Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110032F04Rik |
C |
T |
3: 68,777,402 (GRCm39) |
P121L |
probably damaging |
Het |
4930442H23Rik |
C |
T |
10: 81,018,976 (GRCm39) |
V16I |
unknown |
Het |
4930444P10Rik |
T |
C |
1: 16,139,051 (GRCm39) |
M97V |
probably benign |
Het |
Abcb1a |
A |
T |
5: 8,797,353 (GRCm39) |
|
probably null |
Het |
Abhd5 |
T |
C |
9: 122,197,035 (GRCm39) |
I74T |
probably benign |
Het |
Ankle2 |
T |
A |
5: 110,399,409 (GRCm39) |
F590I |
probably damaging |
Het |
C2cd6 |
T |
C |
1: 59,097,848 (GRCm39) |
S414G |
probably benign |
Het |
Catsperd |
G |
A |
17: 56,968,252 (GRCm39) |
D546N |
probably benign |
Het |
Cep295nl |
G |
T |
11: 118,224,000 (GRCm39) |
H281Q |
possibly damaging |
Het |
Cfap69 |
T |
C |
5: 5,639,164 (GRCm39) |
E670G |
probably damaging |
Het |
Cfh |
A |
T |
1: 140,090,718 (GRCm39) |
V90E |
possibly damaging |
Het |
Cnksr3 |
A |
C |
10: 7,079,021 (GRCm39) |
|
probably null |
Het |
Cntrl |
T |
A |
2: 35,035,077 (GRCm39) |
F901L |
probably benign |
Het |
Coch |
T |
A |
12: 51,645,034 (GRCm39) |
M196K |
probably damaging |
Het |
Crygd |
T |
C |
1: 65,102,369 (GRCm39) |
N34S |
probably damaging |
Het |
Ctdp1 |
A |
T |
18: 80,492,962 (GRCm39) |
I511N |
probably benign |
Het |
Dhx30 |
C |
T |
9: 109,926,186 (GRCm39) |
A142T |
probably damaging |
Het |
Dlg2 |
T |
C |
7: 92,087,284 (GRCm39) |
|
probably null |
Het |
Dmxl1 |
A |
G |
18: 49,998,228 (GRCm39) |
D776G |
probably damaging |
Het |
Dnm3 |
C |
T |
1: 162,149,354 (GRCm39) |
G197D |
probably damaging |
Het |
Eif4g3 |
A |
G |
4: 137,824,190 (GRCm39) |
H91R |
probably damaging |
Het |
Ephb6 |
A |
G |
6: 41,596,258 (GRCm39) |
M844V |
probably damaging |
Het |
Erc1 |
T |
C |
6: 119,773,902 (GRCm39) |
E351G |
probably benign |
Het |
Etfbkmt |
G |
A |
6: 149,045,744 (GRCm39) |
G33R |
probably benign |
Het |
Fnbp4 |
T |
C |
2: 90,588,738 (GRCm39) |
I503T |
probably benign |
Het |
Gm6370 |
A |
T |
5: 146,429,993 (GRCm39) |
Q143L |
probably benign |
Het |
Gnas |
T |
C |
2: 174,141,988 (GRCm39) |
V719A |
possibly damaging |
Het |
H13 |
C |
A |
2: 152,530,873 (GRCm39) |
D219E |
probably damaging |
Het |
Hhatl |
G |
A |
9: 121,618,191 (GRCm39) |
T188I |
possibly damaging |
Het |
Ifi27l2b |
C |
T |
12: 103,422,683 (GRCm39) |
A45T |
probably damaging |
Het |
Kbtbd8 |
T |
C |
6: 95,103,874 (GRCm39) |
C585R |
possibly damaging |
Het |
Limk2 |
A |
G |
11: 3,297,715 (GRCm39) |
S473P |
probably damaging |
Het |
Lrba |
G |
A |
3: 86,267,169 (GRCm39) |
G1620S |
probably benign |
Het |
Lrrtm2 |
T |
C |
18: 35,346,490 (GRCm39) |
T271A |
probably benign |
Het |
Map3k4 |
A |
G |
17: 12,476,871 (GRCm39) |
S759P |
possibly damaging |
Het |
Mybphl |
G |
T |
3: 108,282,952 (GRCm39) |
V247F |
possibly damaging |
Het |
Myh10 |
T |
A |
11: 68,682,815 (GRCm39) |
V1120D |
probably benign |
Het |
Naip1 |
T |
C |
13: 100,569,821 (GRCm39) |
N271S |
probably benign |
Het |
Napepld |
C |
T |
5: 21,875,561 (GRCm39) |
V328I |
probably damaging |
Het |
Nucb1 |
A |
G |
7: 45,148,159 (GRCm39) |
V218A |
probably benign |
Het |
Nup107 |
A |
T |
10: 117,593,238 (GRCm39) |
D813E |
probably benign |
Het |
Or14j3 |
T |
A |
17: 37,901,053 (GRCm39) |
K64* |
probably null |
Het |
Or5g29 |
T |
A |
2: 85,421,279 (GRCm39) |
Y132N |
probably damaging |
Het |
