help  | about  | cite  | software

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:
  • uc032qgb.2,
  • CLTD,
  • CLTD,
  • clathrin, heavy polypeptide-like 1,
  • NM_007098,
  • CHC22,
  • HGNC:2093,
  • OTTHUMG00000150109,
  • clathrin, heavy chain-like 1,
  • CLH22,
  • CLH22,
  • CHC22,
  • CLTCL,
  • CLTCL,
  • CLTCL1
  • identifiers:
  • 8218,
  • ENSG00000070371,
  • CLTCL1

Genome feature

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


Paste the following link
Lists
This Gene is in one list:
PL_GenomicsEngland_GenePanel:Pain_syndromes (24)

Uni Prot Comments Displayer

Protein Atlas Displayer

Gene Expression Atlas Tissues Displayer

Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer

Function

Gene Ontology Displayer

13 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

J Browse Displayer

Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

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

Homologue Displayer

Interactions

Cytoscape Network Displayer

Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

13 Pathways

3740 SN Ps

5 Cross References

15 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results





Funding: InterMine has been developed principally through support of the Wellcome Trust. Complementary projects have been funded by the NIH/NHGRI and the BBSRC.

An ELIXIR-UK resource

© 2002 - 2019 Department of Genetics, University of Cambridge, Downing Street,
Cambridge CB2 3EH, United Kingdom