Evidence map›Paper›PMID 38688916›Full record

ArticleScientific data2024

Mannose-binding lectin gene sequence data in Kelantan population.

Muhamad Aidil Zahidin, Noor Haslina Mohd Noor, Muhammad Farid Johan, Abu Dzarr Abdullah, Zefarina Zulkafli, Hisham Atan Edinur

Erratum issuedOpen access · goldAbstract readDataset
PubMed Full text at PMC Publisher
In one paragraph

Article in Scientific data, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 92% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Muhamad Aidil ZahidinDepartment of Haematology, School of Medical Sciences, Universiti Sains Malaysia (Health Campus), 16150, Kubang Kerian, Kelantan, Malaysia.ORCID 0000-0003-0098-6781
Noor Haslina Mohd NoorDepartment of Haematology, School of Medical Sciences, Universiti Sains Malaysia (Health Campus), 16150, Kubang Kerian, Kelantan, Malaysia. drhaslina@usm.my.
Muhammad Farid JohanDepartment of Haematology, School of Medical Sciences, Universiti Sains Malaysia (Health Campus), 16150, Kubang Kerian, Kelantan, Malaysia.
Abu Dzarr AbdullahDepartment of Internal Medicine, School of Medical Sciences, Universiti Sains Malaysia (Health Campus), 16150, Kubang Kerian, Kelantan, Malaysia.
Zefarina ZulkafliDepartment of Haematology, School of Medical Sciences, Universiti Sains Malaysia (Health Campus), 16150, Kubang Kerian, Kelantan, Malaysia.
Hisham Atan EdinurForensic Science Programme, School of Health Sciences, Universiti Sains Malaysia (Health Campus), 16150, Kubang Kerian, Kelantan, Malaysia.
Universiti Sains Malaysia · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human mannose-binding lectin (MBL) gene encodes a polymorphic protein that plays a crucial role in the innate immune response. Human MBL deficiency is associated with immunodeficiencies, and its variants have been linked to autoimmune and infectious diseases. Despite this significance, gene studies concerning MBL sequencing are uncommon in Malaysia. Therefore, we aimed to preliminary described the human MBL sequencing dataset based on the Kelantan population. Blood samples were collected from 30 unrelated individuals and underwent DNA extraction, genotyping, and sequencing. The sequencing data generated 886 bp, which were deposited in GenBank (ON619541-ON619546). Allelic variants were identified and translated into six MBL haplotypes: HYPA, HYPB, LYPB, LXPB, HXPA, and LXPA. An evolutionary tree was constructed using the haplotype sequences. These findings contribute to the expansion of MBL information within the country, providing a valuable baseline for future research exploring the association between the gene and targeted diseases.

Indexed as

Mannose-Binding LectinAllelesBase SequenceHaplotypesHumansMalaysiaMannose-Binding Lectin

Identifiers

PMID38688916
PMCPMC11061297
OpenAlexW4396558346

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.