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Table 2 Genes expressed in muscle and components of the interactomes of known LGMD genes

From: Whole-exome sequencing identifies novel pathogenic mutations and putative phenotype-influencing variants in Polish limb-girdle muscular dystrophy patients

Gene

Protein

Interactive partner

ANK1

ankyrin 1

RYR1, TTN

ANKRD23

ankyrin repeat domain 23

TTN

ATP1B4

ATPase beta 4 polypeptide

POMT1, POMT2

C1QTNF9

C1q and tumor necrosis factor protein 9

COL6A1, COL6A2

C1QTNF9

C1q and tumor necrosis factor protein 9B

COL6A1, COL6A2

EVC2

Ellis-van Creveld syndrome 2

TOR1AIP1

FYCO1

FYVE and coiled-coil containing 1

LMNA

HECW2

HECT, C2 and WW containing E3 ubiquitin

DYSF

HSPB2

heat shock protein 2

BAG3, CRYAB, FLNC, TCAP, TTN

MLIP

muscular LMNA-interacting protein

LMNA

MYOZ1

myozenin 1

FLNC, TCAP

MYOZ2

myozenin 2

FLNC, TCAP

MYOZ3

myozenin 3

FLNC, TCAP

OPRM1

opioid receptor mu 1

TNPO3

PDLIM7

PDZ and LIM domain 7

BAG3, PLEC

RXRA

retinoid x receptor alpha

TRIM32

SIRT2

sirtuin 2

DMD, DNAJB6

SRRM2

serine/arginine repetitive matrix 2

LMNA, PLEC

SVIL

Supervillin

LMNA

TRIM63

tripartite motif containing 63, E3 ubiquitin protein ligase

DES, FLNC, MYOT, TCAP, TTN