Incidental Mutation 'R7222:Ubr4'
ID 561867
Institutional Source Beutler Lab
Gene Symbol Ubr4
Ensembl Gene ENSMUSG00000066036
Gene Name ubiquitin protein ligase E3 component n-recognin 4
Synonyms p600, A930005E13Rik, LOC381562, D930005K06Rik, Zubr1, 1810009A16Rik
MMRRC Submission 045294-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R7222 (G1)
Quality Score 225.009
Status Validated
Chromosome 4
Chromosomal Location 139107970-139216844 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 139190684 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Threonine at position 905 (S905T)
Ref Sequence ENSEMBL: ENSMUSP00000117419 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000097822] [ENSMUST00000147999] [ENSMUST00000165860]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000097822
AA Change: S4064T
SMART Domains Protein: ENSMUSP00000095433
Gene: ENSMUSG00000066036
AA Change: S4064T

DomainStartEndE-ValueType
low complexity region 5 20 N/A INTRINSIC
low complexity region 414 425 N/A INTRINSIC
low complexity region 530 541 N/A INTRINSIC
low complexity region 555 566 N/A INTRINSIC
low complexity region 571 588 N/A INTRINSIC
low complexity region 600 621 N/A INTRINSIC
low complexity region 1312 1330 N/A INTRINSIC
low complexity region 1642 1655 N/A INTRINSIC
Pfam:zf-UBR 1660 1725 1.9e-9 PFAM
Blast:ZnF_C2H2 1966 1991 6e-8 BLAST
low complexity region 2268 2279 N/A INTRINSIC
low complexity region 2502 2540 N/A INTRINSIC
low complexity region 2725 2735 N/A INTRINSIC
low complexity region 2818 2852 N/A INTRINSIC
low complexity region 2887 2905 N/A INTRINSIC
low complexity region 2928 2942 N/A INTRINSIC
low complexity region 2945 2959 N/A INTRINSIC
low complexity region 2966 2986 N/A INTRINSIC
low complexity region 3063 3091 N/A INTRINSIC
low complexity region 3329 3385 N/A INTRINSIC
low complexity region 3776 3788 N/A INTRINSIC
Pfam:E3_UbLigase_R4 4364 5160 N/A PFAM
Predicted Effect unknown
Transcript: ENSMUST00000147999
AA Change: S905T
SMART Domains Protein: ENSMUSP00000117419
Gene: ENSMUSG00000066036
AA Change: S905T

DomainStartEndE-ValueType
low complexity region 170 226 N/A INTRINSIC
low complexity region 617 629 N/A INTRINSIC
Pfam:E3_UbLigase_R4 1205 1301 4.5e-60 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000165860
AA Change: S4040T

PolyPhen 2 Score 0.271 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000125800
Gene: ENSMUSG00000066036
AA Change: S4040T

DomainStartEndE-ValueType
low complexity region 5 20 N/A INTRINSIC
low complexity region 414 425 N/A INTRINSIC
low complexity region 530 541 N/A INTRINSIC
low complexity region 555 566 N/A INTRINSIC
low complexity region 571 588 N/A INTRINSIC
low complexity region 600 621 N/A INTRINSIC
low complexity region 1312 1330 N/A INTRINSIC
low complexity region 1642 1655 N/A INTRINSIC
Pfam:zf-UBR 1659 1729 4e-13 PFAM
Blast:ZnF_C2H2 1966 1991 5e-8 BLAST
low complexity region 2268 2279 N/A INTRINSIC
low complexity region 2513 2551 N/A INTRINSIC
low complexity region 2736 2746 N/A INTRINSIC
low complexity region 2863 2881 N/A INTRINSIC
low complexity region 2904 2918 N/A INTRINSIC
low complexity region 2921 2935 N/A INTRINSIC
low complexity region 2942 2962 N/A INTRINSIC
low complexity region 3039 3067 N/A INTRINSIC
low complexity region 3305 3361 N/A INTRINSIC
low complexity region 3752 3764 N/A INTRINSIC
Pfam:E3_UbLigase_R4 4340 5136 N/A PFAM
Meta Mutation Damage Score 0.0960 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.7%
