Homo sapiens (human): 429
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Entry
429 CDS
T01001
Symbol
ASCL1, ASH1, HASH1, MASH1, bHLHa46
Name
(RefSeq) achaete-scute family bHLH transcription factor 1
KO
K09067
achaete-scute complex protein
Organism
hsa
Homo sapiens (human)
Disease
H00916
Congenital central hypoventilation syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
429 (ASCL1)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Basic helix-loop-helix (bHLH)
Achaete-Scute
429 (ASCL1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
HLH
DUF6491
TFIIA
Cas9-BH
Motif
Other DBs
NCBI-GeneID:
429
NCBI-ProteinID:
NP_004307
OMIM:
100790
HGNC:
738
Ensembl:
ENSG00000139352
UniProt:
P50553
LinkDB
All DBs
Position
12:102957674..102960513
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AA seq
236 aa
AA seq
DB search
MESSAKMESGGAGQQPQPQPQQPFLPPAACFFATAAAAAAAAAAAAAQSAQQQQQQQQQQ
QQAPQLRPAADGQPSGGGHKSAPKQVKRQRSSSPELMRCKRRLNFSGFGYSLPQQQPAAV
ARRNERERNRVKLVNLGFATLREHVPNGAANKKMSKVETLRSAVEYIRALQQLLDEHDAV
SAAFQAGVLSPTISPNYSNDLNSMAGSPVSSYSSDEGSYDPLSPEEQELLDFTNWF
NT seq
711 nt
NT seq
+upstream
nt +downstream
nt
atggaaagctctgccaagatggagagcggcggcgccggccagcagccccagccgcagccc
cagcagcccttcctgccgcccgcagcctgtttctttgccacggccgcagccgcggcggcc
gcagccgccgcagcggcagcgcagagcgcgcagcagcagcagcagcagcagcagcagcag
cagcaggcgccgcagctgagaccggcggccgacggccagccctcagggggcggtcacaag
tcagcgcccaagcaagtcaagcgacagcgctcgtcttcgcccgaactgatgcgctgcaaa
cgccggctcaacttcagcggctttggctacagcctgccgcagcagcagccggccgccgtg
gcgcgccgcaacgagcgcgagcgcaaccgcgtcaagttggtcaacctgggctttgccacc
cttcgggagcacgtccccaacggcgcggccaacaagaagatgagtaaggtggagacactg
cgctcggcggtcgagtacatccgcgcgctgcagcagctgctggacgagcatgacgcggtg
agcgccgccttccaggcaggcgtcctgtcgcccaccatctcccccaactactccaacgac
ttgaactccatggccggctcgccggtctcatcctactcgtcggacgagggctcttacgac
ccgctcagccccgaggagcaggagcttctcgacttcaccaactggttctga
DBGET
integrated database retrieval system
