Incidental Mutation 'R6860:4933427D14Rik'
| ID |
535454 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
4933427D14Rik
|
| Ensembl Gene |
ENSMUSG00000020807 |
| Gene Name |
RIKEN cDNA 4933427D14 gene |
| Synonyms |
Gm43951 |
| MMRRC Submission |
045025-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R6860 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
72044755-72098308 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 72080412 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Glycine
at position 418
(E418G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000122273
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000108506]
[ENSMUST00000131546]
[ENSMUST00000142530]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000108506
AA Change: E418G
PolyPhen 2
Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000104146
Gene: ENSMUSG00000020807
AA Change: E418G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF4673
|
1 |
954 |
N/A |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000131546
AA Change: E418G
PolyPhen 2
Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000122273
Gene: ENSMUSG00000020807
AA Change: E418G
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
84 |
93 |
N/A |
INTRINSIC |
|
coiled coil region
|
210 |
231 |
N/A |
INTRINSIC |
|
coiled coil region
|
256 |
279 |
N/A |
INTRINSIC |
|
low complexity region
|
291 |
305 |
N/A |
INTRINSIC |
|
low complexity region
|
360 |
377 |
N/A |
INTRINSIC |
|
low complexity region
|
545 |
559 |
N/A |
INTRINSIC |
|
coiled coil region
|
625 |
653 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000142530
|
| SMART Domains |
Protein: ENSMUSP00000115276
Gene: ENSMUSG00000020807
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
84 |
93 |
N/A |
INTRINSIC |
|
coiled coil region
|
210 |
231 |
N/A |
INTRINSIC |
|
coiled coil region
|
256 |
279 |
N/A |
INTRINSIC |
|
low complexity region
|
291 |
305 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.5%
- 20x: 98.3%
|
| Validation Efficiency |
100% (86/86) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 89 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 9930012K11Rik |
C |
A |
14: 70,395,071 (GRCm39) |
V28L |
possibly damaging |
Het |
| Abtb2 |
C |
T |
2: 103,539,770 (GRCm39) |
R712* |
probably null |
Het |
| Acvr1c |
C |
T |
2: 58,177,717 (GRCm39) |
G171S |
probably damaging |
Het |
| Ahctf1 |
G |
T |
1: 179,580,853 (GRCm39) |
A1783E |
probably benign |
Het |
| Anapc4 |
A |
T |
5: 53,006,170 (GRCm39) |
Q149L |
probably damaging |
Het |
| Ankrd27 |
T |
C |
7: 35,327,952 (GRCm39) |
V824A |
possibly damaging |
Het |
| Ankrd31 |
G |
C |
13: 96,968,094 (GRCm39) |
C577S |
probably benign |
Het |
| Apol7c |
T |
C |
15: 77,410,274 (GRCm39) |
N224S |
probably benign |
Het |
| Arl14 |
A |
T |
3: 69,130,029 (GRCm39) |
T59S |
probably benign |
Het |
| Astn1 |
T |
A |
1: 158,440,042 (GRCm39) |
I870K |
probably damaging |
Het |
| B4galt1 |
A |
T |
4: 40,807,796 (GRCm39) |
V335E |
probably benign |
Het |
| C2cd3 |
C |
T |
7: 100,039,448 (GRCm39) |
P216S |
probably benign |
Het |
| Cchcr1 |
C |
A |
17: 35,840,015 (GRCm39) |
N711K |
possibly damaging |
Het |
| Chd2 |
A |
G |
7: 73,147,558 (GRCm39) |
F467L |
possibly damaging |
Het |
| Cntn6 |
A |
T |
6: 104,838,907 (GRCm39) |
E987V |
possibly damaging |
Het |
| Col11a2 |
T |
A |
17: 34,272,572 (GRCm39) |
L286H |
probably damaging |
Het |
| Cwc22 |
C |
T |
2: 77,759,792 (GRCm39) |
R85Q |
possibly damaging |
Het |
| Cyp7a1 |
A |
C |
4: 6,272,587 (GRCm39) |
F209V |
probably damaging |
Het |
| Dmtn |
T |
C |
14: 70,852,322 (GRCm39) |
T189A |
possibly damaging |
Het |
| Dnhd1 |
C |
G |
7: 105,327,473 (GRCm39) |
N777K |
probably benign |
