s526860

• 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	17	3204
	NM_133330.2	NP_579877.1	19	3522
	NM_133331.2	NP_579878.1	18	3342
	NM_133335.3	NP_579890.1	17	3167
	XM_005248001.3	XP_005248058.1	17	3147
	XM_005248002.2	XP_005248059.1	15	3036
	XM_011513557.2	XP_011511859.1	17	3083
	XM_011513560.2	XP_011511862.1	6	785
	XM_017008587.1	XP_016864076.1	8	1050
	XM_017008588.1	XP_016864077.1	7	1780
GenBank mRNA	AB029013.1	-	7	1594
	AF071593.1	-	16	3057
	AF083386.1	-	19	3522
	AF083387.1	-	18	3342
	AF083388.1	-	17	3166
	AF083389.1	-	20	3749
	AF083390.1	-	20	3616
	AF330040.1	-	9	1645
	AJ007042.1	-	17	3790
	AK026939.1	-	1	26
	BC094825.1	-	5	695
	BC144464.1	-	8	950
	BC152412.1	-	7	1629	8862517

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