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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
大鼠
Slc17a8 - solute carrier family 17 member 8
Alias:
Vglut3
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Basic Information
Sequence Homology
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
References Literature
预测能够实现L-谷氨酸跨膜转运体和神经递质跨膜转运体的活性。参与大脑发育;耳蜗发育;和神经视网膜发育。位于几个细胞组件中,包括轴突;树突;和神经节限制端足。帕金森病的生物标志物;耳蜗疾病;坐骨神经病变;短暂脑缺血;和旋毛虫病。这个基因的人类同源物与常染色体显性非综合征性耳聋25有关。与人类SLC17A8(溶质载体家族17成员8)正交。[由基因组资源联盟,2022年4月提供]
Related ID:
NCBI:266767
ENSEMBL:ENSRNOG00000007581
UNIPROT:Q7TSF2
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Related Mouse Models
Reference
266767
2
12
55287 bp
64.75
13
9
Slc17a8 Genetics information (-)
mRatBN7.2
Sequence Homology
Transcripts & Proteins
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#
Transcript
Length(nt)
Exon Count
CDS(bp)
Protein
Length(aa)
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* This data comes from NCBI.
Gene Expression
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Type
Name
MGI
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