Incidental Mutation 'H8562:Urb1'
ID |
44397 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Urb1
|
Ensembl Gene |
ENSMUSG00000039929 |
Gene Name |
URB1 ribosome biogenesis 1 homolog (S. cerevisiae) |
Synonyms |
5730405K23Rik, 4921511H13Rik |
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
H8562 (G3)
of strain
604
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
16 |
Chromosomal Location |
90548415-90607301 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 90566357 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Methionine to Leucine
at position 1477
(M1477L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000114717
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000140920]
|
AlphaFold |
no structure available at present |
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000140158
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000140920
AA Change: M1477L
PolyPhen 2
Score 0.076 (Sensitivity: 0.93; Specificity: 0.85)
|
SMART Domains |
Protein: ENSMUSP00000114717 Gene: ENSMUSG00000039929 AA Change: M1477L
Domain | Start | End | E-Value | Type |
low complexity region
|
8 |
20 |
N/A |
INTRINSIC |
Pfam:Npa1
|
78 |
396 |
1.5e-86 |
PFAM |
low complexity region
|
751 |
761 |
N/A |
INTRINSIC |
low complexity region
|
955 |
966 |
N/A |
INTRINSIC |
low complexity region
|
1126 |
1137 |
N/A |
INTRINSIC |
low complexity region
|
1360 |
1375 |
N/A |
INTRINSIC |
Pfam:NopRA1
|
1670 |
1859 |
3.6e-60 |
PFAM |
low complexity region
|
2029 |
2040 |
N/A |
INTRINSIC |
low complexity region
|
2092 |
2111 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 95.0%
|
Validation Efficiency |
96% (109/114) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 109 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
T |
C |
11: 58,771,717 (GRCm39) |
C400R |
probably damaging |
Het |
4930519F16Rik |
A |
T |
X: 102,299,463 (GRCm39) |
|
noncoding transcript |
Het |
5430402E10Rik |
G |
T |
X: 76,966,340 (GRCm39) |
H117Q |
probably damaging |
Het |
Abca15 |
T |
C |
7: 119,974,077 (GRCm39) |
|
probably benign |
Het |
Abca8a |
A |
G |
11: 109,933,835 (GRCm39) |
I1190T |
probably benign |
Het |
Acmsd |
T |
C |
1: 127,676,795 (GRCm39) |
Y107H |
probably benign |
Het |
Adcy5 |
A |
G |
16: 35,087,551 (GRCm39) |
I471V |
probably damaging |
Het |
Aff2 |
G |
A |
X: 68,892,532 (GRCm39) |
A939T |
unknown |
Het |
Ampd2 |
C |
A |
3: 107,988,427 (GRCm39) |
A11S |
probably benign |
Het |
Aoah |
T |
A |
13: 21,000,694 (GRCm39) |
C43S |
probably damaging |
Het |
Apobec4 |
T |
C |
1: 152,632,925 (GRCm39) |
S318P |
probably damaging |
Het |
Arid2 |
C |
T |
15: 96,267,427 (GRCm39) |
P636S |
possibly damaging |
Het |
Atp13a3 |
A |
T |
16: 30,178,543 (GRCm39) |
C164* |
probably null |
Het |
Avl9 |
G |
A |
6: 56,734,295 (GRCm39) |
A625T |
probably damaging |
Het |
Bco1 |
G |
T |
8: 117,832,386 (GRCm39) |
|
probably benign |
Het |
Brd3 |
C |
T |
2: 27,340,545 (GRCm39) |
G555S |
possibly damaging |
Het |
Brd4 |
A |
T |
17: 32,448,377 (GRCm39) |
|
probably benign |
Het |
Btbd7 |
A |
G |
12: 102,754,561 (GRCm39) |
V735A |
probably benign |
Het |
C2cd2 |
G |
T |
16: 97,680,840 (GRCm39) |
Q325K |
possibly damaging |
Het |
Carmil1 |
A |
G |
13: 24,248,630 (GRCm39) |
V485A |
probably benign |
Het |
Casz1 |
T |
C |
4: 149,017,908 (GRCm39) |
L113P |
probably damaging |
Het |
Ccdc3 |
T |
C |
2: 5,143,016 (GRCm39) |
L91S |
