Incidental Mutation 'IGL02361:Mov10'
ID 290507
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Mov10
Ensembl Gene ENSMUSG00000002227
Gene Name Mov10 RISC complex RNA helicase
Synonyms Mov-10
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.317) question?
Stock # IGL02361
Quality Score
Status
Chromosome 3
Chromosomal Location 104702152-104725879 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 104711437 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000128246 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000002297] [ENSMUST00000106774] [ENSMUST00000106775] [ENSMUST00000136148] [ENSMUST00000166979] [ENSMUST00000168015]
AlphaFold P23249
Predicted Effect probably benign
Transcript: ENSMUST00000002297
SMART Domains Protein: ENSMUSP00000002297
Gene: ENSMUSG00000002227

DomainStartEndE-ValueType
low complexity region 297 312 N/A INTRINSIC
low complexity region 338 353 N/A INTRINSIC
AAA 517 699 5.72e-3 SMART
low complexity region 953 970 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000106774
SMART Domains Protein: ENSMUSP00000102386
Gene: ENSMUSG00000002227

DomainStartEndE-ValueType
low complexity region 297 312 N/A INTRINSIC
low complexity region 338 353 N/A INTRINSIC
AAA 517 699 5.72e-3 SMART
low complexity region 953 970 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000106775
SMART Domains Protein: ENSMUSP00000102387
Gene: ENSMUSG00000002227

DomainStartEndE-ValueType
low complexity region 297 312 N/A INTRINSIC
low complexity region 338 353 N/A INTRINSIC
AAA 517 699 5.72e-3 SMART
low complexity region 953 970 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000136148
Predicted Effect noncoding transcript
Transcript: ENSMUST00000145414
Predicted Effect probably benign
Transcript: ENSMUST00000166979
SMART Domains Protein: ENSMUSP00000126897
Gene: ENSMUSG00000002227

DomainStartEndE-ValueType
low complexity region 61 75 N/A INTRINSIC
low complexity region 370 385 N/A INTRINSIC
low complexity region 411 426 N/A INTRINSIC
AAA 590 772 5.72e-3 SMART
low complexity region 1026 1043 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000168015
SMART Domains Protein: ENSMUSP00000128246
Gene: ENSMUSG00000002227

