Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam17 |
C |
A |
12: 21,390,493 (GRCm39) |
G410C |
probably damaging |
Het |
Adcy3 |
A |
G |
12: 4,254,762 (GRCm39) |
D698G |
probably damaging |
Het |
Afap1 |
T |
A |
5: 36,131,742 (GRCm39) |
N356K |
possibly damaging |
Het |
Afm |
A |
G |
5: 90,671,713 (GRCm39) |
N132D |
probably benign |
Het |
Bsdc1 |
T |
A |
4: 129,359,141 (GRCm39) |
|
probably null |
Het |
Ccdc121rt2 |
T |
G |
5: 112,597,698 (GRCm39) |
Y82D |
not run |
Het |
Ccdc47 |
T |
C |
11: 106,101,143 (GRCm39) |
E173G |
possibly damaging |
Het |
Cit |
T |
G |
5: 116,001,027 (GRCm39) |
F142C |
probably benign |
Het |
Cnga3 |
A |
G |
1: 37,300,852 (GRCm39) |
D524G |
probably damaging |
Het |
Cpne8 |
T |
A |
15: 90,424,450 (GRCm39) |
D313V |
probably damaging |
Het |
Ell3 |
TCTCCTC |
TCTC |
2: 121,269,937 (GRCm39) |
|
probably benign |
Het |
Flrt1 |
C |
A |
19: 7,073,229 (GRCm39) |
L439F |
possibly damaging |
Het |
Gkn1 |
A |
T |
6: 87,325,163 (GRCm39) |
I82N |
probably damaging |
Het |
Gm14410 |
C |
A |
2: 176,885,613 (GRCm39) |
C217F |
probably damaging |
Het |
Gm14412 |
G |
T |
2: 177,007,590 (GRCm39) |
H102N |
probably benign |
Het |
Gm3159 |
A |
T |
14: 4,397,585 (GRCm38) |
|
probably benign |
Het |
Golm2 |
T |
C |
2: 121,764,022 (GRCm39) |
V434A |
probably benign |
Het |
Helz2 |
A |
G |
2: 180,879,782 (GRCm39) |
M612T |
probably benign |
Het |
Iars1 |
T |
A |
13: 49,876,494 (GRCm39) |
I853N |
probably damaging |
Het |
Kcna4 |
A |
C |
2: 107,126,237 (GRCm39) |
I324L |
possibly damaging |
Het |
Kcnh1 |
T |
C |
1: 192,117,183 (GRCm39) |
S690P |
probably damaging |
Het |
Kpna3 |
T |
C |
14: 61,622,182 (GRCm39) |
Y194C |
probably damaging |
Het |
Lrrc56 |
T |
C |
7: 140,789,515 (GRCm39) |
S511P |
probably damaging |
Het |
Ltbp1 |
A |
G |
17: 75,559,351 (GRCm39) |
Y280C |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,420,906 (GRCm39) |
I116T |
probably benign |
Het |
Mmp16 |
A |
T |
4: 18,112,112 (GRCm39) |
N496I |
probably damaging |
Het |
Mon2 |
T |
C |
10: 122,878,236 (GRCm39) |
D229G |
probably benign |
Het |
Or2b2 |
T |
A |
13: 21,887,369 (GRCm39) |
L66Q |
probably damaging |
Het |
Or2j6 |
A |
T |
7: 139,980,377 (GRCm39) |
M194K |
probably damaging |
Het |
Or52s1 |
A |
G |
7: 102,861,186 (GRCm39) |
I40V |
probably benign |
Het |
Or5p61 |
T |
A |
7: 107,758,637 (GRCm39) |
I148F |
probably benign |
Het |
Or5w14 |
G |
T |
2: 87,541,428 (GRCm39) |
T274K |
possibly damaging |
Het |
Pkp1 |
A |
G |
1: 135,817,695 (GRCm39) |
F147L |
possibly damaging |
Het |
Ppp1r3e |
T |
C |
14: 55,114,672 (GRCm39) |
Q30R |
probably damaging |
Het |
Ppp2r5b |
C |
A |
19: 6,282,628 (GRCm39) |
R174L |
probably benign |
Het |
Pramel58 |
A |
G |
5: 94,831,287 (GRCm39) |
D98G |
possibly damaging |
Het |
Qrfprl |
G |
T |
6: 65,433,121 (GRCm39) |
A314S |
possibly damaging |
Het |
Rbm15 |
C |
T |
3: 107,239,459 (GRCm39) |
R313H |
probably damaging |
Het |
Rgs18 |
A |
G |
1: 144,629,603 (GRCm39) |
F219L |
probably damaging |
Het |
Ryr1 |
T |
C |
7: 28,702,985 (GRCm39) |
|
probably null |
Het |
Sirpd |
T |
A |
3: 15,361,723 (GRCm39) |
|
probably null |
Het |
Sirt4 |
T |
G |
5: 115,617,805 (GRCm39) |
I284L |
probably benign |
