Incidental Mutation 'R1263:Sft2d1'
Institutional Source Beutler Lab
Gene Symbol Sft2d1
Ensembl Gene ENSMUSG00000073468
Gene NameSFT2 domain containing 1
MMRRC Submission 039330-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.113) question?
Stock #R1263 (G1)
Quality Score225
Status Not validated
Chromosomal Location8311102-8396852 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 8320638 bp
Amino Acid Change Lysine to Arginine at position 91 (K91R)
Ref Sequence ENSEMBL: ENSMUSP00000117294 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000130782] [ENSMUST00000145276] [ENSMUST00000154553]
Predicted Effect noncoding transcript
Transcript: ENSMUST00000128087
Predicted Effect silent
Transcript: ENSMUST00000130782
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135627
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135964
Predicted Effect noncoding transcript
Transcript: ENSMUST00000140890
Predicted Effect noncoding transcript
Transcript: ENSMUST00000141213
Predicted Effect silent
Transcript: ENSMUST00000145276
Predicted Effect noncoding transcript
Transcript: ENSMUST00000150728
Predicted Effect noncoding transcript
Transcript: ENSMUST00000153406
Predicted Effect probably benign
Transcript: ENSMUST00000154553
AA Change: K91R

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000117294
Gene: ENSMUSG00000073468
AA Change: K91R

Pfam:Got1 43 154 3.5e-41 PFAM
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.4%
  • 20x: 93.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
0610010F05Rik A T 11: 23,620,278 Y207* probably null Het
Abca8b A C 11: 109,941,607 H1231Q possibly damaging Het
Acbd4 T A 11: 103,103,851 probably null Het
Atp13a4 T A 16: 29,471,953 Y226F possibly damaging Het
Brd3 A C 2: 27,462,522 F132C probably damaging Het
Btaf1 A T 19: 36,956,524 N184I probably benign Het
Ccdc180 A G 4: 45,903,887 E351G possibly damaging Het
Ccdc185 A T 1: 182,747,353 Y590* probably null Het
Chil1 G A 1: 134,189,242 E315K probably benign Het
Col6a6 T A 9: 105,709,489 M1778L probably benign Het
Cyp3a59 A C 5: 146,104,711 Y355S probably damaging Het
Cyp4a31 A G 4: 115,574,711 T396A probably benign Het
Dnah6 A T 6: 73,144,965 I1373N probably damaging Het
Dopey2 C A 16: 93,777,386 H1598N probably benign Het
Erich4 T A 7: 25,615,134 K118M probably damaging Het
Gkap1 A T 13: 58,255,773 V179E probably benign Het
Gpr107 T G 2: 31,178,255 I243S possibly damaging Het
Hs3st6 A G 17: 24,758,530 N328S probably damaging Het
Kcnq5 A T 1: 21,479,378 I375N probably damaging Het
Klhdc3 A T 17: 46,676,966 H266Q probably benign Het
Krt71 C T 15: 101,735,466 G446R probably damaging Het
L3mbtl2 A G 15: 81,682,968 T423A probably benign Het
Mical3 T C 6: 120,952,469 E1812G probably damaging Het
Nlrp1a A G 11: 71,097,122 I1174T probably benign Het
Npas2 C A 1: 39,334,768 Q450K possibly damaging Het
Nrp1 T A 8: 128,468,389 I442N probably damaging Het
Olfr1385 A T 11: 49,495,021 M163L probably benign Het
Olfr338 T A 2: 36,376,994 S73T probably damaging Het
Palld TGCGTAGCG TGCG 8: 61,513,457 probably null Het
Pih1d3 A T 1: 31,223,215 I93F probably damaging Het
Pold3 T A 7: 100,119,683 Q36L possibly damaging Het
Polg T C 7: 79,459,786 T428A probably benign Het
Rfx7 T A 9: 72,577,047 V57E possibly damaging Het
Rnf122 T G 8: 31,112,149 M1R probably null Het
Scn10a T A 9: 119,617,733 T1410S probably damaging Het
Serpinb13 T A 1: 107,000,736 V362E probably damaging Het
Setdb1 T C 3: 95,327,611 N927S probably damaging Het
Shprh A G 10: 11,159,530 H327R probably damaging Het
Slc9b2 C A 3: 135,336,395 H478Q probably benign Het
Styxl1 G T 5: 135,753,883 S117R probably damaging Het
Synj2 T C 17: 6,019,359 F150L probably damaging Het
Tep1 C A 14: 50,845,513 V1013L possibly damaging Het
Tgfbi T A 13: 56,630,655 L413Q probably damaging Het
Tmc5 G A 7: 118,666,870 R789Q probably damaging Het
Tonsl T A 15: 76,622,562 I115F possibly damaging Het
Trim38 A G 13: 23,791,134 Y352C probably damaging Het
Txnl4a T A 18: 80,207,321 V44D probably benign Het
Vars2 A G 17: 35,661,609 V39A probably damaging Het
Vmn2r105 A G 17: 20,208,322 C831R probably damaging Het
Vmn2r26 T A 6: 124,050,708 I469N probably benign Het
Vmn2r53 T C 7: 12,581,606 Y762C probably benign Het
Vps13d T A 4: 145,170,348 Q334L probably benign Het
Zfp277 A T 12: 40,364,165 I227N probably damaging Het
Other mutations in Sft2d1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00419:Sft2d1 APN 17 8320605 missense possibly damaging 0.95
PIT4131001:Sft2d1 UTSW 17 8391031 missense possibly damaging 0.46
R0244:Sft2d1 UTSW 17 8319422 missense probably benign 0.05
R0571:Sft2d1 UTSW 17 8326950 splice site probably benign
R3922:Sft2d1 UTSW 17 8318882 missense possibly damaging 0.78
R4388:Sft2d1 UTSW 17 8320637 missense possibly damaging 0.82
R5854:Sft2d1 UTSW 17 8320653 missense probably damaging 0.98
R6833:Sft2d1 UTSW 17 8318875 missense possibly damaging 0.91
R7188:Sft2d1 UTSW 17 8323332 missense possibly damaging 0.59
Predicted Primers PCR Primer

Sequencing Primer
Posted On2014-01-29