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Gene : FAM120C Homo sapiens

Name  ? family with sequence similarity 120C Cytological Location  Xp11.22
Brief Description  family with sequence similarity 120C
Description  This gene encodes a potential transmembrane protein and lies in a region where mutations and deletions have been associated with intellectual disability and autism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]
  • synonyms:
  • HGNC:16949,
  • ORF34,
  • AY150025,
  • FAM120C,
  • OTTHUMG00000021625,
  • CXorf17,
  • NM_017848,
  • ORF34,
  • FLJ20506,
  • uc004dsz.5,
  • CXorf17,
  • chromosome X open reading frame 17
  • identifiers:
  • 54954,
  • ENSG00000184083,
  • FAM120C

Genome feature

Region: gene ? Length: 114961  
Location: X:54068324-54183284 reverse strand Cyto location: Xp11.22


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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

0 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

657 SN Ps

5 Cross References

15 Data Sets

0 Homologues

0 Located Features

97 Rna Seq Results