HOOK1 - hook microtubule tethering protein 1 Gene

Also Known as HK1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 51361

About HOOK1

Cytogenetic location: 1p32.1 Genomic coordinates (GRCh38): 1:59,814,949-59,876,322 (from NCBI)

This gene has 10 transcripts (splice variants), 205 orthologues and 5 paralogues. Broad expression in testis (RPKM 15.7), colon (RPKM 10.0) and 21 other tissues.

Summary

This gene encodes a member of the hook family of coiled-coil proteins, which bind to microtubules and organelles through their N- and C-terminal domains, respectively. The encoded protein localizes to discrete punctuate subcellular structures, and interacts with several members of the Rab GTPase family involved in endocytosis. It is thought to link endocytic membrane trafficking to the microtubule Cytoskeleton. Several alternatively spliced transcript variants have been identified, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]

HOOK1 Products (1)

mRNA Protein Name
NM_015888.6 NP_056972.1 protein Hook homolog 1
Molecular Function GO Annotation Evidence References Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
18799622 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
15471887 GOA
enables protein homodimerization activity IDA
IDA: Inferred from direct assay
32073997 GOA
Biological Process GO Annotation Evidence References Source
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 References 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 cytoplasm IDA
IDA: Inferred from direct assay
15471887 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

HOOK1 Protein Structure

HOOK

HOOK: HOOK protein (9 - 727)

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

protein Hook homolog 1

  • h-hook1

HOOK1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
HOOK1 Q9UJC3 TFIP11 Homo sapiens Q9UBB9 31515488
Intra
HOOK1 Q9UJC3 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
HOOK1 Q9UJC3 TFIP11 Homo sapiens Q9UBB9 25416956
Intra
HOOK1 Q9UJC3 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
HOOK1 Q9UJC3 TFIP11 Homo sapiens Q9UBB9 25416956
Intra
HOOK1 Q9UJC3 ZNF80 Homo sapiens P51504 32296183
Intra
HOOK1 Q9UJC3 ZNF80 Homo sapiens P51504 32296183
Intra
HOOK1 Q9UJC3 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
HOOK1 Q9UJC3 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
HOOK1 Q9UJC3 HOOK3 Homo sapiens Q86VS8
Y2H
32073997
Intra
HOOK1 Q9UJC3 CDK4 Homo sapiens P11802 32296183
Intra
HOOK1 Q9UJC3 CDK4 Homo sapiens P11802 31515488
Intra
HOOK1 Q9UJC3 CDK4 Homo sapiens P11802 25416956
Intra
HOOK1 Q9UJC3 CDK4 Homo sapiens P11802 32296183
Intra
HOOK1 Q9UJC3 TBC1D7 Homo sapiens Q9P0N9 31515488
Intra
HOOK1 Q9UJC3 TBC1D7 Homo sapiens Q9P0N9 25416956
Intra
HOOK1 Q9UJC3 TBC1D7 Homo sapiens Q9P0N9 25416956
Intra
HOOK1 Q9UJC3 NCOR1 Homo sapiens O75376 32814053
Intra
HOOK1 Q9UJC3 NCOR1 Homo sapiens O75376 32814053
Intra
HOOK1 Q9UJC3 NCOR1 Homo sapiens O75376 32814053
Intra
HOOK1 Q9UJC3 PIAS2 Homo sapiens O75928-2 32296183
Intra
HOOK1 Q9UJC3 PIAS2 Homo sapiens O75928-2 32296183
Intra
HOOK1 Q9UJC3 CDC5L Homo sapiens Q99459
Y2H
17043677
Intra
HOOK1 Q9UJC3 ZNF785 Homo sapiens A8K8V0 25416956
Intra
HOOK1 Q9UJC3 ZNF785 Homo sapiens A8K8V0 25416956
Intra
HOOK1 Q9UJC3 ZNF785 Homo sapiens A8K8V0 25416956
Intra
HOOK1 Q9UJC3 ANKRD23 Homo sapiens Q86SG2 32296183
Intra
HOOK1 Q9UJC3 ANKRD23 Homo sapiens Q86SG2 32296183
Intra
HOOK1 Q9UJC3 ZNF655 Homo sapiens Q8N720 32296183
Intra
HOOK1 Q9UJC3 ZNF655 Homo sapiens Q8N720 32296183
Intra
HOOK1 Q9UJC3 SYCE1 Homo sapiens Q8N0S2 25416956
Intra
HOOK1 Q9UJC3 AKTIP Homo sapiens Q9H8T0 25416956
Intra
HOOK1 Q9UJC3 AKTIP Homo sapiens Q9H8T0
Y2H
32073997
Intra
HOOK1 Q9UJC3 LMO2 Homo sapiens P25791 25416956
Intra
HOOK1 Q9UJC3 USP2 Homo sapiens O75604 25416956
Intra
HOOK1 Q9UJC3 BSG Homo sapiens P35613 29423001
Intra
HOOK1 Q9UJC3 BSG Homo sapiens P35613 29423001
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Spermatogenic Failure 16
  • SPGF16

