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Gene : DPY19L2 Homo sapiens

Name  ? dpy-19 like 2 Cytological Location  12q14.2
Brief Description  dpy-19 like 2
Description  The protein encoded by this gene belongs to the dpy-19 family. It is highly expressed in testis, and is required for sperm head elongation and acrosome formation during spermatogenesis. Mutations in this gene are associated with an infertility disorder, spermatogenic failure type 9 (SPGF9). [provided by RefSeq, Dec 2011]
  • synonyms:
  • OTTHUMG00000168712,
  • spermatogenesis associated 34,
  • dpy-19 like 2 (C. elegans),
  • DPY19L2,
  • NM_173812,
  • SPGF9,
  • FLJ32949,
  • SPATA34,
  • HGNC:19414,
  • SPATA34,
  • uc001srp.2
  • identifiers:
  • 283417,
  • ENSG00000177990,
  • DPY19L2

Genome feature

Region: gene ? Length: 110289  
Location: 12:63558913-63669201 reverse strand Cyto location: 12q14.2


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 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

Gene --> GO terms.

 

Other

0 Pathways

3753 SN Ps

5 Cross References

17 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results