Homo sapiens (human): 200186
Help
Entry
200186 CDS
T01001
Symbol
CRTC2, TORC-2, TORC2
Name
(RefSeq) CREB regulated transcription coactivator 2
KO
K16333
CREB-regulated transcription coactivator 2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04151
PI3K-Akt signaling pathway
hsa04152
AMPK signaling pathway
hsa04922
Glucagon signaling pathway
hsa04931
Insulin resistance
hsa05166
Human T-cell leukemia virus 1 infection
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04151 PI3K-Akt signaling pathway
200186 (CRTC2)
04152 AMPK signaling pathway
200186 (CRTC2)
09150 Organismal Systems
09152 Endocrine system
04922 Glucagon signaling pathway
200186 (CRTC2)
09160 Human Diseases
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
200186 (CRTC2)
09167 Endocrine and metabolic disease
04931 Insulin resistance
200186 (CRTC2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
TORC_M
TORC_C
TORC_N
Motif
Other DBs
NCBI-GeneID:
200186
NCBI-ProteinID:
NP_859066
OMIM:
608972
HGNC:
27301
Ensembl:
ENSG00000160741
UniProt:
Q53ET0
Structure
PDB
PDBj
LinkDB
All DBs
Position
1:complement(153947675..153958612)
Genome browser
AA seq
693 aa
AA seq
DB search
MATSGANGPGSATASASNPRKFSEKIALQKQRQAEETAAFEEVMMDIGSTRLQAQKLRLA
YTRSSHYGGSLPNVNQIGSGLAEFQSPLHSPLDSSRSTRHHGLVERVQRDPRRMVSPLRR
YTRHIDSSPYSPAYLSPPPESSWRRTMAWGNFPAEKGQLFRLPSALNRTSSDSALHTSVM
NPSPQDTYPGPTPPSILPSRRGGILDGEMDPKVPAIEENLLDDKHLLKPWDAKKLSSSSS
RPRSCEVPGINIFPSPDQPANVPVLPPAMNTGGSLPDLTNLHFPPPLPTPLDPEETAYPS
LSGGNSTSNLTHTMTHLGISRGMGLGPGYDAPGLHSPLSHPSLQSSLSNPNLQASLSSPQ
PQLQGSHSHPSLPASSLARHVLPTTSLGHPSLSAPALSSSSSSSSTSSPVLGAPSYPAST
PGASPHHRRVPLSPLSLLAGPADARRSQQQLPKQFSPTMSPTLSSITQGVPLDTSKLSTD
QRLPPYPYSSPSLVLPTQPHTPKSLQQPGLPSQSCSVQSSGGQPPGRQSHYGTPYPPGPS
GHGQQSYHRPMSDFNLGNLEQFSMESPSASLVLDPPGFSEGPGFLGGEGPMGGPQDPHTF
NHQNLTHCSRHGSGPNIILTGDSSPGFSKEIAAALAGVPGFEVSAAGLELGLGLEDELRM
EPLGLEGLNMLSDPCALLPDPAVEESFRSDRLQ
NT seq
2082 nt
NT seq
+upstream
nt +downstream
nt
atggcgacgtcgggggcgaacgggcctggttcggccacggcctcggcttccaatccgcgc
aaatttagtgagaagattgcgctgcagaagcagcgtcaggccgaggagacggcggccttc
gaggaggtgatgatggacatcggctccacccggttacaggcccaaaaactgcgactggca
tacacaaggagctctcattatggtgggtctctgcccaatgttaaccagattggctctggc
ctggccgagttccagagccccctccactcacctttggattcatctcggagcactcggcac
catgggctggtggaacgggtgcagcgagatcctcgaagaatggtgtccccacttcgccga
tacacccgccacattgacagctctccctatagtcctgcctacttatctcctcccccagag
tctagctggcgaaggacgatggcctggggcaatttccctgcagagaaggggcagttgttt
cgactaccatctgcacttaacaggacaagctctgactctgcccttcatacaagtgtgatg
aaccccagtccccaggatacctacccaggccccacacctcccagcatcctgcccagccga
cgtgggggtattctggatggtgaaatggaccccaaagtacctgctattgaggagaacttg
ctagatgacaagcatttgctgaagccatgggatgctaagaagctatcctcatcctcttcc
cgacctcggtcctgtgaagtccctggaattaacatctttccatctcctgaccagcctgcc