Validation Efficiency 98% (49/50)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is an E3 ubiquitin-protein ligase that interacts with the retinoblastoma-associated protein in the nucleus and with calcium-bound calmodulin in the cytoplasm. The encoded protein appears to be a cytoskeletal component in the cytoplasm and part of the chromatin scaffold in the nucleus. In addition, this protein is a target of the human papillomavirus type 16 E7 oncoprotein. [provided by RefSeq, Aug 2010]
PHENOTYPE: Mice homozygous for a transgenic gene disruption exhibit neonatal lethality and decreased body size at birth. Mice homozygous for a null mutation display complete embryonic lethality during organogenesis with arrest of vitelline vascular remodeling. [provided by MGI curators]
Allele List at MGI

All alleles(59) : Targeted(2) Gene trapped(56) Transgenic(1)

Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca6 A T 11: 110,082,519 (GRCm39) N1151K probably benign Het
Add3 T C 19: 53,205,277 (GRCm39) V9A unknown Het
Ankar A G 1: 72,705,514 (GRCm39) I832T probably damaging Het
Arhgef10l C A 4: 140,248,580 (GRCm39) W785L probably damaging Het
Atp7b G A 8: 22,512,394 (GRCm39) Q490* probably null Het
Chrna5 A G 9: 54,905,347 (GRCm39) D53G probably benign Het
Clip1 T A 5: 123,749,904 (GRCm39) N993I probably damaging Het
Cyp3a59 A T 5: 146,033,385 (GRCm39) probably null Het
Dnah3 T A 7: 119,670,746 (GRCm39) N651Y probably benign Het
Dop1a T C 9: 86,404,929 (GRCm39) probably null Het
Eva1c AGGGTGTCCTGTACGAAGGACTTCCGGG AGGG 16: 90,701,072 (GRCm39) probably benign Het
Flg T A 3: 93,195,621 (GRCm39) S74T unknown Het
Fras1 T C 5: 96,784,045 (GRCm39) Y850H probably damaging Het
Fras1 A T 5: 96,784,668 (GRCm39) T884S probably benign Het
Fsip2 A G 2: 82,814,015 (GRCm39) T3445A probably benign Het
Herc1 C A 9: 66,374,781 (GRCm39) P3237H probably damaging Het
Ifi35 A G 11: 101,348,341 (GRCm39) N123S probably benign Het
Igkv1-117 A T 6: 68,098,733 (GRCm39) D94V probably damaging Het
Kif1b T C 4: 149,309,614 (GRCm39) D764G probably damaging Het
Lztr1 A G 16: 17,341,996 (GRCm39) E657G possibly damaging Het
Mmd2 G T 5: 142,553,682 (GRCm39) L160I probably benign Het
Muc2 A T 7: 141,290,758 (GRCm39) T15S Het
Muc6 T A 7: 141,214,428 (GRCm39) H2835L unknown Het
Myo1h G A 5: 114,493,322 (GRCm39) probably null Het
Or10v5 C A 19: 11,806,021 (GRCm39) R123L probably damaging Het
Or51ag1 A G 7: 103,155,664 (GRCm39) V163A possibly damaging Het
Or52n4 T C 7: 104,293,937 (GRCm39) D214G probably damaging Het
Or5d43 T A 2: 88,104,809 (GRCm39) M195L probably benign Het
Or5p72 A G 7: 108,021,844 (GRCm39) D22G probably benign Het
Or6c219 A G 10: 129,781,758 (GRCm39) Y58H probably damaging Het
Or7g32 A T 9: 19,388,763 (GRCm39) V261E probably damaging Het
Osbpl7 A G 11: 96,951,364 (GRCm39) T684A probably damaging Het
P2ry14 T C 3: 59,022,803 (GRCm39) K219R probably benign Het
Pde4d A T 13: 109,894,113 (GRCm39) H156L probably damaging Het
Polq G T 16: 36,906,995 (GRCm39) E2319* probably null Het
Ranbp3 T G 17: 57,017,211 (GRCm39) V409G probably damaging Het
Sart3 T C 5: 113,884,717 (GRCm39) D629G probably benign Het
Selenon T A 4: 134,275,288 (GRCm39) T137S possibly damaging Het
Setd2 T A 9: 110,380,530 (GRCm39) D55E Het
Slamf8 G A 1: 172,411,775 (GRCm39) T240I possibly damaging Het
Slc39a10 A G 1: 46,858,452 (GRCm39) L615P possibly damaging Het
Speer1e T A 5: 11,233,080 (GRCm39) N14K probably damaging Het
Tbce T C 13: 14,172,735 (GRCm39) D505G probably damaging Het
Tenm3 C T 8: 48,754,004 (GRCm39) G800R probably damaging Het
