Manteia - Molecule gene

ENSMUSG00000037712

Mus musculus

Features

Gene ID:	ENSMUSG00000037712

Biological name :	Fermt2

Synonyms :	Fermitin family homolog 2 / Fermt2 / Q8CIB5

Possible biological names infered from orthology :	fermitin family member 2 / Q96AC1

Species:	Mus musculus

Chr. number:	14
Strand:	-1
Band:	C1
Gene start:	45458795
Gene end:	45530118

Corresponding Affymetrix probe sets:	10419223 (MoGene1.0st) 1434180_at (Mouse Genome 430 2.0 Array) 1434181_at (Mouse Genome 430 2.0 Array) 1459324_at (Mouse Genome 430 2.0 Array)

Cross references:	Ensembl peptide - ENSMUSP00000120918 Ensembl peptide - ENSMUSP00000153760 Ensembl peptide - ENSMUSP00000044554 Ensembl peptide - ENSMUSP00000118214 NCBI entrez gene - 218952 See in Manteia. MGI - MGI:2385001 RefSeq - XM_006518826 RefSeq - XM_006518827 RefSeq - XM_006518828 RefSeq - NM_146054 RefSeq Peptide - NP_666166 swissprot - Q3TLE2 swissprot - A6X940 swissprot - A6X941 swissprot - Q8CIB5 Ensembl - ENSMUSG00000037712

See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed

Ortholog prediction (from Ensembl)

Ortholog name	ID	Species
F1Q8X5	ENSDARG00000020242	Danio rerio
FERMT2	ENSGALG00000012425	Gallus gallus
FERMT2	ENSG00000073712	Homo sapiens

Paralog prediction (from Ensembl)

Paralog name	ID	Similarity(%)
Fermt1 / P59113 / Fermitin family homolog 1 / Q9BQL6* / fermitin family member 1*	ENSMUSG00000027356	63
Fermt3 / Q8K1B8 / Fermitin family homolog 3 / Q86UX7* / fermitin family member 3*	ENSMUSG00000024965	51

Protein motifs (from Interpro)

Interpro ID	Name
IPR001849	Pleckstrin homology domain
IPR011993	PH-like domain superfamily
IPR014352	FERM/acyl-CoA-binding protein superfamily
IPR019748	FERM central domain
IPR019749	Band 4.1 domain
IPR035963	FERM superfamily, second domain

Gene Ontology (GO)

Type	GO ID	Term	Ev.Code
biological_process	GO:0007155	cell adhesion	IEA
biological_process	GO:0007160	cell-matrix adhesion	IEA
biological_process	GO:0007179	transforming growth factor beta receptor signaling pathway	IEA
biological_process	GO:0007229	integrin-mediated signaling pathway	IEA
biological_process	GO:0008360	regulation of cell shape	IEA
biological_process	GO:0016055	Wnt signaling pathway	ISO
biological_process	GO:0033622	integrin activation	IEA
biological_process	GO:0034446	substrate adhesion-dependent cell spreading	IMP
biological_process	GO:0048041	focal adhesion assembly	IMP
biological_process	GO:0072657	protein localization to membrane	IMP
cellular_component	GO:0001725	stress fiber	IDA
cellular_component	GO:0005634	nucleus	ISO
cellular_component	GO:0005654	nucleoplasm	IEA
cellular_component	GO:0005737	cytoplasm	ISS
cellular_component	GO:0005856	cytoskeleton	IEA
cellular_component	GO:0005886	plasma membrane	IEA
cellular_component	GO:0005925	focal adhesion	ISS
cellular_component	GO:0005938	cell cortex	IEA
cellular_component	GO:0009986	cell surface	IEA
cellular_component	GO:0016020	membrane	IEA
cellular_component	GO:0030054	cell junction	IEA
cellular_component	GO:0031234	extrinsic component of cytoplasmic side of plasma membrane	IEA
cellular_component	GO:0031258	lamellipodium membrane	IEA
cellular_component	GO:0031674	I band	IEA
cellular_component	GO:0031941	filamentous actin	IDA
cellular_component	GO:0042995	cell projection	IEA
molecular_function	GO:0005547	phosphatidylinositol-3,4,5-trisphosphate binding	IEA
molecular_function	GO:0008289	lipid binding	IEA

