ATIC - 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase Gene

Also Known as PURH; AICAR; AICARFT; IMPCHASE; HEL-S-70p

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 471

About ATIC

Cytogenetic location: 2q35 Genomic coordinates (GRCh38): 2:215,312,059-215,368,592 (from NCBI)

This gene has 14 transcripts (splice variants), 226 orthologues and is associated with 67 phenotypes. Ubiquitous expression in lymph node (RPKM 19.1), placenta (RPKM 17.9) and 25 other tissues.

Summary

This gene encodes a bifunctional protein that catalyzes the last two steps of the de novo purine biosynthetic pathway. The N-terminal domain has phosphoribosylaminoimidazolecarboxamide formyltransferase activity, and the C-terminal domain has IMP cyclohydrolase activity. A mutation in this gene results in AICA-ribosiduria. [provided by RefSeq, Sep 2009]

ATIC Products (1)

mRNA Protein Name
NM_004044.7 NP_004035.2 bifunctional purine biosynthesis protein ATIC
Molecular Function GO Annotation Evidence References Source
enables IMP cyclohydrolase activity IDA
IDA: Inferred from direct assay
26588576 GOA
enables protein homodimerization activity IPI
IPI: Inferred from physical interaction
14756553 GOA
Biological Process GO Annotation Evidence References Source
involved in 'de novo' AMP biosynthetic process IDA
IDA: Inferred from direct assay
26588576 GOA
involved in 'de novo' IMP biosynthetic process IDA
IDA: Inferred from direct assay
26588576 GOA
involved in 'de novo' XMP biosynthetic process IDA
IDA: Inferred from direct assay
26588576 GOA
involved in GMP biosynthetic process IDA
IDA: Inferred from direct assay
26588576 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

ATIC Protein Structure

MGS

MGS: MGS-like domain (16 - 130)

AICARFT_IMPCHas

AICARFT_IMPCHas: AICARFT/IMPCHase bienzyme (135 - 462)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 592 a.a.
Protein Preferred Names Protein Names

bifunctional purine biosynthesis protein ATIC

  • 5-aminoimidazole-4-carboxamide-1-beta-D-ribonucleotide transformylase/inosinicase

ATIC Antibodies

Cat. No. 상품명 신청 Reactivity
HY-P81327 ATIC Antibody (YA1072) WB Human, Mouse, Rat
HY-P85553 ATIC Antibody (YA5245) WB Human, Mouse, Rat

Related Diseases

Diseases Alias
Aica-Ribosuria Due To Atic Deficiency
  • Aica-Ribosiduria Due To Atic Deficiency

  • Aicar Transformylase/Imp Cyclohydrolase Deficiency

  • Atic Deficiency

  • Aica-Ribosiduria

  • 5-Amino-4-Imidazole Carboxamide Ribosiduria

  • AICAR

  • Aicar Transformylase Inosine Monophosphate Cyclohydrolase Deficiency

Glomerulopathy With Fibronectin Deposits 2
  • Fibronectin Glomerulopathy

  • GFND2

  • Glomerulopathy With Fibronectin Deposits

  • Familial Glomerular Nephritis With Fibronectin Deposits

  • Familial Lobular Glomerulopathy

  • Gfnd

  • Glomerulopathy With Giant Fibrillar Deposits

  • Glomerular Nephritis, Familial, With Fibronectin Deposits

  • Glomerular Nephritis Familial With Fibronectin Deposits

  • Glomerulopathy, With Fibronectin Deposits

  • Glomerulopathy, With Fibronectin Deposits, Type 2

Pulmonary Plasma Cell Granuloma
  • Plasma Cell Granuloma, Pulmonary

  • Granuloma, Plasma Cell, Pulmonary

  • Lymphocytic Pseudotumor Of Lung

  • Sclerosing Hemangiocytoma Of Lung

Nephrotic Syndrome
  • Finnish Congenital Nephrotic Syndrome

  • Ns - [Nephrotic Syndrome]

  • Nephrosis Syndrome

  • Nephrosis Nos

  • Glomerular Lesion Nephrosis

Epithelioid Inflammatory Myofibroblastic Sarcoma
Inflammatory Myofibroblastic Tumor
  • Inflammatory Fibrosarcoma

