Genopathy
Gene-Disorder Association · Article
Gene
SLC19A2
Solute Carrier Family 19 Member 2
Disorder
Diabetes Mellitus
First reported 1999
Supporting publications 6
Key publication · gene–disorder Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness.Nature genetics · 1999
Key publication · disorder Studies on experimental diabetes mellitus, as produced by organic reagents; oxine diabetes and dithizone diabetes.The Journal of laboratory and clinical medicine · 1950
Manually curated
Association Review

In brief

The association between SLC19A2 (Solute Carrier Family 19 Member 2) and Diabetes Mellitus is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 3
Compounds 0
Trials 0
Publications 6
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Request access
02
Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

Request access
03
SLC19A2

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

Request access
04
Diabetes Mellitus

The disorder

8 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Request access
05
Literature

Reading

6 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

Request access
06
Provenance

References & sources

9 references

Every source and publication cited across this dossier, as one numbered reference list.

Request access