Pathways (from Reactome)

Pathway description

Cell-extracellular matrix interactions

Phenotype (from MGI, Zfin or HPO)

ID	Phenotype	Definition	Genetic BG
MP:0000063	reduced bone density	"decreased mineral content of bone; indicator of bone strength" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:57315]	Show Allelic Composition: Fermt2^tm1.1Gxo/Fermt2^tm1.1Gxo,Tg(Col2a1-cre)1Bhr/0 Genetic Background: B6.Cg-Fermt2^tm1.1Gxo Tg(Col2a1-cre)1Bhr
MP:0000075	absent neurocranium	"missing bones of the skull enclosing the brain" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0000149	abnormal scapula morphology	"malformation of either or both of the large, flat bones of the back part of the shoulder" [J:13049]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0000157	abnormal sternum morphology	"malformed long flat bone of the chest; articulates with clavicle and first seven rib pairs" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:19212]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0000160	kyphosis	"forward curvature of the spine, characterized by extensive flexion. " [J:62023, J:66943, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, cml:Cathleen M. Lutz , Mouse Genome Informatics Curator]	Show Allelic Composition: Whrn^hb/Whrn^hb Genetic Background: involves: BALB/c * C3H/HeH * C57BL/6J
MP:0000165	abnormal hypertrophic chondrocyte zone	"anomaly of the cartilage cell matrix layer " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:58795]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0000166	abnormal chondrocyte morphology	"anomalous structure, organization, or differentiation of nondividing cartilage cells" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:40203]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0000167	reduced chondrocyte numbers	"fewer than normal numbers of nondividing cartilage cells" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:61509]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0000547	short limbs	"reduced average length of the extremities" [MGI:CLS, J:61509]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N Allelic Composition: Fermt2^tm1.1Gxo/Fermt2^tm1.1Gxo,Tg(Col2a1-cre)1Bhr/0 Genetic Background: B6.Cg-Fermt2^tm1.1Gxo Tg(Col2a1-cre)1Bhr
MP:0001265	reduced body size	"smaller than average body weight, height and/or length of an organism compared to controls" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23170]	Show Allelic Composition: Whrn^hb/Whrn^hb Genetic Background: involves: BALB/c * C3H/HeH * C57BL/6J
MP:0001674	abnormal triploblastic development	"abnormal development of the three primary germ layers" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, tc:Teresa Chu , Mouse Genome Informatics Curator]	Show Allelic Composition: Prkg1^tm2.1Naw/Prkg1^tm2.1Naw Genetic Background: involves: 129S1/Sv * 129X1/SvJ
MP:0001732	postnatal growth retardation	"slow or limited development after birth " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]	Show Allelic Composition: Fermt2^tm1.1Gxo/Fermt2^tm1.1Gxo,Tg(Col2a1-cre)1Bhr/0 Genetic Background: B6.Cg-Fermt2^tm1.1Gxo Tg(Col2a1-cre)1Bhr
MP:0001954	respiratory distress	"physical difficulty or inability to breathe" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54931]	Show Allelic Composition: Fermt2^tm1.1Gxo/Fermt2^tm1.1Gxo,Tg(Col2a1-cre)1Bhr/0 Genetic Background: B6.Cg-Fermt2^tm1.1Gxo Tg(Col2a1-cre)1Bhr
MP:0002083	premature death	"death after 3 weeks of age, but before normal life span" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]	Show Allelic Composition: Whrn^hb/Whrn^hb Genetic Background: involves: BALB/c * C3H/HeH * C57BL/6J
