WDR45 (WD repeat domain 45)

2014-11-01  

Identity

HGNC
LOCATION
Xp11.23
LOCUSID
ALIAS
JM5,NBIA4,NBIA5,WDRX1,WIPI-4,WIPI4

Other Information

Locus ID:

NCBI: 11152
MIM: 300526
HGNC: 28912
Ensembl: ENSG00000196998

Variants:

dbSNP: 11152
ClinVar: 11152
TCGA: ENSG00000196998
COSMIC: WDR45

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000196998ENST00000322995Q9Y484
ENSG00000196998ENST00000322995A0A024QYW6
ENSG00000196998ENST00000356463Q9Y484
ENSG00000196998ENST00000367375H0Y329
ENSG00000196998ENST00000376368Q9Y484
ENSG00000196998ENST00000376372Q9Y484
ENSG00000196998ENST00000376372A0A024QYX1
ENSG00000196998ENST00000396681G8JLI5
ENSG00000196998ENST00000419567C9JUS5
ENSG00000196998ENST00000423215C9J7Q8
ENSG00000196998ENST00000465382C9JE01
ENSG00000196998ENST00000471338C9J5L0
ENSG00000196998ENST00000473974C9J471
ENSG00000196998ENST00000474053C9JBX7
ENSG00000196998ENST00000475880C9J0A8
ENSG00000196998ENST00000475977H7C4N7
ENSG00000196998ENST00000476728C9JVT3
ENSG00000196998ENST00000485908C9JYH8
ENSG00000196998ENST00000486337H7C5B4
ENSG00000196998ENST00000634522A0A0U1RR42
ENSG00000196998ENST00000634559A0A0U1RQG6
ENSG00000196998ENST00000634671A0A0U1RQJ7
ENSG00000196998ENST00000634736A0A0U1RRJ9
ENSG00000196998ENST00000634838A0A0U1RR06
ENSG00000196998ENST00000634849A0A0U1RQS7
ENSG00000196998ENST00000634944Q9Y484
ENSG00000196998ENST00000634944A0A024QYX1
ENSG00000196998ENST00000635003A0A0U1RQM7
ENSG00000196998ENST00000635344A0A0U1RRJ2
ENSG00000196998ENST00000635666A0A0U1RQR1
ENSG00000196998ENST00000636049A0A1B0GV56
ENSG00000196998ENST00000636645A0A1Y8EKY4

Expression (GTEx)

0
10
20
30
40
50
60
70
80

Pathways

PathwaySourceExternal ID
Cellular responses to stressREACTOMER-HSA-2262752
MacroautophagyREACTOMER-HSA-1632852

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
369407322023WDR45 mutation dysregulates iron homeostasis by promoting the chaperone-mediated autophagic degradation of ferritin heavy chain in an ER stress/p38 dependent mechanism.1
378197432023Variants in the WDR45 Gene Within the OPA-2 Locus Associate With Isolated X-Linked Optic Atrophy.0
369407322023WDR45 mutation dysregulates iron homeostasis by promoting the chaperone-mediated autophagic degradation of ferritin heavy chain in an ER stress/p38 dependent mechanism.1
378197432023Variants in the WDR45 Gene Within the OPA-2 Locus Associate With Isolated X-Linked Optic Atrophy.0
348181172022Quantitative retrospective natural history modeling of WDR45-related developmental and epileptic encephalopathy - a systematic cross-sectional analysis of 160 published cases.5
348373962022A neurodegeneration gene, WDR45, links impaired ferritinophagy to iron accumulation.12
348181172022Quantitative retrospective natural history modeling of WDR45-related developmental and epileptic encephalopathy - a systematic cross-sectional analysis of 160 published cases.5
348373962022A neurodegeneration gene, WDR45, links impaired ferritinophagy to iron accumulation.12
332517662021Beta-propeller protein-associated neurodegeneration presenting Rett-like features: A case report and literature review.0
343254862021Autophagic defects observed in fibroblasts from a patient with β-propeller protein-associated neurodegeneration.4
347690842021Iron Accumulation and Changes in Cellular Organelles in WDR45 Mutant Fibroblasts.3
332517662021Beta-propeller protein-associated neurodegeneration presenting Rett-like features: A case report and literature review.0
343254862021Autophagic defects observed in fibroblasts from a patient with β-propeller protein-associated neurodegeneration.4
347690842021Iron Accumulation and Changes in Cellular Organelles in WDR45 Mutant Fibroblasts.3
323870082020Phenotypic and Imaging Spectrum Associated With WDR45.11

Citation

Dessen P

WDR45 (WD repeat domain 45)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/75715/css/css/card-gene.css