Incidental Mutation 'R0373:Ubr1'
ID |
30584 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ubr1
|
Ensembl Gene |
ENSMUSG00000027272 |
Gene Name |
ubiquitin protein ligase E3 component n-recognin 1 |
Synonyms |
E3 alpha |
MMRRC Submission |
038579-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.826)
|
Stock # |
R0373 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
2 |
Chromosomal Location |
120690750-120801196 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 120777138 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Asparagine
at position 276
(Y276N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000028728
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028728]
|
AlphaFold |
O70481 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000028728
AA Change: Y276N
PolyPhen 2
Score 0.011 (Sensitivity: 0.96; Specificity: 0.78)
|
SMART Domains |
Protein: ENSMUSP00000028728 Gene: ENSMUSG00000027272 AA Change: Y276N
Domain | Start | End | E-Value | Type |
ZnF_UBR1
|
97 |
167 |
1.24e-35 |
SMART |
Pfam:ClpS
|
221 |
301 |
8e-24 |
PFAM |
low complexity region
|
918 |
936 |
N/A |
INTRINSIC |
low complexity region
|
1017 |
1030 |
N/A |
INTRINSIC |
low complexity region
|
1070 |
1081 |
N/A |
INTRINSIC |
Blast:RING
|
1101 |
1203 |
4e-34 |
BLAST |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000133408
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.1%
- 10x: 95.8%
- 20x: 91.5%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The N-end rule pathway is one proteolytic pathway of the ubiquitin system. The recognition component of this pathway, encoded by this gene, binds to a destabilizing N-terminal residue of a substrate protein and participates in the formation of a substrate-linked multiubiquitin chain. This leads to the eventual degradation of the substrate protein. The protein described in this record has a RING-type zinc finger and a UBR-type zinc finger. Mutations in this gene have been associated with Johanson-Blizzard syndrome. [provided by RefSeq, Jul 2008] PHENOTYPE: Homozygous null mutants have 20% lower body weight and reduced muscle and adipose tissue. Skeletal muscle lacks a mechanism for targeting proteins for rapid catabolism. Aberrant regulation of fatty acid synthase upon starvation is also observed. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930579F01Rik |
A |
T |
3: 137,879,343 (GRCm39) |
L235Q |
probably damaging |
Het |
Aadacl4fm4 |
A |
T |
4: 144,412,790 (GRCm39) |
M50K |
possibly damaging |
Het |
Adam6b |
T |
A |
12: 113,454,275 (GRCm39) |
V364D |
probably benign |
Het |
Akap13 |
T |
C |
7: 75,259,677 (GRCm39) |
L767P |
probably benign |
Het |
Akap13 |
T |
A |
7: 75,380,248 (GRCm39) |
S2193T |
probably damaging |
Het |
Anapc11 |
T |
C |
11: 120,496,203 (GRCm39) |
V69A |
probably benign |
Het |
Ankmy1 |
C |
T |
1: 92,823,912 (GRCm39) |
R118Q |
probably damaging |
Het |
Ankrd27 |
T |
C |
7: 35,337,478 (GRCm39) |
S931P |
probably benign |
Het |
Atp6v1c2 |
G |
A |
12: 17,338,169 (GRCm39) |
R280C |
probably damaging |
Het |
Bbs10 |
T |
A |
10: 111,135,913 (GRCm39) |
I342N |
