CNPY2 - canopy FGF signaling regulator 2 Gene

Homo sapiens

Also known as MSAP; TMEM4; ZSIG9; HP10390

Gene ID: 10330 | Gene type: protein coding

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

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 Cross Intra	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	Reference
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%

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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS02911	CNPY2 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

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

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