Homo sapiens (human): 6925
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Entry
6925 CDS
T01001
Symbol
TCF4, CDG2T, E2-2, FCD2, FECD3, ITF-2, ITF2, PTHS, SEF-2, SEF2, SEF2-1, SEF2-1A, SEF2-1B, SEF2-1D, TCF-4, bHLHb19
Name
(RefSeq) transcription factor 4 isoform b
KO
K15603
transcription factor 4/12
Organism
hsa
Homo sapiens (human)
Disease
H00756
Pitt-Hopkins syndrome
H00960
Fuchs corneal dystrophy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
6925 (TCF4)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Basic helix-loop-helix (bHLH)
Ubiquitous (class A) factors
6925 (TCF4)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
HLH
Motif
Other DBs
NCBI-GeneID:
6925
NCBI-ProteinID:
NP_001356500
OMIM:
602272
HGNC:
11634
UniProt:
P15884
Structure
PDB
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All DBs
Position
18:complement(55222185..55635957)
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AA seq
667 aa
AA seq
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MHHQQRMAALGTDKELSDLLDFSAMFSPPVSSGKNGPTSLASGHFTGSNVEDRSSSGSWG
NGGHPSPSRNYGDGTPYDHMTSRDLGSHDNLSPPFVNSRIQSKTERGSYSSYGRESNLQG
CHQQSLLGGDMDMGNPGTLSPTKPGSQYYQYSSNNPRRRPLHSSAMEVQTKKVRKVPPGL
PSSVYAPSASTADYNRDSPGYPSSKPATSTFPSSFFMQDGHHSSDPWSSSSGMNQPGYAG
MLGNSSHIPQSSSYCSLHPHERLSYPSHSSADINSSLPPMSTFHRSGTNHYSTSSCTPPA
NGTDSIMANRGSGAAGSSQTGDALGKALASIYSPDHTNNSFSSNPSTPVGSPPSLSAGTA
VWSRNGGQASSSPNYEGPLHSLQSRIEDRLERLDDAIHVLRNHAVGPSTAMPGGHGDMHG
IIGPSHNGAMGGLGSGYGTGLLSANRHSLMVGTHREDGVALRGSHSLLPNQVPVPQLPVQ
SATSPDLNPPQDPYRGMPPGLQGQSVSSGSSEIKSDDEGDENLQDTKSSEDKKLDDDKKD
IKSITSNNDDEDLTPEQKAEREKERRMANNARERLRVRDINEAFKELGRMVQLHLKSDKP
QTKLLILHQAVAVILSLEQQVRERNLNPKAACLKRREEEKVSSEPPPLSLAGPHPGMGDA
SNHMGQM
NT seq
2004 nt
NT seq
+upstream
nt +downstream
nt
atgcatcaccaacagcgaatggctgccttagggacggacaaagagctgagtgatttactg
gatttcagtgcgatgttttcacctcctgtgagcagtgggaaaaatggaccaacttctttg
gcaagtggacattttactggctcaaatgtagaagacagaagtagctcagggtcctggggg
aatggaggacatccaagcccgtccaggaactatggagatgggactccctatgaccacatg
accagcagggaccttgggtcacatgacaatctctctccaccttttgtcaattccagaata
caaagtaaaacagaaaggggctcatactcatcttatgggagagaatcaaacttacagggt
tgccaccagcagagtctccttggaggtgacatggatatgggcaacccaggaaccctttcg
cccaccaaacctggttcccagtactatcagtattctagcaataatccccgaaggaggcct
cttcacagtagtgccatggaggtacagacaaagaaagttcgaaaagttcctccaggtttg
ccatcttcagtctatgctccatcagcaagcactgccgactacaatagggactcgccaggc
tatccttcctccaaaccagcaaccagcactttccctagctccttcttcatgcaagatggc
catcacagcagtgacccttggagctcctccagtgggatgaatcagcctggctatgcagga
atgttgggcaactcttctcatattccacagtccagcagctactgtagcctgcatccacat
gaacgtttgagctatccatcacactcctcagcagacatcaattccagtcttcctccgatg
tccactttccatcgtagtggtacaaaccattacagcacctcttcctgtacgcctcctgcc
aacgggacagacagtataatggcaaatagaggaagcggggcagccggcagctcccagact
ggagatgctctggggaaagcacttgcttcgatctattctccagatcacactaacaacagc
ttttcatcaaacccttcaactcctgttggctctcctccatctctctcagcaggcacagct
gtttggtctagaaatggaggacaggcctcatcgtctcctaattatgaaggacccttacac
tctttgcaaagccgaattgaagatcgtttagaaagactggatgatgctattcatgttctc
cggaaccatgcagtgggcccatccacagctatgcctggtggtcatggggacatgcatgga
atcattggaccttctcataatggagccatgggtggtctgggctcagggtatggaaccggc
cttctttcagccaacagacattcactcatggtggggacccatcgtgaagatggcgtggcc
ctgagaggcagccattctcttctgccaaaccaggttccggttccacagcttcctgtccag
tctgcgacttcccctgacctgaacccaccccaggacccttacagaggcatgccaccagga
ctacaggggcagagtgtctcctctggcagctctgagatcaaatccgatgacgagggtgat
gagaacctgcaagacacgaaatcttcggaggacaagaaattagatgacgacaagaaggat
atcaaatcaattactagcaataatgacgatgaggacctgacaccagagcagaaggcagag
cgtgagaaggagcggaggatggccaacaatgcccgagagcgtctgcgggtccgtgacatc
aacgaggctttcaaagagctcggccgcatggtgcagctccacctcaagagtgacaagccc
cagaccaagctcctgatcctccaccaggcggtggccgtcatcctcagtctggagcagcaa
gtccgagaaaggaatctgaatccgaaagctgcgtgtctgaaaagaagggaggaagagaag
gtgtcctcagagcctccccctctctccttggccggcccacaccctggaatgggagacgca
tcgaatcacatgggacagatgtaa
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