MID1
Appearance
gjen i llojit Homo sapiens
nënklasë e
gjen kodues i proteinave[5]
found in taxon
encodes
Midline 1[6]
gene inversion association with
kromozom
strand orientation
genomic start
genomic end
cytogenetic location
Xp22.2[2]
HomoloGene ID
7837[2]
Gene Atlas image
increased expression in
ortholog
expressed in
përputhje e saktë
Reference
- ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ensembl Release 106, ENSG00000101871
- ^ a b c d e f g h i j k l m n o p NCBI Gene, 15 maj 2022, 4281
- ^ UMLS 2023, 15 qershor 2023, inferred by common HGNC mappings on source and on Wikidata
- ^ Online Mendelian Inheritance in Man, 19 gusht 2019
- ^ Ensembl Release 87, ENSG00000101871
- ^ UniProt, 6 korrik 2017, O15344
- ^ Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22, Rasti studimor
- ^ a b c The MID1 gene product in physiology and disease, review article
- ^ Resveratrol induces dephosphorylation of Tau by interfering with the MID1-PP2A complex
- ^ A hormone-dependent feedback-loop controls androgen receptor levels by limiting MID1, a novel translation enhancer and promoter of oncogenic signaling
- ^ a b c HomoloGene build68, 7837
- ^ a b Orthologous MAtrix, https://omabrowser.org/oma/vps/O15344/
- ^ a b c d e f g h i j Bgee, 7 qershor 2024, https://www.bgee.org/gene/ENSG00000101871
- ^ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069