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中文人类
MEGF8 - Multiple EGF Like Domains 8
Alias:
SBP1
CRPT2
EGFL4
C19orf49
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这个基因编码的蛋白质是一个含有几个EGF样结构域、Kelch重复序列和PSI结构域的未知功能的单通过路I型膜蛋白。这个基因的缺陷是导致Carpenter综合征2的原因。已经发现这个基因有两个编码不同异型的转录变异体。[由RefSeq提供，2012年12月]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
MEGF8 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
