Incidental Mutation 'R1768:Wdr17'
ID |
194593 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Wdr17
|
Ensembl Gene |
ENSMUSG00000039375 |
Gene Name |
WD repeat domain 17 |
Synonyms |
B230207L18Rik, 3010002I12Rik |
MMRRC Submission |
039799-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1768 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
55082316-55180014 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 55126689 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glutamic Acid
at position 388
(D388E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000117710
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000127511]
[ENSMUST00000144482]
[ENSMUST00000144711]
[ENSMUST00000150488]
[ENSMUST00000175915]
|
AlphaFold |
E9Q271 |
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126316
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000127511
AA Change: D405E
PolyPhen 2
Score 0.746 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000115550 Gene: ENSMUSG00000039375 AA Change: D405E
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 |
possibly damaging
Transcript: ENSMUST00000144482
AA Change: D92E
PolyPhen 2
Score 0.798 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000134950 Gene: ENSMUSG00000039375 AA Change: D92E
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 |
possibly damaging
Transcript: ENSMUST00000144711
AA Change: D388E
PolyPhen 2
Score 0.840 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000117710 Gene: ENSMUSG00000039375 AA Change: D388E
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 |
possibly damaging
Transcript: ENSMUST00000150488
AA Change: D381E
PolyPhen 2
Score 0.644 (Sensitivity: 0.87; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000122326 Gene: ENSMUSG00000039375 AA Change: D381E
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 |
possibly damaging
Transcript: ENSMUST00000175915
AA Change: D381E
PolyPhen 2
Score 0.837 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000135805 Gene: ENSMUSG00000039375 AA Change: D381E
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 |
0.0827 |
Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.9%
- 10x: 95.3%
- 20x: 92.4%
|
Validation Efficiency |
91% (107/117) |
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: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921524L21Rik |
G |
C |
18: 6,623,470 (GRCm39) |
R60P |
possibly damaging |
Het |
Aox1 |
T |
A |
1: 58,393,354 (GRCm39) |
C1199S |
probably benign |
Het |
Arhgap18 |
G |
A |
10: 26,763,857 (GRCm39) |
M482I |
probably damaging |
Het |
Arhgap18 |
G |
T |
10: 26,763,858 (GRCm39) |
A483S |
probably damaging |
Het |
Arid4a |
G |
A |
12: 71,122,112 (GRCm39) |
S509N |
probably benign |
Het |
BC051019 |
T |
C |
7: 109,322,381 (GRCm39) |
T38A |
probably benign |
Het |
Bcam |
T |
C |
7: 19,499,543 (GRCm39) |
N192S |
probably null |
Het |
Bend5 |
A |
T |
4: 111,311,438 (GRCm39) |
K351* |
probably null |
Het |
Bicdl2 |
T |
A |
17: 23,884,923 (GRCm39) |
M208K |
probably damaging |
Het |
Ccp110 |
A |
T |
7: 118,325,247 (GRCm39) |
|
probably null |
Het |
Cdc6 |
A |
T |
11: 98,803,043 (GRCm39) |
T328S |
probably damaging |
Het |
Cdk5rap2 |
G |
T |
4: 70,225,470 (GRCm39) |
N558K |
probably benign |
Het |
Cdkn1c |
C |
T |
7: 143,012,858 (GRCm39) |
R146K |
probably benign |
Het |
Ceacam18 |
G |
A |
7: 43,297,918 (GRCm39) |
C371Y |
probably benign |
Het |
Cep95 |
T |
A |
11: 106,697,177 (GRCm39) |
C233* |
probably null |
Het |
Chrnd |
A |
G |
1: 87,122,650 (GRCm39) |
I144V |
probably benign |
Het |
Col6a4 |
T |
A |
9: 105,957,299 (GRCm39) |
Q175L |
probably benign |
Het |
Cym |
A |
T |
3: 107,120,816 (GRCm39) |
