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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking ALOX12B and autosomal recessive congenital ichthyosis 2 in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with ALOX12B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to autosomal recessive congenital ichthyosis 2  (DOID:0060710)
  • 0 papers in RGD have been used to annotate ALOX12B


    • An association has been curated linking ALOX12B and autosomal recessive congenital ichthyosis 2 in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with ALOX12B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to autosomal recessive congenital ichthyosis 2  (DOID:0060710)
  • 0 papers in RGD have been used to annotate ALOX12B
  • Curation Notes: ClinVar Annotator: match by term: ALOX12B-related condition | ClinVar Annotator: match by term: Autosomal recessive congenital ichthyosis 2
  • Original References(s): PMID:11773004 PMID:16116617 PMID:16199547 PMID:17139268 PMID:17576681 PMID:18347291 PMID:18414213 PMID:19131948 PMID:19890349 PMID:20222929 PMID:22622417 PMID:23083690 PMID:23621129 PMID:24033266 PMID:25524567 PMID:25741868 PMID:25998749 PMID:26762237 PMID:26863999 PMID:27025581 PMID:28492532 PMID:29687370 PMID:31046801 PMID:31168818 PMID:31642606 PMID:31953843 PMID:32253496 PMID:33435499 PMID:33726816 PMID:34008892 PMID:34379964 PMID:35052464 PMID:36003334 PMID:9536098


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