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Gene : ROGDI Homo sapiens

Name  ? rogdi atypical leucine zipper Cytological Location  16p13.3
Brief Description  rogdi homolog
description  This gene encodes a protein of unknown function. Loss-of-function mutation in this gene cause Kohlschutter-Tonz syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]
  • synonyms:
  • NM_024589,
  • KTZS,
  • uc002cxv.5,
  • ROGDI,
  • AK026039,
  • HGNC:29478,
  • rogdi homolog (Drosophila),
  • OTTHUMG00000129479,
  • FLJ22386,
  • rogdi homolog
  • identifiers:
  • 79641,
  • ENSG00000067836,
  • ROGDI

Genome feature

Region: gene ? Length: 5989  
Location: 16:4796962-4802950 reverse strand Cyto location: 16p13.3


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Function

Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

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)

Mouse Gene --> Allele [Phenotype]

Homology

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Gene --> Orthologues

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

811 SN Ps

5 Cross References

18 Data Sets

6 Homologues

0 Located Features

90 Rna Seq Results