This gene encodes a transcription factor that is required for central nervous system myelination and may regulate oligodendrocyte differentiation. It is thought to act by increasing the expression of genes that effect myelin production but may also directly promote myelin gene expression. Loss of a similar gene in mouse models results in severe demyelination. Alternative splici... See more...

Aliases for MYRF Gene

Aliases for MYRF Gene

  • Myelin Regulatory Factor 2 3 4 5
  • Myelin Gene Regulatory Factor 2 3 4
  • C11orf9 3 4
  • MRF 3 4
  • Chromosome 11 Open Reading Frame 9 2
  • EC 3.4.-.- 4
  • KIAA0954 4
  • 11orf9 3
  • Pqn-47 3
  • MMERV 3
  • Ndt80 3
  • CUGS 3

External Ids for MYRF Gene

Previous HGNC Symbols for MYRF Gene

  • C11orf9

Previous GeneCards Identifiers for MYRF Gene

  • GC11P061521

Summaries for MYRF Gene

Entrez Gene Summary for MYRF Gene

  • This gene encodes a transcription factor that is required for central nervous system myelination and may regulate oligodendrocyte differentiation. It is thought to act by increasing the expression of genes that effect myelin production but may also directly promote myelin gene expression. Loss of a similar gene in mouse models results in severe demyelination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]

GeneCards Summary for MYRF Gene

MYRF (Myelin Regulatory Factor) is a Protein Coding gene. Diseases associated with MYRF include Encephalitis/Encephalopathy, Mild, With Reversible Myelin Vacuolization and Cardiac-Urogenital Syndrome. Gene Ontology (GO) annotations related to this gene include DNA-binding transcription factor activity and peptidase activity. An important paralog of this gene is MYRFL.

UniProtKB/Swiss-Prot Summary for MYRF Gene

  • Myelin regulatory factor: Constitutes a precursor of the transcription factor. Mediates the autocatalytic cleavage that releases the Myelin regulatory factor, N-terminal component that specifically activates transcription of central nervous system (CNS) myelin genes (PubMed:23966832).
  • Myelin regulatory factor, C-terminal: Membrane-bound part that has no transcription factor activity and remains attached to the endoplasmic reticulum membrane following cleavage.
  • Myelin regulatory factor, N-terminal: Transcription factor that specifically activates expression of myelin genes such as MBP, MOG, MAG, DUSP15 and PLP1 during oligodendrocyte (OL) maturation, thereby playing a central role in oligodendrocyte maturation and CNS myelination. Specifically recognizes and binds DNA sequence 5'-CTGGYAC-3' in the regulatory regions of myelin-specific genes and directly activates their expression. Not only required during oligodendrocyte differentiation but is also required on an ongoing basis for the maintenance of expression of myelin genes and for the maintenance of a mature, viable oligodendrocyte phenotype (PubMed:23966832).

Additional gene information for MYRF Gene

No data available for CIViC Summary , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , Rfam classification and piRNA Summary for MYRF Gene