V263E |
probably damaging |
Het |
Cyp2a4 |
G |
T |
7: 26,012,197 (GRCm39) |
V327F |
possibly damaging |
Het |
Dhx29 |
T |
A |
13: 113,084,774 (GRCm39) |
M664K |
probably damaging |
Het |
Dlec1 |
T |
G |
9: 118,975,075 (GRCm39) |
|
probably null |
Het |
Dna2 |
T |
C |
10: 62,792,863 (GRCm39) |
Y293H |
probably benign |
Het |
Dnase1l3 |
T |
A |
14: 7,974,104 (GRCm38) |
N196Y |
probably damaging |
Het |
Eea1 |
T |
A |
10: 95,832,822 (GRCm39) |
D222E |
probably damaging |
Het |
Efcab14 |
A |
T |
4: 115,610,116 (GRCm39) |
|
probably null |
Het |
Entpd5 |
C |
T |
12: 84,432,985 (GRCm39) |
R189H |
probably benign |
Het |
Exoc4 |
A |
T |
6: 33,734,985 (GRCm39) |
K534M |
probably damaging |
Het |
Extl1 |
T |
A |
4: 134,098,449 (GRCm39) |
Y194F |
probably benign |
Het |
Eya1 |
A |
G |
1: 14,323,299 (GRCm39) |
L161S |
possibly damaging |
Het |
Fam163b |
T |
C |
2: 27,002,874 (GRCm39) |
E41G |
possibly damaging |
Het |
Fam180a |
A |
C |
6: 35,292,287 (GRCm39) |
S40A |
probably benign |
Het |
Fbxl4 |
T |
C |
4: 22,385,950 (GRCm39) |
S186P |
probably benign |
Het |
Fbxw19 |
A |
T |
9: 109,323,840 (GRCm39) |
L45* |
probably null |
Het |
Fgf14 |
G |
T |
14: 124,913,924 (GRCm39) |
T69N |
probably benign |
Het |
Flt1 |
A |
G |
5: 147,609,519 (GRCm39) |
Y432H |
probably damaging |
Het |
Frmd4b |
A |
T |
6: 97,283,725 (GRCm39) |
L374Q |
possibly damaging |
Het |
G6pc2 |
T |
A |
2: 69,053,321 (GRCm39) |
V125D |
probably damaging |
Het |
Gm10033 |
T |
C |
8: 69,826,210 (GRCm39) |
I119M |
unknown |
Het |
Gna15 |
A |
T |
10: 81,347,954 (GRCm39) |
L164Q |
probably damaging |
Het |
Gnaz |
C |
A |
10: 74,827,702 (GRCm39) |
D151E |
possibly damaging |
Het |
Has1 |
T |
C |
17: 18,070,562 (GRCm39) |
T120A |
probably benign |
Het |
Hectd4 |
T |
A |
5: 121,496,366 (GRCm39) |
D3919E |
possibly damaging |
Het |
Hs3st5 |
A |
G |
10: 36,709,165 (GRCm39) |
I233M |
probably benign |
Het |
Ilf3 |
T |
C |
9: 21,314,438 (GRCm39) |
|
probably benign |
Het |
Inpp5b |
T |
A |
4: 124,687,069 (GRCm39) |
L765* |
probably null |
Het |
Insr |
A |
T |
8: 3,209,561 (GRCm39) |
I1174N |
probably damaging |
Het |
Kash5 |
T |
A |
7: 44,838,227 (GRCm39) |
|
probably null |
Het |
Kcnq3 |
A |
G |
15: 65,877,755 (GRCm39) |
L445P |
probably damaging |
Het |
Kctd20 |
A |
T |
17: 29,181,824 (GRCm39) |
N159Y |
probably damaging |
Het |
Kctd20 |
A |
T |
17: 29,185,755 (GRCm39) |
D366V |
probably damaging |
Het |
Klk15 |
T |
C |
7: 43,587,757 (GRCm39) |
|
probably benign |
Het |
Lama4 |
T |
G |
10: 38,979,497 (GRCm39) |
N1658K |
possibly damaging |
Het |
Lonrf2 |
G |
A |
1: 38,852,357 (GRCm39) |
P165S |
probably benign |
Het |
Mas1 |
T |
C |
17: 13,060,586 (GRCm39) |
Y279C |
probably damaging |
Het |
Mast2 |
G |
T |
4: 116,164,156 (GRCm39) |
D1747E |
probably damaging |
Het |
Mest |
G |
A |
6: 30,745,138 (GRCm39) |
M235I |
probably benign |
Het |
Mfsd6 |
A |
G |
1: 52,699,964 (GRCm39) |
|
probably null |
Het |
Mllt10 |
T |
A |
2: 18,167,657 (GRCm39) |
S449R |
probably damaging |
Het |
Mon2 |
T |
A |
10: 122,849,668 (GRCm39) |
T1211S |
probably benign |
Het |
Mrnip |
G |
A |
11: 50,067,688 (GRCm39) |
C27Y |
probably damaging |
Het |
Myh15 |
A |
T |
16: 48,983,498 (GRCm39) |
T1538S |
probably benign |
Het |
Nfatc2ip |
A |
G |
7: 125,989,634 (GRCm39) |
V250A |
probably benign |
Het |
Npy1r |
A |
G |
8: 67,157,177 (GRCm39) |
D199G |
possibly damaging |
Het |
Numbl |
A |
G |
7: 26,980,379 (GRCm39) |
T454A |
probably benign |
Het |
Nutm2 |
T |
G |
13: 50,627,152 (GRCm39) |
F436V |
probably damaging |
Het |
Opa1 |
T |
C |
16: 29,439,628 (GRCm39) |
S773P |
probably benign |
Het |
Or12e1 |
T |
A |
2: 87,022,042 (GRCm39) |
S4T |