Het |
| Dusp16 |
A |
T |
6: 134,702,842 (GRCm39) |
C216* |
probably null |
Het |
| Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
| Fbn1 |
T |
C |
2: 125,170,078 (GRCm39) |
N1993S |
probably damaging |
Het |
| Fbxw22 |
A |
G |
9: 109,213,030 (GRCm39) |
S306P |
probably benign |
Het |
| Ferd3l |
T |
C |
12: 33,978,651 (GRCm39) |
S55P |
probably benign |
Het |
| Fpr-rs3 |
A |
G |
17: 20,844,560 (GRCm39) |
S194P |
possibly damaging |
Het |
| Gm19965 |
G |
A |
1: 116,748,609 (GRCm39) |
D97N |
probably benign |
Het |
| Gtpbp2 |
A |
G |
17: 46,478,914 (GRCm39) |
|
probably benign |
Het |
| H3c7 |
G |
T |
13: 23,728,760 (GRCm39) |
V36L |
probably benign |
Het |
| Hcn3 |
A |
C |
3: 89,067,152 (GRCm39) |
I72S |
possibly damaging |
Het |
| Hk3 |
T |
A |
13: 55,162,278 (GRCm39) |
N109Y |
probably damaging |
Het |
| Iqub |
T |
C |
6: 24,505,737 (GRCm39) |
E57G |
possibly damaging |
Het |
| Kcnk3 |
T |
A |
5: 30,779,397 (GRCm39) |
M149K |
possibly damaging |
Het |
| Kcp |
C |
T |
6: 29,505,719 (GRCm39) |
G51D |
probably benign |
Het |
| Kif26a |
C |
A |
12: 112,113,263 (GRCm39) |
A53D |
probably damaging |
Het |
| Lifr |
T |
A |
15: 7,202,418 (GRCm39) |
I353K |
probably benign |
Het |
| Llph |
A |
T |
10: 120,067,189 (GRCm39) |
N102I |
probably damaging |
Het |
| Lmo3 |
C |
A |
6: 138,393,566 (GRCm39) |
R18L |
possibly damaging |
Het |
| Lrrc46 |
T |
C |
11: 96,926,371 (GRCm39) |
E175G |
probably benign |
Het |
| Ltk |
A |
T |
2: 119,585,075 (GRCm39) |
C128* |
probably null |
Het |
| Map1b |
T |
C |
13: 99,571,275 (GRCm39) |
E482G |
probably damaging |
Het |
| Mapk8ip2 |
T |
C |
15: 89,344,655 (GRCm39) |
V740A |
probably damaging |
Het |
| Miga2 |
T |
C |
2: 30,261,175 (GRCm39) |
W157R |
probably benign |
Het |
| Mlip |
A |
G |
9: 77,009,675 (GRCm39) |
*837Q |
probably null |
Het |
| Mroh2a |
G |
T |
1: 88,182,657 (GRCm39) |
R1195L |
possibly damaging |
Het |
| Myl1 |
T |
C |
1: 66,984,217 (GRCm39) |
|
probably benign |
Het |
| Or1l4 |
T |
C |
2: 37,092,189 (GRCm39) |
L312P |
possibly damaging |
Het |
| Or2a5 |
T |
C |
6: 42,873,750 (GRCm39) |
Y122H |
probably benign |
Het |
| Or51ab3 |
A |
G |
7: 103,201,075 (GRCm39) |
I28V |
probably benign |
Het |
| P3h3 |
A |
T |
6: 124,834,331 (GRCm39) |
V107D |
probably benign |
Het |
| Papolb |
A |
T |
5: 142,514,651 (GRCm39) |
S331T |
possibly damaging |
Het |
| Pars2 |
T |
G |
4: 106,511,700 (GRCm39) |
V494G |
probably benign |
Het |
| Pcdhb3 |
C |
A |
18: 37,434,763 (GRCm39) |
T243K |
probably benign |
Het |
| Pde9a |
T |
A |
17: 31,689,698 (GRCm39) |
M415K |
probably damaging |
Het |
| Ppp1r9b |
G |
A |
11: 94,882,974 (GRCm39) |
A201T |
probably benign |
Het |
| Prl |
A |
G |
13: 27,248,942 (GRCm39) |
N197S |
possibly damaging |
Het |
| Prl2c1 |
T |
A |
13: 28,035,724 (GRCm39) |
M32K |
probably benign |
Het |
| Prrt4 |
T |
C |
6: 29,170,737 (GRCm39) |
S572G |
possibly damaging |
Het |
| Psd |
T |
A |
19: 46,310,858 (GRCm39) |
D397V |
probably damaging |
Het |
| Psme2b |
A |
T |
11: 48,836,307 (GRCm39) |
Y213* |
probably null |
Het |
| Ptcd3 |
T |
A |
6: 71,874,094 (GRCm39) |
|
probably null |
Het |
| Ptprk |
T |
G |
10: 28,210,480 (GRCm39) |
F167L |
probably damaging |
Het |
| Rfx7 |
T |
C |
9: 72,524,226 (GRCm39) |
V472A |
probably damaging |
Het |
| Sanbr |
A |
G |
11: 23,575,100 (GRCm39) |
L58P |
probably damaging |
Het |
| Scnn1g |
T |
C |
7: 121,339,576 (GRCm39) |
L125S |
probably damaging |
Het |
| Sec16a |
T |
C |
2: 26,320,124 (GRCm39) |
Y1438C |
probably damaging |
Het |
| Serinc3 |
C |
T |
2: 163,476,366 (GRCm39) |
S155N |
probably benign |
Het |
| Slc3a2 |
A |
T |
19: 8,690,996 (GRCm39) |
V78E |
probably damaging |
Het |
| Slc44a4 |
T |
A |
17: 35,140,044 (GRCm39) |
L23Q |
