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  3. DNAJC21
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IBMDx study

Gene: DNAJC21

Green List (high evidence)
DNAJC21 (DnaJ heat shock protein family (Hsp40) member C21)
EnsemblGeneIds (GRCh38): ENSG00000168724
EnsemblGeneIds (GRCh37): ENSG00000168724
OMIM: 617048, Gene2Phenotype
DNAJC21 is in 9 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Green List (high evidence)

Onset of pancytopenia in early childhood; variable nonspecific somatic abnormalities, including poor growth, microcephaly, and skin anomalies.
Sources: Expert list
Created: 8 Jan 2020, 9:24 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Bone marrow failure syndrome 3, MIM# 617052

Publications

Created: 8 Jan 2020, 9:24 p.m.

Panel version: Imported from Bone Marrow Failure panel version 0.11

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Green
  • IBMDx Study
  • Expert Review Green
  • Expert list
Phenotypes
  • Bone marrow failure syndrome 3, MIM# 617052
OMIM
617048
Clinvar variants
Variants in DNAJC21
Penetrance
None
Panels with this gene

History Filter Activity

10 Dec 2021, Gel status: 3

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: DNAJC21 was added gene: DNAJC21 was added to IBMDx study. Sources: IBMDx Study,Expert Review Green Mode of inheritance for gene: DNAJC21 was set to Unknown Phenotypes for gene: DNAJC21 were set to Bone marrow failure syndrome 3, MIM# 617052