2. Gene
  3. DNAL4 - dynein axonemal light chain 4 Gene

DNAL4 - dynein axonemal light chain 4 Gene

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

Also known as MRMV3; PIG27

Gene ID: 10126 | Gene type: protein coding

About DNAL4

Cytogenetic location: 22q13.1 Genomic coordinates (GRCh38): 22:38,778,508-38,794,143 (from NCBI)

This gene has 4 transcripts (splice variants), 191 orthologues and is associated with 2 phenotypes. Broad expression in testis (RPKM 25.2), thyroid (RPKM 13.3) and 25 other tissues.

Summary

This gene encodes an axonemal dynein LIGHT chain which functions as a component of the outer dynein arms complex. This complex acts as the molecular motor that provides the force to move cilia in an ATP-dependent manner. The encoded protein is expressed in tissues with motile cilia or flagella and may be involved in the movement of sperm flagella. [provided by RefSeq, Dec 2014]

DNAL4 Products(1)

mRNA Protein Name
NM_005740.3 NP_005731.1 dynein axonemal light chain 4
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 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

DNAL4 Protein Structure

Dynein_light

Dynein_light: Dynein light chain type 1 (20 - 105)

  • 0
  • 105 a.a.
Protein Preferred Names Protein Names

dynein axonemal light chain 4

dynein light chain, outer arm 4

DNAL4 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra DNAL4 O96015 NUDT22 Homo sapiens Q9BRQ3
Validated Y2H
32296183
Intra DNAL4 O96015 KRTAP12-3 Homo sapiens P60328
Validated Y2H
32296183
Intra DNAL4 O96015 KRTAP9-8 Homo sapiens Q9BYQ0
Validated Y2H
32296183
Intra DNAL4 O96015 NFATC2IP Homo sapiens Q8NCF5-2
Y2H Prey Pooling
32296183
Intra DNAL4 O96015 NFATC2IP Homo sapiens Q8NCF5-2
Validated Y2H
32296183
Intra DNAL4 O96015 NFATC2IP Homo sapiens Q8NCF5-2
Y2H Array
32296183
Intra DNAL4 O96015 DYNLL1 Homo sapiens P63167
Validated Y2H
32296183
Intra DNAL4 O96015 DYNLL1 Homo sapiens P63167
Anti Tag CoIP
33961781
Intra DNAL4 O96015 CAMK2D Homo sapiens Q13557
Y2H Array
25416956
Intra DNAL4 O96015 CAMK2D Homo sapiens Q13557
Anti Tag CoIP
33961781
Intra DNAL4 O96015 CAMK2D Homo sapiens Q13557
Y2H Array
31515488
Intra DNAL4 O96015 CAMK2D Homo sapiens Q13557
Validated Y2H
25416956
Intra DNAL4 O96015 NTAQ1 Homo sapiens Q96HA8
Validated Y2H
32296183
Intra DNAL4 O96015 CHIC2 Homo sapiens Q9UKJ5
Validated Y2H
32296183
Intra DNAL4 O96015 DYNLL2 Homo sapiens Q96FJ2
Y2H Pooling
16189514
Intra DNAL4 O96015 FHL5 Homo sapiens Q5TD97
Y2H Array
31515488
Intra DNAL4 O96015 DYNLL2 Homo sapiens Q96FJ2
Y2H Array
31515488
Intra DNAL4 O96015 DYNLL2 Homo sapiens Q96FJ2
Y2H Prey Pooling
25416956
Intra DNAL4 O96015 DYNLL2 Homo sapiens Q96FJ2
Validated Y2H
25416956
Intra DNAL4 O96015 FHL5 Homo sapiens Q5TD97
Validated Y2H
32296183
Intra DNAL4 O96015 DYNLL2 Homo sapiens Q96FJ2
Y2H Array
25416956
Intra DNAL4 O96015 DYNLL2 Homo sapiens Q96FJ2
Anti Tag CoIP
33961781
Intra DNAL4 O96015 FHL5 Homo sapiens Q5TD97
Y2H Prey Pooling
32296183
Intra DNAL4 O96015 FHL5 Homo sapiens Q5TD97
Y2H Array
32296183
Intra DNAL4 O96015 GNA14 Homo sapiens O95837
Validated Y2H
25416956
Intra DNAL4 O96015 GNA14 Homo sapiens O95837
Y2H Array
25416956
Intra DNAL4 O96015 NOTCH2NLA Homo sapiens Q7Z3S9
Y2H Array
25416956
Intra DNAL4 O96015 NOTCH2NLA Homo sapiens Q7Z3S9
Y2H Prey Pooling
25416956
Intra DNAL4 O96015 NOTCH2NLA Homo sapiens Q7Z3S9
Validated Y2H
25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Mirror Movements 3

