Incidental Mutation 'R0827:Faim2'
ID 78347
Institutional Source Beutler Lab
Gene Symbol Faim2
Ensembl Gene ENSMUSG00000023011
Gene Name Fas apoptotic inhibitory molecule 2
Synonyms Tmbim2, 2900002L20Rik, Lfg, lifeguard, NMP25
MMRRC Submission 039007-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.139) question?
Stock # R0827 (G1)
Quality Score 93
Status Validated
Chromosome 15
Chromosomal Location 99394893-99426046 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 99422617 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 60 (V60A)
Ref Sequence ENSEMBL: ENSMUSP00000155195 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000023750] [ENSMUST00000231171]
AlphaFold Q8K097
Predicted Effect probably benign
Transcript: ENSMUST00000023750
AA Change: V60A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000023750
Gene: ENSMUSG00000023011
AA Change: V60A

DomainStartEndE-ValueType
Pfam:Bax1-I 101 312 1.6e-36 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000230603
Predicted Effect noncoding transcript
Transcript: ENSMUST00000230837
Predicted Effect probably benign
Transcript: ENSMUST00000231171
AA Change: V60A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Meta Mutation Damage Score 0.0754 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.1%
  • 20x: 93.6%
Validation Efficiency 100% (88/88)
MGI Phenotype PHENOTYPE: A mutation in this gene results in kidney abnormalities including enlargement and dilation. A reduced seizure threshold in response to pharmacological agents is also observed. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 86 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acan T C 7: 78,749,419 (GRCm39) S1397P probably benign Het
Adamts15 T C 9: 30,832,776 (GRCm39) Y253C probably damaging Het
Ankk1 A G 9: 49,333,037 (GRCm39) I149T possibly damaging Het
Ankrd63 A G 2: 118,533,034 (GRCm39) S296P possibly damaging Het
Arpc1b T G 5: 145,062,566 (GRCm39) C227G probably benign Het
B4gat1 A G 19: 5,089,725 (GRCm39) R241G possibly damaging Het
Ccar2 T C 14: 70,377,287 (GRCm39) N751D probably benign Het
Cd55b T C 1: 130,341,973 (GRCm39) I221M probably damaging Het
Cntn5 A G 9: 9,666,943 (GRCm39) V1032A possibly damaging Het
Col11a1 G A 3: 113,932,414 (GRCm39) R113H unknown Het
Colec10 G A 15: 54,325,980 (GRCm39) C270Y probably damaging Het
Ctnnbl1 C T 2: 157,641,337 (GRCm39) probably benign Het
Cyp2j12 T G 4: 96,001,099 (GRCm39) probably benign Het
Dennd5a G A 7: 109,498,938 (GRCm39) T999M probably damaging Het
Dusp13b C A 14: 21,792,839 (GRCm39) V29L probably benign Het
Efr3a A C 15: 65,725,400 (GRCm39) D83A possibly damaging Het
Elmod2 A G 8: 84,043,424 (GRCm39) probably null Het
Eml3 C A 19: 8,915,830 (GRCm39) T640K probably damaging Het
Eps8l1 T C 7: 4,480,388 (GRCm39) V543A possibly damaging Het
Ermn T C 2: 57,938,263 (GRCm39) K117E probably damaging Het
