CANX - calnexin Gene

Also Known as CNX; P90; IP90

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 821

About CANX

Cytogenetic location: 5q35.3 Genomic coordinates (GRCh38): 5:179,678,656-179,731,641 (from NCBI)

This gene has 47 transcripts (splice variants), 1 gene allele, 212 orthologues and 3 paralogues. Ubiquitous expression in thyroid (RPKM 267.4), placenta (RPKM 108.5) and 25 other tissues.

Summary

This gene encodes a member of the calnexin family of molecular chaperones. The encoded protein is a calcium-binding, endoplasmic reticulum (ER)-associated protein that interacts transiently with newly synthesized N-linked glycoproteins, facilitating protein folding and assembly. It may also play a central role in the quality control of protein folding by retaining incorrectly folded protein subunits within the ER for degradation. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jun 2018]

CANX Products (11)

mRNA Protein Name
NM_001024649.2 NP_001019820.1 calnexin isoform d precursor
NM_001363993.1 NP_001350922.1 calnexin isoform a
NM_001363994.1 NP_001350923.1 calnexin isoform b
NM_001363995.1 NP_001350924.1 calnexin isoform c precursor
NM_001363996.1 NP_001350925.1 calnexin isoform d precursor
NM_001363997.1 NP_001350926.1 calnexin isoform d precursor
NM_001363998.1 NP_001350927.1 calnexin isoform e precursor
NM_001363999.1 NP_001350928.1 calnexin isoform f precursor
NM_001364000.1 NP_001350929.1 calnexin isoform g
NM_001364001.1 NP_001350930.1 calnexin isoform g
NM_001746.4 NP_001737.1 calnexin isoform d precursor
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
16361248 GOA
Cellular Component GO Annotation Evidence References Source
located in endoplasmic reticulum IDA
IDA: Inferred from direct assay
14966132 GOA
located in endoplasmic reticulum membrane IDA
IDA: Inferred from direct assay
19723497 GOA
NOT located in extracellular exosome IDA
IDA: Inferred from direct assay
21235781 GOA
located in mitochondria-associated endoplasmic reticulum membrane contact site IDA
IDA: Inferred from direct assay
23455425 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

CANX Protein Structure

Calreticulin

Calreticulin: Calreticulin family (69 - 440)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 592 a.a.
Protein Preferred Names Protein Names

calnexin

  • epididymis secretory sperm binding protein

CANX Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CANX P27824 CYB5R3 Homo sapiens P00387 35271311
Intra
CANX P27824 CYB5R3 Homo sapiens P00387 30021884
Intra
CANX P27824 CNTNAP2 Homo sapiens Q9UHC6-1 22872700
Intra
CANX P27824 CFTR Homo sapiens P13569 12208510
Intra
CANX P27824 RPL12 Homo sapiens P30050 22314232
Intra
CANX P27824 RPL12 Homo sapiens P30050 22314232
Intra
CANX P27824 SEC61A1 Homo sapiens P61619 22314232
Intra
CANX P27824 SEC61A1 Homo sapiens P61619 29568061
Intra
CANX P27824 SEC61A1 Homo sapiens P61619 35271311
Intra
CANX P27824 SSR1 Homo sapiens P43307 22314232
Intra
CANX P27824 SSR1 Homo sapiens P43307 17380188
Intra
CANX P27824 SSR1 Homo sapiens P43307 22314232
Intra
CANX P27824 SSR1 Homo sapiens P43307 29568061
Intra
CANX P27824 SSR1 Homo sapiens P43307 35271311
Intra
CANX P27824 NDRG1 Homo sapiens Q92597 17220478
Cross
CANX P27824 env Human immunodeficiency virus P04578 25170080
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant CANX Proteins

Cat. No. Product Name Accession Purity
HY-P7711 Calnexin Protein, Human (HEK293, His) P27824 (H21-P481) ≥ 95%, as determined by reducing SDS-PAGE.

