Incidental Mutation 'R5997:Spns3'
ID480638
Institutional Source Beutler Lab
Gene Symbol Spns3
Ensembl Gene ENSMUSG00000020798
Gene Namespinster homolog 3
Synonyms9830002I17Rik
MMRRC Submission 044176-MU
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R5997 (G1)
Quality Score225.009
Status Validated
Chromosome11
Chromosomal Location72494919-72550506 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to G at 72539078 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Proline at position 175 (T175P)
Ref Sequence ENSEMBL: ENSMUSP00000090617 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021154] [ENSMUST00000092940]
Predicted Effect probably damaging
Transcript: ENSMUST00000021154
AA Change: T153P

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000021154
Gene: ENSMUSG00000020798
AA Change: T153P

DomainStartEndE-ValueType
low complexity region 9 25 N/A INTRINSIC
Pfam:MFS_1 47 402 2.4e-28 PFAM
Pfam:Sugar_tr 48 225 3.3e-9 PFAM
transmembrane domain 428 450 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000092940
AA Change: T175P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000090617
Gene: ENSMUSG00000020798
AA Change: T175P

DomainStartEndE-ValueType
low complexity region 9 25 N/A INTRINSIC
Pfam:Sugar_tr 44 248 1.5e-11 PFAM
Pfam:OATP 50 388 4.8e-9 PFAM
Pfam:MFS_1 55 425 4.2e-35 PFAM
transmembrane domain 450 472 N/A INTRINSIC
Meta Mutation Damage Score 0.5159 question?
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 99.4%
  • 10x: 97.1%
  • 20x: 90.5%
Validation Efficiency 100% (78/78)
Allele List at MGI
Other mutations in this stock
Total: 78 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700061G19Rik A T 17: 56,876,373 D38V probably benign Het
Abcb9 A T 5: 124,089,815 V121E possibly damaging Het
Adamts20 T A 15: 94,379,747 Y278F probably damaging Het
Adcy7 A T 8: 88,326,392 D972V probably benign Het
Adgrf3 C A 5: 30,198,362 probably null Het
Ahdc1 G T 4: 133,063,895 G816C probably benign Het
Aifm3 A G 16: 17,502,130 K283E probably benign Het
Akap6 T C 12: 52,937,233 probably null Het
Ank1 T C 8: 23,099,662 L593P probably damaging Het
Apol11b T A 15: 77,635,497 T128S probably benign Het
C1qtnf7 C A 5: 43,616,085 T235K probably damaging Het
Camk2a A T 18: 60,977,957 I73F probably damaging Het
Cd109 G T 9: 78,705,062 V1244F possibly damaging Het
Cep164 A G 9: 45,769,463 L1240S possibly damaging Het
Cnga1 T A 5: 72,604,575 D532V probably damaging Het
Cyp4a14 A T 4: 115,496,100 L5* probably null Het
Cyp4a30b A T 4: 115,459,391 K405* probably null Het
Dchs1 T C 7: 105,754,095 D3080G probably benign Het
Ddx1 T C 12: 13,237,799 D168G probably damaging Het
Dhx57 T G 17: 80,245,806 K1231Q probably damaging Het
Dnah14 A G 1: 181,770,105 N3640D probably benign Het
Dock4 T A 12: 40,755,834 L935Q probably damaging Het
Dus2 A T 8: 106,046,066 R269S probably benign Het
E230025N22Rik G A 18: 36,689,108 R201C possibly damaging Het
Erbb3 G A 10: 128,583,185 T269M probably damaging Het
Fam71f2 T A 6: 29,290,424 L267* probably null Het
Fbxo43 T C 15: 36,162,093 R323G probably damaging Het
Fktn A G 4: 53,735,061 H233R probably benign Het
Ftsj3 A T 11: 106,252,251 D412E probably damaging Het
Fzd7 A T 1: 59,484,544 M529L probably benign Het
Fzr1 T A 10: 81,370,826 probably null Het
Ganc T G 2: 120,430,605 V257G possibly damaging Het
Gm4131 T C 14: 62,464,758 K254E probably damaging Het
Gm6583 C T 5: 112,355,008 V277M possibly damaging Het
Gm7347 G T 5: 26,057,249 Y91* probably null Het
Gm9857 G A 3: 108,940,165 probably benign Het
Grpel1 T C 5: 36,465,248 S19P probably benign Het
Gtf3c4 T C 2: 28,833,711 K670E possibly damaging Het
