Homo sapiens (human): 220202
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Entry
220202 CDS
T01001
Symbol
ATOH7, Math5, NCRNA, PHPVAR, RNANC, bHLHa13
Name
(RefSeq) atonal bHLH transcription factor 7
KO
K09083
atonal protein 1/7
Organism
hsa
Homo sapiens (human)
Disease
H02112
Persistent hyperplastic primary vitreous
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
220202 (ATOH7)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Basic helix-loop-helix (bHLH)
Tal/Twist/Atonal/Hen, Atonal
220202 (ATOH7)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
HLH
Motif
Other DBs
NCBI-GeneID:
220202
NCBI-ProteinID:
NP_660161
OMIM:
609875
HGNC:
13907
Ensembl:
ENSG00000179774
UniProt:
Q8N100
F1T0H4
LinkDB
All DBs
Position
10:complement(68230595..68232113)
Genome browser
AA seq
152 aa
AA seq
DB search
MKSCKPSGPPAGARVAPPCAGGTECAGTCAGAGRLESAARRRLAANARERRRMQGLNTAF
DRLRRVVPQWGQDKKLSKYETLQMALSYIMALTRILAEAERFGSERDWVGLHCEHFGRDH
YLPFPGAKLPGESELYSQRLFGFQPEPFQMAT
NT seq
459 nt
NT seq
+upstream
nt +downstream
nt
atgaagtcctgcaagcccagcggcccgccggcgggagcgcgcgttgcacccccgtgcgcg
ggcggcaccgagtgcgcgggcacgtgcgccggggccgggcggctggagagcgcggcgcgc
aggcgcctggcggccaacgcgcgcgagcgccgccgcatgcaggggctcaacactgccttc
gaccgcttacgcagggtggttccccagtggggccaggataaaaagctgtccaagtacgag
accctgcagatggccctgagctacatcatggctctgacccggatcctggccgaggccgag
cgattcggctcggagcgggactgggtgggtctccactgtgagcacttcggccgcgaccac
tacctcccgttcccgggcgcgaagctgccgggcgagagcgagctgtacagccagagactc
ttcggcttccagcccgagcccttccagatggccacctag
DBGET
integrated database retrieval system