probably damaging |
Het |
Cd180 |
A |
G |
13: 102,841,926 (GRCm39) |
K324R |
probably benign |
Het |
Cd200r4 |
A |
G |
16: 44,653,736 (GRCm39) |
T132A |
possibly damaging |
Het |
Cops7a |
A |
G |
6: 124,939,416 (GRCm39) |
|
probably benign |
Het |
Cyp2c29 |
A |
T |
19: 39,298,106 (GRCm39) |
N217I |
probably damaging |
Het |
Dapk1 |
C |
A |
13: 60,909,126 (GRCm39) |
H1246Q |
probably damaging |
Het |
Dmbt1 |
T |
A |
7: 130,713,805 (GRCm39) |
C1450* |
probably null |
Het |
Dnah10 |
T |
A |
5: 124,906,593 (GRCm39) |
M4151K |
probably damaging |
Het |
Dnai1 |
C |
A |
4: 41,629,833 (GRCm39) |
F452L |
possibly damaging |
Het |
Dync1h1 |
T |
C |
12: 110,583,241 (GRCm39) |
M446T |
probably benign |
Het |
Dytn |
A |
C |
1: 63,714,071 (GRCm39) |
S143A |
possibly damaging |
Het |
E130308A19Rik |
T |
A |
4: 59,691,033 (GRCm39) |
L289Q |
possibly damaging |
Het |
Efemp2 |
G |
T |
19: 5,530,677 (GRCm39) |
V250L |
probably benign |
Het |
Elmo1 |
T |
C |
13: 20,465,033 (GRCm39) |
S201P |
probably damaging |
Het |
Fam222b |
T |
A |
11: 78,045,404 (GRCm39) |
C194S |
probably damaging |
Het |
Fam91a1 |
G |
A |
15: 58,298,970 (GRCm39) |
|
probably null |
Het |
Fcf1 |
T |
A |
12: 85,027,386 (GRCm39) |
|
probably benign |
Het |
Fnip1 |
T |
A |
11: 54,371,123 (GRCm39) |
F134L |
probably damaging |
Het |
Fyn |
T |
C |
10: 39,387,950 (GRCm39) |
S69P |
probably benign |
Het |
Gabbr1 |
T |
C |
17: 37,382,841 (GRCm39) |
Y845H |
probably damaging |
Het |
Gfra2 |
C |
T |
14: 71,215,818 (GRCm39) |
T169M |
possibly damaging |
Het |
Gm5435 |
T |
C |
12: 82,542,449 (GRCm39) |
|
noncoding transcript |
Het |
Gm7251 |
A |
G |
13: 49,959,148 (GRCm39) |
Y94H |
probably damaging |
Het |
Gvin3 |
A |
G |
7: 106,202,356 (GRCm39) |
F296S |
probably damaging |
Het |
H2bc15 |
T |
C |
13: 21,938,648 (GRCm39) |
V119A |
probably benign |
Het |
Heatr1 |
T |
A |
13: 12,423,594 (GRCm39) |
N530K |
probably benign |
Het |
Icam5 |
A |
T |
9: 20,946,442 (GRCm39) |
E355V |
probably benign |
Het |
Ighv3-6 |
A |
G |
12: 114,252,158 (GRCm39) |
|
probably benign |
Het |
Intu |
T |
C |
3: 40,647,103 (GRCm39) |
S659P |
probably damaging |
Het |
Ivns1abp |
T |
C |
1: 151,230,446 (GRCm39) |
V198A |
probably damaging |
Het |
Katnb1 |
T |
A |
8: 95,822,138 (GRCm39) |
|
probably benign |
Het |
Kcna5 |
T |
C |
6: 126,510,386 (GRCm39) |
S581G |
probably damaging |
Het |
Kif23 |
A |
G |
9: 61,831,347 (GRCm39) |
V741A |
probably benign |
Het |
Lbr |
A |
T |
1: 181,648,233 (GRCm39) |
|
probably benign |
Het |
Loxhd1 |
A |
C |
18: 77,429,627 (GRCm39) |
T508P |
possibly damaging |
Het |
Lrrk2 |
T |
A |
15: 91,557,561 (GRCm39) |
N26K |
probably benign |
Het |
Ly96 |
A |
T |
1: 16,761,918 (GRCm39) |
K41N |
probably damaging |
Het |
Lypd1 |
C |
T |
1: 125,838,274 (GRCm39) |
|
probably benign |
Het |
Macf1 |
A |
G |
4: 123,359,833 (GRCm39) |
V1817A |
probably benign |
Het |
Mknk2 |
A |
G |
10: 80,504,768 (GRCm39) |
|
probably benign |
Het |
Mmp19 |
A |
T |
10: 128,631,470 (GRCm39) |
I117L |
probably benign |
Het |
Mmrn1 |
G |
A |
6: 60,935,164 (GRCm39) |
G220D |
probably damaging |
Het |
Mtrr |
T |
C |
13: 68,712,496 (GRCm39) |
H630R |
probably damaging |
Het |
Nfat5 |
T |
C |
8: 108,066,014 (GRCm39) |
|
probably benign |
Het |
Ngef |
C |
A |
1: 87,415,529 (GRCm39) |
K288N |
possibly damaging |
Het |
Nkain4 |
T |
C |
2: 180,584,938 (GRCm39) |
E71G |
probably benign |
Het |
Odc1 |
T |
C |
