DOCK7 - dedicator of cytokinesis 7 Gene

Also Known as ZIR2; DEE23; EIEE23

生物種: Homo sapiens

遺伝子タイプ: protein coding

遺伝子ID: 85440

About DOCK7

Cytogenetic location: 1p31.3 Genomic coordinates (GRCh38): 1:62,454,726-62,688,386 (from NCBI)

This gene has 37 transcripts (splice variants), 224 orthologues, 10 paralogues and is associated with 3 phenotypes. Ubiquitous expression in testis (RPKM 8.6), ovary (RPKM 6.0) and 25 other tissues.

Summary

The protein encoded by this gene is a guanine nucleotide exchange factor (GEF) that plays a role in axon formation and neuronal polarization. The encoded protein displays GEF activity toward RAC1 and RAC3 Rho small GTPases but not toward CDC42. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]

DOCK7 Products (7)

mRNA	Protein	Name
NM_001271999.2	NP_001258928.1	dedicator of cytokinesis protein 7 isoform 1
NM_001272000.2	NP_001258929.1	dedicator of cytokinesis protein 7 isoform 3
NM_001272001.2	NP_001258930.1	dedicator of cytokinesis protein 7 isoform 4
NM_001272002.2	NP_001258931.1	dedicator of cytokinesis protein 7 isoform 5
NM_001330614.2	NP_001317543.1	dedicator of cytokinesis protein 7 isoform 6
NM_001367561.1	NP_001354490.1	dedicator of cytokinesis protein 7 isoform 7
NM_033407.4	NP_212132.2	dedicator of cytokinesis protein 7 isoform 2

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	参考文献	由来
enables protein binding	IPI IPI: Inferred from physical interaction	24255178	GOA
enables small GTPase binding	IDA IDA: Inferred from direct assay	16982419	GOA

Biological Process GO Annotation	Evidence	参考文献	由来
involved in activation of GTPase activity	IDA IDA: Inferred from direct assay	16982419	GOA
involved in axonogenesis	IMP IMP: Inferred from mutant phenotype	16982419	GOA
involved in establishment of neuroblast polarity	IMP IMP: Inferred from mutant phenotype	16982419	GOA
involved in microtubule cytoskeleton organization	IMP IMP: Inferred from mutant phenotype	16982419	GOA
involved in neuron projection development	IMP IMP: Inferred from mutant phenotype	16982419	GOA
involved in positive regulation of peptidyl-serine phosphorylation	IMP IMP: Inferred from mutant phenotype	16982419	GOA
involved in positive regulation of vascular associated smooth muscle cell migration	IMP IMP: Inferred from mutant phenotype	22158624	GOA

Cellular Component GO Annotation	Evidence	参考文献	由来
part of COP9 signalosome	IDA IDA: Inferred from direct assay	18850735	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

DOCK7 Protein Structure

DUF3398

DOCK-C2

DHR-2

0
400
800
1200
1600
2000
2109 a.a.

Protein Preferred Names	Protein Names
dedicator of cytokinesis protein 7

DOCK7 Protein-protein interaction Information

Type	タンパク質名	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	参考文献
Intra	DOCK7	Q96N67	LRCH1	Homo sapiens	Q9Y2L9	Anti Tag CoIP	35271311
Intra	DOCK7	Q96N67	LRCH1	Homo sapiens	Q9Y2L9	Anti Tag CoIP	24255178
Intra	DOCK7	Q96N67	NBEAL2	Homo sapiens	Q6ZNJ1	Anti Tag CoIP	29187380
Intra	DOCK7	Q96N67	NBEAL2	Homo sapiens	Q6ZNJ1	Anti Bait CoIP	29187380
Intra	DOCK7	Q96N67	SEC16A	Homo sapiens	O15027	Anti Bait CoIP	29187380
Intra	DOCK7	Q96N67	LRCH4	Homo sapiens	O75427	Anti Tag CoIP	32203420
Intra	DOCK7	Q96N67	LRCH3	Homo sapiens	Q96II8	Anti Tag CoIP	35271311
Intra	DOCK7	Q96N67	LRCH3	Homo sapiens	Q96II8	Anti Tag CoIP	29467281
Intra	DOCK7	Q96N67	LRCH3	Homo sapiens	Q96II8	BioID	29467281
Intra	DOCK7	Q96N67	LRCH3	Homo sapiens	Q96II8	Anti Tag CoIP	24255178

Cross: Cross-species interaction Intra: Intraspecies interaction

DOCK7 抗体

製品番号	製品名	アプリケーション	反応性
HY-P89558	DOCK 7 Antibody (YA8902)	WB, ICC/IF, IF-Tissue, IP, ELISA	human, mouse, rat

