Incidental Mutation 'IGL01797:Faiml'
ID 155385
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Faiml
Ensembl Gene ENSMUSG00000096316
Gene Name Fas apoptotic inhibitory molecule like
Synonyms Gm6432
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.368) question?
Stock # IGL01797
Quality Score
Status
Chromosome 9
Chromosomal Location 99111429-99119292 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 99116442 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Glutamic Acid at position 83 (K83E)
Ref Sequence ENSEMBL: ENSMUSP00000139801 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000178051] [ENSMUST00000188555]
AlphaFold J3QPY3
Predicted Effect probably damaging
Transcript: ENSMUST00000178051
AA Change: K83E

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000137541
Gene: ENSMUSG00000096316
AA Change: K83E

DomainStartEndE-ValueType
Pfam:FAIM1 2 174 2.2e-85 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000188555
AA Change: K83E

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000139801
Gene: ENSMUSG00000096316
AA Change: K83E

DomainStartEndE-ValueType
Pfam:FAIM1 1 176 1.2e-83 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 T C 7: 120,113,760 (GRCm39) V877A probably benign Het
Clcn2 T C 16: 20,531,511 (GRCm39) I178V probably damaging Het
Cnbp A G 6: 87,822,542 (GRCm39) probably benign Het
Coq8a A T 1: 179,997,284 (GRCm39) probably null Het
Dctn2 A G 10: 127,113,182 (GRCm39) D244G possibly damaging Het
Dync1h1 T A 12: 110,618,630 (GRCm39) probably null Het
Efcab15 T C 11: 103,089,794 (GRCm39) Y381C probably damaging Het
Fdx1 A T 9: 51,854,925 (GRCm39) C159* probably null Het
Fgd3 A T 13: 49,443,065 (GRCm39) V169E probably damaging Het
Ice1 G T 13: 70,772,065 (GRCm39) T51K probably damaging Het
Iqca1 A C 1: 90,072,541 (GRCm39) probably null Het
Jup C A 11: 100,272,498 (GRCm39) probably benign Het
Krt84 A G 15: 101,436,915 (GRCm39) V373A possibly damaging Het
Ndst4 T A 3: 125,476,802 (GRCm39) M9K probably damaging Het
Nomo1 T C 7: 45,706,086 (GRCm39) V480A probably damaging Het
Nsun5 A G 5: 135,404,225 (GRCm39) H344R probably damaging Het
Or13a21 A G 7: 139,998,931 (GRCm39) Y252H probably damaging Het
Or1e1f A T 11: 73,855,644 (GRCm39) D70V probably damaging Het
Pjvk T C 2: 76,487,883 (GRCm39) probably benign Het
Prkaa1 G A 15: 5,198,187 (GRCm39) D159N probably damaging Het
Sap130 T A 18: 31,831,721 (GRCm39) I736N probably damaging Het
Tlcd1 A G 11: 78,071,160 (GRCm39) probably null Het
Tpp1 T C 7: 105,398,459 (GRCm39) I286V probably benign Het
Ttll5 T A 12: 86,003,371 (GRCm39) I1069K possibly damaging Het
Ttn T G 2: 76,540,257 (GRCm39) E34243A possibly damaging Het
Uqcr10 A C 11: 4,654,179 (GRCm39) I43S possibly damaging Het
Ush2a T A 1: 187,995,706 (GRCm39) M159K probably damaging Het
Vmn2r121 G A X: 123,041,048 (GRCm39) probably benign Het
Vmn2r30 T A 7: 7,337,195 (GRCm39) D147V probably benign Het
Xntrpc T C 7: 101,739,753 (GRCm39) I559T possibly damaging Het
Zfp268 T A 4: 145,347,241 (GRCm39) N48K probably damaging Het
Other mutations in Faiml
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1745:Faiml UTSW 9 99,116,511 (GRCm39) missense probably benign 0.00
R2137:Faiml UTSW 9 99,114,545 (GRCm39) missense probably benign 0.00
R2275:Faiml UTSW 9 99,111,612 (GRCm39) missense probably benign 0.03
R2939:Faiml UTSW 9 99,114,527 (GRCm39) missense probably damaging 0.96
R2940:Faiml UTSW 9 99,114,527 (GRCm39) missense probably damaging 0.96
R3081:Faiml UTSW 9 99,114,527 (GRCm39) missense probably damaging 0.96
R6258:Faiml UTSW 9 99,114,513 (GRCm39) missense possibly damaging 0.80
R7071:Faiml UTSW 9 99,118,400 (GRCm39) start codon destroyed unknown
R7121:Faiml UTSW 9 99,116,446 (GRCm39) missense probably benign 0.01
R7135:Faiml UTSW 9 99,116,496 (GRCm39) missense probably benign 0.00
R7297:Faiml UTSW 9 99,111,666 (GRCm39) missense probably damaging 0.98
R9353:Faiml UTSW 9 99,116,462 (GRCm39) missense probably damaging 1.00
R9410:Faiml UTSW 9 99,111,587 (GRCm39) missense probably benign 0.43
Posted On 2014-02-04