ENSMUSG00000036817


Mus musculus

Features
Gene ID: ENSMUSG00000036817
  
Biological name :Sun1
  
Synonyms : Q9D666 / Sad1 and UNC84 domain containing 1 / Sun1
  
Possible biological names infered from orthology : O94901
  
Species: Mus musculus
  
Chr. number: 5
Strand: 1
Band: G2
Gene start: 139200637
Gene end: 139249840
  
Corresponding Affymetrix probe sets: 10526897 (MoGene1.0st)   1426666_a_at (Mouse Genome 430 2.0 Array)   1426667_a_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000117679
Ensembl peptide - ENSMUSP00000116364
Ensembl peptide - ENSMUSP00000119582
Ensembl peptide - ENSMUSP00000123211
Ensembl peptide - ENSMUSP00000122785
Ensembl peptide - ENSMUSP00000119587
Ensembl peptide - ENSMUSP00000056655
Ensembl peptide - ENSMUSP00000077756
Ensembl peptide - ENSMUSP00000098086
Ensembl peptide - ENSMUSP00000106506
Ensembl peptide - ENSMUSP00000106507
Ensembl peptide - ENSMUSP00000106508
Ensembl peptide - ENSMUSP00000114488
Ensembl peptide - ENSMUSP00000114514
Ensembl peptide - ENSMUSP00000114869
NCBI entrez gene - 77053     See in Manteia.
MGI - MGI:1924303
RefSeq - XM_017321171
RefSeq - XM_006504767
RefSeq - XM_017321156
RefSeq - XM_017321157
RefSeq - XM_017321158
RefSeq - XM_017321159
RefSeq - XM_017321160
RefSeq - XM_017321161
RefSeq - XM_017321162
RefSeq - XM_017321163
RefSeq - XM_017321164
RefSeq - XM_017321165
RefSeq - XM_017321166
RefSeq - XM_017321167
RefSeq - XM_017321168
RefSeq - XM_017321169
RefSeq - XM_017321170
RefSeq - NM_001256115
RefSeq - NM_001256116
RefSeq - NM_001256117
RefSeq - NM_001256118
RefSeq - NM_024451
RefSeq - XM_006504758
RefSeq - XM_006504762
RefSeq - XM_006504764
RefSeq - XM_006504765
RefSeq - XM_006504766
RefSeq Peptide - NP_001243046
RefSeq Peptide - NP_001243047
RefSeq Peptide - NP_077771
RefSeq Peptide - NP_001243044
RefSeq Peptide - NP_001243045
swissprot - F7AJ01
swissprot - F7BX07
swissprot - D3Z0L7
swissprot - D3YUW9
swissprot - D3Z5Q2
swissprot - Q3TSM1
swissprot - Q9D666
swissprot - D3Z3N5
swissprot - D3Z1X3
swissprot - F6RMJ1
swissprot - F6XYA0
Ensembl - ENSMUSG00000036817
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 sun1ENSDARG00000055350Danio rerio
 SUN1ENSGALG00000003781Gallus gallus
 SUN1ENSG00000164828Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Sun2 / Q8BJS4 / SUN domain-containing protein 2 / Q9UH99* / Sad1 and UNC84 domain containing 2*ENSMUSG0000004252425
Spag4 / Q9JJF2 / Sperm-associated antigen 4 protein / Q9NPE6* / sperm associated antigen 4*ENSMUSG0000003818013
Sun5 / SUN domain-containing protein 5 isoform 1 / Q8TC36* / Sad1 and UNC84 domain containing 5*ENSMUSG0000002748012
Sun3 / Q5SS91 / SUN domain-containing protein 3 / Q8TAQ9* / Sad1 and UNC84 domain containing 3*ENSMUSG0000004098512


Protein motifs (from Interpro)
Interpro ID Name
 IPR008979  Galactose-binding-like domain superfamily
 IPR012919  SUN domain
 IPR018539  SUN domain-containing protein 1
 IPR032680  SUN domain-containing protein 1, N-terminal


