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中文人类
FAM136A - Family With Sequence Similarity 136 Member A
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这个基因编码一个在线粒体中定位的蛋白质，它在不同物种中高度保守。该基因在各种组织中表达，包括人类淋巴母细胞和大鼠的神经感觉上皮。这个基因的突变与家族性梅尼埃病有关，这是一种内耳的慢性疾病。在其他染色体上发现了这个基因的几个假基因。选择性剪接产生了多种转录变异体。[RefSeq，2016年8月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
FAM136A 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
