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

Details

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