ENSMUSG00000075324


Mus musculus

Features
Gene ID: ENSMUSG00000075324
  
Biological name :Fign
  
Synonyms : Fidgetin / Fign / Q9ERZ6
  
Possible biological names infered from orthology : fidgetin, microtubule severing factor / Q5HY92
  
Species: Mus musculus
  
Chr. number: 2
Strand: -1
Band: C1.3
Gene start: 63971507
Gene end: 64098038
  
Corresponding Affymetrix probe sets: 10483150 (MoGene1.0st)   1439602_at (Mouse Genome 430 2.0 Array)   1442873_at (Mouse Genome 430 2.0 Array)   1450268_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000122855
Ensembl peptide - ENSMUSP00000124338
NCBI entrez gene - 60344     See in Manteia.
MGI - MGI:1890647
RefSeq - NM_001267846
RefSeq - NM_021716
RefSeq Peptide - NP_001254775
RefSeq Peptide - NP_068362
swissprot - Q9ERZ6
swissprot - E0CYB7
Ensembl - ENSMUSG00000075324
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 fignENSDARG00000008662Danio rerio
 FIGNENSGALG00000011069Gallus gallus
 FIGNENSG00000182263Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Fignl2 / fidgetin like 2 / A6NMB9*ENSMUSG0000009544036
Fignl1 / Q8BPY9 / Fidgetin-like protein 1 / Q6PIW4* / fidgetin like 1*ENSMUSG0000003545533
Spast / Q9QYY8 / Spastin / Q9UBP0*ENSMUSG0000002406820
A6H690 / 4931409K22Rik / IQ and AAA domain-containing protein 1-like / IQCA1L* / IQ motif containing with AAA domain 1 like*ENSMUSG0000003819914
Iqca / Q9CUL5 / IQ and AAA domain-containing protein 1 / IQCA1* / Q86XH1* / IQ motif containing with AAA domain 1*ENSMUSG0000002630114


Protein motifs (from Interpro)
Interpro ID Name
 IPR003593  AAA+ ATPase domain
 IPR003959  ATPase, AAA-type, core
 IPR003960  ATPase, AAA-type, conserved site
 IPR015415  Vps4 oligomerisation, C-terminal
 IPR027417  P-loop containing nucleoside triphosphate hydrolase


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007049 cell cycle IEA
 biological_processGO:0010569 regulation of double-strand break repair via homologous recombination IBA
 biological_processGO:0051301 cell division IEA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005815 microtubule organizing center IEA
 cellular_componentGO:0005856 cytoskeleton IEA
 cellular_componentGO:0005874 microtubule IEA
 cellular_componentGO:0016363 nuclear matrix IEA
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0005524 ATP binding IEA
 molecular_functionGO:0008022 protein C-terminus binding IPI
 molecular_functionGO:0016887 ATPase activity IBA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000035 abnormal membranous labyrinth "malformations in the complex arrangement of communicating canaliculi and sacs suspended within the cavity of the bony labyrinth of the inner ear" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23837]
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Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0000036 absent semicircular canals "missing organ of balance; consists of three bony tubes within which the semicircular ducts are located" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:23837]
Show

Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

Allelic Composition: Figntm1Frk/Fignfi
Genetic Background: involves: 129S1/Sv * 129X1SvJ * C57BL/6J

 MP:0000458 abnormal mandible morphology "malformation of the lower bony framework of the mouth where the inferior teeth are held" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+
Genetic Background: involves: 129S1/Sv * C57BL/6J

 MP:0000562 polydactyly "greater than 5 digits on one or more autopods" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+
Genetic Background: involves: 129S1/Sv * C57BL/6J

 MP:0000929 open neural tube "incomplete invagination and fusion of the neuroepithelial layer in early development" [MGI:CLS, J:53370, J:62571]
Show

Allelic Composition: Fignfi/Fignfi,Pax3Sp/Pax3Sp
Genetic Background: BR.Cg-Pax3Sp Fignfi

 MP:0001262 decreased body weight "lower than normal average weight " [J:61295]
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Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+
Genetic Background: involves: 129S1/Sv * C57BL/6J

 MP:0001297 microphthalmia "reduced average size of the eyes" [J:18048]
Show

Allelic Composition: Prkdcscid/Prkdcscid,Iduatm1Clk/Iduatm1Clk
Genetic Background: NOD.129(B6)-Prkdcscid Iduatm1Clk/J

Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

Allelic Composition: Figntm1Frk/Fignfi
Genetic Background: involves: 129S1/Sv * 129X1SvJ * C57BL/6J