probably benign |
Het |
Or2d3 |
A |
T |
7: 106,491,184 (GRCm39) |
|
probably null |
Het |
Or2d3 |
G |
T |
7: 106,491,185 (GRCm39) |
L44M |
probably damaging |
Het |
Or2r11 |
A |
G |
6: 42,437,611 (GRCm39) |
L114S |
probably damaging |
Het |
Or2t48 |
A |
G |
11: 58,420,602 (GRCm39) |
L70P |
probably damaging |
Het |
Or51b17 |
A |
G |
7: 103,542,484 (GRCm39) |
S153P |
probably benign |
Het |
Or51m1 |
C |
T |
7: 103,578,932 (GRCm39) |
R301* |
probably null |
Het |
Or52e7 |
A |
G |
7: 104,685,157 (GRCm39) |
S251G |
probably benign |
Het |
Or52i2 |
A |
G |
7: 102,319,508 (GRCm39) |
Y127C |
probably damaging |
Het |
Or8b12c |
T |
A |
9: 37,715,599 (GRCm39) |
Y131N |
probably damaging |
Het |
Pde8a |
G |
C |
7: 80,950,471 (GRCm39) |
|
probably null |
Het |
Pgam1 |
T |
C |
19: 41,906,144 (GRCm39) |
F232S |
probably damaging |
Het |
Pgk1 |
T |
A |
X: 105,243,914 (GRCm39) |
V303E |
possibly damaging |
Het |
Pirb |
A |
T |
7: 3,720,189 (GRCm39) |
C395S |
probably damaging |
Het |
Plxnc1 |
C |
T |
10: 94,680,184 (GRCm39) |
V824I |
probably benign |
Het |
Ppp6r1 |
A |
G |
7: 4,636,691 (GRCm39) |
|
probably null |
Het |
Rapgef4 |
C |
A |
2: 72,056,131 (GRCm39) |
|
probably benign |
Het |
Rars1 |
T |
A |
11: 35,700,465 (GRCm39) |
T539S |
probably damaging |
Het |
Rbm44 |
G |
T |
1: 91,081,679 (GRCm39) |
|
probably null |
Het |
Samd4b |
A |
G |
7: 28,113,317 (GRCm39) |
I216T |
probably benign |
Het |
Serpine2 |
A |
C |
1: 79,794,532 (GRCm39) |
F134V |
probably damaging |
Het |
Shmt1 |
A |
G |
11: 60,683,790 (GRCm39) |
Y341H |
probably damaging |
Het |
Slc23a2 |
C |
A |
2: 131,917,561 (GRCm39) |
V226F |
probably benign |
Het |
Slc23a4 |
A |
G |
6: 34,933,896 (GRCm39) |
I69T |
probably damaging |
Het |
Slc37a1 |
C |
A |
17: 31,552,652 (GRCm39) |
T319K |
possibly damaging |
Het |
Slc6a4 |
A |
T |
11: 76,904,078 (GRCm39) |
T178S |
probably damaging |
Het |
Smarca4 |
G |
A |
9: 21,612,479 (GRCm39) |
A1588T |
possibly damaging |
Het |
Spag17 |
A |
T |
3: 99,934,668 (GRCm39) |
Y650F |
possibly damaging |
Het |
Stab2 |
C |
T |
10: 86,838,872 (GRCm39) |
G65S |
probably damaging |
Het |
Stambpl1 |
C |
G |
19: 34,204,121 (GRCm39) |
N70K |
probably damaging |
Het |
Stip1 |
C |
A |
19: 6,999,165 (GRCm39) |
C471F |
probably damaging |
Het |
Taf1 |
T |
C |
X: 100,584,500 (GRCm39) |
S223P |
probably benign |
Het |
Tchh |
C |
A |
3: 93,350,882 (GRCm39) |
N107K |
possibly damaging |
Het |
Tenm3 |
A |
C |
8: 48,685,139 (GRCm39) |
H2432Q |
probably damaging |
Het |
Tmem243 |
A |
G |
5: 9,168,548 (GRCm39) |
N110S |
probably damaging |
Het |
Toe1 |
A |
T |
4: 116,662,076 (GRCm39) |
I306F |
probably benign |
Het |
Trank1 |
G |
A |
9: 111,221,995 (GRCm39) |
V2911M |
probably damaging |
Het |
Trpm4 |
A |
G |
7: 44,958,036 (GRCm39) |
I811T |
probably damaging |
Het |
Tspear |
T |
A |
10: 77,710,950 (GRCm39) |
|
probably null |
Het |
Ttc28 |
A |
T |
5: 111,425,034 (GRCm39) |
I1589F |
possibly damaging |
Het |
Tubgcp3 |
A |
G |
8: 12,699,686 (GRCm39) |
|
probably benign |
Het |
U2af2 |
C |
A |
7: 5,070,544 (GRCm39) |
R78S |
probably benign |
Het |
Wdr3 |
A |
T |
3: 100,061,186 (GRCm39) |
S261T |
probably benign |
Het |
Zfp667 |
A |
G |
7: 6,308,066 (GRCm39) |
N245D |
possibly damaging |
Het |
Zfp692 |
A |
G |
11: 58,201,002 (GRCm39) |
|
probably benign |
Het |
Zfp729a |
T |
C |
13: 67,767,370 (GRCm39) |
H953R |
probably benign |
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 |
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'- TGTGCTAAAATCTTACACCTCACAGCAG -3'
(R):5'- GAAATCCGAAATTCAGAACACTTGGTCC -3'
Sequencing Primer
(F):5'- GCTGAGCTGATCAAATATTGCCAG -3'
(R):5'- ATTCAGAACACTTGGTCCTTAGTC -3'
|
Posted On |
2014-05-23 |