KEGG   Homo sapiens (human): 79816
Entry
79816             CDS       T01001                                 
Symbol
TLE6, GRG6, OZEMA15, PREMBL
Name
(RefSeq) transducin-like enhancer protein 6 isoform 1
  KO
K04497  groucho
Organism
hsa  Homo sapiens (human)
Pathway
hsa04310  Wnt signaling pathway
hsa04330  Notch signaling pathway
Disease
H01897  Oocyte/zygote/embryo maturation arrest
H02335  Preimplantation embryonic lethality
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    79816 (TLE6)
   04330 Notch signaling pathway
    79816 (TLE6)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04812 Cytoskeleton proteins [BR:hsa04812]
    79816 (TLE6)
Cytoskeleton proteins [BR:hsa04812]
 Eukaryotic cytoskeleton proteins
  Actin filaments / Microfilaments
   Actin-binding proteins
    ADF / Cofilin
     SCMC complex
      79816 (TLE6)
SSDB
Motif
Pfam: Beta-prop_IFT122_1st Beta-prop_EML_2 Beta-prop_THOC3 Beta-prop_WDR5 WD40 Beta-prop_WDR3_1st WD40_Prp19 WDR55 Beta-prop_WDR3_2nd WD40_CDC20-Fz Beta-prop_WDR36-Utp21_2nd Beta-prop_TEP1_2nd WD40_WDHD1_1st DSE1_N WD40_Gbeta Beta-prop_VPS8 WDR90_beta-prop_4th Beta-prop_WDR36-Utp21_1st
Other DBs
NCBI-GeneID: 79816
NCBI-ProteinID: NP_001137458
OMIM: 612399
HGNC: 30788
Ensembl: ENSP00000246112.3
UniProt: Q9H808
Structure
LinkDB
Position
19:2977401..2995179
AA seq 572 aa
MTSRDQPRPKGPPKSTSPCPGISNSESSPTLNYQGILNRLKQFPRFSPHFAAELESIYYS
LHKIQQDVAEHHKQIGNVLQIVESCSQLQGFQSEEVSPAEPASPGTPQQVKDKTLQESSF
EDIMATRSSDWLRRPLGEDNQPETQLFWDKEPWFWHDTLTEQLWRIFAGVHDEKAKPRDR
QQAPGLGQESKAPGSCDPGTDPCPEDASTPRPPEASSSPPEGSQDRNTSWGVVQEPPGRA
SRFLQSISWDPEDFEDAWKRPDALPGQSKRLAVPCKLEKMRILAHGELVLATAISSFTRH
VFTCGRRGIKVWSLTGQVAEDRFPESHLPIQTPGAFLRTCLLSSNSRSLLTGGYNLASVS
VWDLAAPSLHVKEQLPCAGLNCQALDANLDANLAFASFTSGVVRIWDLRDQSVVRDLKGY
PDGVKSIVVKGYNIWTGGPDACLRCWDQRTIMKPLEYQFKSQIMSLSHSPQEDWVLLGMA
NGQQWLQSTSGSQRHMVGQKDSVILSVKFSPFGQWWASVGMDDFLGVYSMPAGTKVFEVP
EMSPVTCCDVSSNNRLVVTGSGEHASVYQITY
NT seq 1719 nt   +upstreamnt  +downstreamnt
atgacctctagggaccagcccagacccaagggccccccgaaaagcacttcgccttgtcct
gggatctcgaactctgagagctctccgacgctgaattatcagggcattctaaatcggctc
aagcagttccccaggttttctcctcattttgctgcggagttggagagcatttactactcg
ctgcacaagatccagcaggatgtggcagaacatcacaagcagataggaaacgtcttacag
attgtggagagctgcagccaactccagggtttccagtctgaggaggtctcacctgctgaa
ccagccagccctgggacgccccagcaggtgaaggacaagaccctgcaggagtcgagcttt
gaggacatcatggccaccaggtcctccgactggctccggcggcctttgggggaggacaat
cagccggagacccagctgttctgggacaaggagccttggttttggcacgacactctgacc
gagcaactctggcggatttttgccggcgtccacgatgagaaggcaaagcccagagacaga
cagcaggcaccaggcctggggcaggaaagcaaggcaccaggatcctgtgacccaggaaca
gacccatgtcctgaagatgcctccacccccaggccacctgaggcctcctccagtccccct
gagggttcccaagacaggaacacaagttggggtgtggtccaggagcctcctggaagagcc
tctcggtttctacagtccatatcctgggaccctgaggactttgaagatgcatggaagagg
ccagatgccttgcccgggcagtcaaagagactcgccgtcccgtgcaaactggaaaagatg
cggatcttggcacacggggagctcgtgctcgccacggccatcagcagcttcacgcggcac
gtgttcacctgtggcagaagaggcatcaaggtgtggagcctgactggacaggtggctgag
gacaggttccctgagagccacctgcctatacagacccctggggccttcctgcgcacctgc
ctgctgtcctcaaacagcaggagcctgctcaccggtggctacaacctggccagcgtgagc
gtgtgggacctggcggcgccctccctgcatgtgaaggagcagttgccctgtgcaggtctc
aactgccaggccctggatgccaacctggatgccaacctggccttcgccagcttcaccagt
ggtgtggtcaggatctgggacctgcgggatcagagtgtggtcagggacctcaagggttat
cctgatggagtcaagagtatcgtggtcaagggctacaacatctggactgggggtccggat
gcctgtctgcggtgctgggaccagaggaccatcatgaaacctctggagtaccaattcaag
tctcagataatgagcctgtcccacagcccccaggaggactgggtgctgctgggcatggcc
aatggccagcagtggctgcaaagcaccagcgggagccagcggcacatggtggggcaaaaa
gacagcgtcatcctgagcgtcaagttctccccctttggccagtggtgggcaagcgttgga
atggacgacttccttggcgtctacagcatgccggcggggacaaaagtgttcgaggtgcct
gagatgtctccagtcacgtgctgtgacgtctcttccaacaaccgcctcgttgtcacaggc
tccggggagcacgcctccgtgtaccagatcacctactga

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