DYNLT1 - dynein light chain Tctex-type 1 Gene

Also Known as CW-1; TCTEL1; TCTEX1; tctex-1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 6993

About DYNLT1

Cytogenetic location: 6q25.3 Genomic coordinates (GRCh38): 6:158,636,474-158,644,743 (from NCBI)

This gene has 3 transcripts (splice variants), 219 orthologues and 5 paralogues. Ubiquitous expression in testis (RPKM 62.3), colon (RPKM 58.0) and 25 other tissues.

Summary

This gene encodes a component of the motor complex, cytoplasmic dynein, which transports cellular cargo along microtubules in the cell. The encoded protein regulates the length of primary cilia which are sensory organelles found on the surface of cells. The protein encoded by this gene interacts with Viral Proteins, like the minor capsid protein L2 of human papillomavirus, and is required for dynein-mediated delivery of the viral nucleic acid to the host nucleus. This protein interacts with oncogenic nucleoporins to disrupt gene regulation and cause leukemic transformation. Pseudogenes of this gene are present on chromosomes 4 and 17. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2014]

DYNLT1 Products (3)

mRNA Protein Name
NM_001291602.2 NP_001278531.1 dynein light chain Tctex-type 1 isoform 2
NM_001291603.2 NP_001278532.1 dynein light chain Tctex-type 1 isoform 3
NM_006519.4 NP_006510.1 dynein light chain Tctex-type 1 isoform 1
Molecular Function GO Annotation Evidence References Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
17965411 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
10644691 GOA
Biological Process GO Annotation Evidence References Source
involved in intracellular transport of viral protein in host cell IMP
IMP: Inferred from mutant phenotype
18647839 GOA
Cellular Component GO Annotation Evidence References Source
part of cytoplasmic dynein complex IDA
IDA: Inferred from direct assay
25205765 GOA
located in cytoplasmic microtubule IDA
IDA: Inferred from direct assay
21262767 GOA
part of dynein complex IPI
IPI: Inferred from physical interaction
24986880 GOA
located in secretory vesicle IDA
IDA: Inferred from direct assay
21262767 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

DYNLT1 Protein Structure

Tctex-1

Tctex-1: Tctex-1 family (15 - 112)

  • 0
  • 100
  • 113 a.a.
Protein Preferred Names Protein Names

dynein light chain Tctex-type 1

  • T-complex testis-specific protein 1 homolog

DYNLT1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
DYNLT1 P63172 PELO Homo sapiens Q9BRX2 32296183
Intra
DYNLT1 P63172 HSPB9 Homo sapiens Q9BQS6
Y2H
15503857
Intra
DYNLT1 P63172 HSPB9 Homo sapiens Q9BQS6 15503857
Intra
DYNLT1 P63172 TCEANC Homo sapiens Q8N8B7-2 32296183
Intra
DYNLT1 P63172 ARID4B Homo sapiens Q4LE39-3 32296183
Intra
DYNLT1 P63172 OLFM3 Homo sapiens Q96PB7-3 32296183
Intra
DYNLT1 P63172 ACOX2 Homo sapiens Q99424 32296183
Intra
DYNLT1 P63172 DYNC1I2 Homo sapiens Q13409-3 32296183
Intra
DYNLT1 P63172 PITX2 Homo sapiens Q99697-2 32296183
Intra
DYNLT1 P63172 DYNLT2B Homo sapiens Q8WW35 32296183
Intra
DYNLT1 P63172 DYNLT2B Homo sapiens Q8WW35
TAP
27173435
Intra
DYNLT1 P63172 CCDC68 Homo sapiens Q9H2F9 32296183
Intra
DYNLT1 P63172 NHSL2 Homo sapiens Q5HYW2 32296183
Intra
DYNLT1 P63172 UXT Homo sapiens Q9UBK9 32296183
Intra
DYNLT1 P63172 NEFL Homo sapiens P07196 32814053
Intra
DYNLT1 P63172 NEFL Homo sapiens P07196 32814053
Intra
DYNLT1 P63172 NEFL Homo sapiens P07196 32814053
Intra
DYNLT1 P63172 HSPB7 Homo sapiens Q9UBY9 32296183
Intra
DYNLT1 P63172 LNX1 Homo sapiens Q8TBB1 32296183
Intra
DYNLT1 P63172 NTAQ1 Homo sapiens Q96HA8 32296183
Intra
DYNLT1 P63172 DYNLT3 Homo sapiens P51808
TAP
27173435
Intra
DYNLT1 P63172 RRAGA Homo sapiens Q7L523 32296183
Intra
DYNLT1 P63172 KLK15 Homo sapiens Q9H2R5 32296183
Intra
DYNLT1 P63172 AARSD1 Homo sapiens Q9BTE6-2 32296183
Intra
DYNLT1 P63172 MARK1 Homo sapiens Q9P0L2 32296183
Cross
DYNLT1 P63172 gag Mason-Pfizer monkey virus P07567 18647839
Cross: Cross-species interaction Intra: Intraspecies interaction

