Details for: NYX

Gene ID: 60506

Symbol: NYX

Ensembl ID: ENSG00000188937

Description: nyctalopin

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

Title: The DNA sequence of the human X chromosome.

PubMed ID: 15772651

DOI: 10.1038/nature03440

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.