Hs02640903_cn

• Gene Symbol: HNRNPH3
• Assay Reference Genome Location: Chr.10:68342275 on build GRCh38
• Cytoband: 10q21.3

Target Gene Details

• Entrez Gene ID: 3189
• Gene Name: heterogeneous nuclear ribonucleoprotein H3
• Gene Aliases: 2H9, HNRPH3
• Location: Chr.10:68331174-68343196 on Build GRCh38
• Assay Gene Location: Within Exon 12

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
HNRNPH3	NM_001322434.1	10	1510	NP_001309363.1
	NM_001322436.1	10	1472	NP_001309365.1
	NM_001322437.1	10	1575	NP_001309366.1
	NM_001322438.1	10	1402	NP_001309367.1
	NM_001322439.1	10	1465	NP_001309368.1
	NM_001322440.1	10	1427	NP_001309369.1
	NM_001322441.1	10	1530	NP_001309370.1
	NM_001322442.1	10	1492	NP_001309371.1
	NM_001322443.1	10	1473	NP_001309372.1
	NM_001322444.1	8	1167	NP_001309373.1
	NM_001322445.1	9	1308	NP_001309374.1
	NM_001322446.1	9	1352	NP_001309375.1
	NM_001322447.1	9	1333	NP_001309376.1
	NM_001322448.1	9	1371	NP_001309377.1
	NM_001322449.1	9	1436	NP_001309378.1
	NM_001322450.1	9	1353	NP_001309379.1
	NM_001322451.1	9	1288	NP_001309380.1
	NM_001322452.1	9	1307	NP_001309381.1
	NM_001322453.1	9	1326	NP_001309382.1
	NM_012207.2	10	1491	NP_036339.1
	NM_021644.3	10	1446	NP_067676.2
	XM_011539742.1	8	1138	XP_011538044.1
	XM_017016168.1	10	1921	XP_016871657.1
	XM_017016169.1	9	1782	XP_016871658.1
	AF052131.1	2	326
	AF132361.1			AAF68849.1
	AF132362.1	8	1392	AAF68850.1
	AF132363.1			AAF68851.1
	AF132364.1			AAF68852.1
	AK091411.1
	AK223441.1			BAD97161.1
	AK291547.1	10	1398
	AL117395.1			CAB55897.1
	BC004511.2			AAH04511.2
	BC039824.1	10	1382	AAH39824.1

Target Gene Details

• Entrez Gene ID: 55680
• Gene Name: RUN and FYVE domain containing 2
• Gene Aliases: RABIP4R, ZFYVE13
• Location: Chr.10:68341107-68407302 on Build GRCh38
• Assay Gene Location: Within Intron 20

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
RUFY2	NR_103475.1
	NR_103476.1
	AB040970.1			BAA96061.1
	AF461266.1			AAL67520.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv950972	Chr.10:68334244 - 68344643 on Build GRCh38	Duplication	HNRNPH3 RUFY2

More Information

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

Panther Classification:

Molecular Function -

RNA splicing factor

Gene Ontology Categories:

Process(es)

mRNA splicing, via spliceosome
RNA processing
RNA splicing
epithelial cell differentiation

Function(s)

nucleotide binding
RNA binding
protein binding
poly(A) RNA binding
metal ion binding