Incidental Mutation 'R1533:Ubr2'
ID |
166784 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ubr2
|
Ensembl Gene |
ENSMUSG00000023977 |
Gene Name |
ubiquitin protein ligase E3 component n-recognin 2 |
Synonyms |
ENSMUSG00000043296, E130209G04Rik, 9930021A08Rik |
MMRRC Submission |
039572-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.891)
|
Stock # |
R1533 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
17 |
Chromosomal Location |
47239221-47321482 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
A to C
at 47278173 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Stop codon
at position 721
(Y721*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000108963
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000113335]
[ENSMUST00000113337]
[ENSMUST00000225599]
|
AlphaFold |
Q6WKZ8 |
Predicted Effect |
probably null
Transcript: ENSMUST00000113335
AA Change: Y721*
|
SMART Domains |
Protein: ENSMUSP00000108961 Gene: ENSMUSG00000023977 AA Change: Y721*
Domain | Start | End | E-Value | Type |
ZnF_UBR1
|
97 |
167 |
3.14e-32 |
SMART |
Pfam:ClpS
|
221 |
302 |
2.4e-23 |
PFAM |
low complexity region
|
635 |
646 |
N/A |
INTRINSIC |
low complexity region
|
749 |
760 |
N/A |
INTRINSIC |
low complexity region
|
872 |
886 |
N/A |
INTRINSIC |
coiled coil region
|
1019 |
1046 |
N/A |
INTRINSIC |
RING
|
1108 |
1213 |
7.66e-1 |
SMART |
low complexity region
|
1221 |
1235 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000113337
AA Change: Y721*
|
SMART Domains |
Protein: ENSMUSP00000108963 Gene: ENSMUSG00000023977 AA Change: Y721*
Domain | Start | End | E-Value | Type |
ZnF_UBR1
|
97 |
167 |
3.14e-32 |
SMART |
Pfam:ClpS
|
222 |
301 |
6.2e-26 |
PFAM |
low complexity region
|
635 |
646 |
N/A |
INTRINSIC |
low complexity region
|
749 |
760 |
N/A |
INTRINSIC |
low complexity region
|
872 |
886 |
N/A |
INTRINSIC |
coiled coil region
|
1019 |
1046 |
N/A |
INTRINSIC |
RING
|
1108 |
1213 |
7.66e-1 |
SMART |
low complexity region
|
1221 |
1235 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000224759
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000225599
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.4%
- 20x: 92.9%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an E3 ubiquitin ligase of the N-end rule proteolytic pathway that targets proteins with destabilizing N-terminal residues for polyubiquitylation and proteasome-mediated degradation. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010] PHENOTYPE: On a mixed genetic background, female homozygotes for a targeted null mutation exhibit embryonic lethality, while males are viable, but sterile due to postnatal testicular degeneration. On an inbred background, both genders die in utero. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
G |
C |
3: 121,928,807 (GRCm39) |
G1340A |
probably benign |
Het |
Ambra1 |
T |
A |
2: 91,717,210 (GRCm39) |
Y836N |
probably damaging |
Het |
Arhgap26 |
A |
T |
18: 39,504,130 (GRCm39) |
H144L |
probably benign |
Het |
B3gnt5 |
A |
G |
16: 19,588,364 (GRCm39) |
I194M |
probably damaging |
Het |
Bltp1 |
G |
T |
3: 37,095,524 (GRCm39) |
G4509V |
probably damaging |
Het |
Bod1l |
A |
T |
5: 41,979,498 (GRCm39) |
C605* |
probably null |
Het |
C2cd3 |
G |
T |
7: 100,055,284 (GRCm39) |
K482N |
possibly damaging |
Het |
Cd300lg |
T |
A |
11: 101,934,047 (GRCm39) |
L98Q |
probably damaging |
Het |
Cerkl |
T |
A |
2: 79,171,701 (GRCm39) |
I386F |
possibly damaging |
Het |
Cfh |
T |
A |
1: 140,028,716 (GRCm39) |
D466V |
possibly damaging |
