Hs01954415_cn

• Gene Symbol: MYO19
• Assay Reference Genome Location: Chr.17:36498528 on build GRCh38
• Cytoband: 17q12

Target Gene Details

• Entrez Gene ID: 80179
• Gene Name: myosin XIX
• Gene Aliases: MYOHD1
• Location: Chr.17:36495636-36535457 on Build GRCh38
• Assay Gene Location: Within Exon 28

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
MYO19	NM_001163735.1	25	3487	NP_001157207.1
	NM_025109.5	21	2887	NP_079385.2
	XM_011525286.1	28	3174	XP_011523588.1
	XM_011525287.1	28	3168	XP_011523589.1
	XM_011525290.2	26	3036	XP_011523592.1
	XM_017025157.1	28	3148	XP_016880646.1
	XM_017025158.1	27	3081	XP_016880647.1
	XM_017025159.1	26	3042	XP_016880648.1
	XM_017025160.1			XP_016880649.1
	XM_017025161.1	26	2966	XP_016880650.1
	AB209035.1	26	4712	BAD92272.1
	AK293903.1
	AK304073.1	25	2838
	AL133017.1	12	3312
	BC008900.2	21	2278	AAH08900.1
	BU543266.1	7	628

Target Gene Details

• Entrez Gene ID: 9326
• Gene Name: zinc finger HIT-type containing 3
• Gene Aliases: TRIP3
• Location: Chr.17:36486627-36499310 on Build GRCh38
• Assay Gene Location: Within Exon 6

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ZNHIT3	NM_001281432.1	5	1282	NP_001268361.1
	NR_104011.1	4	1250
	AK308583.1	4	1178

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3640472	Chr.17:36483375 - 36567136 on Build GRCh38	Gain	PIGW GGNBP2 ZNHIT3 MYO19
esv2763162	Chr.17:36460442 - 36567250 on Build GRCh38	Gain	PIGW GGNBP2 ZNHIT3 MYO19
esv3640471	Chr.17:36461662 - 36600489 on Build GRCh38	Gain	PIGW GGNBP2 ZNHIT3 MYO19 DHRS11
nsv469853	Chr.17:36387554 - 36574537 on Build GRCh38	Gain+Loss	PIGW GGNBP2 ZNHIT3 MYO19 TBC1D3H TBC1D3J TBC1D3F
nsv471697	Chr.17:36357257 - 36574537 on Build GRCh38	Gain	PIGW GGNBP2 ZNHIT3 MYO19 TBC1D3H TBC1D3J TBC1D3F
nsv516100	Chr.17:36459737 - 36549567 on Build GRCh38	Gain+Loss	PIGW GGNBP2 ZNHIT3 MYO19
dgv573e214	Chr.17:36461232 - 36515958 on Build GRCh38	Gain	ZNHIT3 MYO19

More Information

Additional Information:

For this assay, SNP(s) [rs113036400] 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, DGV Variation

Panther Classification:

Molecular Function -

actin binding motor protein

Gene Ontology Categories:

Process(es)

regulation of transcription, DNA-templated

Function(s)

actin binding
ATP binding
ATPase activity
myosin light chain binding
plus-end directed microfilament motor activity
protein binding
metal ion binding
thyroid hormone receptor binding