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  2. Congenital anaemias
  3. C15orf41
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Congenital anaemias

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)

Comment on list classification: Added new-gene-name tag, new approved HGNC gene symbol for C15orf41 is CDIN1
Created: 7 May 2020, 10:51 a.m. | Last Modified: 7 May 2020, 10:51 a.m.
Panel Version: 0.99
Created: 7 May 2020, 10:51 a.m.
Last Modified: 7 May 2020, 10:51 a.m.
Panel version: 0.99

Details

Sources
  • Expert Review Red
  • UKGTN
  • Eligibility statement prior genetic testing
Phenotypes
  • Congenital Dyserythropoietic Anemia
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

Entity classified by Genomics England curator

Catherine Snow (Genomics England)

Gene: c15orf41 has been classified as Red List (Low Evidence).

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

Added New Source

Ellen McDonagh (Genomics England Curator)

C15orf41 was added to Congenital anaemiaspanel. Source: UKGTN

12 Aug 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

C15orf41 was added to Congenital anaemiaspanel. Sources: Eligibility statement prior genetic testing

28 Apr 2015, Gel status: 1

Added New Source

GEL ()

C15orf41 was added to Congenital anaemiaspanel. Sources: UKGTN