DCTN2 - dynactin subunit 2 Gene

Also Known as RBP50; DCTN50; HEL-S-77; DYNAMITIN

生物種: Homo sapiens

遺伝子タイプ: protein coding
遺伝子ID: 10540

About DCTN2

Cytogenetic location: 12q13.3 Genomic coordinates (GRCh38): 12:57,530,051-57,547,192 (from NCBI)

This gene has 33 transcripts (splice variants) and 214 orthologues. Ubiquitous expression in brain (RPKM 42.2), esophagus (RPKM 36.9) and 25 other tissues.

Summary

This gene encodes a 50-kD subunit of dynactin, a macromolecular complex consisting of 10-11 subunits ranging in size from 22 to 150 kD. Dynactin binds to both microtubules and cytoplasmic dynein. It is involved in a diverse array of cellular functions, including ER-to-Golgi transport, the centripetal movement of lysosomes and endosomes, spindle formation, chromosome movement, nuclear positioning, and axonogenesis. This subunit is present in 4-5 copies per dynactin molecule. It contains three short alpha-helical coiled-coil domains that may mediate association with self or Other dynactin subunits. It may interact directly with the largest subunit (p150) of dynactin and may affix p150 in place. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2012]

DCTN2 Products (7)

mRNA Protein Name
NM_001261412.2 NP_001248341.1 dynactin subunit 2 isoform 2
NM_001261413.2 NP_001248342.1 dynactin subunit 2 isoform 3
NM_001348065.2 NP_001334994.1 dynactin subunit 2 isoform 4
NM_001348066.2 NP_001334995.1 dynactin subunit 2 isoform 5
NM_001348067.2 NP_001334996.1 dynactin subunit 2 isoform 6
NM_001348068.2 NP_001334997.1 dynactin subunit 2 isoform 6
NM_006400.5 NP_006391.1 dynactin subunit 2 isoform 1
Molecular Function GO Annotation Evidence 参考文献 由来
enables identical protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
10226031 GOA
enables protein kinase binding IPI
IPI: Inferred from physical interaction
17139249 GOA
enables spectrin binding IDA
IDA: Inferred from direct assay
23704327 GOA
Biological Process GO Annotation Evidence 参考文献 由来
involved in mitotic metaphase chromosome alignment IMP
IMP: Inferred from mutant phenotype
8647893 GOA
involved in mitotic spindle organization IMP
IMP: Inferred from mutant phenotype
8647893 GOA
acts upstream of or within protein localization to centrosome IMP
IMP: Inferred from mutant phenotype
24816561 GOA
Cellular Component GO Annotation Evidence 参考文献 由来
located in centrosome IDA
IDA: Inferred from direct assay
8647893 GOA
part of dynactin complex IDA
IDA: Inferred from direct assay
8647893 GOA
located in kinetochore IDA
IDA: Inferred from direct assay
8647893 GOA
located in vesicle IDA
IDA: Inferred from direct assay
20682791 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

DCTN2 Protein Structure

Dynamitin

Dynamitin: Dynamitin (12 - 399)

