KEGG   Homo sapiens (human): 4901
Entry
4901              CDS       T01001                                 
Symbol
NRL, D14S46E, NRL-MAF, RP27
Name
(RefSeq) neural retina leucine zipper
  KO
K09038  neural retina-specific leucine zipper protein
Organism
hsa  Homo sapiens (human)
Disease
H00527  Retinitis pigmentosa
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    4901 (NRL)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Basic leucine zipper (bZIP)
   AP-1(-like) components, Maf
    4901 (NRL)
SSDB
Motif
Pfam: bZIP_Maf Maf_N bZIP_1 KASH_CCD DivIC APG6_N DUF4407 bZIP_2 DUF4164 PI3K_P85_iSH2
Other DBs
NCBI-GeneID: 4901
NCBI-ProteinID: NP_006168
OMIM: 162080
HGNC: 8002
Ensembl: ENSG00000129535
UniProt: P54845
Position
14:complement(24078662..24114949)
AA seq 237 aa
MALPPSPLAMEYVNDFDLMKFEVKREPSEGRPGPPTASLGSTPYSSVPPSPTFSEPGMVG
ATEGTRPGLEELYWLATLQQQLGAGEALGLSPEEAMELLQGQGPVPVDGPHGYYPGSPEE
TGAQHVQLAERFSDAALVSMSVRELNRQLRGCGRDEALRLKQRRRTLKNRGYAQACRSKR
LQQRRGLEAERARLAAQLDALRAEVARLARERDLYKARCDRLTSSGPGSGDPSHLFL
NT seq 714 nt   +upstreamnt  +downstreamnt
atggccctgccccccagccccctggccatggaatatgtcaatgactttgacttgatgaag
tttgaggtaaagcgggaaccctctgagggccgacctggcccccctacagcctcactgggc
tccacaccttacagctcagtgcctccttcacccaccttcagtgaaccaggcatggtgggg
gcaaccgagggcacccggccaggcctggaggagctgtactggctggctaccctgcagcag
cagctgggggctggggaggcattggggctgagtcctgaagaggccatggagctgctgcag
ggtcagggcccagtccctgttgatgggccccatggctactacccagggagcccagaggag
acaggagcccagcacgtccagctggcagagcggttttccgacgcggcgctggtctcgatg
tctgtgcgggagctaaaccggcagctgcggggctgcgggcgcgacgaggcgctgcggctg
aagcagaggcgccgcacgctgaagaaccgcggctacgcgcaggcctgtcgctccaagcgg
ctgcagcagcggcgcgggctggaggccgagcgcgcccgcctggccgcccagctggacgcg
ctgcgggccgaggtggcccgcctggcccgggagcgcgatctctacaaggctcgctgtgac
cggctaacctcgagcggccccgggtccggggacccctcccacctcttcctctga

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