Homo sapiens (human): 84839
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Entry
84839 CDS
T01001
Symbol
RAX2, ARMD6, CORD11, QRX, RAXL1, RP95
Name
(RefSeq) retina and anterior neural fold homeobox 2
KO
K09333
retina and anterior neural fold homeobox-like protein
Organism
hsa
Homo sapiens (human)
Disease
H00481
Cone-rod dystrophy and cone dystrophy
H00527
Retinitis pigmentosa
H00821
Age-related macular degeneration
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
84839 (RAX2)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Helix-turn-helix
Homeo domain Paired-related
84839 (RAX2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Homeodomain
Homeobox_KN
Motif
Other DBs
NCBI-GeneID:
84839
NCBI-ProteinID:
NP_001306003
OMIM:
610362
HGNC:
18286
Ensembl:
ENSG00000173976
UniProt:
Q96IS3
LinkDB
All DBs
Position
19:complement(3769089..3772228)
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AA seq
184 aa
AA seq
DB search
MFLSPGEGPATEGGGLGPGEEAPKKKHRRNRTTFTTYQLHQLERAFEASHYPDVYSREEL
AAKVHLPEVRVQVWFQNRRAKWRRQERLESGSGAVAAPRLPEAPALPFARPPAMSLPLEP
WLGPGPPAVPGLPRLLGPGPGLQASFGPHAFAPTFADGFALEEASLRLLAKEHAQALDRA
WPPA
NT seq
555 nt
NT seq
+upstream
nt +downstream
nt
atgttcctgagcccgggcgaggggccggcaaccgagggtgggggtctggggccgggcgag
gaggcccccaagaagaagcaccggaggaaccgcaccaccttcaccacctaccagctgcac
cagctggagcgggcgttcgaggcctctcactacccggatgtgtacagccgtgaggagctg
gcagccaaggtgcacctacctgaggtgcgcgtgcaggtgtggttccagaaccgccgggcc
aagtggcgccgccaggagcggctggagtcaggctcgggtgccgtggcagctccgagactc
cccgaggccccagcgctgccgttcgcccgccccccggccatgtcgctgcccctggagccc
tggttgggccccggaccgccggccgtgccaggcctcccccgcctcctgggcccgggcccg
gggctgcaagcgtccttcgggcctcatgcctttgctcccaccttcgcagatggcttcgcc
ctggaggaggcgtccctgcggctgctggccaaggaacatgcacaggctctggacagggcc
tggccgccagcctga
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integrated database retrieval system