CANX Antibodies

Cat. No. Product Name Application Reactivity
HY-P80041 Calnexin Antibody (YA573) WB, ICC/IF, IHC-P, FC Human, Rat
HY-P80578 Calnexin Antibody WB, IHC-F, IHC-P, ICC/IF, ELISA Human, Mouse, Rat
HY-P85072 Calnexin Antibody (YA4764) WB, ICC/IF, ELISA Human
HY-P85072A Calnexin Antibody (YA4764)(PBS only) WB, ICC/IF, ELISA Human
HY-P86146 Calnexin Antibody (YA5838) WB, IHC-P, ICC/IF, IP, ELISA Human

Related Diseases

Diseases Alias
Influenza
  • Flu

  • Influenza With Non-Respiratory Manifestation

  • Influenza With Other Manifestations

  • Influenza, Human

  • Influenza, Susceptibility To

  • Seasonal Influenza, Virus Identified

Myeloperoxidase Deficiency
  • Mpo Deficiency

  • MPOD

Nephrogenic Diabetes Insipidus
  • Vasopressin-Resistant Diabetes Insipidus

  • Diabetes Insipidus, Nephrogenic

  • Diabetes Insipidus Nephrogenic

  • Congenital Nephrogenic Diabetes Insipidus

  • Adh Resistant Diabetes Insipidus

  • Diabetes Insipidus Nephrogenic X-Linked

  • Diabetes Insipidus Nephrogenic Type 1

  • Adh-Resistant Diabetes Insipidus

  • Diabetes Insipidus Renalis

  • Ndi

  • Renal Diabetes Insipidus

  • Familial Nephrogenic Diabetes

  • Antidiuretic-Hormone-Resistant Diabetes Insipidus

  • Adiuretin-Resistant Diabetes Insipidus

  • Ndi - [Nephrogenic Diabetes Insipidus]

  • Diabetes Tenuifluus

  • Adh - [Antidiuretic-Hormone] Resistant Diabetes Insipidus

  • Hereditary Nephrogenic Diabetes Insipidus

  • Familial Nephrogenic Diabetes Insipidus

  • Primary Nephrogenic Diabetes Insipidus

Pseudoachondroplasia
  • PSACH

  • Pseudoachondroplastic Dysplasia

  • Pseudoachondroplastic Spondyloepiphyseal Dysplasia Syndrome

  • Spondyloepiphyseal Dysplasia, Pseudoachondroplastic

  • Pseudoachondroplastic Spondyloepiphyseal Dysplasia

  • Spondyloepiphyseal Dysplasia Pseudoachondroplastic

Cystic Fibrosis
  • Mucoviscidosis

  • CF

  • Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis

  • Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis

  • Cystic Fibrosis Lung Disease, Modifier Of

  • Cystic Fibrosis Of Pancreas

  • Fibrocystic Disease Of Pancreas

  • Cf - [Cystic Fibrosis]

  • Cystic Fibrosis Nos

  • Fibrocystic Disease

  • Fibrocystic Disease Of The Pancreas

  • Mucoviscidosis Of Pancreas

  • Nonproliferative Fibrocystic Disease

  • Pancreatic Cystic Fibrosis

Oculocutaneous Albinism
  • Albinism, Oculocutaneous

  • Oca

  • Albinism Oculocutaneous

  • Oca - [Oculocutaneous Albinism]

Lipase Deficiency, Combined
  • Lipoprotein Lipase Deficiency With Hepatic Triglyceride Lipase Deficiency

