Homo sapiens (human): 54973
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Entry
54973 CDS
T01001
Symbol
INTS11, CPSF3L, CPSF73L, INT11, NEDMLOB, PSF3L, RC-68, RC68
Name
(RefSeq) integrator complex subunit 11
KO
K13148
integrator complex subunit 11 [EC:3.1.27.-]
Organism
hsa
Homo sapiens (human)
Disease
H02470
Neurodevelopmental disorder with structural brain abnormalities
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03041 Spliceosome [BR:
hsa03041
]
54973 (INTS11)
Spliceosome [BR:
hsa03041
]
Other splicing related proteins
Proteins involved in snRNP biogenesis
Integrator complex
54973 (INTS11)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
IntS11_C
Beta-Casp
Lactamase_B_6
RMMBL
Lactamase_B
Lactamase_B_2
Lactamase_B_3
Beta_lactamase3
Motif
Other DBs
NCBI-GeneID:
54973
NCBI-ProteinID:
NP_060341
OMIM:
611354
HGNC:
26052
Ensembl:
ENSG00000127054
UniProt:
Q5TA45
Structure
PDB
PDBj
LinkDB
All DBs
Position
1:complement(1311600..1324660)
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AA seq
600 aa
AA seq
DB search
MPEIRVTPLGAGQDVGRSCILVSIAGKNVMLDCGMHMGFNDDRRFPDFSYITQNGRLTDF
LDCVIISHFHLDHCGALPYFSEMVGYDGPIYMTHPTQAICPILLEDYRKIAVDKKGEANF
FTSQMIKDCMKKVVAVHLHQTVQVDDELEIKAYYAGHVLGAAMFQIKVGSESVVYTGDYN
MTPDRHLGAAWIDKCRPNLLITESTYATTIRDSKRCRERDFLKKVHETVERGGKVLIPVF
ALGRAQELCILLETFWERMNLKVPIYFSTGLTEKANHYYKLFIPWTNQKIRKTFVQRNMF
EFKHIKAFDRAFADNPGPMVVFATPGMLHAGQSLQIFRKWAGNEKNMVIMPGYCVQGTVG
HKILSGQRKLEMEGRQVLEVKMQVEYMSFSAHADAKGIMQLVGQAEPESVLLVHGEAKKM
EFLKQKIEQELRVNCYMPANGETVTLPTSPSIPVGISLGLLKREMAQGLLPEAKKPRLLH
GTLIMKDSNFRLVSSEQALKELGLAEHQLRFTCRVHLHDTRKEQETALRVYSHLKSVLKD
HCVQHLPDGSVTVESVLLQAAAPSEDPGTKVLLVSWTYQDEELGSFLTSLLKKGLPQAPS
NT seq
1803 nt
NT seq
+upstream
nt +downstream
nt
atgcctgagatcagagtcacgcccttgggggccggccaggacgtgggccgaagctgcatc
ctggtctccattgcgggcaagaatgtcatgctggactgtggaatgcacatgggcttcaat
gacgaccgacgcttccctgacttctcctacatcacccagaacggccgcctaacagacttc
ctggactgtgtgatcattagccacttccacctggaccactgcggggcactcccctacttc
agcgagatggtgggctacgacgggcccatctacatgactcaccccacccaggccatctgc
cccatcttgctggaggactaccgcaagatcgccgtagacaagaagggcgaggccaacttc
ttcacctcccagatgatcaaagactgcatgaagaaggtggtggctgtccacctccaccag
acggtccaggtagatgatgagctggagatcaaggcctactatgcaggccacgtgctgggg
gcagccatgttccagattaaagtgggctcagagtctgtggtctacacgggtgattataac
atgaccccagaccgacacttaggagctgcctggattgacaagtgccgccccaacctgctc
atcacagagtccacgtacgccacgaccatccgtgactccaagcgctgccgggagcgagac
ttcctgaagaaagtccacgagaccgtggagcgtggtgggaaggtgctgatacctgtgttc
gcgctgggccgcgcccaggagctctgcatcctcctggagaccttctgggagcgcatgaac
ctgaaggtgcccatctacttctccacggggctgaccgagaaggccaaccactactacaag
ctgttcatcccctggaccaaccagaagatccgcaagactttcgtgcagaggaacatgttt
gagttcaagcacatcaaggccttcgaccgggcttttgctgacaacccaggaccgatggtt
gtgtttgccacgccaggaatgctgcacgctgggcagtccctgcagatcttccggaaatgg
gccggaaacgaaaagaacatggtcatcatgcccggctactgcgtgcagggcaccgtcggc
cacaagatcctcagcgggcagcggaagctcgagatggaggggcggcaggtgctggaggtc
aagatgcaggtggagtacatgtcattcagcgcacacgcggacgccaagggcatcatgcag
ctggtgggccaggcagagccggagagcgtgctgctggtgcatggcgaggccaagaagatg
gagttcctgaagcagaagatcgagcaggagctccgggtcaactgctacatgccggccaat
ggcgagacggtgacgctgcccacaagccccagcatccccgtaggcatctcgctggggctg
ctgaagcgggagatggcgcaggggctgctccctgaggccaagaagcctcggctcctgcac
ggcaccctgatcatgaaggacagcaacttccggctggtgtcctcagagcaagccctcaaa
gagctgggtctggctgagcaccagctgcgcttcacctgccgcgtgcacctgcatgacaca
cgcaaggagcaggagacggcattgcgcgtctacagccacctcaagagcgtcctgaaggac
cactgtgtgcagcacctcccagacggctctgtgactgtggagtccgtcctcctccaggcc
gccgccccttctgaggacccaggcaccaaggtgctgctggtctcctggacctaccaggac
gaggagctggggagcttcctcacatctctgctgaagaagggcctcccccaggcccccagc
tga
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