aatgtgcctgtcctcccacctgccatgaacacggggggctccctacctgacctcaccaac
ctgcactttcccccaccactgcccacccccctggaccctgaagagacagcctaccctagc
ctgagtgggggcaacagtacctccaatttgacccacaccatgactcacctgggcatcagc
aggggcatgggcctgggcccaggctatgatgcaccaggacttcattcacctctcagccac
ccatccctgcagtcctccctaagcaatcccaacctccaggcttccctgagcagtcctcag
ccccagcttcagggctcccacagccacccctctctgcctgcctcctccttggcccgccat
gtactgcccaccacctccctgggccacccctcactcagtgctccggctctctcctcctcc
tcttcctcctcctccacttcatctcctgttttgggcgccccctcttaccctgcttctacc
cctggggcctccccccaccaccgccgtgtgcccctcagccccctgagtttgctcgcgggc
ccagccgacgccagaaggtcccaacagcagctgcccaaacagttttcgccaacaatgtca
cccaccttgtcttccatcactcagggcgtccccctggataccagtaaactgtccactgac
cagcggttacccccatacccatacagctccccaagtctggttctgcctacccagccccac
accccaaagtctctacagcagccagggctgccctctcagtcttgttcagtgcagtcctca
ggtgggcagcccccaggcaggcagtctcattatgggacaccgtacccacctgggcccagt
gggcatgggcaacagtcttaccaccggccaatgagtgacttcaacctggggaatctggag
cagttcagcatggagagcccatcagccagcctggtgctggatccccctggcttttctgaa
gggcctggatttttagggggtgaggggccaatgggtggcccccaggatccccacaccttc
aaccaccagaacttgacccactgttcccgccatggctcagggcctaacatcatcctcaca
ggggactcctctccaggtttctctaaggagattgcagcagccctggccggagtgcctggc
tttgaggtgtcagcagctggattggagctagggcttgggctagaagatgagctgcgcatg
gagccactgggcctggaagggctaaacatgctgagtgacccctgtgccctgctgcctgat
cctgctgtggaggagtcattccgcagtgaccggctccaatga
Homo sapiens (human): 23373
Help
Entry
23373 CDS
T01001
Symbol
CRTC1, MAML2, MECT1, Mam-2, TORC-1, TORC1, WAMTP1
Name
(RefSeq) CREB regulated transcription coactivator 1
KO
K15309
CREB-regulated transcription coactivator 1
Organism
hsa
Homo sapiens (human)
Pathway
hsa05166
Human T-cell leukemia virus 1 infection
Disease
H01508
Salivary gland cancer
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
23373 (CRTC1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
23373 (CRTC1)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial quality control factors
Regulator of mitochondrial biogenesis
Coactivators
23373 (CRTC1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
TORC_M
TORC_C
TORC_N
Motif
Other DBs
NCBI-GeneID:
23373
NCBI-ProteinID:
NP_056136
OMIM:
607536
HGNC:
16062
Ensembl:
ENSG00000105662
UniProt:
Q6UUV9
Structure
PDB
PDBj
LinkDB
All DBs
Position
19:18683680..18782333
Genome browser
AA seq
634 aa
AA seq
DB search
MATSNNPRKFSEKIALHNQKQAEETAAFEEVMKDLSLTRAARLQLQKSQYLQLGPSRGQY
YGGSLPNVNQIGSGTMDLPFQTPFQSSGLDTSRTTRHHGLVDRVYRERGRLGSPHRRPLS
VDKHGRQADSCPYGTMYLSPPADTSWRRTNSDSALHQSTMTPTQPESFSSGSQDVHQKRV
LLLTVPGMEETTSEADKNLSKQAWDTKKTGSRPKSCEVPGINIFPSADQENTTALIPATH
NTGGSLPDLTNIHFPSPLPTPLDPEEPTFPALSSSSSTGNLAANLTHLGIGGAGQGMSTP
GSSPQHRPAGVSPLSLSTEARRQQASPTLSPLSPITQAVAMDALSLEQQLPYAFFTQAGS
QQPPPQPQPPPPPPPASQQPPPPPPPQAPVRLPPGGPLLPSASLTRGPQPPPLAVTVPSS
LPQSPPENPGQPSMGIDIASAPALQQYRTSAGSPANQSPTSPVSNQGFSPGSSPQHTSTL
