1. Gene
  2. DDI1 - DNA damage inducible 1 homolog 1 Gene

DDI1 - DNA damage inducible 1 homolog 1 Gene

Homo sapiens
Gene ID: 414301 | Gene type: protein coding

About DDI1

This gene has 1 transcript (splice variant), 188 orthologues and 4 paralogues.

Summary

Predicted to enable aspartic-type endopeptidase activity. Involved in several processes, including cellular response to hydroxyurea; proteasomal protein catabolic process; and regulation of DNA stability. [provided by Alliance of Genome Resources, Apr 2022]

DDI1 Products(1)

mRNA Protein Name
NM_001001711.3 NP_001001711.1 protein DDI1 homolog 1
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
21516116 GOA
Biological Process GO Annotation Evidence Reference Source
involved in cellular response to hydroxyurea IMP
IMP: Inferred from mutant phenotype
29290612 GOA
involved in proteasomal protein catabolic process IMP
IMP: Inferred from mutant phenotype
29290612 GOA
involved in regulation of DNA stability IMP
IMP: Inferred from mutant phenotype
29290612 GOA
involved in regulation of protein stability IMP
IMP: Inferred from mutant phenotype
29290612 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

DDI1 Protein Structure

ubiquitin

ubiquitin: Ubiquitin family (13 - 77)

Asp_protease

Asp_protease: Aspartyl protease (220 - 343)

  • 0
  • 100
  • 200
  • 300
  • 396 a.a.
Protein Preferred Names Protein Names

protein DDI1 homolog 1

DDI1, DNA-damage inducible 1, homolog 1

DDI1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
DDI1 Q8WTU0 RPP25 Homo sapiens Q9BUL9
Validated Y2H
32296183
Intra
DDI1 Q8WTU0 UBE2K Homo sapiens P61086
Y2H Prey Pooling
25416956
Intra
DDI1 Q8WTU0 UBE2K Homo sapiens P61086
Y2H Array
25416956
Intra
DDI1 Q8WTU0 CYGB Homo sapiens Q8WWM9
Validated Y2H
32296183
Intra
DDI1 Q8WTU0 FAM161B Homo sapiens Q96MY7
Validated Y2H
32296183
Intra
DDI1 Q8WTU0 KLHL42 Homo sapiens Q9P2K6
Validated Y2H
32296183
Intra
DDI1 Q8WTU0 KLHL42 Homo sapiens Q9P2K6
Y2H Array
25416956
Intra
DDI1 Q8WTU0 CCL28 Homo sapiens Q9NRJ3
Validated Y2H
25416956
Intra
DDI1 Q8WTU0 CCL28 Homo sapiens Q9NRJ3
Y2H Array
25416956
Intra
DDI1 Q8WTU0 CCL28 Homo sapiens Q9NRJ3
Y2H Prey Pooling
25416956
Intra
DDI1 Q8WTU0 CCL28 Homo sapiens Q9NRJ3
Validated Y2H
32296183
Intra
DDI1 Q8WTU0 TEKT3 Homo sapiens Q9BXF9
Validated Y2H
32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Ruijs-Aalfs Syndrome

Progeroid Features-Hepatocellular Carcinoma Predisposition Syndrome

RJALS

Ngly1-Deficiency

Deficiency Of N-Glycanase 1

Ngly1-Cddg

Alacrimia-Choreoathetosis-Liver Dysfunction Syndrome

Ngly1 Deficiency

Congenital Disorder Of Deglycosylation

Congenital Disorder Of Glycosylation Type Iv

Congenital Disorder Of Deglycosylation

Cddg

Congenital Disorder Of Glycosylation Type Iv

Cdg1v

Kenny-Caffey Syndrome, Type 2

KCS2

Kenny-Caffey Syndrome Type 2

Autosomal Dominant Kenny-Caffey Syndrome

Kenny Syndrome

Dwarfism, Cortical Thickening Of Tubular Bones, And Transient Hypocalcemia

Dwarfism, Cortical Thickening Of Tubular Bones And Transient Hypocalcemia

Kenny-Caffey Syndrome, Autosomal Dominant

Kenny-Caffey Syndrome 2

Dwarfism With Cortical Thickening Of Tubular Bones And Transient Hypocalcemia

Kenny-Caffey Syndrome

Angelman Syndrome

AS

Happy Puppet Syndrome

Happy Puppet Syndrome, Formerly

Puppetlike Syndrome

Median Arcuate Ligament Syndrome

Celiac Artery Compression Syndrome

Dunbar Syndrome

Mals

Harjola-Marable Syndrome

Marable'S Syndrome

Celiac Axis Syndrome

Childhood Germ Cell Cancer

Pediatric Germ Cell Tumor

Paediatric Germ Cell Cancer

Paediatric Germ Cell Neoplasm

Pediatric Germ Cell Cancer

Pediatric Germ Cell Neoplasm

Kenny-Caffey Syndrome

Kenny Syndrome

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus DDI1 VGNC VGNC:27945
Mus musculus DDI1 MGD MGI:1919079
Rattus norvegicus DDI1 RGD RGD:1559430
Canis familiaris DDI1 VGNC VGNC:39834
Felis catus DDI1 VGNC VGNC:105842
Macaca mulatta DDI1 VGNC VGNC:100923