Incidental Mutation 'R6334:Ubxn7'
ID533162
Institutional Source Beutler Lab
Gene Symbol Ubxn7
Ensembl Gene ENSMUSG00000053774
Gene NameUBX domain protein 7
SynonymsUbxd7
MMRRC Submission
Accession Numbers
Is this an essential gene? Essential (E-score: 1.000) question?
Stock #R6334 (G1)
Quality Score42.0073
Status Validated
Chromosome16
Chromosomal Location32332257-32393747 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) T to A at 32372189 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000110804 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115151]
Predicted Effect probably null
Transcript: ENSMUST00000115151
SMART Domains Protein: ENSMUSP00000110804
Gene: ENSMUSG00000053774

DomainStartEndE-ValueType
low complexity region 2 12 N/A INTRINSIC
Pfam:UBA_4 15 56 4.3e-15 PFAM
UAS 137 260 3.05e-50 SMART
low complexity region 312 328 N/A INTRINSIC
UBX 405 487 1.16e-15 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.5%
Validation Efficiency 100% (64/64)
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2810021J22Rik T A 11: 58,880,114 S141T probably benign Het
Afap1l2 A G 19: 56,917,976 probably null Het
Aox2 C T 1: 58,307,407 Q567* probably null Het
Aqp4 T A 18: 15,393,591 M278L probably benign Het
Atp23 A C 10: 126,887,669 L188R probably benign Het
B230359F08Rik A G 14: 53,795,942 T103A probably damaging Het
Catsperg1 C T 7: 29,206,357 G215D probably benign Het
Cavin4 T C 4: 48,663,824 V68A possibly damaging Het
Ccl4 T C 11: 83,662,678 S6P unknown Het
Cfap46 T C 7: 139,680,831 E117G probably damaging Het
Chek1 A G 9: 36,714,492 S286P possibly damaging Het
Cntn4 G A 6: 106,344,786 V35I probably benign Het
Cntn4 C A 6: 106,506,192 P236Q probably benign Het
Cyp2d40 C A 15: 82,761,552 G84V probably benign Het
Dnah12 A T 14: 26,706,834 H205L possibly damaging Het
Dock1 G A 7: 134,851,576 V845I probably benign Het
Drg1 T C 11: 3,266,292 K7E possibly damaging Het
Eloa G A 4: 136,009,822 P488S probably damaging Het
Evi5 G A 5: 107,820,521 R187* probably null Het
Fam53a T A 5: 33,600,875 L301F probably damaging Het
Fmnl3 T C 15: 99,337,653 K63E probably damaging Het
Gast C A 11: 100,336,612 Q44K probably benign Het
Gm4788 A G 1: 139,773,924 probably null Het
Gng10 T A 4: 59,035,257 V7E probably benign Het
Gtf3c5 G A 2: 28,570,462 T375I probably benign Het
Haus5 C T 7: 30,658,976 W298* probably null Het
Hspa14 A T 2: 3,489,072 probably null Het
Kcna3 T C 3: 107,036,424 M1T probably null Het
Kcnj15 T G 16: 95,296,236 L239R probably damaging Het
Klhl2 G T 8: 64,759,808 D232E probably benign Het
Lamb3 A T 1: 193,335,474 I888F probably damaging Het
Lars C A 18: 42,217,486 M919I probably benign Het
Lfng T C 5: 140,612,767 V247A possibly damaging Het
Lrp1b C T 2: 41,789,033 A16T probably benign Het
Mamdc2 A T 19: 23,363,906 I235N probably damaging Het
Map9 T A 3: 82,383,305 L492Q probably damaging Het
Mcpt8 A G 14: 56,085,147 V14A possibly damaging Het
Myo1b T C 1: 51,768,651 K823R probably null Het
Nbea G T 3: 56,037,149 T598K probably damaging Het
Nrcam C A 12: 44,572,300 H877N probably benign Het
Nrxn2 T C 19: 6,531,292 probably null Het
Nwd2 A T 5: 63,800,253 I309F possibly damaging Het
Phyhd1 G A 2: 30,274,724 probably null Het
Pkp2 C T 16: 16,226,069 T229I probably damaging Het
Plagl2 G A 2: 153,232,691 P97S probably benign Het
Plekhh2 C A 17: 84,566,866 N526K probably benign Het
Plin4 A G 17: 56,103,261 L1217P probably benign Het
Polr3e T C 7: 120,927,999 S67P possibly damaging Het
Postn A G 3: 54,385,282 K757E probably benign Het
Prpf39 T A 12: 65,042,813 probably null Het
Ptprg C T 14: 12,166,832 T745I probably damaging Het
Pxylp1 C G 9: 96,825,254 A292P probably damaging Het
Rpl35 G T 2: 39,001,742 D82E possibly damaging Het
Slc9a1 G A 4: 133,422,208 V782I possibly damaging Het
Syn2 T A 6: 115,263,914 M415K possibly damaging Het
Tmem117 A C 15: 95,011,443 I246L probably benign Het
Tmem221 A T 8: 71,558,784 V9E probably damaging Het
Vmn2r101 G T 17: 19,589,850 M299I possibly damaging Het
Vmn2r103 T A 17: 19,794,082 S379T probably damaging Het
Vmn2r109 T C 17: 20,541,178 N639S probably benign Het
Wdr26 T C 1: 181,203,206 Het
Zfp109 T A 7: 24,228,883 Y367F probably damaging Het
Zfp143 G A 7: 110,086,131 C389Y probably damaging Het
Zfp553 G T 7: 127,236,892 probably null Het
Other mutations in Ubxn7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00821:Ubxn7 APN 16 32369398 missense probably damaging 0.97
IGL02149:Ubxn7 APN 16 32375270 missense probably damaging 1.00
IGL02183:Ubxn7 APN 16 32369383 missense probably damaging 1.00
IGL02690:Ubxn7 APN 16 32381605 missense probably benign 0.01
IGL03133:Ubxn7 APN 16 32381781 missense probably damaging 1.00
R0268:Ubxn7 UTSW 16 32360046 missense probably benign 0.05
R0583:Ubxn7 UTSW 16 32375914 missense probably damaging 1.00
R0635:Ubxn7 UTSW 16 32367417 intron probably benign
R0787:Ubxn7 UTSW 16 32381763 splice site probably benign
R1658:Ubxn7 UTSW 16 32381236 intron probably null
R1916:Ubxn7 UTSW 16 32381759 splice site probably benign
R2070:Ubxn7 UTSW 16 32372469 missense possibly damaging 0.47
R2071:Ubxn7 UTSW 16 32372469 missense possibly damaging 0.47
R3031:Ubxn7 UTSW 16 32375307 missense probably benign 0.34
R3871:Ubxn7 UTSW 16 32381430 missense possibly damaging 0.94
R4994:Ubxn7 UTSW 16 32381504 missense probably damaging 1.00
R5629:Ubxn7 UTSW 16 32332299 missense unknown
R6599:Ubxn7 UTSW 16 32384925 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ACACAGTGCGTTTAAGGTGTG -3'
(R):5'- GCCACACTCTTTGGCCTGTAAG -3'

Sequencing Primer
(F):5'- ACTGGAGCATGGTCACTCTAC -3'
(R):5'- CTTTGGCCTGTAAGAGTAAAATTTCC -3'
Posted On2018-09-04