Het |
Slc25a11 |
A |
G |
11: 70,536,005 (GRCm39) |
V243A |
probably benign |
Het |
Syde1 |
A |
G |
10: 78,425,741 (GRCm39) |
I142T |
probably benign |
Het |
Synj2 |
A |
G |
17: 6,088,098 (GRCm39) |
E1383G |
probably benign |
Het |
Syt4 |
A |
T |
18: 31,573,245 (GRCm39) |
C423* |
probably null |
Het |
Tfr2 |
T |
A |
5: 137,569,986 (GRCm39) |
Y131N |
possibly damaging |
Het |
Tgm1 |
C |
T |
14: 55,949,932 (GRCm39) |
R92Q |
unknown |
Het |
Thoc1 |
A |
T |
18: 9,984,441 (GRCm39) |
D309V |
probably damaging |
Het |
Vmn2r24 |
C |
T |
6: 123,757,422 (GRCm39) |
H97Y |
probably benign |
Het |
Wbp1 |
A |
T |
6: 83,097,176 (GRCm39) |
Y89* |
probably null |
Het |
Wnk1 |
A |
G |
6: 119,926,137 (GRCm39) |
L1358P |
probably benign |
Het |
Zfp14 |
T |
C |
7: 29,738,368 (GRCm39) |
T206A |
possibly damaging |
Het |
Zfp748 |
T |
C |
13: 67,689,608 (GRCm39) |
T551A |
probably benign |
Het |
Zfp9 |
A |
T |
6: 118,441,843 (GRCm39) |
V273E |
probably damaging |
Het |
|
Other mutations in 1110002E22Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0026:1110002E22Rik
|
UTSW |
3 |
137,772,566 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0047:1110002E22Rik
|
UTSW |
3 |
137,772,025 (GRCm39) |
missense |
probably damaging |
0.97 |
R0047:1110002E22Rik
|
UTSW |
3 |
137,772,025 (GRCm39) |
missense |
probably damaging |
0.97 |
R0102:1110002E22Rik
|
UTSW |
3 |
137,773,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R0102:1110002E22Rik
|
UTSW |
3 |
137,773,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R0197:1110002E22Rik
|
UTSW |
3 |
137,775,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:1110002E22Rik
|
UTSW |
3 |
137,771,595 (GRCm39) |
small deletion |
probably benign |
|
R0394:1110002E22Rik
|
UTSW |
3 |
137,773,065 (GRCm39) |
missense |
probably damaging |
0.99 |
R0401:1110002E22Rik
|
UTSW |
3 |
137,776,067 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0496:1110002E22Rik
|
UTSW |
3 |
137,774,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R0591:1110002E22Rik
|
UTSW |
3 |
137,774,704 (GRCm39) |
nonsense |
probably null |
|
R0711:1110002E22Rik
|
UTSW |
3 |
137,773,986 (GRCm39) |
missense |
probably damaging |
0.99 |
R0883:1110002E22Rik
|
UTSW |
3 |
137,775,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R0908:1110002E22Rik
|
UTSW |
3 |
137,775,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R0968:1110002E22Rik
|
UTSW |
3 |
137,772,967 (GRCm39) |
missense |
probably damaging |
0.99 |
R1023:1110002E22Rik
|
UTSW |
3 |
137,772,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R1168:1110002E22Rik
|
UTSW |
3 |
137,773,661 (GRCm39) |
missense |
probably benign |
0.20 |
R1472:1110002E22Rik
|
UTSW |
3 |
137,773,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1538:1110002E22Rik
|
UTSW |
3 |
137,771,162 (GRCm39) |
missense |
probably benign |
0.02 |
R1648:1110002E22Rik
|
UTSW |
3 |
137,775,181 (GRCm39) |
missense |
probably benign |
0.18 |
R1800:1110002E22Rik
|
UTSW |
3 |
137,772,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:1110002E22Rik
|
UTSW |
3 |
137,773,031 (GRCm39) |
missense |
probably damaging |
0.99 |
R1974:1110002E22Rik
|
UTSW |
3 |
137,773,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R1990:1110002E22Rik