Het |
Crtc1 |
A |
T |
8: 70,850,949 (GRCm39) |
I221N |
probably damaging |
Het |
Ctnnbl1 |
T |
C |
2: 157,678,563 (GRCm39) |
S389P |
probably benign |
Het |
Ctsb |
A |
T |
14: 63,376,544 (GRCm39) |
D258V |
probably damaging |
Het |
Cuzd1 |
G |
T |
7: 130,913,432 (GRCm39) |
T395N |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,128,536 (GRCm39) |
T1240A |
probably benign |
Het |
Dok7 |
T |
A |
5: 35,221,671 (GRCm39) |
|
probably null |
Het |
Dscaml1 |
T |
C |
9: 45,361,882 (GRCm39) |
V214A |
probably damaging |
Het |
Enpp6 |
A |
T |
8: 47,518,469 (GRCm39) |
Y199F |
probably benign |
Het |
Entpd5 |
C |
A |
12: 84,441,434 (GRCm39) |
K111N |
probably damaging |
Het |
Fam98a |
A |
G |
17: 75,848,276 (GRCm39) |
L146S |
probably damaging |
Het |
Fhod3 |
A |
T |
18: 25,248,921 (GRCm39) |
I1367F |
probably damaging |
Het |
Fmnl2 |
A |
G |
2: 52,995,549 (GRCm39) |
E424G |
probably damaging |
Het |
Fpr3 |
T |
A |
17: 18,190,922 (GRCm39) |
Y64* |
probably null |
Het |
Fzd6 |
A |
T |
15: 38,895,019 (GRCm39) |
H395L |
probably damaging |
Het |
Gcsh |
T |
A |
8: 117,715,921 (GRCm39) |
H54L |
probably damaging |
Het |
Gsdma |
T |
A |
11: 98,567,210 (GRCm39) |
S437T |
unknown |
Het |
Gzmc |
A |
G |
14: 56,471,376 (GRCm39) |
V55A |
probably damaging |
Het |
Hecw2 |
T |
A |
1: 53,965,704 (GRCm39) |
|
probably null |
Het |
Ifi207 |
A |
G |
1: 173,555,306 (GRCm39) |
V792A |
probably benign |
Het |
Itpr3 |
C |
A |
17: 27,314,534 (GRCm39) |
N661K |
possibly damaging |
Het |
Jmy |
A |
T |
13: 93,577,819 (GRCm39) |
I783N |
probably benign |
Het |
Kcmf1 |
T |
C |
6: 72,820,003 (GRCm39) |
E281G |
possibly damaging |
Het |
Klra3 |
G |
C |
6: 130,310,107 (GRCm39) |
R138G |
probably benign |
Het |
Lgr6 |
T |
A |
1: 135,032,670 (GRCm39) |
Y70F |
possibly damaging |
Het |
Lnx1 |
T |
G |
5: 74,780,678 (GRCm39) |
D330A |
probably damaging |
Het |
Lrp5 |
T |
C |
19: 3,664,234 (GRCm39) |
N106S |
probably benign |
Het |
Mamdc4 |
C |
A |
2: 25,459,759 (GRCm39) |
R135L |
possibly damaging |
Het |
Mcm3ap |
A |
G |
10: 76,340,121 (GRCm39) |
E1464G |
probably damaging |
Het |
Megf8 |
T |
C |
7: 25,034,280 (GRCm39) |
V666A |
possibly damaging |
Het |
Mettl3 |
T |
A |
14: 52,534,385 (GRCm39) |
E331D |
probably benign |
Het |
Mphosph9 |
T |
C |
5: 124,405,204 (GRCm39) |
K789R |
probably damaging |
Het |
Mtf2 |
T |
C |
5: 108,239,995 (GRCm39) |
L234P |
probably damaging |
Het |
Ncdn |
C |
A |
4: 126,642,491 (GRCm39) |
E389* |
probably null |
Het |
Ndor1 |
A |
G |
2: 25,139,279 (GRCm39) |
S231P |
probably damaging |
Het |
Nelfa |
T |
G |
5: 34,056,215 (GRCm39) |
K483Q |
probably damaging |
Het |
Odad1 |
T |
A |
7: 45,592,282 (GRCm39) |
M354K |
probably benign |
Het |
Opn1sw |
C |
T |
6: 29,378,923 (GRCm39) |
R243Q |
probably benign |
Het |
Or13a24 |
T |
A |
7: 140,155,034 (GRCm39) |
|
probably null |
Het |
Or9e1 |
A |
G |
11: 58,732,792 (GRCm39) |
N284S |
probably damaging |
Het |
Pik3cd |
T |
C |
4: 149,739,653 (GRCm39) |
E584G |
probably damaging |
Het |
Plcb3 |
A |
T |
19: 6,935,041 (GRCm39) |
M870K |
possibly damaging |
Het |
Poc5 |
A |
G |
13: 96,528,152 (GRCm39) |
D16G |
probably damaging |
Het |
Prpf40a |
A |
G |
2: 53,035,852 (GRCm39) |
I633T |
probably damaging |
Het |
Ptpn13 |
G |
T |
5: 103,704,044 (GRCm39) |
E1359* |
probably null |
Het |
Ptprr |
C |
A |
10: 116,024,113 (GRCm39) |
Y4* |
probably null |
Het |
Rbm45 |
T |
C |
2: 76,202,503 (GRCm39) |
|
probably null |
Het |
Rfng |
C |
T |
11: 120,672,687 (GRCm39) |
W320* |
probably null |
Het |
Rgs6 |
G |
T |
12: 83,138,547 (GRCm39) |
