Incidental Mutation 'IGL01621:Fbxo38'
ID 92617
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fbxo38
Ensembl Gene ENSMUSG00000042211
Gene Name F-box protein 38
Synonyms SP329, 6030410I24Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01621
Quality Score
Status
Chromosome 18
Chromosomal Location 62637226-62681766 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) G to A at 62655595 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000047541 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000048688]
AlphaFold Q8BMI0
Predicted Effect probably benign
Transcript: ENSMUST00000048688
SMART Domains Protein: ENSMUSP00000047541
Gene: ENSMUSG00000042211

DomainStartEndE-ValueType
Pfam:F-box 29 66 2.6e-5 PFAM
SCOP:d1fqva2 127 357 6e-4 SMART
low complexity region 493 525 N/A INTRINSIC
low complexity region 598 610 N/A INTRINSIC
low complexity region 705 728 N/A INTRINSIC
low complexity region 736 753 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
0610040J01Rik C T 5: 64,055,726 (GRCm39) T154I possibly damaging Het
4933434E20Rik T A 3: 89,971,809 (GRCm39) M56K possibly damaging Het
Abca6 A G 11: 110,075,534 (GRCm39) L1319S probably damaging Het
Adh4 C T 3: 138,134,788 (GRCm39) probably benign Het
Aloxe3 A G 11: 69,020,839 (GRCm39) N188S probably benign Het
Ap1s1 G A 5: 137,070,658 (GRCm39) R119* probably null Het
Apc2 T G 10: 80,142,035 (GRCm39) L318R probably damaging Het
Atg101 A G 15: 101,184,976 (GRCm39) S33G possibly damaging Het
Atp8a2 A T 14: 60,253,317 (GRCm39) probably benign Het
Bpifb9b C A 2: 154,158,871 (GRCm39) probably null Het
Braf A T 6: 39,623,787 (GRCm39) probably benign Het
Cabp5 A G 7: 13,135,189 (GRCm39) D43G probably damaging Het
Cfap46 T C 7: 139,186,523 (GRCm39) N2462S unknown Het
Cit C T 5: 116,130,662 (GRCm39) probably benign Het
Cpa4 T C 6: 30,574,415 (GRCm39) V68A probably damaging Het
Cyp2j5 T C 4: 96,517,791 (GRCm39) I474V probably benign Het
Dennd1a C A 2: 37,734,821 (GRCm39) D49Y probably damaging Het
Dlg5 T C 14: 24,198,289 (GRCm39) D1525G probably damaging Het
Dnajc18 C T 18: 35,813,893 (GRCm39) R292H probably benign Het
Dync2h1 A G 9: 7,140,897 (GRCm39) probably null Het
E2f6 A G 12: 16,875,369 (GRCm39) D268G probably benign Het
Evi2b T A 11: 79,407,126 (GRCm39) T150S probably damaging Het
F13b A G 1: 139,431,589 (GRCm39) D53G probably benign Het
Flnb C T 14: 7,950,470 (GRCm38) P2596L probably damaging Het
Fyco1 A G 9: 123,656,247 (GRCm39) probably benign Het
Gm21759 A G 5: 8,229,775 (GRCm39) probably benign Het
Gtse1 A G 15: 85,759,283 (GRCm39) N597S probably benign Het
Hcn3 G T 3: 89,055,030 (GRCm39) S739Y probably damaging Het
Ighv9-4 T A 12: 114,263,612 (GRCm39) N107I probably damaging Het
Inava C A 1: 136,147,513 (GRCm39) A402S probably damaging Het
Iqub T C 6: 24,446,211 (GRCm39) K738E probably benign Het
Itga6 A T 2: 71,656,000 (GRCm39) D308V probably benign Het
Klf12 T C 14: 100,260,585 (GRCm39) Y48C probably damaging Het
Klhdc9 A G 1: 171,186,384 (GRCm39) *351Q probably null Het
Krt40 A T 11: 99,433,694 (GRCm39) N97K probably damaging Het
Lrit1 A C 14: 36,782,112 (GRCm39) T262P probably damaging Het