Terf2ip T C 8: 112,738,547 (GRCm39) V145A possibly damaging Het
Tmprss7 T C 16: 45,511,256 (GRCm39) I41V probably benign Het
Traj49 A T 14: 54,406,160 (GRCm39) N6I Het
Trim30a T C 7: 104,070,639 (GRCm39) probably null Het
Unc93a2 A G 17: 7,643,866 (GRCm39) S148P probably damaging Het
Zfp948 T A 17: 21,808,102 (GRCm39) H431Q probably damaging Het
Zfyve1 A G 12: 83,601,779 (GRCm39) F525L probably benign Het
Other mutations in Ubr4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00087:Ubr4 APN 4 139,192,633 (GRCm39) missense possibly damaging 0.46
IGL00336:Ubr4 APN 4 139,155,877 (GRCm39) missense probably damaging 1.00
IGL00586:Ubr4 APN 4 139,182,495 (GRCm39) missense possibly damaging 0.95
IGL00659:Ubr4 APN 4 139,148,556 (GRCm39) missense probably damaging 1.00
IGL00766:Ubr4 APN 4 139,168,077 (GRCm39) missense probably damaging 1.00
IGL00819:Ubr4 APN 4 139,203,593 (GRCm39) missense possibly damaging 0.92
IGL00833:Ubr4 APN 4 139,120,470 (GRCm39) critical splice donor site probably null
IGL01126:Ubr4 APN 4 139,129,866 (GRCm39) missense probably benign 0.04
IGL01311:Ubr4 APN 4 139,206,356 (GRCm39) missense possibly damaging 0.66
IGL01349:Ubr4 APN 4 139,208,039 (GRCm39) missense unknown
IGL01388:Ubr4 APN 4 139,187,554 (GRCm39) missense possibly damaging 0.76
IGL01417:Ubr4 APN 4 139,138,111 (GRCm39) missense probably damaging 0.99
IGL01446:Ubr4 APN 4 139,165,351 (GRCm39) splice site probably benign
IGL01449:Ubr4 APN 4 139,140,047 (GRCm39) missense probably damaging 0.98
IGL01545:Ubr4 APN 4 139,170,140 (GRCm39) splice site probably benign
IGL01568:Ubr4 APN 4 139,148,684 (GRCm39) missense probably damaging 1.00
IGL01596:Ubr4 APN 4 139,189,845 (GRCm39) splice site probably benign
IGL01621:Ubr4 APN 4 139,168,094 (GRCm39) nonsense probably null
IGL01639:Ubr4 APN 4 139,144,655 (GRCm39) missense probably damaging 0.99
IGL01655:Ubr4 APN 4 139,135,107 (GRCm39) missense probably damaging 1.00
IGL01710:Ubr4 APN 4 139,145,772 (GRCm39) missense possibly damaging 0.81
IGL01830:Ubr4 APN 4 139,199,811 (GRCm39) missense probably damaging 0.99
IGL01862:Ubr4 APN 4 139,204,469 (GRCm39) missense possibly damaging 0.66
IGL01868:Ubr4 APN 4 139,139,989 (GRCm39) nonsense probably null
IGL01874:Ubr4 APN 4 139,120,600 (GRCm39) splice site probably benign
IGL01889:Ubr4 APN 4 139,189,783 (GRCm39) nonsense probably null
IGL01891:Ubr4 APN 4 139,163,571 (GRCm39) critical splice donor site probably null
IGL01980:Ubr4 APN 4 139,156,913 (GRCm39) missense probably damaging 0.99
IGL02126:Ubr4 APN 4 139,180,052 (GRCm39) critical splice donor site probably null
IGL02153:Ubr4 APN 4 139,187,471 (GRCm39) nonsense probably null
IGL02173:Ubr4 APN 4 139,164,381 (GRCm39) splice site probably null
IGL02214:Ubr4 APN 4 139,155,894 (GRCm39) missense possibly damaging 0.95
IGL02214:Ubr4 APN 4 139,189,138 (GRCm39) critical splice acceptor site probably null
IGL02220:Ubr4 APN 4 139,115,746 (GRCm39) missense probably benign 0.01
IGL02246:Ubr4 APN 4 139,186,414 (GRCm39) missense possibly damaging 0.89
IGL02264:Ubr4 APN 4 139,182,939 (GRCm39) nonsense probably null
IGL02273:Ubr4 APN 4 139,199,889 (GRCm39) missense possibly damaging 0.94
IGL02316:Ubr4 APN 4 139,200,489 (GRCm39) missense possibly damaging 0.46
IGL02328:Ubr4 APN 4 139,206,233 (GRCm39) missense probably damaging 0.97
IGL02476:Ubr4 APN 4 139,148,560 (GRCm39) nonsense probably null
IGL02477:Ubr4 APN 4 139,163,516 (GRCm39) missense probably damaging 0.98
IGL02544:Ubr4 APN 4 139,142,429 (GRCm39) missense probably damaging 1.00
