Incidental Mutation 'R0600:Wdr17'
ID |
55312 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Wdr17
|
Ensembl Gene |
ENSMUSG00000039375 |
Gene Name |
WD repeat domain 17 |
Synonyms |
B230207L18Rik, 3010002I12Rik |
MMRRC Submission |
038789-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0600 (G1)
|
Quality Score |
219 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
55082316-55180014 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 55114530 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Threonine
at position 662
(I662T)
|
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 benign
Transcript: ENSMUST00000127511
AA Change: I686T
PolyPhen 2
Score 0.201 (Sensitivity: 0.92; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000115550 Gene: ENSMUSG00000039375 AA Change: I686T
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 benign
Transcript: ENSMUST00000144482
|
SMART Domains |
Protein: ENSMUSP00000134950 Gene: ENSMUSG00000039375
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 benign
Transcript: ENSMUST00000144711
AA Change: I669T
PolyPhen 2
Score 0.094 (Sensitivity: 0.93; Specificity: 0.85)
|
SMART Domains |
Protein: ENSMUSP00000117710 Gene: ENSMUSG00000039375 AA Change: I669T
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: I662T
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000122326 Gene: ENSMUSG00000039375 AA Change: I662T
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 benign
Transcript: ENSMUST00000175915
AA Change: I662T
PolyPhen 2
Score 0.332 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000135805 Gene: ENSMUSG00000039375 AA Change: I662T
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 |
0.6467 |
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.1%
- 20x: 93.5%
|
Validation Efficiency |
99% (95/96) |
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: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057M21Rik |
A |
G |
7: 130,959,389 (GRCm39) |
S150P |
probably damaging |
Het |
5530400C23Rik |
T |
G |
6: 133,270,174 (GRCm39) |
|
probably benign |
Het |
Ahctf1 |
A |
C |
1: 179,591,033 (GRCm39) |
|
probably null |
Het |
Ang5 |
T |
C |
14: 44,200,206 (GRCm39) |
V90A |
probably benign |
Het |
Ano9 |
C |
T |
7: 140,684,623 (GRCm39) |
G442R |
probably damaging |
Het |
Apaf1 |
G |
A |
10: 90,895,914 (GRCm39) |
T386I |
probably damaging |
Het |
Apob |
C |
A |
12: 8,056,440 (GRCm39) |
H1608N |
probably damaging |
Het |
Arhgap12 |
C |
A |
18: 6,064,433 (GRCm39) |
|
probably benign |
Het |
Asxl1 |
T |
A |
2: 153,241,824 (GRCm39) |
D791E |
probably benign |
Het |
Avl9 |
T |
C |
6: 56,713,891 (GRCm39) |
V383A |
probably benign |
Het |
Btbd1 |
A |
C |
7: 81,465,754 (GRCm39) |
D197E |
probably damaging |
Het |
Camta2 |
T |
C |
11: 70,564,785 (GRCm39) |
I938V |
possibly damaging |
Het |
Ccn5 |
G |
A |
2: 163,667,233 (GRCm39) |
C78Y |
probably damaging |
Het |
Cdca7 |
C |
A |
2: 72,313,811 (GRCm39) |
A200D |
possibly damaging |
Het |
Cep104 |
A |
T |
4: 154,091,249 (GRCm39) |
Y923F |
possibly damaging |
Het |
