Incidental Mutation 'R8919:Wdr90'
| ID |
679164 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Wdr90
|
| Ensembl Gene |
ENSMUSG00000073434 |
| Gene Name |
WD repeat domain 90 |
| Synonyms |
3230401M21Rik |
| MMRRC Submission |
068706-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.107)
|
| Stock # |
R8919 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
17 |
| Chromosomal Location |
26063745-26080475 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 26076146 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Cysteine
at position 104
(R104C)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000079461]
[ENSMUST00000176923]
|
| AlphaFold |
Q6ZPG2 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000079461
AA Change: R516C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000078426
Gene: ENSMUSG00000073434
AA Change: R516C
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
32 |
53 |
N/A |
INTRINSIC |
|
Pfam:DUF667
|
60 |
183 |
5e-26 |
PFAM |
|
Pfam:DUF667
|
210 |
271 |
3.7e-9 |
PFAM |
|
low complexity region
|
381 |
396 |
N/A |
INTRINSIC |
|
WD40
|
478 |
519 |
5.94e0 |
SMART |
|
WD40
|
522 |
565 |
3.2e0 |
SMART |
|
WD40
|
572 |
612 |
3.3e1 |
SMART |
|
WD40
|
687 |
725 |
1.15e1 |
SMART |
|
WD40
|
728 |
766 |
5.75e-1 |
SMART |
|
WD40
|
768 |
808 |
9.24e-4 |
SMART |
|
WD40
|
811 |
850 |
4.13e0 |
SMART |
|
WD40
|
853 |
892 |
4.62e-1 |
SMART |
|
WD40
|
950 |
993 |
1.07e1 |
SMART |
|
WD40
|
996 |
1035 |
5.75e-1 |
SMART |
|
WD40
|
1040 |
1077 |
1.58e-2 |
SMART |
|
WD40
|
1290 |
1334 |
5.23e-3 |
SMART |
|
WD40
|
1337 |
1378 |
1.27e-1 |
SMART |
|
WD40
|
1384 |
1419 |
1.83e2 |
SMART |
|
WD40
|
1422 |
1469 |
3.08e0 |
SMART |
|
WD40
|
1472 |
1509 |
9.9e0 |
SMART |
|
WD40
|
1568 |
1607 |
9.02e-7 |
SMART |
|
WD40
|
1610 |
1655 |
5.75e-1 |
SMART |
|
WD40
|
1659 |
1697 |
2.98e-1 |
SMART |
|
WD40
|
1700 |
1749 |
6.14e1 |
SMART |
|
WD40
|
1850 |
1888 |
1.92e-1 |
SMART |
|
| Predicted Effect |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000176923
AA Change: R498C
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000135420
Gene: ENSMUSG00000073434
AA Change: R498C
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
32 |
53 |
N/A |
INTRINSIC |
|
Pfam:DUF667
|
60 |
252 |
5.1e-14 |
PFAM |
|
low complexity region
|
363 |
378 |
N/A |
INTRINSIC |
|
WD40
|
460 |
501 |
5.94e0 |
SMART |
|
WD40
|
504 |
547 |
3.2e0 |
SMART |
|
WD40
|
554 |
594 |
3.3e1 |
SMART |
|
WD40
|
669 |
707 |
1.15e1 |
SMART |
|
WD40
|
710 |
748 |
5.75e-1 |
SMART |
|
WD40
|
750 |
790 |
9.24e-4 |
SMART |
|
WD40
|
793 |
832 |
4.13e0 |
SMART |
|
WD40
|
835 |
874 |
4.62e-1 |
SMART |
|
WD40
|
932 |
975 |
1.07e1 |
SMART |
|
WD40
|
978 |
1017 |
5.75e-1 |
SMART |
|
WD40
|
1022 |
1059 |
1.58e-2 |
SMART |
|
WD40
|
1272 |
1316 |
5.23e-3 |
SMART |
|
WD40
|
1319 |
1360 |
1.27e-1 |
SMART |
|
WD40
|
1366 |
1401 |
1.83e2 |
SMART |
|
WD40
|
1404 |
1451 |
3.08e0 |
SMART |
|
WD40
|
1454 |
1491 |
9.9e0 |
SMART |
|
WD40
|
1550 |
1589 |
9.02e-7 |
SMART |
|
WD40
|
1592 |
1637 |
5.75e-1 |
SMART |
|
WD40
|
1641 |
1679 |
2.98e-1 |
SMART |
|
WD40
|
1682 |
1731 |
6.14e1 |
SMART |
|
WD40
|
1832 |
1870 |
1.92e-1 |
SMART |
|
| Meta Mutation Damage Score |
0.0852 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
| Validation Efficiency |
99% (81/82) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 82 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aadat |
