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中文人类
SLC26A4 - Solute Carrier Family 26 Member 4
Alias:
EVA
PDS
DFNB4
TDH2B
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这种基因的突变与Pendred综合症有关，这是最常见的综合征性耳聋形式，是一种常染色体隐性疾病。它与SLC26A3基因高度相似；它们具有相似的基因组结构，该基因位于SLC26A3基因的3'端。编码的蛋白质与硫酸盐转运蛋白具有同源性。[由RefSeq，2008年7月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
SLC26A4 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