probably damaging |
Het |
| Slco5a1 |
C |
T |
1: 12,951,420 (GRCm39) |
|
probably benign |
Het |
| Slit1 |
A |
G |
19: 41,605,154 (GRCm39) |
M899T |
probably benign |
Het |
| Sorl1 |
A |
G |
9: 41,933,688 (GRCm39) |
I1094T |
probably benign |
Het |
| Spag9 |
T |
A |
11: 93,972,196 (GRCm39) |
L258Q |
probably benign |
Het |
| Strip1 |
T |
C |
3: 107,526,252 (GRCm39) |
E488G |
possibly damaging |
Het |
| Stx18 |
G |
A |
5: 38,262,235 (GRCm39) |
D30N |
possibly damaging |
Het |
| Sync |
T |
C |
4: 129,181,583 (GRCm39) |
|
probably null |
Het |
| Syncrip |
A |
G |
9: 88,358,849 (GRCm39) |
V220A |
probably damaging |
Het |
| Tagln2 |
T |
C |
1: 172,333,476 (GRCm39) |
I110T |
probably benign |
Het |
| Taok1 |
T |
C |
11: 77,432,627 (GRCm39) |
T729A |
probably benign |
Het |
| Tgfbrap1 |
C |
T |
1: 43,106,759 (GRCm39) |
V75I |
possibly damaging |
Het |
| Tnfrsf21 |
A |
G |
17: 43,327,957 (GRCm39) |
T24A |
probably benign |
Het |
| Tnxb |
T |
A |
17: 34,932,131 (GRCm39) |
D2221E |
probably damaging |
Het |
| Triml1 |
A |
G |
8: 43,583,603 (GRCm39) |
S333P |
probably damaging |
Het |
| Trp53bp1 |
C |
A |
2: 121,029,594 (GRCm39) |
R1862L |
probably damaging |
Het |
| Tsc22d1 |
T |
G |
14: 76,655,732 (GRCm39) |
I737S |
possibly damaging |
Het |
| U2af2 |
A |
T |
7: 5,082,273 (GRCm39) |
K462N |
possibly damaging |
Het |
| Ubap2 |
A |
C |
4: 41,233,631 (GRCm39) |
N86K |
probably damaging |
Het |
| Uso1 |
A |
G |
5: 92,343,207 (GRCm39) |
K764E |
probably benign |
Het |
| Vmn1r192 |
T |
A |
13: 22,372,122 (GRCm39) |
M33L |
probably benign |
Het |
|
| Other mutations in 4933427D14Rik |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00707:4933427D14Rik
|
APN |
11 |
72,069,330 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01643:4933427D14Rik
|
APN |
11 |
72,082,414 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02004:4933427D14Rik
|
APN |
11 |
72,082,423 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
IGL02308:4933427D14Rik
|
APN |
11 |
72,093,308 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02378:4933427D14Rik
|
APN |
11 |
72,080,424 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02715:4933427D14Rik
|
APN |
11 |
72,089,714 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03330:4933427D14Rik
|
APN |
11 |
72,050,254 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03384:4933427D14Rik
|
APN |
11 |
72,086,673 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
BB002:4933427D14Rik
|
UTSW |
11 |
72,071,327 (GRCm39) |
missense |
probably benign |
0.31 |
|
BB012:4933427D14Rik
|
UTSW |
11 |
72,071,327 (GRCm39) |
missense |
probably benign |
0.31 |
|
IGL03047:4933427D14Rik
|
UTSW |
11 |
72,057,552 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0114:4933427D14Rik
|
UTSW |
11 |
72,086,625 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0526:4933427D14Rik
|
UTSW |
11 |
72,060,609 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0653:4933427D14Rik
|
UTSW |
11 |
72,066,371 (GRCm39) |
nonsense |
probably null |
|
|
R0669:4933427D14Rik
|
UTSW |
11 |
72,089,671 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R0729:4933427D14Rik
|
UTSW |
11 |
72,050,281 (GRCm39) |
missense |
probably benign |
0.07 |
|
R1797:4933427D14Rik
|
UTSW |
11 |
72,089,285 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R3973:4933427D14Rik
|
UTSW |
11 |
72,089,567 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4744:4933427D14Rik
|
UTSW |
11 |
72,066,365 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4897:4933427D14Rik
|
UTSW |
11 |
72,082,342 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5023:4933427D14Rik
|
UTSW |
11 |
72,057,581 (GRCm39) |
missense |
probably benign |
0.07 |
|