C |
T |
8: 60,993,158 (GRCm39) |
T373I |
possibly damaging |
Het |
| Abca13 |
T |
C |
11: 9,241,653 (GRCm39) |
L1172P |
possibly damaging |
Het |
| Abcg2 |
A |
G |
6: 58,661,326 (GRCm39) |
Y459C |
probably benign |
Het |
| AC125199.3 |
T |
C |
16: 88,609,061 (GRCm39) |
N4D |
possibly damaging |
Het |
| Acad8 |
A |
G |
9: 26,910,785 (GRCm39) |
M3T |
probably benign |
Het |
| Acsbg3 |
A |
C |
17: 57,189,218 (GRCm39) |
I209L |
probably benign |
Het |
| Adcyap1r1 |
C |
T |
6: 55,474,080 (GRCm39) |
T472I |
probably damaging |
Het |
| Ank3 |
A |
T |
10: 69,840,671 (GRCm39) |
K1890N |
possibly damaging |
Het |
| Asic1 |
G |
A |
15: 99,569,826 (GRCm39) |
C49Y |
probably benign |
Het |
| Atp1a1 |
T |
C |
3: 101,498,547 (GRCm39) |
N215S |
probably damaging |
Het |
| C87436 |
A |
G |
6: 86,422,774 (GRCm39) |
Y116C |
probably damaging |
Het |
| Car5a |
T |
C |
8: 122,671,519 (GRCm39) |
D5G |
probably benign |
Het |
| Ccdc169 |
T |
C |
3: 55,058,368 (GRCm39) |
|
probably null |
Het |
| Ccdc93 |
A |
G |
1: 121,426,970 (GRCm39) |
R586G |
probably damaging |
Het |
| Cep295 |
A |
G |
9: 15,238,007 (GRCm39) |
V131A |
probably damaging |
Het |
| Cox5a |
A |
G |
9: 57,436,329 (GRCm39) |
D60G |
possibly damaging |
Het |
| Cpne6 |
A |
T |
14: 55,750,104 (GRCm39) |
E78D |
probably benign |
Het |
| Cyp2u1 |
T |
C |
3: 131,089,114 (GRCm39) |
E390G |
probably damaging |
Het |
| Dab2 |
C |
A |
15: 6,465,271 (GRCm39) |
N707K |
|
Het |
| Dock10 |
A |
T |
1: 80,483,147 (GRCm39) |
D2101E |
probably benign |
Het |
| Duoxa2 |
G |
A |
2: 122,132,357 (GRCm39) |
|
probably null |
Het |
| Eif4a3 |
T |
C |
11: 119,190,758 (GRCm39) |
D22G |
probably benign |
Het |
| Fhip1b |
T |
C |
7: 105,037,477 (GRCm39) |
T369A |
possibly damaging |
Het |
| Fubp3 |
A |
G |
2: 31,482,476 (GRCm39) |
|
probably null |
Het |
| Gm10330 |
A |
G |
12: 23,829,887 (GRCm39) |
L98P |
probably benign |
Het |
| Gm5108 |
A |
G |
5: 68,134,299 (GRCm39) |
*102W |
probably null |
Het |
| Gpr149 |
A |
C |
3: 62,438,478 (GRCm39) |
S560A |
probably damaging |
Het |
| Haspin |
T |
C |
11: 73,027,430 (GRCm39) |
D553G |
probably benign |
Het |
| Hsf1 |
C |
T |
15: 76,382,051 (GRCm39) |
H104Y |
probably benign |
Het |
| Ifi203 |
T |
C |
1: 173,756,494 (GRCm39) |
T430A |
unknown |
Het |
| Itih2 |
G |
A |
2: 10,102,822 (GRCm39) |
Q771* |
probably null |
Het |
| Kazald1 |
T |
A |
19: 45,065,395 (GRCm39) |
L92Q |
probably damaging |
Het |
| Krt19 |
T |
C |
11: 100,031,980 (GRCm39) |
E324G |
probably damaging |
Het |
| Lrrc28 |
A |
T |
7: 67,268,833 (GRCm39) |
V79E |
possibly damaging |
Het |
| Ltn1 |
T |
A |
16: 87,178,381 (GRCm39) |
Q1616L |
probably damaging |
Het |
| Mdc1 |
A |
G |
17: 36,158,843 (GRCm39) |
K408E |
probably benign |
Het |
| Nalcn |
A |
T |
14: 123,561,284 (GRCm39) |
M738K |
probably benign |
Het |
| Ncoa4 |
T |
C |
14: 31,894,848 (GRCm39) |
L125P |
probably damaging |
Het |
| Ncor2 |
G |
T |
5: 125,106,253 (GRCm39) |
R810S |
|
Het |
| Neb |
C |
T |
2: 52,127,141 (GRCm39) |
G348D |
|
Het |
| Nfat5 |
T |
A |
8: 108,095,228 (GRCm39) |
F1156L |
probably damaging |
Het |
| Oit3 |
G |
A |
10: 59,277,468 (GRCm39) |
T13I |
unknown |
Het |
| Opa1 |
A |
C |
16: 29,424,340 (GRCm39) |
Q230P |
probably damaging |
Het |
| Or10j3b |
T |
C |
1: 173,044,064 (GRCm39) |
I282T |