GSVFGDAYYEQQMAARQANALSHQLEQFNMMENAISSSSLYSPGSTLNYSQAAMMGLTGS
HGSLPDSQQLGYASHSGIPNIILTVTGESPPSLSKELTSSLAGVGDVSFDSDSQFPLDEL
KIDPLTLDGLHMLNDPDMVLADPATEDTFRMDRL
NT seq
1905 nt
NT seq
+upstream
nt +downstream
nt
atggcgacttcgaacaatccgcggaaattcagcgagaagatcgcgctgcacaatcagaag
caggcggaggagacggcggccttcgaggaggtcatgaaggacctgagcctgacgcgggcc
gcgcggctccagctccagaaatcccagtacctgcaactgggccccagccgaggccagtac
tatggcgggtccctgcccaacgtgaaccagatcgggagtggcaccatggacctgcccttc
cagacccccttccaatcctcgggcctggacaccagccggaccacccggcaccatgggctg
gtggacagggtgtaccgggagcgtggccggctcggctccccacaccgccggcccctgtca
gtggacaaacacggacggcaggccgacagctgcccctatggcaccatgtacctctcacca
cccgcggacaccagctggagaaggaccaattctgactccgccctgcaccagagcacaatg
acgcccacgcagccagaatcctttagcagtgggtcccaggacgtgcaccagaaaagagtc
ttactgttaacagtcccaggaatggaagagaccacatcagaggcagacaaaaacctttcc
aagcaagcatgggacaccaagaagacggggtccaggcccaagtcctgtgaggtccccgga
atcaacatcttcccgtctgccgaccaggaaaacactacagccctgatccccgccacccac
aacacaggggggtccctgcccgacctgaccaacatccacttcccctccccgctcccgacc
ccgctggaccccgaggagcccaccttccctgcactgagcagctccagcagcaccggcaac
ctcgcggccaacctgacgcacctgggcatcggtggcgccggccagggaatgagcacacct
ggctcctctccacagcaccgcccagctggcgtcagccccctgtccctgagcacagaggca
aggcgtcagcaggcatcgcccaccctgtccccgctgtcacccatcactcaggctgtagcc
atggacgccctgtctctggagcagcagctgccctacgccttcttcacccaggcgggctcc
cagcagccaccgccgcagccccagcccccgccgcctcctccacccgcgtcccagcagcca
ccacccccgccacccccacaggcgcccgtccgcctgccccctggtggccccctgttgccc
agcgccagcctgactcgtgggccacagccgcccccgcttgcagtcacggtaccgtcctct
ctcccccagtcccccccagagaaccctggccagccatcgatggggatcgacatcgcctcg
gcgccggctctgcagcagtaccgcactagcgccggctccccggccaaccagtctcccacc
tcgccagtctccaatcaaggcttctccccagggagctccccgcaacacacttccaccctg
ggcagcgtgtttggggacgcgtactatgagcagcagatggcggccaggcaggccaatgct
ctgtcccaccagctggagcagttcaacatgatggagaacgccatcagctccagcagcctg
tacagcccgggctccacactcaactactcgcaggcggccatgatgggcctcacgggcagc
cacgggagcctgccggactcgcagcaactgggatacgccagccacagtggcatccccaac
atcatcctcacagtgacaggagagtccccccccagcctctctaaagaactgaccagctct
ctggccggggtcggcgacgtcagcttcgactccgacagccagtttcccctggacgaactc
aagatcgaccccctgaccctcgacggactgcacatgctcaacgaccccgacatggttctg
gccgacccagccaccgaggacaccttccggatggaccgcctgtga
Homo sapiens (human): 64784
Help
Entry
64784 CDS
T01001
Symbol
CRTC3, TORC-3, TORC3
Name
(RefSeq) CREB regulated transcription coactivator 3
KO
K16334
CREB-regulated transcription coactivator 3
Organism
hsa
Homo sapiens (human)
Pathway
hsa05166
Human T-cell leukemia virus 1 infection
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
64784 (CRTC3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
TORC_M
TORC_C
TORC_N
Motif
Other DBs
NCBI-GeneID:
64784
NCBI-ProteinID:
NP_073606
OMIM:
608986
HGNC:
26148
Ensembl:
ENSG00000140577
UniProt:
