Incidental Mutation 'R5943:Strn'
ID 460452
Institutional Source Beutler Lab
Gene Symbol Strn
Ensembl Gene ENSMUSG00000024077
Gene Name striatin, calmodulin binding protein
Synonyms
MMRRC Submission 044135-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.565) question?
Stock # R5943 (G1)
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 78957327-79043990 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 78977276 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Phenylalanine at position 211 (V211F)
Ref Sequence ENSEMBL: ENSMUSP00000024881 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000024881] [ENSMUST00000145910]
AlphaFold O55106
Predicted Effect probably damaging
Transcript: ENSMUST00000024881
AA Change: V211F

PolyPhen 2 Score 0.965 (Sensitivity: 0.78; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000024881
Gene: ENSMUSG00000024077
AA Change: V211F

DomainStartEndE-ValueType
low complexity region 85 101 N/A INTRINSIC
low complexity region 178 195 N/A INTRINSIC
low complexity region 223 231 N/A INTRINSIC
low complexity region 259 276 N/A INTRINSIC
WD40 299 338 6.04e-8 SMART
WD40 352 391 2.42e-7 SMART
WD40 405 444 1.21e-7 SMART
WD40 493 539 1.28e1 SMART
WD40 542 581 4.4e-10 SMART
WD40 584 627 2.48e-4 SMART
Predicted Effect unknown
Transcript: ENSMUST00000145480
AA Change: V214F
SMART Domains Protein: ENSMUSP00000117663
Gene: ENSMUSG00000024077
AA Change: V214F

DomainStartEndE-ValueType
low complexity region 60 76 N/A INTRINSIC
low complexity region 153 171 N/A INTRINSIC
low complexity region 227 235 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000145910
AA Change: V364F

PolyPhen 2 Score 0.956 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000120830
Gene: ENSMUSG00000024077
AA Change: V364F

