人类

FAM111A - FAM111 Trypsin Like Peptidase A

Alias:
KCS2
GCLEB
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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细胞周期调节的,并且具有核定位。蛋白质的C端与胰蛋白酶样肽酶具有同源性,并包含一个与增殖细胞核抗原(PCNA)共定位所必需的PCNA相互作用肽(PIP)盒。这个基因的减少表达会导致DNA复制缺陷,这与这个基因在猴病毒40(SV40)病毒复制中的作用一致。这个基因的突变与肯尼-卡费综合征(KCS)2型和更严重的骨颅硬化症(OCS,也称为Gracile骨发育异常)有关,两者都以矮小身材、甲状旁腺功能减退、骨发育异常和低钙血症为特征。可变剪接导致多个转录变异体。[由RefSeq,2015年8月提供]

Basic Information

NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
33
6
12184 bp
70.20
178
3
5
14

FAM111A Genetics information (+)

GRCh38

Sequence Homology

Related Diseases and Mutations

#
Disease
Anatomical Category
Score
Mutations
No data available

Transcripts & Proteins

Table View
Tile View
#
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
Alphabetical

Interactions

Acting
Regulation
Detail
Mechanism
Target
Residues
Reference
Score
No data available

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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