Inherited bleeding disorders

Gene: LMAN1

Green List (high evidence)

LMAN1 (lectin, mannose binding 1)
EnsemblGeneIds (GRCh38): ENSG00000074695
EnsemblGeneIds (GRCh37): ENSG00000074695
OMIM: 601567, Gene2Phenotype
LMAN1 is in 3 panels

2 reviews

Louise Daugherty (Genomics England Curator)

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Combined factor V and VIII deficiency

BRIDGE consortium (NIHRBR-RD)

Green List (high evidence)

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Combined factor V and VIII deficiency

Variants in this GENE are reported as part of current diagnostic practice

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • BRIDGE Study Tier 1 Gene
Phenotypes
  • Combined factor V and VIII deficiency
OMIM
601567
Clinvar variants
Variants in LMAN1
Penetrance
Complete
Panels with this gene

History Filter Activity

19 Dec 2016, Gel status: 4

panel promoted to version 1

Louise Daugherty (Genomics England Curator)

Revised 19 December 2016

19 Dec 2016, Gel status: 4

Added New Source

Louise Daugherty (Genomics England Curator)

LMAN1 was added to Inherited bleeding disorderspanel. Source: Expert Review Green

9 Sep 2016, Gel status: 0

Created

Ellen McDonagh (Genomics England Curator)

LMAN1 was created by ellenmcdonagh

9 Sep 2016, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

LMAN1 was added to Inherited bleeding disorderspanel. Sources: BRIDGE Study Tier 1 Gene