1. Gene
  2. HOOK3 - hook microtubule tethering protein 3 Gene

HOOK3 - hook microtubule tethering protein 3 Gene

Homo sapiens

Also known as HK3

Gene ID: 84376 | Gene type: protein coding

About HOOK3

Cytogenetic location: 8p11.21 Genomic coordinates (GRCh38): 8:42,896,978-43,030,535 (from NCBI)

This gene has 6 transcripts (splice variants), 217 orthologues, 5 paralogues and is associated with 77 phenotypes. Ubiquitous expression in thyroid (RPKM 6.6), fat (RPKM 4.5) and 25 other tissues.

Summary

Hook proteins are cytosolic coiled-coil proteins that contain conserved N-terminal domains, which attach to microtubules, and more divergent C-terminal domains, which mediate binding to organelles. The Drosophila Hook protein is a component of the endocytic compartment.[supplied by OMIM, Apr 2004]

HOOK3 Products(1)

mRNA Protein Name
NM_032410.4 NP_115786.1 protein Hook homolog 3
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables dynactin binding IDA
IDA: Inferred from direct assay
27482052 GOA
enables dynein intermediate chain binding IDA
IDA: Inferred from direct assay
27482052 GOA
enables dynein light chain binding IPI
IPI: Inferred from physical interaction
27482052 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
18799622 GOA
enables microtubule binding IDA
IDA: Inferred from direct assay
11238449 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
17237231 GOA
Biological Process GO Annotation Evidence Reference Source
involved in Golgi localization IMP
IMP: Inferred from mutant phenotype
11238449 GOA
involved in cytoplasmic microtubule organization IMP
IMP: Inferred from mutant phenotype
11238449 GOA
involved in early endosome to late endosome transport IMP
IMP: Inferred from mutant phenotype
18799622 GOA
involved in endosome organization IMP
IMP: Inferred from mutant phenotype
18799622 GOA
involved in endosome to lysosome transport IMP
IMP: Inferred from mutant phenotype
18799622 GOA
involved in lysosome organization IMP
IMP: Inferred from mutant phenotype
18799622 GOA
involved in protein localization to perinuclear region of cytoplasm IMP
IMP: Inferred from mutant phenotype
32073997 GOA
Cellular Component GO Annotation Evidence Reference Source
part of FHF complex IDA
IDA: Inferred from direct assay
18799622 GOA
part of HOPS complex IDA
IDA: Inferred from direct assay
18799622 GOA
located in cis-Golgi network IDA
IDA: Inferred from direct assay
11238449 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

HOOK3 Protein Structure

HOOK

HOOK: HOOK protein (6 - 717)

  • 0
  • 200
  • 400
  • 600
  • 718 a.a.
Protein Preferred Names Protein Names

protein Hook homolog 3

h-hook3

HOOK3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
HOOK3 Q86VS8 PNMA5 Homo sapiens Q96PV4 32296183
Intra
HOOK3 Q86VS8 PNMA5 Homo sapiens Q96PV4 32296183
Intra
HOOK3 Q86VS8 PNMA5 Homo sapiens Q96PV4 32296183
Intra
HOOK3 Q86VS8 CTIF Homo sapiens O43310-2 32296183
Intra
HOOK3 Q86VS8 CTIF Homo sapiens O43310-2 32296183
Intra
HOOK3 Q86VS8 KRT13 Homo sapiens P13646 32296183
Intra
HOOK3 Q86VS8 KRT13 Homo sapiens P13646 32296183
Intra
HOOK3 Q86VS8 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
HOOK3 Q86VS8 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
HOOK3 Q86VS8 MSR1 Homo sapiens P21757 17237231
Intra
HOOK3 Q86VS8 MSR1 Homo sapiens P21757 17237231
Intra
HOOK3 Q86VS8 KRT27 Homo sapiens Q7Z3Y8 32296183
Intra
HOOK3 Q86VS8 KRT27 Homo sapiens Q7Z3Y8 32296183
Intra
HOOK3 Q86VS8 AKTIP Homo sapiens Q9H8T0
Y2H
32073997
Intra
HOOK3 Q86VS8 HOOK1 Homo sapiens Q9UJC3
Y2H
32073997
Intra
HOOK3 Q86VS8 HOOK1 Homo sapiens Q9UJC3 33961781
Intra
HOOK3 Q86VS8 HOOK1 Homo sapiens Q9UJC3 32296183
Intra
HOOK3 Q86VS8 HOOK1 Homo sapiens Q9UJC3 28514442
Intra
HOOK3 Q86VS8 HOOK1 Homo sapiens Q9UJC3 32296183
Intra
HOOK3 Q86VS8 HOOK1 Homo sapiens Q9UJC3 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Small Intestine Neuroendocrine Neoplasm

Small Intestine Neuroendocrine Tumor

Neuroendocrine Tumor Of The Small Intestine

Net Of The Small Intestine

Neuroendocrine Neoplasm Of The Small Intestine

Neuroendocrine Tumor Of Small Bowel

Small Intestinal Neuroendocrine Neoplasm

Dystonia 6, Torsion

DYT6

Torsion Dystonia 6

Dystonia 6

Idiopathic Torsion Dystonia Of Mixed Type

Primary Dystonia, Dyt6 Type

Torsion Dystonia, Adult-Onset, Mixed Type

Dyt-Thap1

Adolescent-Onset Dystonia Of Mixed Type

Torsion Dystonia Adult Onset Mixed Type

Dyt6 Dystonia

Thap1 Dystonia

Generalized Cervical And Upper-Limb-Onset Dystonia

Adult-Onset Torsion Dystonia Mixed Type

Autosomal Dominant Torsion Dystonia 6

Dystonia-6

Torsion Dystonia Type 6

Dystonia, Type 6, Torsion

Hermansky-Pudlak Syndrome 9

HPS9

Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial

Delta Storage Pool Disease

Hermansky-Pudlak Syndrome, Type 9

Platelet Storage Pool Deficiency

Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells

Small Intestine Benign Neoplasm

Neoplasm Of Small Intestine

Small Intestinal Neoplasm

Neoplasm Of The Small Intestine

Small Bowel Cancer

Small Intestine Cancer

Malignant Neoplasm Of Small Intestine, Unspecified

Malignant Tumour Of Small Bowel

Malignant Tumour Of Small Intestine

Primary Malignant Neoplasm Of Meckel Diverticulum

Spinal Muscular Atrophy With Lower Extremity Predominant

Spinal Muscular Atrophy With Lower Extremity Predominance

Autosomal Dominant Childhood-Onset Proximal Spinal Muscular Atrophy With Contractures

Kugelberg-Welander Syndrome, Autosomal Dominant

Lower Extremity-Predominant Autosomal Dominant Proximal Spinal Muscular Atrophy With Contractures

Sma-Led

Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant

Spinal Muscular Atrophy, Juvenile, Proximal, Autosomal Dominant

Spinal Muscular Atrophy, Lower Extremity, Autosomal Dominant

Spinal Muscular Atrophy, Lower Extremity, Dominant

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
Mus musculus HOOK3 MGD MGI:2443554
Rattus norvegicus HOOK3 RGD RGD:1560960
Macaca mulatta HOOK3 VGNC VGNC:73433
Bos taurus HOOK3 VGNC VGNC:50090
Canis familiaris HOOK3 VGNC VGNC:41742
Felis catus HOOK3 VGNC VGNC:62834