Cep135 |
G |
C |
5: 76,769,152 (GRCm39) |
V601L |
probably benign |
Het |
Ces2b |
G |
A |
8: 105,562,542 (GRCm39) |
G291S |
probably benign |
Het |
Col6a6 |
C |
T |
9: 105,638,639 (GRCm39) |
G1400D |
probably damaging |
Het |
Cyth2 |
T |
C |
7: 45,462,541 (GRCm39) |
E1G |
probably damaging |
Het |
Dand5 |
A |
T |
8: 85,542,921 (GRCm39) |
L185Q |
probably damaging |
Het |
Dck |
T |
C |
5: 88,929,080 (GRCm39) |
V253A |
probably benign |
Het |
Ddx20 |
A |
G |
3: 105,586,396 (GRCm39) |
S650P |
probably damaging |
Het |
Dicer1 |
G |
A |
12: 104,673,123 (GRCm39) |
P799S |
probably damaging |
Het |
Dst |
C |
T |
1: 34,228,200 (GRCm39) |
P1606L |
probably damaging |
Het |
Eya2 |
G |
A |
2: 165,611,157 (GRCm39) |
C477Y |
probably damaging |
Het |
Fip1l1 |
T |
A |
5: 74,756,503 (GRCm39) |
N498K |
probably damaging |
Het |
Flt4 |
C |
T |
11: 49,527,166 (GRCm39) |
|
probably benign |
Het |
Galntl6 |
T |
C |
8: 58,290,217 (GRCm39) |
|
probably null |
Het |
Gda |
A |
T |
19: 21,411,667 (GRCm39) |
F44I |
possibly damaging |
Het |
Gli2 |
G |
A |
1: 118,768,119 (GRCm39) |
R703C |
probably damaging |
Het |
Golgb1 |
T |
A |
16: 36,736,633 (GRCm39) |
L1960Q |
probably damaging |
Het |
Gramd1b |
T |
C |
9: 40,219,651 (GRCm39) |
D341G |
probably damaging |
Het |
Grid2 |
G |
T |
6: 63,480,419 (GRCm39) |
A78S |
probably benign |
Het |
Hao2 |
A |
T |
3: 98,790,876 (GRCm39) |
|
probably benign |
Het |
Hook3 |
A |
G |
8: 26,609,014 (GRCm39) |
V10A |
probably benign |
Het |
Kif20a |
A |
G |
18: 34,762,262 (GRCm39) |
E425G |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,403,252 (GRCm39) |
D2107G |
probably benign |
Het |
Lrriq3 |
T |
C |
3: 154,893,373 (GRCm39) |
I358T |
possibly damaging |
Het |
Mad2l2 |
A |
G |
4: 148,225,381 (GRCm39) |
D17G |
possibly damaging |
Het |
Mastl |
G |
T |
2: 23,023,358 (GRCm39) |
T455K |
probably benign |
Het |
Mkln1 |
G |
T |
6: 31,409,862 (GRCm39) |
|
probably benign |
Het |
Mmp1b |
A |
T |
9: 7,387,947 (GRCm39) |
Y16N |
possibly damaging |
Het |
Mmp24 |
C |
T |
2: 155,634,517 (GRCm39) |
A79V |
probably benign |
Het |
Mrps35 |
T |
A |
6: 146,972,232 (GRCm39) |
C292S |
possibly damaging |
Het |
Myom1 |
T |
C |
17: 71,427,643 (GRCm39) |
F1435L |
possibly damaging |
Het |
Nars2 |
C |
T |
7: 96,689,130 (GRCm39) |
H351Y |
probably damaging |
Het |
Nat2 |
A |
T |
8: 67,953,919 (GRCm39) |
I10F |
probably damaging |
Het |
Nfix |
G |
A |
8: 85,453,155 (GRCm39) |
R300C |
probably damaging |
Het |
Olfm5 |
A |
T |
7: 103,803,076 (GRCm39) |
Y462* |
probably null |
Het |
Or13p5 |
C |
T |
4: 118,591,986 (GRCm39) |
H87Y |
probably damaging |
Het |
Or1j12 |
C |
A |
2: 36,342,660 (GRCm39) |
A21E |
probably benign |
Het |
Or2w3 |
C |
A |
11: 58,556,986 (GRCm39) |
F200L |
probably damaging |
Het |
Or4c122 |
C |
A |
2: 89,079,742 (GRCm39) |
E87* |
probably null |
Het |
Or4e1 |
T |
C |
14: 52,700,966 (GRCm39) |
I167V |
probably benign |
Het |
Or5p70 |
T |
A |
7: 107,994,438 (GRCm39) |
I37N |
probably damaging |
Het |
Or7g35 |
T |
C |
9: 19,496,600 (GRCm39) |
S256P |
possibly damaging |
Het |