DomainStartEndE-ValueType
low complexity region 17 45 N/A INTRINSIC
Pfam:Striatin 48 177 4.2e-50 PFAM
low complexity region 238 254 N/A INTRINSIC
low complexity region 331 348 N/A INTRINSIC
low complexity region 376 384 N/A INTRINSIC
low complexity region 412 429 N/A INTRINSIC
WD40 452 491 6.04e-8 SMART
WD40 505 544 2.42e-7 SMART
WD40 558 597 1.21e-7 SMART
WD40 646 692 1.28e1 SMART
WD40 695 734 4.4e-10 SMART
WD40 737 780 2.48e-4 SMART
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.5%
  • 10x: 97.7%
  • 20x: 93.1%
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice heterozygous for a knock-out allele exhibit increased blood pressure and circulating aldosterone when fed a liberal salt diet. No mice could be generated that were homozygous for the allele. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 65 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aars2 C A 17: 45,828,637 (GRCm39) Q671K probably benign Het
Acaa2 A G 18: 74,925,453 (GRCm39) H72R probably damaging Het
Acad8 A G 9: 26,910,740 (GRCm39) L18P probably benign Het
Acap3 T C 4: 155,983,879 (GRCm39) V115A possibly damaging Het
Adamts9 T C 6: 92,880,767 (GRCm39) T503A probably benign Het
Adcy1 T C 11: 7,111,337 (GRCm39) F876S probably damaging Het
Adgrv1 T C 13: 81,534,985 (GRCm39) E5760G probably damaging Het
Ankrd26 A T 6: 118,482,707 (GRCm39) I1631K probably damaging Het
Ccdc150 A G 1: 54,339,526 (GRCm39) T457A probably benign Het
Cd163 T C 6: 124,306,561 (GRCm39) *1160R probably null Het
Cdc6 T C 11: 98,811,589 (GRCm39) S517P probably damaging Het
Cenpf A T 1: 189,392,166 (GRCm39) D555E possibly damaging Het
Cfap251 A G 5: 123,424,420 (GRCm39) T205A probably benign Het
Clcn1 T A 6: 42,269,900 (GRCm39) I241N probably damaging Het
Clrn2 A T 5: 45,621,061 (GRCm39) I152F probably benign Het
Col4a4 A G 1: 82,502,737 (GRCm39) I349T unknown Het
Coq8b T A 7: 26,933,428 (GRCm39) F96L probably damaging Het
Cp A T 3: 20,018,470 (GRCm39) N58I probably benign Het
Dcst1 A T 3: 89,263,718 (GRCm39) probably null Het
Dhrs3 A T 4: 144,646,546 (GRCm39) M199L possibly damaging Het
Dido1 A T 2: 180,303,675 (GRCm39) S1410T probably benign Het
Dnase1l2 C T 17: 24,661,721 (GRCm39) A13T probably damaging Het
Duox1 G A 2: 122,163,916 (GRCm39) R861Q probably benign Het
Eya2 A G 2: 165,566,609 (GRCm39) H220R probably damaging Het
Fas T G 19: 34,297,987 (GRCm39) probably null Het
Fezf1 T A 6: 23,246,948 (GRCm39) K295* probably null Het
Gldn T G 9: 54,245,721 (GRCm39) I424R possibly damaging Het
Gnptab T C 10: 88,269,376 (GRCm39) V693A probably benign Het
Gsdma A T 11: 98,563,852 (GRCm39) T269S probably benign Het
Hectd4 A T 5: 121,460,357 (GRCm39) T2209S probably benign Het
Hoxd3 A G 2: 74,577,173 (GRCm39) N351S probably benign Het
Itpkc T A 7: 26,912,404 (GRCm39) N581I possibly damaging Het
Kank3 G T 17: 34,037,375 (GRCm39) E226D probably damaging Het
Krtap5-1 A G 7: 141,850,788 (GRCm39) S7P unknown Het
Lrriq3 A G 3: 154,869,587 (GRCm39) Y304C probably damaging Het
Man2a1 A G 17: 64,932,375 (GRCm39) K154R probably benign Het
Mdn1 T C 4: 32,678,330 (GRCm39) S653P probably damaging Het
Mri1 A T 8: 84,980,948 (GRCm39) L194* probably null Het
Mtus1 T C 8: 41,537,302 (GRCm39) E138G probably benign Het
Myo3b G A 2: 70,117,285 (GRCm39) R906Q probably benign Het
Nckipsd C T 9: 108,689,435 (GRCm39) P199S possibly damaging Het
Or52n5 T A 7: 104,587,850 (GRCm39) I39N possibly damaging Het
Or9i16 C T 19: 13,865,116 (GRCm39) V153I possibly damaging Het
Pacsin1 T C 17: 27,925,045 (GRCm39) L253P probably damaging Het
Pcca T A 14: 122,896,188 (GRCm39) I268N probably damaging Het
Pcdhga8 A G 18: 37,949,565 (GRCm39) D327G probably damaging Het
Pcnx4 A G 12: 72,626,232 (GRCm39) H1146R probably damaging Het
Pnma8b T C 7: 16,680,362 (GRCm39) S449P probably benign Het
Psmb9 T C 17: 34,403,265 (GRCm39) E61G probably damaging Het
Pxylp1 A G 9: 96,721,203 (GRCm39) Y101H probably damaging Het
Radil A G 5: 142,471,213 (GRCm39) I1044T probably damaging Het
Rnf43 G A 11: 87,622,561 (GRCm39) R554H probably damaging Het
Sp5 A T 2: 70,305,659 (GRCm39) Q17L probably null Het
Spmip1 T A 6: 29,471,908 (GRCm39) L128Q possibly damaging Het
Sult3a1 A G 10: 33,742,637 (GRCm39) D88G probably damaging Het
Trim14 T C 4: 46,522,136 (GRCm39) I180M probably benign Het
Tsnax C A 8: 125,751,278 (GRCm39) S90* probably null Het
Ttn A G 2: 76,798,780 (GRCm39) M498T probably benign Het
Vmn1r198 T A 13: 22,539,367 (GRCm39) Y195* probably null Het
