2. Gene
  3. CEP20 - centrosomal protein 20 Gene

CEP20 - centrosomal protein 20 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as FOPNL; FOR20; C16orf63; PHSECRG2

Gene ID: 123811 | Gene type: protein coding

About 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.

Summary

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

CEP20 Products(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

CEP20 Protein Structure

FOP_dimer

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

  • 0
  • 100
  • 174 a.a.
Protein Preferred Names Protein Names

centrosomal protein 20

FGFR1OP N-terminal like

Related Diseases

Diseases Alias
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
Diseases Alias
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

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS02509 CEP20 Human Pre-designed siRNA Set A / Unkown

Orthologs Information

Species Symbol Source 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