probably damaging |
Het |
Calhm2 |
T |
C |
19: 47,121,389 (GRCm39) |
D260G |
possibly damaging |
Het |
Camk2a |
A |
G |
18: 61,091,310 (GRCm39) |
E264G |
probably damaging |
Het |
Ccdc146 |
T |
A |
5: 21,524,543 (GRCm39) |
M270L |
probably benign |
Het |
Cdc16 |
A |
G |
8: 13,829,264 (GRCm39) |
T517A |
probably benign |
Het |
Ces1g |
T |
C |
8: 94,057,821 (GRCm39) |
H160R |
probably benign |
Het |
Chst4 |
T |
C |
8: 110,757,026 (GRCm39) |
N196S |
probably damaging |
Het |
Ciz1 |
A |
T |
2: 32,257,479 (GRCm39) |
N175Y |
probably damaging |
Het |
Cyb5r4 |
G |
A |
9: 86,909,093 (GRCm39) |
V57I |
probably damaging |
Het |
Cyth3 |
A |
G |
5: 143,670,181 (GRCm39) |
|
probably benign |
Het |
Def6 |
A |
G |
17: 28,439,154 (GRCm39) |
E255G |
probably damaging |
Het |
Dhtkd1 |
T |
G |
2: 5,916,681 (GRCm39) |
Q665P |
probably damaging |
Het |
Dsg3 |
A |
C |
18: 20,672,804 (GRCm39) |
D825A |
probably damaging |
Het |
Eif3m |
T |
C |
2: 104,835,345 (GRCm39) |
T242A |
probably benign |
Het |
Emilin3 |
A |
G |
2: 160,751,737 (GRCm39) |
F101L |
probably benign |
Het |
Epha7 |
A |
G |
4: 28,935,700 (GRCm39) |
|
probably null |
Het |
Fbxo45 |
A |
T |
16: 32,057,223 (GRCm39) |
Y224N |
probably damaging |
Het |
Fhod3 |
A |
T |
18: 25,223,161 (GRCm39) |
M836L |
possibly damaging |
Het |
Fut4 |
C |
A |
9: 14,662,506 (GRCm39) |
V263F |
probably damaging |
Het |
Ggt1 |
C |
T |
10: 75,415,104 (GRCm39) |
T206M |
probably benign |
Het |
Gls |
T |
C |
1: 52,227,858 (GRCm39) |
R79G |
probably damaging |
Het |
Grhl1 |
T |
C |
12: 24,631,514 (GRCm39) |
S156P |
probably benign |
Het |
Ipo8 |
C |
T |
6: 148,676,540 (GRCm39) |
S983N |
probably benign |
Het |
Kcna7 |
C |
T |
7: 45,058,868 (GRCm39) |
A385V |
probably damaging |
Het |
Kpnb1 |
A |
T |
11: 97,075,916 (GRCm39) |
L40Q |
probably damaging |
Het |
Matn1 |
A |
T |
4: 130,677,417 (GRCm39) |
S209C |
probably damaging |
Het |
Mcc |
A |
G |
18: 44,608,289 (GRCm39) |
I501T |
probably benign |
Het |
Mdp1 |
A |
T |
14: 55,896,832 (GRCm39) |
F104L |
probably damaging |
Het |
Mib2 |
A |
T |
4: 155,740,745 (GRCm39) |
N626K |
probably damaging |
Het |
Mrgprh |
T |
C |
17: 13,095,843 (GRCm39) |
S28P |
possibly damaging |
Het |
Mup-ps23 |
T |
A |
4: 61,774,386 (GRCm39) |
|
noncoding transcript |
Het |
Myh15 |
A |
G |
16: 49,003,322 (GRCm39) |
T1794A |
possibly damaging |
Het |
Myo18a |
C |
G |
11: 77,711,868 (GRCm39) |
P680A |
probably benign |
Het |
Myom2 |
G |
T |
8: 15,148,419 (GRCm39) |
D532Y |
possibly damaging |
Het |
Ndufaf5 |
A |
G |
2: 140,012,801 (GRCm39) |
N57S |
probably benign |
Het |
Nectin3 |
C |
T |
16: 46,278,550 (GRCm39) |
V282M |
probably damaging |
Het |
Nup188 |
G |
T |
2: 30,221,000 (GRCm39) |
D997Y |
probably damaging |
Het |
Olfm3 |
T |
C |
3: 114,916,454 (GRCm39) |
V462A |
probably damaging |
Het |
Opcml |
A |
G |
9: 28,724,694 (GRCm39) |
H164R |
possibly damaging |
Het |
Or14a259 |
A |
T |
7: 86,013,013 (GRCm39) |
C177* |
probably null |
Het |
Or4c120 |
A |
T |
2: 89,000,757 (GRCm39) |
F266L |
probably benign |
Het |
Or8u9 |
A |
C |
2: 86,002,050 (GRCm39) |
F37C |
probably damaging |
Het |
