s536465

• Gene Symbol: WHSC1
• Gene Name: Wolf-Hirschhorn syndrome candidate 1
• Gene Aliases: MMSET, NSD2, REIIBP, TRX5, WHS
• Chromosome Location: Chr.4: 1871357 - 1982207 on Build GRCh38
• UniGene ID: Hs.113876
• Species: Human
• Species Specific ID (Flybase ID): -

siRNA Details

Gene Symbol: WHSC1
Interrogated Sequence		Translated Protein	Targeted Exon(s)	siRNA Location	IMAGE Clone ID
RefSeq	NM_001042424.2	NP_001035889.1	2	596
	NM_007331.1	NP_015627.1	4	914
	NM_133330.2	NP_579877.1	4	914
	NM_133331.2	NP_579878.1	3	734
	NM_133334.2	NP_579889.1	1	449
	NM_133335.3	NP_579890.1	2	559
	XM_005248001.3	XP_005248058.1	2	539
	XM_005248002.2	XP_005248059.1	2	635
	XM_005248005.2	XP_005248062.1	2	635
	XM_006713914.3	XP_006713977.1	3	804
	XM_011513557.2	XP_011511859.1	2	475
GenBank mRNA	AF071593.1	-	1	449
	AF071594.1	-	1	449
	AF083386.1	-	4	914
	AF083387.1	-	3	734
	AF083388.1	-	2	558
	AF083389.1	-	4	914
	AF083390.1	-	4	914
	AF083391.1	-	4	914
	AJ007042.1	-	2	1182
	AK289697.1	-	3	581
	AY694128.1	-	1	431
	BC020545.1	-	2	531
	BC052254.1	-	2	538
	BC141815.1	-	2	629
	CX866583.1	-	2	625

More Information

Gene Ontology Categories:

Process(es)

negative regulation of transcription from RNA polymerase II promoter
membranous septum morphogenesis
atrial septum primum morphogenesis
atrial septum secundum morphogenesis
double-strand break repair via nonhomologous end joining
transcription, DNA-templated
anatomical structure morphogenesis
histone H3-K36 methylation
chromatin modification
histone H4-K20 methylation
positive regulation of isotype switching to IgA isotypes
bone development
regulation of establishment of protein localization
regulation of double-strand break repair via nonhomologous end joining

Function(s)

chromatin binding
protein binding
zinc ion binding
histone-lysine N-methyltransferase activity
histone methyltransferase activity (H4-K20 specific)
sequence-specific DNA binding