probably damaging |
Het |
| Or52k2 |
T |
A |
7: 102,253,711 (GRCm39) |
I50N |
probably damaging |
Het |
| Or5p66 |
A |
G |
7: 107,886,289 (GRCm39) |
F15L |
probably damaging |
Het |
| Or5w12 |
A |
C |
2: 87,502,567 (GRCm39) |
L48W |
probably damaging |
Het |
| Or6c5b |
G |
T |
10: 129,246,082 (GRCm39) |
M282I |
probably benign |
Het |
| Parpbp |
T |
C |
10: 87,946,189 (GRCm39) |
H410R |
probably null |
Het |
| Pex5l |
A |
G |
3: 33,007,333 (GRCm39) |
V481A |
probably damaging |
Het |
| Plekhh3 |
C |
A |
11: 101,057,225 (GRCm39) |
R344L |
probably benign |
Het |
| Prrc2b |
T |
C |
2: 32,104,953 (GRCm39) |
V1477A |
probably benign |
Het |
| Ptp4a2 |
G |
A |
4: 129,738,945 (GRCm39) |
G94S |
possibly damaging |
Het |
| Ptprk |
T |
A |
10: 28,359,203 (GRCm39) |
Y598* |
probably null |
Het |
| Rfx5 |
C |
A |
3: 94,864,475 (GRCm39) |
T207N |
probably damaging |
Het |
| Rnase2b |
A |
G |
14: 51,400,347 (GRCm39) |
T143A |
possibly damaging |
Het |
| Scn1a |
A |
G |
2: 66,168,330 (GRCm39) |
V92A |
probably benign |
Het |
| Shank2 |
C |
A |
7: 143,965,265 (GRCm39) |
P958T |
probably damaging |
Het |
| Slc13a1 |
A |
G |
6: 24,108,194 (GRCm39) |
I294T |
probably damaging |
Het |
| Slc4a8 |
A |
T |
15: 100,712,421 (GRCm39) |
E1084D |
probably benign |
Het |
| Smurf1 |
T |
A |
5: 144,820,422 (GRCm39) |
R549* |
probably null |
Het |
| Spmip10 |
T |
C |
18: 56,725,537 (GRCm39) |
F66L |
probably damaging |
Het |
| Sprr2b |
T |
C |
3: 92,225,032 (GRCm39) |
C93R |
unknown |
Het |
| Tcn2 |
G |
T |
11: 3,873,569 (GRCm39) |
S259Y |
probably damaging |
Het |
| Tent4a |
G |
T |
13: 69,651,828 (GRCm39) |
T531N |
possibly damaging |
Het |
| Tle1 |
A |
G |
4: 72,076,525 (GRCm39) |
S168P |
possibly damaging |
Het |
| Tnfrsf1b |
C |
T |
4: 144,950,150 (GRCm39) |
G264D |
probably damaging |
Het |
| Tnks2 |
T |
A |
19: 36,823,088 (GRCm39) |
N118K |
probably damaging |
Het |
| Topaz1 |
G |
T |
9: 122,626,930 (GRCm39) |
|
probably benign |
Het |
| Traf3ip1 |
A |
G |
1: 91,443,796 (GRCm39) |
|
probably benign |
Het |
| Ttk |
A |
G |
9: 83,721,322 (GRCm39) |
E69G |
probably damaging |
Het |
| Tulp3 |
T |
C |
6: 128,310,966 (GRCm39) |
D87G |
probably benign |
Het |
| Usp38 |
C |
T |
8: 81,708,479 (GRCm39) |
G1033D |
probably damaging |
Het |
| Usp44 |
T |
A |
10: 93,693,775 (GRCm39) |
N707K |
probably benign |
Het |
| Vipas39 |
T |
A |
12: 87,305,858 (GRCm39) |
R112* |
probably null |
Het |
| Vmn1r185 |
A |
C |
7: 26,311,206 (GRCm39) |
S100A |
probably damaging |
Het |
| Vmn1r209 |
T |
C |
13: 22,990,223 (GRCm39) |
M156V |
probably benign |
Het |
| Vmn1r3 |
G |
A |
4: 3,184,863 (GRCm39) |
T148I |
probably benign |
Het |
| Wdr41 |
G |
A |
13: 95,151,620 (GRCm39) |
R260H |
probably benign |
Het |
| Wnk2 |
A |
T |
13: 49,221,711 (GRCm39) |
H1183Q |
possibly damaging |
Het |
| Zfp667 |
A |
T |
7: 6,308,256 (GRCm39) |
H308L |
possibly damaging |
Het |
| Zfp952 |
A |
G |
17: 33,220,628 (GRCm39) |
N18D |
possibly damaging |
Het |
|
| Other mutations in Wdr90 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00418:Wdr90
|
APN |
17 |
26,068,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01118:Wdr90
|
APN |
17 |
26,073,661 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01964:Wdr90
|
APN |
17 |
26,067,383 (GRCm39) |
missense |
probably benign |
|
|
IGL02116:Wdr90
|
APN |
17 |
26,078,466 (GRCm39) |
