Loss	TM4SF19-TCTEX1D2 SDHAP2 ZDHHC19 SDHAP1 LOC105374301 TCTEX1D2 APOD SLC51A TM4SF19-AS1 MIR570 TM4SF19 ACAP2 TFRC MIR6829 PPP1R2 PCYT1A MUC20 MUC4 TNK2 LOC105374299 LOC105374297 LOC101929697 LINC00885 LINC00969

More Information

• Set Membership: Intragenic, Exonic, DGV Variation