Mcoln1 T C 8: 3,560,910 (GRCm39) Y411H probably damaging Het
Mfsd4a A G 1: 131,981,881 (GRCm39) S149P probably benign Het
Minar2 A G 18: 59,195,458 (GRCm39) M1V probably null Het
Mipep A G 14: 61,033,614 (GRCm39) probably benign Het
Mslnl A G 17: 25,962,641 (GRCm39) probably benign Het
N4bp2 A T 5: 65,948,267 (GRCm39) H299L probably damaging Het
Nbn C T 4: 15,965,221 (GRCm39) P190S probably benign Het
Nos1 T A 5: 118,083,949 (GRCm39) I1253N probably damaging Het
Nup210 G T 6: 91,007,099 (GRCm39) F572L probably damaging Het
Or10k2 T C 8: 84,268,247 (GRCm39) V158A probably benign Het
Or1e30 T C 11: 73,678,103 (GRCm39) F113S probably damaging Het
Or2y11 T C 11: 49,442,964 (GRCm39) L130P probably damaging Het
P4htm T A 9: 108,460,935 (GRCm39) E106V probably damaging Het
Pcdhb20 C T 18: 37,637,860 (GRCm39) H129Y possibly damaging Het
Pdcd6ip T C 9: 113,514,490 (GRCm39) E240G probably benign Het
Pex5l T C 3: 33,069,110 (GRCm39) probably null Het
Plcd1 T C 9: 118,905,246 (GRCm39) N181S probably damaging Het
Plekhg6 G T 6: 125,349,062 (GRCm39) L412M probably damaging Het
Ppp1r13b T A 12: 111,801,526 (GRCm39) Q386L possibly damaging Het
Pramel25 T C 4: 143,520,502 (GRCm39) F85L probably benign Het
Prpf40b A G 15: 99,207,926 (GRCm39) probably benign Het
Rdh11 C T 12: 79,233,187 (GRCm39) probably null Het
Ripor3 A T 2: 167,839,172 (GRCm39) S110T probably damaging Het
Sec24d G A 3: 123,087,807 (GRCm39) probably null Het
Secisbp2l T C 2: 125,615,131 (GRCm39) S165G probably benign Het
Shank1 C T 7: 43,991,889 (GRCm39) A698V unknown Het
Shank1 T C 7: 44,001,023 (GRCm39) M914T unknown Het
Slc22a3 T C 17: 12,677,379 (GRCm39) Q263R probably benign Het
Smc1a C A X: 150,819,125 (GRCm39) Q647K probably damaging Het
Sohlh1 A G 2: 25,736,873 (GRCm39) probably benign Het
Tacc2 C A 7: 130,331,498 (GRCm39) T484K probably damaging Het
Ubr4 G T 4: 139,168,094 (GRCm39) E2825* probably null Het
Wbp2nl G A 15: 82,192,806 (GRCm39) M163I probably benign Het
Zfp69 T A 4: 120,788,697 (GRCm39) K206M probably damaging Het
Zswim3 G A 2: 164,663,440 (GRCm39) R640H probably damaging Het
Other mutations in Fbxo38
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00911:Fbxo38 APN 18 62,663,871 (GRCm39) missense possibly damaging 0.59
IGL01384:Fbxo38 APN 18 62,655,487 (GRCm39) missense probably damaging 0.98
IGL01443:Fbxo38 APN 18 62,666,741 (GRCm39) missense probably damaging 1.00
IGL01515:Fbxo38 APN 18 62,651,642 (GRCm39) missense probably benign 0.00
IGL01975:Fbxo38 APN 18 62,648,484 (GRCm39) missense probably damaging 1.00
IGL02148:Fbxo38 APN 18 62,669,298 (GRCm39) missense probably benign 0.02
IGL02390:Fbxo38 APN 18 62,666,660 (GRCm39) missense probably damaging 1.00
IGL03040:Fbxo38 APN 18 62,660,323 (GRCm39) missense probably damaging 1.00
IGL03088:Fbxo38 APN 18 62,655,543 (GRCm39) missense possibly damaging 0.86
IGL03290:Fbxo38 APN 18 62,659,234 (GRCm39) missense probably benign 0.08
FR4976:Fbxo38 UTSW 18 62,648,418 (GRCm39) small deletion probably benign
R0526:Fbxo38 UTSW 18 62,639,051 (GRCm39) missense probably damaging 1.00
R0529:Fbxo38 UTSW 18 62,639,057 (GRCm39) missense probably damaging 1.00
