Sequence of MYRF_HUMAN
EC Number:3.4
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
Other sequences found for EC No. 3.4
General information:
Sequence
0 MEVVDETEAL QRFFEGHDIN GALEPSNIDT SILEEYISKE DASDLCFPDI SAPASSASYS
60 HGQPAMPGSS GVHHLSPPGG GPSPGRHGPL PPPGYGTPLN CNNNNGMGAA PKPFPGGTGP
120 PIKAEPKAPY APGTLPDSPP DSGSEAYSPQ QVNEPHLLRT ITPETLCHVG VPSRLEHPPP
180 PPAHLPGPPP PPPPPPHYPV LQRDLYMKAE PPIPHYAAMG QGLVPTDLHH TQQSQMLHQL
240 LQQHGAELPT HPSKKRKHSE SPPSTLNAQM LNGMIKQEPG TVTALPLHPT RAPSPPWPPQ
300 GPLSPGPGSL PLSIARVQTP PWHPPGAPSP GLLQDSDSLS GSYLDPNYQS IKWQPHQQNK
360 WATLYDANYK ELPMLTYRVD ADKGFNFSVG DDAFVCQKKN HFQVTVYIGM LGEPKYVKTP
420 EGLKPLDCFY LKLHGVKLEA LNQSINIEQS QSDRSKRPFN PVTVNLPPEQ VTKVTVGRLH
480 FSETTANNMR KKGKPNPDQR YFMLVVALQA HAQNQNYTLA AQISERIIVR ASNPGQFESD
540 SDVLWQRAQV PDTVFHHGRV GINTDRPDEA LVVHGNVKVM GSLMHPSDLR AKEHVQEVDT
600 TEQLKRISRM RLVHYRYKPE FAASAGIEAT APETGVIAQE VKEILPEAVK DTGDMVFANG
660 KTIENFLVVN KERIFMENVG AVKELCKLTD NLETRIDELE RWSHKLAKLR RLDSLKSTGS
720 SGAFSHAGSQ FSRAGSVPHK KRPPKVASKS SSVVPDQACI SQRFLQGTII ALVVVMAFSV
780 VSMSTLYVLS LRTEEDLVDT DGSFAVSTSC LLALLRPQPP GGSEALCPWS SQSFGTTQLR
840 QSPLTTGLPG IQPSLLLVTT SLTSSAPGSA VRTLDMCSSH PCPVICCSSP TTNPTTGPSL
900 GPSFNPGHVL SPSPSPSTNR SGPSQMALLP VTNIRAKSWG LSVNGIGHSK HHKSLEPLAS
960 PAVPFPGGQG KAKNSPSLGF HGRARRGALQ SSVGPAEPTW AQGQSASLLA EPVPSLTSIQ
1020 VLENSMSITS QYCAPGDACR PGNFTYHIPV SSGTPLHLSL TLQMNSSSPV SVVLCSLRSK
1080 EEPCEEGSLP QSLHTHQDTQ GTSHRWPITI LSFREFTYHF RVALLGQANC SSEALAQPAT
1140 DYHFHFYRLC D
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Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
192994
Stoehr H.,Marquardt A.,White K.,Weber B.H.F.
cDNA cloning and genomic structure of a novel gene (C11orf9) localized to chromosome 11q12-->q13.1 which encodes a highly conserved, potential membrane-associated protein.
Cytogenet. Cell Genet.
88
211-216
2000
192995
Nagase T.,Ishikawa K.,Suyama M.,Kikuno R.,Hirosawa M.,Miyajima N.,Tanaka A.,Kotani H.,Nomura N.,Ohara O.
Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
DNA Res.
6
63-70
1999
192996
Nakajima D.,Okazaki N.,Yamakawa H.,Kikuno R.,Ohara O.,Nagase T.
Construction of expression-ready cDNA clones for KIAA genes: manual curation of 330 KIAA cDNA clones.
DNA Res.
9
99-106
2002
192998
Cooper P.R.,Nowak N.J.,Higgins M.J.,Church D.M.,Shows T.B.
Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes.
Genomics
49
419-429
1998
192999
Choudhary C.,Kumar C.,Gnad F.,Nielsen M.L.,Rehman M.,Walther T.C.,Olsen J.V.,Mann M.
Lysine acetylation targets protein complexes and co-regulates major cellular functions.
Science
325
834-840
2009
193000
Li Z.,Park Y.,Marcotte E.M.
A bacteriophage tailspike domain promotes self-cleavage of a human membrane-bound transcription factor, the myelin regulatory factor MYRF.
PLoS Biol.
11
0-0
2013
193001
Kurahashi H.,Azuma Y.,Masuda A.,Okuno T.,Nakahara E.,Imamura T.,Saitoh M.,Mizuguchi M.,Shimizu T.,Ohno K.,Okumura A.
MYRF is associated with encephalopathy with reversible myelin vacuolization.
Ann. Neurol.
83
98-106
2018
193002
Pinz H.,Pyle L.C.,Li D.,Izumi K.,Skraban C.,Tarpinian J.,Braddock S.R.,Telegrafi A.,Monaghan K.G.,Zackai E.,Bhoj E.J.
De novo variants in Myelin regulatory factor (MYRF) as candidates of a new syndrome of cardiac and urogenital anomalies.
Am. J. Med. Genet. A
176
969-972
2018
193003
Chitayat D.,Shannon P.,Uster T.,Nezarati M.M.,Schnur R.E.,Bhoj E.J.
An additional individual with a de novo variant in myelin regulatory factor (MYRF) with cardiac and urogenital anomalies: Further proof of causality: Comments on the article by Pinz et al.
Am. J. Med. Genet. A
176
2041-2043
2018
193004
Qi H.,Yu L.,Zhou X.,Wynn J.,Zhao H.,Guo Y.,Zhu N.,Kitaygorodsky A.,Hernan R.,Aspelund G.,Lim F.Y.,Crombleholme T.,Cusick R.,Azarow K.,Danko M.E.,Chung D.,Warner B.W.,Mychaliska G.B.,Potoka D.,Wagner A.J.,ElFiky M.,Wilson J.M.,Nickerson D.,Bamshad M.,High F.A.,Longoni M.,Donahoe P.K.,Chung W.K.,Shen Y.
De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders.
PLoS Genet.
14
0-0
2018
193005
Chen B.,Zhu Y.,Ye S.,Zhang R.
Structure of the DNA-binding domain of human myelin-gene regulatory factor reveals its potential protein-DNA recognition mode.
J. Struct. Biol.
203
170-178
2018