V294L |
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,169,002 (GRCm39) |
|
probably null |
Het |
Ruvbl2 |
T |
A |
7: 45,073,566 (GRCm39) |
N313I |
probably damaging |
Het |
Sema4g |
G |
A |
19: 44,981,256 (GRCm39) |
V70M |
probably damaging |
Het |
Siglec1 |
T |
C |
2: 130,918,078 (GRCm39) |
T969A |
probably benign |
Het |
Slc22a27 |
T |
A |
19: 7,844,348 (GRCm39) |
T431S |
possibly damaging |
Het |
Slc25a16 |
G |
A |
10: 62,756,643 (GRCm39) |
R38H |
probably damaging |
Het |
Slc38a6 |
T |
C |
12: 73,391,626 (GRCm39) |
V296A |
probably benign |
Het |
Slc39a11 |
C |
T |
11: 113,196,748 (GRCm39) |
V212I |
probably damaging |
Het |
Sltm |
A |
G |
9: 70,493,948 (GRCm39) |
K782E |
probably damaging |
Het |
Styxl1 |
T |
A |
5: 135,799,175 (GRCm39) |
Y23F |
probably damaging |
Het |
Svs4 |
T |
C |
2: 164,120,148 (GRCm39) |
I20V |
unknown |
Het |
Syt14 |
G |
T |
1: 192,613,084 (GRCm39) |
T572K |
possibly damaging |
Het |
Tbc1d5 |
A |
T |
17: 51,227,603 (GRCm39) |
I214N |
possibly damaging |
Het |
Tm9sf3 |
A |
G |
19: 41,227,223 (GRCm39) |
S283P |
probably benign |
Het |
Tmtc1 |
C |
T |
6: 148,147,208 (GRCm39) |
|
probably null |
Het |
Ttll7 |
T |
A |
3: 146,602,422 (GRCm39) |
N73K |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,602,802 (GRCm39) |
K18473N |
probably damaging |
Het |
Vmn1r14 |
T |
A |
6: 57,211,286 (GRCm39) |
I288N |
probably damaging |
Het |
Vmn2r103 |
T |
C |
17: 19,993,662 (GRCm39) |
I13T |
probably benign |
Het |
Vps13a |
A |
T |
19: 16,678,494 (GRCm39) |
Y1162* |
probably null |
Het |
Vps51 |
C |
A |
19: 6,121,497 (GRCm39) |
R175L |
probably benign |
Het |
Zfp523 |
C |
A |
17: 28,423,473 (GRCm39) |
S149R |
probably benign |
Het |
Zik1 |
A |
G |
7: 10,224,053 (GRCm39) |
I348T |
possibly damaging |
Het |
Znfx1 |
T |
A |
2: 166,898,708 (GRCm39) |
H72L |
probably benign |
Het |
|
Other mutations in Ubr2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00324:Ubr2
|
APN |
17 |
47,296,986 (GRCm39) |
splice site |
probably benign |
|
IGL00332:Ubr2
|
APN |
17 |
47,301,916 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00518:Ubr2
|
APN |
17 |
47,303,922 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00693:Ubr2
|
APN |
17 |
47,283,907 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00785:Ubr2
|
APN |
17 |
47,255,791 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01144:Ubr2
|
APN |
17 |
47,268,247 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01459:Ubr2
|
APN |
17 |
47,241,435 (GRCm39) |
splice site |
probably benign |
|
IGL01637:Ubr2
|
APN |
17 |
47,267,580 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01710:Ubr2
|
APN |
17 |
47,254,335 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01726:Ubr2
|
APN |
17 |
47,303,907 (GRCm39) |
splice site |
probably benign |
|
IGL01925:Ubr2
|
APN |
17 |
47,265,875 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01960:Ubr2
|
APN |
17 |
47,284,893 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02170:Ubr2
|
APN |
17 |
47,278,123 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02308:Ubr2
|
APN |
17 |
47,245,119 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02387:Ubr2
|
APN |
17 |
47,274,076 (GRCm39) |
missense |
probably benign |
|
IGL02696:Ubr2
|
APN |
17 |
47,274,691 (GRCm39) |
missense |
probably benign |
|
IGL02726:Ubr2
|
APN |
17 |
47,283,847 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02750:Ubr2
|
APN |
17 |
47,280,208 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02934:Ubr2
|
APN |
17 |