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001503 ossification IEA
 biological_processGO:0006998 nuclear envelope organization IBA
 biological_processGO:0007129 synapsis IMP
 biological_processGO:0007283 spermatogenesis IEA
 biological_processGO:0009612 response to mechanical stimulus IEA
 biological_processGO:0021817 nucleokinesis involved in cell motility in cerebral cortex radial glia guided migration IMP
 biological_processGO:0030154 cell differentiation IEA
 biological_processGO:0051321 meiotic cell cycle IEA
 biological_processGO:0051642 centrosome localization IMP
 biological_processGO:0070197 meiotic attachment of telomere to nuclear envelope IMP
 biological_processGO:0090286 cytoskeletal anchoring at nuclear membrane IBA
 biological_processGO:0090292 nuclear matrix anchoring at nuclear membrane ISO
 cellular_componentGO:0002080 acrosomal membrane IDA
 cellular_componentGO:0002081 outer acrosomal membrane IEA
 cellular_componentGO:0005634 nucleus IDA
 cellular_componentGO:0005635 nuclear envelope TAS
 cellular_componentGO:0005637 nuclear inner membrane IEA
 cellular_componentGO:0005639 integral component of nuclear inner membrane IEA
 cellular_componentGO:0005737 cytoplasm IDA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0031410 cytoplasmic vesicle IEA
 cellular_componentGO:0031965 nuclear membrane ISO
 cellular_componentGO:0034993 meiotic nuclear membrane microtubule tethering complex IEA
 cellular_componentGO:0043231 intracellular membrane-bounded organelle ISO
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0005521 lamin binding IDA
 molecular_functionGO:0043495 protein membrane anchor IBA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000852 small cerebellum "reduced size of cerebellum" [MGI:CLS, J:17203, J:67524]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj,Sun2tm1.1Cyh/Sun2+
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0000854 abnormal cerebellum development "malformed or incomplete differentiation of the part of the metencephalon that lies dorsal to the pons and medulla behind the brain stem and controls balance for walking and standing, modulates the force and range of movement and is involved in the learning of motor skills " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0000857 abnormal cerebellar foliation "malformation of small offshoots of the cerebellar lobules" [Principles of Neural Science:ISBN 0-8385-8034-3, J:52951]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0000872 abnormal external granule cell layer "malformation of the transient layer of the cerebellar cortex which is composed of the dividing and migrating granule cells" [tc:Teresa Chu , Mouse Genome Informatics Curator]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj,Sun2tm1.1Cyh/Sun2+
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0000877 abnormal Purkinje cell "any structural anomaly of the neurons located at the interface of the molecular and internal granule layers of the cerebellar cortex; these inhibitory neurons provide the output of the cerebellar cortex through axons that project into the white matter, and extensive dendritic trees from the Purkinje cells extend upward in a single plane into the molecular layer where they synapse with parallel fibers of granule cells" [J:46140, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj,Sun2tm1.1Cyh/Sun2+
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

Allelic Composition: Sun1tm1.1Ktj/Sun1+,Sun2tm1.1Cyh/Sun2tm1.1Cyh
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0000885 ectopic Purkinje cell "Purkinje cell body resides in places other than the Purkinje cell layer in the cerebellum" [MGI:tc, J:60896]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj,Sun2tm1.1Cyh/Sun2+
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0000890 thin cerebellar molecular layer "reduced width of the outer of the three cortical layers of the cerebellum" [J:46854]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj,Sun2tm1.1Cyh/Sun2+
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0001127 small ovary "reduced size of the female reproductive gland containing the germ cells" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:35782]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

 MP:0001147 small testis "reduced size of the male reproductive glands" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:58959]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: C57BL/6J * FVB/N

 MP:0001262 decreased body weight "lower than normal average weight " [J:61295]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0001393 ataxia "inability to coordinate voluntary muscular movements" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:67231]
Show

Allelic Composition: Spo11tm2.1Rdco/Spo11tm2.1Rdco
Genetic Background: B6.129S6-Spo11tm2.1Rdco

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj,Sun2tm1.1Cyh/Sun2+
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 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]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj,Sun2tm1.1Cyh/Sun2+
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0001407 short stride length "reduced average distance between steps" [J:34193]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj,Sun2tm1.1Cyh/Sun2+
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 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: Sun1tm1Mhan/Sun1tm1Mhan,Sun2tm1Mhan/Sun2tm1Mhan
Genetic Background: involves: 129S6/SvEvTac

 MP:0001925 male infertility "inability of male to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: C57BL/6J * FVB/N

 MP:0001926 female infertility "inability of female to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:34193]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: C57BL/6J * FVB/N

 MP:0002108 abnormal muscle morphology "abnormal development of muscle tissue resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

Allelic Composition: Sun1tm1Mhan/Sun1tm1Mhan,Sun2tm1Mhan/Sun2tm1Mhan
Genetic Background: involves: 129S6/SvEvTac

Allelic Composition: Sun1tm1Mhan/Sun1tm1Mhan,Sun2tm1Mhan/Sun2+
Genetic Background: involves: 129S6/SvEvTac

Allelic Composition: Sun1tm1Mhan/Sun1+,Sun2tm1Mhan/Sun2tm1Mhan
Genetic Background: involves: 129S6/SvEvTac

 MP:0002175 low brain weight "lower than average weight of the brain" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0002777 absent ovarian follicles "lack of the sac-like structures in the ovaries that surround the ova" [J:42612, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: C57BL/6J * FVB/N

 MP:0004399 abnormal cochlear outer hair cell morphology "any structural abnormality in the sensory cells of the organ of Corti which are in synaptic contact with sensory as well as efferent fibers of the auditory nerve; there are three rows of columnar outer hair cells largely surrounded by cortilymph and supporting phalangeal cells; the apical end of each cell is anchored to the cuticular plate and about 100 stereocilia arranged in a V-shaped pattern extend from the cell s surface through the cuticular plate into the tectorial membrane" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

 MP:0004404 cochlear outer hair cell degeneration "degeneration or loss of the columnar outer hair sensory cells of the organ of Corti" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

 MP:0004805 absent oocytes "absence of mature germ cells in the female" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: C57BL/6J * FVB/N

