Incidental Mutation 'R5426:Wdr17'
ID |
426889 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Wdr17
|
Ensembl Gene |
ENSMUSG00000039375 |
Gene Name |
WD repeat domain 17 |
Synonyms |
B230207L18Rik, 3010002I12Rik |
MMRRC Submission |
042992-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R5426 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
55082316-55180014 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 55134434 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glycine to Arginine
at position 349
(G349R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000122326
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000127511]
[ENSMUST00000144482]
[ENSMUST00000144711]
[ENSMUST00000150488]
[ENSMUST00000175915]
|
AlphaFold |
E9Q271 |
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126316
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000127511
AA Change: G373R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000115550 Gene: ENSMUSG00000039375 AA Change: G373R
Domain | Start | End | E-Value | Type |
WD40
|
72 |
112 |
8.55e-8 |
SMART |
WD40
|
162 |
202 |
1.58e2 |
SMART |
WD40
|
205 |
252 |
4.26e1 |
SMART |
WD40
|
255 |
298 |
1.15e0 |
SMART |
WD40
|
383 |
422 |
1.59e-7 |
SMART |
WD40
|
425 |
465 |
2.39e0 |
SMART |
WD40
|
468 |
509 |
5.52e-2 |
SMART |
WD40
|
511 |
550 |
4.14e-6 |
SMART |
WD40
|
555 |
595 |
5.14e-11 |
SMART |
WD40
|
598 |
638 |
6.58e-9 |
SMART |
WD40
|
641 |
681 |
6.28e-6 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000144482
AA Change: G60R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000134950 Gene: ENSMUSG00000039375 AA Change: G60R
Domain | Start | End | E-Value | Type |
Blast:WD40
|
16 |
65 |
2e-24 |
BLAST |
WD40
|
70 |
109 |
1.59e-7 |
SMART |
WD40
|
112 |
152 |
2.39e0 |
SMART |
WD40
|
155 |
196 |
5.52e-2 |
SMART |
WD40
|
198 |
237 |
4.14e-6 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000144711
AA Change: G356R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000117710 Gene: ENSMUSG00000039375 AA Change: G356R
Domain | Start | End | E-Value | Type |
WD40
|
72 |
112 |
8.55e-8 |
SMART |
WD40
|
194 |
235 |
7.64e1 |
SMART |
WD40
|
238 |
281 |
1.15e0 |
SMART |
WD40
|
366 |
405 |
1.59e-7 |
SMART |
WD40
|
408 |
448 |
2.39e0 |
SMART |
WD40
|
451 |
492 |
5.52e-2 |
SMART |
WD40
|
494 |
533 |
4.14e-6 |
SMART |
WD40
|
538 |
578 |
5.14e-11 |
SMART |
WD40
|
581 |
621 |
6.58e-9 |
SMART |
WD40
|
624 |
664 |
6.28e-6 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000150488
AA Change: G349R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000122326 Gene: ENSMUSG00000039375 AA Change: G349R
Domain | Start | End | E-Value | Type |
WD40
|
48 |
88 |
8.55e-8 |
SMART |
WD40
|
138 |
178 |
1.58e2 |
SMART |
WD40
|
181 |
228 |
4.26e1 |
SMART |
WD40
|
231 |
274 |
1.15e0 |
SMART |
WD40
|
359 |
398 |
1.59e-7 |
SMART |
WD40
|
401 |
441 |
2.39e0 |
SMART |
WD40
|
444 |
485 |
5.52e-2 |
SMART |
WD40
|
487 |
526 |
4.14e-6 |
SMART |
WD40
|
531 |
571 |
5.14e-11 |
SMART |
WD40
|
574 |
614 |
6.58e-9 |
SMART |
WD40
|
617 |
657 |
6.28e-6 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000175915
AA Change: G349R
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000135805 Gene: ENSMUSG00000039375 AA Change: G349R
