Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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4281 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Midline 1 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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MID1 |
SynonymsGene synonyms aliases
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BBBG1, FXY, GBBB, GBBB1, MIDIN, OGS1, OS, OSX, RNF59, TRIM18, XPRF, ZNFXY |
ChromosomeChromosome number
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X |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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Xp22.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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 |
rs147106995 |
G>A |
Conflicting-interpretations-of-pathogenicity, benign |
Missense variant, genic downstream transcript variant, coding sequence variant |
rs375668839 |
AAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA |
Benign, benign-likely-benign, conflicting-interpretations-of-pathogenicity |
Intron variant |
rs387906719 |
C>A |
Pathogenic |
Stop gained, coding sequence variant |
rs398123341 |
T>C,G |
Uncertain-significance, pathogenic |
Genic downstream transcript variant, missense variant, coding sequence variant |
rs398123342 |
->G |
Pathogenic |
Genic downstream transcript variant, frameshift variant, coding sequence variant |
rs398123343 |
T>- |
Pathogenic |
Genic downstream transcript variant, frameshift variant, coding sequence variant |
rs745554420 |
G>A |
Pathogenic |
Genic downstream transcript variant, stop gained, coding sequence variant |
rs786200982 |
->ATCA |
Pathogenic |
Stop gained, genic downstream transcript variant, coding sequence variant |
rs797044786 |
->TTGT |
Pathogenic |
Genic downstream transcript variant, frameshift variant, coding sequence variant |
rs1555894390 |
G>- |
Likely-pathogenic |
Genic downstream transcript variant, frameshift variant, coding sequence variant |
rs1555895704 |
G>A |
Pathogenic |
Genic downstream transcript variant, stop gained, coding sequence variant |
rs1555895725 |
C>G |
Pathogenic |
Genic downstream transcript variant, splice acceptor variant |
rs1555899082 |
C>T |
Pathogenic |
Intron variant |
rs1556001856 |
G>T |
Likely-pathogenic |
Genic downstream transcript variant, stop gained, coding sequence variant |
rs1556001968 |
C>T |
Likely-pathogenic |
Genic downstream transcript variant, stop gained, coding sequence variant |
rs1556002004 |
CTGCGGAAAC>- |
Pathogenic |
Genic downstream transcript variant, intron variant, splice acceptor variant, coding sequence variant |
rs1556003095 |
->CAAT |
Pathogenic |
Genic downstream transcript variant, stop gained, coding sequence variant |
rs1556003200 |
G>- |
Likely-pathogenic |
Genic downstream transcript variant, frameshift variant, coding sequence variant |
rs1556004366 |
C>G |
Pathogenic |
Genic downstream transcript variant, missense variant, coding sequence variant |
rs1556004400 |
T>C |
Uncertain-significance, likely-pathogenic |
Genic downstream transcript variant, missense variant, coding sequence variant |
rs1569265497 |
G>- |
Pathogenic |
Coding sequence variant, frameshift variant, genic downstream transcript variant |
rs1569268013 |
->C |
Pathogenic |
Coding sequence variant, frameshift variant, genic downstream transcript variant |
rs1569268029 |
CT>- |
Pathogenic |
Coding sequence variant, frameshift variant, genic downstream transcript variant |
rs1569270016 |
A>G |
Likely-pathogenic |
Coding sequence variant, missense variant, genic downstream transcript variant |
rs1569270035 |
ATC>- |
Pathogenic |
Coding sequence variant, inframe deletion, genic downstream transcript variant |
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miRNAmiRNA information provided by mirtarbase database.
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Transcription factors
|
Transcription factor |
Regulation |
Reference |
AR |
Unknown |
24913494 |
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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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 |
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Sequence |
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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.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Agenesis of corpus callosum |
Agenesis of corpus callosum |
rs754914260, rs1057519053, rs1057519056, rs1057519054, rs1057519055, rs1057519057, rs1384496494, rs1599017933 |
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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 |
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Cryptorchidism |
Cryptorchidism |
rs121912555, rs104894697, rs104894698, rs398122886 |
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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 |
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Opitz gbbb syndrome, x-linked |
Opitz GBBB Syndrome, X-Linked |
rs1569270035, rs1569268013, rs28934611, rs104894865, rs104894866, rs1569268029, rs387906719, rs398123342, rs745554420, rs1556001856, rs1556001968, rs1556003095, rs1556003200, rs1556004366, rs1555894390, rs1555895704, rs1555895725, rs1569265497 |
9718340, 15558842, 17221865, 9354791, 11030761, 20181585, 15121778, 12833403 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Dysphagia |
Deglutition Disorders |
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Frontal bossing |
Frontal bossing |
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Gastroesophageal reflux disease |
Gastroesophageal reflux disease |
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High palate |
Byzanthine arch palate |
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Hypospadias |
Hypospadias |
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Imperforate anus |
Anus, Imperforate |
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