Evidence map›Paper›PMID 33603160›Full record

ArticleEuropean journal of human genetics : EJHG2021

Further delineation of BCAP31-linked intellectual disability: description of 17 new families with LoF and missense variants.

Sandra Whalen, Marie Shaw, Cyril Mignot, Delphine Héron, Sandra Chantot Bastaraud, Cecile Cieuta Walti, Jan Liebelt, Frances Elmslie, Patrick Yap, Jane Hurst and 30 more

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in European journal of human genetics : EJHG, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Expanding the Spectrum ofNeurology. Genetics · 2026
    Article
  4. Article
  5. An X-Linked Ataxia Syndrome in a Family with Hearing Loss Associated with a Novel Variant in the BCAP31 Gene.Movement disorders : official journal of the Movement Disorder Society · 2025
    Article
  6. Whole exome sequencing reveals a dual diagnosis ofMolecular genetics and metabolism reports · 2024
    Article
  7. Review
  8. Case Report: The first Korean familial case ofFrontiers in pediatrics · 2024
    Article
  9. Article
  10. Complex Diagnostics of Non-Specific Intellectual Developmental Disorder.International journal of molecular sciences · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

40 authors at 20 institutions in 9 countries.

Sandra WhalenUF de Génétique Clinique et Centre de Reference Anomalies du Développement et Syndromes Malformatifs, APHP, Sorbonne Université, Hôpital Trousseau, Paris, France. Sandra.whalen@aphp.fr.ORCID 0000-0001-9156-5047
Marie ShawAdelaide Medical School and Robinson Research Institute, The University of Adelaide, Adelaide, SA, 5005, Australia.
Cyril MignotDépartement de Génétique et de Cytogénétique et Centre de Référence Déficiences Intellectuelles de Causes Rares, APHP, Sorbonne Université, Paris, France.
Delphine HéronDépartement de Génétique et de Cytogénétique et Centre de Référence Déficiences Intellectuelles de Causes Rares, APHP, Sorbonne Université, Paris, France.
Sandra Chantot BastaraudDépartement de Génétique, UF de Génétique Chromosomique, APHP, Hôpital Armand Trousseau, Paris, France.
Cecile Cieuta WaltiInstitut Jérôme Lejeune, Paris, France.
Jan LiebeltSouth Australian Clinical Genetics Service, Women's and Children's Hospital, Adelaide, SA, Australia.
Frances ElmslieSouth West Thames Regional Genetics Service, St George's University Hospitals, London, UK.ORCID 0000-0002-2508-9107
Patrick YapGenetic Health Service New Zealand (Northern Hub), Auckland, New Zealand.
Jane HurstDepartment of Clinical Genetics, Great Ormond Street Hospital For Children NHS Foundation Trust, London, UK.
Elisabeth ForsytheDepartment of Clinical Genetics, Great Ormond Street Hospital For Children NHS Foundation Trust, London, UK.
Brian KirmseDivision of Medical Genetics, Department of Pediatrics, University of Mississippi Medical Center, Jackson, MS, USA.
Jillian OzmoreMedical Genetics, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
Alessandro Mauro SpinelliMedical Genetics Unit, University of Modena and Reggio Emilia, Modena, Italy.ORCID 0000-0003-1902-8209
Olga CalabreseMedical Genetics Unit, University of Modena and Reggio Emilia, Modena, Italy.
Thierry Billette de VillemeurSorbonne Université, Service de Neuropédiatrie, Hôpital Trousseau, APHP, SU, Inserm, Paris, France.
Anne Claude TabetUF de Cytogénétique, Département de Génétique, APHP, Hôpital Robert Debré, Paris, France.
Jonathan LevyUF de Cytogénétique, Département de Génétique, APHP, Hôpital Robert Debré, Paris, France.
Agnes GuetService de Néonatologie et Pédiatrie, APHP, Hôpital Louis-Mourier, Colombes, France.
Manoëlle KossorotoffDépartement de Neurologie Pédiatrique, AP-HP, Hôpital Necker-Enfants-Malades, Paris, France.ORCID 0000-0002-0813-9045
Benjamin KamienGenetic Services of Western Australia, King Edward Memorial Hospital, Subiaco, WA, Australia.
Jenny MortonWest Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Birmingham Women's and Children's Hospitals NHS Foundation Trust, Birmingham, UK.
Anne McCabeWest Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Birmingham Women's and Children's Hospitals NHS Foundation Trust, Birmingham, UK.
Elise Brischoux-BoucherCentre de Génétique Humaine, Université de Franche-Comté, Besançon, France.ORCID 0000-0002-4816-1431
Annick Raas-RothschildInstitute for Rare Diseases, Edmond and Lily Safra Children Hospital, Sheba Medical Center, Ramat Gan, Israel.
Antonella PiniChild Neurology and Psychiatry Unit, IRCCS Istituto delle Scienze Neurologiche, Bologna, Italy.
Renée CarrollAdelaide Medical School and Robinson Research Institute, The University of Adelaide, Adelaide, SA, 5005, Australia.
Jessica N HartleyBiochemistry & Medical Genetics, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.ORCID 0000-0002-4221-8820
Care4Rare Canada Consortium
Patrick FroskBiochemistry & Medical Genetics, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.ORCID 0000-0002-9673-795X
Anne SlavotinekMedical Genetics, Benioff Children's Hospital Oakland, Division of Genetics, Department of Pediatrics, University of California, UCSF Benioff Children's Hospital, San Francisco, CA, USA.
Kristen TruxalDivision of Genetic and Genomic Medicine, Nationwide Children's Hospital and Research Institute, The Ohio State University, Columbus, OH, USA.
Carroll JenniferDivision of Genetic and Genomic Medicine, Nationwide Children's Hospital and Research Institute, The Ohio State University, Columbus, OH, USA.ORCID 0000-0002-1087-8664
Annelies DheedeneCenter for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
Hong CuiGeneDx, Gaithersburg, MD, USA.
Vishal KumarDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, CA, USA.
Glen ThomsonDepartment of Paediatric Radiology, Starship Children's Hospital, Auckland, New Zealand.
Florence RiccardiDépartement de génétique médicale, AP-HM, Hôpital d'enfants La Timone, Marseille, France.
Jozef Gecz *Adelaide Medical School and Robinson Research Institute, The University of Adelaide, Adelaide, SA, 5005, Australia.ORCID 0000-0002-7884-6861
Laurent Villard *Département de génétique médicale, AP-HM, Hôpital d'enfants La Timone, Marseille, France.ORCID 0000-0001-6657-5008
University of Calgary · CAUniversity of Toronto · CASorbonne Université · FRInserm · FRUniversity of British Columbia · CAAssistance Publique – Hôpitaux de Paris · FRBirmingham Women’s and Children’s NHS Foundation Trust · GBGreat Ormond Street Hospital for Children NHS Foundation Trust · GBNationwide Children's Hospital · USThe University of Adelaide · AUUniversity of Manitoba · CAUniversity of Modena and Reggio Emilia · ITUniversity of Ottawa · CAAgricultural Research Institute of Ontario · CADartmouth–Hitchcock Medical Center · USGhent University Hospital · BEHôpital Louis-Mourier · FRHôpital Necker-Enfants Malades · FRIstituto delle Scienze Neurologiche di Bologna · ITKing Edward Memorial Hospital · AU