Domain | Start | End | E-Value | Type |
WD40
|
48 |
88 |
8.55e-8 |
SMART |
WD40
|
138 |
178 |
1.58e2 |
SMART |
WD40
|
181 |
228 |
4.26e1 |
SMART |
WD40
|
231 |
274 |
1.15e0 |
SMART |
WD40
|
359 |
398 |
1.59e-7 |
SMART |
WD40
|
401 |
441 |
2.39e0 |
SMART |
WD40
|
444 |
485 |
5.52e-2 |
SMART |
WD40
|
487 |
526 |
4.14e-6 |
SMART |
WD40
|
531 |
571 |
5.14e-11 |
SMART |
WD40
|
574 |
614 |
6.58e-9 |
SMART |
WD40
|
617 |
657 |
6.28e-6 |
SMART |
|
Meta Mutation Damage Score |
0.3416 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.6%
|
Validation Efficiency |
97% (85/88) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a WD repeat-containing protein. It is abundantly expressed in retina and testis, and is thought to be a candidate gene for retinal disease. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2009]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
T |
A |
9: 124,056,633 (GRCm39) |
H122L |
probably damaging |
Het |
9330182O14Rik |
G |
A |
15: 40,011,932 (GRCm39) |
M90I |
unknown |
Het |
9330182O14Rik |
G |
A |
15: 40,011,933 (GRCm39) |
D91N |
unknown |
Het |
Abca13 |
T |
A |
11: 9,240,722 (GRCm39) |
S862T |
probably damaging |
Het |
Acyp2 |
C |
T |
11: 30,456,354 (GRCm39) |
E98K |
possibly damaging |
Het |
Adgb |
C |
A |
10: 10,226,004 (GRCm39) |
A1405S |
probably benign |
Het |
Adpgk |
T |
A |
9: 59,204,832 (GRCm39) |
V86E |
probably damaging |
Het |
Agfg2 |
G |
C |
5: 137,666,020 (GRCm39) |
P80A |
probably damaging |
Het |
Akap11 |
G |
A |
14: 78,736,304 (GRCm39) |
Q1829* |
probably null |
Het |
Aldh1l1 |
G |
A |
6: 90,536,281 (GRCm39) |
R62Q |
probably benign |
Het |
Amd1 |
G |
T |
10: 40,166,183 (GRCm39) |
D265E |
probably damaging |
Het |
Aox4 |
A |
T |
1: 58,259,253 (GRCm39) |
Q106L |
probably damaging |
Het |
Arap2 |
A |
T |
5: 62,800,159 (GRCm39) |
N1289K |
probably benign |
Het |
Arhgef12 |
T |
C |
9: 42,897,880 (GRCm39) |
S874G |
probably damaging |
Het |
Ccdc166 |
T |
C |
15: 75,853,945 (GRCm39) |
Q45R |
possibly damaging |
Het |
Cdc45 |
C |
T |
16: 18,614,647 (GRCm39) |
R205H |
probably damaging |
Het |
Cdk14 |
A |
G |
5: 4,938,975 (GRCm39) |
S388P |
possibly damaging |
Het |
Chgb |
A |
T |
2: 132,635,453 (GRCm39) |
Q465L |
possibly damaging |
Het |
Commd9 |
T |
A |
2: 101,729,220 (GRCm39) |
W109R |
probably damaging |
Het |
Cspg4b |
G |
A |
13: 113,505,587 (GRCm39) |
V2239I |
probably benign |
Het |
Cyp2b9 |
T |
C |
7: 25,887,080 (GRCm39) |
V163A |
probably benign |
Het |
Dcpp2 |
T |
A |
17: 24,118,287 (GRCm39) |
H27Q |
possibly damaging |
Het |
Ddn |
T |
A |
15: 98,704,347 (GRCm39) |
E315V |
possibly damaging |
Het |
Defb29 |
C |
A |
2: 152,380,868 (GRCm39) |
C47F |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,281,366 (GRCm39) |
M2809T |
possibly damaging |
Het |
Dock4 |
A |
T |
12: 40,795,744 (GRCm39) |
I854F |
probably damaging |
Het |
Dsg4 |
T |
C |
18: 20,591,541 (GRCm39) |
Y427H |
probably damaging |
Het |
E130114P18Rik |
C |
T |
4: 97,578,907 (GRCm39) |
A23T |
unknown |
Het |
Flacc1 |
T |
A |
1: 58,706,045 (GRCm39) |
K275* |
probably null |
Het |
Gemin5 |
A |
G |
11: 58,016,113 (GRCm39) |
S1297P |
probably benign |
Het |
Gm10309 |
A |
C |
17: 86,806,161 (GRCm39) |
|
probably benign |
Het |
Gpatch11 |
T |
A |
17: 79,148,663 (GRCm39) |
S155R |