F830045P16Rik A G 2: 129,314,696 (GRCm39) S194P probably benign Het
Fancd2 G A 6: 113,563,210 (GRCm39) probably null Het
Fbxo43 A T 15: 36,163,115 (GRCm39) S31T possibly damaging Het
Gab2 G A 7: 96,949,539 (GRCm39) R411Q probably damaging Het
Gpm6a A T 8: 55,511,918 (GRCm39) D264V probably damaging Het
H1f6 A G 13: 23,880,204 (GRCm39) D119G probably benign Het
Hsp90aa1 T C 12: 110,659,129 (GRCm39) E556G probably benign Het
Ifi203 A T 1: 173,756,029 (GRCm39) probably benign Het
Iqca1 C A 1: 90,070,453 (GRCm39) G133V probably null Het
Kcnc3 A G 7: 44,244,630 (GRCm39) T307A probably damaging Het
Kin C A 2: 10,095,187 (GRCm39) probably benign Het
Knl1 T C 2: 118,919,382 (GRCm39) probably benign Het
Lrp4 G A 2: 91,325,386 (GRCm39) V1404M probably damaging Het
Lrrc71 T A 3: 87,649,952 (GRCm39) probably null Het
Med13l T C 5: 118,864,312 (GRCm39) probably benign Het
Mfap5 A G 6: 122,497,879 (GRCm39) D39G probably damaging Het
Mlxipl T C 5: 135,161,592 (GRCm39) S504P probably benign Het
Myo3a T G 2: 22,448,227 (GRCm39) Y1D probably damaging Het
Nek1 A G 8: 61,558,682 (GRCm39) probably benign Het
Nfkbiz T C 16: 55,636,730 (GRCm39) R524G probably damaging Het
Npbwr1 T C 1: 5,987,008 (GRCm39) T169A possibly damaging Het
Nuggc T C 14: 65,846,340 (GRCm39) Y84H probably damaging Het
Nxph3 G A 11: 95,402,252 (GRCm39) S54L probably benign Het
Or13a21 A G 7: 139,999,380 (GRCm39) F102S probably damaging Het
Or9e1 T C 11: 58,732,597 (GRCm39) I219T probably damaging Het
Ostn A G 16: 27,143,381 (GRCm39) N70D probably damaging Het
Pate7 A T 9: 35,689,147 (GRCm39) L12Q probably damaging Het
Pcdhb2 G A 18: 37,428,710 (GRCm39) V228I possibly damaging Het
Pnpla6 A T 8: 3,567,618 (GRCm39) M109L possibly damaging Het
Ppil6 T A 10: 41,370,500 (GRCm39) probably benign Het
Prss46 A G 9: 110,680,500 (GRCm39) N215S probably benign Het
Ptprd A T 4: 76,047,152 (GRCm39) D371E probably damaging Het
Ripor2 T A 13: 24,878,169 (GRCm39) F315I probably damaging Het
Rmi2 G A 16: 10,653,104 (GRCm39) G51S probably damaging Het
Scg3 A G 9: 75,590,979 (GRCm39) I10T possibly damaging Het
Scn9a T A 2: 66,366,468 (GRCm39) K761* probably null Het
Scyl2 A G 10: 89,493,727 (GRCm39) L347P possibly damaging Het
Sh3d21 A G 4: 126,046,064 (GRCm39) probably benign Het
Shc1 T A 3: 89,334,090 (GRCm39) probably null Het
Slbp A G 5: 33,801,166 (GRCm39) S182P probably damaging Het
Slc24a1 C T 9: 64,835,472 (GRCm39) G885D probably benign Het
Slc24a3 T C 2: 145,360,412 (GRCm39) probably benign Het
Sowahb T G 5: 93,191,145 (GRCm39) N525H probably damaging Het
Sppl3 T A 5: 115,220,392 (GRCm39) C101* probably null Het
Srsf5 A G 12: 80,996,314 (GRCm39) K163E probably damaging Het
Sult2a4 A G 7: 13,718,886 (GRCm39) I119T probably benign Het
Svep1 A G 4: 58,053,113 (GRCm39) probably benign Het
Tas1r3 G A 4: 155,945,326 (GRCm39) R632W probably benign Het
Tlr4 T A 4: 66,752,117 (GRCm39) probably null Het
Tmf1 A C 6: 97,135,011 (GRCm39) L1001* probably null Het
