KEGG   Neogale vison (American mink): 122891699
Entry
122891699         CDS       T08764                                 
Symbol
TCF7
Name
(RefSeq) transcription factor 7 isoform X1
  KO
K02620  transcription factor 7
Organism
nvs  Neogale vison (American mink)
Pathway
nvs04310  Wnt signaling pathway
nvs04390  Hippo signaling pathway
nvs04520  Adherens junction
nvs04550  Signaling pathways regulating pluripotency of stem cells
nvs04916  Melanogenesis
nvs04934  Cushing syndrome
nvs04936  Alcoholic liver disease
nvs05132  Salmonella infection
nvs05165  Human papillomavirus infection
nvs05167  Kaposi sarcoma-associated herpesvirus infection
nvs05200  Pathways in cancer
nvs05210  Colorectal cancer
nvs05213  Endometrial cancer
nvs05215  Prostate cancer
nvs05216  Thyroid cancer
nvs05217  Basal cell carcinoma
nvs05221  Acute myeloid leukemia
nvs05224  Breast cancer
nvs05225  Hepatocellular carcinoma
nvs05226  Gastric cancer
nvs05412  Arrhythmogenic right ventricular cardiomyopathy
Brite
KEGG Orthology (KO) [BR:nvs00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    122891699 (TCF7)
   04390 Hippo signaling pathway
    122891699 (TCF7)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04520 Adherens junction
    122891699 (TCF7)
   04550 Signaling pathways regulating pluripotency of stem cells
    122891699 (TCF7)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    122891699 (TCF7)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    122891699 (TCF7)
  09162 Cancer: specific types
   05210 Colorectal cancer
    122891699 (TCF7)
   05225 Hepatocellular carcinoma
    122891699 (TCF7)
   05226 Gastric cancer
    122891699 (TCF7)
   05216 Thyroid cancer
    122891699 (TCF7)
   05221 Acute myeloid leukemia
    122891699 (TCF7)
   05217 Basal cell carcinoma
    122891699 (TCF7)
   05215 Prostate cancer
    122891699 (TCF7)
   05213 Endometrial cancer
    122891699 (TCF7)
   05224 Breast cancer
    122891699 (TCF7)
  09172 Infectious disease: viral
   05167 Kaposi sarcoma-associated herpesvirus infection
    122891699 (TCF7)
   05165 Human papillomavirus infection
    122891699 (TCF7)
  09171 Infectious disease: bacterial
   05132 Salmonella infection
    122891699 (TCF7)
  09166 Cardiovascular disease
   05412 Arrhythmogenic right ventricular cardiomyopathy
    122891699 (TCF7)
  09167 Endocrine and metabolic disease
   04936 Alcoholic liver disease
    122891699 (TCF7)
   04934 Cushing syndrome
    122891699 (TCF7)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:nvs03000]
    122891699 (TCF7)
Transcription factors [BR:nvs03000]
 Eukaryotic type
  beta-Scaffold factors with minor groove contacts
   HMG TCF-1
    122891699 (TCF7)
SSDB
Motif
Pfam: CTNNB1_binding HMG_box HMG_box_2 HMG_WDHD1
Other DBs
NCBI-GeneID: 122891699
NCBI-ProteinID: XP_044083497
LinkDB
Position
1:complement(244413567..244445127)
AA seq 567 aa
MPQLDSGGGGAGGGDDLGAPDELLAFQDEGEEQDDKSRDSAAGPERDLAELKSSLVNESE
GAAGGAGVPGAGTGARDEAEVGGEALGREHASQRLFPDKLPESLEDGLKAPECASGMYKD
TVYSAFNLLMHYPPPSGAGQHPQPQPPLHNKASQPAHSVPQLSPLYEHFSSPHPTPAPAD
ISQKQGVHRPLQTPDLSGFYSLTSGSMGQLPHTVSWPSPPLYPLSPSCGYRQHFPAPTAA
PGAPYPRFTHPSLMLGSGVPGHPAAIPHPAIVPPSGKQELQPYDRSLKTQAESKVEKEAK
KPTIKKPLNAFMLYMKEMRAKVIAECTLKESAAINQILGRRWHALSREEQAKYYELARKE
RQLHMQLYPGWSARDNYGKKKRRSREKHQESNTDPGSPKKCRARFGLNQQTDWCGPCRRK
KKCIRYLPGEGRCPSPVPSDDSAVGCPGSPAPEDSPSYLLLPHLPTELLASPAEPAPTSP
GLSAALSLPAPWTPPGPPQHPAEYTGATRGISETGSLACTGHLAASRGPSSERKRQSPKA
HGNWPGALLPPSQGPGPGDFRGCTTSA
NT seq 1704 nt   +upstreamnt  +downstreamnt
atgccgcagctggactccggagggggcggcgcgggcgggggcgacgacctgggcgcgcct
gacgaactgctggccttccaggacgagggcgaggagcaggacgacaagagtcgcgacagc
gccgcgggccccgagcgcgacctggccgagctcaagtcgtcgctggtcaatgagtccgag
ggcgcggcgggcggcgcgggggtcccgggggccggcaccggggcccgcgacgaggcggag
gtcgggggtgaggcgctcggacgggagcacgcttcgcagagacttttccccgacaaactt
ccagagtctctggaggacggcctgaaggccccggagtgcgccagcggcatgtacaaagac
accgtctactccgccttcaatctgctcatgcactaccctcccccctcgggagcagggcag
cacccccagccgcagcccccgctgcacaacaaggccagtcaaccagcccacagcgtccca
caactctctcctctctatgaacatttcagcagtccacaccctacacctgcaccagccgac
atcagccagaaacaaggagttcacaggcctctacagacccccgacctctctggcttctac
tctttgacctcaggcagcatgggacaactcccccacactgtgagctggcccagtcctcct
ctctaccccttgtccccttcctgcggatatagacagcacttccctgcccccactgcagcc
cctggcgccccctaccccaggttcacccacccatccctgatgctgggctctggtgtacct
ggtcaccctgcagccatcccccacccggccatcgtacctccctcagggaagcaggaactg
cagccgtatgaccggagcctgaagacacaggcagaatccaaggtggaaaaggaggccaag
aagccaaccatcaagaagcccctcaacgccttcatgctgtacatgaaggagatgagagcc
aaggtcattgcagagtgcacactcaaggagagtgctgccatcaaccagatcttgggtcga
aggtggcatgcactgtctcgggaagagcaagccaagtattatgagctggcccgaaaggag
aggcagctgcacatgcagctgtacccaggctggtcagcgcgggacaattatgggaagaag
aaaaggcggtctcgggaaaagcaccaggaatccaacacagaccctggctcgcctaagaaa
tgccgtgctcgctttggcctcaaccagcagacggattggtgtggtccgtgcaggaggaaa
aagaaatgcattcggtacttacccggagaaggccgctgccccagccccgttccttccgat
gacagtgctgtaggctgccccgggtccccagcccccgaggactcgccctcatacctcctg
ctgccccacctccccacagaactgcttgctagtcctgcggagccagcgcctacatcacca
gggctctcggccgctctcagcctcccagccccctggactcccccaggccctccccagcac
cctgcagagtacacaggtgcaacgagaggaatctcagagacaggcagcctagcatgcaca
gggcacctggctgcctccaggggcccatcctccgagaggaagcgacagagccccaaagca
catggaaactggccaggggccctgttacctccctctcagggaccaggcccaggagacttc
cgaggctgcacaacttctgcctga

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