abnormal extracellular matrix morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the structure lying external to one or more cells, which provides structural support for cells or tissues; in mammals, the extracellular matrix is completely external to the cell (Mammalian Phenotype Ontology, MP_0013258)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013258
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Genes

34 gene mutations causing the abnormal extracellular matrix morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADM adrenomedullin
ANTXR1 anthrax toxin receptor 1
CAV2 caveolin 2
COL13A1 collagen, type XIII, alpha 1
COL18A1 collagen, type XVIII, alpha 1
COL4A1 collagen, type IV, alpha 1
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
FKTN fukutin
FLRT3 fibronectin leucine rich transmembrane protein 3
FN1 fibronectin 1
FOXC1 forkhead box C1
FRAS1 Fraser extracellular matrix complex subunit 1
HSPG2 heparan sulfate proteoglycan 2
ILK integrin-linked kinase
ISPD isoprenoid synthase domain containing
ITGA6 integrin, alpha 6
ITGB8 integrin, beta 8
LAMA2 laminin, alpha 2
LAMA4 laminin, alpha 4
LAMA5 laminin, alpha 5
LAMC1 laminin, gamma 1 (formerly LAMB2)
LAMC2 laminin, gamma 2
MMP14 matrix metallopeptidase 14 (membrane-inserted)
MYO7A myosin VIIA
NID1 nidogen 1
P4HA1 prolyl 4-hydroxylase, alpha polypeptide I
PLOD3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
PXDN peroxidasin
RECK reversion-inducing-cysteine-rich protein with kazal motifs
RTL1 retrotransposon-like 1
SLC31A1 solute carrier family 31 (copper transporter), member 1
SPINT1 serine peptidase inhibitor, Kunitz type 1