Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,226,959 (GRCm39) |
S572P |
probably damaging |
Het |
Abca13 |
T |
C |
11: 9,247,833 (GRCm39) |
Y2527H |
probably damaging |
Het |
Abcc5 |
A |
G |
16: 20,241,173 (GRCm39) |
I4T |
possibly damaging |
Het |
Adamts12 |
C |
T |
15: 11,317,365 (GRCm39) |
T1355I |
probably benign |
Het |
Aloxe3 |
A |
G |
11: 69,018,353 (GRCm39) |
T117A |
probably benign |
Het |
Asb15 |
A |
G |
6: 24,556,555 (GRCm39) |
I17V |
probably benign |
Het |
Atf2 |
A |
G |
2: 73,672,777 (GRCm39) |
V194A |
probably benign |
Het |
Capn7 |
T |
C |
14: 31,071,779 (GRCm39) |
V221A |
probably benign |
Het |
Cct4 |
C |
T |
11: 22,946,420 (GRCm39) |
T162I |
probably benign |
Het |
Cdc40 |
A |
T |
10: 40,717,439 (GRCm39) |
H417Q |
probably damaging |
Het |
Celf1 |
A |
G |
2: 90,833,588 (GRCm39) |
I115V |
probably benign |
Het |
Ces3a |
A |
G |
8: 105,783,056 (GRCm39) |
Y395C |
probably damaging |
Het |
Cfh |
C |
A |
1: 140,033,204 (GRCm39) |
C798F |
probably damaging |
Het |
Clstn3 |
T |
C |
6: 124,435,088 (GRCm39) |
T313A |
probably benign |
Het |
Crmp1 |
T |
A |
5: 37,436,229 (GRCm39) |
M329K |
probably benign |
Het |
Csf2ra |
C |
T |
19: 61,215,491 (GRCm39) |
A76T |
possibly damaging |
Het |
Cspg4 |
T |
A |
9: 56,795,727 (GRCm39) |
V1154E |
possibly damaging |
Het |
Cyp2a4 |
A |
T |
7: 26,014,188 (GRCm39) |
N455I |
probably benign |
Het |
Cyp4a32 |
T |
G |
4: 115,468,234 (GRCm39) |
M268R |
probably benign |
Het |
Dcaf13 |
T |
A |
15: 38,993,615 (GRCm39) |
I236N |
probably damaging |
Het |
Dennd2a |
A |
G |
6: 39,500,397 (GRCm39) |
I56T |
probably damaging |
Het |
Eif2d |
T |
A |
1: 131,098,793 (GRCm39) |
S530R |
probably benign |
Het |
Ep300 |
T |
A |
15: 81,532,715 (GRCm39) |
M1651K |
unknown |
Het |
Epha3 |
G |
A |
16: 63,418,657 (GRCm39) |
T596I |
probably damaging |
Het |
Fam171a2 |
C |
T |
11: 102,329,628 (GRCm39) |
C377Y |
possibly damaging |
Het |
Fat4 |
T |
A |
3: 39,054,385 (GRCm39) |
N4142K |
probably damaging |
Het |
Galnt5 |
C |
A |
2: 57,904,937 (GRCm39) |
S500Y |
probably damaging |
Het |
Gas6 |
A |
G |
8: 13,521,456 (GRCm39) |
V431A |
probably benign |
Het |
Gm7544 |
C |
T |
1: 82,933,502 (GRCm39) |
C56Y |
unknown |
Het |
Golgb1 |
T |
A |
16: 36,733,281 (GRCm39) |
L884I |
possibly damaging |
Het |
Gpatch2l |
T |
G |
12: 86,312,025 (GRCm39) |
|
probably null |
Het |
Gpr33 |
T |
C |
12: 52,070,050 (GRCm39) |
T330A |
probably benign |
Het |
H2bw2 |
G |
A |
X: 135,828,471 (GRCm39) |
R120K |
unknown |
Het |
Ifi205 |
A |
G |
1: 173,855,874 (GRCm39) |
M52T |
possibly damaging |
Het |
Ino80 |
A |
T |
2: 119,210,495 (GRCm39) |
D1346E |
probably benign |
Het |
Ino80c |
T |
C |
18: 24,241,836 (GRCm39) |
K183R |
unknown |
Het |
Itgal |
G |
T |
7: 126,906,047 (GRCm39) |
R379L |
probably benign |
Het |
Itih3 |
T |
A |
14: 30,636,730 (GRCm39) |
T582S |
probably benign |
Het |
Kcnb2 |
T |
C |
1: 15,781,251 (GRCm39) |
S708P |
possibly damaging |
Het |
Kcnt1 |
A |
T |
2: 25,806,011 (GRCm39) |
Y1200F |
probably benign |
Het |
L3mbtl4 |
G |
A |
17: 68,948,537 (GRCm39) |
D473N |
probably benign |
Het |
Lama1 |
T |
G |
17: 68,024,169 (GRCm39) |
I89R |
|
Het |
Lama2 |
A |
G |
10: 27,142,630 (GRCm39) |
I616T |
probably benign |
Het |
Lipm |
A |
C |
19: 34,093,881 (GRCm39) |
D266A |
probably benign |
Het |
Lrrc4c |
A |
T |
2: 97,460,106 (GRCm39) |
H244L |
probably benign |
Het |
Lrrtm3 |
T |
C |
10: 63,923,925 (GRCm39) |
E414G |
probably damaging |
Het |
Ltbp4 |
A |
G |
7: 27,029,192 (GRCm39) |
V231A |
unknown |
Het |
