CAPN1 - calpain 1 Gene

Also Known as CANP; muCL; CANP1; SPG76; CANPL1; muCANP

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 823

About CAPN1

Cytogenetic location: 11q13.1 Genomic coordinates (GRCh38): 11:65,181,373-65,212,006 (from NCBI)

This gene has 28 transcripts (splice variants), 229 orthologues, 20 paralogues and is associated with 2 phenotypes. Ubiquitous expression in esophagus (RPKM 94.2), skin (RPKM 48.8) and 24 other tissues.

Summary

The calpains, calcium-activated neutral proteases, are nonlysosomal, intracellular cysteine proteases. The mammalian calpains include ubiquitous, stomach-specific, and muscle-specific proteins. The ubiquitous Enzymes consist of heterodimers with distinct large, catalytic subunits associated with a common small, regulatory subunit. This gene encodes the large subunit of the ubiquitous enzyme, calpain 1. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]

CAPN1 Products (3)

mRNA Protein Name
NM_001198868.2 NP_001185797.1 calpain-1 catalytic subunit
NM_001198869.2 NP_001185798.1 calpain-1 catalytic subunit
NM_005186.4 NP_005177.2 calpain-1 catalytic subunit

CAPN1 Protein Structure

Peptidase_C2

Peptidase_C2: Calpain family cysteine protease (55 - 354)

Calpain_III

Calpain_III: Calpain large subunit, domain III (365 - 519)

EF-hand_8

EF-hand_8: EF-hand domain pair (557 - 610)

EF-hand_6

EF-hand_6: EF-hand domain (622 - 645)

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

calpain-1 catalytic subunit

  • CANP 1

CAPN1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CAPN1 P07384 EZR Homo sapiens P15311 22805611
Intra
CAPN1 P07384 CMPK1 Homo sapiens P30085-3 32814053
Intra
CAPN1 P07384 CMPK1 Homo sapiens P30085-3 32814053
Intra
CAPN1 P07384 CMPK1 Homo sapiens P30085-3 32814053
Intra
CAPN1 P07384 STAT3 Homo sapiens P40763
Y2H
21988832
Intra
CAPN1 P07384 OPTN Homo sapiens Q96CV9 32814053
Intra
CAPN1 P07384 OPTN Homo sapiens Q96CV9 32814053
Intra
CAPN1 P07384 OPTN Homo sapiens Q96CV9 32814053
Intra
CAPN1 P07384 PTPN1 Homo sapiens P18031 19712109
Intra
CAPN1 P07384 PTPN1 Homo sapiens P18031 19712109
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant CAPN1 Proteins

Cat. No. Product Name Accession Purity
HY-P72113 CAPN1 Protein, Human (His) P07384 (M1-A714) ≥ 90%, as determined by reducing SDS-PAGE.

CAPN1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P80443 Calpain 1 Antibody (YA815) ICC/IF, IHC-P, FC Human, Mouse, Rat
HY-P83990 Calpain 1 Antibody (YA3687) WB, IHC-P, FC, ELISA Human
HY-P83990A Calpain 1 Antibody (YA3687)(PBS only) WB, IHC-P, FC, ELISA Human

Related Diseases

Diseases Alias
Spastic Paraplegia 76, Autosomal Recessive
  • SPG76

  • Autosomal Recessive Spastic Paraplegia Type 76

  • Hereditary Spastic Paraplegia 76

  • Autosomal Recessive Spastic Paraplegia 76

  • Paraplegia, Spastic, Autosomal Recessive, Type 76

Paraplegia
  • Paraplegia, Lower

  • Severe Or Complete Loss Of Motor Function In The Lower Extremities And Lower Portions Of The Trunk

Spasticity
Machado-Joseph Disease
  • SCA3

  • MJD

  • Spinocerebellar Ataxia 3

  • Azorean Disease

  • Spinocerebellar Ataxia Type 3

  • Spinocerebellar Atrophy

  • Azorean Neurologic Disease

  • Spinopontine Atrophy

  • Nigrospinodentatal Degeneration

  • Spinocerebellar Atrophy Iii

  • Spinocerebellar Atrophy Type 3

  • Azorean Ataxia

  • Azorean Disease Of The Nervous System

  • Machado Disease

  • Nigro-Spino-Dentatal Degeneration With Nuclear Ophthalmoplegia

  • Disease, Machado-Joseph

  • Ataxia, Spinocerebellar

Spastic Paraplegia 79, Autosomal Recessive
  • Early-Onset Progressive Neurodegeneration-Blindness-Ataxia-Spasticity Syndrome

  • SPG79

  • Neurodegeneration With Optic Atrophy, Childhood-Onset

  • Ndgoa

  • Hereditary Spastic Paraplegia 79

  • Spastic Paraplegia 79 Autosomal Recessive

  • Doid:0112344

  • Neurodegeneration, With Optic Atrophy, Childhood-Onset

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2a
  • Leyden-Moebius Muscular Dystrophy

