Hs02771808_cn

• Gene Symbol: SEPT2
• Assay Reference Genome Location: Chr.2:241326062 on build GRCh38
• Cytoband: 2q37.3

Target Gene Details

• Entrez Gene ID: 4735
• Gene Name: septin 2
• Gene Aliases: DIFF6, NEDD-5, NEDD5, Pnutl3, hNedd5
• Location: Chr.2:241315187-241354027 on Build GRCh38
• Assay Gene Location: Within Exon 9

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SEPT2	NM_001008491.2	4	621	NP_001008491.1
	NM_001008492.2	4	303	NP_001008492.1
	NM_001282972.1	4	352	NP_001269901.1
	NM_001282973.1	6	546	NP_001269902.1
	NM_001321029.1	4	337	NP_001307958.1
	NM_001321030.1	4	335	NP_001307959.1
	NM_001321031.1	5	438	NP_001307960.1
	NM_001321032.1	3	218	NP_001307961.1
	NM_001321033.1	5	454	NP_001307962.1
	NM_001321034.1	5	453	NP_001307963.1
	NM_001321035.1	4	319	NP_001307964.1
	NM_004404.4	3	218	NP_004395.1
	NM_006155.2	3	520	NP_006146.1
	XM_011511237.1	3	168	XP_011509539.1
	XM_011511238.1			XP_011509540.1
	XM_011511240.1			XP_011509542.1
	XM_017004189.1	5	413	XP_016859678.1
	XM_017004190.1	5	348	XP_016859679.1
	XM_017004191.1	5	413	XP_016859680.1
	XM_017004192.1	5	413	XP_016859681.1
	XM_017004193.1	3	218	XP_016859682.1
	XM_017004194.1	5	368	XP_016859683.1
	XM_017004195.1	5	572	XP_016859684.1
	XM_017004196.1	5	454	XP_016859685.1
	XM_017004197.1	4	269	XP_016859686.1
	XM_017004198.1	4	331	XP_016859687.1
	XM_017004199.1	5	370	XP_016859688.1
	XM_017004200.1	4	333	XP_016859689.1
	XM_017004201.1	4	455	XP_016859690.1
	XM_017004202.1	3	437	XP_016859691.1
	XM_017004203.1	4	261	XP_016859692.1
	XM_017004204.1	3	176	XP_016859693.1
	XM_017004205.1	5	368	XP_016859694.1
	XM_017004206.1	4	269	XP_016859695.1
	XM_017004207.1	1	70	XP_016859696.1
	XM_017004208.1	4	264	XP_016859697.1
	XM_017004209.1	3	151	XP_016859698.1
	XM_017004210.1			XP_016859699.1
	XM_017004211.1			XP_016859700.1
	XM_017004212.1			XP_016859701.1
	XM_017004213.1	5	413	XP_016859702.1
	AF038404.1	3	157	AAB92377.1
	AK294563.1	4	260
	BC014455.1	4	500	AAH14455.1
	BC033559.1	6	524	AAH33559.1
	BG721140.1	3	218
	BI561073.1	3	434
	BX648000.1	4	237
	CN282712.1	3	251
	D28540.1	2	141	BAA05893.1
	D63878.1	3	337
	DA444624.1	5	377
	DA544741.1	4	322
	DB035463.1
	DB091579.1	3	218
	DB095611.1	3	454
	DB224668.1	5	458
	DB277926.1	5	354
	HY043466.1	4	325

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3594827	Chr.2:241325760 - 241335933 on Build GRCh38	Gain	SEPT2
esv3594826	Chr.2:241322580 - 241339193 on Build GRCh38	Gain	SEPT2
esv2445970	Chr.2:241325547 - 241326920 on Build GRCh38	Deletion	SEPT2
esv2721993	Chr.2:241326089 - 241326797 on Build GRCh38	Deletion	SEPT2

More Information

• Set Membership: Intragenic, Exonic, DGV Variation

Panther Classification:

Molecular Function -

cytoskeletal protein

Gene Ontology Categories:

Process(es)

regulation of L-glutamate transport
mitotic nuclear division
smoothened signaling pathway
neuron projection development
regulation of protein localization
cilium assembly
regulation of catalytic activity
cell division
cell-cell adhesion

Function(s)

protein binding
GTP binding
enzyme regulator activity
protein complex scaffold
cadherin binding involved in cell-cell adhesion