Genes in panel
STRs in panel
Prev Next

COVID-19 research

Gene: STAT5B

Green List (high evidence)

STAT5B (signal transducer and activator of transcription 5B)
EnsemblGeneIds (GRCh38): ENSG00000173757
EnsemblGeneIds (GRCh37): ENSG00000173757
OMIM: 604260, Gene2Phenotype
STAT5B is in 9 panels

7 reviews

Ivone Leong (Genomics England Curator)

Green List (high evidence)

IUIS: Inheritance - AR (causes STAT5b deficiency. T cells: Modestly decreased, reduced Treg number and function. B cells: Normal. Ig: hypergammaglobulinemia, increased IgE. Associated with growth-hormone insensitive dwarfism; dysmorphic features; eczema; lymphocytic interstitial pneumonitis; prominent autoimmunity), AD dominant-negative (causes STAT5b deficiency. T cells and B cells are normal. Increased IgE. Associated with Growth-failure; eczema (no immune defects compared to AR STAT5 deficiency)).
Created: 15 Apr 2020, 12:09 p.m. | Last Modified: 15 Apr 2020, 12:09 p.m.
Panel Version: 0.103

Mode of inheritance
BOTH monoallelic and biallelic, autosomal or pseudoautosomal

Publications

Tracy Briggs (Manchester Genomic Medicine Centre)

Green List (high evidence)

YES- this is covered on our targeted exome
Created: 17 Sep 2019, 3:18 p.m. | Last Modified: 17 Sep 2019, 3:18 p.m.
Panel Version: 1.94

Eleanor Williams (Genomics England Curator)

Green List (high evidence)

Comment on list classification: Changing this gene from Amber to Green as there are >3 independant cases providing association of this gene and the disorder
Created: 3 May 2018, 9:59 p.m.
In OMIM this gene is associated with Growth hormone insensitivity with immunodeficiency 245590. They report that in Kofoed et al. (2003) (PMID: 13679528) a patient is described with a homozygous ala630-to-pro mutation (A630P) in the STATB gene and a combined phenotype of GH insensitivity and immunodeficiency consistent with the presence of a defect in the JAK/STAT system. Cohen et al. (2006) (PMID: 16920911) further investigated this patient and observed immune dysregulation with decreased numbers of regulatory CD4+/CD25-high T cells (Tregs). Hwa et al. (2005) (PMID: 15827093) report a 16.4-year-old Turkish girl with postnatal growth retardation and insensitivity to growth hormone, who also had recurrent pulmonary infections and a bleeding diathesis due to defective thrombocyte aggregation, and a homozygous 1-bp insertion in the STAT5B gene. The insertion resulted in a frame shift, leading to early protein termination and consequent lack of immunodetectable STAT5b protein. Vidarsdottir et al. (2006) (PMID: 16787985) report a 30-year-old man born in the Dutch Antilles who had short stature and delayed puberty with normal GH and GHBP levels, an elevated plasma prolactin level, and extremely low levels of IGF1, IGFBP3, and acid-labile subunit identified homozygosity for a 1-bp insertion in the STAT5B gene . The authors stated that the patient was diagnosed with congenital ichthyosis at birth and had hemorrhagic varicella at 16 years of age, but had NO history of pulmonary or immunologic problems. Bernasconi et al. (2006) (PMID:17030597) report a 16-year-old girl with severe postnatal growth failure, GH insensitivity, and immunodeficiency and homozygosity for a nonsense mutation in the STAT5B gene. Hwa et al. (2007) (PMID: 17389811) report 2 Kuwaiti sisters from a consanguineous family with severe postnatal growth retardation, normal GH and GHBP levels, and no mutation in the GH receptor gene, Hwa et al. (2007) (PMID: 17389811) identified homozygosity for a 1-bp deletion in the STAT5B gene (604260.0005). In addition to GHI, siblings 2 and 1 presented with, respectively, a diagnosis of juvenile idiopathic arthritis and recurrent pulmonary infections. A PubMed search also finds Pugliese-Pires et al (2010) (PMID: 20538865) who report 2 male siblings with GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction with a novel STAT5B mutation. Both siblings were homozygous for a 4 bp deletion in STAT5B. One sibling also had a heterozygous missense mutation in the GHR gene. Rating this gene green because there are >3 cases of plausable disease causing mutations in the STAT5B gene.
Created: 2 May 2018, 1:59 p.m.
Comment on phenotypes: Added MIM ID to first phenotype
Created: 2 May 2018, 10:21 a.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Publications

Louise Daugherty (Genomics England Curator)

Green List (high evidence)