MP:0002543	brachyphalangia	"abnormally short phalanges" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0002544	brachydactyly	"abnormally short digits" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0002657	chondrodystrophy	"abnormal development of the cartilage primordia of long bones, resulting in abnormally short extremities but normal head and trunk" [il:Ira Lu , Mouse Genome Informatics Curator]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0002764	short tibia	" reduced length of the medial and larger bone of the lower leg" [J:12736, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0003055	abnormal epiphyseal plate morphology	"malformed or absent cartilagenous center of ossification on the long bones permitting growth of the bone in both directions during development" [MeSH:National Library of Medicine - Medical Subject Headings, 2003]	Show Allelic Composition: Fermt2^tm1.1Gxo/Fermt2^tm1.1Gxo,Tg(Col2a1-cre)1Bhr/0 Genetic Background: B6.Cg-Fermt2^tm1.1Gxo Tg(Col2a1-cre)1Bhr
MP:0003109	short femur	"reduced length of the long bone of the thigh" [ava:Anna V. Anagnostopoulos, Mouse Genome Informatics Curator, Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0003419	delayed endochondral bone ossification	"late onset of bone formation in bones that form from cartilage" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:94631]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N Allelic Composition: Fermt2^tm1.1Gxo/Fermt2^tm1.1Gxo,Tg(Col2a1-cre)1Bhr/0 Genetic Background: B6.Cg-Fermt2^tm1.1Gxo Tg(Col2a1-cre)1Bhr
MP:0003566	abnormal cell adhesion	"altered ability of a cell to adhere to another cell or to a non-cellular component of the environment" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]	Show Allelic Composition: Prkg1^tm2.1Naw/Prkg1^tm2.1Naw Genetic Background: involves: 129S1/Sv * 129X1/SvJ
MP:0003662	abnormal proliferative zone	"germinal layer of the epiphyseal plate where cells are actively dividing as well as producing extracellular matrix" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:96254]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0003886	abnormal embryonic epiblast morphology	"anomaly in the development/organization of the tissue that gives rise to the ectoderm, endoderm and mesoderm of the embryo proper" [brs:Beverly Richards-Smith, Mouse Genome Informatics Curator]	Show Allelic Composition: Prkg1^tm2.1Naw/Prkg1^tm2.1Naw Genetic Background: involves: 129S1/Sv * 129X1/SvJ
MP:0004321	short sternum	"reduced length of the long flat bone of the chest which articulates with clavicle and first seven rib pairs" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0004337	clavicle hypoplasia	"underdevelopment or reduced size, usually due to a reduced number of cells, of one or both of the doubly curved long bone that forms part of the shoulder girdle and articulates with the sternum and the scapula" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0004338	small clavicle	"reduced size of one or both of the doubly curved long bone that forms part of the shoulder girdle and articulates with the sternum and the scapula" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0004340	short scapula	"reduced length of either or both of the large, flat bones of the back part of the shoulder" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0004351	short humerus	"reduced length of one or both of the bones of the forelimb that articulates with the scapula above and the radius and ulna below" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0004355	short radius	"reduced length of the short bone of the lateral forearm" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0004359	short ulna	"reduced length of the medial and larger of the two bones of the forearm" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0004610	small vertebrae	"reduced size of the bony segments of the spinal column" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]	Show Allelic Composition: Fermt2^tm1.1Gxo/Fermt2^tm1.1Gxo,Tg(Col2a1-cre)1Bhr/0 Genetic Background: B6.Cg-Fermt2^tm1.1Gxo Tg(Col2a1-cre)1Bhr
MP:0004626	vertebral compression	"appearance of vertebrae that are flattened laterally along the whole length such that they appear pressed together and take up less rostrocaudal space " [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]	Show Allelic Composition: Fermt2^tm1.1Gxo/Fermt2^tm1.1Gxo,Tg(Col2a1-cre)1Bhr/0 Genetic Background: B6.Cg-Fermt2^tm1.1Gxo Tg(Col2a1-cre)1Bhr
