Homo sapiens (human): 9442
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Entry
9442 CDS
T01001
Symbol
MED27, CRAP34, CRSP34, CRSP8, MED3, NEDSCAC, TRAP37
Name
(RefSeq) mediator complex subunit 27
KO
K15170
mediator of RNA polymerase II transcription subunit 27
Organism
hsa
Homo sapiens (human)
Pathway
hsa04919
Thyroid hormone signaling pathway
Disease
H02470
Neurodevelopmental disorder with structural brain abnormalities
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09152 Endocrine system
04919 Thyroid hormone signaling pathway
9442 (MED27)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03021 Transcription machinery [BR:
hsa03021
]
9442 (MED27)
Transcription machinery [BR:
hsa03021
]
Eukaryotic type
RNA polymerase II system
Mediator complex
Other mediators
9442 (MED27)
BRITE hierarchy
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Ortholog
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Gene cluster
GFIT
Motif
Pfam:
Med27
Motif
Other DBs
NCBI-GeneID:
9442
NCBI-ProteinID:
NP_004260
OMIM:
605044
HGNC:
2377
Ensembl:
ENSG00000160563
UniProt:
Q6P2C8
Structure
PDB
PDBj
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All DBs
Position
9:complement(131860112..132079867)
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AA seq
311 aa
AA seq
DB search
MADVINVSVNLEAFSQAISAIQALRSSVSRVFDCLKDGMRNKETLEGREKAFIAHFQDNL
HSVNRDLNELERLSNLVGKPSENHPLHNSGLLSLDPVQDKTPLYSQLLQAYKWSNKLQYH
AGLASGLLNQQSLKRSANQMGVSAKRRPKAQPTTLVLPPQYVDDVISRIDRMFPEMSIHL
SRPNGTSAMLLVTLGKVLKVIVVMRSLFIDRTIVKGYNENVYTEDGKLDIWSKSNYQVFQ
KVTDHATTALLHYQLPQMPDVVVRSFMTWLRSYIKLFQAPCQRCGKFLQDGLPPTWRDFR
TLEAFHDTCRQ
NT seq
936 nt
NT seq
+upstream
nt +downstream
nt
atggcggacgtgataaatgtcagtgtgaacctggaggccttttcccaggccattagtgcc
atccaggcgctgcgctccagcgtgagcagggtgttcgactgcctgaaggatgggatgcgg
aacaaggagacgctggagggccgggagaaggcctttattgcgcacttccaggacaactta
cattcggtcaaccgggacctcaatgagctggaacgtctgagcaatctggtaggcaagcca
tctgagaaccatcctcttcataacagtgggctgttaagcctggatcctgtgcaggacaaa
actcctctctatagtcaactccttcaagcatataagtggtcaaacaagttgcagtaccat
gcaggactagcatctggccttttaaatcagcagtcattgaagcgttccgctaatcagatg
ggagtatctgccaaacgtagaccaaaggctcagcccacaactcttgtcctaccacctcaa
tatgttgatgatgtgatcagccgcattgacaggatgtttcctgaaatgtccatccactta
tccagacccaatggaacatcagcaatgcttctggtgaccttgggaaaggtgttgaaagtg
atcgtcgtcatgcggagcctgttcattgatcgaacaatagtaaagggatataacgagaat
gtctacacagaagatggcaagcttgatatatggtccaaatccaactatcaagtattccag
aaggtgacagaccatgccaccactgccctgctccactatcagctgccccagatgccggat
gtcgtggtccgatccttcatgacctggttaagaagttacataaagctgttccaggccccg
tgccagcgctgcgggaagtttctgcaggacggccttcccccgacatggagggatttccga
accctcgaagccttccatgacacctgccggcagtag
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