 MP:0001306 small lens "reduced size of the transparent structure of the eye responsible for focusing light rays" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840]
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Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+
Genetic Background: involves: 129S1/Sv * C57BL/6J

 MP:0001312 abnormal cornea morphology "malformation or absence of the transparent anterior portion of the fibrous coat of the eye that serves as the chief refractory structure " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+
Genetic Background: involves: 129S1/Sv * C57BL/6J

 MP:0001314 corneal opacity "complete or partial clouding of the cornea" [jte:Janan T. Eppig , Mouse Genome Informatics, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+
Genetic Background: involves: 129S1/Sv * C57BL/6J

 MP:0001347 absent lacrimal glands "missing the glands that secrete tears" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, tc:Teresa Chu , Mouse Genome Informatics Curator]
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Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+
Genetic Background: involves: 129S1/Sv * C57BL/6J

 MP:0001386 abnormal maternal nurturing "failure of mothers to tend offspring" [J:39801]
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Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+
Genetic Background: involves: 129S1/Sv * C57BL/6J

 MP:0001395 bi-directional circling "circling behavior exhibited in both clockwise and counterclockwise directions" [cml:Cathleen M. Lutz , Mouse Genome Informatics Curator]
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Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0001405 impaired coordination "reduced ability to execute integrated movements of muscle" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+
Genetic Background: involves: 129S1/Sv * C57BL/6J

 MP:0001488 increased startle reflex "reduced threshold or more severe reflex response to variable stimuli, often auditory; usually measured by amplitude of whole body flinch" [What s Wrong With My Mouse?:ISBN 0-471-31639-3, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+
Genetic Background: involves: 129S1/Sv * C57BL/6J

 MP:0001575 cyanosis "a dark bluish or purple skin discoloration resulting from deficient oxygenation of the blood" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60159]
Show

Allelic Composition: Gata3tm2Gsv/Gata3+
Genetic Background: either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)

 MP:0001732 postnatal growth retardation "slow or limited development after birth " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0001851 eye inflammation "local accumulation of fluid, plasma proteins, and leukocytes in the eye" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0001852 conjunctivitis "inflammation of the mucous membrane that lines the inner surface of the eyelids" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60896]
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Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0001921 reduced fertility "diminished ability to produce live offspring" [J:65030]
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Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+
Genetic Background: involves: 129S1/Sv * C57BL/6J

 MP:0001954 respiratory distress "physical difficulty or inability to breathe" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54931]
Show

Allelic Composition: Gata3tm2Gsv/Gata3+
Genetic Background: either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)

 MP:0001967 deafness "inability to hear" [J:57651]
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Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0002116 abnormal craniofacial bone morphology "abnormal development of cranial or facial bones resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+
Genetic Background: involves: 129S1/Sv * C57BL/6J

 MP:0002428 abnormal semicircular canal "anomaly of the organ of balance composed of three long bony tubes of the labyrinth" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Figntm1Frk/Fignfi
Genetic Background: involves: 129S1/Sv * 129X1SvJ * C57BL/6J

 MP:0002730 head shaking "compulsive movement of the head in the horizontal plane" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:274]
Show

Allelic Composition: Prkdcscid/Prkdcscid,Iduatm1Clk/Iduatm1Clk
Genetic Background: NOD.129(B6)-Prkdcscid Iduatm1Clk/J

Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

Allelic Composition: Figntm1Frk/Fignfi
Genetic Background: involves: 129S1/Sv * 129X1SvJ * C57BL/6J

 MP:0003077 abnormal cell cycle "failure to progress or abnormal progression through the stages of of the cell cycle" [smb:Susan M. Bello, Mouse Genome Informatics Curator, J:91266]
Show

Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0003161 absent lateral semicircular canal 
Show

Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0003312 abnormal locomotor coordination "reduced ability of an animal to maintain skillful and effective interaction of movements while engaging in locomotor activity" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0004045 abnormal cell cycle checkpoint function "anomaly in the amount of time spent at the points in the cell cycle (end of G1 phase, end of G2 phase, and during metaphase) which prevent the cell from progressing to the next phase when conditions are unfavorable" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Gt(ROSA)26Sortm1(GRN)Pvd/Gt(ROSA)26Sortm1(GRN)Pvd,Tg(Pgk1-cre)1Lni/0,Tg(SOD1*G93A)1Gur/0
Genetic Background: B6J.Cg-Tg(Pgk1-cre)1Lni Gt(ROSA)26Sortm1(GRN)Pvd Tg(SOD1*G93A)1Gur