Pacrg |
A |
G |
17: 10,622,347 (GRCm39) |
I209T |
probably damaging |
Het |
Pcf11 |
T |
C |
7: 92,310,423 (GRCm39) |
M522V |
probably benign |
Het |
Pck1 |
T |
A |
2: 172,995,183 (GRCm39) |
M1K |
probably null |
Het |
Pcm1 |
G |
T |
8: 41,729,148 (GRCm39) |
E707* |
probably null |
Het |
Pcsk5 |
G |
A |
19: 17,632,213 (GRCm39) |
R318W |
probably damaging |
Het |
Phf11d |
A |
T |
14: 59,590,793 (GRCm39) |
M188K |
possibly damaging |
Het |
Ppip5k2 |
A |
T |
1: 97,668,262 (GRCm39) |
C615* |
probably null |
Het |
Prkdc |
T |
A |
16: 15,609,791 (GRCm39) |
S3132T |
probably damaging |
Het |
Prl2c5 |
A |
T |
13: 13,357,609 (GRCm39) |
|
probably benign |
Het |
Prpsap2 |
A |
G |
11: 61,631,826 (GRCm39) |
I177T |
possibly damaging |
Het |
Rad50 |
A |
G |
11: 53,541,346 (GRCm39) |
S1297P |
probably damaging |
Het |
Rasip1 |
T |
A |
7: 45,284,668 (GRCm39) |
N678K |
possibly damaging |
Het |
Rubcn |
A |
G |
16: 32,656,350 (GRCm39) |
S544P |
probably damaging |
Het |
Rwdd2a |
A |
T |
9: 86,456,453 (GRCm39) |
T210S |
possibly damaging |
Het |
Scd2 |
A |
G |
19: 44,291,479 (GRCm39) |
D306G |
probably damaging |
Het |
Sema3b |
T |
C |
9: 107,480,117 (GRCm39) |
N207S |
probably benign |
Het |
Sf3b2 |
C |
T |
19: 5,324,852 (GRCm39) |
D845N |
probably damaging |
Het |
Sipa1l2 |
C |
A |
8: 126,191,149 (GRCm39) |
C947F |
probably damaging |
Het |
Slc12a1 |
A |
T |
2: 125,067,951 (GRCm39) |
T1013S |
probably damaging |
Het |
Slc18a2 |
A |
T |
19: 59,275,799 (GRCm39) |
I461L |
probably benign |
Het |
Slc1a6 |
C |
A |
10: 78,637,756 (GRCm39) |
Y427* |
probably null |
Het |
Slc30a4 |
A |
T |
2: 122,531,319 (GRCm39) |
I231K |
probably damaging |
Het |
Sos1 |
G |
T |
17: 80,761,192 (GRCm39) |
A168D |
probably damaging |
Het |
Spata31f1a |
T |
C |
4: 42,851,161 (GRCm39) |
I332V |
probably benign |
Het |
Sptb |
T |
C |
12: 76,668,145 (GRCm39) |
S651G |
probably benign |
Het |
Stk36 |
T |
C |
1: 74,672,779 (GRCm39) |
L1007P |
probably damaging |
Het |
Tek |
A |
T |
4: 94,692,578 (GRCm39) |
N229Y |
probably damaging |
Het |
Tep1 |
A |
G |
14: 51,074,225 (GRCm39) |
F1887L |
possibly damaging |
Het |
Tet1 |
A |
T |
10: 62,713,988 (GRCm39) |
C602* |
probably null |
Het |
Tnfrsf19 |
A |
G |
14: 61,209,485 (GRCm39) |
S262P |
possibly damaging |
Het |
Trim5 |
T |
C |
7: 103,914,891 (GRCm39) |
I393V |
probably benign |
Het |
Trpm6 |
A |
G |
19: 18,830,951 (GRCm39) |
E1272G |
probably benign |
Het |
Ttc21b |
A |
T |
2: 66,018,670 (GRCm39) |
Y1246N |
probably damaging |
Het |
Ttll3 |
T |
A |
6: 113,375,738 (GRCm39) |
L151H |
probably damaging |
Het |
U2surp |
C |
T |
9: 95,366,496 (GRCm39) |
V470I |
probably benign |
Het |
Uggt1 |
A |
G |
1: 36,218,751 (GRCm39) |
S59P |
probably benign |
Het |
Unc45a |
T |
C |
7: 79,976,092 (GRCm39) |
T796A |
probably damaging |
Het |
Unc5b |
C |
A |
10: 60,614,719 (GRCm39) |
V193F |
possibly damaging |
Het |
Upp1 |
G |
T |
11: 9,079,590 (GRCm39) |
M50I |
probably benign |
Het |
Vps18 |
C |
T |
2: 119,124,386 (GRCm39) |
R438C |
probably damaging |
Het |
Zfp715 |
T |
C |
7: 42,948,760 (GRCm39) |
Y400C |
possibly damaging |
Het |
Zfp955b |
