Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Abcc9 |
A |
T |
6: 142,640,251 (GRCm39) |
L79H |
probably damaging |
Het |
Alb |
A |
G |
5: 90,623,143 (GRCm39) |
T601A |
probably benign |
Het |
Aldh1l2 |
A |
T |
10: 83,331,816 (GRCm39) |
L776* |
probably null |
Het |
Ank3 |
A |
G |
10: 69,823,329 (GRCm39) |
K666R |
|
Het |
Ankrd17 |
T |
C |
5: 90,391,986 (GRCm39) |
T1895A |
possibly damaging |
Het |
Ankrd17 |
C |
T |
5: 90,416,508 (GRCm39) |
R1108Q |
probably damaging |
Het |
Ap2a2 |
T |
C |
7: 141,207,815 (GRCm39) |
F738L |
probably benign |
Het |
Ap4m1 |
T |
A |
5: 138,175,445 (GRCm39) |
C319* |
probably null |
Het |
Arsj |
C |
T |
3: 126,232,745 (GRCm39) |
T497M |
probably damaging |
Het |
Begain |
G |
T |
12: 108,999,918 (GRCm39) |
S284R |
probably damaging |
Het |
Bicc1 |
A |
T |
10: 70,785,917 (GRCm39) |
N408K |
probably benign |
Het |
Cacybp |
T |
C |
1: 160,031,208 (GRCm39) |
M207V |
possibly damaging |
Het |
Cct8l1 |
A |
G |
5: 25,721,336 (GRCm39) |
D17G |
probably benign |
Het |
Cd1d1 |
C |
A |
3: 86,905,939 (GRCm39) |
|
probably null |
Het |
Chd3 |
C |
T |
11: 69,251,200 (GRCm39) |
C554Y |
probably damaging |
Het |
Chsy1 |
A |
G |
7: 65,821,499 (GRCm39) |
D578G |
probably damaging |
Het |
Col6a6 |
T |
C |
9: 105,663,300 (GRCm39) |
Q79R |
possibly damaging |
Het |
Cpne4 |
A |
T |
9: 104,563,738 (GRCm39) |
R38S |
probably damaging |
Het |
Cyp3a57 |
A |
G |
5: 145,318,159 (GRCm39) |
D380G |
probably benign |
Het |
Dnah6 |
A |
T |
6: 72,998,261 (GRCm39) |
S4054T |
probably benign |
Het |
Emb |
G |
T |
13: 117,357,096 (GRCm39) |
|
probably benign |
Het |
Eml5 |
T |
C |
12: 98,762,837 (GRCm39) |
R1648G |
probably benign |
Het |
Fam117b |
A |
T |
1: 60,020,740 (GRCm39) |
M537L |
probably benign |
Het |
Fcrl2 |
C |
T |
3: 87,164,906 (GRCm39) |
V207I |
possibly damaging |
Het |
Ffar1 |
A |
G |
7: 30,560,457 (GRCm39) |
S147P |
probably benign |
Het |
Fgfr3 |
G |
A |
5: 33,885,216 (GRCm39) |
R110Q |
probably benign |
Het |
Frmd6 |
T |
A |
12: 70,933,865 (GRCm39) |
|
probably null |
Het |
Fry |
A |
G |
5: 150,401,403 (GRCm39) |
R356G |
|
Het |
Fsip2 |
A |
G |
2: 82,811,039 (GRCm39) |
R2453G |
possibly damaging |
Het |
Glipr1l3 |
G |
A |
10: 111,983,923 (GRCm39) |
T181I |
probably benign |
Het |
Hoxc10 |
A |
G |
15: 102,879,382 (GRCm39) |
I301V |
possibly damaging |
Het |
Igf2bp2 |
T |
A |
16: 21,883,895 (GRCm39) |
D463V |
probably damaging |
Het |
Ints13 |
T |
C |
6: 146,467,129 (GRCm39) |
D194G |
probably null |
Het |
Kif5c |
A |
T |
2: 49,622,792 (GRCm39) |
E548V |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,357,979 (GRCm39) |
D350G |
probably damaging |
Het |
Lrrc61 |
T |
C |
6: 48,545,245 (GRCm39) |
S23P |
possibly damaging |
Het |
Mcpt4 |
T |
C |
14: 56,299,134 (GRCm39) |
M35V |
probably damaging |
Het |
Mical1 |
T |
A |
10: 41,357,302 (GRCm39) |
M369K |
possibly damaging |
Het |
Mre11a |
T |
A |
9: 14,736,514 (GRCm39) |
F548L |
probably benign |
Het |
Muc20 |
C |
T |
16: 32,614,471 (GRCm39) |
C302Y |
possibly damaging |
Het |
Nlgn1 |
T |
C |
3: 25,488,622 (GRCm39) |
D571G |
probably damaging |
Het |
Nup88 |
T |
C |
11: 70,858,756 (GRCm39) |
K131E |