Funding

Sharing Aggregate Genomics Research Findings with Diverse Participants: A Pilot Study of an Innovative Design StrategyU01HG009599 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KOENIG, BARBARA A., KWOK, PUI-YAN · 2017 to 2021
$16.3M
NHGRI NIH HHS U01 HG009599
6 · The paper itself

Abstract

The BCAP31 gene, located at Xq28, encodes BAP31, which plays a role in ER-to-Golgi anterograde transport. To date, BCAP31 pathogenic variants have been reported in 12 male cases from seven families (six loss of function (LoF) and one missense). Patients had severe intellectual disability (ID), dystonia, deafness, and central hypomyelination, delineating a so-called deafness, dystonia and cerebral hypomyelination syndrome (DDCH). Female carriers are mostly asymptomatic but may present with deafness. BCAP31 is flanked by the SLC6A8 and ABCD1 genes. Contiguous deletions of BCAP31 and ABCD1 and/or SLC6A8 have been described in 12 patients. Patients with deletions including BCAP31 and SLC6A8 have the same phenotype as BCAP31 patients. Patients with deletions of BCAP31 and ABCD1 have contiguous ABCD1 and DXS1375E/BCAP31 deletion syndrome (CADDS), and demonstrate a more severe neurological phenotype with cholestatic liver disease and early death. We report 17 novel families, 14 with intragenic BCAP31 variants (LoF and missense) and three with a deletion of BCAP31 and adjacent genes (comprising two CADDS patients, one male and one symptomatic female). Our study confirms the phenotype reported in males with intragenic LoF variants and shows that males with missense variants exhibit a milder phenotype. Most patients with a LoF pathogenic BCAP31 variant have permanent or transient liver enzyme elevation. We further demonstrate that carrier females (n = 10) may have a phenotype comprising LD, ID, and/or deafness. The male with CADDS had a severe neurological phenotype, but no cholestatic liver disease, and the symptomatic female had moderate ID and cholestatic liver disease.

Indexed as

Loss of Function MutationPhenotypeAdolescentAdultChildChild, PreschoolDeafnessFemaleHereditary Central Nervous System Demyelinating DiseasesHumansIntellectual DisabilityMaleMembrane ProteinsMutation, MissensePedigreeSyndromeBCAP31 protein, humanMembrane Proteins

Identifiers

PMID33603160
PMCPMC8440520
OpenAlexW3130280597

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.