Q6UUV7
Q8TEF4
LinkDB
All DBs
Position
15:90529923..90645345
Genome browser
AA seq
619 aa
AA seq
DB search
MAASPGSGSANPRKFSEKIALHTQRQAEETRAFEQLMTDLTLSRVQFQKLQQLRLTQYHG
GSLPNVSQLRSSASEFQPSFHQADNVRGTRHHGLVERPSRNRFHPLHRRSGDKPGRQFDG
SAFGANYSSQPLDESWPRQQPPWKDEKHPGFRLTSALNRTNSDSALHTSALSTKPQDPYG
GGGQSAWPAPYMGFCDGENNGHGEVASFPGPLKEENLLNVPKPLPKQLWETKEIQSLSGR
PRSCDVGGGNAFPHNGQNLGLSPFLGTLNTGGSLPDLTNLHYSTPLPASLDTTDHHFGSM
SVGNSVNNIPAAMTHLGIRSSSGLQSSRSNPSIQATLNKTVLSSSLNNHPQTSVPNASAL
HPSLRLFSLSNPSLSTTNLSGPSRRRQPPVSPLTLSPGPEAHQGFSRQLSSTSPLAPYPT
SQMVSSDRSQLSFLPTEAQAQVSPPPPYPAPQELTQPLLQQPRAPEAPAQQPQAASSLPQ
SDFQLLPAQGSSLTNFFPDVGFDQQSMRPGPAFPQQVPLVQQGSRELQDSFHLRPSPYSN
CGSLPNTILPEDSSTSLFKDLNSALAGLPEVSLNVDTPFPLEEELQIEPLSLDGLNMLSD
SSMGLLDPSVEETFRADRL
NT seq
1860 nt
NT seq
+upstream
nt +downstream
nt
atggccgcctcgccgggctcgggcagcgccaacccgcggaagttcagtgagaagatcgcg
ctgcacacgcagagacaggccgaggagacgcgggccttcgagcagctcatgaccgacctc
accctgtcgcgggttcaatttcagaagcttcagcaactgcgccttacacagtaccatgga
ggatccttaccaaatgtgagccagctgcggagcagtgcgtcagagtttcagccgtcattt
caccaagctgataatgttcggggaacccgccatcacgggctggtggagaggccatccagg
aaccgcttccaccccctccaccgaaggtctggggacaagccagggcgacaatttgatggt
agtgcttttggagccaattattcctcacagcctctggatgagagttggccaaggcagcag
cctccttggaaagacgaaaagcatcctgggttcaggctgacatctgcacttaacaggacc
aattctgattctgctcttcacacgagtgctctgagtaccaagccccaggacccctatgga
ggagggggccagtcggcctggcctgccccatacatgggtttctgtgatggtgagaataat
ggacatggggaagtagcatctttccctggcccattgaaagaagagaatctgttaaatgtt
ccgaagccactgccaaaacaactgtgggagaccaaggagattcagtccctgtcaggacgc
cctcgatcctgtgatgttggaggtggcaatgcttttccacataatggtcaaaacctaggc
ctctcacccttcttggggaccttgaacactggagggtcattgccagatctaaccaacctc
cactactcgacacccctgccagcctccctggacaccaccgaccaccactttggcagtatg
agtgtggggaatagtgtgaacaacatcccagctgctatgacccacctgggtataagaagc
tcctctggtctccagagttctcggagtaacccctccatccaagccacgctcaataagact
gtgctttcctcttccttaaataaccacccacagacatctgttcccaacgcatctgctctt
cacccttcgctccgtctgttttcccttagcaacccatctctttccaccacaaacctgagc
ggcccgtctcggcgtcggcagcctcccgtcagccctctcacgctttctcctggccctgaa
gcacatcaaggtttcagcagacagctgtcttcaaccagcccactggccccatatcctacc
tcccagatggtgtcctcagaccgaagccaactttcctttctgcccacagaagctcaagcc
caggtgtcgccgccacccccttaccctgcaccccaggagctcacccagcccctcctgcag
cagccccgcgcccctgaggcccctgcccagcagccccaggcagcctcctcactgccacag
tcagactttcagcttctcccggcccagggctcatctttgaccaacttcttcccagatgtg
ggttttgaccagcagtccatgaggccaggccctgcctttcctcaacaggtgcctctggtg
caacaaggttcccgagaactgcaggactcttttcatttgagaccaagcccgtattccaac
tgcgggagtctcccgaacaccatcctgccagaagactccagcaccagcctgttcaaagac
ctcaacagtgcgctggcaggcctgcctgaggtcagcctgaacgtggacactccatttcca
ctggaagaggagctgcagattgaacccctgagcctggacggactcaacatgttaagtgac
tccagcatgggcctgctggacccctctgttgaagagacgtttcgagctgacagactgtga
DBGET
integrated database retrieval system