47,268,266 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02959:Ubr2
|
APN |
17 |
47,286,877 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03018:Ubr2
|
APN |
17 |
47,264,972 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03343:Ubr2
|
APN |
17 |
47,262,844 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4280001:Ubr2
|
UTSW |
17 |
47,255,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R0044:Ubr2
|
UTSW |
17 |
47,303,911 (GRCm39) |
splice site |
probably benign |
|
R0044:Ubr2
|
UTSW |
17 |
47,303,911 (GRCm39) |
splice site |
probably benign |
|
R0446:Ubr2
|
UTSW |
17 |
47,294,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R0513:Ubr2
|
UTSW |
17 |
47,297,705 (GRCm39) |
nonsense |
probably null |
|
R0565:Ubr2
|
UTSW |
17 |
47,266,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R0600:Ubr2
|
UTSW |
17 |
47,278,174 (GRCm39) |
missense |
probably damaging |
0.99 |
R0690:Ubr2
|
UTSW |
17 |
47,249,579 (GRCm39) |
missense |
probably damaging |
0.97 |
R0710:Ubr2
|
UTSW |
17 |
47,249,607 (GRCm39) |
missense |
probably damaging |
0.96 |
R0761:Ubr2
|
UTSW |
17 |
47,294,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R0798:Ubr2
|
UTSW |
17 |
47,280,102 (GRCm39) |
splice site |
probably benign |
|
R0862:Ubr2
|
UTSW |
17 |
47,278,009 (GRCm39) |
nonsense |
probably null |
|
R0947:Ubr2
|
UTSW |
17 |
47,252,038 (GRCm39) |
missense |
probably damaging |
0.99 |
R0972:Ubr2
|
UTSW |
17 |
47,245,187 (GRCm39) |
splice site |
probably null |
|
R1500:Ubr2
|
UTSW |
17 |
47,297,615 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1514:Ubr2
|
UTSW |
17 |
47,311,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R1554:Ubr2
|
UTSW |
17 |
47,283,877 (GRCm39) |
missense |
probably benign |
|
R1575:Ubr2
|
UTSW |
17 |
47,243,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R1602:Ubr2
|
UTSW |
17 |
47,251,987 (GRCm39) |
missense |
probably benign |
0.30 |
R1941:Ubr2
|
UTSW |
17 |
47,284,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R1966:Ubr2
|
UTSW |
17 |
47,265,845 (GRCm39) |
missense |
probably benign |
0.05 |
R2041:Ubr2
|
UTSW |
17 |
47,296,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R2067:Ubr2
|
UTSW |
17 |
47,274,071 (GRCm39) |
critical splice donor site |
probably null |
|
R2111:Ubr2
|
UTSW |
17 |
47,274,071 (GRCm39) |
critical splice donor site |
probably null |
|
R2189:Ubr2
|
UTSW |
17 |
47,254,290 (GRCm39) |
missense |
probably benign |
0.01 |
R2219:Ubr2
|
UTSW |
17 |
47,296,968 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2307:Ubr2
|
UTSW |
17 |
47,277,141 (GRCm39) |
nonsense |
probably null |
|
R3426:Ubr2
|
UTSW |
17 |
47,279,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R3428:Ubr2
|
UTSW |
17 |
47,279,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R3608:Ubr2
|
UTSW |
17 |
47,255,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R4080:Ubr2
|
UTSW |
17 |
47,299,648 (GRCm39) |
missense |
probably benign |
0.05 |
R4330:Ubr2
|
UTSW |
17 |
47,278,204 (GRCm39) |
missense |
probably null |
1.00 |
R4383:Ubr2
|
UTSW |
17 |
47,250,313 (GRCm39) |
missense |
probably benign |
0.01 |
R4460:Ubr2
|
UTSW |
17 |
47,255,971 (GRCm39) |
critical splice donor site |
probably null |
|
R4794:Ubr2
|
UTSW |
17 |
47,241,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R4902:Ubr2
|
UTSW |
17 |
47,296,922 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4913:Ubr2
|
UTSW |
17 |
47,270,385 (GRCm39) |
splice site |
probably null |
|
R5092:Ubr2
|
UTSW |
17 |
47,280,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R5209:Ubr2