T |
C |
17: 33,521,496 (GRCm39) |
Y322H |
probably benign |
Het |
|
Other mutations in Ubr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00552:Ubr1
|
APN |
2 |
120,705,888 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL00570:Ubr1
|
APN |
2 |
120,771,574 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL00990:Ubr1
|
APN |
2 |
120,761,353 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01124:Ubr1
|
APN |
2 |
120,745,386 (GRCm39) |
missense |
probably benign |
|
IGL01346:Ubr1
|
APN |
2 |
120,703,603 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01368:Ubr1
|
APN |
2 |
120,771,612 (GRCm39) |
splice site |
probably benign |
|
IGL01539:Ubr1
|
APN |
2 |
120,756,494 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL01862:Ubr1
|
APN |
2 |
120,764,823 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01965:Ubr1
|
APN |
2 |
120,705,879 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01984:Ubr1
|
APN |
2 |
120,751,867 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02184:Ubr1
|
APN |
2 |
120,730,989 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02208:Ubr1
|
APN |
2 |
120,776,830 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02415:Ubr1
|
APN |
2 |
120,801,084 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02517:Ubr1
|
APN |
2 |
120,694,854 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02614:Ubr1
|
APN |
2 |
120,701,460 (GRCm39) |
splice site |
probably benign |
|
IGL02627:Ubr1
|
APN |
2 |
120,771,472 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02718:Ubr1
|
APN |
2 |
120,745,364 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02741:Ubr1
|
APN |
2 |
120,771,572 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02939:Ubr1
|
APN |
2 |
120,711,664 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03081:Ubr1
|
APN |
2 |
120,791,637 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL03310:Ubr1
|
APN |
2 |
120,694,898 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03370:Ubr1
|
APN |
2 |
120,725,641 (GRCm39) |
missense |
probably benign |
|
I1329:Ubr1
|
UTSW |
2 |
120,764,775 (GRCm39) |
splice site |
probably benign |
|
R0022:Ubr1
|
UTSW |
2 |
120,791,654 (GRCm39) |
splice site |
probably benign |
|
R0345:Ubr1
|
UTSW |
2 |
120,734,584 (GRCm39) |
splice site |
probably null |
|
R0393:Ubr1
|
UTSW |
2 |
120,737,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R0543:Ubr1
|
UTSW |
2 |
120,711,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R0559:Ubr1
|
UTSW |
2 |
120,778,364 (GRCm39) |
nonsense |
probably null |
|
R0723:Ubr1
|
UTSW |
2 |
120,711,582 (GRCm39) |
nonsense |
probably null |
|
R1178:Ubr1
|
UTSW |
2 |
120,756,510 (GRCm39) |
nonsense |
probably null |
|
R1401:Ubr1
|
UTSW |
2 |
120,786,125 (GRCm39) |
missense |
probably benign |
0.01 |
R1485:Ubr1
|
UTSW |
2 |
120,791,579 (GRCm39) |
missense |
probably benign |
0.03 |
R1572:Ubr1
|
UTSW |
2 |
120,765,800 (GRCm39) |
splice site |
probably benign |
|
R1920:Ubr1
|
UTSW |
2 |
120,761,449 (GRCm39) |
missense |
probably benign |
0.11 |
R1921:Ubr1
|
UTSW |
2 |
120,761,449 (GRCm39) |
missense |
