Heterocephalus glaber (naked mole-rat): 101707882
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Entry
101707882 CDS
T02812
Symbol
Tcf7
Name
(RefSeq) transcription factor 7 (T-cell specific, HMG-box)
KO
K02620
transcription factor 7
Organism
hgl
Heterocephalus glaber (naked mole-rat)
Pathway
hgl04310
Wnt signaling pathway
hgl04390
Hippo signaling pathway
hgl04520
Adherens junction
hgl04550
Signaling pathways regulating pluripotency of stem cells
hgl04916
Melanogenesis
hgl04934
Cushing syndrome
hgl04936
Alcoholic liver disease
hgl05132
Salmonella infection
hgl05165
Human papillomavirus infection
hgl05167
Kaposi sarcoma-associated herpesvirus infection
hgl05200
Pathways in cancer
hgl05210
Colorectal cancer
hgl05213
Endometrial cancer
hgl05215
Prostate cancer
hgl05216
Thyroid cancer
hgl05217
Basal cell carcinoma
hgl05221
Acute myeloid leukemia
hgl05224
Breast cancer
hgl05225
Hepatocellular carcinoma
hgl05226
Gastric cancer
hgl05412
Arrhythmogenic right ventricular cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
hgl00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
101707882 (Tcf7)
04390 Hippo signaling pathway
101707882 (Tcf7)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04520 Adherens junction
101707882 (Tcf7)
04550 Signaling pathways regulating pluripotency of stem cells
101707882 (Tcf7)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
101707882 (Tcf7)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
101707882 (Tcf7)
09162 Cancer: specific types
05210 Colorectal cancer
101707882 (Tcf7)
05225 Hepatocellular carcinoma
101707882 (Tcf7)
05226 Gastric cancer
101707882 (Tcf7)
05216 Thyroid cancer
101707882 (Tcf7)
05221 Acute myeloid leukemia
101707882 (Tcf7)
05217 Basal cell carcinoma
101707882 (Tcf7)
05215 Prostate cancer
101707882 (Tcf7)
05213 Endometrial cancer
101707882 (Tcf7)
05224 Breast cancer
101707882 (Tcf7)
09172 Infectious disease: viral
05167 Kaposi sarcoma-associated herpesvirus infection
101707882 (Tcf7)
05165 Human papillomavirus infection
101707882 (Tcf7)
09171 Infectious disease: bacterial
05132 Salmonella infection
101707882 (Tcf7)
09166 Cardiovascular disease
05412 Arrhythmogenic right ventricular cardiomyopathy
101707882 (Tcf7)
09167 Endocrine and metabolic disease
04936 Alcoholic liver disease
101707882 (Tcf7)
04934 Cushing syndrome
101707882 (Tcf7)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hgl03000
]
101707882 (Tcf7)
Transcription factors [BR:
hgl03000
]
Eukaryotic type
beta-Scaffold factors with minor groove contacts
HMG TCF-1
101707882 (Tcf7)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
CTNNB1_binding
HMG_box
HMG_box_2
HMG_WDHD1
Motif
Other DBs
NCBI-GeneID:
101707882
NCBI-ProteinID:
XP_012934372
UniProt:
A0AAX6R3M6
LinkDB
All DBs
Position
Un
AA seq
416 aa
AA seq
DB search
MPQLDSGGAGGGDDLGAPDELLAFQDEGEEQDDKSRDSTAGPERDLAELKSSLVNESEGA
AGGAGAREAGGAASGEAEVGPEALGREHSSQRLFGDKLPESLEDGLKAPECASGMYKETV
YSAFNLLMHYPAPSGAGQHPQPQPPLHKASQPPHSVPQLSPLYEHFSSPHPTQAPVDISQ
KQGVHRPLQTPDLSSFYSLTSGSMGQLPHTVSWPSPPLYPLSPSCGYRQHFPAPTAAPGA
PYPRFTHPSLMLGSGVPGHPAAIPHPAIVPSSGKQDLQPYDRSLKTQAESKAEKEAKKPT
IKKPLNAFMLYMKEMRAKVIAECTLKESAAINQILGRRWHALSREEQAKYYELARKERQL
HMQLYPGWSARDNYGKKKRRSREKHQESTTGGKRNALGTYPEKAAAPAPFLPMTVL
NT seq
1251 nt
NT seq
+upstream
nt +downstream
nt
atgccgcagctggactcgggcggcgcgggcggcggcgacgacctgggcgcgcccgatgag
ctgctggccttccaggacgagggcgaggagcaggacgacaagagccgcgacagcaccgcg
ggccccgagcgcgacctggccgagctcaagtcgtcgctcgtgaacgagtccgagggcgcg
gccgggggcgcaggggcccgggaggccgggggcgcagcgagcggcgaggccgaggtcggg
cccgaggctctcgggcgggagcacagttcgcagagactcttcggcgacaaacttccagag
tcgctggaggacggcctgaaggccccggagtgcgccagcggcatgtacaaagagaccgtc
tactccgccttcaatctgctcatgcactacccggccccctcgggcgcagggcagcacccc
cagccgcagcccccgctgcacaaggccagccaacccccccacagcgtcccccaactctct
cctctctacgaacatttcagcagcccacaccccacgcaggcccctgtggacatcagccag
aaacaaggagttcacaggcccctacagactcctgacctctccagcttctactctctgacc
tcaggcagcatgggacagctgccccacactgtgagctggcccagccctcctctctacccc
ctgtccccttcctgcggatatagacagcacttccctgcccccaccgcagcccctggcgcc
ccctaccccaggttcacccacccgtccctgatgctgggctctggtgtacctggtcaccca
gcagccatcccccacccagccatcgtgccttcctcagggaagcaggacttgcagccgtat
gaccgcagcctgaagacccaggcagaatccaaggcagagaaggaggctaagaagccaacc
atcaagaagcccctcaatgcgttcatgctgtacatgaaggagatgagagccaaggtcatt
gcagagtgcacactcaaggagagcgctgctatcaaccagatcctgggtcgcaggtggcat
gcactgtctcgggaagagcaggccaagtattatgagctggcccgcaaggaaaggcagctg
cacatgcagctgtacccaggctggtcagcgcgggacaactacgggaagaagaagaggcgc
tcgagggagaagcaccaggaatccaccacaggaggaaaaagaaatgcactcggtacttac
ccggagaaggccgctgccccagccccgttccttccgatgacagtgctctag
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