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Gene : CEP19 Homo sapiens

Name  ? centrosomal protein 19 Cytological Location  3q29
Brief Description  centrosomal protein 19
Description  The protein encoded by this gene localizes to centrosomes and primary cilia and co-localizes with a marker for the mother centriole. This gene resides in a region of human chromosome 3 that is linked to morbid obesity. A homozygous knockout of the orthologous gene in mouse resulted in mice with morbid obesity, hyperphagy, glucose intolerance, and insulin resistance. Mutations in this gene cause morbid obesity and spermatogenic failure (MOSPGF). This gene has a pseudogene on human chromosome 2. [provided by RefSeq, Apr 2014]
  • synonyms:
  • chromosome 3 open reading frame 34,
  • NM_032898,
  • centrosomal protein 19kDa,
  • HGNC:28209,
  • BC007827,
  • C3orf34,
  • C3orf34,
  • uc011btw.3,
  • MGC14126,
  • MOSPGF,
  • OTTHUMG00000153933,
  • CEP19
  • identifiers:
  • 84984,
  • ENSG00000174007,
  • CEP19

Genome feature

Region: gene ? Length: 6018  
Location: 3:196706273-196712290 reverse strand Cyto location: 3q29


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

3753 SN Ps

5 Cross References

17 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results