IGL02622:Ubr4 APN 4 139,194,561 (GRCm39) nonsense probably null
IGL02679:Ubr4 APN 4 139,186,445 (GRCm39) missense probably damaging 0.99
IGL02728:Ubr4 APN 4 139,196,122 (GRCm39) missense probably damaging 1.00
IGL02754:Ubr4 APN 4 139,138,095 (GRCm39) missense probably damaging 0.99
IGL02754:Ubr4 APN 4 139,120,470 (GRCm39) critical splice donor site probably null
IGL02892:Ubr4 APN 4 139,144,642 (GRCm39) missense probably damaging 0.96
IGL02897:Ubr4 APN 4 139,199,819 (GRCm39) missense probably damaging 0.97
IGL02946:Ubr4 APN 4 139,152,606 (GRCm39) missense probably damaging 1.00
IGL02964:Ubr4 APN 4 139,135,131 (GRCm39) missense possibly damaging 0.84
IGL03059:Ubr4 APN 4 139,207,987 (GRCm39) missense probably damaging 0.98
IGL03068:Ubr4 APN 4 139,137,041 (GRCm39) missense probably benign 0.02
IGL03087:Ubr4 APN 4 139,177,668 (GRCm39) nonsense probably null
IGL03116:Ubr4 APN 4 139,206,892 (GRCm39) splice site probably benign
IGL03212:Ubr4 APN 4 139,137,074 (GRCm39) missense probably benign 0.13
IGL03228:Ubr4 APN 4 139,156,909 (GRCm39) missense probably damaging 1.00
IGL03292:Ubr4 APN 4 139,167,746 (GRCm39) missense probably damaging 1.00
IGL03388:Ubr4 APN 4 139,142,343 (GRCm39) missense probably damaging 0.98
IGL03393:Ubr4 APN 4 139,179,989 (GRCm39) missense probably damaging 1.00
IGL03409:Ubr4 APN 4 139,127,240 (GRCm39) nonsense probably null
Aqua_regia UTSW 4 139,180,030 (GRCm39) nonsense probably null
Eats UTSW 4 139,190,886 (GRCm39) missense probably damaging 0.97
Hardened UTSW 4 139,196,158 (GRCm39) missense probably damaging 1.00
Stoney UTSW 4 139,171,998 (GRCm39) missense probably damaging 1.00
Uber UTSW 4 139,206,373 (GRCm39) critical splice donor site probably null
BB001:Ubr4 UTSW 4 139,194,587 (GRCm39) missense unknown
BB011:Ubr4 UTSW 4 139,194,587 (GRCm39) missense unknown
P0019:Ubr4 UTSW 4 139,179,092 (GRCm39) missense probably damaging 1.00
PIT4544001:Ubr4 UTSW 4 139,129,871 (GRCm39) missense possibly damaging 0.93
R0001:Ubr4 UTSW 4 139,179,099 (GRCm39) missense probably damaging 1.00
R0002:Ubr4 UTSW 4 139,118,211 (GRCm39) missense probably damaging 1.00
R0006:Ubr4 UTSW 4 139,158,960 (GRCm39) missense probably benign 0.03
R0006:Ubr4 UTSW 4 139,158,960 (GRCm39) missense probably benign 0.03
R0008:Ubr4 UTSW 4 139,157,487 (GRCm39) missense probably damaging 1.00
R0027:Ubr4 UTSW 4 139,127,704 (GRCm39) missense probably damaging 0.99
R0027:Ubr4 UTSW 4 139,127,704 (GRCm39) missense probably damaging 0.99
R0030:Ubr4 UTSW 4 139,154,104 (GRCm39) missense probably damaging 1.00
R0044:Ubr4 UTSW 4 139,164,369 (GRCm39) splice site probably benign
R0044:Ubr4 UTSW 4 139,164,369 (GRCm39) splice site probably benign
R0088:Ubr4 UTSW 4 139,168,125 (GRCm39) missense probably damaging 1.00
R0131:Ubr4 UTSW 4 139,191,362 (GRCm39) missense possibly damaging 0.66
R0184:Ubr4 UTSW 4 139,172,573 (GRCm39) missense probably damaging 1.00
R0219:Ubr4 UTSW 4 139,157,568 (GRCm39) missense possibly damaging 0.64
R0227:Ubr4 UTSW 4 139,158,960 (GRCm39) missense probably benign 0.03
R0270:Ubr4 UTSW 4 139,206,746 (GRCm39) splice site probably benign
R0285:Ubr4 UTSW 4 139,168,112 (GRCm39) missense probably damaging 1.00
R0322:Ubr4 UTSW 4 139,149,729 (GRCm39) missense probably damaging 1.00
R0363:Ubr4 UTSW 4 139,119,171 (GRCm39) missense probably damaging 0.98
R0393:Ubr4 UTSW 4 139,138,171 (GRCm39) splice site probably benign
R0450:Ubr4 UTSW 4 139,157,534 (GRCm39) missense probably benign 0.14
