SRP54, signal recognition particle 54, 6729

N. diseases: 96; N. variants: 4
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0272170
Disease: Shwachman syndrome
Shwachman syndrome
0.510 Biomarker disease BEFREE Interestingly, SBDS, DNAJC21, EFL1 and SRP54 are involved in ribosome biogenesis: SBDS, through direct interaction with EFL1, promotes the release of the eukaryotic initiation factor 6 (eIF6) during ribosome maturation, DNAJC21 stabilizes the 80S ribosome, and SRP54 facilitates protein trafficking. 30413969 2019
CUI: C0272170
Disease: Shwachman syndrome
Shwachman syndrome
0.510 GermlineCausalMutation disease ORPHANET Using trio whole-exome sequencing (WES) in an sbds-negative SDS family and candidate gene sequencing in additional SBDS-negative SDS cases or molecularly undiagnosed IBMFS cases, we identified 3 independent patients, each of whom carried a de novo missense variant in srp54 (encoding signal recognition particle 54 kDa). 28972538 2017
CUI: C0272170
Disease: Shwachman syndrome
Shwachman syndrome
0.510 Biomarker disease CTD_human
Neutropenia, Severe Congenital, Autosomal Dominant 1
0.300 GermlineCausalMutation disease ORPHANET Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond-like syndrome. 29914977 2018
CUI: C0027947
Disease: Neutropenia
Neutropenia
0.110 GeneticVariation disease BEFREE In conclusion, autosomal dominant mutations in SRP54, a key member of the cotranslation protein-targeting pathway, lead to syndromic neutropenia with a Shwachman-Diamond-like phenotype. 28972538 2017
CUI: C0027947
Disease: Neutropenia
Neutropenia
0.110 Biomarker disease HPO
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
CUI: C4692625
Disease: SHWACHMAN-DIAMOND SYNDROME 1
SHWACHMAN-DIAMOND SYNDROME 1
0.100 CausalMutation disease CLINVAR Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features. 28972538 2017
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
0.100 Biomarker phenotype HPO
CUI: C0002871
Disease: Anemia
Anemia
0.100 Biomarker disease HPO
CUI: C0002874
Disease: Aplastic Anemia
Aplastic Anemia
0.100 Biomarker disease HPO
CUI: C0007642
Disease: Cellulitis
Cellulitis
0.100 Biomarker phenotype HPO
CUI: C0011334
Disease: Dental caries
Dental caries
0.100 Biomarker disease HPO
Diabetes Mellitus, Insulin-Dependent
0.100 Biomarker disease HPO
CUI: C0011991
Disease: Diarrhea
Diarrhea
0.100 Biomarker phenotype HPO
CUI: C0013336
Disease: Dwarfism
Dwarfism
0.100 Biomarker disease HPO
CUI: C0013595
Disease: Eczema
Eczema
0.100 Biomarker disease HPO
CUI: C0014457
Disease: Eosinophilia
Eosinophilia
0.100 Biomarker disease HPO
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
0.100 Biomarker disease HPO
CUI: C0015967
Disease: Fever
Fever
0.100 Biomarker phenotype HPO
CUI: C0017574
Disease: Gingivitis
Gingivitis
0.100 Biomarker disease HPO
CUI: C0018916
Disease: Hemangioma
Hemangioma
0.100 Biomarker disease HPO
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly
0.100 Biomarker phenotype HPO
CUI: C0020757
Disease: Ichthyoses
Ichthyoses
0.100 Biomarker disease HPO
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.100 Biomarker disease HPO