Puma concolor (puma): 112861082
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Entry
112861082 CDS
T08890
Symbol
TCF7
Name
(RefSeq) transcription factor 7 isoform X1
KO
K02620
transcription factor 7
Organism
pcoo
Puma concolor (puma)
Pathway
pcoo04310
Wnt signaling pathway
pcoo04390
Hippo signaling pathway
pcoo04520
Adherens junction
pcoo04550
Signaling pathways regulating pluripotency of stem cells
pcoo04916
Melanogenesis
pcoo04934
Cushing syndrome
pcoo04936
Alcoholic liver disease
pcoo05132
Salmonella infection
pcoo05165
Human papillomavirus infection
pcoo05167
Kaposi sarcoma-associated herpesvirus infection
pcoo05200
Pathways in cancer
pcoo05210
Colorectal cancer
pcoo05213
Endometrial cancer
pcoo05215
Prostate cancer
pcoo05216
Thyroid cancer
pcoo05217
Basal cell carcinoma
pcoo05221
Acute myeloid leukemia
pcoo05224
Breast cancer
pcoo05225
Hepatocellular carcinoma
pcoo05226
Gastric cancer
pcoo05412
Arrhythmogenic right ventricular cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
pcoo00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
112861082 (TCF7)
04390 Hippo signaling pathway
112861082 (TCF7)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04520 Adherens junction
112861082 (TCF7)
04550 Signaling pathways regulating pluripotency of stem cells
112861082 (TCF7)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
112861082 (TCF7)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
112861082 (TCF7)
09162 Cancer: specific types
05210 Colorectal cancer
112861082 (TCF7)
05225 Hepatocellular carcinoma
112861082 (TCF7)
05226 Gastric cancer
112861082 (TCF7)
05216 Thyroid cancer
112861082 (TCF7)
05221 Acute myeloid leukemia
112861082 (TCF7)
05217 Basal cell carcinoma
112861082 (TCF7)
05215 Prostate cancer
112861082 (TCF7)
05213 Endometrial cancer
112861082 (TCF7)
05224 Breast cancer
112861082 (TCF7)
09172 Infectious disease: viral
05167 Kaposi sarcoma-associated herpesvirus infection
112861082 (TCF7)
05165 Human papillomavirus infection
112861082 (TCF7)
09171 Infectious disease: bacterial
05132 Salmonella infection
112861082 (TCF7)
09166 Cardiovascular disease
05412 Arrhythmogenic right ventricular cardiomyopathy
112861082 (TCF7)
09167 Endocrine and metabolic disease
04936 Alcoholic liver disease
112861082 (TCF7)
04934 Cushing syndrome
112861082 (TCF7)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
pcoo03000
]
112861082 (TCF7)
Transcription factors [BR:
pcoo03000
]
Eukaryotic type
beta-Scaffold factors with minor groove contacts
HMG TCF-1
112861082 (TCF7)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
HMG_box
CTNNB1_binding
HMG_box_2
HMG_WDHD1
Motif
Other DBs
NCBI-GeneID:
112861082
NCBI-ProteinID:
XP_025780141
UniProt:
A0A6P6HX75
LinkDB
All DBs
Position
Unknown
AA seq
283 aa
AA seq
DB search
MYKDTVYSAFNLLMHYPPPSGAGQHPQPQPPLHNKASQPAHSVPQLSPLYEHFSSPHPTP
APADISQKQVHRPLQTPDLSGFYSLTSGSMGQLPHTVSWPSPPLYPLSPSCGYRQHFPAP
TAAPGAPYPRFTHPSLMLGSGVPGHPAAIPHPAIVPPSGKQELQPYDRSLKTQAESKAEK
EAKKPTIKKPLNAFMLYMKEMRAKVIAECTLKESAAINQILGRRWHALSREEQAKYYELA
RKERQLHMQLYPGWSARDNYGKKKRRSREKHQESNTDNSLHYS
NT seq
852 nt
NT seq
+upstream
nt +downstream
nt
atgtacaaagacaccgtctactcggccttcaatctgcttatgcactacccacccccttcg
ggagcagggcagcacccccagccgcagcccccactgcacaacaaggccagtcagccagcc
cacagcgtcccacagctctctcctctctatgaacatttcagcagcccacaccctacacct
gcaccagccgacatcagccagaagcaagttcacaggcctctgcagacccctgacctctct
ggcttctactctctgacctcaggcagcatgggacagcttccccacaccgtgagctggccc
agccctcctctctaccccctgtccccttcctgcggatatagacagcacttccctgccccc
actgcagcccctggcgccccctaccccaggttcacccacccatccctgatgctaggctcc
ggtgtgcctggtcaccctgcagccatcccccacccggctatcgtacctccctcaggcaag
caggagctgcagccatatgaccgtagcctgaagacacaggcggaatccaaggcagagaaa
gaggccaagaagccaaccatcaagaagcctctcaatgccttcatgctgtacatgaaggag
atgagagccaaggtcattgcagagtgtacactcaaggagagtgctgccatcaaccagatc
ctgggccgcaggtggcacgcgctgtctcgggaagagcaggccaagtattatgagctggcc
cgaaaagagaggcagctgcacatgcagctctacccaggctggtcggcgcgtgacaactat
gggaagaaaaagaggcggtcacgagaaaagcaccaggagtccaacacagataactctctt
cactattcctag
DBGET
integrated database retrieval system