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

DDI1 - DNA damage inducible 1 homolog 1 Gene

中文名称:DNA 损伤诱导 1 同系物 1

种属: Homo sapiens

基因 ID: 414301 | 基因类型: protein coding

关于 DDI1

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

功能概要

预测启用天冬氨酸型内肽酶活性。参与多个过程,包括细胞对羟基脲的反应;蛋白酶体蛋白质分解代谢过程;和 DNA 稳定性的调节。 [由基因组资源联盟提供,2022 年 4 月]

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 基因产物(1)

mRNA Protein Name
NM_001001711.3 NP_001001711.1 protein DDI1 homolog 1

DDI1 蛋白结构

ubiquitin

ubiquitin: Ubiquitin family (13 - 77)

Asp_protease

Asp_protease: Aspartyl protease (220 - 343)

  • 0
  • 100
  • 200
  • 300
  • 396 a.a.
蛋白主名 其他名称

protein DDI1 homolog 1

DDI1, DNA-damage inducible 1, homolog 1

关联疾病

疾病名称 别名
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

疾病名称 别名
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

直系同源

种属 基因名 来源 基因 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