DomainStartEndE-ValueType
low complexity region 297 312 N/A INTRINSIC
low complexity region 338 353 N/A INTRINSIC
AAA 517 699 5.72e-3 SMART
low complexity region 953 970 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000196161
Predicted Effect noncoding transcript
Transcript: ENSMUST00000196211
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Homozygous knockout is embryonic lethal. Heterozygous knockout leads to reduced dendritic branching of neurons, which affects anxiety- and/or activity-related behavior. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aqp1 A C 6: 55,322,498 (GRCm39) L164F possibly damaging Het
Bfsp1 T C 2: 143,673,907 (GRCm39) E261G probably damaging Het
Brinp2 A G 1: 158,074,748 (GRCm39) C458R probably damaging Het
Cacng3 T G 7: 122,271,169 (GRCm39) M58R possibly damaging Het
Cfap43 A T 19: 47,885,852 (GRCm39) C254* probably null Het
Cnga1 T C 5: 72,774,061 (GRCm39) probably null Het
Dis3 A T 14: 99,317,148 (GRCm39) Y765* probably null Het
Dpep1 T A 8: 123,926,957 (GRCm39) S260R probably benign Het
Elmod1 A G 9: 53,838,842 (GRCm39) L106P probably damaging Het
Fut10 A G 8: 31,691,398 (GRCm39) Y81C probably damaging Het
Fzd10 T A 5: 128,678,932 (GRCm39) D217E possibly damaging Het
Gap43 T C 16: 42,160,871 (GRCm39) probably benign Het
Gigyf1 T C 5: 137,517,989 (GRCm39) probably benign Het
Gpc5 C T 14: 115,370,699 (GRCm39) R175* probably null Het
Gpi-ps T C 8: 5,690,896 (GRCm39) noncoding transcript Het
Kcna1 C A 6: 126,619,869 (GRCm39) Q150H probably damaging Het
Lama5 A T 2: 179,835,677 (GRCm39) C1225* probably null Het
Lrrc25 A T 8: 71,070,477 (GRCm39) D86V probably benign Het
Madd A T 2: 90,992,543 (GRCm39) V1043E probably benign Het
Mzb1 T A 18: 35,782,250 (GRCm39) H46L possibly damaging Het
Nek10 A T 14: 14,843,856 (GRCm38) Q193L probably damaging Het
Nos3 A T 5: 24,572,621 (GRCm39) I187F probably damaging Het
Or4c1 T A 2: 89,133,526 (GRCm39) M137L probably benign Het
Or5p53 T A 7: 107,533,484 (GRCm39) Y252* probably null Het
Or6c69c A G 10: 129,911,143 (GRCm39) Y288C probably damaging Het
Pgap1 T C 1: 54,551,975 (GRCm39) T486A probably benign Het
Prdm9 C T 17: 15,783,109 (GRCm39) V58M probably damaging Het
Prkd2 A G 7: 16,581,583 (GRCm39) Y146C probably damaging Het
Psmd9 G T 5: 123,386,379 (GRCm39) R175I probably damaging Het
Pxdn A G 12: 30,049,188 (GRCm39) D618G probably damaging Het
Rgs6 A T 12: 82,665,393 (GRCm39) probably benign Het
Rrm2 G T 12: 24,761,438 (GRCm39) probably benign Het
Shank3 T C 15: 89,388,536 (GRCm39) V376A probably damaging Het
Slc5a10 A G 11: 61,610,666 (GRCm39) probably null Het
Slfn3 A T 11: 83,104,068 (GRCm39) Q313L possibly damaging Het
Sptbn1 A T 11: 30,060,783 (GRCm39) F2062L probably damaging Het
Tbc1d10a T C 11: 4,165,047 (GRCm39) V500A probably benign Het
Tcea1 T C 1: 4,966,570 (GRCm39) probably benign Het
Thsd7a T C 6: 12,348,192 (GRCm39) probably benign Het
Tm9sf4 C T 2: 153,029,570 (GRCm39) T173M probably benign Het
Tmtc2 T C 10: 105,107,387 (GRCm39) T709A probably benign Het
Zfp385b T C 2: 77,280,647 (GRCm39) E97G probably damaging Het
Zim1 A T 7: 6,685,873 (GRCm39) probably null Het
Other mutations in Mov10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00498:Mov10 APN 3 104,708,263 (GRCm39) splice site probably benign
IGL01111:Mov10 APN 3 104,708,721 (GRCm39) missense possibly damaging 0.71
IGL01315:Mov10 APN 3 104,703,261 (GRCm39) missense probably damaging 0.98
IGL01463:Mov10 APN 3 104,707,640 (GRCm39) missense probably damaging 1.00
IGL02114:Mov10 APN 3 104,702,634 (GRCm39) unclassified probably benign
IGL02354:Mov10 APN 3 104,711,437 (GRCm39) splice site probably benign
IGL02692:Mov10 APN 3 104,708,119 (GRCm39) nonsense probably null
IGL03104:Mov10 APN 3 104,704,623 (GRCm39) missense probably damaging 1.00
IGL03121:Mov10 APN 3 104,708,318 (GRCm39) missense probably benign
P0040:Mov10 UTSW 3 104,711,995 (GRCm39) missense probably damaging 1.00
R0025:Mov10 UTSW 3 104,711,919 (GRCm39) missense probably damaging 1.00
R0270:Mov10 UTSW 3 104,702,721 (GRCm39) missense probably benign 0.09
R0747:Mov10 UTSW 3 104,709,812 (GRCm39) missense probably benign 0.41
R1434:Mov10 UTSW 3 104,702,490 (GRCm39) missense probably damaging 1.00
R1482:Mov10 UTSW 3 104,711,862 (GRCm39) missense probably damaging 0.98
R1594:Mov10 UTSW 3 104,702,727 (GRCm39) missense probably damaging 1.00
R1656:Mov10 UTSW 3 104,706,912 (GRCm39) missense probably benign 0.03
R1739:Mov10 UTSW 3 104,707,598 (GRCm39) missense probably damaging 0.98
R1785:Mov10 UTSW 3 104,725,432 (GRCm39) missense possibly damaging 0.73
R1786:Mov10 UTSW 3 104,725,432 (GRCm39) missense possibly damaging 0.73
R1911:Mov10 UTSW 3 104,708,876 (GRCm39) splice site probably benign
R1962:Mov10 UTSW 3 104,704,293 (GRCm39) missense probably damaging 1.00
R1993:Mov10 UTSW 3 104,706,735 (GRCm39) missense probably damaging 1.00
R2095:Mov10 UTSW 3 104,708,847 (GRCm39) missense probably damaging 1.00
R2138:Mov10 UTSW 3 104,711,558 (GRCm39) missense probably benign 0.00
R3107:Mov10 UTSW 3 104,707,040 (GRCm39) missense probably damaging 1.00
R4241:Mov10 UTSW 3 104,704,592 (GRCm39) missense probably benign 0.45
R4280:Mov10 UTSW 3 104,707,095 (GRCm39) missense probably damaging 0.98
R4474:Mov10 UTSW 3 104,725,781 (GRCm39) missense probably damaging 1.00
R5227:Mov10 UTSW 3 104,709,894 (GRCm39) missense probably benign
R5391:Mov10 UTSW 3 104,709,849 (GRCm39) missense probably benign 0.12
R5704:Mov10 UTSW 3 104,706,912 (GRCm39) missense probably benign 0.03
R5819:Mov10 UTSW 3 104,708,828 (GRCm39) missense probably damaging 1.00
R5842:Mov10 UTSW 3 104,706,695 (GRCm39) splice site probably benign
R6059:Mov10 UTSW 3 104,725,266 (GRCm39) utr 3 prime probably benign
R6692:Mov10 UTSW 3 104,725,360 (GRCm39) missense probably damaging 0.97
R7226:Mov10 UTSW 3 104,708,328 (GRCm39) missense probably damaging 1.00
R7426:Mov10 UTSW 3 104,707,368 (GRCm39) splice site probably null
R7633:Mov10 UTSW 3 104,704,381 (GRCm39) missense possibly damaging 0.93
R7637:Mov10 UTSW 3 104,703,201 (GRCm39) missense probably benign 0.26
R7869:Mov10 UTSW 3 104,711,994 (GRCm39) missense probably damaging 1.00
R8684:Mov10 UTSW 3 104,711,690 (GRCm39) missense probably benign
R9008:Mov10 UTSW 3 104,707,332 (GRCm39) missense probably benign 0.09
R9127:Mov10 UTSW 3 104,711,659 (GRCm39) nonsense probably null
R9559:Mov10 UTSW 3 104,708,277 (GRCm39) missense
R9587:Mov10 UTSW 3 104,711,899 (GRCm39) missense probably benign 0.11
R9602:Mov10 UTSW 3 104,708,284 (GRCm39) missense probably benign 0.18
R9606:Mov10 UTSW 3 104,707,664 (GRCm39) missense probably benign 0.00
R9708:Mov10 UTSW 3 104,704,613 (GRCm39) missense probably benign
Posted On 2015-04-16