KEGG   Heterocephalus glaber (naked mole-rat): 101707882
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)
SSDB
Motif
Pfam: CTNNB1_binding HMG_box HMG_box_2
Other DBs
NCBI-GeneID: 101707882
NCBI-ProteinID: XP_012934372
Position
Un
AA seq 416 aa
MPQLDSGGAGGGDDLGAPDELLAFQDEGEEQDDKSRDSTAGPERDLAELKSSLVNESEGA
AGGAGAREAGGAASGEAEVGPEALGREHSSQRLFGDKLPESLEDGLKAPECASGMYKETV
YSAFNLLMHYPAPSGAGQHPQPQPPLHKASQPPHSVPQLSPLYEHFSSPHPTQAPVDISQ
KQGVHRPLQTPDLSSFYSLTSGSMGQLPHTVSWPSPPLYPLSPSCGYRQHFPAPTAAPGA
PYPRFTHPSLMLGSGVPGHPAAIPHPAIVPSSGKQDLQPYDRSLKTQAESKAEKEAKKPT
IKKPLNAFMLYMKEMRAKVIAECTLKESAAINQILGRRWHALSREEQAKYYELARKERQL
HMQLYPGWSARDNYGKKKRRSREKHQESTTGGKRNALGTYPEKAAAPAPFLPMTVL
NT seq 1251 nt   +upstreamnt  +downstreamnt
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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