about
P688
MID1 and MID2 homo- and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, alpha 4, to microtubules: implications for the clinical variability of X-linked Opitz GBBB syndrome and other developmental disordersThe Opitz syndrome gene product, MID1, associates with microtubulesTRIM27 negatively regulates NOD2 by ubiquitination and proteasomal degradationCytokine activation of p38 mitogen-activated protein kinase and apoptosis is opposed by alpha-4 targeting of protein phosphatase 2A for site-specific dephosphorylation of MEK3.Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22Active transport of the ubiquitin ligase MID1 along the microtubules is regulated by protein phosphatase 2A
P921
description
humanes Protein
@de
mammalian protein found in Homo sapiens
@en
menselijk eiwit
@nl
protein
@id
proteinë
@sq
protèin
@ace
protéine humaine
@fr
بروتين بشري
@ar
name
Midline 1
@en
Midline 1
@nl
type
label
Midline 1
@en
Midline 1
@nl
altLabel
E3 ubiquitin-protein ligase Midline-1
@en
MID1
@en
Midin
@en
Opitz/BBB syndrome
@en
RING finger protein 59
@en
RING finger protein Midline-1
@en
RING-type E3 ubiquitin transferase Midline-1
@en
midline 1 RING finger protein
@en
putative transcription factor XPRF
@en
tripartite motif protein TRIM18
@en
prefLabel
Midline 1
@en
Midline 1
@nl
P361
P527
P637
P638
P680
P681
P682
P705
P352
P637
P31
P352
P361
P527
P637
NP_001092094
NP_001180206
NP_001180207
NP_001180208
NP_001180209
NP_001334662
P638
P680
P681
P682
P702
P703
P705
ENSP00000312678
ENSP00000370156
ENSP00000370157
ENSP00000370159
ENSP00000370162
ENSP00000370164
ENSP00000391154
ENSP00000414521
ENSP00000483707
ENSP00000484712