1. Gene
  2. YRDC - yrdC N6-threonylcarbamoyltransferase domain containing Gene

YRDC - yrdC N6-threonylcarbamoyltransferase domain containing Gene

Homo sapiens

Also known as IRIP; SUA5; DRIP3; GAMOS10

Gene ID: 79693 | Gene type: protein coding

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

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