TUBD1 - tubulin delta 1 Gene

Also Known as TUBD

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 51174

About TUBD1

Cytogenetic location: 17q23.1 Genomic coordinates (GRCh38): 17:59,859,479-59,892,943 (from NCBI)

This gene has 16 transcripts (splice variants), 204 orthologues and 23 paralogues. Ubiquitous expression in esophagus (RPKM 3.8), thyroid (RPKM 3.7) and 25 other tissues.

Summary

Predicted to enable GTP binding activity. Predicted to be a structural constituent of Cytoskeleton. Predicted to be involved in microtubule Cytoskeleton organization; mitotic cell cycle; and positive regulation of smoothened signaling pathway. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

TUBD1 Products (6)

mRNA Protein Name
NM_001193609.2 NP_001180538.1 tubulin delta chain isoform 2
NM_001193610.2 NP_001180539.1 tubulin delta chain isoform 3
NM_001193611.2 NP_001180540.1 tubulin delta chain isoform 4
NM_001193612.2 NP_001180541.1 tubulin delta chain isoform 5
NM_001193613.2 NP_001180542.1 tubulin delta chain isoform 6
NM_016261.4 NP_057345.2 tubulin delta chain isoform 1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
33961781 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

TUBD1 Protein Structure

Tubulin

Tubulin: Tubulin/FtsZ family, GTPase domain (3 - 225)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 453 a.a.
Protein Preferred Names Protein Names

tubulin delta chain

  • delta-tubulin

TUBD1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
TUBD1 Q9UJT1 CCT6B Homo sapiens Q92526 33961781
Cross: Cross-species interaction Intra: Intraspecies interaction

TUBD1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P83669 delta Tubulin Antibody WB, IHC-P Human, Mouse

Related Diseases

Diseases Alias
Ciliary Dyskinesia, Primary, 27
  • Primary Ciliary Dyskinesia 27

  • CILD27

  • Ciliary Dyskinesia, Primary, 27, Without Situs Inversus

  • Primary Ciliary Dyskinesia 27 Without Situs Inversus

  • Primary Ciliary Dyskinesia 27 With Or Without Situs Inversus

  • Dyskinesia, Ciliary, Primary, 27

Atrial Septal Defect 6
  • ASD6

  • Atrial Heart Septal Defect 6

  • Septal Defect, Atrial, Type 6

Orofaciodigital Syndrome Ix
  • OFD9

  • Orofaciodigital Syndrome With Retinal Abnormalities

  • Oral-Facial-Digital Syndrome With Retinal Abnormalities

  • Orofaciodigital Syndrome 9

  • Oral-Facial-Digital Syndrome Type 9

  • Ofds Ix

  • Oral-Facial-Digital Syndrome, Type Ix

  • Ofd Syndrome 9

  • Ofds 9

  • Oral Facial Digital Syndrome 9

  • Oral Facial Digital Syndrome Type 9

  • Orofaciodigital Syndrome Type 9

  • Orofaciodigital Syndrome, Type Ix

Seckel Syndrome 7
  • SCKL7

  • Microcephalic Primordial Dwarfism, Dauber Type

  • Seckel Syndrome, Type 7

Retinitis Pigmentosa 83
  • RP83

  • Retinitis Pigmentosa, Type 83

Weaver Syndrome
  • Wss

  • Weaver-Smith Syndrome

  • WVS

  • Weaver-Like Syndrome

  • Weaver-Williams Syndrome

  • Camptodactyly-Overgrowth-Unusual Facies Syndrome

  • Camptodactyly - Overgrowth - Unusual Facies

  • Ezh2 Related Overgrowth

  • Overgrowth Syndrome With Accelerated Skeletal Maturation, Unusual Facies, And Camptodactyly

  • Weaver Smith Syndrome

  • Weaver Like Syndrome

  • Weaver Williams Syndrome

  • Camptodactyly-Overgrowth-Unusual Facies

  • Weaver Syndrome 1

  • Weaver Syndrome 2

  • Wvs1

  • Wvs2

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

Orthologs Information

Species Symbol Source ID
Felis catus TUBD1 VGNC VGNC:66702
Rattus norvegicus TUBD1 RGD RGD:1311967
Macaca mulatta TUBD1 VGNC VGNC:79052
Mus musculus TUBD1 MGD MGI:1891826
Canis familiaris TUBD1 VGNC VGNC:47992
Bos taurus TUBD1 VGNC VGNC:36510
Others TUBD1 NCBI