Associated with
Other Information
Genular Protein ID: 3096782673
Symbol: NYX_HUMAN
Name: Nyctalopin
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 11062472
Title: The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
PubMed ID: 11062472
DOI: 10.1038/81627
PubMed ID: 11062471
Title: Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
PubMed ID: 11062471
DOI: 10.1038/81619
PubMed ID: 15772651
PubMed ID: 15489334
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PubMed ID: 15489334
DOI: 10.1101/gr.2596504
Sequence Information:
- Length: 476
- Mass: 51470
- Checksum: 4B9D85132AC63D37
- Sequence:
MLVLLLHAVV LGLPSAWAVG ACARACPAAC ACSTVERGCS VRCDRAGLLR VPAELPCEAV SIDLDRNGLR FLGERAFGTL PSLRRLSLRH NNLSFITPGA FKGLPRLAEL RLAHNGDLRY LHARTFAALS RLRRLDLAAC RLFSVPERLL AELPALRELA AFDNLFRRVP GALRGLANLT HAHLERGRIE AVASSSLQGL RRLRSLSLQA NRVRAVHAGA FGDCGVLEHL LLNDNLLAEL PADAFRGLRR LRTLNLGGNA LDRVARAWFA DLAELELLYL DRNSIAFVEE GAFQNLSGLL ALHLNGNRLT VLAWVAFQPG FFLGRLFLFR NPWCCDCRLE WLRDWMEGSG RVTDVPCASP GSVAGLDLSQ VTFGRSSDGL CVDPEELNLT TSSPGPSPEP AATTVSRFSS LLSKLLAPRV PVEEAANTTG GLANASLSDS LSSRGVGGAG RQPWFLLASC LLPSVAQHVV FGLQMD
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.