Or8d2b |
T |
A |
9: 38,789,111 (GRCm39) |
I213N |
probably damaging |
Het |
Or8g20 |
A |
T |
9: 39,396,284 (GRCm39) |
F85L |
probably benign |
Het |
Otog |
A |
T |
7: 45,900,819 (GRCm39) |
|
probably benign |
Het |
Pdcd2l |
A |
T |
7: 33,892,232 (GRCm39) |
D212E |
possibly damaging |
Het |
Pex5 |
T |
C |
6: 124,381,596 (GRCm39) |
N213S |
probably benign |
Het |
Pkn3 |
C |
T |
2: 29,971,146 (GRCm39) |
P238S |
probably benign |
Het |
Pramel32 |
A |
T |
4: 88,547,536 (GRCm39) |
I45K |
probably damaging |
Het |
Prl2b1 |
A |
T |
13: 27,574,723 (GRCm39) |
|
probably null |
Het |
Ptprb |
A |
T |
10: 116,204,712 (GRCm39) |
I1849L |
possibly damaging |
Het |
Rasal3 |
G |
T |
17: 32,612,500 (GRCm39) |
S787Y |
probably damaging |
Het |
Scn2a |
T |
A |
2: 65,532,177 (GRCm39) |
D596E |
possibly damaging |
Het |
Sdhd |
A |
T |
9: 50,515,064 (GRCm39) |
V9D |
possibly damaging |
Het |
Serinc5 |
T |
C |
13: 92,844,565 (GRCm39) |
S436P |
probably damaging |
Het |
Slc27a1 |
C |
T |
8: 72,036,808 (GRCm39) |
P348L |
probably damaging |
Het |
Slc28a2b |
A |
T |
2: 122,344,879 (GRCm39) |
I162F |
probably damaging |
Het |
Smg1 |
G |
A |
7: 117,759,606 (GRCm39) |
|
probably benign |
Het |
Sorl1 |
A |
T |
9: 41,955,196 (GRCm39) |
|
probably benign |
Het |
Sprtn |
T |
A |
8: 125,626,957 (GRCm39) |
H112Q |
probably damaging |
Het |
Tasor2 |
A |
T |
13: 3,626,054 (GRCm39) |
F1299I |
probably benign |
Het |
Tet2 |
A |
G |
3: 133,173,363 (GRCm39) |
M1633T |
probably benign |
Het |
Tet2 |
T |
A |
3: 133,173,486 (GRCm39) |
D1592V |
probably benign |
Het |
Tmem68 |
A |
T |
4: 3,569,667 (GRCm39) |
C8S |
probably damaging |
Het |
Tnrc6a |
T |
A |
7: 122,771,039 (GRCm39) |
I943N |
probably benign |
Het |
Trib2 |
A |
T |
12: 15,844,069 (GRCm39) |
V191D |
probably damaging |
Het |
Tsc22d4 |
T |
C |
5: 137,760,917 (GRCm39) |
S113P |
probably damaging |
Het |
Ttc21b |
T |
C |
2: 66,069,914 (GRCm39) |
R250G |
probably damaging |
Het |
Ubr2 |
T |
C |
17: 47,278,174 (GRCm39) |
Y721C |
probably damaging |
Het |
Ubtfl1 |
A |
T |
9: 18,320,660 (GRCm39) |
I63F |
probably damaging |
Het |
Ush1c |
G |
A |
7: 45,874,332 (GRCm39) |
P171S |
probably benign |
Het |
Utp20 |
A |
T |
10: 88,603,323 (GRCm39) |
N1843K |
probably damaging |
Het |
Vangl1 |
A |
G |
3: 102,074,253 (GRCm39) |
Y285H |
probably damaging |
Het |
Virma |
A |
G |
4: 11,498,769 (GRCm39) |
D70G |
probably damaging |
Het |
Vmn2r102 |
T |
C |
17: 19,898,277 (GRCm39) |
F431L |
probably benign |
Het |
Wdr87-ps |
T |
A |
7: 29,232,690 (GRCm39) |
|
noncoding transcript |
Het |
Zfp160 |
G |
A |
17: 21,247,268 (GRCm39) |
R606H |
probably benign |
Het |
Zfp369 |
C |
T |
13: 65,444,248 (GRCm39) |
R464C |
probably damaging |
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 |
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 |
R5426: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'- TCATGATGGCTAATGAGACGGCG -3'
(R):5'- AGAGAGCCTCTGAGTTACTCACATTCC -3'
Sequencing Primer
(F):5'- GACGGCGTAAGAATTATAACTCC -3'
(R):5'- AGTTACTCACATTCCTTCATAACTTC -3'
|
Posted On |
2013-07-11 |