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Gene : CHRDL1 Homo sapiens

Name  ? chordin like 1 Cytological Location  Xq23
Brief Description  chordin like 1
Description  This gene encodes an antagonist of bone morphogenetic protein 4. The encoded protein may play a role in topographic retinotectal projection and in the regulation of retinal angiogenesis in response to hypoxia. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jan 2009]
  • synonyms:
  • MGCN,
  • CHRDL1,
  • VOPT,
  • MGC1,
  • NRLN1,
  • megalocornea 1 (X-linked),
  • dA141H5.1,
  • OTTHUMG00000022199,
  • CHL,
  • MGC1,
  • HGNC:29861,
  • CHL,
  • NM_145234,
  • NRLN1,
  • AL049176,
  • uc065arx.1
  • identifiers:
  • 91851,
  • ENSG00000101938,
  • CHRDL1

Genome feature

Region: gene ? Length: 121962  
Location: X:110673856-110795817 reverse strand Cyto location: Xq23


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

2 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

3753 SN Ps

5 Cross References

19 Data Sets

2 Homologues

0 Located Features

97 Rna Seq Results