12: 17,598,038 (GRCm39) |
Y122H |
probably benign |
Het |
Or1e25 |
T |
C |
11: 73,494,273 (GRCm39) |
I289T |
probably damaging |
Het |
Or2d2 |
C |
A |
7: 106,728,448 (GRCm39) |
A51S |
probably benign |
Het |
Or8g51 |
C |
A |
9: 38,609,206 (GRCm39) |
G156V |
probably damaging |
Het |
Osbpl3 |
A |
T |
6: 50,324,446 (GRCm39) |
N190K |
probably benign |
Het |
Osgepl1 |
T |
C |
1: 53,354,198 (GRCm39) |
V54A |
probably damaging |
Het |
Otogl |
T |
C |
10: 107,746,817 (GRCm39) |
Y19C |
probably benign |
Het |
Pop1 |
T |
C |
15: 34,530,358 (GRCm39) |
S919P |
probably benign |
Het |
Pramel21 |
T |
A |
4: 143,341,920 (GRCm39) |
|
probably benign |
Het |
Prl8a9 |
A |
G |
13: 27,746,584 (GRCm39) |
|
probably benign |
Het |
Prr14l |
A |
T |
5: 32,951,072 (GRCm39) |
V1907D |
probably damaging |
Het |
Ptprn |
T |
C |
1: 75,231,264 (GRCm39) |
T547A |
possibly damaging |
Het |
Rdh14 |
G |
T |
12: 10,444,709 (GRCm39) |
V187F |
probably damaging |
Het |
Rev1 |
A |
G |
1: 38,095,848 (GRCm39) |
L853P |
probably damaging |
Het |
Robo4 |
T |
C |
9: 37,317,106 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
A |
G |
13: 11,732,027 (GRCm39) |
|
probably benign |
Het |
Sec16a |
G |
A |
2: 26,331,517 (GRCm39) |
P166L |
probably benign |
Het |
Slc6a19 |
G |
A |
13: 73,848,243 (GRCm39) |
|
probably benign |
Het |
Slco4c1 |
T |
A |
1: 96,770,210 (GRCm39) |
T285S |
probably benign |
Het |
Speg |
G |
T |
1: 75,392,241 (GRCm39) |
A1633S |
probably benign |
Het |
Srpk1 |
T |
A |
17: 28,821,707 (GRCm39) |
T236S |
probably benign |
Het |
Stxbp5 |
T |
C |
10: 9,645,187 (GRCm39) |
N262S |
probably benign |
Het |
Suco |
T |
C |
1: 161,680,420 (GRCm39) |
E317G |
probably damaging |
Het |
Syk |
A |
G |
13: 52,794,657 (GRCm39) |
N441D |
probably damaging |
Het |
Syt17 |
T |
C |
7: 118,007,292 (GRCm39) |
K334R |
probably benign |
Het |
Sytl5 |
A |
T |
X: 9,826,335 (GRCm39) |
H436L |
probably benign |
Het |
Tasor2 |
A |
T |
13: 3,627,000 (GRCm39) |
S983R |
probably damaging |
Het |
Thada |
A |
G |
17: 84,753,972 (GRCm39) |
L333P |
probably damaging |
Het |
Thap12 |
T |
C |
7: 98,364,314 (GRCm39) |
Y161H |
probably damaging |
Het |
Thbs2 |
C |
T |
17: 14,891,715 (GRCm39) |
V941I |
probably benign |
Het |
Tktl1 |
A |
T |
X: 73,225,470 (GRCm39) |
E72V |
probably damaging |
Het |
Tm4sf5 |
T |
A |
11: 70,396,338 (GRCm39) |
|
probably benign |
Het |
Vcp |
T |
A |
4: 42,982,596 (GRCm39) |
I699F |
probably damaging |
Het |
Vmn1r232 |
T |
C |
17: 21,133,656 (GRCm39) |
T315A |
probably benign |
Het |
Vmn2r100 |
T |
A |
17: 19,741,752 (GRCm39) |
W155R |
possibly damaging |
Het |
Vmn2r19 |
T |
C |
6: 123,292,861 (GRCm39) |
I301T |
possibly damaging |
Het |
Wwc2 |
A |
G |
8: 48,373,701 (GRCm39) |
V55A |
possibly damaging |
Het |
Xirp2 |
A |
G |
2: 67,345,801 (GRCm39) |
T2681A |
probably benign |
Het |
Zfp39 |
C |
A |
11: 58,791,512 (GRCm39) |
L58F |
probably damaging |
Het |
Zfp612 |
T |
C |
8: 110,816,670 (GRCm39) |
F587L |
probably damaging |
Het |
Zfp810 |
T |
C |
9: 22,190,387 (GRCm39) |
R174G |
probably benign |
Het |
Zfta |
A |
G |
19: 7,400,286 (GRCm39) |
K251E |
probably benign |
Het |
|
Other mutations in Urb1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00715:Urb1
|
APN |
16 |
90,550,209 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00915:Urb1
|
APN |
16 |
90,575,986 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01108:Urb1
|
APN |
