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Search references for RNASEH2C. Phrases containing RNASEH2C
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Protein-coding gene in the species Homo sapiens
Ribonuclease H2 subunit C is a protein that in humans is encoded by the RNASEH2C gene. RNase H2 is composed of a single catalytic subunit (A) and two non-catalytic
RNASEH2C
Medical condition
nine have been identified to date, namely: TREX1, RNASEH2A, RNASEH2B, RNASEH2C (which together encode the ribonuclease H2 enzyme complex), SAMHD1, ADAR1
Aicardi–Goutières_syndrome
Autoimmune disease in which the immune system attacks healthy tissue
RAG1, RAG2, DNASE1, SHOC2, KRAS, PTPN11, PTEN, BLK, RNASEH2A, RNASEH2B, RNASEH2C, Complement component 1qA, Complement component 1qB, Complement component
Lupus
Disorders or diseases of the brain
syndrome, a hereditary disease caused by mutations in the TREX1, RNASEH2B, RNASEH2C, RNASEH2A, ADAR1, SAMHD1, IFIH1, LSM11, or RNU7-1 gene. Infectious disease-associated
Encephalopathy
Protein-coding gene in the species Homo sapiens
RNASEH2A and another accessory subunit, RNASEH2C. Structurally, RNASEH2B forms a stable heterodimer with RNASEH2C, contributing to an interwoven triple
RNASEH2B
syndrome TP63 dominant Aicardi–Goutières syndrome TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, IFIH1 1:19,500,000 Albinism 1:18,000-20,000 Alexander disease
List_of_genetic_disorders
Enzyme family
trimeric H2 complex RNASEH2B, a structural subunit of the trimeric H2 complex RNASEH2C, a structural subunit of the trimeric H2 complex In addition, genetic material
Ribonuclease_H
Protein-coding gene in the species Homo sapiens
enzyme (RNaseH2). The other two subunits are the non-catalytic RNASEH2B and RNASEH2C. RNaseH2 is the major source of ribonuclease H activity in mammalian cells
RNASEH2A
Medical condition
RAG1, RAG2, DNASE1, SHOC2, KRAS, PTPN11, PTEN, BLK, RNASEH2A, RNASEH2B, RNASEH2C, Complement component 1qA, Complement component 1qB, Complement component
Childhood-onset systemic lupus erythematosus
Childhood-onset_systemic_lupus_erythematosus
Aicardi–Goutières syndrome 2; 610181; RNASEH2B Aicardi–Goutières syndrome 3; 610329; RNASEH2C Aicardi–Goutières syndrome 4; 610333; RNASEH2A Aicardi–Goutières syndrome
List_of_OMIM_disorder_codes
Human gene
childhood genetic disorder caused by certain mutations in the TREX1, RNASEH2B, RNASEH2C, RNASEH2A, ADAR1, SAMHD1, IFIH1, LSM11, or RNU7-1 gene. Symptoms of the
IFI44L
13836 RNASEH2A HGNC:18518; O75792 13837 RNASEH2B HGNC:25671; Q5TBB1 13838 RNASEH2C HGNC:24116; Q8TDP1 13839 RNASEK HGNC:33911; Q6P5S7 13840 RNASEL HGNC:10050;
List of human protein-coding genes 7
List_of_human_protein-coding_genes_7
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RNASEH2C
RNASEH2C
RNASEH2C
RNASEH2C
RNASEH2C
RNASEH2C
RNASEH2C
RNASEH2C
RNASEH2C
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