Homo sapiens (human): 6938
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Entry
6938 CDS
T01001
Symbol
TCF12, CRS3, HEB, HH26, HTF4, HsT17266, TCF-12, bHLHb20, p64
Name
(RefSeq) transcription factor 12
KO
K15603
transcription factor 4/12
Organism
hsa
Homo sapiens (human)
Disease
H00255
Hypogonadotropic hypogonadism
H02160
Craniosynostoses
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
6938 (TCF12)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Basic helix-loop-helix (bHLH)
Ubiquitous (class A) factors
6938 (TCF12)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
HLH
Motif
Other DBs
NCBI-GeneID:
6938
NCBI-ProteinID:
NP_001309086
OMIM:
600480
HGNC:
11623
Ensembl:
ENSG00000140262
UniProt:
Q99081
Structure
PDB
PDBj
LinkDB
All DBs
Position
15:56918090..57291310
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AA seq
682 aa
AA seq
DB search
MNPQQQRMAAIGTDKELSDLLDFSAMFSPPVNSGKTRPTTLGSSQFSGSGIDERGGTTSW
GTSGQPSPSYDSSRGFTDSPHYSDHLNDSRLGAHEGLSPTPFMNSNLMGKTSERGSFSLY
SRDTGLPGCQSSLLRQDLGLGSPAQLSSSGKPGTAYYSFSATSSRRRPLHDSAALDPLQA
KKVRKVPPGLPSSVYAPSPNSDDFNRESPSYPSPKPPTSMFASTFFMQDGTHNSSDLWSS
SNGMSQPGFGGILGTSTSHMSQSSSYGNLHSHDRLSYPPHSVSPTDINTSLPPMSSFHRG
STSSSPYVAASHTPPINGSDSILGTRGNAAGSSQTGDALGKALASIYSPDHTSSSFPSNP
STPVGSPSPLTGTSQWPRPGGQAPSSPSYENSLHSLQSRMEDRLDRLDDAIHVLRNHAVG
PSTSLPAGHSDIHSLLGPSHNAPIGSLNSNYGGSSLVASSRSASMVGTHREDSVSLNGNH
SVLSSTVTTSSTDLNHKTQENYRGGLQSQSGTVVTTEIKTENKEKDENLHEPPSSDDMKS
DDESSQKDIKVSSRGRTSSTNEDEDLNPEQKIEREKERRMANNARERLRVRDINEAFKEL
GRMCQLHLKSEKPQTKLLILHQAVAVILSLEQQVRERNLNPKAACLKRREEEKVSAVSAE
PPTTLPGTHPGLSETTNPMGHM
NT seq
2049 nt
NT seq
+upstream
nt +downstream
nt
atgaatccccagcaacaacgcatggccgctatagggaccgacaaggagctgagcgaccta
ctggacttcagtgcgatgttttccccacctgttaatagtgggaaaactagaccaactaca
ctgggaagcagtcaattcagtggatcaggtattgatgaaagaggaggtacaacatcttgg
ggaacaagtggtcaaccaagtccttcctatgattcatctagaggttttacagacagccct
cattacagtgatcacttgaatgacagtcgattaggagcccatgaaggcttgtccccaaca
cctttcatgaactcaaatctgatgggaaaaacatcagagagaggctcattttccctgtac
agcagagatactggattaccaggctgtcaatctagtctcctgagacaagatctggggctt
gggagcccagcacagctatcttcttcaggaaaacctgggacagcatactattcattctct
gctacaagttccaggaggagaccactccatgactctgcagcgcttgatcccttgcaagca
aaaaaagtcagaaaggtgcctcctggtttgccttcttctgtatatgcaccatccccaaat
tcagatgatttcaaccgtgaatctcctagttatccatctcctaagccaccaaccagtatg
ttcgctagcactttctttatgcaagatgggacccacaattcttctgacctttggagttca
tcaaatgggatgagccagcctggttttggtggaattctggggacctccacttcccacatg
tctcaatccagtagttatggcaaccttcattcacatgaccgcttgagttatcctccacac
tcagtttcaccaacagacataaacacgagtcttccaccaatgtccagctttcatcgcggc
agtaccagcagttcaccttacgttgctgcctcacacactcctcccatcaatggatcagac
agcattctaggaaccagagggaatgctgctggaagctcacagacaggtgatgcacttgga
aaggctttggcatctatttattctcctgaccataccagcagtagttttccgtcaaatcca
tcaacaccagttggatcaccttcacctctcacaggtaccagtcagtggccaagacctgga
gggcaagcaccttcatccccaagctatgaaaactcactccactccctgcagtctcgaatg
gaggatcgtttagacagactggatgatgcaatccatgtgctgcggaaccatgctgtggga
ccttccaccagtttgcctgctggtcacagtgatatacatagtttattgggaccatcccat
aatgcaccaattggaagcctcaattcaaactatggaggatcaagccttgttgcaagcagt
cgatcagcttcaatggttggaactcatcgggaagactctgtcagtctcaatggcaatcat
tcagtcctgtctagtacagtcactacttcaagcacagacctgaaccataaaacacaagaa
aattatagaggtggcttgcaaagtcagtctggaactgttgttacaacagaaatcaagact
gaaaacaaagaaaaggatgaaaaccttcatgaacctccttcatcagatgacatgaagtca
gatgatgaatcctcccaaaaagatatcaaggtttcatctagaggcagaacaagcagtact
aatgaagatgaggatttgaaccctgaacagaagatagaaagggagaaggagaggcggatg
gctaacaatgccagagaacgcttacgcgtgcgggatattaatgaagcattcaaagagctt
ggccgaatgtgtcagcttcacttgaagagtgaaaaaccccaaacaaaactccttattctt
catcaagccgtggcagtcatccttagtctagaacagcaagtcagagagaggaaccttaac
cccaaagcagcctgccttaagagaagggaagaagaaaaagtttctgccgtatcggcagag
ccgccaaccacactgccaggaacccatcctgggcttagtgaaactaccaaccctatgggt
catatgtaa
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