R0504:Ubr4 UTSW 4 139,133,889 (GRCm39) missense probably damaging 1.00
R0504:Ubr4 UTSW 4 139,208,149 (GRCm39) critical splice donor site probably null
R0510:Ubr4 UTSW 4 139,157,534 (GRCm39) missense probably benign 0.14
R0513:Ubr4 UTSW 4 139,144,186 (GRCm39) missense possibly damaging 0.74
R0517:Ubr4 UTSW 4 139,119,435 (GRCm39) missense probably benign 0.00
R0558:Ubr4 UTSW 4 139,154,213 (GRCm39) missense probably benign 0.09
R0617:Ubr4 UTSW 4 139,206,373 (GRCm39) critical splice donor site probably null
R0636:Ubr4 UTSW 4 139,163,613 (GRCm39) splice site probably null
R0637:Ubr4 UTSW 4 139,126,926 (GRCm39) missense probably damaging 1.00
R0652:Ubr4 UTSW 4 139,128,637 (GRCm39) missense probably damaging 0.99
R0691:Ubr4 UTSW 4 139,151,217 (GRCm39) missense probably damaging 1.00
R0729:Ubr4 UTSW 4 139,212,631 (GRCm39) missense possibly damaging 0.66
R0735:Ubr4 UTSW 4 139,155,339 (GRCm39) splice site probably null
R0751:Ubr4 UTSW 4 139,164,509 (GRCm39) splice site probably benign
R0789:Ubr4 UTSW 4 139,137,582 (GRCm39) critical splice donor site probably null
R0825:Ubr4 UTSW 4 139,206,887 (GRCm39) critical splice donor site probably null
R0828:Ubr4 UTSW 4 139,177,864 (GRCm39) splice site probably benign
R1052:Ubr4 UTSW 4 139,182,771 (GRCm39) missense possibly damaging 0.83
R1184:Ubr4 UTSW 4 139,164,509 (GRCm39) splice site probably benign
R1222:Ubr4 UTSW 4 139,115,782 (GRCm39) splice site probably null
R1258:Ubr4 UTSW 4 139,154,225 (GRCm39) missense probably damaging 1.00
R1321:Ubr4 UTSW 4 139,187,434 (GRCm39) missense possibly damaging 0.46
R1385:Ubr4 UTSW 4 139,129,923 (GRCm39) missense probably benign 0.00
R1450:Ubr4 UTSW 4 139,195,339 (GRCm39) missense probably damaging 1.00
R1470:Ubr4 UTSW 4 139,148,537 (GRCm39) splice site probably null
R1470:Ubr4 UTSW 4 139,148,537 (GRCm39) splice site probably null
R1474:Ubr4 UTSW 4 139,156,890 (GRCm39) missense probably damaging 1.00
R1479:Ubr4 UTSW 4 139,153,151 (GRCm39) missense possibly damaging 0.95
R1534:Ubr4 UTSW 4 139,155,462 (GRCm39) missense possibly damaging 0.95
R1546:Ubr4 UTSW 4 139,144,238 (GRCm39) nonsense probably null
R1785:Ubr4 UTSW 4 139,151,256 (GRCm39) missense probably damaging 1.00
R1786:Ubr4 UTSW 4 139,151,256 (GRCm39) missense probably damaging 1.00
R1789:Ubr4 UTSW 4 139,120,364 (GRCm39) missense probably damaging 1.00
R1796:Ubr4 UTSW 4 139,155,907 (GRCm39) missense probably benign 0.25
R1800:Ubr4 UTSW 4 139,135,274 (GRCm39) missense probably damaging 0.99
R1801:Ubr4 UTSW 4 139,179,874 (GRCm39) splice site probably null
R1827:Ubr4 UTSW 4 139,153,008 (GRCm39) critical splice acceptor site probably null
R1887:Ubr4 UTSW 4 139,182,871 (GRCm39) missense probably damaging 1.00
R1966:Ubr4 UTSW 4 139,178,555 (GRCm39) critical splice acceptor site probably null
R2010:Ubr4 UTSW 4 139,207,963 (GRCm39) missense possibly damaging 0.92
R2049:Ubr4 UTSW 4 139,204,518 (GRCm39) missense probably damaging 0.97
R2069:Ubr4 UTSW 4 139,206,851 (GRCm39) missense possibly damaging 0.66
R2114:Ubr4 UTSW 4 139,156,922 (GRCm39) nonsense probably null
R2140:Ubr4 UTSW 4 139,204,518 (GRCm39) missense probably damaging 0.97
R2141:Ubr4 UTSW 4 139,204,518 (GRCm39) missense probably damaging 0.97
R2142:Ubr4 UTSW 4 139,204,518 (GRCm39) missense probably damaging 0.97
R2168:Ubr4 UTSW 4 139,137,960 (GRCm39) missense probably benign 0.25
R2237:Ubr4 UTSW 4 139,170,101 (GRCm39) missense probably damaging 1.00
R2249:Ubr4 UTSW 4 139,176,232 (GRCm39) missense probably damaging 1.00
R2261:Ubr4 UTSW 4 139,140,773 (GRCm39) missense probably damaging 0.99
