2. Gene
  3. SEPTIN2 - septin 2 Gene

SEPTIN2 - septin 2 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as DIFF6; NEDD5; SEPT2; NEDD-5; Pnutl3; hNedd5

Gene ID: 4735 | Gene type: protein coding

About SEPTIN2

Cytogenetic location: 2q37.3 Genomic coordinates (GRCh38): 2:241,315,355-241,354,027 (from NCBI)

This gene has 45 transcripts (splice variants), 225 orthologues and 12 paralogues. Ubiquitous expression in fat (RPKM 77.8), thyroid (RPKM 76.6) and 25 other tissues.

Summary

Enables identical protein binding activity. Predicted to be involved in several processes, including cilium assembly; regulation of exocytosis; and smoothened signaling pathway. Predicted to act upstream of or within regulation of L-glutamate import across plasma membrane and regulation of protein localization. Located in several cellular components, including cytoskeleton; photoreceptor connecting cilium; and sperm annulus. Part of septin complex. [provided by Alliance of Genome Resources, Apr 2022]

SEPTIN2 Products(31)

mRNA Protein Name
NM_001008491.3 NP_001008491.1 septin-2 isoform a
NM_001008492.3 NP_001008492.1 septin-2 isoform a
NM_001282972.2 NP_001269901.1 septin-2 isoform b
NM_001282973.2 NP_001269902.1 septin-2 isoform c
NM_001321029.2 NP_001307958.1 septin-2 isoform d
NM_001321030.3 NP_001307959.1 septin-2 isoform a
NM_001321031.2 NP_001307960.1 septin-2 isoform a
NM_001321032.2 NP_001307961.1 septin-2 isoform a
NM_001321033.3 NP_001307962.1 septin-2 isoform a
NM_001321034.2 NP_001307963.1 septin-2 isoform a
NM_001321035.2 NP_001307964.1 septin-2 isoform a
NM_001349287.2 NP_001336216.1 septin-2 isoform e
NM_001349288.2 NP_001336217.1 septin-2 isoform c
NM_001349289.2 NP_001336218.1 septin-2 isoform a
NM_001349290.2 NP_001336219.1 septin-2 isoform a
NM_001349291.2 NP_001336220.1 septin-2 isoform a
NM_001349302.2 NP_001336231.1 septin-2 isoform f
NM_001349304.2 NP_001336233.1 septin-2 isoform g
NM_001349305.2 NP_001336234.1 septin-2 isoform g
NM_001349306.2 NP_001336235.1 septin-2 isoform g
NM_001349307.2 NP_001336236.1 septin-2 isoform h
NM_001349308.2 NP_001336237.1 septin-2 isoform h
NM_001349309.2 NP_001336238.1 septin-2 isoform h
NM_001349310.2 NP_001336239.1 septin-2 isoform h
NM_001349311.2 NP_001336240.1 septin-2 isoform h
NM_001349312.2 NP_001336241.1 septin-2 isoform h
NM_001349313.2 NP_001336242.1 septin-2 isoform h
NM_001349314.2 NP_001336243.1 septin-2 isoform h
NM_001349315.2 NP_001336244.1 septin-2 isoform h
NM_004404.5 NP_004395.1 septin-2 isoform a
NM_006155.3 NP_006146.1 septin-2 isoform a
Gene Ontology
  • Molecular Function
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
17637674 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
10321247 GOA
Cellular Component GO Annotation Evidence Reference Source
located in axoneme IDA
IDA: Inferred from direct assay
23572511 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
10942595 GOA
located in non-motile cilium IDA
IDA: Inferred from direct assay
23572511 GOA
located in nucleus IDA
IDA: Inferred from direct assay
10942595 GOA
located in photoreceptor connecting cilium IDA
IDA: Inferred from direct assay
23572511 GOA
part of septin complex IDA
IDA: Inferred from direct assay
23572511 GOA
located in sperm annulus IDA
IDA: Inferred from direct assay
25588830 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SEPTIN2 Protein Structure

Septin

Septin: Septin (34 - 312)

