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Gene : CLTCL1 Homo sapiens

Name  ? clathrin heavy chain like 1 Cytological Location  22q11.21
Brief Description  clathrin heavy chain like 1
Description  This gene is a member of the clathrin heavy chain family and encodes a major protein of the polyhedral coat of coated pits and vesicles. Chromosomal aberrations involving this gene are associated with meningioma, DiGeorge syndrome, and velo-cardio-facial syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2009]
  • synonyms:
  • CHC22,
  • clathrin, heavy polypeptide-like 1,
  • CLTCL1,
  • CLTD,
  • OTTHUMG00000150109,
  • CHC22,
  • NM_007098,
  • CLH22,
  • HGNC:2093,
  • clathrin, heavy chain-like 1,
  • CLTCL,
  • CLH22,
  • uc032qgb.2,
  • CLTCL,
  • CLTD
  • identifiers:
  • 8218,
  • ENSG00000070371,
  • CLTCL1

Genome feature

Region: gene ? Length: 112247  
Location: 22:19179473-19291719 reverse strand Cyto location: 22q11.21


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Function

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> GO terms.

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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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Expression

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

Gene Ontology

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Other

3756 SN Ps

5 Cross References

16 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results