1. Panels
  2. Incidentalome_PREGEN_DRAFT
  3. ABL1
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Incidentalome_PREGEN_DRAFT

Gene: ABL1

Red List (low evidence)
ABL1 (ABL proto-oncogene 1, non-receptor tyrosine kinase)
EnsemblGeneIds (GRCh38): ENSG00000097007
EnsemblGeneIds (GRCh37): ENSG00000097007
OMIM: 189980, Gene2Phenotype
ABL1 is in 7 panels

1 review

Tony Roscioli (New South Wales Health Pathology)

Red List (low evidence)

A cause of a Mendelian disorder that could present in fetal life
Created: 4 Dec 2020, 3:45 a.m. | Last Modified: 4 Dec 2020, 3:45 a.m.
Panel Version: 0.3
Created: 4 Dec 2020, 3:45 a.m.
Last Modified: 4 Dec 2020, 3:45 a.m.
Panel version: 0.3

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • NSW Health Pathology
OMIM
189980
Clinvar variants
Variants in ABL1
Penetrance
None
Panels with this gene

History Filter Activity

7 Dec 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: abl1 has been classified as Red List (Low Evidence).

7 Dec 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: abl1 has been classified as Red List (Low Evidence).

9 Nov 2020, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: ABL1 was added gene: ABL1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology Mode of inheritance for gene: ABL1 was set to Unknown