Homo sapiens (human): 50674
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Entry
50674 CDS
T01001
Symbol
NEUROG3, Atoh5, Math4B, NGN-3, bHLHa7, ngn3
Name
(RefSeq) neurogenin 3
KO
K08028
neurogenin 3
Organism
hsa
Homo sapiens (human)
Pathway
hsa04950
Maturity onset diabetes of the young
Disease
H01174
Congenital diarrhea
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09167 Endocrine and metabolic disease
04950 Maturity onset diabetes of the young
50674 (NEUROG3)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
50674 (NEUROG3)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Basic helix-loop-helix (bHLH)
Tal/Twist/Atonal/Hen, Atonal
50674 (NEUROG3)
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
HLH
Umbravirus_LDM
Motif
Other DBs
NCBI-GeneID:
50674
NCBI-ProteinID:
NP_066279
OMIM:
604882
HGNC:
13806
Ensembl:
ENSG00000122859
UniProt:
Q9Y4Z2
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Position
10:complement(69571485..69573422)
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AA seq
214 aa
AA seq
DB search
MTPQPSGAPTVQVTRETERSFPRASEDEVTCPTSAPPSPTRTRGNCAEAEEGGCRGAPRK
LRARRGGRSRPKSELALSKQRRSRRKKANDRERNRMHNLNSALDALRGVLPTFPDDAKLT
KIETLRFAHNYIWALTQTLRIADHSLYALEPPAPHCGELGSPGGSPGDWGSLYSPVSQAG
SLSPAASLEERPGLLGATFSACLSPGSLAFSDFL
NT seq
645 nt
NT seq
+upstream
nt +downstream
nt
atgacgcctcaaccctcgggtgcgcccactgtccaagtgacccgtgagacggagcggtcc
ttccccagagcctcggaagacgaagtgacctgccccacgtccgccccgcccagccccact
cgcacacgggggaactgcgcagaggcggaagagggaggctgccgaggggccccgaggaag
ctccgggcacggcgcgggggacgcagccggcctaagagcgagttggcactgagcaagcag
cgacggagtcggcgaaagaaggccaacgaccgcgagcgcaatcgaatgcacaacctcaac
tcggcactggacgccctgcgcggtgtcctgcccaccttcccagacgacgcgaagctcacc
aagatcgagacgctgcgcttcgcccacaactacatctgggcgctgactcaaacgctgcgc
atagcggaccacagcttgtacgcgctggagccgccggcgccgcactgcggggagctgggc
agcccaggcggttcccccggggactgggggtccctctactccccagtctcccaggctggc
agcctgagtcccgccgcgtcgctggaggagcgacccgggctgctgggggccaccttttcc
gcctgcttgagcccaggcagtctggctttctcagattttctgtga
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