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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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人类
GRIN1 - Glutamate Ionotropic Receptor NMDA Type Subunit 1
Alias:
NR1
MRD8
GluN1
NMDA1
DEE101
NDHMSD
NDHMSR
NMD-R1
NMDAR1
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码的蛋白质是N-甲基-D-天冬氨酸受体的关键亚基,该受体属于谷氨酸受体通道超家族,是一个具有多个亚基的异质性蛋白质复合体,用于形成配体门控离子通道。这些亚基在突触的可塑性中起着关键作用,被认为与记忆和学习有关。细胞特异性因子被认为可以控制不同异构体的表达,这可能有助于亚基的功能多样性。已经描述了可替代剪接的转录变异体。[由RefSeq,2008年7月提供]
Related ID:
NCBI:2902
ENSEMBL:ENSG00000176884
HGNC:4584
UNIPROT:Q05586
OMIM:138249
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
2902
9
20
29603 bp
105.37
848
8
29
26
GRIN1 Genetics information (+)
GRCh38
Sequence Homology
Related Diseases and Mutations
#
Disease
Anatomical Category
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No data available
Transcripts & Proteins
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Transcript
Length(nt)
Exon Count
CDS(bp)
Protein
Length(aa)
No data available
* This data comes from NCBI.
Gene Expression
Tissue-specific RNA expression
Organ
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Alphabetical
Cell-specific RNA expression
Organ
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Type
Name
MGI
Strain of Origin
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Mutations
No data available
Related Drugs
Name
CAS Number
Status
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Link
No data available
References Literature
Title
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Journal
Year
IF
No Data Found!
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