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  2. Early onset pancytopenia and red cell disorders
  3. C15orf41
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Early onset pancytopenia and red cell disorders

Gene: C15orf41

Red List (low evidence)
C15orf41 (chromosome 15 open reading frame 41)
EnsemblGeneIds (GRCh38): ENSG00000186073
EnsemblGeneIds (GRCh37): ENSG00000186073
OMIM: 615626, Gene2Phenotype
C15orf41 is in 2 panels

1 review

Catherine Snow (Genomics England)

Added new-gene-name tag, new approved HGNC gene symbol for C15orf41 is CDIN1
Created: 7 May 2020, 10:50 a.m. | Last Modified: 7 May 2020, 10:50 a.m.
Panel Version: 0.260
Created: 7 May 2020, 10:50 a.m.
Last Modified: 7 May 2020, 10:50 a.m.
Panel version: 0.260

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • UKGTN
  • Eligibility statement prior genetic testing
Phenotypes
  • Congenital Dyserythropoietic Anemia
  • N/A
Tags
new-gene-name
OMIM
615626
Clinvar variants
Variants in C15orf41
Penetrance
Complete
Panels with this gene

History Filter Activity

7 May 2020, Gel status: 1

Added Tag

Catherine Snow (Genomics England)

Tag new-gene-name tag was added to gene: C15orf41.

30 Sep 2015, Gel status: 1

Set Mode of Inheritance

Ellen McDonagh (Genomics England Curator)

Model of inheritance for gene C15orf41 was set to BIALLELIC, autosomal or pseudoautosomal

30 Sep 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

C15orf41 was added to Early onset pancytopenia and red cell disorderspanel. Source: UKGTN

12 Aug 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

C15orf41 was added to Early onset pancytopenia and red cell disorderspanel. Sources: Eligibility statement prior genetic testing