|
UTSW |
3 |
137,771,419 (GRCm39) |
nonsense |
probably null |
|
R1991:1110002E22Rik
|
UTSW |
3 |
137,771,419 (GRCm39) |
nonsense |
probably null |
|
R2102:1110002E22Rik
|
UTSW |
3 |
137,770,934 (GRCm39) |
missense |
probably damaging |
0.99 |
R2761:1110002E22Rik
|
UTSW |
3 |
137,773,541 (GRCm39) |
missense |
probably damaging |
0.99 |
R2899:1110002E22Rik
|
UTSW |
3 |
137,771,443 (GRCm39) |
missense |
probably benign |
0.00 |
R3618:1110002E22Rik
|
UTSW |
3 |
137,774,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R3904:1110002E22Rik
|
UTSW |
3 |
137,772,400 (GRCm39) |
missense |
probably benign |
0.15 |
R3955:1110002E22Rik
|
UTSW |
3 |
137,773,834 (GRCm39) |
missense |
probably benign |
0.00 |
R4520:1110002E22Rik
|
UTSW |
3 |
137,776,027 (GRCm39) |
missense |
probably damaging |
0.99 |
R4619:1110002E22Rik
|
UTSW |
3 |
137,775,520 (GRCm39) |
missense |
probably damaging |
0.99 |
R4736:1110002E22Rik
|
UTSW |
3 |
137,774,246 (GRCm39) |
missense |
probably damaging |
0.99 |
R4752:1110002E22Rik
|
UTSW |
3 |
137,775,751 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4777:1110002E22Rik
|
UTSW |
3 |
137,771,503 (GRCm39) |
missense |
probably benign |
0.09 |
R4780:1110002E22Rik
|
UTSW |
3 |
137,771,131 (GRCm39) |
missense |
probably benign |
0.02 |
R4824:1110002E22Rik
|
UTSW |
3 |
137,771,437 (GRCm39) |
missense |
probably benign |
0.00 |
R4829:1110002E22Rik
|
UTSW |
3 |
137,774,780 (GRCm39) |
missense |
probably damaging |
0.99 |
R4965:1110002E22Rik
|
UTSW |
3 |
137,775,433 (GRCm39) |
missense |
probably benign |
|
R5206:1110002E22Rik
|
UTSW |
3 |
137,772,272 (GRCm39) |
missense |
probably benign |
0.00 |
R5212:1110002E22Rik
|
UTSW |
3 |
137,771,611 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5373:1110002E22Rik
|
UTSW |
3 |
137,773,396 (GRCm39) |
missense |
probably benign |
|
R5374:1110002E22Rik
|
UTSW |
3 |
137,773,396 (GRCm39) |
missense |
probably benign |
|
R5506:1110002E22Rik
|
UTSW |
3 |
137,773,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R5528:1110002E22Rik
|
UTSW |
3 |
137,772,260 (GRCm39) |
missense |
probably benign |
|
R5536:1110002E22Rik
|
UTSW |
3 |
137,772,149 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5587:1110002E22Rik
|
UTSW |
3 |
137,771,170 (GRCm39) |
missense |
probably benign |
|
R5759:1110002E22Rik
|
UTSW |
3 |
137,774,419 (GRCm39) |
missense |
probably benign |
|
R5933:1110002E22Rik
|
UTSW |
3 |
137,776,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R5957:1110002E22Rik
|
UTSW |
3 |
137,775,922 (GRCm39) |
missense |
probably benign |
|
R6092:1110002E22Rik
|
UTSW |
3 |
137,774,701 (GRCm39) |
missense |
probably benign |
0.02 |
R6305:1110002E22Rik
|
UTSW |
3 |
137,773,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R6457:1110002E22Rik
|
UTSW |
3 |
137,772,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R6469:1110002E22Rik
|
UTSW |
3 |
137,772,736 (GRCm39) |
missense |
probably damaging |
0.97 |
R6499:1110002E22Rik
|
UTSW |
3 |
137,774,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R6527:1110002E22Rik
|
UTSW |
3 |
137,773,288 (GRCm39) |
missense |
probably damaging |
0.99 |
R6580:1110002E22Rik
|
UTSW |
3 |