DYNLT1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P83518 Dynein Light Chain Tctex Type 1 Antibody (YA3263) WB, IHC-F, IHC-P, ICC/IF, FC, IP Human, Mouse, Rat
HY-P83518A Dynein Light Chain Tctex Type 1 Antibody (YA3263)(PBS only) WB, IHC-F, IHC-P, ICC/IF, FC, IP Human, Mouse, Rat

Related Diseases

Diseases Alias
Glaucomatocyclitic Crisis
  • Posner-Schlossman Syndrome

  • Terrien-Viel Syndrome

Pulmonary Hypertension
  • Primary Pulmonary Hypertension

  • Hypertension Pulmonary

  • Hypertension, Pulmonary

  • Hypertension, Pulmonary, Primary

  • Idiopathic Pulmonary Hypertension

  • Idiopathic Pulmonary Arterial Hypertension

  • Pulmonary Htn - [Hypertension]

Nonparalytic Poliomyelitis
  • Acute Nonparalytic Poliomyelitis

  • Non-Paralytic Aseptic Meningitis

Neutrophilic Dermatosis, Acute Febrile
  • Sweet Syndrome

  • Acute Febrile Neutrophilic Dermatosis

  • Ss

  • AFND

  • Pyrin-Associated Autoinflammatory Disease

  • PAAND

  • Gomm-Button Disease

  • Sweet'S Syndrome

  • Gomm Button Disease

  • Sweets Syndrome

  • Acromelic Frontonasal Dysostosis

  • Sweet Disease

Paralytic Poliomyelitis
  • Poliomyelitis, Paralytic

Dermatitis, Atopic, 3
  • ATOD3

  • Dermatitis, Atopic, Susceptibility To, 3

  • Atopic Dermatitis 3

  • Dermatitis, Atopic, With Asthma

  • Dermatitis, Atopic 3

  • Atopic Dermatitis With Asthma

Lissencephaly
  • Pachygyria

  • Broad Gyri Of Cerebrum

  • Large Gyri Of Cerebrum

  • Macrogyria

Bardet-Biedl Syndrome
  • Bbs

  • Biedl-Bardet Syndrome

Behcet Syndrome
  • Behcet Disease

  • Behcet'S Syndrome

  • Behcet'S Disease

  • Behçet Disease

  • Bd

  • Adamantiades-Behcet Disease

  • Triple Symptom Complex

  • Behçet'S Disease

  • Behet'S Syndrome

  • Bd Syndrome

  • Behçet Syndrome

  • Behçet'S Syndrome

  • Behcet Triple Symptom Complex

  • Malignant Aphthosis

  • Old Silk Route Disease

  • Adamantiades-Behçet Disease

Primary Ciliary Dyskinesia
  • Immotile Cilia Syndrome

  • Kartagener Syndrome

  • Dextrocardia Bronchiectasis And Sinusitis

  • Pcd

  • Ciliary Motility Disorders

  • Ciliary Motility Disorder

  • Immotile Ciliary Syndrome

  • Ciliary Dyskinesia Primary

  • Ics

  • Polynesian Bronchiectasis

  • Dextrocardia-Bronchiectasis-Sinusitis Syndrome

  • Immotile Cilia Syndrome, Kartagener Type

  • Primary Ciliary Dyskinesia And Situs Inversus

  • Primary Ciliary Dyskinesia, Kartagener Type

  • Siewert Syndrome

  • Dyskinesia, Ciliary, Primary

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

Orthologs Information

Species Symbol Source ID
Macaca mulatta DYNLT1 VGNC VGNC:81062
Felis catus DYNLT1 VGNC VGNC:61684
Rattus norvegicus DYNLT1 RGD RGD:620261
Canis familiaris DYNLT1 VGNC VGNC:54841
Others DYNLT1 NCBI