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中文人类
PRR12 - Proline Rich 12
Alias:
NOC
KIAA1205
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这个基因编码一个富含脯氨酸的蛋白质，包含两个A-T钩状DNA结合结构域。在人类患者中，染色体易位和该基因与含锌指蛋白、含1个MIZ型（基因ID：57178）之间的基因融合可能导致智力障碍和神经精神障碍。该基因在胚胎小鼠大脑中的富集表达提示，该基因可能在神经系统发育中发挥作用。[RefSeq，2016年7月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
PRR12 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