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

dynactin subunit 2

  • 50 kDa dynein-associated polypeptide

DCTN2 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
DCTN2 Q13561 CENPH Homo sapiens Q9H3R5 32296183
Intra
DCTN2 Q13561 CENPH Homo sapiens Q9H3R5 32296183
Intra
DCTN2 Q13561 BORCS6 Homo sapiens Q96GS4 32296183
Intra
DCTN2 Q13561 BORCS6 Homo sapiens Q96GS4 32296183
Intra
DCTN2 Q13561 BORCS6 Homo sapiens Q96GS4 33961781
Intra
DCTN2 Q13561 BORCS6 Homo sapiens Q96GS4 32296183
Intra
DCTN2 Q13561 ABI2 Homo sapiens Q9NYB9-2 32296183
Intra
DCTN2 Q13561 KIFC3 Homo sapiens Q9BVG8-5 32296183
Intra
DCTN2 Q13561 RABGEF1 Homo sapiens Q9UJ41-4 32296183
Intra
DCTN2 Q13561 KIFC3 Homo sapiens Q9BVG8 25416956
Intra
DCTN2 Q13561 KIFC3 Homo sapiens Q9BVG8 25416956
Intra
DCTN2 Q13561 VPS33A Homo sapiens Q96AX1 32814053
Intra
DCTN2 Q13561 VPS33A Homo sapiens Q96AX1 32814053
Intra
DCTN2 Q13561 VPS33A Homo sapiens Q96AX1 32814053
Intra
DCTN2 Q13561 CCDC172 Homo sapiens P0C7W6 31515488
Intra
DCTN2 Q13561 CCDC172 Homo sapiens P0C7W6 25416956
Cross
DCTN2 Q13561 y14_sars Human SARS coronavirus Q7TLC7 22046132
Cross
DCTN2 Q13561 y14_sars Human SARS coronavirus Q7TLC7 22046132
Cross
DCTN2 Q13561 ns6_sars Human SARS coronavirus P59634 22046132
Cross
DCTN2 Q13561 ns6_sars Human SARS coronavirus P59634 22046132
Intra
DCTN2 Q13561 BLOC1S1 Homo sapiens P78537 32296183
Intra
DCTN2 Q13561 BLOC1S1 Homo sapiens P78537 32296183
Intra
DCTN2 Q13561 PDCD6 Homo sapiens O75340 26950892
Intra
DCTN2 Q13561 PDCD6 Homo sapiens O75340 26950892
Intra
DCTN2 Q13561 SMARCD1 Homo sapiens Q96GM5 32296183
Intra
DCTN2 Q13561 GADD45A Homo sapiens P24522 32296183
Intra
DCTN2 Q13561 GADD45A Homo sapiens P24522 32296183
Intra
DCTN2 Q13561 BLOC1S6 Homo sapiens Q9UL45 25416956
Intra
DCTN2 Q13561 BLOC1S6 Homo sapiens Q9UL45 25416956
Intra
DCTN2 Q13561 BLOC1S2 Homo sapiens Q6QNY1 32296183
Intra
DCTN2 Q13561 BLOC1S2 Homo sapiens Q6QNY1 32296183
Intra
DCTN2 Q13561 BLOC1S2 Homo sapiens Q6QNY1 32296183
Intra
DCTN2 Q13561 HTT Homo sapiens P42858
Y2H
17500595
Intra
DCTN2 Q13561 TXLNB Homo sapiens Q8N3L3 32296183
Intra
DCTN2 Q13561 CAPZA2 Homo sapiens P47755 35271311
Intra
DCTN2 Q13561 DCTN1 Homo sapiens Q14203
TAP
27173435
Intra
DCTN2 Q13561 CAPZA2 Homo sapiens P47755
TAP
27173435
Intra
DCTN2 Q13561 DCTN1 Homo sapiens Q14203 33961781
Intra
DCTN2 Q13561 DCTN1 Homo sapiens Q14203 35271311
Intra
DCTN2 Q13561 MAPRE3 Homo sapiens Q9UPY8 27107012
Intra
DCTN2 Q13561 MAPRE3 Homo sapiens Q9UPY8
SLC
27107012
Intra
DCTN2 Q13561 MAPRE3 Homo sapiens Q9UPY8 27107012
Intra
DCTN2 Q13561 RINT1 Homo sapiens Q6NUQ1 32296183
Intra
DCTN2 Q13561 RINT1 Homo sapiens Q6NUQ1 32296183
Intra
DCTN2 Q13561 RINT1 Homo sapiens Q6NUQ1 32296183
Intra
DCTN2 Q13561 USHBP1 Homo sapiens Q8N6Y0 32296183
Intra
DCTN2 Q13561 CEP44 Homo sapiens Q9C0F1 32296183
Intra
DCTN2 Q13561 CEP44 Homo sapiens Q9C0F1 32296183
Intra
DCTN2 Q13561 CEP44 Homo sapiens Q9C0F1 32296183
Intra
DCTN2 Q13561 COG3 Homo sapiens Q96JB2-2 32296183
Intra
DCTN2 Q13561 COG3 Homo sapiens Q96JB2-2 32296183
Intra
DCTN2 Q13561 COG3 Homo sapiens Q96JB2-2 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

DCTN2 抗体

製品番号 製品名 アプリケーション 反応性
HY-P810970 Dynactin p50 Antibody WB, IHC-P Human, Mouse, Rat

関連疾患

Diseases Alias
Charcot-Marie-Tooth Disease
  • Cmt

  • Hmsn

  • Hereditary Motor And Sensory Neuropathy

  • Pma

  • Cmt - Charcot-Marie-Tooth Disease

  • Charcot Marie Tooth Disease

  • Charcot-Marie-Tooth Hereditary Neuropathy

  • Charcot-Marie-Tooth Syndrome

  • Peroneal Muscular Atrophy

  • Hereditary Motor And Sensory Neuropathies

Neuronopathy, Distal Hereditary Motor, Type Viib
  • HMN7B

  • Hmn Viib

  • Dhmn7b

  • Neuropathy, Distal Hereditary Motor, Type Viib

  • Distal Hereditary Motor Neuronopathy Type 7b

  • Distal Hereditary Motor Neuropathy Type Viib

  • Neuronopathy, Distal Hereditary Motor, Type 7b

  • Neuropathy, Distal Hereditary Motor, With Vocal Cord Paralysis, Type Viib

  • Lower Motor Neuron Disease, Dynactin Type

  • Distal Spinal Muscular Atrophy With Vocal Cord Paralysis Type 7b

  • Harper-Young Myopathy

  • Neuronopathy, Distal Hereditary Motor, 7b

  • Distal Hereditary Motor Neuropathy With Vocal Cord Paralysis Type Viib

  • Lower Motor Neuron Disease Dynactin Type

  • Plmnd

  • Progressive Lower Motor Neuron Disease

  • Neuropathy, Motor, Distal, Hereditary, Type Viib

Distal Hereditary Motor Neuronopathy Type 7
  • Dhmn7

  • Dhmnvpy

  • Distal Spinal Muscular Atrophy With Vocal Cord Paralysis

Perry Syndrome
  • Parkinsonism With Alveolar Hypoventilation And Mental Depression

  • PERRYS

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

Congenital Nervous System Abnormality
  • Congenital Neurologic Anomaly

  • Congenital Nervous System Disorder

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

Orthologs Information

生物種 Symbol 由来 ID
Macaca mulatta DCTN2 VGNC VGNC:71751
Felis catus DCTN2 VGNC VGNC:61378
Canis familiaris DCTN2 VGNC VGNC:39817
Rattus norvegicus DCTN2 RGD RGD:1303182
Mus musculus DCTN2 MGD MGI:107733
Bos taurus DCTN2 VGNC VGNC:27929
Others DCTN2 NCBI