CKAP4 - cytoskeleton associated protein 4 Gene

Also Known as p63; CLIMP63; CLIMP-63; ERGIC-63

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 10970

About CKAP4

Cytogenetic location: 12q23.3 Genomic coordinates (GRCh38): 12:106,237,881-106,248,020 (from NCBI)

This gene has 3 transcripts (splice variants), 192 orthologues and 7 paralogues. Ubiquitous expression in bone marrow (RPKM 41.9), placenta (RPKM 30.9) and 25 other tissues.

Summary

Enables RNA binding activity. Located in several cellular components, including lipid droplet; nuclear speck; and rough endoplasmic reticulum. [provided by Alliance of Genome Resources, Apr 2022]

CKAP4 Products (1)

mRNA Protein Name
NM_006825.4 NP_006816.2 cytoskeleton-associated protein 4
Molecular Function GO Annotation Evidence Références Source
enables protein binding IPI
IPI: Inferred from physical interaction
28514442 GOA
Cellular Component GO Annotation Evidence Références Source
located in endoplasmic reticulum IDA
IDA: Inferred from direct assay
19401338 GOA
located in lipid droplet IDA
IDA: Inferred from direct assay
14741744 GOA
located in rough endoplasmic reticulum IDA
IDA: Inferred from direct assay
24454821 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
Protein Preferred Names Protein Names

cytoskeleton-associated protein 4

  • 63 kDa membrane protein

Recombinant CKAP4 Proteins

Cat. No. Nom du produit Accession Pureté
HY-P700976 CKAP4 Protein, Human (His) Q07065 (H128-V602) ≥ 90%, as determined by reducing SDS-PAGE.

CKAP4 Anticorps

Cat. No. Nom du produit Application Reactivity
HY-P810724 CKAP4 Antibody (YA9968) WB, ICC/IF, FC Human
HY-P84944 CKAP4 Antibody WB Human, Mouse

Related Diseases

Diseases Alias
Cystitis
  • Infective Cystitis

  • Urocystitis

  • Pyocystitis

Bladder Exstrophy
  • Exstrophy Of The Bladder

  • Classic Exstrophy Of The Bladder

Axenfeld-Rieger Syndrome, Type 1
  • Axenfeld-Rieger Syndrome Type 1

  • RIEG1

  • Rieg

  • Rgs

  • Rieger Syndrome Type 1

  • Rieger Syndrome, Type 1

  • Axenfeld-Rieger Syndrome 1

  • Iridogoniodysgenesis With Somatic Anomalies

Retinitis Pigmentosa 20
  • RP20

  • Retinitis Pigmentosa, Type 20

Spastic Paraplegia 36, Autosomal Dominant
  • SPG36

  • Hereditary Spastic Paraplegia 36

  • Autosomal Dominant Spastic Paraplegia Type 36

  • Autosomal Dominant Spastic Paraplegia 36

Interstitial Cystitis
  • Bladder Pain Syndrome

  • Painful Bladder Syndrome

  • Ulcerative Cystitis

  • Ic/Bps

  • Ic/Pbs

  • Interstitial Cystitis/Bladder Pain Syndrome

  • Interstitial Cystitis/Painful Bladder Syndrome

  • Cystitis, Interstitial

  • Chronic Interstitial Cystitis

  • Pelvic Congestion Syndrome

  • Trigonitis

Amelogenesis Imperfecta
  • Ai

  • Congenital Enamel Hypoplasia

  • Al - [Amelogenesis Imperfecta]

Hereditary Spastic Paraplegia
  • Familial Spastic Paraplegia

  • Hereditary Spastic Paraparesis

  • Strumpell-Lorrain Disease

  • Familial Spastic Paraparesis

  • Hsp

  • Spg

  • Strümpell-Lorrain Disease

  • Spastic Paraplegia, Hereditary

  • French Settlement Disease

  • Strumpell-Lorrain Syndrome

  • Fsp

  • Spastic Paraplegia, Familial

  • Spastic Paraplegia Hereditary

  • Spastic Paraplegia 3, Autosomal Dominant

  • Spastic Paraparesis

  • Hereditary Spastic Paralysis

  • Familial Spastic Paralysis

  • Hereditary Spastic Ataxia

Cone-Rod Dystrophy 2
  • Cone-Rod Dystrophy

  • CORD2

  • Cone-Rod Retinal Dystrophy

  • Rcrd2

  • Cone-Rod Retinal Dystrophy 2

  • Crd2

  • Cord

  • Crd

  • Retinal Cone-Rod Dystrophy

  • Cone-Rod Retinal Dystrophy-2

  • Retinal Cone-Rod Dystrophy 2

  • Tapetoretinal Degeneration

  • Cone-Rod Degeneration

  • Cone Rod Dystrophy

  • Dystrophy, Cone-Rod

  • Dystrophy, Cone-Rod, Type 2

  • Retinitis Pigmentosa

  • Retinitis Pigmentosa 2

  • Progressive Cone-Rod Dystrophy

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
Canis familiaris CKAP4 VGNC VGNC:39288
Felis catus CKAP4 VGNC VGNC:83533
Mus musculus CKAP4 MGD MGI:2444926
Bos taurus CKAP4 VGNC VGNC:27382
Rattus norvegicus CKAP4 RGD RGD:1311989
Macaca mulatta CKAP4 VGNC VGNC:71190
Others CKAP4 NCBI