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SPINT2

SPINT2

Protein-coding gene in the species Homo sapiens

inhibitor 2 is an enzyme inhibitor that in humans is encoded by the SPINT2 gene. SPINT2 is a transmembrane protein with two extracellular Kunitz domains

SPINT2

Congenital tufting enteropathy

Medical condition

cell adhesion molecule (EpCAM) on chromosome 2 (2p21) and SPINT2 on chromosome 19. SPINT2 is a Kunitz-type protease inhibitor. The mutation in the EpCAM

Congenital tufting enteropathy

Congenital_tufting_enteropathy

Kunitz domain

InterPro Domain

include: AMBP, APLP2, APP COL6A3, COL7A1, COL28A1 PAPLN, SPINLW1, SPINT1, SPINT2, SPINT3, SPINT4 TFPI, TFPI2 WFDC6, WFDC8, WFIKKN1, WFIKKN2 Several plant

Kunitz domain

Kunitz_domain

Inter-alpha-trypsin inhibitor

ITIH2, ITIH3, ITIH4 and one light chain selected from the group AMBP or SPINT2. They function as protease inhibitors. IαI form complexes with hyaluronan

Inter-alpha-trypsin inhibitor

Inter-alpha-trypsin_inhibitor

Hepatocyte growth factor receptor

Mammalian protein found in Homo sapiens

epigenetic inactivation of hepatocyte growth factor activator inhibitor type 2/SPINT2 in papillary and clear cell renal cell carcinoma". Cancer Res. 65 (11):

Hepatocyte growth factor receptor

Hepatocyte_growth_factor_receptor

List of human protein-coding genes 7

15709 SPINK14 HGNC:33825; Q6IE38 15710 SPINT1 HGNC:11246; O43278 15711 SPINT2 HGNC:11247; O43291 15712 SPINT3 HGNC:11248; P49223 15713 SPINT4 HGNC:16130;

List of human protein-coding genes 7

List_of_human_protein-coding_genes_7

List of OMIM disorder codes

610187; ZFPM2 Diarrhea 3, secretory sodium, congenital, syndromic; 270420; SPINT2 Diarrhea 4, malabsorptive, congenital; 610370; NEUROG3 Diarrhea 5, with

List of OMIM disorder codes

List_of_OMIM_disorder_codes