missense |
probably benign |
0.12 |
|
IGL02172:Wdr90
|
APN |
17 |
26,069,408 (GRCm39) |
missense |
probably benign |
0.22 |
|
IGL02716:Wdr90
|
APN |
17 |
26,076,194 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL02961:Wdr90
|
APN |
17 |
26,067,649 (GRCm39) |
nonsense |
probably null |
|
|
IGL03229:Wdr90
|
APN |
17 |
26,064,437 (GRCm39) |
splice site |
probably benign |
|
|
IGL03367:Wdr90
|
APN |
17 |
26,066,765 (GRCm39) |
splice site |
probably benign |
|
|
IGL03098:Wdr90
|
UTSW |
17 |
26,078,961 (GRCm39) |
intron |
probably benign |
|
|
R0111:Wdr90
|
UTSW |
17 |
26,067,418 (GRCm39) |
splice site |
probably benign |
|
|
R0454:Wdr90
|
UTSW |
17 |
26,079,023 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0457:Wdr90
|
UTSW |
17 |
26,079,459 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0488:Wdr90
|
UTSW |
17 |
26,067,591 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0622:Wdr90
|
UTSW |
17 |
26,074,632 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0671:Wdr90
|
UTSW |
17 |
26,065,367 (GRCm39) |
missense |
probably benign |
0.04 |
|
R0799:Wdr90
|
UTSW |
17 |
26,079,104 (GRCm39) |
missense |
probably benign |
0.38 |
|
R1177:Wdr90
|
UTSW |
17 |
26,065,028 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R1460:Wdr90
|
UTSW |
17 |
26,079,422 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R1468:Wdr90
|
UTSW |
17 |
26,073,027 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1468:Wdr90
|
UTSW |
17 |
26,073,027 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1544:Wdr90
|
UTSW |
17 |
26,068,284 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R2057:Wdr90
|
UTSW |
17 |
26,074,173 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2087:Wdr90
|
UTSW |
17 |
26,065,577 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2159:Wdr90
|
UTSW |
17 |
26,070,715 (GRCm39) |
missense |
probably benign |
|
|
R2208:Wdr90
|
UTSW |
17 |
26,079,362 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2345:Wdr90
|
UTSW |
17 |
26,078,136 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2391:Wdr90
|
UTSW |
17 |
26,070,429 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2394:Wdr90
|
UTSW |
17 |
26,070,429 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2520:Wdr90
|
UTSW |
17 |
26,074,326 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3798:Wdr90
|
UTSW |
17 |
26,069,472 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3979:Wdr90
|
UTSW |
17 |
26,078,252 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4111:Wdr90
|
UTSW |
17 |
26,068,342 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4326:Wdr90
|
UTSW |
17 |
26,072,705 (GRCm39) |
missense |
probably benign |
0.25 |
|
R4459:Wdr90
|
UTSW |
17 |
26,079,976 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4697:Wdr90
|
UTSW |
17 |
26,074,337 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4735:Wdr90
|
UTSW |
17 |
26,078,424 (GRCm39) |
missense |
probably benign |
|
|
R4907:Wdr90
|
UTSW |
17 |
26,079,624 (GRCm39) |
intron |
probably benign |
|
|
R5070:Wdr90
|
UTSW |
17 |
26,065,307 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5230:Wdr90
|
UTSW |
17 |
26,074,277 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5268:Wdr90
|
UTSW |
17 |
26,069,819 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5287:Wdr90
|
UTSW |
17 |
26,080,441 (GRCm39) |
