Homo sapiens (human): 4901
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
bZIP_Maf
Maf_N
bZIP_1
KASH_CCD
DivIC
APG6_N
bZIP_2
DUF4407
PI3K_P85_iSH2
DUF4164
Motif
Other DBs
NCBI-GeneID:
4901
NCBI-ProteinID:
NP_006168
OMIM:
162080
HGNC:
8002
Ensembl:
ENSG00000129535
UniProt:
P54845
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All DBs
Position
14:complement(24078662..24114949)
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AA seq
237 aa
AA seq
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MALPPSPLAMEYVNDFDLMKFEVKREPSEGRPGPPTASLGSTPYSSVPPSPTFSEPGMVG
ATEGTRPGLEELYWLATLQQQLGAGEALGLSPEEAMELLQGQGPVPVDGPHGYYPGSPEE
TGAQHVQLAERFSDAALVSMSVRELNRQLRGCGRDEALRLKQRRRTLKNRGYAQACRSKR
LQQRRGLEAERARLAAQLDALRAEVARLARERDLYKARCDRLTSSGPGSGDPSHLFL
NT seq
714 nt
NT seq
+upstream
nt +downstream
nt
atggccctgccccccagccccctggccatggaatatgtcaatgactttgacttgatgaag
tttgaggtaaagcgggaaccctctgagggccgacctggcccccctacagcctcactgggc
tccacaccttacagctcagtgcctccttcacccaccttcagtgaaccaggcatggtgggg
gcaaccgagggcacccggccaggcctggaggagctgtactggctggctaccctgcagcag
cagctgggggctggggaggcattggggctgagtcctgaagaggccatggagctgctgcag
ggtcagggcccagtccctgttgatgggccccatggctactacccagggagcccagaggag
acaggagcccagcacgtccagctggcagagcggttttccgacgcggcgctggtctcgatg
tctgtgcgggagctaaaccggcagctgcggggctgcgggcgcgacgaggcgctgcggctg
aagcagaggcgccgcacgctgaagaaccgcggctacgcgcaggcctgtcgctccaagcgg
ctgcagcagcggcgcgggctggaggccgagcgcgcccgcctggccgcccagctggacgcg
ctgcgggccgaggtggcccgcctggcccgggagcgcgatctctacaaggctcgctgtgac
cggctaacctcgagcggccccgggtccggggacccctcccacctcttcctctga
DBGET
integrated database retrieval system
