Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
A |
G |
2: 68,559,935 (GRCm39) |
T242A |
probably benign |
Het |
Adam24 |
A |
T |
8: 41,133,404 (GRCm39) |
I291L |
probably benign |
Het |
Adamts16 |
G |
A |
13: 70,927,637 (GRCm39) |
|
probably benign |
Het |
Adcy8 |
C |
A |
15: 64,694,056 (GRCm39) |
R407L |
possibly damaging |
Het |
Aldh3b2 |
C |
T |
19: 4,031,133 (GRCm39) |
P461S |
probably benign |
Het |
Araf |
T |
C |
X: 20,717,912 (GRCm39) |
F144L |
probably benign |
Het |
Atp11b |
G |
T |
3: 35,861,091 (GRCm39) |
D193Y |
probably damaging |
Het |
Atp6v1b2 |
C |
A |
8: 69,555,411 (GRCm39) |
|
probably null |
Het |
Bclaf1 |
T |
A |
10: 20,215,624 (GRCm39) |
|
probably benign |
Het |
Cadps |
A |
G |
14: 12,465,935 (GRCm38) |
Y987H |
probably benign |
Het |
Capn6 |
T |
G |
X: 142,587,785 (GRCm39) |
T498P |
possibly damaging |
Het |
Ccdc153 |
T |
A |
9: 44,154,314 (GRCm39) |
L47Q |
probably damaging |
Het |
Ccdc180 |
G |
T |
4: 45,948,856 (GRCm39) |
|
probably null |
Het |
Cep162 |
G |
T |
9: 87,126,384 (GRCm39) |
T176K |
probably benign |
Het |
Cpsf2 |
A |
G |
12: 101,956,088 (GRCm39) |
D297G |
probably benign |
Het |
Entpd8 |
T |
C |
2: 24,975,028 (GRCm39) |
M453T |
probably damaging |
Het |
Eprs1 |
T |
A |
1: 185,099,734 (GRCm39) |
L18Q |
probably damaging |
Het |
Fem1b |
G |
T |
9: 62,704,020 (GRCm39) |
C413* |
probably null |
Het |
Flrt1 |
T |
A |
19: 7,072,723 (GRCm39) |
D608V |
probably damaging |
Het |
Fstl5 |
C |
A |
3: 76,389,659 (GRCm39) |
N285K |
probably damaging |
Het |
Golga1 |
T |
C |
2: 38,913,183 (GRCm39) |
D543G |
probably benign |
Het |
Hivep2 |
A |
G |
10: 14,004,107 (GRCm39) |
H235R |
probably damaging |
Het |
Htr2c |
G |
C |
X: 145,977,186 (GRCm39) |
W325C |
probably damaging |
Het |
Htr2c |
G |
T |
X: 145,977,188 (GRCm39) |
C326F |
probably damaging |
Het |
Ifit1bl2 |
G |
T |
19: 34,596,630 (GRCm39) |
L329M |
possibly damaging |
Het |
Igsf9b |
T |
C |
9: 27,244,792 (GRCm39) |
S920P |
probably damaging |
Het |
Macroh2a1 |
C |
T |
13: 56,232,075 (GRCm39) |
G235S |
probably damaging |
Het |
Mcm8 |
T |
A |
2: 132,662,041 (GRCm39) |
I125K |
possibly damaging |
Het |
Micall1 |
C |
T |
15: 79,014,036 (GRCm39) |
R644W |
probably damaging |
Het |
Myo16 |
G |
A |
8: 10,644,905 (GRCm39) |
D1746N |
possibly damaging |
Het |
Myo9a |
A |
G |
9: 59,801,463 (GRCm39) |
E1887G |
probably benign |
Het |
Nbn |
A |
G |
4: 15,970,904 (GRCm39) |
T296A |
probably benign |
Het |
Nckap1l |
T |
C |
15: 103,364,361 (GRCm39) |
|
probably null |
Het |
Neb |
T |
C |
2: 52,123,007 (GRCm39) |
R3734G |
probably benign |
Het |
Nup93 |
C |
T |
8: 95,030,819 (GRCm39) |
T305I |
probably benign |
Het |
Or5bw2 |
A |
T |
7: 6,573,802 (GRCm39) |
M271L |
probably benign |
Het |
P2ry4 |
A |
G |
X: 99,637,553 (GRCm39) |
L115P |
probably damaging |
Het |
Pmepa1 |
G |
A |
2: 173,069,926 (GRCm39) |
R210W |
probably damaging |
Het |
Ppp1r26 |
T |
C |
2: 28,343,798 (GRCm39) |
F1143L |
possibly damaging |
Het |
Ppp1r3c |
C |
A |
19: 36,711,098 (GRCm39) |
R224L |
probably benign |
Het |
Pwwp2b |
T |
C |
7: 138,835,104 (GRCm39) |
C182R |
probably damaging |
