Incidental Mutation 'IGL02419:Misp'
ID 292602
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Misp
Ensembl Gene ENSMUSG00000035852
Gene Name mitotic spindle positioning
Synonyms 9130017N09Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.075) question?
Stock # IGL02419
Quality Score
Chromosome 10
Chromosomal Location 79656853-79666286 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to G at 79663705 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000151839 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000046833] [ENSMUST00000169041] [ENSMUST00000218687] [ENSMUST00000219305] [ENSMUST00000219734]
AlphaFold Q9D279
Predicted Effect probably benign
Transcript: ENSMUST00000046833
SMART Domains Protein: ENSMUSP00000048893
Gene: ENSMUSG00000035852

low complexity region 262 284 N/A INTRINSIC
Pfam:AKAP2_C 294 643 2.2e-140 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000169041
SMART Domains Protein: ENSMUSP00000130071
Gene: ENSMUSG00000035852

low complexity region 262 284 N/A INTRINSIC
Pfam:AKAP2_C 294 643 1.7e-150 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000218531
Predicted Effect probably benign
Transcript: ENSMUST00000218687
Predicted Effect probably benign
Transcript: ENSMUST00000219305
Predicted Effect probably benign
Transcript: ENSMUST00000219734
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is an actin-bundling protein involved in determining cell morphology and mitotic progression. The encoded protein is required for the proper positioning of the mitotic spindle. Two transcript variants, one protein-coding and the other non-protein coding, have been found for this gene. [provided by RefSeq, Feb 2016]
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933402J07Rik T C 8: 88,312,727 (GRCm39) F171L possibly damaging Het
Abca2 A G 2: 25,336,849 (GRCm39) N2291D probably benign Het
Adamts9 A G 6: 92,773,978 (GRCm39) V1145A probably benign Het
Adcy2 A G 13: 69,130,482 (GRCm39) V135A probably benign Het
Akr1c14 A T 13: 4,130,617 (GRCm39) probably null Het
Aptx G T 4: 40,691,032 (GRCm39) A229E probably benign Het
Ash1l T C 3: 88,892,872 (GRCm39) S1584P probably benign Het
Catsper3 A T 13: 55,955,881 (GRCm39) T329S possibly damaging Het
Cntrl A G 2: 35,024,055 (GRCm39) D27G probably damaging Het
Cobll1 A T 2: 64,981,392 (GRCm39) I98K probably damaging Het
Ctdp1 T C 18: 80,463,799 (GRCm39) K79R probably damaging Het
Cwf19l2 T C 9: 3,418,777 (GRCm39) probably null Het
Cyp11b2 A T 15: 74,722,904 (GRCm39) F498Y probably damaging Het
Dnpep A G 1: 75,292,332 (GRCm39) I162T probably damaging Het
Efcab9 T C 11: 32,472,950 (GRCm39) I166V probably benign Het
Ep400 A T 5: 110,845,242 (GRCm39) probably null Het
Gata6 G A 18: 11,054,220 (GRCm39) G50R probably damaging Het
Gm9631 G A 11: 121,834,478 (GRCm39) Het
Grifin T C 5: 140,550,455 (GRCm39) T20A probably benign Het
Hnf4a A T 2: 163,408,202 (GRCm39) I352F probably damaging Het
Ifi204 T C 1: 173,576,946 (GRCm39) T552A possibly damaging Het
Ifi205 C T 1: 173,845,180 (GRCm39) A201T probably damaging Het
Kcnk6 A G 7: 28,924,627 (GRCm39) V259A probably benign Het
Kif21b A G 1: 136,079,005 (GRCm39) N451S probably benign Het
Klhl24 T A 16: 19,926,118 (GRCm39) Y215* probably null Het
Lyst G A 13: 13,835,541 (GRCm39) C1741Y probably benign Het
Mical1 A G 10: 41,358,273 (GRCm39) K429E possibly damaging Het
Mon2 T C 10: 122,852,352 (GRCm39) N1007S probably benign Het
Or10v1 A T 19: 11,874,186 (GRCm39) Y267F probably benign Het
Or14a260 C A 7: 85,984,870 (GRCm39) V245F probably damaging Het
Or51v8 A T 7: 103,319,682 (GRCm39) C185* probably null Het
Or8k41 T A 2: 86,313,259 (GRCm39) I276F probably damaging Het
Pex6 C A 17: 47,035,361 (GRCm39) T840N possibly damaging Het
Prox1 C T 1: 189,893,327 (GRCm39) A373T probably benign Het
Rapgef3 G T 15: 97,648,171 (GRCm39) N679K probably benign Het
Serpina3n T C 12: 104,379,777 (GRCm39) V390A possibly damaging Het
Sirpb1a A G 3: 15,491,398 (GRCm39) F23S probably benign Het
Slc44a3 T C 3: 121,283,906 (GRCm39) T449A probably benign Het
Smad6 G A 9: 63,860,800 (GRCm39) probably benign Het
Sos2 C T 12: 69,663,764 (GRCm39) M573I probably benign Het
St8sia1 A T 6: 142,774,661 (GRCm39) I306N probably damaging Het
Tnks1bp1 T C 2: 84,902,125 (GRCm39) S1674P possibly damaging Het
Trim47 G A 11: 115,997,027 (GRCm39) R576W probably damaging Het
Wdr86 A T 5: 24,927,702 (GRCm39) I79N probably damaging Het
Wwp2 T A 8: 108,276,447 (GRCm39) V473D probably damaging Het
Zc3h12a T C 4: 125,013,581 (GRCm39) T428A probably benign Het
Zfp592 A G 7: 80,687,993 (GRCm39) E973G probably damaging Het
Other mutations in Misp
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02565:Misp APN 10 79,662,177 (GRCm39) missense probably benign 0.33
IGL02901:Misp APN 10 79,662,771 (GRCm39) missense possibly damaging 0.70
R1118:Misp UTSW 10 79,662,969 (GRCm39) missense probably benign 0.01
R1421:Misp UTSW 10 79,662,681 (GRCm39) missense probably damaging 1.00
R1656:Misp UTSW 10 79,661,777 (GRCm39) missense possibly damaging 0.75
R2864:Misp UTSW 10 79,662,872 (GRCm39) missense probably benign 0.05
R3786:Misp UTSW 10 79,661,795 (GRCm39) missense probably benign 0.23
R5035:Misp UTSW 10 79,663,790 (GRCm39) missense probably benign 0.01
R5503:Misp UTSW 10 79,662,552 (GRCm39) missense probably damaging 1.00
R5594:Misp UTSW 10 79,662,977 (GRCm39) missense probably damaging 1.00
R5982:Misp UTSW 10 79,663,728 (GRCm39) nonsense probably null
R6066:Misp UTSW 10 79,662,146 (GRCm39) missense possibly damaging 0.66
R6236:Misp UTSW 10 79,662,956 (GRCm39) missense probably benign 0.00
R7103:Misp UTSW 10 79,662,999 (GRCm39) missense probably damaging 1.00
R8170:Misp UTSW 10 79,662,300 (GRCm39) missense probably benign 0.39
R8479:Misp UTSW 10 79,663,750 (GRCm39) missense possibly damaging 0.91
R8961:Misp UTSW 10 79,663,823 (GRCm39) missense probably benign 0.01
R9430:Misp UTSW 10 79,661,675 (GRCm39) missense probably benign
Posted On 2015-04-16