probably damaging |
Het |
Nwd2 |
A |
G |
5: 63,962,306 (GRCm39) |
D630G |
probably damaging |
Het |
Or3a1 |
A |
G |
11: 74,225,193 (GRCm39) |
L288P |
probably damaging |
Het |
Or5h19 |
C |
T |
16: 58,856,678 (GRCm39) |
V141M |
probably benign |
Het |
Or6c212 |
A |
T |
10: 129,558,881 (GRCm39) |
C177* |
probably null |
Het |
Pdzd8 |
A |
T |
19: 59,289,219 (GRCm39) |
L727* |
probably null |
Het |
Pi16 |
T |
A |
17: 29,546,852 (GRCm39) |
N475K |
probably benign |
Het |
Pikfyve |
G |
A |
1: 65,307,901 (GRCm39) |
A1826T |
probably damaging |
Het |
Plxna1 |
A |
T |
6: 89,314,138 (GRCm39) |
S768T |
probably benign |
Het |
Plxnc1 |
T |
A |
10: 94,700,599 (GRCm39) |
R656* |
probably null |
Het |
Poglut1 |
A |
G |
16: 38,349,850 (GRCm39) |
W308R |
probably damaging |
Het |
Prmt9 |
T |
G |
8: 78,285,663 (GRCm39) |
V165G |
probably benign |
Het |
Ptch2 |
A |
G |
4: 116,961,969 (GRCm39) |
E102G |
probably damaging |
Het |
Rpn2 |
G |
T |
2: 157,141,500 (GRCm39) |
A303S |
possibly damaging |
Het |
Rttn |
A |
C |
18: 89,078,576 (GRCm39) |
H1334P |
probably damaging |
Het |
Septin3 |
A |
T |
15: 82,163,739 (GRCm39) |
D32V |
probably damaging |
Het |
Sftpa1 |
G |
T |
14: 40,854,417 (GRCm39) |
M1I |
probably null |
Het |
Slc15a2 |
G |
A |
16: 36,574,080 (GRCm39) |
T591I |
probably benign |
Het |
Slc18a2 |
C |
T |
19: 59,262,791 (GRCm39) |
T252I |
probably benign |
Het |
Smchd1 |
A |
G |
17: 71,694,071 (GRCm39) |
F1225L |
probably damaging |
Het |
Swt1 |
A |
G |
1: 151,286,767 (GRCm39) |
S242P |
possibly damaging |
Het |
Tcaim |
C |
A |
9: 122,647,928 (GRCm39) |
H148N |
probably damaging |
Het |
Tgfbr3l |
T |
C |
8: 4,299,640 (GRCm39) |
V141A |
probably damaging |
Het |
Ticrr |
A |
G |
7: 79,330,735 (GRCm39) |
D711G |
probably damaging |
Het |
Trim45 |
A |
T |
3: 100,832,319 (GRCm39) |
Q184L |
possibly damaging |
Het |
Tyw1 |
G |
A |
5: 130,298,065 (GRCm39) |
R202Q |
probably damaging |
Het |
Usp25 |
G |
A |
16: 76,904,843 (GRCm39) |
R803H |
probably damaging |
Het |
Vmn2r71 |
T |
A |
7: 85,273,442 (GRCm39) |
M752K |
probably damaging |
Het |
Wdr35 |
G |
A |
12: 9,071,826 (GRCm39) |
V893I |
probably benign |
Het |
Zdhhc7 |
G |
T |
8: 120,814,494 (GRCm39) |
P105Q |
probably damaging |
Het |
Zfp316 |
A |
G |
5: 143,250,046 (GRCm39) |
|
probably null |
Het |
Zfp454 |
G |
C |
11: 50,764,537 (GRCm39) |
N298K |
possibly damaging |
Het |
Zfp7 |
TGCGGGAAAGGTTTCCACCTGAGCG |
TGCG |
15: 76,774,800 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Sppl2c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00814:Sppl2c
|
APN |
11 |
104,077,805 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02326:Sppl2c
|
APN |
11 |
104,078,099 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02479:Sppl2c
|
APN |
11 |
104,077,763 (GRCm39) |
missense |
probably benign |
|
H8786:Sppl2c
|
UTSW |
11 |
104,077,691 (GRCm39) |
missense |
probably benign |
0.04 |
R0083:Sppl2c
|
UTSW |
11 |
104,077,358 (GRCm39) |
missense |
probably benign |
0.00 |
R1625:Sppl2c
|
UTSW |
11 |
104,077,995 (GRCm39) |
missense |
probably damaging |
0.98 |
R1913:Sppl2c
|
UTSW |
11 |
104,078,715 (GRCm39) |
missense |
probably benign |
0.15 |