 MP:0004509 abnormal pelvic girdle bone morphology "any structural anomaly of the bones of the pelvis by which the limbs attach to the axial skeleton " [MGI:cwg "Carroll-Ann W. Goldsmith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0004748 increased susceptibility to age-related hearing loss "greater than normal loss of hearing associated with advancing age, manifest as reduced ability to perceive or discriminate sounds; the pattern and age of onset vary" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0005542 corneal vascularization "formation of blood vessels in the cornea, which normally lacks vessels" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0006071 abnormal retinal progenitor morphology "anomoly in the proliferation or differentiation of the cells that give rise to the various cells of the retina" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:92622:]
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Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0006097 abnormal cerebellar lobule formation "anomaly in the formation of the lobes of the cerebellum" [smb:Susan M Bello, Mouse Genome Informatics Curator, anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, J:65410]
Show

Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0008919 fused tarsal bones "anomaly of the eight bones of the instep of the paw/foot resulting in some or all the bones being joined together" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0009772 abnormal retinal development "anomaly in any of the steps during embryogenesis that produce the nerve layer lining in the back of the eye which senses light, and creates impulses that travel through the optic nerve to the brain" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0009890 cleft secondary palate "congenital fissure of the tissues normally uniting to form the secondary palate" [PMID:16680722]
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Allelic Composition: Gata3tm2Gsv/Gata3+
Genetic Background: either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)

Allelic Composition: Akap8Gt(XG068)Byg/Akap8+,Fignfi/Fignfi
Genetic Background: involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6

Allelic Composition: Akap8Gt(XG068)Byg/Akap8Gt(XG068)Byg,Fignfi/Fign+
Genetic Background: involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6

Allelic Composition: Fignfi/Fignfi
Genetic Background: involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6

Allelic Composition: Fignfi/Fignfi
Genetic Background: involves: 129S1/SvImJ * C57BL/6

 MP:0011085 complete postnatal lethality "premature death anytime between the neonatal period and weaning age of all organisms of a given genotype in a population (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
Show

Allelic Composition: Gata3tm2Gsv/Gata3+
Genetic Background: either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)

 MP:0011086 partial postnatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms anytime between the neonatal period and weaning age (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
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Allelic Composition: Prkdcscid/Prkdcscid,Iduatm1Clk/Iduatm1Clk
Genetic Background: NOD.129(B6)-Prkdcscid Iduatm1Clk/J

 MP:0011088 partial neonatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms within the neonatal period after birth (Mus: P0)" [MGI:csmith]
Show

Allelic Composition: Gata3tm2Gsv/Gata3+
Genetic Background: either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)

 MP:0011091 complete prenatal lethality "death of all organisms of a given genotype in a population between fertilization and birth (Mus: approximately E18.5)" [MGI:csmith]
Show

Allelic Composition: Fignfi/Fignfi,Pax3Sp/Pax3Sp
Genetic Background: BR.Cg-Pax3Sp Fignfi

 MP:0011101 partial prenatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between fertilization and birth (Mus: approximately E18.5)" [MGI:csmith]
Show

Allelic Composition: Prkdcscid/Prkdcscid,Iduatm1Clk/Iduatm1Clk
Genetic Background: NOD.129(B6)-Prkdcscid Iduatm1Clk/J

 MP:0013387 Meibomian gland hypertrophy "increase in the bulk size of the meibum-secreting modified lobulated sebaceous glands located at the rim of the eyelids inside the tarsal plate due to cell enlargement" [MGI:Anna]
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Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0013447 Harderian gland hypertrophy "increase in the bulk size, due to cell enlargement, of the sebaceous gland that is located behind the eyeball and excretes fluid that facilitates movement of the nictitating membrane" [MGI:Anna]
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Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0030233 absent mandibular canal "absence of the canal that is normally located within the internal aspect of the mandible and contains the inferior alveolar nerve, artery and the vein" [MGI:anna]
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Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0030235 absent mandibular foramen "absence of the opening that is normally located on the medial surface of the ramus of the mandible and forms the entrance to the mandibular canal" [MGI:anna]
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Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

 MP:0030237 absent mental foramen "absence of the small opening located on the anterior surface of the mandible; normally, the mental nerve, a terminal branch of inferior alveolar nerve, and the mental artery leave the mandibular canal through it" [MGI:anna]
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Allelic Composition: Fignfi/Fignfi
Genetic Background: mixed

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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