utr 5 prime |
probably benign |
|
|
R5382:Wdr90
|
UTSW |
17 |
26,064,572 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5511:Wdr90
|
UTSW |
17 |
26,063,995 (GRCm39) |
unclassified |
probably benign |
|
|
R5545:Wdr90
|
UTSW |
17 |
26,064,830 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5707:Wdr90
|
UTSW |
17 |
26,076,166 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5973:Wdr90
|
UTSW |
17 |
26,065,381 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5973:Wdr90
|
UTSW |
17 |
26,064,107 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6385:Wdr90
|
UTSW |
17 |
26,067,504 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6481:Wdr90
|
UTSW |
17 |
26,064,885 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7078:Wdr90
|
UTSW |
17 |
26,068,623 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7214:Wdr90
|
UTSW |
17 |
26,064,367 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7288:Wdr90
|
UTSW |
17 |
26,065,286 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7304:Wdr90
|
UTSW |
17 |
26,070,480 (GRCm39) |
missense |
probably benign |
0.10 |
|
R7309:Wdr90
|
UTSW |
17 |
26,079,676 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7391:Wdr90
|
UTSW |
17 |
26,065,502 (GRCm39) |
missense |
probably benign |
0.08 |
|
R7622:Wdr90
|
UTSW |
17 |
26,073,083 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7646:Wdr90
|
UTSW |
17 |
26,079,104 (GRCm39) |
missense |
probably benign |
0.38 |
|
R7772:Wdr90
|
UTSW |
17 |
26,080,465 (GRCm39) |
start gained |
probably benign |
|
|
R7779:Wdr90
|
UTSW |
17 |
26,065,300 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7780:Wdr90
|
UTSW |
17 |
26,065,300 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7781:Wdr90
|
UTSW |
17 |
26,065,300 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7782:Wdr90
|
UTSW |
17 |
26,065,300 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7812:Wdr90
|
UTSW |
17 |
26,071,532 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7870:Wdr90
|
UTSW |
17 |
26,079,513 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7911:Wdr90
|
UTSW |
17 |
26,069,723 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8126:Wdr90
|
UTSW |
17 |
26,067,951 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R8260:Wdr90
|
UTSW |
17 |
26,064,141 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8315:Wdr90
|
UTSW |
17 |
26,064,399 (GRCm39) |
missense |
probably benign |
0.21 |
|
R8938:Wdr90
|
UTSW |
17 |
26,076,146 (GRCm39) |
missense |
|
|
|
R8940:Wdr90
|
UTSW |
17 |
26,076,146 (GRCm39) |
missense |
|
|
|
R9038:Wdr90
|
UTSW |
17 |
26,076,200 (GRCm39) |
missense |
|
|
|
R9079:Wdr90
|
UTSW |
17 |
26,076,403 (GRCm39) |
missense |
|
|
|
R9401:Wdr90
|
UTSW |
17 |
26,064,750 (GRCm39) |
small insertion |
probably benign |
|
|
R9471:Wdr90
|
UTSW |
17 |
26,080,015 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R9642:Wdr90
|
UTSW |
17 |
26,072,694 (GRCm39) |
critical splice donor site |
probably null |
|
|
X0064:Wdr90
|
UTSW |
17 |
26,067,537 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Wdr90
|
UTSW |
17 |
26,079,470 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GCTTATTGGCACATTACCGTCC -3'
(R):5'- TTCCTTGGCCATACCGACAAG -3'
Sequencing Primer
(F):5'- TTGCCCACACCGCAGAG -3'
(R):5'- ACAAGGTACATGCCTGCTG -3'
|
| Posted On |
2021-08-02 |
Incidental Mutation