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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
LOXHD1 - Lipoxygenase Homology PLAT Domains 1
Alias:
LH2D1
DFNB77
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码一个高度保守的蛋白质,其由PLAT(多囊蛋白/脂质氧化酶/α毒素)结构域组成,被认为涉及将蛋白质靶向到质膜。研究表明,这个基因在内耳的机械敏感毛细胞中表达,这个基因的突变导致听觉缺陷,表明这个基因对正常毛细胞功能是必不可少的。对人类有耳聋症状的家庭的筛查发现,这个基因中的一个突变导致了DFNB77,这是一种进行性的常染色体隐性非综合征性听力损失(ARNSHL)。已经注意到这个基因有不同的剪接转录变异体,编码不同的异构体。[RefSeq,2010年3月提供]
Related ID:
NCBI:125336
ENSEMBL:ENSG00000167210
HGNC:26521
UNIPROT:Q8IVV2
OMIM:613072
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
125336
21
41
180260 bp
235.68
1853
7
7
5
LOXHD1 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
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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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