YRDC - yrdC N6-threonylcarbamoyltransferase domain containing Gene

Also Known as IRIP; SUA5; DRIP3; GAMOS10

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 79693

About YRDC

Cytogenetic location: 1p34.3 Genomic coordinates (GRCh38): 1:37,802,945-37,808,208 (from NCBI)

This gene has 1 transcript (splice variant), 205 orthologues and is associated with 2 phenotypes. Ubiquitous expression in bone marrow (RPKM 17.4), testis (RPKM 11.7) and 25 other tissues.

Summary

Predicted to enable nucleotidyltransferase activity and tRNA binding activity. Acts upstream of or within negative regulation of transport. Predicted to be located in membrane and mitochondrion. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

YRDC Products (1)

mRNA Protein Name
NM_024640.4 NP_078916.3 threonylcarbamoyl-AMP synthase precursor

YRDC Protein Structure

Sua5_yciO_yrdC

Sua5_yciO_yrdC: Telomere recombination (77 - 255)

  • 0
  • 100
  • 200
  • 279 a.a.
Protein Preferred Names Protein Names

threonylcarbamoyl-AMP synthase

  • dopamine receptor interacting protein 3

Related Diseases

Diseases Alias
Galloway-Mowat Syndrome 10

  • GAMOS10
Galloway-Mowat Syndrome

  • Galloway Mowat Syndrome

  • Galloway Syndrome

  • Hiatal Hernia-Microcephaly-Nephrosis, Galloway Type

  • Microcephaly Nephrosis Syndrome

  • Microcephaly, Hiatal Hernia, And Nephrotic Syndrome

  • Nephrosis Neuronal Dysmigration Syndrome

  • Microcephaly-Hiatus Hernia-Nephrotic Syndrome

  • Nephrosis-Neuronal Dysmigration Syndrome
Ischemia

  • Acute Coronary Syndrome
Congenital Hypothyroidism

  • Cretinism

  • Neonatal Hypothyroidism

  • Ch

  • Cht

  • Congenital Myxedema

  • Myxedema, Congenital

  • Endemic Cretinism

  • Congenital Iodine-Deficiency Syndrome

  • Fetal Iodine Deficiency Syndrome

  • Congenital Iodine-Deficiency Hypothyroidism Nos
Refractory Hairy Cell Leukemia
Polymicrogyria

  • Pmg
Microcephaly

  • Microencephaly

  • Microcephalus

  • Microcephalic

  • Nanocephaly

  • Congenital Microcephaly

  • Brain Hypoplasia

  • Brain Nondevelopment

  • Cephalic Hypoplasia

  • Undeveloped Cerebrum

  • Undeveloped Brain

  • Micrencephalon

  • Micrencephaly
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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (2)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-Q66655 YRDC-IN-1 / Unkown
HY-RS15934 YRDC Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Canis familiaris YRDC VGNC VGNC:48502
Rattus norvegicus YRDC RGD RGD:708492
Mus musculus YRDC MGD MGI:2387201
Macaca mulatta YRDC VGNC VGNC:79751
Bos taurus YRDC VGNC VGNC:37038
Felis catus YRDC VGNC VGNC:80406
Others YRDC NCBI