Incidental Mutation 'R1635:Fbxo42'
ID173054
Institutional Source Beutler Lab
Gene Symbol Fbxo42
Ensembl Gene ENSMUSG00000028920
Gene NameF-box protein 42
Synonyms6720460I06Rik
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.286) question?
Stock #R1635 (G1)
Quality Score225
Status Not validated
Chromosome4
Chromosomal Location141147913-141204062 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 141200529 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Alanine at position 707 (T707A)
Ref Sequence ENSEMBL: ENSMUSP00000030757 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000030757]
Predicted Effect probably damaging
Transcript: ENSMUST00000030757
AA Change: T707A

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000030757
Gene: ENSMUSG00000028920
AA Change: T707A

DomainStartEndE-ValueType
FBOX 50 90 2.64e-4 SMART
Pfam:Kelch_5 114 159 7.3e-9 PFAM
Pfam:Kelch_4 118 174 6.1e-10 PFAM
Pfam:Kelch_3 130 182 4e-11 PFAM
Pfam:Kelch_5 228 268 8.2e-10 PFAM
Pfam:Kelch_1 231 274 6.3e-8 PFAM
Pfam:Kelch_2 231 277 5.1e-10 PFAM
Pfam:Kelch_3 241 285 2.9e-8 PFAM
low complexity region 363 376 N/A INTRINSIC
low complexity region 458 471 N/A INTRINSIC
low complexity region 508 513 N/A INTRINSIC
low complexity region 567 595 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.0%
  • 20x: 91.9%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Members of the F-box protein family, such as FBXO42, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (SKP1A; MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Dec 2010]
Allele List at MGI
Other mutations in this stock
Total: 95 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca2 A T 2: 25,444,856 I1947F probably benign Het
Adgrd1 G T 5: 129,128,907 V182F probably damaging Het
Agmat A G 4: 141,747,069 D87G probably damaging Het
AI182371 T C 2: 35,088,737 probably null Het
Anapc1 G T 2: 128,628,532 H1559Q probably damaging Het
Ankar T C 1: 72,650,138 Y1278C probably damaging Het
Arhgef2 A T 3: 88,639,321 probably null Het
Arsi G A 18: 60,916,651 G202E probably benign Het
Banp A T 8: 122,001,011 I130F probably damaging Het
C130050O18Rik G T 5: 139,414,493 R100S probably benign Het
Carmil3 A G 14: 55,496,282 T374A possibly damaging Het
Cc2d2a T A 5: 43,722,470 W1076R probably damaging Het
Cdc34 T G 10: 79,688,054 S235A probably benign Het
Cdh8 G T 8: 99,031,024 H647Q probably damaging Het
Cdk1 A T 10: 69,338,547 L282Q probably damaging Het
Ceacam3 A G 7: 17,159,977 D471G probably damaging Het
Cltc A T 11: 86,757,279 I4N probably benign Het
Cntfr T A 4: 41,658,816 E305V probably damaging Het
Cwh43 T A 5: 73,434,310 I496N probably damaging Het
Cyp2f2 A G 7: 27,129,724 N218S probably benign Het
D16Ertd472e A G 16: 78,546,504 probably null Het
Dab2 A G 15: 6,429,870 Q400R possibly damaging Het
Dapl1 A T 2: 59,496,562 I51F probably benign Het
Drc7 G A 8: 95,074,332 probably null Het
Etl4 A G 2: 20,806,408 T1101A probably damaging Het
Fam83c C A 2: 155,830,051 R488M possibly damaging Het
Fam96b A T 8: 104,640,988 I108N possibly damaging Het
Fcmr A T 1: 130,876,185 probably null Het
Fer1l6 G C 15: 58,647,081 K1687N probably damaging Het
Fgd4 G A 16: 16,475,029 R275* probably null Het
Fxr2 G A 11: 69,641,313 C87Y possibly damaging Het
Gja4 A T 4: 127,312,679 I97N probably damaging Het
Gm136 A G 4: 34,750,919 probably null Het
Gm14496 A G 2: 182,001,044 D836G possibly damaging Het
Gm8882 A G 6: 132,363,006 probably null Het
Grm3 T A 5: 9,511,520 T777S probably damaging Het
Guca2b A G 4: 119,657,715 Y50H probably damaging Het
Herc2 C T 7: 56,136,667 P1587S probably benign Het
Hmcn1 C T 1: 150,669,558 S2766N probably benign Het
Idi2 T A 13: 8,959,419 I224K probably damaging Het
Kmt2a A T 9: 44,824,369 probably benign Het
Lonp2 A T 8: 86,713,450 M693L possibly damaging Het
Megf8 G T 7: 25,346,747 M1525I possibly damaging Het
Mgme1 T C 2: 144,279,098 V276A possibly damaging Het
Mief2 G T 11: 60,731,408 W268L probably damaging Het
Mpped1 C T 15: 83,791,990 probably benign Het
Mreg T C 1: 72,192,197 N34S probably benign Het
Myf6 T C 10: 107,494,673 Y11C probably damaging Het
Myh9 C A 15: 77,771,167 Q1196H probably benign Het
Myh9 A T 15: 77,775,899 D56E probably benign Het
Myo5c A T 9: 75,277,075 R949S probably benign Het