Tnnt2 A G 1: 135,771,534 (GRCm39) probably benign Het
Trank1 G A 9: 111,178,485 (GRCm39) probably benign Het
Trdn A T 10: 33,275,154 (GRCm39) probably benign Het
Trmt6 A T 2: 132,657,754 (GRCm39) V34E probably damaging Het
Trrap T C 5: 144,751,640 (GRCm39) F1699L probably benign Het
Ttk A G 9: 83,725,968 (GRCm39) R250G probably benign Het
Ttn T A 2: 76,640,248 (GRCm39) I13787F probably damaging Het
Uggt1 T A 1: 36,195,394 (GRCm39) probably null Het
Ugt2b35 T A 5: 87,155,989 (GRCm39) probably benign Het
Ugt2b36 C A 5: 87,214,234 (GRCm39) R470L possibly damaging Het
Unk A G 11: 115,943,935 (GRCm39) D352G possibly damaging Het
Vmn2r77 G T 7: 86,451,224 (GRCm39) C370F probably damaging Het
Vmn2r85 A G 10: 130,265,387 (GRCm39) I32T possibly damaging Het
Zfp637 A G 6: 117,822,405 (GRCm39) I178V possibly damaging Het
Zfp943 A G 17: 22,211,071 (GRCm39) probably null Het
Zyg11a A G 4: 108,067,239 (GRCm39) probably benign Het
Other mutations in Faim2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01906:Faim2 APN 15 99,412,314 (GRCm39) missense probably damaging 1.00
IGL02820:Faim2 APN 15 99,419,138 (GRCm39) missense probably benign 0.02
IGL02989:Faim2 APN 15 99,418,243 (GRCm39) splice site probably benign
R1171:Faim2 UTSW 15 99,398,135 (GRCm39) missense probably benign 0.05
R1678:Faim2 UTSW 15 99,418,217 (GRCm39) missense possibly damaging 0.92
R1785:Faim2 UTSW 15 99,410,423 (GRCm39) missense probably damaging 1.00
R2004:Faim2 UTSW 15 99,398,127 (GRCm39) missense possibly damaging 0.87
R2063:Faim2 UTSW 15 99,412,314 (GRCm39) missense probably damaging 1.00
R3401:Faim2 UTSW 15 99,418,229 (GRCm39) missense probably damaging 0.98
R4242:Faim2 UTSW 15 99,398,082 (GRCm39) missense probably damaging 1.00
R4664:Faim2 UTSW 15 99,422,582 (GRCm39) missense probably benign
R4664:Faim2 UTSW 15 99,422,581 (GRCm39) critical splice donor site probably null
R4665:Faim2 UTSW 15 99,422,582 (GRCm39) missense probably benign
R4665:Faim2 UTSW 15 99,422,581 (GRCm39) critical splice donor site probably null
R4719:Faim2 UTSW 15 99,425,460 (GRCm39) critical splice donor site probably null
R4952:Faim2 UTSW 15 99,419,109 (GRCm39) missense possibly damaging 0.51
R5973:Faim2 UTSW 15 99,419,132 (GRCm39) missense probably benign
R7162:Faim2 UTSW 15 99,419,048 (GRCm39) critical splice donor site probably null
R7305:Faim2 UTSW 15 99,411,814 (GRCm39) missense probably damaging 0.99
R7601:Faim2 UTSW 15 99,398,147 (GRCm39) missense probably damaging 1.00
R7979:Faim2 UTSW 15 99,408,515 (GRCm39) missense possibly damaging 0.67
R8495:Faim2 UTSW 15 99,408,473 (GRCm39) missense probably benign 0.08
R9277:Faim2 UTSW 15 99,419,097 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- CCTCCAAAGCCACTGACTACTGTTC -3'
(R):5'- GCAAGTCTCTACTCCTGGCAACTC -3'

Sequencing Primer
(F):5'- GACTACTGTTCTGCACAACTG -3'
(R):5'- TCTGGCTCTACTCTACAGCTC -3'
Posted On 2013-10-16