人类

ALPL - Alkaline Phosphatase, Biomineralization Associated

Alias:
HOPS
HPPA
HPPC
HPPI
HPPO
TNAP
TNALP
APTNAP
TNSALP
AP-TNAP
TNS-ALP
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码碱性磷酸酶家族的蛋白质成员。至少有四种不同的但相关的碱性磷酸酶:肠、胎盘、胎盘样和肝/骨/肾(组织特异性)。前三者位于2号染色体上,而组织特异性形式位于1号染色体上。这个基因的产物是一种膜结合的糖基化酶,没有在任何特定组织中表达,因此被称为酶的组织特异性形式。替代剪接导致多种转录变体,至少有一种编码前原蛋白,经过蛋白酶处理生成成熟的酶。这种酶可能在骨矿化中发挥作用。这个基因的突变已与低磷酸酶血症相关,这是一种以高钙血症和骨骼缺陷为特征的疾病。[由RefSeq提供,2015年10月]

Basic Information

NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
7
12
69427 bp
57.30
956
10
14
50

ALPL Genetics information (+)

GRCh38

Sequence Homology

Related Diseases and Mutations

#
Disease
Anatomical Category
Score
Mutations
No data available

Transcripts & Proteins

Table View
Tile View
#
Transcript
Length(nt)
Exon Count
CDS(bp)
Protein
Length(aa)
No data available
* This data comes from NCBI.

Gene Expression

Tissue-specific RNA expression

Organ
Abundance
Alphabetical

Cell-specific RNA expression

Organ
Abundance
Alphabetical

Interactions

Acting
Regulation
Detail
Mechanism
Target
Residues
Reference
Score
No data available

Related Mouse Models

Type
Name
MGI
Strain of Origin
Publications
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
Link
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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