1. Panels
  2. Fetal hydrops
  3. SPTB
STRs in panel
Prev Next
Regions in panel
Prev Next

Fetal hydrops

Gene: SPTB

No list
SPTB (spectrin beta, erythrocytic)
EnsemblGeneIds (GRCh38): ENSG00000070182
EnsemblGeneIds (GRCh37): ENSG00000070182
OMIM: 182870, Gene2Phenotype
SPTB is in 4 panels

1 review

Irina Adamena (Children's Clinical University Hospital)

Green List (high evidence)

Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Created: 11 Apr 2024, 4:12 p.m.

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
Nonimmune hydrops fetalis

Publications

Created: 11 Apr 2024, 4:12 p.m.

Panel version: 1.64

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
Phenotypes
  • Nonimmune hydrops fetalis
OMIM
182870
Clinvar variants
Variants in SPTB
Penetrance
None
Publications
Panels with this gene

History Filter Activity

11 Apr 2024, Gel status: 0

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Irina Adamena (Children's Clinical University Hospital)

gene: SPTB was added gene: SPTB was added to Fetal hydrops. Sources: Literature Mode of inheritance for gene: SPTB was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: SPTB were set to PMID: 33082562 Phenotypes for gene: SPTB were set to Nonimmune hydrops fetalis Review for gene: SPTB was set to GREEN