関連疾患

Diseases	Alias
Developmental And Epileptic Encephalopathy 23	DEE23 Epileptic Encephalopathy, Early Infantile, 23 Eiee23 Early-Onset Epileptic Encephalopathy-Cortical Blindness-Intellectual Disability-Facial Dysmorphism Syndrome Epilepsy-Cortical Blindness-Intellectual Disability-Facial Dysmorphism Syndrome Developmental And Epileptic Encephalopathy, 23 Early Infantile Epileptic Encephalopathy 23
Hypobetalipoproteinemia, Familial, 2	Familial Hypobetalipoproteinemia 2 FHBL2 Hypolipidemia, Familial, Combined Combined Familial Hypolipidemia Combined Hypobetalipoproteinemia Familial Hypobetalipoproteinemia, Familial, Type 2
Cortical Blindness	Blindness, Cortical
Visual Cortex Disease	Visual Cortex Dysfunction Visual Cortex Disorder Visual Cortical Disorder Disease Of Visual Cortex
Visual Pathway Disease	Disorder Of Visual Pathways
Night Blindness, Congenital Stationary, Autosomal Dominant 3	Congenital Stationary Night Blindness Autosomal Dominant 3 CSNBAD3 Night Blindness, Congenital Stationary, Nougaret Type Nougaret Type Congenital Stationary Night Blindness Congenital Stationary Night Blindness Nougaret Type Hemeralopia Congenital Essential Blindness, Night, Stationary, Congenital, Autosomal Dominant, Type 3
Generalized Epilepsy With Febrile Seizures Plus, Type 7	Febrile Seizures, Familial, 3b GEFSP7 GEFS+7 Generalized Epilepsy With Febrile Seizures Plus 7 Gefs+, Type 7 Generalised Epilepsy With Febrile Seizures Plus 7 Generalised Epilepsy With Febrile Seizures Plus Type 7 Generalized Epilepsy With Febrile Seizures Plus Type 7 FEB3B Familial Febrile Convulsions 3 Gefs+ Type 7 Epilepsy, Generalized, With Febrile Seizures Plus, Type 7 Generalized Epilepsy With Febrile Seizures Plus, 7
Pitt-Hopkins-Like Syndrome 2	PTHSL2 Mesh D006985 Mesh D008607
Developmental And Epileptic Encephalopathy	Encephalopathy, Developmental And Epileptic
Developmental And Epileptic Encephalopathy 2	Epileptic Encephalopathy, Early Infantile, 2 DEE2 Eiee2 Issx2 Developmental And Epileptic Encephalopathy, 2 Infantile Spasm Syndrome, X-Linked 2 Early Infantile Epileptic Encephalopathy 2 X-Linked Infantile Spasm Syndrome 2 Atypical Rett Syndrome Cdkl5-Related Atypical Rett Syndrome Hanefeld Variant Infantile Spasm Syndrome X-Linked 2 Rett Syndrome Early-Onset Seizure Variant Rett Syndrome Variant With Infantile Spasms Encephalopathy, Epileptic, Early Infantile, Type 2
Adams-Oliver Syndrome	Adams Oliver Syndrome Aos Congenital Scalp Defects With Distal Limb Reduction Anomalies Aplasia Cutis Congenita With Terminal Transverse Limb Defects Congenital Scalp Defects With Distal Limb Anomalies Limb, Scalp And Skull Defects Limb Scalp And Skull Defects Absence Defect Of Limbs, Scalp, And Skull
Early Infantile Epileptic Encephalopathy	Early Infantile Epileptic Encephalopathy With Burst-Suppression Early Infantile Epileptic Encephalopathy With Suppression Bursts Eiee Early Infantile Epileptic Encephalopathy With Suppression-Bursts Ohtahara Syndrome Encephalopathy, Epileptic, Early Infantile

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

Pre-clinical Phase

Bioactive Molecules (3)

製品番号	製品名	製品効果	純度	Rare Diseases
HY-RS03929	DOCK7 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown
HY-RS21558	Dock7 Mouse Pre-designed siRNA Set A	Pre-designed Set	/	Unkown
HY-RS28076	Dock7 Rat Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

生物種	Symbol	由来	ID
Macaca mulatta	DOCK7	VGNC	VGNC:71864
Bos taurus	DOCK7	VGNC	VGNC:28161
Felis catus	DOCK7	VGNC	VGNC:61576
Mus musculus	DOCK7	MGD	MGI:1914549
Rattus norvegicus	DOCK7	RGD	RGD:1309790
Canis familiaris	DOCK7	VGNC	VGNC:40051
Others	DOCK7	NCBI