Incidental Mutation 'R5540:Fbxo38'
ID 435933
Institutional Source Beutler Lab
Gene Symbol Fbxo38
Ensembl Gene ENSMUSG00000042211
Gene Name F-box protein 38
Synonyms SP329, 6030410I24Rik
MMRRC Submission 043098-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R5540 (G1)
Quality Score 220
Status Not validated
Chromosome 18
Chromosomal Location 62637226-62681766 bp(-) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) A to G at 62647864 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 null
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
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.6%
  • 20x: 96.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 74 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700008O03Rik A G 7: 44,012,371 (GRCm39) S15P probably damaging Het
Actl7a A T 4: 56,744,388 (GRCm39) H305L probably benign Het
Adam26b C A 8: 43,974,654 (GRCm39) C116F probably damaging Het
Adgrl2 A G 3: 148,543,198 (GRCm39) probably null Het
Akr1b10 A G 6: 34,371,047 (GRCm39) T238A probably damaging Het
Akr1c18 A G 13: 4,187,178 (GRCm39) V186A probably benign Het
Alpk3 G A 7: 80,745,184 (GRCm39) V1311M probably damaging Het
Aox1 A G 1: 58,143,569 (GRCm39) N1229S probably benign Het
Apobec3 T A 15: 79,782,120 (GRCm39) N43K probably benign Het
Arid1a A C 4: 133,407,765 (GRCm39) D2247E unknown Het
Asph A G 4: 9,635,906 (GRCm39) L77S probably damaging Het
Cd300ld T A 11: 114,878,231 (GRCm39) T94S probably damaging Het
Celf2 T C 2: 6,558,743 (GRCm39) T382A probably benign Het
Cfap54 C T 10: 92,808,470 (GRCm39) A1402T possibly damaging Het
Chrnb1 A T 11: 69,686,476 (GRCm39) V48E probably benign Het
Col6a5 T A 9: 105,739,975 (GRCm39) E2548V probably benign Het
Crebrf A G 17: 26,961,071 (GRCm39) D56G possibly damaging Het
Dctn5 A G 7: 121,734,275 (GRCm39) T40A probably benign Het
Dmxl2 A T 9: 54,301,141 (GRCm39) N2323K probably benign Het
Dync1h1 A G 12: 110,627,384 (GRCm39) Q4021R probably benign Het
Dyrk1a T G 16: 94,486,202 (GRCm39) probably null Het
Ephb3 T A 16: 21,039,610 (GRCm39) F454Y probably damaging Het
Flg T C 3: 93,184,923 (GRCm39) F15S probably damaging Het
Fndc3b G A 3: 27,555,651 (GRCm39) P301L probably damaging Het
Fpr-rs7 C T 17: 20,334,356 (GRCm39) G45R probably damaging Het
Garin3 A G 11: 46,295,715 (GRCm39) N29S probably damaging Het
Gfi1 T A 5: 107,867,991 (GRCm39) T360S probably damaging Het
Grik4 T C 9: 42,432,243 (GRCm39) H918R probably damaging Het
Hpx A G 7: 105,241,119 (GRCm39) S385P possibly damaging Het
Kdm5b A G 1: 134,558,979 (GRCm39) D1501G probably damaging Het
Kif20b A T 19: 34,915,860 (GRCm39) M546L probably benign Het
Map3k9 G T 12: 81,819,587 (GRCm39) N222K probably damaging Het
Me1 A G 9: 86,561,926 (GRCm39) L53P possibly damaging Het
Mis18bp1 T C 12: 65,195,520 (GRCm39) E748G possibly damaging Het
Morc3 T A 16: 93,644,268 (GRCm39) N186K probably benign Het
Mtor A G 4: 148,539,165 (GRCm39) T221A probably benign Het
Muc6 A G 7: 141,235,850 (GRCm39) probably null Het
Myh8 C A 11: 67,177,266 (GRCm39) T444N probably benign Het
Myo7b A G 18: 32,140,143 (GRCm39) Y216H probably damaging Het
Myom1 G A 17: 71,416,782 (GRCm39) V1382M probably damaging Het
Nbeal2 A T 9: 110,460,801 (GRCm39) Y1718N probably damaging Het
Npc1l1 A G 11: 6,164,546 (GRCm39) S1168P probably damaging Het
Or4c58 A G 2: 89,675,011 (GRCm39) F102S probably damaging Het
Or4d2 T A 11: 87,784,511 (GRCm39) K80* probably null Het
Or51f5 C T 7: 102,424,136 (GRCm39) A135V probably benign Het
Or5an9 T A 19: 12,187,824 (GRCm39) I298N probably damaging Het
Or6c8b G T 10: 128,882,364 (GRCm39) D189E probably damaging Het
Pcdha4 C A 18: 37,087,890 (GRCm39) A691E probably benign Het
Pde6a T G 18: 61,364,438 (GRCm39) F165V probably damaging Het
Ptpn14 A T 1: 189,578,561 (GRCm39) M340L probably benign Het
Rnasel G T 1: 153,630,890 (GRCm39) E469* probably null Het
Rsph3a T G 17: 8,164,790 (GRCm39) L50R probably benign Het
Rusc2 A G 4: 43,423,975 (GRCm39) Y1043C probably damaging Het
Serpinb6b A T 13: 33,161,541 (GRCm39) K86* probably null Het
Serpine1 T C 5: 137,092,063 (GRCm39) T392A probably benign Het
Shcbp1 A T 8: 4,794,529 (GRCm39) D421E probably damaging Het
Slc24a1 A G 9: 64,855,863 (GRCm39) V348A unknown Het
Slc26a7 A G 4: 14,506,621 (GRCm39) F605L probably benign Het
Slc66a1 A T 4: 139,027,655 (GRCm39) L229Q probably damaging Het
Spag17 A C 3: 99,963,588 (GRCm39) E1102A possibly damaging Het
Stab2 A G 10: 86,683,989 (GRCm39) V2390A probably benign Het
Stk11 A G 10: 79,961,883 (GRCm39) I35V probably benign Het
Stk24 T C 14: 121,531,693 (GRCm39) D321G possibly damaging Het
Tbx4 A T 11: 85,801,994 (GRCm39) N209I possibly damaging Het
Tmem225 T C 9: 40,060,681 (GRCm39) L80P probably damaging Het
Tnfrsf4 C T 4: 156,098,380 (GRCm39) T17I probably benign Het
Traf3ip1 G A 1: 91,429,037 (GRCm39) R268Q probably benign Het
Trhde T A 10: 114,636,497 (GRCm39) I237F probably benign Het
Ugt2a1 A T 5: 87,633,915 (GRCm39) W231R probably damaging Het
Vash1 ACTGCTGCTGCTGCTGCTGC ACTGCTGCTGCTGCTGC 12: 86,726,831 (GRCm39) probably benign Het
Vps16 T A 2: 130,284,305 (GRCm39) D685E probably benign Het
Washc4 A G 10: 83,409,657 (GRCm39) D602G probably damaging Het
Wdr59 A G 8: 112,211,816 (GRCm39) L377P possibly damaging Het
Wdr81 T C 11: 75,339,896 (GRCm39) E1364G 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
IGL01621:Fbxo38 APN 18 62,655,595 (GRCm39) splice site probably benign
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
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
Predicted Primers PCR Primer
(F):5'- GGGCAAACACAGGATTTAACTTTTC -3'
(R):5'- TTCAGGCCCAGCACATGATG -3'

Sequencing Primer
(F):5'- GTTTTACATCTGTTTCCACCAAAAC -3'
(R):5'- CCCAGCACATGATGAGAGGAC -3'
Posted On 2016-10-24