|
UTSW |
17 |
47,279,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R5226:Ubr2
|
UTSW |
17 |
47,294,196 (GRCm39) |
missense |
probably benign |
0.04 |
R5250:Ubr2
|
UTSW |
17 |
47,241,368 (GRCm39) |
missense |
probably benign |
0.01 |
R5437:Ubr2
|
UTSW |
17 |
47,274,623 (GRCm39) |
missense |
probably benign |
0.00 |
R5607:Ubr2
|
UTSW |
17 |
47,245,126 (GRCm39) |
nonsense |
probably null |
|
R5848:Ubr2
|
UTSW |
17 |
47,267,581 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6089:Ubr2
|
UTSW |
17 |
47,293,218 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6382:Ubr2
|
UTSW |
17 |
47,268,241 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6552:Ubr2
|
UTSW |
17 |
47,277,194 (GRCm39) |
splice site |
probably null |
|
R6630:Ubr2
|
UTSW |
17 |
47,262,910 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6892:Ubr2
|
UTSW |
17 |
47,245,034 (GRCm39) |
missense |
probably damaging |
0.99 |
R6936:Ubr2
|
UTSW |
17 |
47,283,957 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7039:Ubr2
|
UTSW |
17 |
47,321,139 (GRCm39) |
missense |
probably benign |
0.01 |
R7050:Ubr2
|
UTSW |
17 |
47,272,528 (GRCm39) |
missense |
probably benign |
0.30 |
R7078:Ubr2
|
UTSW |
17 |
47,266,779 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7126:Ubr2
|
UTSW |
17 |
47,284,982 (GRCm39) |
splice site |
probably null |
|
R7219:Ubr2
|
UTSW |
17 |
47,246,360 (GRCm39) |
nonsense |
probably null |
|
R7262:Ubr2
|
UTSW |
17 |
47,311,665 (GRCm39) |
missense |
probably damaging |
0.97 |
R7352:Ubr2
|
UTSW |
17 |
47,241,352 (GRCm39) |
missense |
probably benign |
0.19 |
R7366:Ubr2
|
UTSW |
17 |
47,266,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R7449:Ubr2
|
UTSW |
17 |
47,275,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R7496:Ubr2
|
UTSW |
17 |
47,301,917 (GRCm39) |
critical splice donor site |
probably null |
|
R7759:Ubr2
|
UTSW |
17 |
47,296,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R7869:Ubr2
|
UTSW |
17 |
47,301,934 (GRCm39) |
missense |
probably benign |
0.00 |
R7916:Ubr2
|
UTSW |
17 |
47,279,308 (GRCm39) |
critical splice donor site |
probably null |
|
R8236:Ubr2
|
UTSW |
17 |
47,262,835 (GRCm39) |
missense |
probably benign |
|
R8376:Ubr2
|
UTSW |
17 |
47,253,721 (GRCm39) |
missense |
probably benign |
0.07 |
R9026:Ubr2
|
UTSW |
17 |
47,245,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R9216:Ubr2
|
UTSW |
17 |
47,292,285 (GRCm39) |
missense |
probably benign |
0.36 |
R9339:Ubr2
|
UTSW |
17 |
47,284,865 (GRCm39) |
missense |
probably benign |
0.30 |
R9558:Ubr2
|
UTSW |
17 |
47,262,843 (GRCm39) |
missense |
probably benign |
|
R9606:Ubr2
|
UTSW |
17 |
47,245,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R9644:Ubr2
|
UTSW |
17 |
47,266,706 (GRCm39) |
critical splice donor site |
probably null |
|
R9731:Ubr2
|
UTSW |
17 |
47,274,071 (GRCm39) |
critical splice donor site |
probably null |
|
X0027:Ubr2
|
UTSW |
17 |
47,311,555 (GRCm39) |
missense |
probably damaging |
0.99 |
X0061:Ubr2
|
UTSW |
17 |
47,281,037 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1177:Ubr2
|
UTSW |
17 |
47,311,692 (GRCm39) |
missense |
possibly damaging |
0.76 |
Z1177:Ubr2
|
UTSW |
17 |
47,270,435 (GRCm39) |
missense |
probably benign |
|
Z1177:Ubr2
|
UTSW |
17 |
47,321,069 (GRCm39) |
missense |
probably benign |
0.33 |
|
Predicted Primers |
PCR Primer
(F):5'- CTCACCCACAAGCATGATGATGAGG -3'
(R):5'- GCAGCGAAATTCATAGCCGTGTCC -3'
Sequencing Primer
(F):5'- AGGTAGAGCATCTCTTCGATCAG -3'
(R):5'- CTCTTGGCAGCCACATGATATAG -3'
|
Posted On |
2014-04-13 |