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Gene : NAGA Homo sapiens

Name  ? alpha-N-acetylgalactosaminidase Cytological Location  22q13.2
Brief Description  alpha-N-acetylgalactosaminidase
description  NAGA encodes the lysosomal enzyme alpha-N-acetylgalactosaminidase, which cleaves alpha-N-acetylgalactosaminyl moieties from glycoconjugates. Mutations in NAGA have been identified as the cause of Schindler disease types I and II (type II also known as Kanzaki disease). [provided by RefSeq, Jul 2008]
  • synonyms:
  • HGNC:7631,
  • D22S674,
  • uc003bbw.5,
  • alpha-galactosidase B,
  • GALB,
  • OTTHUMG00000151276,
  • N-acetylgalactosaminidase, alpha-,
  • NM_000262,
  • NAGA,
  • D22S674
  • identifiers:
  • 4668,
  • ENSG00000198951,
  • NAGA

Genome feature

Region: gene ? Length: 12563  
Location: 22:42058334-42070896 reverse strand Cyto location: 22q13.2


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Function

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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

2011 SN Ps

5 Cross References

20 Data Sets

6 Homologues

0 Located Features

90 Rna Seq Results