Genomics for MYRF Gene

GeneHancer (GH) Regulatory Elements for MYRF Gene

Promoters and enhancers for MYRF Gene
GeneHancer (GH) Identifier GH Type GH
Score
GH Sources Gene Association Score Total Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor
Binding Sites
Gene Targets
GH11J061752 Promoter/Enhancer 2.8 EPDnew FANTOM5 Ensembl ENCODE CraniofacialAtlas dbSUPER 768.9 +3.4 3400 7.8 SP1 CTCF RBPJ SMARCE1 NR2F1 NR2F6 MIXL1 MYC NFYC HLF MYRF MYRF-AS1 CPSF7 CSKMT MTA2 TMEM138 TUT1 GANAB AHNAK TTC9C
GH11J061751 Promoter/Enhancer 0.9 Ensembl dbSUPER 759 -1.3 -1336 1.4 DPF2 CTCF RCOR2 ZBTB48 ZNF766 ZKSCAN1 ZNF623 BCOR ZFHX2 ZMYM3 MYRF MYRF-AS1 piR-48834
GH11J061679 Promoter/Enhancer 2.3 EPDnew Ensembl ENCODE CraniofacialAtlas dbSUPER 22 -70.7 -70705 4.4 ZNF785 ZNF24 ZBTB40 CTCF SIX5 MLX RBPJ USF2 NR2F6 CREB1 DAGLA GANAB MYRF EML3 TMEM138 INTS5 MYRF-AS1 TMEM109 RN7SL23P EEF1G
GH11J061693 Promoter/Enhancer 1.8 FANTOM5 Ensembl ENCODE CraniofacialAtlas dbSUPER 20.9 -54.7 -54713 8.5 CTCF POLR2A USF2 ZNF217 MYC MAX MNT NCOA3 MAFK TFE3 MYRF MYRF-AS1 DAGLA SYT7 FTH1 CYB561A3 VWCE SDHAF2 DDB1 CPSF7
GH11J061728 Enhancer 1.1 Ensembl ENCODE 25.1 -21.5 -21536 6.6 CTCF TCF7L2 USF2 MYC CC2D1A HLF L3MBTL2 MAX ZNF121 DACH1 MYRF DAGLA MYRF-AS1 TMEM258 FEN1 MIR611 SYT7 piR-48834
- Elite GeneHancer and/or Elite GeneHancer-gene association Download GeneHancer data from 2017 publication | Request up-to-date GeneHancer data (full dataset)

GeneHancers around MYRF on UCSC Golden Path with GeneCards custom track

Genomic Locations for MYRF Gene

Genomic Locations for MYRF Gene
chr11:61,752,637-61,788,518
(GRCh38/hg38)
Size:
35,882 bases
Orientation:
Plus strand
chr11:61,520,114-61,555,990
(GRCh37/hg19)
Size:
35,877 bases
Orientation:
Plus strand

Genomic View for MYRF Gene

Genes around MYRF on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
MYRF Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for MYRF Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for MYRF Gene

Proteins for MYRF Gene

  • Protein details for MYRF Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    Q9Y2G1-MYRF_HUMAN
    Recommended name:
    Myelin regulatory factor
    Protein Accession:
    Q9Y2G1
    Secondary Accessions:
    • O43582
    • Q9P1Q6

    Protein attributes for MYRF Gene

    Size:
    1151 amino acids
    Molecular mass:
    124397 Da
    Quaternary structure:
    • Homotrimer (PubMed:23966832). Interacts (via C-terminal region) with TMEM98; the interaction inhibits MYRF self-cleavage (By similarity).
    SequenceCaution:
    • Sequence=BAA76798.2; Type=Erroneous initiation; Note=Translation N-terminally shortened.; Evidence={ECO:0000305};

    Three dimensional structures from OCA and Proteopedia for MYRF Gene

    Alternative splice isoforms for MYRF Gene

    UniProtKB/Swiss-Prot:

neXtProt entry for MYRF Gene

Post-translational modifications for MYRF Gene

  • Myelin regulatory factor, C-terminal: Glycosylated.
  • Myelin regulatory factor: Follows autocatalytic cleavage via the peptidase S74 domain. Autoprocessing is apparently constitutive and is essential for transcriptional activity (PubMed:23966832). Autocatalytic cleavage is inhibited by interaction with TMEM98 (By similarity).
  • Glycosylation at Asn919, Thr932, Ser938, Ser942, Ser954, Ser960, Asn1043, Asn1065, and Asn1129
  • Modification sites at PhosphoSitePlus

No data available for DME Specific Peptides for MYRF Gene

Domains & Families for MYRF Gene

Gene Families for MYRF Gene

Human Protein Atlas (HPA):
  • Plasma proteins
  • Predicted membrane proteins
  • Transcription factors