16 |
90,589,702 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01122:Urb1
|
APN |
16 |
90,601,346 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01387:Urb1
|
APN |
16 |
90,554,649 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01484:Urb1
|
APN |
16 |
90,574,448 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01606:Urb1
|
APN |
16 |
90,557,347 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01989:Urb1
|
APN |
16 |
90,566,474 (GRCm39) |
splice site |
probably benign |
|
IGL02516:Urb1
|
APN |
16 |
90,569,583 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03018:Urb1
|
APN |
16 |
90,585,044 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03165:Urb1
|
APN |
16 |
90,577,192 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03216:Urb1
|
APN |
16 |
90,585,002 (GRCm39) |
missense |
probably benign |
0.00 |
H8786:Urb1
|
UTSW |
16 |
90,566,357 (GRCm39) |
missense |
probably benign |
0.08 |
R0064:Urb1
|
UTSW |
16 |
90,576,028 (GRCm39) |
missense |
probably benign |
|
R0064:Urb1
|
UTSW |
16 |
90,576,028 (GRCm39) |
missense |
probably benign |
|
R0359:Urb1
|
UTSW |
16 |
90,588,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R0386:Urb1
|
UTSW |
16 |
90,593,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R0508:Urb1
|
UTSW |
16 |
90,580,150 (GRCm39) |
splice site |
probably benign |
|
R0517:Urb1
|
UTSW |
16 |
90,574,310 (GRCm39) |
nonsense |
probably null |
|
R0704:Urb1
|
UTSW |
16 |
90,573,095 (GRCm39) |
missense |
probably benign |
0.31 |
R0755:Urb1
|
UTSW |
16 |
90,576,026 (GRCm39) |
missense |
probably benign |
|
R0755:Urb1
|
UTSW |
16 |
90,570,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R0783:Urb1
|
UTSW |
16 |
90,607,185 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0833:Urb1
|
UTSW |
16 |
90,592,336 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0836:Urb1
|
UTSW |
16 |
90,592,336 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0970:Urb1
|
UTSW |
16 |
90,566,335 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1144:Urb1
|
UTSW |
16 |
90,573,206 (GRCm39) |
splice site |
probably null |
|
R1344:Urb1
|
UTSW |
16 |
90,566,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R1418:Urb1
|
UTSW |
16 |
90,566,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R1453:Urb1
|
UTSW |
16 |
90,593,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Urb1
|
UTSW |
16 |
90,548,902 (GRCm39) |
missense |
probably benign |
0.34 |
R1470:Urb1
|
UTSW |
16 |
90,548,902 (GRCm39) |
missense |
probably benign |
0.34 |
R1520:Urb1
|
UTSW |
16 |
90,571,633 (GRCm39) |
missense |
probably benign |
0.00 |
R1521:Urb1
|
UTSW |
16 |
90,550,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R1598:Urb1
|
UTSW |
16 |
90,574,328 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1617:Urb1
|
UTSW |
16 |
90,557,340 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1625:Urb1
|
UTSW |
16 |
90,570,936 (GRCm39) |
critical splice donor site |
probably null |
|
R1640:Urb1
|
UTSW |
16 |
90,569,514 (GRCm39) |
missense |
probably benign |
0.00 |
R1664:Urb1
|
UTSW |
16 |
90,584,970 (GRCm39) |
critical splice donor site |
probably null |
|
R1672:Urb1
|
UTSW |
16 |
90,584,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R1694:Urb1
|
UTSW |
16 |
90,563,928 (GRCm39) |
missense |
probably benign |
|
R1856:Urb1
|
UTSW |
16 |
90,558,583 (GRCm39) |
missense |
probably benign |
0.00 |