  • Acephalic Spermatozoa Syndrome

  • Spermatozoa, Acephalic

Male Infertility Due To Acephalic Spermatozoa
  • Acephalic Spermatozoa Syndrome

Metanephric Adenoma
Renal Adenoma
  • Renal Cell Adenoma

Cranioectodermal Dysplasia 1
  • Sensenbrenner Syndrome

  • CED1

  • Levin Syndrome I

  • Cranio-Ectodermal Dysplasia

  • Dysplasia, Cranioectodermal, Type 1

  • Cranioectodermal Dysplasia

Ceroid Lipofuscinosis, Neuronal, 3
  • Batten Disease

  • Juvenile Neuronal Ceroid Lipofuscinosis

  • Neuronal Ceroid Lipofuscinosis 3

  • CLN3

  • Jncl

  • Spielmeyer-Vogt Disease

  • Vogt-Spielmeyer Disease

  • Spielmeyer-Sjogren Disease

  • Cln3 Disease

  • Neuronal Ceroid Lipofuscinosis, Juvenile

  • Cln3 Disease, Juvenile

  • Spielmeyer Sjogren Disease

  • Vogt Spielmeyer Disease

  • Batten-Mayou Disease

  • Batten-Spielmeyer-Vogt Disease

  • Cln3-Related Neuronal Ceroid-Lipofuscinosis

  • Juvenile Batten Disease

  • Juvenile Cerebroretinal Degeneration

  • Classic Juvenile Ncl

  • Classic Juvenile Neuronal Ceroid Lipofuscinosis

  • Juvenile Ncl

  • Lipofuscinosis, Ceroid, Neuronal, Type 3

Neuronal Ceroid Lipofuscinosis
  • Hereditary Ceroid Lipofuscinosis

  • Batten Disease

  • Ncl

  • Neuronal Ceroid-Lipofuscinoses

  • Lipofuscinosis, Ceroid, Neuronal

  • Juvenile Neuronal Ceroid Lipofuscinosis

  • Cerebromacular Dystrophy

  • Cerebromacular Degeneration

  • Ceroid-Lipofuscinosis

  • Ncl - [Neuronal Ceroid Lipofuscinosis]

  • Amaurotic Familial Idiocy

  • Amaurotic Idiocy

  • Amaurotic Idiot

  • Neuronal Lipofuscinosis

  • Pigmentary Retinal Lipoid Neuronal Heredodegeneration

Spermatogenic Failure
  • Azoospermia

  • Spgf

  • Spermatogenic Failure, Susceptibility To

  • Absent Sperm

  • Aspermatogenesis

  • Infertility Due To Azoospermia

  • Hypospermatogenesis

  • Azoospermatism

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 HOOK1 MGD MGI:1925213
Rattus norvegicus HOOK1 RGD RGD:1309987
Canis familiaris HOOK1 VGNC VGNC:41740
Macaca mulatta HOOK1 VGNC VGNC:73424
Bos taurus HOOK1 VGNC VGNC:29905
Felis catus HOOK1 VGNC VGNC:62832
Others HOOK1 NCBI