Protein Domains for MYRF Gene

Suggested Antigen Peptide Sequences for MYRF Gene

GenScript: Design optimal peptide antigens:
  • cDNA FLJ59324 (B4DHB2_HUMAN)
  • Myelin gene regulatory factor (MRF_HUMAN)

Graphical View of Domain Structure for InterPro Entry

Q9Y2G1

UniProtKB/Swiss-Prot:

MYRF_HUMAN :
  • Myelin regulatory factor, N-terminal: The nuclear localization signals mediate translocation to the nucleus.
  • Belongs to the MRF family.
Domain:
  • Myelin regulatory factor, N-terminal: The nuclear localization signals mediate translocation to the nucleus.
  • Myelin regulatory factor: The peptidase S74 domain, also named Intramolecular Chaperone Auto-processed (ICA) domain or Intramolecuar Chaperone Domain (ICD), has protease activity and mediates autocatalytic processing of the protein to generate the Myelin regulatory factor, N-terminal active transcription factor and the Myelin regulatory factor, C-terminal components.
Family:
  • Belongs to the MRF family.
genes like me logo Genes that share domains with MYRF: view

Function for MYRF Gene

Molecular function for MYRF Gene

UniProtKB/Swiss-Prot Function:
Myelin regulatory factor: Constitutes a precursor of the transcription factor. Mediates the autocatalytic cleavage that releases the Myelin regulatory factor, N-terminal component that specifically activates transcription of central nervous system (CNS) myelin genes (PubMed:23966832).
UniProtKB/Swiss-Prot Function:
Myelin regulatory factor, C-terminal: Membrane-bound part that has no transcription factor activity and remains attached to the endoplasmic reticulum membrane following cleavage.
UniProtKB/Swiss-Prot Function:
Myelin regulatory factor, N-terminal: Transcription factor that specifically activates expression of myelin genes such as MBP, MOG, MAG, DUSP15 and PLP1 during oligodendrocyte (OL) maturation, thereby playing a central role in oligodendrocyte maturation and CNS myelination. Specifically recognizes and binds DNA sequence 5'-CTGGYAC-3' in the regulatory regions of myelin-specific genes and directly activates their expression. Not only required during oligodendrocyte differentiation but is also required on an ongoing basis for the maintenance of expression of myelin genes and for the maintenance of a mature, viable oligodendrocyte phenotype (PubMed:23966832).

Enzyme Numbers (IUBMB) for MYRF Gene

Phenotypes From GWAS Catalog for MYRF Gene

Gene Ontology (GO) - Molecular Function for MYRF Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific ISM 19274049
GO:0003677 DNA binding IEA --
GO:0003700 DNA-binding transcription factor activity IBA 21873635
GO:0008233 peptidase activity IEA --
GO:0016787 hydrolase activity IEA --
genes like me logo Genes that share ontologies with MYRF: view
genes like me logo Genes that share phenotypes with MYRF: view

Human Phenotype Ontology for MYRF Gene

HPO Id HPO Name Alternative Ids Definition Synonyms

Animal Model Products

CRISPR Products

Inhibitory RNA Products

  • Search GeneCopoeia for shRNA, lentivirus and/or AAV clone products for MYRF

Clone Products

No data available for Animal Models , Transcription Factor Targets and HOMER Transcription for MYRF Gene

Localization for MYRF Gene

Subcellular locations from UniProtKB/Swiss-Prot for MYRF Gene

Myelin regulatory factor: Endoplasmic reticulum membrane; Single-pass membrane protein.
Myelin regulatory factor, N-terminal: Nucleus. Cytoplasm. Note=Translocates from the cytoplasm to the nucleus upon autocatalytic cleavage. {ECO:0000269 PubMed:23966832}.
Myelin regulatory factor, C-terminal: Endoplasmic reticulum membrane; Single-pass membrane protein.

