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中文人类
SLC1A4 - Solute Carrier Family 1 Member 4
Alias:
SATT
ASCT1
SPATCCM
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这个基因编码的蛋白质是一种依赖钠的中性氨基酸转运蛋白，负责丙氨酸、丝氨酸、半胱氨酸和苏氨酸的运输。这个基因的缺陷与发育延迟、小头畸形和智力障碍有关。[由RefSeq，2017年1月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
SLC1A4 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