  • Lpl And Htgl Deficiency

  • Lpl And Hl Deficiency

  • Familial Lipase Maturation Factor 1 Deficiency

  • Lipase Deficiency Combined

  • Combined Lipase Deficiency

  • Familial Lmf1 Deficiency

  • CLD

Long Qt Syndrome
  • Romano-Ward Syndrome

  • Long Q-T Syndrome

  • Lqt

  • Qt Syndrome, Long

  • Congenital Long Qt Syndrome

  • Familial Long Qt Syndrome

Congenital Disorder Of Glycosylation, Type Iib
  • CDG2B

  • CDGIIB

  • Glucosidase I Deficiency

  • Congenital Disorder Of Glycosylation Type Iib

  • Cdg Iib

  • Mogs-Cdg

  • Cdg Syndrome Type Iib

  • Cdg-Iib

  • Carbohydrate Deficient Glycoprotein Syndrome Type Iib

  • Congenital Disorder Of Glycosylation Type 2b

  • Glucosidase 1 Deficiency

  • Type Iib Congenital Disorder Of Glycosylation

  • Glycosylation, Congenital Disorder Of, Type Iib

Mast Cell Neoplasm
  • Mastocytoma

  • Mast Cell Proliferative Disease

  • Mast Cell Tumor

  • Benign Mastocytoma

Retinitis Pigmentosa 77
  • RP77

  • Retinitis Pigmentosa, Type 77

Charcot-Marie-Tooth Disease
  • Cmt

  • Hmsn

  • Hereditary Motor And Sensory Neuropathy

  • Pma

  • Cmt - Charcot-Marie-Tooth Disease

  • Charcot Marie Tooth Disease

  • Charcot-Marie-Tooth Hereditary Neuropathy

  • Charcot-Marie-Tooth Syndrome

  • Peroneal Muscular Atrophy

  • Hereditary Motor And Sensory Neuropathies

Charcot-Marie-Tooth Disease And Deafness
  • Charcot-Marie-Tooth Disease Type 1e

  • CMT1E

  • Charcot-Marie-Tooth Disease Type 1

  • Hereditary Motor And Sensory Neuropathy Type 1

  • Charcot-Marie-Tooth Disease, Demyelinating, Type 1e

  • Charcot-Marie-Tooth Disease, Type I

  • Charcot-Marie-Tooth Neuropathy And Deafness, Autosomal Dominant

  • Charcot-Marie-Tooth Disease, Type 1e

  • Charcot-Marie-Tooth Disease Demyelinating Type 1e

  • Autosomal Dominant Demyelinating Charcot-Marie-Tooth Disease

  • Cmt1

  • Charcot-Marie-Tooth Neuropathy Type 1

  • Autosomal Dominant Charcot-Marie-Tooth Neuropathy And Deafness

  • Charcot-Marie-Tooth Disease-Deafness

  • Charcot-Marie-Tooth Type 1

  • Hmsn1

  • Hereditary Motor And Sensory Neuropathy 1

  • Cmt 1e

  • Charcot Marie Tooth Disease Type 1e

  • Charcot-Marie-Tooth Disease-Deafness Syndrome

  • Charcot-Marie-Tooth Disease-Hearing Loss Syndrome

  • Charcot-Marie-Tooth Disease 1e

  • Charcot-Marie-Tooth Disease And Deafness Autosomal Dominant

  • Charcot-Marie-Tooth Neuropathy Type 1e

  • Charcot-Marie-Tooth Disease, Type Ie

  • Hereditary Motor And Sensory Neuropathy Type I

Legionnaire Disease
  • Legionnaires' Disease

  • Legionnaires Disease

  • Legionnaire Disease, Susceptibility To

  • Legionella

  • Legionella Pneumonia

  • Infection By Legionella Pneumophilia

  • Legionnaire'S Disease

  • Legionellosis

  • Legionaire Disease, Susceptibility To

  • Legionnaires Pneumonia

Legionellosis
  • Legionella Infection

  • Pontiac Fever

  • Legionnaires' Disease

  • Infection By Legionella Pneumophilia

  • Legionella Pneumophila Infection

Marfan Syndrome
  • MFS

  • Mfs1

  • Marfan'S Syndrome

  • Marfan Syndrome Type 1

  • Marfan Syndrome, Type I

  • Mass Phenotype

  • Contractural Arachnodactyly

  • Mass Syndrome

  • Octd

  • Overlap Connective Tissue Disease

  • Marfanoid Hypermobility Syndrome

  • Marfan Disease

Dystonia
  • Dystonic Disease

  • Dystonic Disorder

  • Dystonia Disorders

  • Neuroleptic Dyskinesia

Esophageal Adenosquamous Carcinoma
Hypertrophic Neuropathy Of Dejerine-Sottas
  • Dejerine-Sottas Disease

