Homo sapiens (human): 79816
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Entry
79816 CDS
T01001
Symbol
TLE6, GRG6, OZEMA15, PREMBL
Name
(RefSeq) TLE family member 6, subcortical maternal complex member
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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
WD40
Motif
Other DBs
NCBI-GeneID:
79816
NCBI-ProteinID:
NP_001137458
OMIM:
612399
HGNC:
30788
Ensembl:
ENSG00000104953
UniProt:
Q9H808
LinkDB
All DBs
Position
19:2977401..2995179
Genome browser
AA seq
572 aa
AA seq
DB search
MTSRDQPRPKGPPKSTSPCPGISNSESSPTLNYQGILNRLKQFPRFSPHFAAELESIYYS
LHKIQQDVAEHHKQIGNVLQIVESCSQLQGFQSEEVSPAEPASPGTPQQVKDKTLQESSF
EDIMATRSSDWLRRPLGEDNQPETQLFWDKEPWFWHDTLTEQLWRIFAGVHDEKAKPRDR
QQAPGLGQESKAPGSCDPGTDPCPEDASTPRPPEASSSPPEGSQDRNTSWGVVQEPPGRA
SRFLQSISWDPEDFEDAWKRPDALPGQSKRLAVPCKLEKMRILAHGELVLATAISSFTRH
VFTCGRRGIKVWSLTGQVAEDRFPESHLPIQTPGAFLRTCLLSSNSRSLLTGGYNLASVS
VWDLAAPSLHVKEQLPCAGLNCQALDANLDANLAFASFTSGVVRIWDLRDQSVVRDLKGY
PDGVKSIVVKGYNIWTGGPDACLRCWDQRTIMKPLEYQFKSQIMSLSHSPQEDWVLLGMA
NGQQWLQSTSGSQRHMVGQKDSVILSVKFSPFGQWWASVGMDDFLGVYSMPAGTKVFEVP
EMSPVTCCDVSSNNRLVVTGSGEHASVYQITY
NT seq
1719 nt
NT seq
+upstream
nt +downstream
nt
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
DBGET
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