R2264:Ubr4 UTSW 4 139,147,684 (GRCm39) splice site probably benign
R2353:Ubr4 UTSW 4 139,160,984 (GRCm39) missense possibly damaging 0.48
R2437:Ubr4 UTSW 4 139,200,853 (GRCm39) missense possibly damaging 0.90
R2496:Ubr4 UTSW 4 139,200,516 (GRCm39) unclassified probably benign
R2896:Ubr4 UTSW 4 139,182,955 (GRCm39) splice site probably null
R2922:Ubr4 UTSW 4 139,206,811 (GRCm39) missense possibly damaging 0.66
R2972:Ubr4 UTSW 4 139,133,847 (GRCm39) missense probably benign 0.22
R2973:Ubr4 UTSW 4 139,133,847 (GRCm39) missense probably benign 0.22
R2989:Ubr4 UTSW 4 139,190,869 (GRCm39) missense possibly damaging 0.89
R3176:Ubr4 UTSW 4 139,149,166 (GRCm39) missense probably benign 0.03
R3276:Ubr4 UTSW 4 139,149,166 (GRCm39) missense probably benign 0.03
R3772:Ubr4 UTSW 4 139,180,011 (GRCm39) missense possibly damaging 0.89
R3844:Ubr4 UTSW 4 139,186,437 (GRCm39) missense probably damaging 0.99
R3873:Ubr4 UTSW 4 139,151,301 (GRCm39) missense probably damaging 1.00
R3900:Ubr4 UTSW 4 139,206,373 (GRCm39) critical splice donor site probably null
R3951:Ubr4 UTSW 4 139,120,405 (GRCm39) missense probably damaging 1.00
R4020:Ubr4 UTSW 4 139,179,116 (GRCm39) missense probably damaging 0.98
R4178:Ubr4 UTSW 4 139,120,725 (GRCm39) missense probably damaging 1.00
R4308:Ubr4 UTSW 4 139,199,820 (GRCm39) missense possibly damaging 0.46
R4378:Ubr4 UTSW 4 139,137,751 (GRCm39) missense possibly damaging 0.76
R4400:Ubr4 UTSW 4 139,189,167 (GRCm39) missense possibly damaging 0.66
R4421:Ubr4 UTSW 4 139,189,167 (GRCm39) missense possibly damaging 0.66
R4462:Ubr4 UTSW 4 139,145,813 (GRCm39) missense possibly damaging 0.47
R4583:Ubr4 UTSW 4 139,108,164 (GRCm39) missense possibly damaging 0.82
R4611:Ubr4 UTSW 4 139,126,890 (GRCm39) missense possibly damaging 0.93
R4664:Ubr4 UTSW 4 139,133,829 (GRCm39) missense possibly damaging 0.56
R4671:Ubr4 UTSW 4 139,163,502 (GRCm39) missense possibly damaging 0.66
R4672:Ubr4 UTSW 4 139,138,027 (GRCm39) missense probably damaging 0.99
R4673:Ubr4 UTSW 4 139,138,027 (GRCm39) missense probably damaging 0.99
R4696:Ubr4 UTSW 4 139,135,983 (GRCm39) missense probably benign 0.09
R4701:Ubr4 UTSW 4 139,198,647 (GRCm39) missense possibly damaging 0.66
R4705:Ubr4 UTSW 4 139,177,840 (GRCm39) missense probably damaging 1.00
R4726:Ubr4 UTSW 4 139,209,890 (GRCm39) missense possibly damaging 0.46
R4728:Ubr4 UTSW 4 139,151,190 (GRCm39) missense probably damaging 1.00
R4783:Ubr4 UTSW 4 139,149,044 (GRCm39) missense possibly damaging 0.85
R4833:Ubr4 UTSW 4 139,129,857 (GRCm39) missense probably damaging 0.98
R4892:Ubr4 UTSW 4 139,155,828 (GRCm39) missense probably benign 0.14
R4936:Ubr4 UTSW 4 139,123,877 (GRCm39) missense probably damaging 0.98
R5000:Ubr4 UTSW 4 139,163,480 (GRCm39) missense probably damaging 0.98
R5114:Ubr4 UTSW 4 139,137,934 (GRCm39) missense probably damaging 0.99
R5189:Ubr4 UTSW 4 139,137,960 (GRCm39) missense probably benign 0.25
R5197:Ubr4 UTSW 4 139,195,408 (GRCm39) missense probably damaging 1.00
R5213:Ubr4 UTSW 4 139,129,877 (GRCm39) nonsense probably null
R5219:Ubr4 UTSW 4 139,204,543 (GRCm39) nonsense probably null
R5346:Ubr4 UTSW 4 139,155,802 (GRCm39) missense probably damaging 0.97
R5368:Ubr4 UTSW 4 139,124,839 (GRCm39) intron probably benign
R5442:Ubr4 UTSW 4 139,135,083 (GRCm39) missense probably damaging 1.00
R5527:Ubr4 UTSW 4 139,208,099 (GRCm39) missense possibly damaging 0.83
R5548:Ubr4 UTSW 4 139,187,401 (GRCm39) missense probably damaging 0.97
R5568:Ubr4 UTSW 4 139,119,349 (GRCm39) missense probably damaging 0.99