Me3 |
G |
T |
7: 89,385,927 (GRCm39) |
R92L |
probably damaging |
Het |
Mroh7 |
T |
G |
4: 106,541,115 (GRCm39) |
I1175L |
probably benign |
Het |
Muc16 |
A |
G |
9: 18,553,258 (GRCm39) |
M4345T |
probably benign |
Het |
Mug2 |
A |
G |
6: 122,017,529 (GRCm39) |
Y422C |
possibly damaging |
Het |
N6amt1 |
T |
G |
16: 87,164,454 (GRCm39) |
S214A |
possibly damaging |
Het |
Ogfrl1 |
G |
A |
1: 23,422,063 (GRCm39) |
Q24* |
probably null |
Het |
Or12e14 |
A |
T |
2: 87,677,406 (GRCm39) |
T264S |
probably benign |
Het |
Or1ad6 |
T |
A |
11: 50,860,152 (GRCm39) |
Y102* |
probably null |
Het |
Or2ag2b |
T |
C |
7: 106,417,551 (GRCm39) |
L87P |
possibly damaging |
Het |
Or4f14 |
G |
A |
2: 111,742,435 (GRCm39) |
P280L |
probably damaging |
Het |
Or4k6 |
A |
C |
14: 50,475,448 (GRCm39) |
V298G |
possibly damaging |
Het |
Or4x13 |
A |
G |
2: 90,231,803 (GRCm39) |
D266G |
probably damaging |
Het |
Or6b6 |
A |
G |
7: 106,571,353 (GRCm39) |
M66T |
probably benign |
Het |
Or7g23 |
A |
C |
9: 19,086,642 (GRCm39) |
M110R |
possibly damaging |
Het |
Or8g23 |
T |
A |
9: 38,971,465 (GRCm39) |
I166L |
probably benign |
Het |
Or8k3 |
C |
T |
2: 86,058,557 (GRCm39) |
G253R |
probably damaging |
Het |
Oser1 |
A |
T |
2: 163,253,364 (GRCm39) |
D48E |
probably benign |
Het |
Piwil4 |
G |
A |
9: 14,613,691 (GRCm39) |
P867L |
probably damaging |
Het |
Pla2g6 |
C |
T |
15: 79,189,898 (GRCm39) |
|
probably null |
Het |
Plxna1 |
A |
G |
6: 89,334,584 (GRCm39) |
L15P |
unknown |
Het |
Ppan |
C |
T |
9: 20,803,140 (GRCm39) |
T404I |
probably benign |
Het |
Pros1 |
C |
A |
16: 62,748,433 (GRCm39) |
Y635* |
probably null |
Het |
Rabep2 |
G |
A |
7: 126,043,342 (GRCm39) |
R414Q |
probably benign |
Het |
Rbms3 |
T |
A |
9: 116,651,894 (GRCm39) |
E201V |
probably damaging |
Het |
Robo4 |
A |
C |
9: 37,314,105 (GRCm39) |
I119L |
probably benign |
Het |
S100b |
A |
T |
10: 76,095,820 (GRCm39) |
D66V |
probably damaging |
Het |
Serpina1f |
A |
G |
12: 103,656,101 (GRCm39) |
S376P |
probably damaging |
Het |
Slc24a4 |
T |
C |
12: 102,193,350 (GRCm39) |
|
probably null |
Het |
Slc30a6 |
T |
C |
17: 74,730,424 (GRCm39) |
V438A |
probably benign |
Het |
Sobp |
A |
G |
10: 42,897,804 (GRCm39) |
S594P |
probably benign |
Het |
Tcstv1b |
A |
G |
13: 120,634,994 (GRCm39) |
E92G |
probably damaging |
Het |
Tmem45b |
T |
C |
9: 31,339,334 (GRCm39) |
D213G |
probably benign |
Het |
Topbp1 |
T |
A |
9: 103,200,543 (GRCm39) |
D525E |
probably benign |
Het |
Trim30c |
G |
T |
7: 104,037,472 (GRCm39) |
L165I |
probably benign |
Het |
Unc13b |
A |
T |
4: 43,174,023 (GRCm39) |
D1617V |
unknown |
Het |
Ush1c |
A |
G |
7: 45,878,679 (GRCm39) |
L112P |
probably damaging |
Het |
Vipr1 |
T |
A |
9: 121,490,539 (GRCm39) |
I195N |
probably damaging |
Het |
Vmn2r38 |
A |
C |
7: 9,078,354 (GRCm39) |
V676G |
probably damaging |
Het |
Vmn2r87 |
A |
T |
10: 130,307,992 (GRCm39) |
Y749N |
probably damaging |
Het |
Vps13d |
A |
T |
4: 144,842,073 (GRCm39) |
S2615R |
|
Het |
Whrn |
A |
G |
4: 63,334,330 (GRCm39) |
V828A |
possibly damaging |
Het |
Zbp1 |
A |
G |
2: 173,050,958 (GRCm39) |
V304A |
probably benign |
Het |
Zeb2 |
A |
T |
2: 44,886,359 (GRCm39) |
N899K |
probably benign |
Het |
Zfp148 |
T |
C |
16: 33,317,511 (GRCm39) |
S728P |
possibly damaging |
Het |
Zfp518a |
T |
A |
19: 40,902,207 (GRCm39) |
I712N |
possibly damaging |
Het |
Zfp683 |
T |
C |
4: 133,786,211 (GRCm39) |
V446A |
probably benign |
Het |
Zranb3 |
A |
T |
1: 127,891,588 (GRCm39) |
V796D |
possibly damaging |
Het |
|