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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
人类
MCOLN1 - Mucolipin TRP Cation Channel 1
Alias:
ML1
ML4
MG-2
MLIV
MST080
TRPML1
MSTP080
TRP-ML1
TRPM-L1
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码瞬时受体电位(TRP)阳离子通道基因家族的成员。该跨膜蛋白定位在内质网膜上,包括溶酶体,并在晚期内吞途径和调节溶酶体分泌中发挥作用。该通道对Ca(2+)、Fe(2+)、Na(+)、K(+)和H(+)具有通透性,并受到Ca(2+)浓度变化的影响。该基因的突变导致Ⅳ型粘脂病。[RefSeq,2009年10月提供]
Related ID:
NCBI:57192
ENSEMBL:ENSG00000090674
HGNC:13356
UNIPROT:Q9GZU1
OMIM:605248
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
57192
1
14
11386 bp
65.02
648
2
5
33
MCOLN1 Genetics information (+)
GRCh38
Sequence Homology
Related Diseases and Mutations
#
Disease
Anatomical Category
Score
Mutations
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
Abundance
Alphabetical
Cell-specific RNA expression
Organ
Abundance
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Interactions
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Acting
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Residues
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Score
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Related Mouse Models
Type
Name
MGI
Strain of Origin
Publications
Mutations
No data available
Related Drugs
Name
CAS Number
Status
Phase
Link
No data available
References Literature
Title
PMID
Journal
Year
IF
No Data Found!
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