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MID1 (midline 1)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4281
Gene nameGene Name - the full gene name approved by the HGNC.
Midline 1
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
MID1
SynonymsGene synonyms aliases
BBBG1, FXY, GBBB, GBBB1, MIDIN, OGS1, OS, OSX, RNF59, TRIM18, XPRF, ZNFXY
ChromosomeChromosome number
X
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xp22.2
SummarySummary of gene provided in NCBI Entrez Gene.
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
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs28934611 A>G Pathogenic Coding sequence variant, missense variant, genic downstream transcript variant
rs104894865 C>A,G,T Pathogenic Coding sequence variant, stop gained, missense variant
rs104894866 A>G Pathogenic Coding sequence variant, missense variant, genic downstream transcript variant
rs138558359 G>A Conflicting-interpretations-of-pathogenicity Coding sequence variant, missense variant, genic downstream transcript variant
rs138629923 G>A Conflicting-interpretations-of-pathogenicity, benign Coding sequence variant, synonymous variant, genic downstream transcript variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT031316 hsa-miR-18a-5p Sequencing 20371350
MIRT045601 hsa-miR-149-5p CLASH 23622248
MIRT038328 hsa-miR-130b-5p CLASH 23622248
MIRT437876 hsa-miR-135b-5p Luciferase reporter assay, Western blot 23623609
MIRT535941 hsa-miR-922 PAR-CLIP 22012620
Transcription factors
Transcription factor Regulation Reference
AR Unknown 24913494
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000226 Process Microtubule cytoskeleton organization TAS 10077590
GO:0005515 Function Protein binding IPI 19549727, 21516116, 25416956, 25910212, 26496610, 31515488, 32296183
GO:0005819 Component Spindle IEA
GO:0005829 Component Cytosol TAS
GO:0005874 Component Microtubule IDA 11806752
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID O15344
Protein name E3 ubiquitin-protein ligase Midline-1 (EC 2.3.2.27) (Midin) (Putative transcription factor XPRF) (RING finger protein 59) (RING finger protein Midline-1) (RING-type E3 ubiquitin transferase Midline-1) (Tripartite motif-containing protein 18)
Protein function Has E3 ubiquitin ligase activity towards IGBP1, promoting its monoubiquitination, which results in deprotection of the catalytic subunit of protein phosphatase PP2A, and its subsequent degradation by polyubiquitination. {ECO:0000269|PubMed:10400
PDB 2DQ5 , 2FFW , 2JUN , 5IM8 , 7QRY
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13445 zf-RING_UBOX
10 57
RING-type zinc-finger
Domain
PF00643 zf-B_box
171 212
B-box zinc finger
Domain
PF18568 COS
323 374
TRIM C-terminal subgroup One Signature domain
Domain
PF00041 fn3
380 475
Fibronectin type III domain
Domain
PF13765 PRY
486 527
SPRY-associated domain
Family
PF00622 SPRY
540 655
SPRY domain
Family
Sequence
METLESELTCPICLELFEDPLLLPCAHSLCFNCAHRILVSHCATNESVESITAFQCPTCR
HVITLSQRGLDGLKRNVTLQNIIDRFQKASVSGPNSPSETRRERAFDANTMTSAEKVLCQ
FCDQDPAQDAVKTCVTCEVSYCDECLKATHPNKKPFTGHRLIEPIPDSHIRGLMCLEHED
EKVNMYCVTDDQLICALCKLVGRHRDHQVAAL
SERYDKLKQNLESNLTNLIKRNTELETL
LAKLIQTCQHVEVNASRQEAKLTEECDLLIEIIQQRRQIIGTKIKEGKVMRLRKLAQQIA
NCKQCIERSASLISQAEHSLKENDHARFLQTAKNITERVSMATASSQVLIPEINLNDTFD
TFALDFSREKKLLE
CLDYLTAPNPPTIREELCTASYDTITVHWTSDDEFSVVSYELQYTI
FTGQANVVSLCNSADSWMIVPNIKQNHYTVHGLQSGTKYIFMVKAINQAGSRSSE
PGKLK
TNSQPFKLDPKSAHRKLKVSHDNLTVERDESSSKKSHTPERFTSQGSYGVAGNVFIDSGR
HYWEVVISGSTWYAIGLAYKSAPKHEWIGKNSASWALCRCNNNWVVRHNSKEIPIEPAPH
LRRVGILLDYDNGSIAFYDALNSIHLYTFDVAFAQPVCPTFTVWNKCLTIITGLP
IPDHL
DCTEQLP
Sequence length 667
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Ubiquitin mediated proteolysis   Interferon gamma signaling
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Agenesis of corpus callosum Agenesis of corpus callosum rs754914260, rs1057519053, rs1057519056, rs1057519054, rs1057519055, rs1057519057, rs1384496494, rs1599017933
Congenital heart defects Congenital Heart Defects rs267607101, rs121434422, rs387906498, rs397509416, rs587777371, rs587777372, rs587777374, rs367537998, rs797044882, rs886041730, rs768027510, rs1064793873, rs1555447012, rs1554263268, rs1554263321, rs1555223294, rs782051102, rs1555896779, rs1555896778, rs1555897088, rs374016704, rs1555446983, rs1479104927, rs1562443558, rs755445139, rs1581616817, rs1581655293, rs1899172049
Cryptorchidism Cryptorchidism rs121912555, rs104894697, rs104894698, rs398122886
Developmental delay Global developmental delay rs28941770, rs199469464, rs281865469, rs143747297, rs398123009, rs587777428, rs786205133, rs606231459, rs797044854, rs797045027, rs864309504, rs878853160, rs886039902, rs886042046, rs886041291, rs886041382, rs1057518991, rs1057518699, rs753254213, rs748294403, rs762552974, rs1135401795, rs1553121073, rs1553122926, rs1364690005, rs1554086554, rs1554210415, rs1554168326, rs1554776342, rs1553873247, rs1567860112, rs779009256, rs1557447255, rs1564568350, rs780011005, rs1597464953, rs1200336864, rs1569513017, rs1587459606, rs1570332505, rs748888652, rs1575155995, rs2087029320, rs1589669105, rs1601769604, rs1184981709, rs749201074
Unknown
Disease name Disease term dbSNP ID References
Dysphagia Deglutition Disorders
Frontal bossing Frontal bossing
Gastroesophageal reflux disease Gastroesophageal reflux disease
High palate Byzanthine arch palate

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