probably benign |
0.11 |
R1997:Ubr1
|
UTSW |
2 |
120,776,754 (GRCm39) |
critical splice donor site |
probably null |
|
R2129:Ubr1
|
UTSW |
2 |
120,773,034 (GRCm39) |
missense |
probably benign |
0.35 |
R2147:Ubr1
|
UTSW |
2 |
120,694,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R2191:Ubr1
|
UTSW |
2 |
120,756,528 (GRCm39) |
missense |
probably damaging |
0.96 |
R2288:Ubr1
|
UTSW |
2 |
120,739,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3409:Ubr1
|
UTSW |
2 |
120,793,929 (GRCm39) |
missense |
probably benign |
0.02 |
R3930:Ubr1
|
UTSW |
2 |
120,746,951 (GRCm39) |
missense |
probably benign |
0.20 |
R3979:Ubr1
|
UTSW |
2 |
120,693,168 (GRCm39) |
missense |
probably benign |
0.11 |
R4172:Ubr1
|
UTSW |
2 |
120,777,103 (GRCm39) |
splice site |
probably null |
|
R4173:Ubr1
|
UTSW |
2 |
120,777,103 (GRCm39) |
splice site |
probably null |
|
R4174:Ubr1
|
UTSW |
2 |
120,777,103 (GRCm39) |
splice site |
probably null |
|
R4241:Ubr1
|
UTSW |
2 |
120,764,867 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4366:Ubr1
|
UTSW |
2 |
120,801,084 (GRCm39) |
utr 5 prime |
probably benign |
|
R4371:Ubr1
|
UTSW |
2 |
120,725,547 (GRCm39) |
splice site |
probably null |
|
R4449:Ubr1
|
UTSW |
2 |
120,776,862 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4533:Ubr1
|
UTSW |
2 |
120,772,963 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4656:Ubr1
|
UTSW |
2 |
120,756,494 (GRCm39) |
missense |
probably benign |
0.35 |
R4765:Ubr1
|
UTSW |
2 |
120,793,923 (GRCm39) |
nonsense |
probably null |
|
R4928:Ubr1
|
UTSW |
2 |
120,745,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R4987:Ubr1
|
UTSW |
2 |
120,794,047 (GRCm39) |
missense |
probably benign |
0.00 |
R5033:Ubr1
|
UTSW |
2 |
120,742,478 (GRCm39) |
critical splice donor site |
probably null |
|
R5108:Ubr1
|
UTSW |
2 |
120,793,903 (GRCm39) |
missense |
probably benign |
0.20 |
R5118:Ubr1
|
UTSW |
2 |
120,712,745 (GRCm39) |
missense |
probably benign |
0.20 |
R5211:Ubr1
|
UTSW |
2 |
120,723,651 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5215:Ubr1
|
UTSW |
2 |
120,734,525 (GRCm39) |
missense |
probably benign |
0.00 |
R5449:Ubr1
|
UTSW |
2 |
120,793,981 (GRCm39) |
missense |
probably benign |
|
R5452:Ubr1
|
UTSW |
2 |
120,698,783 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5582:Ubr1
|
UTSW |
2 |
120,745,888 (GRCm39) |
missense |
probably benign |
|
R5610:Ubr1
|
UTSW |
2 |
120,722,593 (GRCm39) |
missense |
probably benign |
0.04 |
R5637:Ubr1
|
UTSW |
2 |
120,793,998 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5808:Ubr1
|
UTSW |
2 |
120,791,573 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5845:Ubr1
|
UTSW |
2 |
120,734,486 (GRCm39) |
missense |
probably benign |
|
R5979:Ubr1
|
UTSW |
2 |
120,776,863 (GRCm39) |
missense |
probably benign |
0.07 |
R6044:Ubr1
|
UTSW |
2 |
120,693,202 (GRCm39) |
missense |
probably benign |
0.38 |
R6146:Ubr1
|
UTSW |
2 |
120,723,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R6252:Ubr1
|
UTSW |
2 |
120,737,376 (GRCm39) |
missense |
probably benign |
0.21 |
R6389:Ubr1
|
UTSW |
2 |
120,711,520 (GRCm39) |