Hist1h2bf G A 13: 23,574,103 probably benign Het
Hmcn1 G T 1: 150,704,173 Q1938K possibly damaging Het
Hnrnpk T C 13: 58,399,157 D71G probably damaging Het
Hspa4l G A 3: 40,767,979 R311H probably damaging Het
Igkv3-5 T A 6: 70,663,704 F56L probably benign Het
Igkv6-20 T A 6: 70,335,914 T92S possibly damaging Het
Krt8 C T 15: 102,000,594 V200I possibly damaging Het
Lamb2 A T 9: 108,480,388 T66S possibly damaging Het
Lamp3 A G 16: 19,701,028 L135S probably benign Het
Lrguk A G 6: 34,129,143 Y701C probably damaging Het
Mcc G T 18: 44,449,321 L588M probably damaging Het
Mcidas T A 13: 112,998,586 L234Q probably damaging Het
Mtmr14 T A 6: 113,280,614 L208Q probably damaging Het
Myof A G 19: 37,905,299 F1139L possibly damaging Het
Nlrp14 C A 7: 107,182,496 T300K probably benign Het
Olfr1474 A G 19: 13,471,506 I179V probably benign Het
Olfr165 T A 16: 19,407,944 H24L probably benign Het
Olfr716 A T 7: 107,147,328 E4V possibly damaging Het
Olfr890 A T 9: 38,143,801 Y217F probably damaging Het
Orc2 A G 1: 58,472,388 I354T probably damaging Het
Pard3b G T 1: 62,076,409 S140I probably damaging Het
Pcgf5 A G 19: 36,434,603 D49G probably benign Het
Pcsk6 T C 7: 65,959,293 F388S probably damaging Het
Prokr2 A C 2: 132,381,442 I60S probably damaging Het
Rab33b A G 3: 51,484,479 T50A possibly damaging Het
Rbms3 T C 9: 116,719,389 D61G probably damaging Het
Rhcg T A 7: 79,600,514 K274* probably null Het
Rnf112 C T 11: 61,451,022 V319M possibly damaging Het
Rnf44 A T 13: 54,682,800 S265T possibly damaging Het
Sf3a3 A G 4: 124,722,058 D168G probably damaging Het
Sik2 A G 9: 50,895,342 probably null Het
Slco1a5 T A 6: 142,253,113 L275F probably benign Het
Smtnl1 T C 2: 84,815,378 H383R probably damaging Het
Togaram1 A G 12: 64,995,538 T1174A probably benign Het
Tradd C T 8: 105,260,645 E10K possibly damaging Het
Ttc7b A T 12: 100,373,560 Y579N probably damaging Het
Uncx G A 5: 139,547,589 G470R probably damaging Het
Vav3 T A 3: 109,501,461 M177K probably damaging Het
Wfs1 A T 5: 36,967,750 I599N probably damaging Het
Zfp454 G A 11: 50,873,622 H217Y probably damaging Het
Other mutations in Spns3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00822:Spns3 APN 11 72499353 critical splice donor site probably null
IGL02731:Spns3 APN 11 72529577 missense probably damaging 1.00
IGL03400:Spns3 APN 11 72499675 missense possibly damaging 0.65
R0948:Spns3 UTSW 11 72545940 missense probably damaging 1.00
R1807:Spns3 UTSW 11 72538340 nonsense probably null
R2151:Spns3 UTSW 11 72545961 splice site probably benign
R2393:Spns3 UTSW 11 72550233 start gained probably benign
R3703:Spns3 UTSW 11 72499530 splice site probably benign
R4207:Spns3 UTSW 11 72538361 missense probably damaging 1.00
R4685:Spns3 UTSW 11 72537270 missense probably damaging 1.00
R4932:Spns3 UTSW 11 72499495 missense possibly damaging 0.47
R5009:Spns3 UTSW 11 72537201 missense probably damaging 1.00
R5041:Spns3 UTSW 11 72536547 missense possibly damaging 0.46
R6179:Spns3 UTSW 11 72499523 missense probably damaging 1.00
R6277:Spns3 UTSW 11 72529640 missense possibly damaging 0.75
R7635:Spns3 UTSW 11 72539034 critical splice donor site probably null
X0017:Spns3 UTSW 11 72505065 missense possibly damaging 0.53
Z1176:Spns3 UTSW 11 72529582 nonsense probably null
Z1176:Spns3 UTSW 11 72536654 missense probably damaging 1.00
Z1176:Spns3 UTSW 11 72545890 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGTATACACCCAAGGAAACAGG -3'
(R):5'- TCACGAGGTCCCTTTTACGC -3'

Sequencing Primer
(F):5'- CCCAAGGAAACAGGCTCAGAG -3'
(R):5'- GGTCCCTTTTACGCCCCCTG -3'
Posted On2017-06-26