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中文人类
LOXL3 - Lysyl Oxidase Like 3
Alias:
LOXL
MYP28
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这个基因编码赖氨氧化酶，可能作为胺氧化酶发挥作用，并在胶原蛋白和弹性蛋白的交联形成中发挥作用。在小鼠中删除相关基因导致新生儿死亡，腭裂，脊柱畸形和胶原组织缺陷。在这个基因中发现了一个突变，存在于一个患有Stickler综合症的家庭中。[由RefSeq，2016年9月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
LOXL3 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