R0789:Fbxo38 UTSW 18 62,648,570 (GRCm39) missense possibly damaging 0.84
R1232:Fbxo38 UTSW 18 62,643,882 (GRCm39) missense probably damaging 1.00
R1857:Fbxo38 UTSW 18 62,648,489 (GRCm39) missense probably damaging 1.00
R1859:Fbxo38 UTSW 18 62,648,489 (GRCm39) missense probably damaging 1.00
R1872:Fbxo38 UTSW 18 62,650,094 (GRCm39) missense probably benign 0.01
R2114:Fbxo38 UTSW 18 62,639,711 (GRCm39) missense possibly damaging 0.71
R2910:Fbxo38 UTSW 18 62,652,878 (GRCm39) missense probably benign 0.01
R2911:Fbxo38 UTSW 18 62,652,878 (GRCm39) missense probably benign 0.01
R3406:Fbxo38 UTSW 18 62,647,914 (GRCm39) missense probably damaging 0.99
R3731:Fbxo38 UTSW 18 62,648,399 (GRCm39) small deletion probably benign
R3792:Fbxo38 UTSW 18 62,666,533 (GRCm39) splice site probably null
R3848:Fbxo38 UTSW 18 62,648,144 (GRCm39) missense possibly damaging 0.87
R3948:Fbxo38 UTSW 18 62,662,615 (GRCm39) splice site probably benign
R4151:Fbxo38 UTSW 18 62,648,399 (GRCm39) small deletion probably benign
R4323:Fbxo38 UTSW 18 62,648,232 (GRCm39) missense probably benign
R4456:Fbxo38 UTSW 18 62,659,320 (GRCm39) missense probably damaging 1.00
R4786:Fbxo38 UTSW 18 62,662,745 (GRCm39) missense probably damaging 1.00
R4829:Fbxo38 UTSW 18 62,651,662 (GRCm39) missense probably benign
R4959:Fbxo38 UTSW 18 62,655,578 (GRCm39) missense probably benign 0.45
R5274:Fbxo38 UTSW 18 62,648,140 (GRCm39) missense probably damaging 0.98
R5288:Fbxo38 UTSW 18 62,674,042 (GRCm39) missense probably benign
R5384:Fbxo38 UTSW 18 62,674,042 (GRCm39) missense probably benign
R5385:Fbxo38 UTSW 18 62,674,042 (GRCm39) missense probably benign
R5448:Fbxo38 UTSW 18 62,655,528 (GRCm39) missense possibly damaging 0.59
R5540:Fbxo38 UTSW 18 62,647,864 (GRCm39) critical splice donor site probably null
R5588:Fbxo38 UTSW 18 62,659,248 (GRCm39) missense probably damaging 1.00
R5617:Fbxo38 UTSW 18 62,639,042 (GRCm39) missense probably damaging 1.00
R5636:Fbxo38 UTSW 18 62,644,089 (GRCm39) missense possibly damaging 0.80
R5769:Fbxo38 UTSW 18 62,648,036 (GRCm39) missense probably benign 0.10
R6254:Fbxo38 UTSW 18 62,638,571 (GRCm39) splice site probably null
R6315:Fbxo38 UTSW 18 62,669,218 (GRCm39) nonsense probably null
R6517:Fbxo38 UTSW 18 62,666,634 (GRCm39) missense probably damaging 1.00
R6673:Fbxo38 UTSW 18 62,666,986 (GRCm39) missense probably damaging 1.00
R6974:Fbxo38 UTSW 18 62,639,740 (GRCm39) missense possibly damaging 0.95
R7022:Fbxo38 UTSW 18 62,669,295 (GRCm39) missense probably damaging 1.00
R7175:Fbxo38 UTSW 18 62,648,544 (GRCm39) missense probably benign 0.11
R8013:Fbxo38 UTSW 18 62,663,882 (GRCm39) missense possibly damaging 0.63
R8815:Fbxo38 UTSW 18 62,666,587 (GRCm39) missense probably damaging 1.00
R8885:Fbxo38 UTSW 18 62,659,272 (GRCm39) missense probably damaging 0.99
R9240:Fbxo38 UTSW 18 62,651,632 (GRCm39) nonsense probably null
R9427:Fbxo38 UTSW 18 62,644,160 (GRCm39) missense probably benign 0.00
R9750:Fbxo38 UTSW 18 62,674,061 (GRCm39) missense probably benign 0.14
R9796:Fbxo38 UTSW 18 62,674,055 (GRCm39) missense possibly damaging 0.92
Z1177:Fbxo38 UTSW 18 62,648,535 (GRCm39) missense probably damaging 1.00
Posted On 2013-12-09