  • Lgmd2a

  • Limb-Girdle Muscular Dystrophy Due To Calpain Deficiency

  • Muscular Dystrophy, Limb-Girdle, Type 2a

  • Pelvofemoral Muscular Dystrophy

  • Primary Calpainopathy

Ichthyosis
  • Ichthyoses

  • Non-Syndromic Ichthyosis

  • Congenital Ichthyosis

Malaria
  • Malaria, Susceptibility To

  • Malaria, Resistance To

  • Malaria, Cerebral

  • Cerebral Malaria

  • Malaria, Severe, Susceptibility To

  • Malaria, Severe, Resistance To

  • Malaria, Cerebral, Susceptibility To

  • Induced Malaria

  • Malaria, Vivax, Protection Against

  • Malaria, Severe

  • Malaria, Cerebral, Reduced Risk Of

  • Malaria, Protection Against

  • Resistance To Malaria Due To G6pd Deficiency

  • Malaria Due To G6pd Deficiency

  • Malarial Encephalitis

  • CM

  • Malaria Cerebral

  • Susceptibility To Malaria

  • Acute Pernicious Fever

  • Aestivo-Autumnal Fever

  • Aestivo Autumnal Malaria

  • Chagres Fever

  • Continued Malaria Fever

  • Estivo-Autumnal Fever

  • Estivo-Autumnal Malaria

  • Estivo-Autumnal Malarial Fever

  • Falciparum Fever

  • Malignant Tertian Fever

  • Malignant Tertian Malaria

  • Pernicious Intermittent Fever

  • Pernicious Malaria

  • Quotidian Malaria

  • Subtertian Fever

  • Subtertian Malaria Fever

  • Subtertian Malignant Tertian Malaria

  • Tropical Malaria

  • Algid Malaria

  • Bilious Haemoglobinuric Fever

  • Black Water Fever

  • Blackwater Fever

  • Malarial Blackwater Fever

  • Severe Malarial Falciparum

  • West African Fever

  • Malarial Haematinuria

  • Haemoglobinuric Fever

  • Haemoglobinuric Malaria

  • Severe Plasmodium Falciparum Malaria

  • Malarial Haemoglobinuria

  • Malarial Haematuria

  • Falciparum Malaria [Malignant Tertian]

  • Malaria Tropica

  • Malarial Shock

  • Chagres Virus Disease

  • Malignant Malaria

  • Mtm - [Malignant Tertian Malaria]

  • Tm -[Malignant Tertian Malaria]

  • Panama Fever

  • St - [Subtertian Malaria]

  • Malarial Quotidian

  • Benign Tertian Malaria

  • Tertian Ague

  • Vivax Fever

  • Plasmodium Vivax Malaria Nos

  • Btm - [Benign Tertian Malaria]

  • Bt - [Benign Tertian Malaria]

  • Vivax Malaria

  • Benign Tertian Vivax Malaria

  • Tertian Malaria

  • Quartan Malaria

  • Quartan Ague

  • Quartan Fever

  • Plasmodium Malariae Malaria Nos

  • Quartan Malarial

  • Malaria By Plasmodium Malariae

  • Malariae Malaria

  • Ovale Tertian Malaria

  • Plasmodium Ovale Fever

  • Malaria Fever By Plasmodium Ovale

  • Ovale Malaria

  • Malaria By Plasmodium Ovale

  • Malarial Ovale

  • Marsh Fever

  • Remittent Congestive Fever

  • Coastal Fever

  • Remittent Gastric Fever

  • Miasmatic Fever

  • Congestive Remittent Fever

  • Intermittent Fever

  • Jungle Fever

  • Paludism

  • Cameroon Fever

  • Ague

  • Corsican Fever

  • Intermittent Bilious Fever

  • Disease Due To Plasmodiidae

  • Malarial Fever

  • Plasmodiosis

  • Remittent Fever

  • Roman Fever

  • Malaria Fever Nos

  • Malaria Nos

  • Paludal Fever

  • Clinically Diagnosed Malaria

  • Clinically Diagnosed Malaria Without Parasitological Confirmation

  • Congestive Fever

  • Malarial Cachexia

  • Marsh Cachexia

  • Paludal Cachexia

  • Recurrent Malaria

  • Remittent Malaria

Autosomal Recessive Limb-Girdle Muscular Dystrophy
  • Muscular Dystrophy, Limb-Girdle, Autosomal Recessive

Cataract
  • Cataracts

  • Cat - [Cataract]

  • Cataract Form

  • Lens Opacity

  • Lens Opacities

Spastic Ataxia
  • Spax

  • Ataxia, Spastic

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

Alzheimer Disease, Familial, 1
  • Alzheimer Disease

  • Alzheimer'S Disease

  • Presenile And Senile Dementia

  • AD1

  • Alzheimer Disease, Susceptibility To

  • Alzheimer Disease, Late-Onset, Susceptibility To

  • Alzheimer Disease 1, Familial

  • AD

  • Familial Alzheimer Disease

  • Alzheimer Disease, Late-Onset

  • Alzheimers Dementia

  • Alzheimer Dementia

  • Alzheimer Sclerosis

  • Alzheimer Syndrome

  • Alzheimer-Type Dementia

  • Dat

  • Primary Senile Degenerative Dementia

  • Sdat

  • Alzheimer Disease 1

  • Autosomal Dominant Alzheimer Disease

  • Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy

  • Late Onset Alzheimer Disease

  • Alzheimers Disease

  • Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy

  • Late-Onset Alzheimers Disease

  • Alzheimer'S Disease Pathway Kegg

  • Dementia Due To Alzheimer'S Disease

  • Alzheimer Disease Type 1

  • Alzheimers

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
Macaca mulatta CAPN1 VGNC VGNC:70529
Rattus norvegicus CAPN1 RGD RGD:2267
Mus musculus CAPN1 MGD MGI:88263
Felis catus CAPN1 VGNC VGNC:60348
Bos taurus CAPN1 VGNC VGNC:26740
Canis familiaris CAPN1 VGNC VGNC:38698
Others CAPN1 NCBI