Subcellular locations from

COMPARTMENTS
Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for MYRF gene
Compartment Confidence
nucleus 5
endoplasmic reticulum 4
cytosol 4
golgi apparatus 4

Subcellular locations from the

Human Protein Atlas (HPA)
  • Cytosol (2)
  • Nucleoplasm (2)
See all subcellular structures

Gene Ontology (GO) - Cellular Components for MYRF Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005634 nucleus ISS,IBA --
GO:0005654 nucleoplasm IDA --
GO:0005737 cytoplasm IBA 21873635
GO:0005783 endoplasmic reticulum IEA --
GO:0005789 endoplasmic reticulum membrane ISS --
genes like me logo Genes that share ontologies with MYRF: view

Pathways & Interactions for MYRF Gene

PathCards logo

SuperPathways for MYRF Gene

No Data Available

Interacting Proteins for MYRF Gene

STRING Interaction Network Preview (showing top 5 STRING interactants - click image to see top 25)
STRING Interaction Network
Selected Interacting proteins: ENSP00000278836 Q9Y2G1-MYRF_HUMAN for MYRF Gene via STRING IID

Gene Ontology (GO) - Biological Process for MYRF Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0006355 regulation of transcription, DNA-templated IEA --
GO:0006357 regulation of transcription by RNA polymerase II IEA --
GO:0006508 proteolysis IEA --
GO:0014003 oligodendrocyte development ISS --
GO:0016540 protein autoprocessing ISS --
genes like me logo Genes that share ontologies with MYRF: view

No data available for Pathways by source and SIGNOR curated interactions for MYRF Gene

Drugs & Compounds for MYRF Gene

No Compound Related Data Available

Transcripts for MYRF Gene

mRNA/cDNA for MYRF Gene

CRISPR Products

Inhibitory RNA Products

  • Search GeneCopoeia for shRNA, lentivirus and/or AAV clone products for MYRF

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for MYRF Gene

ExUns: 1 ^ 2 ^ 3 ^ 4 ^ 5 ^ 6 ^ 7 ^ 8a · 8b ^ 9a · 9b ^ 10 ^ 11 ^ 12a · 12b ^ 13a · 13b ^ 14a · 14b · 14c ^ 15 ^ 16 ^ 17a · 17b ^ 18a · 18b ^
SP1:
SP2:
SP3:
SP4:
SP5:
SP6:
SP7:
SP8:
SP9:
SP10:
SP11:
SP12: - - - - - - - -
SP13:
SP14:
SP15:
SP16:
SP17:
SP18:
SP19:

ExUns: 19a · 19b ^ 20a · 20b ^ 21 ^ 22 ^ 23a · 23b ^ 24a · 24b · 24c · 24d ^ 25a · 25b · 25c · 25d · 25e ^ 26a · 26b · 26c ^ 27 ^ 28 ^ 29a · 29b ^ 30
SP1: -
SP2: -
SP3: -
SP4: - -
SP5: -
SP6:
SP7:
SP8:
SP9: -
SP10:
SP11: -
SP12: - - - - - - - - - -
SP13:
SP14:
SP15:
SP16:
SP17: - -
SP18:
SP19:

Relevant External Links for MYRF Gene

GeneLoc Exon Structure for
MYRF
ECgene alternative splicing isoforms for
MYRF

Expression for MYRF Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and CGAP SAGE for MYRF Gene

mRNA expression in embryonic tissues and stem cells from LifeMap Discovery

mRNA differential expression in normal tissues according to GTEx for MYRF Gene

This gene is overexpressed in Brain - Spinal cord (cervical c-1) (x8.6), Brain - Substantia nigra (x5.5), Stomach (x4.2), and Brain - Hippocampus (x4.1).

Protein differential expression in normal tissues from HIPED for MYRF Gene

This gene is overexpressed in Cerebrospinal fluid (49.9) and Urinary Bladder (19.1).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB, MaxQB, and MOPED for MYRF Gene



Protein tissue co-expression partners for MYRF Gene

NURSA nuclear receptor signaling pathways regulating expression of MYRF Gene:

MYRF

SOURCE GeneReport for Unigene cluster for MYRF Gene:

Hs.473109

mRNA Expression by UniProt/SwissProt for MYRF Gene:

Q9Y2G1-MYRF_HUMAN
Tissue specificity: Expressed in lung, ARPE-19 cell line, brainstem, uterus and, to a lesser extent, in basal ganglion and liver. Weakly expressed in cerebellum and retina.