  • 0
  • 100
  • 200
  • 300
  • 361 a.a.
Protein Preferred Names Protein Names

septin-2

epididymis secretory sperm binding protein

SEPTIN2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
SEPTIN2 Q15019 SEPTIN5 Homo sapiens Q99719
Anti Tag CoIP
35271311
Intra
SEPTIN2 Q15019 SEPTIN5 Homo sapiens Q99719
Validated Y2H
25416956
Intra
SEPTIN2 Q15019 SEPTIN5 Homo sapiens Q99719
Y2H Array
25416956
Intra
SEPTIN2 Q15019 SEPTIN5 Homo sapiens Q99719
Anti Tag CoIP
33961781
Intra
SEPTIN2 Q15019 SEPTIN6 Homo sapiens Q14141
Anti Tag CoIP
35271311
Intra
SEPTIN2 Q15019 SEPTIN6 Homo sapiens Q14141
Y2H Pooling
16189514
Intra
SEPTIN2 Q15019 SEPTIN6 Homo sapiens Q14141
Anti Tag CoIP
33961781
Intra
SEPTIN2 Q15019 SEPTIN6 Homo sapiens Q14141
IF
25588830
Intra
SEPTIN2 Q15019 SEPTIN6 Homo sapiens Q14141
Validated Y2H
25416956
Intra
SEPTIN2 Q15019 SEPTIN9 Homo sapiens Q9UHD8
Anti Tag CoIP
35271311
Intra
SEPTIN2 Q15019 SEPTIN9 Homo sapiens Q9UHD8
Anti Tag CoIP
33961781
Cross: Cross-species interaction Intra: Intraspecies interaction

SEPTIN2 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82509 Septin 2 Antibody (YA2254) WB, IHC-P, ICC/IF, IP, FC Human, Mouse, Rat

Related Diseases

Diseases Alias
Integrative Agnosia
Pineal Region Meningioma

Pineal Meningioma
Progressive Myoclonus Epilepsy 10

Early-Onset Lafora Body Disease

Epm10
Acquired Color Blindness

Acquired Color Vision Deficiencies

Acquired Color Vision Deficiency

Acquired Colour Blindness

Acquired Colour Vision Deficiencies

Acquired Colour Vision Deficiency
Amyotrophic Neuralgia

Neuralgic Amyotrophy

Brachial Plexus Neuritis

Neuralgic Shoulder Amyotrophy

Acute Brachial Plexus Neuritis

Immune Brachial Plexus Neuropathy

Mononeuritis Multiplex With Brachial Predilection

Parsonage-Turner Syndrome
Brachial Plexus Neuropathy

Brachial Plexopathy

Brachial Plexus Neuropathies

Brachial Plexus Disorder

Bpn - [Brachial Plexus Neuropathy]

Brachial Plexus Disease

Neuropathic Plexus Brachialis

Brachial Plexus Syndrome

Brachial Plexus Irritation

Brachial Plexus Lesion

Brachial Plexus Pressure

Compression Of Brachial Plexus
Intracranial Hypotension
Joubert Syndrome 1

Joubert Syndrome

Jbts

Cerebellooculorenal Syndrome 1

JBTS1

Joubert-Boltshauser Syndrome

Cerebelloparenchymal Disorder Iv

Cpd4

Cors1

Joubert Syndrome And Related Disorders

Jsrd

Familial Aplasia Of The Vermis

Joubert Syndrome Related Disorders

Js

Cerebellar Vermis Agenesis

Cerebelloparenchymal Disorder 4

Agenesis Of Cerebellar Vermis

Cerebello-Oculo-Renal Syndrome

Cors

Joubert-Bolthauser Syndrome

Cpd Iv

Classic Joubert Syndrome

Joubert Syndrome Type A

Pure Joubert Syndrome

Cerebello-Oculo-Renal Syndrome 1

Joubert Syndrome-1

Joubert Syndrome, Type 1

Joubert'S Syndrome
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS12682 SEPTIN2 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Felis catus SEPTIN2 VGNC VGNC:68451
Rattus norvegicus SEPTIN2 RGD RGD:620056
Macaca mulatta SEPTIN2 VGNC VGNC:77359
Bos taurus SEPTIN2 VGNC VGNC:34454
Canis familiaris SEPTIN2 VGNC VGNC:46014
Mus musculus SEPTIN2 MGD MGI:97298