• Thumbnail for RNASEH2B
    Ribonuclease H2, subunit B is a protein in humans that is encoded by the RNASEH2B gene. RNase H2 is composed of a single catalytic subunit (A) and two non-catalytic...
    7 KB (885 words) - 19:06, 19 February 2025
  • Thumbnail for Aicardi–Goutières syndrome
    of which nine have been identified to date, namely: TREX1, RNASEH2A, RNASEH2B, RNASEH2C (which together encode the ribonuclease H2 enzyme complex), SAMHD1...
    30 KB (3,342 words) - 11:26, 22 August 2024
  • Thumbnail for Lupus
    receptor gene, RAG1, RAG2, DNASE1, SHOC2, KRAS, PTPN11, PTEN, BLK, RNASEH2A, RNASEH2B, RNASEH2C, Complement component 1qA, Complement component 1qB, Complement...
    137 KB (14,899 words) - 20:19, 12 May 2025
  • Aicardi–Goutières syndrome, a hereditary disease caused by mutations in the TREX1, RNASEH2B, RNASEH2C, RNASEH2A, ADAR1, SAMHD1, IFIH1, LSM11, or RNU7-1 gene. Infectious...
    16 KB (1,635 words) - 22:19, 17 January 2025
  • Thumbnail for Ribonuclease H
    (monomeric) subtype RNASEH2A, the catalytic subunit of the trimeric H2 complex RNASEH2B, a structural subunit of the trimeric H2 complex RNASEH2C, a structural...
    54 KB (5,823 words) - 20:53, 22 July 2024
  • ADULT syndrome TP63 dominant Aicardi–Goutières syndrome TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, IFIH1 1:19,500,000 Albinism 1:18,000-20,000 Alexander...
    43 KB (995 words) - 17:02, 21 January 2025
  • FASLG, FAS, RAG1, RAG2, DNASE1, SHOC2, KRAS, PTPN11, PTEN, BLK, RNASEH2A, RNASEH2B, RNASEH2C, Complement component 1qA, Complement component 1qB, Complement...
    84 KB (10,375 words) - 13:49, 18 April 2025
  • 13827 RNASEH1 HGNC:18466 O60930 13828 RNASEH2A HGNC:18518 O75792 13829 RNASEH2B HGNC:25671 Q5TBB1 13830 RNASEH2C HGNC:24116 Q8TDP1 13831 RNASEK HGNC:33911...
    282 KB (17 words) - 09:28, 10 February 2025
  • Thumbnail for RNASEH2A
    ribonuclease H enzyme (RNaseH2). The other two subunits are the non-catalytic RNASEH2B and RNASEH2C. RNaseH2 is the major source of ribonuclease H activity in...
    5 KB (582 words) - 01:59, 17 April 2022
  • Thumbnail for IFI44L
    mutation in the RNASEH2B gene. In addition to this mutation, 5 patients had a c.529G>A,p.A177T mutation in exon 7 of their two RNASEH2B genes. In this...
    70 KB (9,189 words) - 21:56, 27 March 2025
  • Thumbnail for C13orf42
    consists of several pseudogenes along with ribonuclease H2 subunit B (RNASEH2B), uncharacterized LOC107984554, and family with sequence similarity 124...
    22 KB (1,651 words) - 22:02, 8 January 2024
  • dominant and recessive; 225750; TREX1 Aicardi–Goutières syndrome 2; 610181; RNASEH2B Aicardi–Goutières syndrome 3; 610329; RNASEH2C Aicardi–Goutières syndrome...
    234 KB (18,877 words) - 18:07, 24 March 2025
  • Thumbnail for RNASEH2C
    RJ, Cerritelli SM (2009). "Contributions of the two accessory subunits, RNASEH2B and RNASEH2C, to the activity and properties of the human RNase H2 complex"...
    3 KB (343 words) - 00:47, 4 March 2023