Evidence on tissue expression from TISSUES for MYRF Gene

  • Nervous system(4.9)
  • Muscle(2.4)
genes like me logo Genes that share expression patterns with MYRF: view

No data available for Phenotype-based relationships between genes and organs from Gene ORGANizer for MYRF Gene

Orthologs for MYRF Gene

This gene was present in the common ancestor of animals.

Orthologs for MYRF Gene

Organism Taxonomy Gene Similarity Type Details
chimpanzee
(Pan troglodytes)
Mammalia MYRF 33
  • 100 (a)
OneToOne
C11H11orf9 32
  • 96.69 (n)
dog
(Canis familiaris)
Mammalia MYRF 33
  • 90 (a)
OneToOne
C18H11orf9 32
  • 89.83 (n)
cow
(Bos Taurus)
Mammalia MYRF 33 32
  • 89.67 (n)
OneToOne
rat
(Rattus norvegicus)
Mammalia Myrf 32
  • 86.88 (n)
mouse
(Mus musculus)
Mammalia Myrf 17 33 32
  • 86.58 (n)
platypus
(Ornithorhynchus anatinus)
Mammalia MYRF 33
  • 63 (a)
OneToOne
chicken
(Gallus gallus)
Aves C5H11ORF9 32
  • 73.76 (n)
MYRF 33
  • 67 (a)
OneToOne
lizard
(Anolis carolinensis)
Reptilia MYRF 33
  • 64 (a)
OneToOne
tropical clawed frog
(Silurana tropicalis)
Amphibia myrf 32
  • 65.14 (n)
zebrafish
(Danio rerio)
Actinopterygii myrf 33 32
  • 62.41 (n)
OneToOne
fruit fly
(Drosophila melanogaster)
Insecta CG3328 33
  • 20 (a)
OneToMany
worm
(Caenorhabditis elegans)
Secernentea pqn-47 33
  • 25 (a)
ManyToMany
F21A10.2 33
  • 23 (a)
ManyToMany
sea squirt
(Ciona savignyi)
Ascidiacea -- 33
  • 56 (a)
OneToMany
Species where no ortholog for MYRF was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Ashbya gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • African clawed frog (Xenopus laevis)
  • African malaria mosquito (Anopheles gambiae)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • baker's yeast (Saccharomyces cerevisiae)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • bread mold (Neurospora crassa)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • fission yeast (Schizosaccharomyces pombe)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • K. lactis yeast (Kluyveromyces lactis)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • oppossum (Monodelphis domestica)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • rainbow trout (Oncorhynchus mykiss)
  • rice (Oryza sativa)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • soybean (Glycine max)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • thale cress (Arabidopsis thaliana)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • wheat (Triticum aestivum)

Evolution for MYRF Gene

ENSEMBL:
Gene Tree for MYRF (if available)
TreeFam:
Gene Tree for MYRF (if available)
Aminode:
Evolutionary constrained regions (ECRs) for MYRF: view image

Paralogs for MYRF Gene

Paralogs for MYRF Gene

(1) SIMAP similar genes for MYRF Gene using alignment to 3 proteins:

  • MRF_HUMAN
  • B4DHB2_HUMAN
  • O60428_HUMAN
genes like me logo Genes that share paralogs with MYRF: view