MP:0004686	decreased length of long bones	"reduced end-to-end length of the several elongated bones of the extremities" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N Allelic Composition: Fermt2^tm1.1Gxo/Fermt2^tm1.1Gxo,Tg(Col2a1-cre)1Bhr/0 Genetic Background: B6.Cg-Fermt2^tm1.1Gxo Tg(Col2a1-cre)1Bhr
MP:0005508	abnormal skeleton morphology	"malformation of the bony framework of the body in vertebrates" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N Allelic Composition: Fermt2^tm1.1Gxo/Fermt2^tm1.1Gxo,Tg(Col2a1-cre)1Bhr/0 Genetic Background: B6.Cg-Fermt2^tm1.1Gxo Tg(Col2a1-cre)1Bhr
MP:0006279	abnormal limb development	"anomaly in the formation of the limbs" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0006397	disorganized long bone epiphyseal plate	"a lack of the regular arrangement of the cells or zones of the epiphyseal plate" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0008273	abnormal intramembranous bone ossification	"anomaly in the process of the formation of bone in which osteoblasts secrete a collage-proteoglycan matrix that binds calcium salts and becomes calcified; intramembranous ossification is the way flat bones are formed" [GO:0001957]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0008817	hematoma	"an abnormal localized accumulation of clotted or partially clotted blood in an organ or a soft tissue space as a result of localized hemorrhage" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0010082	sternebra fusion	"appearance of one or more sternebrae as a single structure" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0010103	small thoracic cage	"reduced size of the bony and cartilaginous structure enclosing the thoracic cavity, consisting of the thoracic vertebrae, ribs, costal cartilages, and sternum" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]	Show Allelic Composition: Fermt2^tm1.1Gxo/Fermt2^tm1.1Gxo,Tg(Col2a1-cre)1Bhr/0 Genetic Background: B6.Cg-Fermt2^tm1.1Gxo Tg(Col2a1-cre)1Bhr
MP:0010879	decreased trabecular bone volume	"decrease in the amount of space occupied by trabecular bone tissue in the skeleton" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]	Show Allelic Composition: Fermt2^tm1.1Gxo/Fermt2^tm1.1Gxo,Tg(Col2a1-cre)1Bhr/0 Genetic Background: B6.Cg-Fermt2^tm1.1Gxo Tg(Col2a1-cre)1Bhr
MP:0011087	complete neonatal lethality	"death of all organisms of a given genotype in a population within the neonatal period after birth (Mus: P0)" [MGI:csmith]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0011096	complete embryonic lethality before somite formation	"death of all organisms of a given genotype in a population between the point of implantation and somite formation (Mus: E4.5 to less than E8)" [MGI:csmith]	Show Allelic Composition: Prkg1^tm2.1Naw/Prkg1^tm2.1Naw Genetic Background: involves: 129S1/Sv * 129X1/SvJ Allelic Composition: Fermt2^{Gt(AM0293)Wtsi}/Fermt2^{Gt(AM0293)Wtsi} Genetic Background: involves: 129P2/OlaHsd * C57BL/6
MP:0012279	wide sternum	"an increase in the width of the long flat bone of the chest that articulates with the clavicle and first seven rib pairs" [MGI:anna]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0013624	decreased femur compact bone thickness	"reduced width of the superficial layer of compact bone at the midpoint of the femur" [MGI:csmith]	Show Allelic Composition: Fermt2^tm1.1Gxo/Fermt2^tm1.1Gxo,Tg(Col2a1-cre)1Bhr/0 Genetic Background: B6.Cg-Fermt2^tm1.1Gxo Tg(Col2a1-cre)1Bhr
MP:0014101	decreased chondrocyte proliferation	"decreased amount of multiplication or reproduction of chondrocytes by cell division, resulting in the expansion of their population" [GO:0035988]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N
MP:0014103	increased chondrocyte apoptosis	"increased number of chondrocytes undergoing programmed cell death" [MGI:csmith]	Show Allelic Composition: Usp42^{tm2a(EUCOMM)Wtsi}/Usp42^{tm2a(EUCOMM)Wtsi} Genetic Background: involves: C57BL/6 * C57BL/6N

Interacting proteins (from Reactome)

Interactor ID	Name	Interaction type
ENSMUSG00000006219	Fblim1 / Q71FD7 / Filamin-binding LIM protein 1 / Q8WUP2*	/ complex / reaction

1 s.

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