Or6c35 |
A |
T |
10: 129,168,794 (GRCm39) |
T15S |
probably damaging |
Het |
Or8g52 |
A |
G |
9: 39,630,678 (GRCm39) |
S52G |
possibly damaging |
Het |
Pabpc2 |
T |
C |
18: 39,907,602 (GRCm39) |
I289T |
probably benign |
Het |
Patj |
T |
C |
4: 98,393,991 (GRCm39) |
F975L |
probably benign |
Het |
Pcdhb17 |
A |
G |
18: 37,618,218 (GRCm39) |
T3A |
probably benign |
Het |
Piezo2 |
T |
C |
18: 63,248,108 (GRCm39) |
E464G |
probably benign |
Het |
Pkd1 |
T |
A |
17: 24,800,341 (GRCm39) |
V3034D |
probably damaging |
Het |
Pld2 |
A |
G |
11: 70,447,944 (GRCm39) |
E869G |
probably damaging |
Het |
Plek |
T |
A |
11: 16,945,311 (GRCm39) |
L29F |
possibly damaging |
Het |
Prelp |
A |
G |
1: 133,842,416 (GRCm39) |
L243P |
probably damaging |
Het |
Rapgef5 |
T |
A |
12: 117,621,930 (GRCm39) |
D231E |
probably benign |
Het |
Riok1 |
A |
G |
13: 38,244,016 (GRCm39) |
E514G |
probably benign |
Het |
Rmdn2 |
T |
C |
17: 79,928,790 (GRCm39) |
M14T |
probably benign |
Het |
Rorb |
G |
A |
19: 18,939,499 (GRCm39) |
Q228* |
probably null |
Het |
Scmh1 |
T |
A |
4: 120,340,827 (GRCm39) |
M171K |
probably damaging |
Het |
Scn9a |
A |
G |
2: 66,392,809 (GRCm39) |
L261P |
probably damaging |
Het |
Senp7 |
A |
T |
16: 55,971,652 (GRCm39) |
N263I |
probably benign |
Het |
Slc11a1 |
G |
T |
1: 74,419,041 (GRCm39) |
A162S |
probably benign |
Het |
Slc6a17 |
A |
G |
3: 107,384,685 (GRCm39) |
V305A |
probably damaging |
Het |
Snph |
A |
T |
2: 151,435,422 (GRCm39) |
V502E |
probably damaging |
Het |
Sost |
G |
T |
11: 101,854,892 (GRCm39) |
A139E |
possibly damaging |
Het |
Srp54a |
A |
T |
12: 55,136,061 (GRCm39) |
E25D |
probably benign |
Het |
Tmeff1 |
T |
A |
4: 48,636,940 (GRCm39) |
C213S |
probably damaging |
Het |
Tmem232 |
A |
T |
17: 65,807,180 (GRCm39) |
Y4* |
probably null |
Het |
Tmem63c |
T |
G |
12: 87,103,361 (GRCm39) |
I45S |
probably benign |
Het |
Ttbk1 |
C |
T |
17: 46,757,998 (GRCm39) |
G879S |
probably damaging |
Het |
Ugt1a7c |
A |
G |
1: 88,022,952 (GRCm39) |
H37R |
probably damaging |
Het |
Vmn1r236 |
T |
C |
17: 21,507,053 (GRCm39) |
L57P |
probably damaging |
Het |
Wnk2 |
T |
A |
13: 49,192,453 (GRCm39) |
E675V |
unknown |
Het |
Wnt10b |
T |
C |
15: 98,674,609 (GRCm39) |
T43A |
probably damaging |
Het |
Wnt8a |
C |
A |
18: 34,680,163 (GRCm39) |
T176K |
probably benign |
Het |
Zfp937 |
T |
A |
2: 150,080,452 (GRCm39) |
C161S |
probably damaging |
Het |
|
Other mutations in Parg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01324:Parg
|
APN |
14 |
32,018,142 (GRCm39) |
splice site |
probably benign |
|
IGL01879:Parg
|
APN |
14 |
31,993,579 (GRCm39) |
splice site |
probably benign |
|
IGL02391:Parg
|
APN |
14 |
31,984,638 (GRCm39) |
splice site |
probably null |
|
IGL02451:Parg
|
APN |
14 |
31,964,186 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02598:Parg
|
APN |
14 |
31,936,281 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02899:Parg
|
APN |
14 |
31,960,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R0112:Parg
|
UTSW |
14 |
31,924,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R0167:Parg
|
UTSW |
14 |
31,939,693 (GRCm39) |
critical splice donor site |
probably null |
|
R0514:Parg
|
UTSW |
14 |
31,976,517 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0834:Parg
|
UTSW |
