ID I0IUI6_HUMAN Unreviewed; 66 AA. AC I0IUI6; DT 13-JUN-2012, integrated into UniProtKB/TrEMBL. DT 13-JUN-2012, sequence version 1. DT 29-OCT-2014, entry version 5. DE SubName: Full=Retinitis pigmentosa 1-like 1 protein {ECO:0000313|EMBL:BAM08935.1}; DE Flags: Fragment; GN Name=RP1L1 {ECO:0000313|EMBL:BAM08935.1}; OS Homo sapiens (Human). OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; OC Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; OC Catarrhini; Hominidae; Homo. OX NCBI_TaxID=9606 {ECO:0000313|EMBL:BAM08935.1}; RN [1] {ECO:0000313|EMBL:BAM08935.1} RP NUCLEOTIDE SEQUENCE. RX PubMed=22605915; RA Kabuto T., Takahashi H., Goto-Fukuura Y., Igarashi T., Akahori M., RA Kameya S., Iwata T., Mizota A., Yamaki K., Miyake Y., Takahashi H.; RT "A new mutation in the RP1L1 gene in a patient with occult macular RT dystrophy associated with a depolarizing pattern of focal macular RT electroretinograms."; RL Mol. Vis. 18:1031-1039(2012). CC --------------------------------------------------------------------------- CC Copyrighted by the UniProt Consortium, see https://www.uniprot.org/terms CC Distributed under the Creative Commons Attribution (CC BY 4.0) License CC --------------------------------------------------------------------------- DR EMBL; AB684329; BAM08935.1; -; Genomic_DNA. DR NextBio; 35531934; -. PE 4: Predicted; FT NON_TER 1 1 {ECO:0000313|EMBL:BAM08935.1}. FT NON_TER 66 66 {ECO:0000313|EMBL:BAM08935.1}. SQ SEQUENCE 66 AA; 6717 MW; ED1558DAC09160FC CRC64; DQLDSGLWEL TWSQALPDLG SHAMTENFTP TSSCGVDISS GSGGSGESSV PCAMDGTLVT QGTELP //