possibly damaging |
Het |
Grin2b |
C |
A |
6: 135,709,366 (GRCm39) |
Q1393H |
probably damaging |
Het |
Heatr5b |
C |
T |
17: 79,081,142 (GRCm39) |
C1370Y |
probably damaging |
Het |
Hmcn2 |
C |
T |
2: 31,226,556 (GRCm39) |
T177I |
possibly damaging |
Het |
Ildr1 |
A |
T |
16: 36,529,981 (GRCm39) |
I123F |
probably damaging |
Het |
Kalrn |
A |
T |
16: 34,083,023 (GRCm39) |
V644D |
probably damaging |
Het |
Kifap3 |
A |
G |
1: 163,607,440 (GRCm39) |
M1V |
probably null |
Het |
Klhl11 |
A |
G |
11: 100,354,942 (GRCm39) |
L293P |
probably damaging |
Het |
Klrc3 |
G |
A |
6: 129,618,513 (GRCm39) |
S98L |
probably benign |
Het |
Lrrc37 |
A |
T |
11: 103,511,586 (GRCm39) |
H127Q |
unknown |
Het |
Med12l |
G |
A |
3: 59,156,143 (GRCm39) |
M1220I |
probably damaging |
Het |
Ms4a7 |
C |
T |
19: 11,303,166 (GRCm39) |
|
probably null |
Het |
Mybpc2 |
A |
G |
7: 44,159,253 (GRCm39) |
V599A |
probably benign |
Het |
Naalad2 |
T |
C |
9: 18,258,815 (GRCm39) |
N487D |
probably benign |
Het |
Nat8f7 |
T |
G |
6: 85,684,805 (GRCm39) |
S12R |
probably benign |
Het |
Nefm |
T |
A |
14: 68,357,515 (GRCm39) |
|
probably benign |
Het |
Nlrp5 |
T |
C |
7: 23,117,626 (GRCm39) |
V450A |
probably damaging |
Het |
Nps |
G |
A |
7: 134,870,376 (GRCm39) |
|
probably null |
Het |
Or13c7d |
A |
G |
4: 43,770,168 (GRCm39) |
I281T |
probably benign |
Het |
Or2ag16 |
C |
A |
7: 106,351,773 (GRCm39) |
S274I |
probably benign |
Het |
Or4a74 |
T |
C |
2: 89,440,083 (GRCm39) |
Y121C |
probably damaging |
Het |
Or4b13 |
T |
A |
2: 90,082,955 (GRCm39) |
K126* |
probably null |
Het |
Or5e1 |
T |
C |
7: 108,354,924 (GRCm39) |
L287P |
possibly damaging |
Het |
Or5h24 |
G |
T |
16: 58,918,665 (GRCm39) |
P230Q |
possibly damaging |
Het |
Or5p67 |
T |
C |
7: 107,922,017 (GRCm39) |
N289D |
probably damaging |
Het |
Oxct2a |
C |
A |
4: 123,216,506 (GRCm39) |
G292W |
possibly damaging |
Het |
Pramel32 |
T |
A |
4: 88,547,647 (GRCm39) |
|
probably benign |
Het |
Prr27 |
T |
C |
5: 87,998,744 (GRCm39) |
|
probably benign |
Het |
Ptx3 |
T |
C |
3: 66,128,143 (GRCm39) |
M68T |
probably damaging |
Het |
Rufy1 |
A |
G |
11: 50,312,561 (GRCm39) |
L131S |
probably damaging |
Het |
Septin7 |
T |
A |
9: 25,197,986 (GRCm39) |
I100N |
possibly damaging |
Het |
Sgms2 |
T |
C |
3: 131,135,446 (GRCm39) |
I143V |
probably benign |
Het |
Slc25a34 |
A |
G |
4: 141,350,877 (GRCm39) |
V44A |
probably damaging |
Het |
Slc28a3 |
T |
A |
13: 58,710,968 (GRCm39) |
D518V |
probably damaging |
Het |
Slc6a7 |
C |
T |
18: 61,136,308 (GRCm39) |
|
probably null |
Het |
Slco4a1 |
C |
A |
2: 180,113,028 (GRCm39) |
A420D |
possibly damaging |
Het |
Smap1 |
T |
C |
1: 23,888,471 (GRCm39) |
T180A |
probably benign |
Het |
Specc1l |
T |
C |
10: 75,103,384 (GRCm39) |
S920P |
probably benign |
Het |
Tgtp2 |
A |
G |
11: 48,950,083 (GRCm39) |
M163T |
probably benign |
Het |
Tiam1 |
G |
T |
16: 89,662,280 (GRCm39) |
Q613K |
possibly damaging |
Het |
Vsig10l |
T |
A |
7: 43,114,247 (GRCm39) |
S190T |
probably damaging |
Het |
Vwa3b |
A |
G |
1: 37,154,752 (GRCm39) |
Y512C |
probably damaging |
Het |
Wdfy3 |
T |
A |
5: 102,067,312 (GRCm39) |
N1207Y |
probably damaging |
Het |
Wdr70 |
A |
G |
15: 7,951,586 (GRCm39) |
L417S |
possibly damaging |
Het |
Wdr81 |
A |
