Photoreceptor cell-specific nuclear receptor (redirect from NR2E3)
(PNR), also known as NR2E3 (nuclear receptor subfamily 2, group E, member 3), is a protein that in humans is encoded by the NR2E3 gene. PNR is a member...
12 KB (1,414 words) - 09:30, 25 July 2024
condition. This condition is caused by autosomal recessive mutations in the NR2E3 gene, located in chromosome 15. Diagnosis of Goldmann–Favre syndrome can...
13 KB (1,273 words) - 10:41, 8 December 2023
induced by several transcription factors, including RORbeta, OTX2, NRL, CRX, NR2E3 and TRbeta2. The S cone fate represents the default photoreceptor program;...
26 KB (2,939 words) - 03:11, 2 September 2024
SEMA4A Retinitis pigmentosa-35 610599 PRCD Retinitis pigmentosa-36 611131 NR2E3 Retinitis pigmentosa-37 268000 MERTK Retinitis pigmentosa-38 268000 USH2A...
63 KB (6,440 words) - 22:03, 21 August 2024
Homologue of the Drosophila tailless gene NR2E1 NR2E3 PNR Photoreceptor cell-specific nuclear receptor NR2E3 F COUP/EAR NR2F1 COUP-TFI Chicken ovalbumin upstream...
74 KB (6,683 words) - 09:55, 12 September 2024
TULP1, CA4, HPRPF3, ABCA4, EYS, CERKL, FSCN2, TOPORS, SNRNP200, PRCD, NR2E3, MERTK, USH2A, PROM1, KLHL7, CNGB1, TTC8, ARL6, DHDDS, BEST1, LRAT, SPARA7...
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P49116 10789 NR2C2AP HGNC:30763 Q86WQ0 10790 NR2E1 HGNC:7973 Q9Y466 10791 NR2E3 HGNC:7974 Q9Y5X4 10792 NR2F1 HGNC:7975 P10589 10793 NR2F2 HGNC:7976 P24468...
282 KB (17 words) - 07:55, 20 June 2024
ENSG00000112333 Nuclear receptor Known motif – High-throughput in vitro [643] AAGTCA NR2E3 ENSG00000278570 Nuclear receptor Known motif – High-throughput in vitro...
374 KB (81 words) - 02:10, 23 September 2023
mouse retinal degeneration model rd7 is caused by an L1 insertion in the Nr2e3 gene. In 2021, a study proposed that L1 elements may be responsible for...
26 KB (2,837 words) - 15:03, 3 August 2024
Mitton KP, Swaroop A (Aug 2004). "Photoreceptor-specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors". Human Molecular...
36 KB (4,270 words) - 10:03, 25 July 2024
AV, Stone EM, Jacobson SG, Swaroop A (Nov 2004). "Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome". Human Mutation. 24 (5): 439...
9 KB (1,095 words) - 14:20, 24 December 2023
Y., Lambert, P., Xu, W., and Ahlquist, P. Orphan Nuclear Receptor PNR/NR2E3 Stimulates p53 Functions by Enhancing p53 Acetylation. Mol. Cell. Biol....
9 KB (1,045 words) - 19:39, 11 February 2024
Hanna, David B. (1 February 2000). "Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate". Nature...
25 KB (2,526 words) - 13:58, 14 August 2024
acetylcholinesterase deficiency; 603034; COLQ Enhanced S-cone syndrome; 268100; NR2E3 Enlarged vestibular aqueduct; 600791; FOXI1 Enlarged vestibular aqueduct;...
234 KB (18,877 words) - 15:43, 9 May 2024