137,772,386 (GRCm39) |
missense |
probably benign |
0.00 |
R6693:1110002E22Rik
|
UTSW |
3 |
137,774,915 (GRCm39) |
missense |
probably benign |
0.00 |
R6751:1110002E22Rik
|
UTSW |
3 |
137,771,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R6852:1110002E22Rik
|
UTSW |
3 |
137,770,930 (GRCm39) |
nonsense |
probably null |
|
R6920:1110002E22Rik
|
UTSW |
3 |
137,773,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R7001:1110002E22Rik
|
UTSW |
3 |
137,771,272 (GRCm39) |
missense |
probably benign |
|
R7145:1110002E22Rik
|
UTSW |
3 |
137,775,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R7238:1110002E22Rik
|
UTSW |
3 |
137,775,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:1110002E22Rik
|
UTSW |
3 |
137,771,237 (GRCm39) |
missense |
probably benign |
|
R7425:1110002E22Rik
|
UTSW |
3 |
137,771,456 (GRCm39) |
missense |
probably benign |
0.00 |
R7487:1110002E22Rik
|
UTSW |
3 |
137,772,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R7557:1110002E22Rik
|
UTSW |
3 |
137,774,044 (GRCm39) |
nonsense |
probably null |
|
R7663:1110002E22Rik
|
UTSW |
3 |
137,771,887 (GRCm39) |
missense |
probably damaging |
0.98 |
R7743:1110002E22Rik
|
UTSW |
3 |
137,774,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R8181:1110002E22Rik
|
UTSW |
3 |
137,774,156 (GRCm39) |
missense |
probably damaging |
0.99 |
R8264:1110002E22Rik
|
UTSW |
3 |
137,773,543 (GRCm39) |
missense |
probably damaging |
0.99 |
R8273:1110002E22Rik
|
UTSW |
3 |
137,772,211 (GRCm39) |
missense |
probably benign |
|
R8434:1110002E22Rik
|
UTSW |
3 |
137,773,021 (GRCm39) |
missense |
probably damaging |
0.97 |
R8530:1110002E22Rik
|
UTSW |
3 |
137,774,586 (GRCm39) |
missense |
probably damaging |
0.99 |
R8754:1110002E22Rik
|
UTSW |
3 |
137,771,798 (GRCm39) |
missense |
probably benign |
|
R8808:1110002E22Rik
|
UTSW |
3 |
137,775,874 (GRCm39) |
missense |
probably benign |
0.01 |
R8891:1110002E22Rik
|
UTSW |
3 |
137,772,520 (GRCm39) |
nonsense |
probably null |
|
R9026:1110002E22Rik
|
UTSW |
3 |
137,770,909 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9177:1110002E22Rik
|
UTSW |
3 |
137,775,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R9250:1110002E22Rik
|
UTSW |
3 |
137,772,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R9291:1110002E22Rik
|
UTSW |
3 |
137,772,464 (GRCm39) |
missense |
probably benign |
0.02 |
R9293:1110002E22Rik
|
UTSW |
3 |
137,771,839 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9307:1110002E22Rik
|
UTSW |
3 |
137,771,183 (GRCm39) |
missense |
probably benign |
0.04 |
R9439:1110002E22Rik
|
UTSW |
3 |
137,772,048 (GRCm39) |
missense |
probably benign |
0.00 |
R9509:1110002E22Rik
|
UTSW |
3 |
137,771,595 (GRCm39) |
small deletion |
probably benign |
|
R9582:1110002E22Rik
|
UTSW |
3 |
137,772,766 (GRCm39) |
missense |
probably damaging |
0.99 |
R9599:1110002E22Rik
|
UTSW |
3 |
137,774,267 (GRCm39) |
missense |
probably benign |
0.16 |
R9613:1110002E22Rik
|
UTSW |
3 |
137,771,126 (GRCm39) |
missense |
probably damaging |
0.98 |
R9670:1110002E22Rik
|
UTSW |
3 |
137,770,894 (GRCm39) |
missense |
probably benign |
|
X0003:1110002E22Rik
|
UTSW |
3 |
137,774,857 (GRCm39) |
missense |
probably damaging |
1.00 |
|