Vmn2r70 T C 7: 85,215,199 (GRCm39) T112A probably benign Het
Wwc2 T C 8: 48,443,137 (GRCm39) N32S possibly damaging Het
Yme1l1 G T 2: 23,058,342 (GRCm39) R158L probably damaging Het
Zc2hc1c C A 12: 85,336,483 (GRCm39) H47N probably damaging Het
Zc3h10 C A 10: 128,381,396 (GRCm39) probably benign Het
Zfp825 T C 13: 74,629,007 (GRCm39) R170G probably benign Het
Other mutations in Strn
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00722:Strn APN 17 78,999,849 (GRCm39) missense possibly damaging 0.89
IGL02165:Strn APN 17 78,995,049 (GRCm39) missense probably damaging 1.00
IGL02424:Strn APN 17 78,991,780 (GRCm39) missense probably damaging 1.00
IGL02473:Strn APN 17 78,991,722 (GRCm39) missense possibly damaging 0.71
IGL03306:Strn APN 17 78,974,652 (GRCm39) missense probably damaging 0.98
R0053:Strn UTSW 17 78,964,363 (GRCm39) missense possibly damaging 0.92
R0053:Strn UTSW 17 78,964,363 (GRCm39) missense possibly damaging 0.92
R0165:Strn UTSW 17 78,984,803 (GRCm39) missense possibly damaging 0.89
R1156:Strn UTSW 17 78,964,360 (GRCm39) missense probably damaging 0.99
R1191:Strn UTSW 17 78,999,855 (GRCm39) missense possibly damaging 0.82
R1256:Strn UTSW 17 78,972,046 (GRCm39) critical splice donor site probably null
R1700:Strn UTSW 17 78,999,831 (GRCm39) missense probably damaging 1.00
R1878:Strn UTSW 17 78,984,755 (GRCm39) missense possibly damaging 0.81
R1897:Strn UTSW 17 78,990,271 (GRCm39) missense probably benign 0.01
R1912:Strn UTSW 17 78,991,824 (GRCm39) missense probably damaging 1.00
R1975:Strn UTSW 17 78,999,928 (GRCm39) splice site probably null
R2357:Strn UTSW 17 78,963,028 (GRCm39) missense probably damaging 1.00
R3054:Strn UTSW 17 78,990,321 (GRCm39) missense probably damaging 0.99
R3693:Strn UTSW 17 78,964,421 (GRCm39) missense probably damaging 1.00
R3694:Strn UTSW 17 78,964,421 (GRCm39) missense probably damaging 1.00
R3695:Strn UTSW 17 78,964,421 (GRCm39) missense probably damaging 1.00
R3941:Strn UTSW 17 78,965,369 (GRCm39) missense probably damaging 0.99
R4431:Strn UTSW 17 79,043,891 (GRCm39) missense probably damaging 1.00
R4570:Strn UTSW 17 78,984,801 (GRCm39) missense possibly damaging 0.95
R4678:Strn UTSW 17 78,984,780 (GRCm39) missense probably damaging 1.00
R4729:Strn UTSW 17 78,965,390 (GRCm39) missense probably damaging 0.98
R4947:Strn UTSW 17 78,969,208 (GRCm39) missense probably damaging 0.98
R5470:Strn UTSW 17 78,964,374 (GRCm39) missense probably benign 0.01
R5710:Strn UTSW 17 78,995,028 (GRCm39) missense probably damaging 1.00
R6173:Strn UTSW 17 79,008,298 (GRCm39) missense probably damaging 1.00
R6800:Strn UTSW 17 78,977,787 (GRCm39) intron probably benign
R6846:Strn UTSW 17 79,043,886 (GRCm39) missense probably damaging 0.97
R7716:Strn UTSW 17 78,963,204 (GRCm39) missense probably damaging 0.99
R7746:Strn UTSW 17 78,984,801 (GRCm39) missense probably benign 0.11
R7950:Strn UTSW 17 78,977,852 (GRCm39) missense
R7997:Strn UTSW 17 78,991,672 (GRCm39) missense probably benign 0.01
R8344:Strn UTSW 17 78,980,076 (GRCm39) missense probably damaging 1.00
R9074:Strn UTSW 17 79,043,790 (GRCm39) missense probably benign 0.00
R9523:Strn UTSW 17 78,967,575 (GRCm39) missense probably benign 0.17
R9538:Strn UTSW 17 78,972,219 (GRCm39) missense possibly damaging 0.68
RF006:Strn UTSW 17 78,984,700 (GRCm39) frame shift probably null
RF008:Strn UTSW 17 78,984,716 (GRCm39) frame shift probably null
RF017:Strn UTSW 17 78,984,717 (GRCm39) frame shift probably null
RF018:Strn UTSW 17 78,984,712 (GRCm39) frame shift probably null
RF031:Strn UTSW 17 78,984,706 (GRCm39) frame shift probably null
RF035:Strn UTSW 17 78,984,714 (GRCm39) frame shift probably null
RF036:Strn UTSW 17 78,984,706 (GRCm39) frame shift probably null
RF038:Strn UTSW 17 78,984,711 (GRCm39) frame shift probably null
RF039:Strn UTSW 17 78,984,707 (GRCm39) frame shift probably null
RF044:Strn UTSW 17 78,984,717 (GRCm39) frame shift probably null
RF045:Strn UTSW 17 78,984,711 (GRCm39) frame shift probably null
RF047:Strn UTSW 17 78,984,703 (GRCm39) frame shift probably null
RF047:Strn UTSW 17 78,984,699 (GRCm39) frame shift probably null
RF048:Strn UTSW 17 78,984,716 (GRCm39) frame shift probably null
X0022:Strn UTSW 17 79,008,378 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TTAAGGAAGCGGATGTGTGC -3'
(R):5'- GACATTCTTTCTCGTGTAGTGATTC -3'

Sequencing Primer
(F):5'- CAGACTGTGTGCTCTCTGAG -3'
(R):5'- TTTCTCGTGTAGTGATTCCATTAAC -3'
Posted On 2017-02-28