 MP:0004852 decreased testis weight "reduced average weight of the male reproductive glands" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: C57BL/6J * FVB/N

 MP:0004901 decreased male germ cell number "reduced numbers of male germ cells whether they are undifferentiated or fully differentiated" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

 MP:0004996 abnormal CNS synapse formation "any anomaly in the process of generating the initial connections between an axon and effector tissue or neuron" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj,Sun2tm1.1Cyh/Sun2+
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0005159 azoospermia "absence of living spermatozoa " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: C57BL/6J * FVB/N

 MP:0005168 abnormal female meiosis "malfunction in the process of nuclear division that results in ova with one half the normal chromosome number of the original cell" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

 MP:0005169 abnormal male meiosis "malfunction in the process of nuclear division that results in sperm with one half the normal chromosome number of the original cell" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: C57BL/6J * FVB/N

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: Not Specified

Allelic Composition: Sun1tm1Mhan/Sun1tm1Mhan
Genetic Background: B6.129S6-Sun1tm1Mhan

Allelic Composition: Sun1tm1Mhan/Sun1tm1Mhan
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J

Allelic Composition: Rad21ltm1Yow/Rad21ltm1Yow,Sun1tm1Mhan/Sun1tm1Mhan
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj

 MP:0006358 absent pinna reflex "complete failure to respond to an auditory stimulus by a characteristic ear twitch" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

 MP:0006379 abnormal spermatocyte morphology "anomaly in the number or structure of male germ cells that through meiosis give rise to spermatids " [ISBN:0-8036-0655-99 "Taber s Cyclopedic Medical Dictionary, 19th edition", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

 MP:0008261 arrest of male meiosis "cessation of the progression of the process of nuclear division that results in sperm with one half the normal chromosome number of the original cell" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: C57BL/6J * FVB/N

 MP:0008572 abnormal Purkinje cell dendrite morphology "any strucutral anomaly of the Purkinje cell body projections with hundreds of parallel spiny branches reaching up into the molecular layer" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj,Sun2tm1.1Cyh/Sun2+
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0009267 abnormal cerebellum fissure morphology "any structural anomaly of the deep furrows which divide the lobules of the cerebellum, including the postcentral, primary and secondary furrows" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj,Sun2tm1.1Cyh/Sun2+
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0009268 absent cerebellum fissure "absence of the deep furrows which divide the lobules of the cerebellum, including the postcentral, primary and secondary furrows" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0009451 abnormal chromosome pairing during meiosis "an anomaly in the highly specific side-by-side association of homologous chromosomes during first prophase of meiosis" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

Allelic Composition: Sun1tm1Mhan/Sun1tm1Mhan
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J

Allelic Composition: Rad21ltm1Yow/Rad21ltm1Yow,Sun1tm1Mhan/Sun1tm1Mhan
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj

 MP:0009703 decreased birth body size "reduction in average body size at birth compared to controls" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Sun1tm1Mhan/Sun1tm1Mhan,Sun2tm1Mhan/Sun2tm1Mhan
Genetic Background: involves: 129S6/SvEvTac

 MP:0009719 reduced cerebellar foliation "the cerebellar lobules are reduced in size or number" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj,Sun2tm1.1Cyh/Sun2+
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0010008 abnormal Purkinje cell migration "defective or impaired movement of immature Purkinje cells from the ventricular zone of the fourth ventricle to the forming Purkinje cell layer during development of the cerebellar cortex" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj,Sun2tm1.1Cyh/Sun2+
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 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: Sun1tm1Mhan/Sun1tm1Mhan,Sun2tm1Mhan/Sun2tm1Mhan
Genetic Background: involves: 129S6/SvEvTac

 MP:0011089 complete perinatal lethality "death of all organisms of a given genotype in a population within the perinatal period (Mus: E18.5 through postnatal day 1)" [MGI:csmith]
Show

Allelic Composition: Sun1tm1.1Ktj/Sun1tm1.1Ktj
Genetic Background: involves: 129/Sv * C57BL/6 * C57BL/6N

 MP:0011967 increased or absent threshold for auditory brainstem response "increase in the value at which one or more sound frequencies or broadband clicks first elicits a recordable response generated by electrical activity of neurons in the ascending auditory system, or complete lack of a recordable response at any frequency or broadband click" [MGI:csmith]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

 MP:0013507 increased ovary apotosis "increase in the timing or the number of ovary cells undergoing programmed cell death" [MGI:csmith]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

 MP:0013601 increased testis apoptosis "increase in the number of cells of the male reproductive glands undergoing programmed cell death" [MGI:Anna]
Show

Allelic Composition: ApcMin/ApcMin,Ppardtm1.1Rev/Ppardtm1.1Rev
Genetic Background: involves: C57BL/6J

 MP:0030024 abnormal meiotic attachment of telomere to nuclear envelope "any anomaly in the meiotic cell cycle process in which physical connections are formed between telomeric heterochromatin and the nuclear envelope, facilitating bouquet formation" [GO:0070197]
Show

Allelic Composition: Sun1tm1Mhan/Sun1tm1Mhan
Genetic Background: B6.129S6-Sun1tm1Mhan

  


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






 

0 s.

 
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