14 |
31,936,511 (GRCm39) |
splice site |
probably benign |
|
R1140:Parg
|
UTSW |
14 |
32,018,200 (GRCm39) |
missense |
probably benign |
0.01 |
R1480:Parg
|
UTSW |
14 |
31,931,585 (GRCm39) |
nonsense |
probably null |
|
R1611:Parg
|
UTSW |
14 |
31,960,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R1912:Parg
|
UTSW |
14 |
31,932,497 (GRCm39) |
missense |
probably damaging |
0.99 |
R1916:Parg
|
UTSW |
14 |
31,930,184 (GRCm39) |
splice site |
probably benign |
|
R1983:Parg
|
UTSW |
14 |
31,939,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R2007:Parg
|
UTSW |
14 |
31,932,531 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2275:Parg
|
UTSW |
14 |
32,017,195 (GRCm39) |
missense |
probably damaging |
0.98 |
R2942:Parg
|
UTSW |
14 |
31,931,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R4206:Parg
|
UTSW |
14 |
31,976,493 (GRCm39) |
missense |
probably benign |
0.07 |
R4482:Parg
|
UTSW |
14 |
31,984,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R4512:Parg
|
UTSW |
14 |
31,984,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R4519:Parg
|
UTSW |
14 |
31,931,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R4611:Parg
|
UTSW |
14 |
31,996,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R4831:Parg
|
UTSW |
14 |
31,924,408 (GRCm39) |
missense |
probably benign |
0.00 |
R4876:Parg
|
UTSW |
14 |
31,993,625 (GRCm39) |
missense |
probably damaging |
0.98 |
R5298:Parg
|
UTSW |
14 |
31,924,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R5606:Parg
|
UTSW |
14 |
31,984,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R5782:Parg
|
UTSW |
14 |
31,996,862 (GRCm39) |
nonsense |
probably null |
|
R5878:Parg
|
UTSW |
14 |
31,939,619 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6373:Parg
|
UTSW |
14 |
31,931,454 (GRCm39) |
splice site |
probably null |
|
R6436:Parg
|
UTSW |
14 |
31,993,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R6530:Parg
|
UTSW |
14 |
31,931,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R7285:Parg
|
UTSW |
14 |
31,932,465 (GRCm39) |
missense |
probably damaging |
0.98 |
R7348:Parg
|
UTSW |
14 |
31,972,036 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7455:Parg
|
UTSW |
14 |
31,931,432 (GRCm39) |
missense |
probably benign |
|
R7780:Parg
|
UTSW |
14 |
31,930,758 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7887:Parg
|
UTSW |
14 |
31,939,619 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7968:Parg
|
UTSW |
14 |
31,936,327 (GRCm39) |
missense |
possibly damaging |
0.57 |
R8153:Parg
|
UTSW |
14 |
31,984,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R8494:Parg
|
UTSW |
14 |
31,930,978 (GRCm39) |
missense |
probably benign |
0.04 |
R8717:Parg
|
UTSW |
14 |
31,932,492 (GRCm39) |
missense |
probably benign |
0.00 |
R8781:Parg
|
UTSW |
14 |
31,936,400 (GRCm39) |
missense |
probably benign |
0.33 |
R8826:Parg
|
UTSW |
14 |
31,931,175 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9357:Parg
|
UTSW |
14 |
31,996,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R9423:Parg
|
UTSW |
14 |
31,939,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R9662:Parg
|
UTSW |
14 |
31,971,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R9666:Parg
|
UTSW |
14 |
31,964,294 (GRCm39) |
missense |
probably damaging |
1.00 |
|