  • Dejerine-Sottas Syndrome

  • Charcot-Marie-Tooth Disease Type 3

  • DSS

  • Hereditary Motor And Sensory Neuropathy Type Iii

  • Hmsn3

  • Dejerine-Sottas Neuropathy

  • Hmsn Iii

  • Charcot-Marie-Tooth Disease, Type 3

  • Cmt3

  • Dsn

  • Hmsn 3

  • Hereditary Motor And Sensory Neuropathy Type 3

  • Hereditary Motor And Sensory Neuropathy 3

  • Hypertrophic Neuropathy Of Infancy

  • Charcot-Marie-Tooth Disease Demyelinating Type 4f

  • Charcot-Marie-Tooth Disease Type 4f

  • Charcot-Marie-Tooth Neuropathy Type 4f

  • Cmt4f

  • Hereditary Motor And Sensory Neuropathy Iii

  • Charcot-Marie-Tooth Disease, Demyelinating, Type 4f

Long Qt Syndrome 2
  • LQT2

  • Long Qt Syndrome, Acquired, Reduced Susceptibility To

  • Long Qt Syndrome 1/2

  • Long Qt Syndrome 2/3

  • Long Qt Syndrome 2/5

  • Long Qt Syndrome 2, Acquired, Susceptibility To

  • Long Qt Syndrome, Acquired, Reduced

  • Long Qt Syndrome Type 2

  • Long Qt Syndrome 2/9

  • Lqt1/2

  • Lqt2/3

  • Lqt2/5

  • Lqt2/9

  • Susceptibility To Acquired Long Qt Syndrome 2

  • Long Qt Syndrome-2

  • Qt Syndrome, Long, Type 2

  • Long Qt Syndrome 1-2

  • Long Qt Syndrome 2-3

  • Long Qt Syndrome 2-5

  • Long Qt Syndrome 9

Hyperekplexia
  • Hereditary Hyperekplexia

  • Kok Disease

  • Congenital Stiff Man Syndrome

  • Familial Startle Disease

  • Sthe

  • Stiff-Baby Syndrome

  • Hereditary Hyperexplexia

  • Startle Disease

  • Exaggerated Startle Reaction

  • Hyperexplexia Hereditary

  • Startle Disease, Familial

  • Startle Reaction, Exaggerated

  • Stiff-Man Syndrome, Congenital

  • Stiff-Person Syndrome, Congenital

  • Congenital Stiff-Man Syndrome

  • Congenital Stiff-Person Syndrome

  • Familial Hyperekplexia

  • Startle Syndrome

  • Stiff Baby Syndrome

  • Hyperekplexia, Hereditary

  • Stiff-Person Syndrome

Congenital Disorder Of Glycosylation, Type In
  • Congenital Disorder Of Glycosylation

  • CDG1N

  • Congenital Disorders Of Glycosylation

  • Cdg In

  • Cdgin

  • Congenital Disorder Of Glycosylation 1n

  • Carbohydrate-Deficient Glycoprotein Syndrome

  • Cdg

  • Rft1-Cdg

  • Cdg-In

  • Congenital Disorder Of Glycosylation Type In

  • Carbohydrate Deficient Glycoprotein Syndrome

  • Cdg Syndrome

  • Congenital Disorder Of Glycosylation In

  • Carbohydrate-Deficient Glycoprotein Syndromes

  • Cdg Syndrome Type In

  • Carbohydrate Deficient Glycoprotein Syndrome Type In

  • Congenital Disorder Of Glycosylation Type 1n

  • Man5glcnac2-Pp-Dol Flippase Deficiency

  • Glycosylation, Congenital Disorder Of

  • Glycosylation, Congenital Disorder Of, Type In

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

Amyotrophic Lateral Sclerosis 1
  • Amyotrophic Lateral Sclerosis

  • ALS

  • Lou Gehrig Disease

  • Amyotrophic Lateral Sclerosis Type 1

  • Charcot Disease

  • ALS1

  • Amyotrophic Lateral Sclerosis, Susceptibility To

  • Fals

  • Lou Gehrig'S Disease

  • Mnd

  • Motor Neuron Disease

  • Familial Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis 1, Familial

  • Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

  • Motor Neuron Disease, Bulbar

  • Motor Neurone Disease

  • Amyotrophic Lateral Sclerosis With Dementia

  • Dementia With Amyotrophic Lateral Sclerosis

  • Motor Neuron Disease, Amyotrophic Lateral Sclerosis

  • Sclerosis, Lateral, Amyotrophic

  • Sclerosis, Lateral, Amyotrophic, Type 1

  • Amyotrophic Sclerosis

  • Als - [Amyotrophic Lateral Sclerosis]

  • Wasting Palsy

  • Amyotrophic Paralysis

  • Amyotrophy Lateral Sclerosis

  • Wasting Paralysis

  • Spinal Progressive Amyotrophy

  • Progressive Atrophic Paralysis

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

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
Bos taurus CANX VGNC VGNC:26736
Macaca mulatta CANX VGNC VGNC:70527
Felis catus CANX VGNC VGNC:60345
Rattus norvegicus CANX RGD RGD:2266
Canis familiaris CANX VGNC VGNC:38695
Mus musculus CANX MGD MGI:88261
Others CANX NCBI