MRMV3

Mirror Movements, Type 3
Mirror Movements 1

Congenital Mirror Movement Disorder

Bimanual Synergia

Congenital Mirror Movements

Familial Congenital Controlateral Synkinesia

Familial Congenital Mirror Movements

Hereditary Congenital Controlateral Synkinesia

Hereditary Congenital Mirror Movements

Isolated Congenital Controlateral Synkinesia

Isolated Congenital Mirror Movements

Mirror Movements

MRMV1

Mirror Movements 1 And/Or Agenesis Of The Corpus Callosum

Mirror Movements, Congenital

Bimanual Synkinesis

Cmm

Mirror Movements, Type 1
Expressive Language Disorder

Developmental Expressive Language Disorder
Necrotizing Ulcerative Gingivitis

Acute Necrotizing Ulcerative Gingivitis

Anug

Vincent Angina

Vincent'S Disease

Acute Necrotising Ulcerative Gingivitis

Acute Necrotising Ulcerative Gingivostomatitis

Acute Necrotizing Ulcerative Gingivostomatitis

Acute Ulceromembranous Gingivitis

Angina - Vincents

Early Acute Necrotising Gingivitis

Trench Mouth

Vincent'S Angina

Vincent'S Angina - Pharyngitis

Vincent'S Infection, Any Site

Acute Membranous Gingivitis

Fusospirillary Gingivitis

Fusospirillosis

Phagedenic Gingivitis

Vincent'S Gingivitis

Vincent'S Infection

Vincent'S Stomatitis

Gingivitis, Necrotizing Ulcerative
Suppurative Otitis Media

Otitis Media With Effusion - Purulent

Purulent Otitis Media

Otitis Media, Suppurative
Klippel-Feil Syndrome

Cervical Vertebral Fusion

Congenital Dystrophia Brevicollis

Cervical Fusion Syndrome

Klippel-Feil Deformity

Autosomal Dominant Klippel-Feil Syndrome

Congenital Synostosis Of Cervical Vertebrae

Klippel-Feil And Turner Syndrome

Klippel-Feil Deformity, Deafness And Facial Asymmetry

Klippel Feil Syndrome

Cervical Vertebral Fusion Syndrome

Dystrophia Brevicollis Congenita

Fusion Of Cervical Vertebrae

Kfs

Klippel-Feil Sequence

Vertebral Cervical Fusion Syndrome

Klippel-Feil Syndrome, Autosomal Dominant

Klippel-Feil Malformation

Isolated Klippel-Feil Syndrome
Dandy-Walker Syndrome

Dandy-Walker Malformation

DWS

Atresia Of Foramina Of Magendie And Luschka

Dandy-Walker Complex

Dandy-Walker Cyst

Dandy-Walker Deformity

Dandy Walker Cyst

Dw Complex

Dandy-Walker Syndrome Or Malformation

Dandy-Walker Variant

Mega Cisterna Magna

Dwm

Hydrocephalus, Internal, Dandy-Walker Type

Hydrocephalus, Noncommunicating, Dandy-Walker Type

Luschka-Magendie Foramina Atresia

Isolated Dandy-Walker Malformation

Mega-Cisterna Magna

Dandy Walker Variant

Atresia Of Foramen Of Luschka

Atresia Of Foramen Of Magendie

Congenital Blockage Of Foramen Magendie
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
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-RS03892 DNAL4 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Macaca mulatta DNAL4 VGNC VGNC:71945
Rattus norvegicus DNAL4 RGD RGD:1309099
Bos taurus DNAL4 VGNC VGNC:56196
Mus musculus DNAL4 MGD MGI:1859217
Felis catus DNAL4 VGNC VGNC:82472
Canis familiaris DNAL4 VGNC VGNC:40022