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  2. CEP20 - centrosomal protein 20 Gene

CEP20 - centrosomal protein 20 Gene

中文名称:中心体蛋白 20

种属: Homo sapiens

同用名: FOPNL; FOR20; C16orf63; PHSECRG2

基因 ID: 123811 | 基因类型: protein coding

关于 CEP20

Cytogenetic location: 16p13.11 Genomic coordinates (GRCh38): 16:15,865,719-15,888,603 (from NCBI)

This gene has 9 transcripts (splice variants), 1 gene allele and 196 orthologues. Ubiquitous expression in thyroid (RPKM 17.8), esophagus (RPKM 13.1) and 25 other tissues.

功能概要

实现相同的蛋白质结合活性。参与纤毛组装。位于中心粒卫星和核质中。 [由基因组资源联盟提供,2022 年 4 月]

Enables identical protein binding activity. Involved in cilium assembly. Located in centriolar satellite and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

CEP20 基因产物(6)

mRNA Protein Name
NM_001304497.2 NP_001291426.1 centrosomal protein 20 isoform 2
NM_001304498.2 NP_001291427.1 centrosomal protein 20 isoform 3
NM_001304499.2 NP_001291428.1 centrosomal protein 20 isoform 4
NM_001304500.2 NP_001291429.1 centrosomal protein 20 isoform 5
NM_001304502.2 NP_001291431.1 centrosomal protein 20 isoform 6
NM_144600.4 NP_653201.1 centrosomal protein 20 isoform 1
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables identical protein binding IPI
IPI: 通过物理相互作用推断
20551181 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
32296183 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in cilium assembly IMP
IMP: 通过突变表型推断
15616553 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in centriolar satellite IDA
IDA: 通过直接分析推断
15616553 GOA
located in centrosome IDA
IDA: 通过直接分析推断
21399614 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

CEP20 蛋白结构

FOP_dimer

FOP_dimer: FOP N terminal dimerisation domain (50 - 113)

  • 0
  • 100
  • 174 a.a.
蛋白主名 其他名称

centrosomal protein 20

FGFR1OP N-terminal like

CEP20 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
CEP20 Q96NB1 OFD1 Homo sapiens O75665 33961781
种属内
CEP20 Q96NB1 CEP20 Homo sapiens Q96NB1
FPS
31837246
种属内
CEP20 Q96NB1 PCM1 Homo sapiens Q15154 20551181
种属内
CEP20 Q96NB1 CEP20 Homo sapiens Q96NB1 20551181
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Orofaciodigital Syndrome I

OFD1

Orofaciodigital Syndrome 1

Oral-Facial-Digital Syndrome, Type I

Oral-Facial-Digital Syndrome 1

Ofds I

Papillon-Leage And Psaume Syndrome

Papillon-Leage-Psaume Syndrome

Oral-Facial-Digital Syndrome Type 1

Orofaciodigital Syndrome Type 1

Orofaciodigital Syndromes

Orofaciodigital Syndrome Type I

Oral-Facial-Digital Syndrome Type I

Ofd Syndrome 1

Ofds 1

Oral Facial Digital Syndrome 1

Oral Facial Digital Syndrome Type 1

Papillon-League-Psaume Syndrome

Ofdi

Ofdsi

Orofaciodigital Syndrome, Type I

Orofaciodigital Syndrome

Oral-Facial-Digital Syndrome

Orofaciodigital Syndromes

Ofd

Oral Facial Digital Syndromes

Oral-Facial-Digital Syndromes

Dysplasia Linguofacialis

Ofds

Oro-Facio-Digital Syndrome

Orodigitofacial Dysostosis

Orodigitofacial Syndrome

Oral Facial Digital Syndrome

Orofaciodigital Syndrome I

Lissencephaly

Pachygyria

Broad Gyri Of Cerebrum

Large Gyri Of Cerebrum

Macrogyria

疾病名称 别名
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

直系同源

种属 基因名 来源 基因 ID
Canis familiaris CEP20 VGNC VGNC:40939
Macaca mulatta CEP20 VGNC VGNC:99500
Bos taurus CEP20 VGNC VGNC:29072
Rattus norvegicus CEP20 RGD RGD:1305823
Mus musculus CEP20 MGD MGI:1913336
Felis catus CEP20 VGNC VGNC:80574