Kirrel3/NEPH2 Products

Description

NEPH2 is a member of the nephrin-like protein family, which includes NEPH1 (KIRREL; MIM 607428) and NEPH3 (MIM 607762). The cytoplasmic domains of these proteins interact with the C terminus of podocin (NPHS2; MIM 604766), and the genes are expressed in kidney podocytes, cells involved in ensuring size- and charge-selective ultrafiltration (Sellin et al., 2003 [PubMed 12424224]).[supplied by OMIM]

Bioinformatics

Entrez	84623 Human
Uniprot	NP_115920 Human NP_115920.1 Human NM_032531 Human
Product By Gene ID	84623
Alternate Names	nephrin-like 2 Nephrin-like protein 2 kin of IRRE-like protein 3 Kin of irregular chiasm-like protein 3 KIRREPRO4502 NEPH2MGC126850 KIAA1867MGC126824 MRD4 kin of IRRE like 3 (Drosophila)

Diseases related to Kirrel3/NEPH2

Discover more about diseases related to Kirrel3/NEPH2.

Tissue Adhesions
Proteinuria Of Undiagnosed Cause
Nervousness
Nephrotic Syndrome
Autistic Disorder
Congenital Nephrotic Syndrome
Muscular Fasciculation
Jacobsen Distal 11q Deletion Syndrome
Schizophrenia
Kidney Failure
Language Delays
Mental Disorders
Child Development Disorders, Pervasive
Congenital Anomaly Of Brain
Kidney Diseases
Chromosomal Translocation
Chromosome Breakage

Pathways for Kirrel3/NEPH2

View related products by pathway and learn more about each of the pathways below.

Cell Recognition
Glomerular Filtration
Cell-cell Adhesion
Cell Adhesion
Cell Death
Brain Development
Myoblast Fusion
Axonal Fasciculation

PTMs for Kirrel3/NEPH2

Learn more about PTMs related to Kirrel3/NEPH2.

Cleavage

Bioinformatics Tool for Kirrel3/NEPH2

Discover related pathways, diseases and genes to Kirrel3/NEPH2. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.