Gene Gene information from NCBI Gene database.
Entrez ID 248
Gene name Alkaline phosphatase, intestinal
Gene symbol ALPI
Synonyms (NCBI Gene)
IAP
Chromosome 2
Chromosome location 2q37.1
Summary There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The intestinal alkaline phosphatase gene encodes a digestive brush-border enzyme. This enzyme is a comp
miRNA miRNA information provided by mirtarbase database.
98
miRTarBase ID miRNA Experiments Reference
MIRT019330 hsa-miR-148b-3p Microarray 17612493
MIRT029513 hsa-miR-26b-5p Microarray 19088304
MIRT695519 hsa-miR-3200-5p HITS-CLIP 23313552
MIRT695518 hsa-miR-4682 HITS-CLIP 23313552
MIRT695517 hsa-miR-6128 HITS-CLIP 23313552
Transcription factors Transcription factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
KLF4 Activation 12919939
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
GO ID Ontology Definition Evidence Reference
GO:0000287 Function Magnesium ion binding ISS
GO:0002020 Function Protease binding IPI 18307834
GO:0004035 Function Alkaline phosphatase activity IBA
GO:0004035 Function Alkaline phosphatase activity IEA
GO:0004035 Function Alkaline phosphatase activity ISS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
171740 437 ENSG00000163295
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P09923
Protein name Intestinal-type alkaline phosphatase (IAP) (Intestinal alkaline phosphatase) (EC 3.1.3.1)
Protein function Alkaline phosphatase that can hydrolyze various phosphate compounds.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00245 Alk_phosphatase 52 487 Alkaline phosphatase Domain
Sequence
Sequence length 528
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Thiamine metabolism
Folate biosynthesis
Metabolic pathways
Biosynthesis of cofactors
  Synthesis of PA
Post-translational modification: synthesis of GPI-anchored proteins
Digestion
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
28
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
ALPI-related disorder Uncertain significance; Benign; Likely benign rs148157889, rs773517600, rs10195208, rs61736995, rs143128875, rs201251145, rs115079894, rs61732026, rs7559279, rs376843697, rs61732024, rs148298725, rs73007641, rs145542166, rs145002990
View all (10 more)
RCV003946389
RCV003399706
RCV003919632
RCV003921852
RCV003981561
RCV003904083
RCV003914290
RCV003914296
RCV003916950
RCV003963863
RCV003964173
RCV003931634
RCV003941435
RCV003941578
RCV003941703
RCV003937256
RCV003926879
RCV003926888
RCV003926974
RCV003926985
RCV003932289
RCV003979261
RCV003962011
RCV003976302
RCV004750463
Inflammatory bowel disease Uncertain significance rs201573533, rs201841252 RCV004560521
RCV004560532
Uterine carcinosarcoma Benign rs2272421 RCV005927799
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Ataxia Telangiectasia Inhibit 30920104
Breast Neoplasms Associate 19563669
Carcinoma Renal Cell Associate 17922292
Cardiovascular Diseases Associate 40334645
Colitis Ulcerative Inhibit 22783049
Colorectal Neoplasms Associate 19686745, 25037223, 27520705, 33660894, 34797333
Crohn Disease Stimulate 18045591
Crohn Disease Inhibit 22783049
Crohn Disease Associate 28103724, 30558547, 35872023
Diabetes Mellitus Type 2 Associate 31915470