AN3
MCID: ANR046
MIFTS: 18

Aniridia 3 (AN3)

Categories: Eye diseases, Genetic diseases, Nephrological diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Aniridia 3

MalaCards integrated aliases for Aniridia 3:

Name: Aniridia 3 57 72 29 6
An3 57 72
Aniridia, Type 3 39

Characteristics:

OMIM®:

57 (Updated 05-Apr-2021)
Inheritance:
autosomal dominant

Miscellaneous:
progressive decreased visual acuity due to gradual development of cataract caused by exposure to sun
based on report of one 4-generation chinese family (last curated october 2016)


HPO:

31
aniridia 3:
Inheritance autosomal dominant inheritance


Classifications:



External Ids:

OMIM® 57 617142
OMIM Phenotypic Series 57 PS106210
MeSH 44 D015783

Summaries for Aniridia 3

UniProtKB/Swiss-Prot : 72 Aniridia 3: A form of aniridia, a congenital, bilateral, panocular disorder characterized by complete absence of the iris or extreme iris hypoplasia. Aniridia is not just an isolated defect in iris development but it is associated with macular and optic nerve hypoplasia, cataract, corneal changes, nystagmus. Visual acuity is generally low but is unrelated to the degree of iris hypoplasia. Glaucoma is a secondary problem causing additional visual loss over time.

MalaCards based summary : Aniridia 3, also known as an3, is related to endometrial adenocarcinoma. An important gene associated with Aniridia 3 is TRIM44 (Tripartite Motif Containing 44). Related phenotypes are glaucoma and cataract

More information from OMIM: 617142 PS106210

Related Diseases for Aniridia 3

Diseases in the Aniridia 1 family:

Aniridia 2 Aniridia 3
Pax6-Related Aniridia

Diseases related to Aniridia 3 via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 1, show less)
# Related Disease Score Top Affiliating Genes
1 endometrial adenocarcinoma 10.0

Symptoms & Phenotypes for Aniridia 3

Human phenotypes related to Aniridia 3:

31 (showing 3, show less)
# Description HPO Frequency HPO Source Accession
1 glaucoma 31 occasional (7.5%) HP:0000501
2 cataract 31 HP:0000518
3 progressive visual loss 31 HP:0000529

Symptoms via clinical synopsis from OMIM®:

57 (Updated 05-Apr-2021)
Head And Neck Eyes:
cataract
glaucoma (in some patients)
decreased visual acuity, progressive
bilateral defects of the iris

Clinical features from OMIM®:

617142 (Updated 05-Apr-2021)

Drugs & Therapeutics for Aniridia 3

Search Clinical Trials , NIH Clinical Center for Aniridia 3

Genetic Tests for Aniridia 3

Genetic tests related to Aniridia 3:

# Genetic test Affiliating Genes
1 Aniridia 3 29 TRIM44

Anatomical Context for Aniridia 3

Publications for Aniridia 3

Articles related to Aniridia 3:

(showing 4, show less)
# Title Authors PMID Year
1
Variants in TRIM44 Cause Aniridia by Impairing PAX6 Expression. 6 57
26394807 2015
2
Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie Syndrome. 61
27124303 2016
3
Ex vivo expansion and transplantation of limbal epithelial stem cells. 61
18554721 2008
4
Amniotic membrane transplantation with or without limbal allografts for corneal surface reconstruction in patients with limbal stem cell deficiency. 61
9565039 1998

Variations for Aniridia 3

ClinVar genetic disease variations for Aniridia 3:

6 (showing 1, show less)
# Gene Name Type Significance ClinVarId dbSNP ID Position
1 TRIM44 NM_017583.6(TRIM44):c.463G>A (p.Gly155Arg) SNV Pathogenic 264710 rs886039241 GRCh37: 11:35685122-35685122
GRCh38: 11:35663574-35663574

UniProtKB/Swiss-Prot genetic disease variations for Aniridia 3:

72 (showing 1, show less)
# Symbol AA change Variation ID SNP ID
1 TRIM44 p.Gly155Arg VAR_077853 rs886039241

Expression for Aniridia 3

Search GEO for disease gene expression data for Aniridia 3.

Pathways for Aniridia 3

GO Terms for Aniridia 3

Sources for Aniridia 3

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 05-Apr-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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