Ncapg2 TAA TA 12: 116,434,685 probably null Het
Nfx1 T A 4: 40,977,004 V226E probably benign Het
Nlrp10 T A 7: 108,924,530 K581M possibly damaging Het
Nmd3 T G 3: 69,739,984 I273S probably benign Het
Olfr1264 A T 2: 90,021,970 I32N possibly damaging Het
P4hb T C 11: 120,571,616 E88G probably damaging Het
Pcnx3 A T 19: 5,665,745 H1444Q probably benign Het
Pdia4 A T 6: 47,799,199 F421L possibly damaging Het
Picalm T A 7: 90,191,251 S538T probably damaging Het
Ppp2r2b T A 18: 43,059,210 I11F probably benign Het
Ptk7 C T 17: 46,573,534 E757K possibly damaging Het
Rbm22 T G 18: 60,561,268 C24W probably damaging Het
Rev3l A G 10: 39,806,662 D288G probably damaging Het
Rgs18 T A 1: 144,754,053 H156L probably benign Het
Rnf213 A G 11: 119,442,579 I2871M probably damaging Het
Rrm2b A T 15: 37,945,084 M137K probably damaging Het
Rrp12 A T 19: 41,868,785 D1183E probably benign Het
Sacs G A 14: 61,203,828 V1108M probably damaging Het
Scube2 A T 7: 109,843,214 D270E possibly damaging Het
Serpina3a T A 12: 104,116,478 F170Y probably damaging Het
Serpinb3b T C 1: 107,154,673 E287G probably benign Het
Slamf8 C T 1: 172,584,619 V130M probably damaging Het
Slc5a3 T C 16: 92,077,396 S114P possibly damaging Het
Sos1 T A 17: 80,422,679 probably null Het
Sox10 A T 15: 79,156,460 D293E probably damaging Het
Sphk1 A G 11: 116,535,770 D177G probably damaging Het
Sphkap T G 1: 83,278,400 M543L probably benign Het
Syt13 A T 2: 92,953,415 K343N probably damaging Het
Tatdn3 A G 1: 191,060,176 M34T probably benign Het
Timd4 T G 11: 46,842,162 V305G possibly damaging Het
Tnnc2 T C 2: 164,777,592 I111V probably benign Het
Togaram2 C T 17: 71,697,851 P301L probably benign Het
Trpc3 T C 3: 36,640,627 N726S probably damaging Het
Tspear T A 10: 77,870,419 L341H possibly damaging Het
Ugt1a5 T A 1: 88,166,083 probably benign Het
Ulk3 A T 9: 57,593,160 probably null Het
Unc5d T A 8: 28,760,749 I297L probably benign Het
Usp20 A G 2: 31,018,818 I804V probably benign Het
Usp22 G T 11: 61,161,318 C278* probably null Het
Usp53 A T 3: 122,934,223 N903K probably benign Het
V1rd19 T C 7: 24,003,387 F93L probably benign Het
Zdbf2 T A 1: 63,304,334 V624E possibly damaging Het
Zfyve16 A T 13: 92,509,020 S1073T probably damaging Het
Zkscan8 T C 13: 21,526,595 H115R possibly damaging Het
Other mutations in Fbxo42
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00769:Fbxo42 APN 4 141180449 missense probably damaging 1.00
IGL02331:Fbxo42 APN 4 141167846 missense probably benign 0.08
IGL02989:Fbxo42 APN 4 141199534 missense probably damaging 1.00
IGL03047:Fbxo42 UTSW 4 141199542 missense possibly damaging 0.92
R0158:Fbxo42 UTSW 4 141200329 missense probably benign 0.26
R0295:Fbxo42 UTSW 4 141200497 missense probably damaging 1.00
R0671:Fbxo42 UTSW 4 141195239 missense probably damaging 1.00
R1321:Fbxo42 UTSW 4 141167849 missense probably benign 0.01
R1437:Fbxo42 UTSW 4 141167854 missense probably benign 0.00
R1459:Fbxo42 UTSW 4 141167762 missense probably benign
R1585:Fbxo42 UTSW 4 141198106 splice site probably benign
R2849:Fbxo42 UTSW 4 141200510 missense probably damaging 1.00
R4288:Fbxo42 UTSW 4 141167896 missense probably damaging 1.00
R4431:Fbxo42 UTSW 4 141200550 missense probably damaging 0.99
R4556:Fbxo42 UTSW 4 141199010 missense probably damaging 1.00
R4701:Fbxo42 UTSW 4 141199809 missense probably benign 0.00
R5071:Fbxo42 UTSW 4 141198945 missense probably damaging 1.00
R5072:Fbxo42 UTSW 4 141198945 missense probably damaging 1.00
R5249:Fbxo42 UTSW 4 141199024 missense probably damaging 1.00
R5796:Fbxo42 UTSW 4 141199789 missense probably benign 0.00
R6366:Fbxo42 UTSW 4 141199949 missense probably benign 0.01
R7197:Fbxo42 UTSW 4 141200085 missense probably benign
R7339:Fbxo42 UTSW 4 141200144 missense possibly damaging 0.95
R7468:Fbxo42 UTSW 4 141199606 missense possibly damaging 0.95
R7605:Fbxo42 UTSW 4 141199818 missense probably benign
R7619:Fbxo42 UTSW 4 141200362 missense possibly damaging 0.69
X0063:Fbxo42 UTSW 4 141195281 missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- GCCATCAAAGCGATGTCATCCAAAG -3'
(R):5'- GGATTTAATCCCAGCCTGGAGCAAG -3'

Sequencing Primer
(F):5'- ATGTGGGTAAACCCTTGTACCAG -3'
(R):5'- CTGGAGCAAGTTAGGCATGG -3'
Posted On2014-04-24