ALPL (alkaline phosphatase, biomineralization associated)

2003-05-01  

Identity

HGNC
LOCATION
1p36.12
LOCUSID
ALIAS
AP-TNAP,APTNAP,HOPS,HPPA,HPPC,HPPI,HPPO,TNALP,TNAP,TNSALP
FUSION GENES

Other Information

Locus ID:

NCBI: 249
MIM: 171760
HGNC: 438
Ensembl: ENSG00000162551

Variants:

dbSNP: 249
ClinVar: 249
TCGA: ENSG00000162551
COSMIC: ALPL

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000162551ENST00000374830B1ANL0
ENSG00000162551ENST00000374832P05186
ENSG00000162551ENST00000374832A0A024RAG0
ENSG00000162551ENST00000374840P05186
ENSG00000162551ENST00000374840A0A024RAG0
ENSG00000162551ENST00000539907P05186
ENSG00000162551ENST00000540617P05186

Expression (GTEx)

0
100
200
300
400
500
600

Pathways

PathwaySourceExternal ID
Thiamine metabolismKEGGko00730
Folate biosynthesisKEGGko00790
Thiamine metabolismKEGGhsa00730
Folate biosynthesisKEGGhsa00790
Metabolic pathwaysKEGGhsa01100
Metabolism of proteinsREACTOMER-HSA-392499
Post-translational protein modificationREACTOMER-HSA-597592
Post-translational modification: synthesis of GPI-anchored proteinsREACTOMER-HSA-163125

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
364443962023Not just a carrier: Clinical presentation and management of patients with heterozygous disease-causing alkaline phosphatase (ALPL) variants identified through expanded carrier screening.1
367928312023Early elevated alkaline phosphatase as a surrogate biomarker of ongoing metabolic bone disease of prematurity.3
371920152023Promotion effect of FGF23 on osteopenia in congenital scoliosis through FGFr3/TNAP/OPN pathway.2
372774512023Association between changes in serum alkaline phosphatase levels and radiographic progression in ankylosing spondylitis.0
373516502023Musculoskeletal pain and muscular weakness as the main symptoms of adult hypophosphatasia in a Spanish cohort: clinical characterization and identification of a new ALPL gene variant.2
382344252023Systemic effects of hypophosphatasia characterization of two novel variants in the ALPL gene.0
364443962023Not just a carrier: Clinical presentation and management of patients with heterozygous disease-causing alkaline phosphatase (ALPL) variants identified through expanded carrier screening.1
367928312023Early elevated alkaline phosphatase as a surrogate biomarker of ongoing metabolic bone disease of prematurity.3
371920152023Promotion effect of FGF23 on osteopenia in congenital scoliosis through FGFr3/TNAP/OPN pathway.2
372774512023Association between changes in serum alkaline phosphatase levels and radiographic progression in ankylosing spondylitis.0
373516502023Musculoskeletal pain and muscular weakness as the main symptoms of adult hypophosphatasia in a Spanish cohort: clinical characterization and identification of a new ALPL gene variant.2
382344252023Systemic effects of hypophosphatasia characterization of two novel variants in the ALPL gene.0
342137432022Clinical, biochemical and genetic findings in adult patients with chronic hypophosphatasemia.3
344480002022Expression of the Adipocyte Progenitor Markers MSCA1 and CD36 is Associated With Adipose Tissue Function in Children.5
349359512022ALPL Genotypes in Patients With Atypical Femur Fractures or Other Biochemical and Clinical Signs of Hypophosphatasia.2

Citation

Dessen P

ALPL (alkaline phosphatase, biomineralization associated)

Atlas Genet Cytogenet Oncol Haematol. 2003-05-01

Online version: http://atlasgeneticsoncology.org/gene/623/tumors-explorer/meetings/meetings/