Evidence map›Paper›PMID 30622326›Full record

ArticleEuropean journal of human genetics : EJHG2019

Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomalies.

Max Krall, Stephanie Htun, Rhonda E Schnur, Alice S Brooks, Laura Baker, Alejandra de Alba Campomanes, Ryan E Lamont, Karen W Gripp, Care 4 Rare Canada Consortium, Dina Schneidman-Duhovny and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Novel BiallelicGenes · 2025
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Generation ofDevelopment & reproduction · 2023
    Article
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  17. Review
  18. Review
  19. Article
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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

13 authors at 4 institutions in 4 countries.

Max KrallDept. Pediatrics, Division of Genetics, University of California, San Francisco, San Francisco, CA, 94143-2711, USA.
Stephanie HtunDept. Pediatrics, Division of Genetics, University of California, San Francisco, San Francisco, CA, 94143-2711, USA.
Rhonda E SchnurGeneDx, Gaithersburg, MD, 20877, USA.
Alice S BrooksDepartment of Clinical Genetics, ErasmusMC University Medical Center, 3015CN, Rotterdam, The Netherlands.
Laura BakerDivision of Medical Genetics, A.I. du Pont Hospital for Children/Nemours, Wilmington, DE, 19803, USA.
Alejandra de Alba CampomanesDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA, 94143, USA.
Ryan E LamontDepartment of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, Canada.
Karen W GrippDivision of Medical Genetics, A.I. du Pont Hospital for Children/Nemours, Wilmington, DE, 19803, USA.
Care 4 Rare Canada Consortium
Dina Schneidman-DuhovnySchool of Computer Science and Engineering, The Hebrew University of Jerusalem, Jerusalem, Israel.
A Micheil InnesDepartment of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, Canada.ORCID http://orcid.org/0000-0001-9881-5467
Grazia M S ManciniDepartment of Clinical Genetics, ErasmusMC University Medical Center, 3015CN, Rotterdam, The Netherlands.
Anne M SlavotinekDept. Pediatrics, Division of Genetics, University of California, San Francisco, San Francisco, CA, 94143-2711, USA. anne.slavotinek@ucsf.edu.
University of California, San Francisco · USErasmus MC · NLUniversity of Calgary · CAHebrew University of Jerusalem · IL

Funding

Gene Discovery in Human Anopthalmia/MicropthalmiaR21EY022779 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SLAVOTINEK, ANNE M. · 2012 to 2013
$421k
NEI NIH HHS R21 EY022779
6 · The paper itself

Abstract

The Integrator complex subunit 1 (INTS1) is a component of the integrator complex that comprises 14 subunits and associates with RPB1 to catalyze endonucleolytic cleavage of nascent snRNAs and assist RNA polymerase II in promoter-proximal pause-release on protein-coding genes. We present five patients, including two sib pairs, with biallelic sequence variants in INTS1. The patients manifested absent or severely limited speech, an abnormal gait, hypotonia and cataracts. Exome sequencing revealed biallelic variants in INTS1 in all patients. One sib pair demonstrated a missense variant, p.(Arg77Cys), and a frameshift variant, p.(Arg1800Profs*20), another sib pair had a homozygous missense variant, p.(Pro1874Leu), and the fifth patient had a frameshift variant, p.(Leu1764Cysfs*16) and a missense variant, p.(Leu2164Pro). We also report additional clinical data on three previously described individuals with a homozygous, loss of function variant, p.(Ser1784*) in INTS1 that shared cognitive delays, cataracts and dysmorphic features with these patients. Several of the variants affected the protein C-terminus and preliminary modeling showed that the p.(Pro1874Leu) and p.(Leu2164Pro) variants may interfere with INTS1 helix folding. In view of the cataracts observed, we performed in-situ hybridization and demonstrated expression of ints1 in the zebrafish eye. We used Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/Cas9 to make larvae with biallelic insertion/deletion (indel) variants in ints1. The mutant larvae developed typically through gastrulation, but sections of the eye showed abnormal lens development. The distinctive phenotype associated with biallelic variants in INTS1 points to dysfunction of the integrator complex as a mechanism for intellectual disability, eye defects and craniofacial anomalies.

Indexed as

AdolescentAdultAnimalsCataractChildChild, PreschoolCraniofacial AbnormalitiesDevelopmental DisabilitiesExome SequencingFemaleFrameshift MutationGastrulationHumansInfantLens, CrystallineMaleWnt1 ProteinWNT1 protein, human

Identifiers

PMID30622326
PMCPMC6460580
OpenAlexW2908647573

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.