ELFN1 - extracellular leucine rich repeat and fibronectin type III domain containing 1 Gene

Homo sapiens

Also known as PPP1R28

Gene ID: 392617 | Gene type: protein coding

About ELFN1

Cytogenetic location: 7p22.3 Genomic coordinates (GRCh38): 7:1,666,064-1,747,946 (from NCBI)

This gene has 4 transcripts (splice variants), 247 orthologues, 22 paralogues and is associated with 1 phenotype. Broad expression in liver (RPKM 1.3), kidney (RPKM 0.9) and 14 other tissues.

Summary

Predicted to enable protein Phosphatase Inhibitor activity. Predicted to be involved in synapse organization. Predicted to be located in dendrite and excitatory synapse. Predicted to be active in extracellular matrix and extracellular space. [provided by Alliance of Genome Resources, Apr 2022]

ELFN1 Products(3)

mRNA	Protein	Name
NM_001128636.4	NP_001122108.1	protein ELFN1 precursor
NM_001394187.1	NP_001381116.1	protein ELFN1 precursor
NM_001394188.1	NP_001381117.1	protein ELFN1 precursor

ELFN1 Protein Structure

LRR_8

0
200
400
600
828 a.a.

Protein Preferred Names

Protein Names

protein ELFN1

extracellular leucine-rich repeat and fibronectin type III containing 1

Recombinant ELFN1 Proteins

Cat. No.	Product Name	Accession	Purity
HY-P78958	ELFN1 Protein, Human (CHO, His)	P0C7U0 (D28-Y418 )	≥95%

Related Diseases

Diseases

Alias

Congenital Stationary Night Blindness

Night Blindness, Congenital Stationary	Congenital Essential Nyctalopia
Oguchi Disease	Blindness, Night, Stationary, Congenital

Attention Deficit-Hyperactivity Disorder

Attention Deficit Hyperactivity Disorder	ADHD
Attention Deficit Disorder	Attention Deficit-Hyperactivity Disorder, Susceptibility To
Attention Deficit Disorder With Hyperactivity	Hyperkinetic Disorder
Hyperactivity Of Childhood	Attention-Deficit/Hyperactivity Disorder
Add	Addh
Attention Deficit	Attention Deficit Disorder Of Childhood With Hyperactivity
Attention Deficit Disorder With Hyperactivity Syndrome	Hyperkinetic Syndrome
Attention-Deficit Hyperactivity Disorder	Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type
Disturbance Of Activity And Attention	Disorder Of Activity And Attention
Adhd - [Attention Deficit Hyperactivity Disorder]	Hyperkinetic Disorders
Disorder Of Activity And Attention With Hyperkinesia	Attention Deficit Syndrome With Hyperactivity

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

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS04303	ELFN1 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	ELFN1	RGD	RGD:1308787
Macaca mulatta	ELFN1	VGNC	VGNC:72204
Bos taurus	ELFN1	VGNC	VGNC:28431
Mus musculus	ELFN1	MGD	MGI:2442479
Felis catus	ELFN1	VGNC	VGNC:80569

Name
Email *

	Sorry, but the email address you supplied was invalid.