Gene rating submitted by Kimberly Gilmour and Austen Worth on behalf of London North GLH for the GMS Immunology specialist test group. As discussed with the GMS Immunology Specialist Test Group during webex call 28th March 2019 and confirmed in follow up email 6th September the Specialist Test Group all agreed there is enough evidence to rate this gene Green.
Created: 17 Sep 2019, 3:18 p.m. | Last Modified: 17 Sep 2019, 3:18 p.m.
Panel Version: 1.94
Gene rating submitted by Tracy Briggs, David Gokhale and Abigal Rousseau on behalf of North West GLH for the GMS Immunology specialist test group. As discussed with the GMS Immunology Specialist Test Group during webex call 28th March 2019 and confirmed in follow up email on 20th June the Specialist Test Group all agreed there is enough evidence to rate this gene Green.
Created: 17 Sep 2019, 3:18 p.m. | Last Modified: 17 Sep 2019, 3:18 p.m.
Panel Version: 1.94
Reviewed gene as Green. Red ratings highly likely to be historical ratings made in view of the panel (SCID). This panel will be retired when this PID panel is V. In view of poor growth, recurrent infections and T-cell abnormalities associated to STAT5B variants, these are appropriate phenotypes for the PID panel so gene should be Green
Created: 11 Jul 2018, 4:26 p.m.
OriginaI Metadata from IUIS classification table (February, 2018) downloaded 20180614. IUIS Genetic defect (original gene symbol in IUIS download): STAT5B .PanelApp HGNC gene symbol check: STAT5B . IUIS Disease: STAT5b deficiency . IUIS Inheritance: AR .T cells: N/A, .B cells: Normal, .IUIS Other affected cells: N/A. IUIS Associated features: Growth-hormone insensitive dwarfism, dysmorphic features, eczema, lymphocytic interstitial pneumonitis, autoimmunity. IUIS Major category: Combined immunodeficiencies with associated or syndromic features. IUIS Subcategory: Other Combined immunodeficiencies with associated or syndromic features
Created: 2 Jul 2018, 10:35 a.m.
This gene was present in the original PanelApp PID panel dataset (review in April 2018) rated as Red. The gene is present in the external expert immunodeficiency diagnostic gene list(s) GOSH or GRID. In this combined PID panel, this gene has been rated as AMBER and needs further curational review to assess pertinence prior to v1.
Created: 19 Apr 2018, 2:07 p.m.
Original metadata downloaded from ESID Registry. ESID_Gene_original: STAT5b, PanelApp HGNC gene symbol check: STAT5B, ESID classification: Main_category/ Sub_category/ PID_Diagnosis Combined immunodeficiencies / Combined immunodeficiency (CID) / Combined immunodeficiency
Created: 17 Apr 2018, 12:29 p.m.
Original metadata supplied by GRID. GRID Gene Symbol HGNC PanelApp check: STAT5B, GRID_Gene_Symbol: STAT5B, GRID_Transcript_ENS_Community submitted: ENST00000293328, GRID_Transcript_RefSeq: NM_012448.3, GRID_Transcript_ENS_used_on_Production: ENST00000293328
Created: 17 Apr 2018, 12:12 p.m.

Peter Arkwright (Royal Manchester Foundation Trust)

Red List (low evidence)

Kimberly Gilmour (Great Ormond Street Hopsital)

Green List (high evidence)

agree with green gene
Created: 17 Sep 2019, 3:18 p.m. | Last Modified: 17 Sep 2019, 3:18 p.m.
Panel Version: 1.94
agree, CID with growth problems
Created: 20 Oct 2015, 1:44 p.m.

Sophie Hambleton (Newcastle University)

Red List (low evidence)

Not linked to SCID
Created: 19 Oct 2015, 7:52 p.m.

Details

Mode of Inheritance
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • IUIS Classification December 2029
Phenotypes
  • Combined immunodeficiency
  • T-B+ SCID
  • Growth-hormone insensitive dwarfism, dysmorphic features, eczema, lymphocytic interstitial pneumonitis, autoimmunity
  • Growth hormone insensitivity with immunodeficiency 245590
  • Combined immunodeficiencies with associated or syndromic features
OMIM
604260
Clinvar variants
Variants in STAT5B
Penetrance
None
Publications
Panels with this gene

History Filter Activity

15 Apr 2020, Gel status: 3

Added New Source, Set mode of inheritance

Ivone Leong (Genomics England Curator)

Source IUIS Classification December 2029 was added to STAT5B. Mode of inheritance for gene STAT5B was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal

1 Apr 2020, Gel status: 3

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

Ellen McDonagh (Genomics England Curator)

gene: STAT5B was added gene: STAT5B was added to Viral susceptibility. Sources: Expert Review Green,ESID Registry 20171117,North West GLH,Victorian Clinical Genetics Services,GRID V2.0,NHS GMS,GOSH PID v.8.0,London North GLH,SCID v1.6,IUIS Classification February 2018 Mode of inheritance for gene: STAT5B was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: STAT5B were set to 13679528; 20538865; 16787985; 17030597; 26703237; 15827093; 17389811; 16920911 Phenotypes for gene: STAT5B were set to Combined immunodeficiency; T-B+ SCID; Growth-hormone insensitive dwarfism, dysmorphic features, eczema, lymphocytic interstitial pneumonitis, autoimmunity; Growth hormone insensitivity with immunodeficiency 245590; Combined immunodeficiencies with associated or syndromic features