R2001:Urb1
|
UTSW |
16 |
90,559,232 (GRCm39) |
missense |
probably benign |
0.30 |
R2196:Urb1
|
UTSW |
16 |
90,571,144 (GRCm39) |
missense |
probably benign |
0.01 |
R2850:Urb1
|
UTSW |
16 |
90,571,144 (GRCm39) |
missense |
probably benign |
0.01 |
R3009:Urb1
|
UTSW |
16 |
90,571,686 (GRCm39) |
missense |
probably benign |
0.09 |
R3104:Urb1
|
UTSW |
16 |
90,592,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R3105:Urb1
|
UTSW |
16 |
90,592,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R3106:Urb1
|
UTSW |
16 |
90,592,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R3160:Urb1
|
UTSW |
16 |
90,594,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Urb1
|
UTSW |
16 |
90,594,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R3900:Urb1
|
UTSW |
16 |
90,580,264 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4014:Urb1
|
UTSW |
16 |
90,566,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R4036:Urb1
|
UTSW |
16 |
90,584,974 (GRCm39) |
missense |
probably benign |
|
R4332:Urb1
|
UTSW |
16 |
90,571,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R4448:Urb1
|
UTSW |
16 |
90,566,282 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4581:Urb1
|
UTSW |
16 |
90,585,034 (GRCm39) |
missense |
probably benign |
0.04 |
R4593:Urb1
|
UTSW |
16 |
90,584,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Urb1
|
UTSW |
16 |
90,573,159 (GRCm39) |
missense |
probably benign |
0.43 |
R4659:Urb1
|
UTSW |
16 |
90,573,017 (GRCm39) |
missense |
probably damaging |
0.96 |
R4672:Urb1
|
UTSW |
16 |
90,569,522 (GRCm39) |
missense |
probably benign |
|
R4681:Urb1
|
UTSW |
16 |
90,601,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R4771:Urb1
|
UTSW |
16 |
90,550,406 (GRCm39) |
missense |
probably benign |
0.00 |
R4790:Urb1
|
UTSW |
16 |
90,566,443 (GRCm39) |
nonsense |
probably null |
|
R4798:Urb1
|
UTSW |
16 |
90,554,715 (GRCm39) |
missense |
probably benign |
0.12 |
R4809:Urb1
|
UTSW |
16 |
90,556,730 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4850:Urb1
|
UTSW |
16 |
90,592,302 (GRCm39) |
nonsense |
probably null |
|
R4916:Urb1
|
UTSW |
16 |
90,580,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R4969:Urb1
|
UTSW |
16 |
90,602,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Urb1
|
UTSW |
16 |
90,553,059 (GRCm39) |
missense |
probably benign |
0.00 |
R5111:Urb1
|
UTSW |
16 |
90,548,905 (GRCm39) |
missense |
probably benign |
0.00 |
R5122:Urb1
|
UTSW |
16 |
90,548,983 (GRCm39) |
nonsense |
probably null |
|
R5184:Urb1
|
UTSW |
16 |
90,580,162 (GRCm39) |
critical splice donor site |
probably null |
|
R5199:Urb1
|
UTSW |
16 |
90,589,636 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5436:Urb1
|
UTSW |
16 |
90,589,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R5767:Urb1
|
UTSW |
16 |
90,573,051 (GRCm39) |
missense |
probably benign |
0.00 |
R5812:Urb1
|
UTSW |
16 |
90,601,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R5872:Urb1
|
UTSW |
16 |
90,569,652 (GRCm39) |
nonsense |
probably null |
|
R6052:Urb1
|
UTSW |
16 |
90,559,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R6063:Urb1
|
UTSW |
16 |
90,585,985 (GRCm39) |
missense |
probably benign |
0.02 |
R6065:Urb1
|
UTSW |
16 |
90,600,220 (GRCm39) |
missense |
probably benign |
0.03 |
R6181:Urb1
|
UTSW |
16 |
90,575,982 (GRCm39) |
missense |
probably benign |
0.00 |
R6268:Urb1
|
UTSW |
16 |
90,550,807 (GRCm39) |