R5639:Ubr4 UTSW 4 139,179,959 (GRCm39) missense possibly damaging 0.66
R5643:Ubr4 UTSW 4 139,171,998 (GRCm39) missense probably damaging 1.00
R5663:Ubr4 UTSW 4 139,155,894 (GRCm39) missense possibly damaging 0.95
R5755:Ubr4 UTSW 4 139,187,406 (GRCm39) missense possibly damaging 0.66
R5781:Ubr4 UTSW 4 139,195,407 (GRCm39) missense probably damaging 1.00
R5784:Ubr4 UTSW 4 139,152,529 (GRCm39) missense probably damaging 1.00
R5817:Ubr4 UTSW 4 139,196,158 (GRCm39) missense probably damaging 1.00
R5872:Ubr4 UTSW 4 139,152,641 (GRCm39) missense probably damaging 0.98
R5891:Ubr4 UTSW 4 139,135,937 (GRCm39) nonsense probably null
R5901:Ubr4 UTSW 4 139,178,565 (GRCm39) missense probably damaging 1.00
R5958:Ubr4 UTSW 4 139,182,949 (GRCm39) missense probably damaging 1.00
R5974:Ubr4 UTSW 4 139,148,389 (GRCm39) splice site probably null
R6065:Ubr4 UTSW 4 139,148,549 (GRCm39) missense probably damaging 1.00
R6109:Ubr4 UTSW 4 139,144,675 (GRCm39) missense probably damaging 0.99
R6207:Ubr4 UTSW 4 139,148,559 (GRCm39) missense probably damaging 1.00
R6265:Ubr4 UTSW 4 139,179,951 (GRCm39) missense possibly damaging 0.90
R6319:Ubr4 UTSW 4 139,136,200 (GRCm39) missense possibly damaging 0.84
R6342:Ubr4 UTSW 4 139,156,850 (GRCm39) missense possibly damaging 0.88
R6434:Ubr4 UTSW 4 139,156,949 (GRCm39) missense probably damaging 1.00
R6437:Ubr4 UTSW 4 139,124,525 (GRCm39) critical splice donor site probably null
R6481:Ubr4 UTSW 4 139,159,062 (GRCm39) missense probably damaging 0.97
R6502:Ubr4 UTSW 4 139,171,982 (GRCm39) missense probably damaging 1.00
R6546:Ubr4 UTSW 4 139,141,705 (GRCm39) missense probably damaging 0.99
R6603:Ubr4 UTSW 4 139,182,897 (GRCm39) missense probably benign 0.17
R6648:Ubr4 UTSW 4 139,180,030 (GRCm39) nonsense probably null
R6649:Ubr4 UTSW 4 139,200,935 (GRCm39) missense possibly damaging 0.66
R6653:Ubr4 UTSW 4 139,200,935 (GRCm39) missense possibly damaging 0.66
R6668:Ubr4 UTSW 4 139,192,652 (GRCm39) missense probably damaging 1.00
R6770:Ubr4 UTSW 4 139,216,493 (GRCm39) missense unknown
R6772:Ubr4 UTSW 4 139,194,541 (GRCm39) nonsense probably null
R6857:Ubr4 UTSW 4 139,213,362 (GRCm39) missense possibly damaging 0.90
R6869:Ubr4 UTSW 4 139,194,538 (GRCm39) missense possibly damaging 0.93
R6912:Ubr4 UTSW 4 139,185,545 (GRCm39) critical splice donor site probably null
R6943:Ubr4 UTSW 4 139,164,442 (GRCm39) nonsense probably null
R6970:Ubr4 UTSW 4 139,133,839 (GRCm39) nonsense probably null
R6976:Ubr4 UTSW 4 139,120,388 (GRCm39) missense probably damaging 0.98
R7000:Ubr4 UTSW 4 139,141,715 (GRCm39) missense probably damaging 1.00
R7017:Ubr4 UTSW 4 139,120,401 (GRCm39) missense probably damaging 0.99
R7165:Ubr4 UTSW 4 139,177,824 (GRCm39) missense
R7241:Ubr4 UTSW 4 139,170,725 (GRCm39) missense probably damaging 1.00
R7343:Ubr4 UTSW 4 139,140,749 (GRCm39) missense probably benign 0.09
R7367:Ubr4 UTSW 4 139,180,002 (GRCm39) missense unknown
R7393:Ubr4 UTSW 4 139,154,096 (GRCm39) missense probably damaging 1.00
R7432:Ubr4 UTSW 4 139,115,693 (GRCm39) missense probably damaging 1.00
R7448:Ubr4 UTSW 4 139,189,778 (GRCm39) missense unknown
R7502:Ubr4 UTSW 4 139,139,983 (GRCm39) missense possibly damaging 0.72
R7514:Ubr4 UTSW 4 139,179,966 (GRCm39) missense unknown
R7526:Ubr4 UTSW 4 139,149,728 (GRCm39) missense probably benign 0.00
R7529:Ubr4 UTSW 4 139,149,728 (GRCm39) missense probably benign 0.00
R7666:Ubr4 UTSW 4 139,140,791 (GRCm39) missense possibly damaging 0.81
R7699:Ubr4 UTSW 4 139,136,178 (GRCm39) nonsense probably null