Variants for MYRF Gene

Sequence variations from dbSNP and Humsavar for MYRF Gene

SNP ID Clin Chr 11 pos Variation AA Info Type
rs1057518279 uncertain-significance, pathogenic, not specified, CARDIAC-UROGENITAL SYNDROME 61,779,931(+) G/A splice_donor_variant
rs1382225004 pathogenic, CARDIAC-UROGENITAL SYNDROME 61,779,333(+) G/A coding_sequence_variant, missense_variant
rs1565286228 pathogenic, CARDIAC-UROGENITAL SYNDROME 61,766,173(+) GCACCGGGCCCCCCATC/T 5_prime_UTR_variant, coding_sequence_variant, frameshift, genic_upstream_transcript_variant
rs1565295286 pathogenic, ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION 61,774,059(+) A/G coding_sequence_variant, missense_variant
rs1565295395 pathogenic, CARDIAC-UROGENITAL SYNDROME 61,774,104(+) AGA/AGAGA coding_sequence_variant, frameshift

Structural Variations from Database of Genomic Variants (DGV) for MYRF Gene

Variant ID Type Subtype PubMed ID
nsv343 CNV insertion 18451855
nsv528697 CNV loss 19592680
nsv832179 CNV loss 17160897
nsv952459 CNV deletion 24416366

Variation tolerance for MYRF Gene

Residual Variation Intolerance Score: 10.9% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 3.27; 52.92% of all genes are more intolerant (likely to be disease-causing)

Additional Variant Information for MYRF Gene

SNPedia medical, phenotypic, and genealogical associations of SNPs for
MYRF

SNP Genotyping and Copy Number Assay Products

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for MYRF Gene

Disorders for MYRF Gene

MalaCards: The human disease database

(6) MalaCards diseases for MYRF Gene - From: OMIM, ClinVar, DISEASES, and GeneCards

- elite association - COSMIC cancer census association via MalaCards
Search MYRF in MalaCards View complete list of genes associated with diseases

UniProtKB/Swiss-Prot

MYRF_HUMAN
  • Encephalitis/encephalopathy, mild, with reversible myelin vacuolization (MMERV) [MIM:618113]: An autosomal dominant disease characterized by episodes of acute encephalitis associated with impaired consciousness, delirious behavior, seizures, and reversible splenial lesions observed on diffusion magnetic resonance imaging. Most patients completely recover and there are no neurologic sequelae. MMERV occurs in children and is frequently associated with a trigger, such as a febrile illness. {ECO:0000269 PubMed:29265453}. Note=The disease may be caused by mutations affecting the gene represented in this entry.
  • Cardiac-urogenital syndrome (CUGS) [MIM:618280]: An autosomal dominant syndrome characterized by partial anomalous pulmonary venous return, tracheal anomalies, pulmonary hypoplasia, congenital diaphragmatic hernia, thyroid fibrosis, thymic involution, cleft spleen, penoscrotal hypospadias, and cryptorchidism. {ECO:0000269 PubMed:29446546, ECO:0000269 PubMed:30070761, ECO:0000269 PubMed:30532227}. Note=The disease is caused by mutations affecting the gene represented in this entry.

Additional Disease Information for MYRF

genes like me logo Genes that share disorders with MYRF: view

No data available for Genatlas for MYRF Gene

Publications for MYRF Gene

  1. 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. (PMID: 10828591) Stöhr H … Weber BH (Cytogenetics and cell genetics 2000) 2 3 4 56
  2. De novo variants in Myelin regulatory factor (MYRF) as candidates of a new syndrome of cardiac and urogenital anomalies. (PMID: 29446546) Pinz H … Bhoj EJ (American journal of medical genetics. Part A 2018) 3 4 56
  3. De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders. (PMID: 30532227) Qi H … Shen Y (PLoS genetics 2018) 3 4 56
  4. MYRF is associated with encephalopathy with reversible myelin vacuolization. (PMID: 29265453) Kurahashi H … Okumura A (Annals of neurology 2018) 3 4 56
  5. A Bacteriophage tailspike domain promotes self-cleavage of a human membrane-bound transcription factor, the myelin regulatory factor MYRF. (PMID: 23966832) Li Z … Marcotte EM (PLoS biology 2013) 3 4 56

Products for MYRF Gene

Sources for MYRF Gene