R5057:4933427D14Rik
|
UTSW |
11 |
72,057,581 (GRCm39) |
missense |
probably benign |
0.07 |
|
R5100:4933427D14Rik
|
UTSW |
11 |
72,057,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5497:4933427D14Rik
|
UTSW |
11 |
72,056,360 (GRCm39) |
missense |
probably benign |
0.22 |
|
R5556:4933427D14Rik
|
UTSW |
11 |
72,066,026 (GRCm39) |
splice site |
probably null |
|
|
R5631:4933427D14Rik
|
UTSW |
11 |
72,067,590 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R5683:4933427D14Rik
|
UTSW |
11 |
72,093,266 (GRCm39) |
missense |
probably benign |
|
|
R5742:4933427D14Rik
|
UTSW |
11 |
72,056,379 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R6247:4933427D14Rik
|
UTSW |
11 |
72,049,768 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6267:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6296:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7023:4933427D14Rik
|
UTSW |
11 |
72,069,229 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7328:4933427D14Rik
|
UTSW |
11 |
72,060,606 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7514:4933427D14Rik
|
UTSW |
11 |
72,086,628 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7544:4933427D14Rik
|
UTSW |
11 |
72,089,765 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7925:4933427D14Rik
|
UTSW |
11 |
72,071,327 (GRCm39) |
missense |
probably benign |
0.31 |
|
R8204:4933427D14Rik
|
UTSW |
11 |
72,057,606 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8280:4933427D14Rik
|
UTSW |
11 |
72,086,667 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R8316:4933427D14Rik
|
UTSW |
11 |
72,059,612 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R8366:4933427D14Rik
|
UTSW |
11 |
72,067,521 (GRCm39) |
nonsense |
probably null |
|
|
R8384:4933427D14Rik
|
UTSW |
11 |
72,057,591 (GRCm39) |
missense |
probably benign |
0.08 |
|
R8722:4933427D14Rik
|
UTSW |
11 |
72,080,422 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8944:4933427D14Rik
|
UTSW |
11 |
72,049,851 (GRCm39) |
splice site |
probably benign |
|
|
R9749:4933427D14Rik
|
UTSW |
11 |
72,080,521 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
X0063:4933427D14Rik
|
UTSW |
11 |
72,067,595 (GRCm39) |
missense |
probably benign |
|
|
X0065:4933427D14Rik
|
UTSW |
11 |
72,080,401 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
Z1176:4933427D14Rik
|
UTSW |
11 |
72,049,826 (GRCm39) |
missense |
probably benign |
0.12 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,089,360 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,089,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,067,535 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,080,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,086,538 (GRCm39) |
frame shift |
probably null |
|
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,086,569 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,086,590 (GRCm39) |
frame shift |
probably null |
|
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,086,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,089,308 (GRCm39) |
missense |
probably benign |
0.13 |
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,089,308 (GRCm39) |
missense |
probably benign |
0.13 |
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,086,590 (GRCm39) |
frame shift |
probably null |
|
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,086,569 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,086,538 (GRCm39) |
frame shift |
probably null |
|
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,086,536 (GRCm39) |
frame shift |
probably null |
|