Het |
Reln |
A |
G |
5: 22,192,076 (GRCm39) |
F1455L |
possibly damaging |
Het |
Rufy1 |
C |
T |
11: 50,288,611 (GRCm39) |
|
probably null |
Het |
Samd9l |
T |
C |
6: 3,376,910 (GRCm39) |
H117R |
probably benign |
Het |
Sfxn4 |
C |
T |
19: 60,839,458 (GRCm39) |
G200E |
probably damaging |
Het |
Sipa1l3 |
T |
A |
7: 29,077,364 (GRCm39) |
K803* |
probably null |
Het |
Smim23 |
C |
A |
11: 32,771,870 (GRCm39) |
Q65H |
probably damaging |
Het |
Spata18 |
A |
T |
5: 73,824,244 (GRCm39) |
I156L |
possibly damaging |
Het |
Sppl2b |
G |
A |
10: 80,701,451 (GRCm39) |
V389M |
probably damaging |
Het |
Srbd1 |
T |
C |
17: 86,292,651 (GRCm39) |
I973V |
probably damaging |
Het |
Ssx2ip |
C |
T |
3: 146,123,531 (GRCm39) |
P10L |
probably damaging |
Het |
Taf2 |
A |
C |
15: 54,928,042 (GRCm39) |
D120E |
possibly damaging |
Het |
Tanc1 |
T |
C |
2: 59,555,068 (GRCm39) |
L42S |
probably benign |
Het |
Tex15 |
C |
A |
8: 34,061,265 (GRCm39) |
H232N |
probably benign |
Het |
Tg |
A |
T |
15: 66,545,860 (GRCm39) |
Q194L |
probably damaging |
Het |
Tnfrsf22 |
C |
T |
7: 143,198,513 (GRCm39) |
|
probably null |
Het |
Tro |
A |
T |
X: 149,438,477 (GRCm39) |
M60K |
probably benign |
Het |
Ttc38 |
G |
A |
15: 85,728,704 (GRCm39) |
V219I |
probably benign |
Het |
U2af2 |
T |
C |
7: 5,078,672 (GRCm39) |
I417T |
probably damaging |
Het |
Ube2r2 |
C |
T |
4: 41,174,044 (GRCm39) |
H61Y |
probably benign |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Vmn1r113 |
C |
T |
7: 20,521,832 (GRCm39) |
S208F |
probably damaging |
Het |
Wdr35 |
A |
G |
12: 9,024,955 (GRCm39) |
K16E |
possibly damaging |
Het |
Wwp1 |
A |
T |
4: 19,641,745 (GRCm39) |
Y437N |
probably damaging |
Het |
Zdhhc4 |
A |
C |
5: 143,306,162 (GRCm39) |
W189G |
probably damaging |
Het |
Zfp512 |
A |
T |
5: 31,622,919 (GRCm39) |
K73N |
probably damaging |
Het |
|
Other mutations in Ptafr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00707:Ptafr
|
APN |
4 |
132,307,569 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02643:Ptafr
|
APN |
4 |
132,307,437 (GRCm39) |
missense |
probably benign |
0.28 |
R0035:Ptafr
|
UTSW |
4 |
132,306,864 (GRCm39) |
missense |
probably benign |
0.15 |
R0035:Ptafr
|
UTSW |
4 |
132,306,864 (GRCm39) |
missense |
probably benign |
0.15 |
R0346:Ptafr
|
UTSW |
4 |
132,307,390 (GRCm39) |
nonsense |
probably null |
|
R0455:Ptafr
|
UTSW |
4 |
132,307,396 (GRCm39) |
missense |
probably benign |
0.00 |
R1982:Ptafr
|
UTSW |
4 |
132,307,296 (GRCm39) |
missense |
probably damaging |
0.99 |
R4051:Ptafr
|
UTSW |
4 |
132,307,305 (GRCm39) |
missense |
probably benign |
0.23 |
R5499:Ptafr
|
UTSW |
4 |
132,306,646 (GRCm39) |
missense |
probably damaging |
0.98 |
R5979:Ptafr
|
UTSW |
4 |
132,306,616 (GRCm39) |
missense |
probably benign |
0.03 |
R6755:Ptafr
|
UTSW |
4 |
132,306,657 (GRCm39) |
missense |
probably benign |
0.09 |
R7577:Ptafr
|
UTSW |
4 |
132,307,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R9228:Ptafr
|
UTSW |
4 |
132,306,613 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
Z1176:Ptafr
|
UTSW |
4 |
132,307,273 (GRCm39) |
missense |
probably benign |
0.00 |
|