missense |
probably benign |
0.03 |
R6600:Ubr1
|
UTSW |
2 |
120,745,880 (GRCm39) |
missense |
probably benign |
0.00 |
R6670:Ubr1
|
UTSW |
2 |
120,754,611 (GRCm39) |
critical splice donor site |
probably null |
|
R6731:Ubr1
|
UTSW |
2 |
120,786,121 (GRCm39) |
missense |
probably null |
0.99 |
R6836:Ubr1
|
UTSW |
2 |
120,727,156 (GRCm39) |
splice site |
probably null |
|
R6994:Ubr1
|
UTSW |
2 |
120,794,074 (GRCm39) |
missense |
probably benign |
|
R7121:Ubr1
|
UTSW |
2 |
120,705,979 (GRCm39) |
missense |
probably benign |
0.00 |
R7204:Ubr1
|
UTSW |
2 |
120,734,558 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7209:Ubr1
|
UTSW |
2 |
120,693,246 (GRCm39) |
missense |
probably benign |
0.04 |
R7434:Ubr1
|
UTSW |
2 |
120,693,161 (GRCm39) |
missense |
probably benign |
|
R7457:Ubr1
|
UTSW |
2 |
120,748,309 (GRCm39) |
missense |
probably benign |
0.35 |
R7464:Ubr1
|
UTSW |
2 |
120,720,255 (GRCm39) |
critical splice donor site |
probably null |
|
R7519:Ubr1
|
UTSW |
2 |
120,705,925 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7574:Ubr1
|
UTSW |
2 |
120,703,672 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8030:Ubr1
|
UTSW |
2 |
120,764,855 (GRCm39) |
missense |
probably damaging |
0.99 |
R8085:Ubr1
|
UTSW |
2 |
120,764,898 (GRCm39) |
nonsense |
probably null |
|
R8221:Ubr1
|
UTSW |
2 |
120,791,585 (GRCm39) |
missense |
probably damaging |
0.97 |
R8241:Ubr1
|
UTSW |
2 |
120,793,937 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8291:Ubr1
|
UTSW |
2 |
120,741,596 (GRCm39) |
missense |
probably benign |
|
R8293:Ubr1
|
UTSW |
2 |
120,693,202 (GRCm39) |
missense |
probably benign |
0.38 |
R8420:Ubr1
|
UTSW |
2 |
120,701,476 (GRCm39) |
missense |
probably benign |
|
R8489:Ubr1
|
UTSW |
2 |
120,711,548 (GRCm39) |
missense |
probably benign |
0.42 |
R8708:Ubr1
|
UTSW |
2 |
120,696,964 (GRCm39) |
missense |
probably benign |
0.27 |
R8856:Ubr1
|
UTSW |
2 |
120,734,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R8995:Ubr1
|
UTSW |
2 |
120,697,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R9153:Ubr1
|
UTSW |
2 |
120,756,469 (GRCm39) |
missense |
probably benign |
0.00 |
R9155:Ubr1
|
UTSW |
2 |
120,754,615 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9156:Ubr1
|
UTSW |
2 |
120,703,603 (GRCm39) |
critical splice donor site |
probably null |
|
R9194:Ubr1
|
UTSW |
2 |
120,778,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R9320:Ubr1
|
UTSW |
2 |
120,727,000 (GRCm39) |
missense |
probably benign |
0.04 |
R9401:Ubr1
|
UTSW |
2 |
120,765,765 (GRCm39) |
missense |
probably benign |
0.06 |
R9430:Ubr1
|
UTSW |
2 |
120,734,506 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9515:Ubr1
|
UTSW |
2 |
120,703,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R9623:Ubr1
|
UTSW |
2 |
120,764,820 (GRCm39) |
missense |
probably benign |
0.06 |
R9703:Ubr1
|
UTSW |
2 |
120,732,092 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- CTGGGCTTTAGTGACCCACACTTC -3'
(R):5'- ATTGGTTTAGCTGCCCCGTGTC -3'
Sequencing Primer
(F):5'- CTTTAGTGACCCACACTTCATAAAGG -3'
(R):5'- cccgtttttgttgttgttgttc -3'
|
Posted On |
2013-04-24 |