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,080,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,067,535 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,089,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,089,360 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,089,360 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,089,308 (GRCm39) |
missense |
probably benign |
0.13 |
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,086,590 (GRCm39) |
frame shift |
probably null |
|
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,086,569 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,086,538 (GRCm39) |
frame shift |
probably null |
|
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,080,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,067,535 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,089,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,089,360 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,089,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,067,535 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,080,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,086,538 (GRCm39) |
frame shift |
probably null |
|
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,086,569 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,086,590 (GRCm39) |
frame shift |
probably null |
|
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,086,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,089,308 (GRCm39) |
missense |
probably benign |
0.13 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,089,308 (GRCm39) |
missense |
probably benign |
0.13 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,086,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,086,590 (GRCm39) |
frame shift |
probably null |
|
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,086,569 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,086,538 (GRCm39) |
frame shift |
probably null |
|
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,080,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,067,535 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,089,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,089,360 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,089,308 (GRCm39) |
missense |
probably benign |
0.13 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,086,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,086,590 (GRCm39) |
frame shift |
probably null |
|
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,086,569 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,086,538 (GRCm39) |
frame shift |
probably null |
|
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,080,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,067,535 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,089,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,089,360 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,089,308 (GRCm39) |
missense |
probably benign |
0.13 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,086,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,086,590 (GRCm39) |
frame shift |
probably null |
|
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,086,569 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,086,538 (GRCm39) |
frame shift |
probably null |
|
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,080,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,067,535 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,089,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,089,360 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATCCCACTTCCTAGGATGAGG -3'
(R):5'- TGACTAAAATCATACGCTAGTGGG -3'
Sequencing Primer
(F):5'- GATCCAGAAATGCACAGATGTC -3'
(R):5'- TCATACGCTAGTGGGATAAACTAAG -3'
|
| Posted On |
2018-09-12 |
Incidental Mutation