C |
11: 75,341,722 (GRCm39) |
S1182A |
possibly damaging |
Het |
Zfp458 |
A |
T |
13: 67,405,256 (GRCm39) |
C391* |
probably null |
Het |
Zfp638 |
A |
G |
6: 83,953,396 (GRCm39) |
E1167G |
probably damaging |
Het |
Zfp763 |
T |
A |
17: 33,238,569 (GRCm39) |
D192V |
probably benign |
Het |
Zfp853 |
T |
G |
5: 143,274,624 (GRCm39) |
Q332P |
unknown |
Het |
|
Other mutations in Wdr17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00309:Wdr17
|
APN |
8 |
55,140,746 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00496:Wdr17
|
APN |
8 |
55,112,614 (GRCm39) |
splice site |
probably benign |
|
IGL01318:Wdr17
|
APN |
8 |
55,125,585 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01347:Wdr17
|
APN |
8 |
55,104,380 (GRCm39) |
missense |
probably benign |
|
IGL01654:Wdr17
|
APN |
8 |
55,115,914 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02010:Wdr17
|
APN |
8 |
55,112,738 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02085:Wdr17
|
APN |
8 |
55,140,771 (GRCm39) |
nonsense |
probably null |
|
IGL02205:Wdr17
|
APN |
8 |
55,149,335 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02375:Wdr17
|
APN |
8 |
55,149,423 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02705:Wdr17
|
APN |
8 |
55,101,250 (GRCm39) |
splice site |
probably null |
|
IGL02719:Wdr17
|
APN |
8 |
55,146,089 (GRCm39) |
splice site |
probably null |
|
IGL03051:Wdr17
|
APN |
8 |
55,104,349 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03131:Wdr17
|
APN |
8 |
55,149,302 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03172:Wdr17
|
APN |
8 |
55,114,515 (GRCm39) |
missense |
probably damaging |
0.96 |
enthralled
|
UTSW |
8 |
55,112,716 (GRCm39) |
missense |
possibly damaging |
0.85 |
riveted
|
UTSW |
8 |
55,085,522 (GRCm39) |
missense |
probably benign |
0.00 |
thrilled
|
UTSW |
8 |
55,149,303 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03138:Wdr17
|
UTSW |
8 |
55,102,178 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4458001:Wdr17
|
UTSW |
8 |
55,126,614 (GRCm39) |
nonsense |
probably null |
|
R0011:Wdr17
|
UTSW |
8 |
55,125,536 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0011:Wdr17
|
UTSW |
8 |
55,125,536 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0124:Wdr17
|
UTSW |
8 |
55,088,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R0226:Wdr17
|
UTSW |
8 |
55,116,043 (GRCm39) |
missense |
probably benign |
0.08 |
R0270:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0271:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0288:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0321:Wdr17
|
UTSW |
8 |
55,149,303 (GRCm39) |
critical splice donor site |
probably null |
|
R0464:Wdr17
|
UTSW |
8 |
55,123,427 (GRCm39) |
splice site |
probably benign |
|
R0479:Wdr17
|
UTSW |
8 |
55,104,456 (GRCm39) |
splice site |
probably null |
|
R0488:Wdr17
|
UTSW |
8 |
55,146,087 (GRCm39) |
unclassified |
probably benign |
|
R0552:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0553:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0600:Wdr17
|
UTSW |
8 |
55,114,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R0621:Wdr17
|
UTSW |
8 |
55,096,226 (GRCm39) |
missense |
probably benign |
0.18 |
R0655:Wdr17
|
UTSW |
8 |
