Bos taurus Gene: MID1
Summary
InnateDB Gene IDBG-639068.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MID1
Gene Name midline-1
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000010152
Encoded Proteins
midline 1 (Opitz/BBB syndrome)
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
InnateDB Annotation from Orthologs
Summary
[Homo sapiens] MID1 was identified in a systematic screen for positive regulators of innate immune responses.
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000101871:
The protein encoded by this gene is a member of the tripartite motif (TRIM) family, also known as the 'RING-B box-coiled coil' (RBCC) subgroup of RING finger proteins. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein forms homodimers which associate with microtubules in the cytoplasm. The protein is likely involved in the formation of multiprotein structures acting as anchor points to microtubules. Mutations in this gene have been associated with the X-linked form of Opitz syndrome, which is characterized by midline abnormalities such as cleft lip, laryngeal cleft, heart defects, hypospadias, and agenesis of the corpus callosum. This gene was also the first example of a gene subject to X inactivation in human while escaping it in mouse. Multiple different transcript variants are generated by alternate splicing; however, the full-length nature of some of the variants has not been determined. [provided by RefSeq, Jul 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome X:139791005-139928580
Strand Forward strand
Band
Transcripts
ENSBTAT00000013398 ENSBTAP00000013398
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 23 interaction(s) predicted by orthology.
Predicted by orthology
Total 23 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0008017 microtubule binding
GO:0008270 zinc ion binding
GO:0031625 ubiquitin protein ligase binding
GO:0042803 protein homodimerization activity
GO:0046872 metal ion binding
GO:0046982 protein heterodimerization activity
GO:0051219 phosphoprotein binding
Biological Process
GO:0007026 negative regulation of microtubule depolymerization
GO:0032874 positive regulation of stress-activated MAPK cascade
GO:0035372 protein localization to microtubule
Cellular Component
GO:0005622 intracellular
GO:0005737 cytoplasm
GO:0005874 microtubule
GO:0005881 cytoplasmic microtubule
GO:0015630 microtubule cytoskeleton
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
KEGG
Ubiquitin mediated proteolysis pathway
Ubiquitin mediated proteolysis pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL E1BAD8
UniProt Splice Variant
Entrez Gene 534604
UniGene Bt.58809
RefSeq NM_001192822 XM_005228472 XM_005228473 XM_005228474 XM_005228475 XM_005228476 XM_005228477
HUGO HGNC:7095
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02075420
GenPept
RNA Seq Atlas 534604