Rheumatoid Arthritis
  • RA

  • Arthritis, Rheumatoid

  • Rheumatoid Arthritis, Susceptibility To

  • Arthritis Or Polyarthritis, Rheumatic

  • Atrophic Arthritis

  • Rheumatism Arthritis

  • Rheumatoid Polyarthritis

Charcot-Marie-Tooth Disease, X-Linked Recessive, 5
  • CMTX5

  • Rosenberg-Chutorian Syndrome

  • Charcot-Marie-Tooth Disease X-Linked Recessive 5

  • Optic Atrophy, Polyneuropathy, And Deafness

  • Charcot-Marie-Tooth Neuropathy X-Linked Recessive 5

  • Cmt5x

  • X-Linked Charcot-Marie-Tooth Disease Type 5

  • Charcot-Marie-Tooth Neuropathy, X-Linked Recessive, 5

  • Optic Atrophy Polyneuropathy Deafness

  • Optic Atrophy With Polyneuropathy And Deafness

  • Charcot-Marie-Tooth Disease, X-Linked Recessive, Type 5

Arts Syndrome
  • ARTS

  • Mrxsarts

  • Ataxia, Fatal X-Linked, With Deafness And Loss Of Vision

  • Mrxs18

  • Lethal Ataxia With Deafness And Optic Atrophy

  • Fatal X-Linked Ataxia With Deafness And Loss Of Vision

  • Mental Retardation, X-Linked, Syndromic, Arts Type

  • Mental Retardation, X-Linked, Syndromic 18

  • Syndromic X-Linked Mental Retardation 18

  • Syndromic X-Linked Mental Retardation Arts Type

  • Lethal Ataxia-Deafness-Optic Atrophy

  • X-Linked Fatal Ataxia With Deafness And Loss Of Vision

  • Ataxia-Deafness-Optic Atrophy, Lethal

  • Lethal Ataxia With Hearing Loss And Optic Atrophy

  • Art

Childhood Osteosarcoma
  • Pediatric Osteosarcoma

Lesch-Nyhan Syndrome
  • Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency

  • LNS

  • Hprt Deficiency

  • Complete Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency

  • Hypoxanthine Guanine Phosphoribosyltransferase Deficiency

  • X-Linked Hyperuricemia

  • Choreoathetosis Self-Mutilation Syndrome

  • Hprt1 Deficiency

  • Hprt Deficiency, Complete

  • Deficiency Of Imp Pyrophosphorylase

  • Hgprt Deficiency

  • Lesch-Nyhan Disease

  • Hypoxanthine Guanine Phosphoribosyltransferase 1 Deficiency

  • Hg-Prt Deficiency

  • Hypoxanthine-Guanine-Phosphoribosyltransferase Deficiency

  • Lesch - Nyhan Syndrome

  • Hprt1 Disorders

  • Lesch Nyhan Syndrome

  • Complete Hprt Deficiency Complete

  • Lesch Nyhan Disease

  • Complete Hprt Deficiency

  • Deficiency Of Guanine Phosphoribosyltransferase

  • Deficiency Of Hypoxanthine Phosphoribosyltransferase

  • Hypoxanthine Phosphoribosyltransferase Deficiency

  • Juvenile Gout, Choreoathetosis, Mental Retardation Syndrome

  • Juvenile Hyperuricemia Syndrome

  • Lnd

  • Primary Hyperuricemia Syndrome

  • Total Hprt Deficiency

  • Total Hypoxanthine-Guanine Phosphoribosyl Transferase Deficiency

  • X-Linked Primary Hyperuricemia

  • X-Linked Uric Aciduria Enzyme Defect

  • Hprt Complete Deficiency

  • Hprt Deficiency Grade Iv

  • Hypoxanthine Guanine Phosphoribosyltransferase Complete Deficiency

  • Hypoxanthine Guanine Phosphoribosyltransferase Deficiency, Grade Iv

  • Hypoxanthine-Guanine Phosphoribosyltransferase 1 Deficiency

  • Hprt - [ Hypoxanthine-Guanine Phosphoribosyltransferase] Complete Deficiency

  • Total Hgprt - [Hypoxanthine-Guanine Phosphoribosyltransferase] Deficiency

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 ATIC VGNC VGNC:26264
Rattus norvegicus ATIC RGD RGD:70879
Canis familiaris ATIC VGNC VGNC:38229
Felis catus ATIC VGNC VGNC:80144
Macaca mulatta ATIC VGNC VGNC:70172
Mus musculus ATIC MGD MGI:1351352
Others ATIC NCBI