55,102,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R0730:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0789:Wdr17
|
UTSW |
8 |
55,112,607 (GRCm39) |
splice site |
probably benign |
|
R0854:Wdr17
|
UTSW |
8 |
55,156,916 (GRCm39) |
missense |
probably benign |
|
R0879:Wdr17
|
UTSW |
8 |
55,114,516 (GRCm39) |
missense |
probably benign |
0.08 |
R1462:Wdr17
|
UTSW |
8 |
55,123,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Wdr17
|
UTSW |
8 |
55,123,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R1497:Wdr17
|
UTSW |
8 |
55,125,536 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1589:Wdr17
|
UTSW |
8 |
55,156,942 (GRCm39) |
intron |
probably benign |
|
R1618:Wdr17
|
UTSW |
8 |
55,092,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R1768:Wdr17
|
UTSW |
8 |
55,126,689 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1778:Wdr17
|
UTSW |
8 |
55,143,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R1819:Wdr17
|
UTSW |
8 |
55,143,159 (GRCm39) |
missense |
probably benign |
0.18 |
R1913:Wdr17
|
UTSW |
8 |
55,140,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R2129:Wdr17
|
UTSW |
8 |
55,085,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Wdr17
|
UTSW |
8 |
55,125,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R2309:Wdr17
|
UTSW |
8 |
55,096,283 (GRCm39) |
missense |
probably benign |
|
R3882:Wdr17
|
UTSW |
8 |
55,092,536 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4097:Wdr17
|
UTSW |
8 |
55,088,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R4372:Wdr17
|
UTSW |
8 |
55,092,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R4380:Wdr17
|
UTSW |
8 |
55,101,442 (GRCm39) |
intron |
probably benign |
|
R4480:Wdr17
|
UTSW |
8 |
55,117,999 (GRCm39) |
critical splice donor site |
probably null |
|
R4654:Wdr17
|
UTSW |
8 |
55,134,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R4656:Wdr17
|
UTSW |
8 |
55,134,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R4669:Wdr17
|
UTSW |
8 |
55,143,083 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4719:Wdr17
|
UTSW |
8 |
55,092,911 (GRCm39) |
missense |
probably benign |
0.33 |
R4912:Wdr17
|
UTSW |
8 |
55,082,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R5000:Wdr17
|
UTSW |
8 |
55,118,161 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5073:Wdr17
|
UTSW |
8 |
55,143,271 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5176:Wdr17
|
UTSW |
8 |
55,106,913 (GRCm39) |
critical splice donor site |
probably null |
|
R5194:Wdr17
|
UTSW |
8 |
55,140,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5270:Wdr17
|
UTSW |
8 |
55,096,221 (GRCm39) |
missense |
probably benign |
0.20 |
R5300:Wdr17
|
UTSW |
8 |
55,134,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R5325:Wdr17
|
UTSW |
8 |
55,112,716 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5336:Wdr17
|
UTSW |
8 |
55,085,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R5394:Wdr17
|
UTSW |
8 |
55,092,524 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5424:Wdr17
|
UTSW |
8 |
55,134,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R5425:Wdr17
|
UTSW |
8 |
55,134,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R5548:Wdr17
|
UTSW |
8 |
55,156,886 (GRCm39) |
missense |
probably damaging |
0.97 |
R5681:Wdr17
