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中文人类
PEPD - Peptidase D
Alias:
PROLIDASE
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这个基因编码肽酶家族的成员。蛋白质形成同源二聚体，水解具有C端脯氨酸或羟脯氨酸残基的二肽或三肽。该酶在脯氨酸的循环利用中起着重要作用，可能是胶原产生过程中的限速步骤。这个基因的突变导致脯氨酰酶缺乏，其特点是排泄大量含有脯氨酸的二肽和三肽。已发现这个基因有多种转录变异体，编码不同的异构体。[RefSeq，2009年10月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
PEPD Genetics information (-)
GRCh38
Sequence Homology
Related Diseases and Mutations
#
Disease
Anatomical Category
Score
Mutations
Transcripts & Proteins
Table View
Tile View
#
Transcript
Length(nt)
Exon Count
CDS(bp)
Protein
Length(aa)
* 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
Related Mouse Models
Type
Name
MGI
Strain of Origin
Publications
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Link
References Literature
Title
PMID
Journal
Year
IF