R7700:Ubr4 UTSW 4 139,136,178 (GRCm39) nonsense probably null
R7726:Ubr4 UTSW 4 139,186,231 (GRCm39) missense unknown
R7753:Ubr4 UTSW 4 139,197,603 (GRCm39) missense unknown
R7810:Ubr4 UTSW 4 139,142,394 (GRCm39) missense
R7837:Ubr4 UTSW 4 139,120,462 (GRCm39) nonsense probably null
R7868:Ubr4 UTSW 4 139,187,344 (GRCm39) missense unknown
R7872:Ubr4 UTSW 4 139,120,373 (GRCm39) missense possibly damaging 0.94
R7887:Ubr4 UTSW 4 139,135,121 (GRCm39) missense probably damaging 0.99
R7924:Ubr4 UTSW 4 139,194,587 (GRCm39) missense unknown
R7980:Ubr4 UTSW 4 139,145,717 (GRCm39) missense
R7982:Ubr4 UTSW 4 139,155,519 (GRCm39) critical splice donor site probably null
R8005:Ubr4 UTSW 4 139,139,941 (GRCm39) missense probably damaging 0.98
R8054:Ubr4 UTSW 4 139,195,413 (GRCm39) missense unknown
R8094:Ubr4 UTSW 4 139,168,007 (GRCm39) missense probably damaging 0.97
R8151:Ubr4 UTSW 4 139,130,112 (GRCm39) missense probably damaging 0.97
R8183:Ubr4 UTSW 4 139,209,782 (GRCm39) missense unknown
R8252:Ubr4 UTSW 4 139,200,528 (GRCm39) missense unknown
R8505:Ubr4 UTSW 4 139,156,880 (GRCm39) missense
R8519:Ubr4 UTSW 4 139,143,958 (GRCm39) missense probably damaging 0.97
R8716:Ubr4 UTSW 4 139,196,164 (GRCm39) missense unknown
R8720:Ubr4 UTSW 4 139,208,149 (GRCm39) critical splice donor site probably null
R8749:Ubr4 UTSW 4 139,129,935 (GRCm39) missense probably damaging 0.98
R8768:Ubr4 UTSW 4 139,149,076 (GRCm39) missense
R8789:Ubr4 UTSW 4 139,137,494 (GRCm39) missense possibly damaging 0.76
R8879:Ubr4 UTSW 4 139,137,829 (GRCm39) missense probably benign 0.06
R8937:Ubr4 UTSW 4 139,190,886 (GRCm39) missense probably damaging 0.97
R9006:Ubr4 UTSW 4 139,172,003 (GRCm39) critical splice donor site probably null
R9116:Ubr4 UTSW 4 139,145,785 (GRCm39) missense
R9134:Ubr4 UTSW 4 139,127,755 (GRCm39) critical splice donor site probably null
R9251:Ubr4 UTSW 4 139,177,636 (GRCm39) missense
R9340:Ubr4 UTSW 4 139,182,763 (GRCm39) missense unknown
R9384:Ubr4 UTSW 4 139,194,631 (GRCm39) missense unknown
R9389:Ubr4 UTSW 4 139,153,235 (GRCm39) missense
R9393:Ubr4 UTSW 4 139,212,613 (GRCm39) missense unknown
R9531:Ubr4 UTSW 4 139,135,217 (GRCm39) missense probably benign 0.00
R9573:Ubr4 UTSW 4 139,148,450 (GRCm39) missense
R9604:Ubr4 UTSW 4 139,159,827 (GRCm39) critical splice donor site probably null
R9613:Ubr4 UTSW 4 139,149,073 (GRCm39) missense
R9623:Ubr4 UTSW 4 139,159,024 (GRCm39) missense probably benign 0.00
R9651:Ubr4 UTSW 4 139,206,859 (GRCm39) missense unknown
R9685:Ubr4 UTSW 4 139,191,341 (GRCm39) missense unknown
R9698:Ubr4 UTSW 4 139,167,975 (GRCm39) missense
R9700:Ubr4 UTSW 4 139,119,388 (GRCm39) missense probably damaging 0.97
R9727:Ubr4 UTSW 4 139,140,735 (GRCm39) missense probably damaging 0.98
R9766:Ubr4 UTSW 4 139,194,595 (GRCm39) missense unknown
T0975:Ubr4 UTSW 4 139,179,092 (GRCm39) missense probably damaging 1.00
X0028:Ubr4 UTSW 4 139,137,582 (GRCm39) critical splice donor site probably null
Z1176:Ubr4 UTSW 4 139,137,456 (GRCm39) missense probably damaging 1.00
Z1176:Ubr4 UTSW 4 139,129,971 (GRCm39) missense probably benign 0.04
Z1176:Ubr4 UTSW 4 139,127,696 (GRCm39) missense probably damaging 1.00
Z1177:Ubr4 UTSW 4 139,177,792 (GRCm39) missense
Z1186:Ubr4 UTSW 4 139,137,964 (GRCm39) missense probably benign 0.02
Predicted Primers PCR Primer
(F):5'- TGGGCCATCAAAACTGCATG -3'
(R):5'- CGTACTTCTCGGTCAAGTAGAG -3'

Sequencing Primer
(F):5'- AACTCTCACCTTGTGCTG -3'
(R):5'- CTTCTCGGTCAAGTAGAGACGGTG -3'
Posted On 2019-06-26