|
UTSW |
8 |
55,115,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R5722:Wdr17
|
UTSW |
8 |
55,113,806 (GRCm39) |
critical splice donor site |
probably null |
|
R5894:Wdr17
|
UTSW |
8 |
55,149,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R5906:Wdr17
|
UTSW |
8 |
55,092,503 (GRCm39) |
missense |
probably benign |
0.33 |
R6038:Wdr17
|
UTSW |
8 |
55,085,346 (GRCm39) |
critical splice donor site |
probably null |
|
R6038:Wdr17
|
UTSW |
8 |
55,085,346 (GRCm39) |
critical splice donor site |
probably null |
|
R6391:Wdr17
|
UTSW |
8 |
55,114,495 (GRCm39) |
missense |
probably benign |
0.04 |
R6605:Wdr17
|
UTSW |
8 |
55,134,559 (GRCm39) |
missense |
probably benign |
0.16 |
R6892:Wdr17
|
UTSW |
8 |
55,126,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R7019:Wdr17
|
UTSW |
8 |
55,134,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R7257:Wdr17
|
UTSW |
8 |
55,085,522 (GRCm39) |
missense |
probably benign |
0.00 |
R7481:Wdr17
|
UTSW |
8 |
55,114,371 (GRCm39) |
missense |
probably benign |
|
R7868:Wdr17
|
UTSW |
8 |
55,149,302 (GRCm39) |
critical splice donor site |
probably null |
|
R7939:Wdr17
|
UTSW |
8 |
55,140,677 (GRCm39) |
missense |
probably damaging |
0.98 |
R7962:Wdr17
|
UTSW |
8 |
55,113,806 (GRCm39) |
critical splice donor site |
probably null |
|
R8017:Wdr17
|
UTSW |
8 |
55,091,403 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8122:Wdr17
|
UTSW |
8 |
55,118,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R8226:Wdr17
|
UTSW |
8 |
55,146,155 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8251:Wdr17
|
UTSW |
8 |
55,110,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R8413:Wdr17
|
UTSW |
8 |
55,115,953 (GRCm39) |
missense |
probably benign |
0.08 |
R8534:Wdr17
|
UTSW |
8 |
55,101,265 (GRCm39) |
missense |
probably benign |
0.08 |
R8708:Wdr17
|
UTSW |
8 |
55,093,127 (GRCm39) |
intron |
probably benign |
|
R9116:Wdr17
|
UTSW |
8 |
55,114,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R9258:Wdr17
|
UTSW |
8 |
55,112,654 (GRCm39) |
nonsense |
probably null |
|
R9351:Wdr17
|
UTSW |
8 |
55,143,057 (GRCm39) |
missense |
probably benign |
0.00 |
R9475:Wdr17
|
UTSW |
8 |
55,088,512 (GRCm39) |
missense |
probably benign |
0.00 |
R9546:Wdr17
|
UTSW |
8 |
55,112,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R9547:Wdr17
|
UTSW |
8 |
55,112,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R9635:Wdr17
|
UTSW |
8 |
55,101,375 (GRCm39) |
missense |
probably damaging |
0.98 |
V5088:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
V5622:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
V5622:Wdr17
|
UTSW |
8 |
55,146,131 (GRCm39) |
missense |
possibly damaging |
0.85 |
X0022:Wdr17
|
UTSW |
8 |
55,092,529 (GRCm39) |
missense |
probably benign |
0.04 |
X0066:Wdr17
|
UTSW |
8 |
55,126,595 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Wdr17
|
UTSW |
8 |
55,123,414 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Wdr17
|
UTSW |
8 |
55,096,220 (GRCm39) |
missense |
probably benign |
0.03 |
|
Predicted Primers |
PCR Primer
(F):5'- GGCTACCTAGTTGAGTTACTTAGATG -3'
(R):5'- TAAGTCCTGCCTAATTTTCAGCCAC -3'
Sequencing Primer
(F):5'- GAGTTACTTAGATGAGCTAGTTGAAC -3'
(R):5'- ACACTGAGTTTTATGCTCATTTTTGG -3'
|
Posted On |
2016-09-01 |