missense |
probably benign |
0.03 |
R6429:Urb1
|
UTSW |
16 |
90,559,318 (GRCm39) |
splice site |
probably null |
|
R6572:Urb1
|
UTSW |
16 |
90,584,302 (GRCm39) |
missense |
probably benign |
0.37 |
R6606:Urb1
|
UTSW |
16 |
90,607,156 (GRCm39) |
missense |
probably benign |
0.00 |
R6730:Urb1
|
UTSW |
16 |
90,575,971 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6838:Urb1
|
UTSW |
16 |
90,578,994 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7237:Urb1
|
UTSW |
16 |
90,588,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R7238:Urb1
|
UTSW |
16 |
90,549,003 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7339:Urb1
|
UTSW |
16 |
90,569,461 (GRCm39) |
critical splice donor site |
probably benign |
|
R7341:Urb1
|
UTSW |
16 |
90,569,461 (GRCm39) |
critical splice donor site |
probably benign |
|
R7361:Urb1
|
UTSW |
16 |
90,571,656 (GRCm39) |
missense |
probably damaging |
0.99 |
R7365:Urb1
|
UTSW |
16 |
90,569,461 (GRCm39) |
critical splice donor site |
probably benign |
|
R7366:Urb1
|
UTSW |
16 |
90,569,461 (GRCm39) |
critical splice donor site |
probably benign |
|
R7440:Urb1
|
UTSW |
16 |
90,584,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R7530:Urb1
|
UTSW |
16 |
90,558,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R7553:Urb1
|
UTSW |
16 |
90,589,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R7557:Urb1
|
UTSW |
16 |
90,569,461 (GRCm39) |
critical splice donor site |
probably benign |
|
R7603:Urb1
|
UTSW |
16 |
90,569,461 (GRCm39) |
critical splice donor site |
probably benign |
|
R7607:Urb1
|
UTSW |
16 |
90,569,461 (GRCm39) |
critical splice donor site |
probably benign |
|
R7609:Urb1
|
UTSW |
16 |
90,569,461 (GRCm39) |
critical splice donor site |
probably benign |
|
R7610:Urb1
|
UTSW |
16 |
90,569,461 (GRCm39) |
critical splice donor site |
probably benign |
|
R7612:Urb1
|
UTSW |
16 |
90,594,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R7613:Urb1
|
UTSW |
16 |
90,569,461 (GRCm39) |
critical splice donor site |
probably benign |
|
R7684:Urb1
|
UTSW |
16 |
90,583,006 (GRCm39) |
nonsense |
probably null |
|
R8029:Urb1
|
UTSW |
16 |
90,576,040 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8324:Urb1
|
UTSW |
16 |
90,588,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Urb1
|
UTSW |
16 |
90,571,513 (GRCm39) |
missense |
probably benign |
0.00 |
R8785:Urb1
|
UTSW |
16 |
90,600,311 (GRCm39) |
missense |
probably benign |
0.07 |
R8914:Urb1
|
UTSW |
16 |
90,607,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R8959:Urb1
|
UTSW |
16 |
90,571,005 (GRCm39) |
missense |
probably benign |
0.26 |
R9005:Urb1
|
UTSW |
16 |
90,550,678 (GRCm39) |
missense |
probably benign |
0.01 |
R9126:Urb1
|
UTSW |
16 |
90,566,290 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9195:Urb1
|
UTSW |
16 |
90,589,638 (GRCm39) |
missense |
probably benign |
0.03 |
R9276:Urb1
|
UTSW |
16 |
90,569,463 (GRCm39) |
splice site |
probably benign |
|
R9534:Urb1
|
UTSW |
16 |
90,583,096 (GRCm39) |
missense |
possibly damaging |
0.54 |
Z1177:Urb1
|
UTSW |
16 |
90,571,750 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Urb1
|
UTSW |
16 |
90,550,771 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- AGCCTTCCAAACAAGTGGCAGG -3'
(R):5'- TGCGTCAGCTCATCAGAAAGTTCC -3'
Sequencing Primer
(F):5'- GGTCCTTGGTTTAACACACACAG -3'
(R):5'- ATGATTGGACCATGTGCCAC -3'
|
Posted On |
2013-06-11 |