R2037:Sppl2c
|
UTSW |
11 |
104,077,307 (GRCm39) |
missense |
probably benign |
0.23 |
R2869:Sppl2c
|
UTSW |
11 |
104,078,141 (GRCm39) |
missense |
probably benign |
0.21 |
R2869:Sppl2c
|
UTSW |
11 |
104,078,141 (GRCm39) |
missense |
probably benign |
0.21 |
R2871:Sppl2c
|
UTSW |
11 |
104,078,141 (GRCm39) |
missense |
probably benign |
0.21 |
R2871:Sppl2c
|
UTSW |
11 |
104,078,141 (GRCm39) |
missense |
probably benign |
0.21 |
R2873:Sppl2c
|
UTSW |
11 |
104,078,141 (GRCm39) |
missense |
probably benign |
0.21 |
R3009:Sppl2c
|
UTSW |
11 |
104,078,141 (GRCm39) |
missense |
probably benign |
0.21 |
R3010:Sppl2c
|
UTSW |
11 |
104,078,141 (GRCm39) |
missense |
probably benign |
0.21 |
R3011:Sppl2c
|
UTSW |
11 |
104,078,141 (GRCm39) |
missense |
probably benign |
0.21 |
R4698:Sppl2c
|
UTSW |
11 |
104,079,141 (GRCm39) |
missense |
probably benign |
0.21 |
R4718:Sppl2c
|
UTSW |
11 |
104,079,141 (GRCm39) |
missense |
probably benign |
0.21 |
R4841:Sppl2c
|
UTSW |
11 |
104,078,478 (GRCm39) |
missense |
probably benign |
0.06 |
R4842:Sppl2c
|
UTSW |
11 |
104,078,478 (GRCm39) |
missense |
probably benign |
0.06 |
R5248:Sppl2c
|
UTSW |
11 |
104,077,407 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5288:Sppl2c
|
UTSW |
11 |
104,078,127 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5300:Sppl2c
|
UTSW |
11 |
104,077,901 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5384:Sppl2c
|
UTSW |
11 |
104,078,127 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5386:Sppl2c
|
UTSW |
11 |
104,078,127 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5427:Sppl2c
|
UTSW |
11 |
104,078,693 (GRCm39) |
missense |
probably benign |
0.01 |
R5452:Sppl2c
|
UTSW |
11 |
104,078,126 (GRCm39) |
missense |
probably benign |
|
R5796:Sppl2c
|
UTSW |
11 |
104,078,619 (GRCm39) |
missense |
probably benign |
0.00 |
R6112:Sppl2c
|
UTSW |
11 |
104,077,963 (GRCm39) |
missense |
probably benign |
0.00 |
R6452:Sppl2c
|
UTSW |
11 |
104,079,017 (GRCm39) |
missense |
probably benign |
0.01 |
R6476:Sppl2c
|
UTSW |
11 |
104,077,595 (GRCm39) |
missense |
probably benign |
|
R7368:Sppl2c
|
UTSW |
11 |
104,078,430 (GRCm39) |
missense |
probably damaging |
0.99 |
R7871:Sppl2c
|
UTSW |
11 |
104,079,342 (GRCm39) |
splice site |
probably null |
|
R7896:Sppl2c
|
UTSW |
11 |
104,077,956 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7991:Sppl2c
|
UTSW |
11 |
104,078,640 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7991:Sppl2c
|
UTSW |
11 |
104,078,189 (GRCm39) |
missense |
probably benign |
0.00 |
R8035:Sppl2c
|
UTSW |
11 |
104,078,192 (GRCm39) |
missense |
probably benign |
0.01 |
R8221:Sppl2c
|
UTSW |
11 |
104,077,710 (GRCm39) |
missense |
probably damaging |
0.99 |
R8243:Sppl2c
|
UTSW |
11 |
104,078,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R8462:Sppl2c
|
UTSW |
11 |
104,077,532 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8474:Sppl2c
|
UTSW |
11 |
104,078,963 (GRCm39) |
missense |
probably benign |
0.00 |
R9507:Sppl2c
|
UTSW |
11 |
104,078,153 (GRCm39) |
missense |
probably benign |
0.00 |
R9672:Sppl2c
|
UTSW |
11 |
104,077,344 (GRCm39) |
missense |
probably damaging |
0.99 |
|