Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:79827
  • Symbol:CLMP
  • Description:CXADR like membrane protein

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Disease_Term Source Rank Other Values
Congenital short bowel syndrome, 615237 (3) OMIM high
  • Genome region :11q24.1
  • OMIM_ID :611693OMIM gene ID
  • OMIM_ID :615237OMIM phenotype ID
Proteinuria in chronic kidney disease GWAS high