CNPY2 - canopy FGF signaling regulator 2 Gene

Also Known as MSAP; TMEM4; ZSIG9; HP10390

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 10330

About CNPY2

Cytogenetic location: 12q13.3 Genomic coordinates (GRCh38): 12:56,309,844-56,316,346 (from NCBI)

This gene has 12 transcripts (splice variants), 93 orthologues and 2 paralogues. Ubiquitous expression in prostate (RPKM 22.5), adrenal (RPKM 21.4) and 25 other tissues.

Summary

Predicted to be active in endoplasmic reticulum. [provided by Alliance of Genome Resources, Apr 2022]

CNPY2 Products (2)

mRNA Protein Name
NM_001190991.3 NP_001177920.1 protein canopy homolog 2 isoform 2 precursor
NM_014255.7 NP_055070.1 protein canopy homolog 2 isoform 1 precursor

CNPY2 Protein Structure

DUF3456

DUF3456: TLR4 regulator and MIR-interacting MSAP (26 - 172)

  • 0
  • 100
  • 182 a.a.
Protein Preferred Names Protein Names

protein canopy homolog 2

  • MIR-interacting saposin-like protein

CNPY2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CNPY2 Q9Y2B0 ADRA2C Homo sapiens P18825
Y2H Prey Pooling
32296183
Intra
CNPY2 Q9Y2B0 ADRA2C Homo sapiens P18825
Y2H Array
32296183
Intra
CNPY2 Q9Y2B0 MYLIP Homo sapiens Q8WY64
Y2H
12826659
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant CNPY2 Proteins

Cat. No. Product Name Accession Purity
HY-P76839 CNPY2 Protein, Human (HEK293, His) Q9Y2B0-1 (R21-S178) ≥ 95%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
Fanconi Anemia, Complementation Group C

  • Fanconi Anemia Complementation Group C

  • FANCC

  • Facc

  • Fac

  • Fa3

  • Fanconi Pancytopenia Type 3

  • Fanconi Pancytopenia, Type 3

  • Faces Syndrome

  • Facial Features , Anorexia, Cachexia, Eye And Skin Anomalies

  • Friedman-Goodman Syndrome

  • Abnormality Of The Face
Craniosynostosis

  • Premature Closure Of Cranial Sutures

  • Craniostenosis

  • Craniosynostosis Syndrome

  • Cso

  • Craniosynostoses

  • Congenital Ossification Of Cranial Sutures

  • Congenital Ossification Of Sutures Of Skull

  • Craniostosis

  • Imperfect Fusion Of Skull

  • Congenital Imperfect Closure Skull

  • Imperfect Closure Skull

  • Premature Closure Cranium Sutures

  • Deficiency Of Craniofacial Axis
Cataract 34, Multiple Types

  • Cataract, Autosomal Recessive Congenital 3

  • Cataract 34 Multiple Types

  • CTRCT34

  • Catc3

  • Cataract 34, Multiple Types, With Or Without Microcornea

  • Autosomal Recessive Congenital Cataract 3

  • Cataract 34 Multiple Types With Or Without Microcornea

  • Cataract, Multiple Types, Type 34
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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (3)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS02911 CNPY2 Human Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS19998 Cnpy2 Mouse Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS26501 Cnpy2 Rat Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Rattus norvegicus CNPY2 RGD RGD:1589072
Mus musculus CNPY2 MGD MGI:1928477
Others CNPY2 NCBI