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 |
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 |
Sppl2c |
G |
A |
11: 104,078,561 (GRCm39) |
G454S |
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 Rttn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00595:Rttn
|
APN |
18 |
88,992,464 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00788:Rttn
|
APN |
18 |
88,990,633 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00929:Rttn
|
APN |
18 |
89,047,059 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01392:Rttn
|
APN |
18 |
89,013,737 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01395:Rttn
|
APN |
18 |
89,147,894 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01701:Rttn
|
APN |
18 |
89,082,339 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02136:Rttn
|
APN |
18 |
89,064,252 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02151:Rttn
|
APN |
18 |
89,038,329 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02165:Rttn
|
APN |
18 |
89,061,165 (GRCm39) |
missense |
probably benign |
|
IGL02228:Rttn
|
APN |
18 |
89,060,355 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02276:Rttn
|
APN |
18 |
89,066,578 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02612:Rttn
|
APN |
18 |
88,991,750 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02645:Rttn
|
APN |
18 |
89,128,810 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02716:Rttn
|
APN |
18 |
89,066,541 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02820:Rttn
|
APN |
18 |
89,047,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02961:Rttn
|
APN |
18 |
89,071,697 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02973:Rttn
|
APN |
18 |
88,990,618 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03027:Rttn
|
APN |
18 |
88,997,814 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03082:Rttn
|
APN |
18 |
89,002,072 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03121:Rttn
|
APN |
18 |
88,993,875 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03135:Rttn
|
APN |
18 |
89,033,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03328:Rttn
|
APN |
18 |
89,061,152 (GRCm39) |
missense |
probably benign |
0.19 |
Fascisti
|
UTSW |
18 |
89,027,584 (GRCm39) |
splice site |
probably benign |
|
marcher
|
UTSW |
18 |
89,056,070 (GRCm39) |
missense |
probably damaging |
0.99 |
militaristi
|
UTSW |
18 |
89,029,040 (GRCm39) |
missense |
probably damaging |
1.00 |
Thoughtless
|
UTSW |
18 |
89,032,735 (GRCm39) |
missense |
probably damaging |
1.00 |
twister
|
UTSW |
18 |
89,064,286 (GRCm39) |
critical splice donor site |
probably null |
|
Vermiculus
|
UTSW |
18 |
89,108,557 (GRCm39) |
missense |
probably benign |
|
R0062:Rttn
|
UTSW |
18 |
89,029,090 (GRCm39) |
critical splice donor site |
probably null |
|
R0062:Rttn
|
UTSW |
18 |
89,029,090 (GRCm39) |
critical splice donor site |
probably null |
|
R0310:Rttn
|
UTSW |
18 |
89,027,584 (GRCm39) |
splice site |
probably benign |
|
R0330:Rttn
|
UTSW |
18 |
89,004,204 (GRCm39) |
splice site |
probably null |
|
R0363:Rttn
|
UTSW |
18 |
89,029,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R0485:Rttn
|
UTSW |
18 |
89,108,543 (GRCm39) |
splice site |
probably benign |
|
R0590:Rttn
|
UTSW |
18 |
88,997,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Rttn
|
UTSW |
18 |
89,061,090 (GRCm39) |
missense |
probably benign |
0.00 |
R0604:Rttn
|
UTSW |
18 |
88,995,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R0631:Rttn
|
UTSW |
18 |
89,007,670 (GRCm39) |
missense |
probably benign |
0.00 |
R0882:Rttn
|
UTSW |
18 |
88,991,813 (GRCm39) |
nonsense |
probably null |
|
R0885:Rttn
|
UTSW |
18 |
89,001,934 (GRCm39) |
missense |
probably benign |
0.03 |
R0900:Rttn
|
UTSW |
18 |
89,119,815 (GRCm39) |
missense |
probably benign |
0.13 |
R1077:Rttn
|
UTSW |
18 |
89,082,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R1444:Rttn
|
UTSW |
18 |
89,060,991 (GRCm39) |
missense |
probably benign |
0.04 |
R1460:Rttn
|
UTSW |
18 |
89,127,481 (GRCm39) |
splice site |
probably benign |
|
R1517:Rttn
|
UTSW |
18 |
89,131,474 (GRCm39) |
missense |
probably benign |
0.01 |
R1630:Rttn
|
UTSW |
18 |
89,061,078 (GRCm39) |
missense |
probably benign |
0.02 |
R1632:Rttn
|
UTSW |
18 |
89,027,460 (GRCm39) |
missense |
probably benign |
0.18 |
R1722:Rttn
|
UTSW |
18 |
88,991,655 (GRCm39) |
missense |
probably benign |
0.34 |
R1755:Rttn
|
UTSW |
18 |
89,027,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R1881:Rttn
|
UTSW |
18 |
89,033,336 (GRCm39) |
missense |
probably damaging |
0.96 |
R1971:Rttn
|
UTSW |
18 |
89,108,557 (GRCm39) |
missense |
probably benign |
|
R2035:Rttn
|
UTSW |
18 |
89,038,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Rttn
|
UTSW |
18 |
89,004,197 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2191:Rttn
|
UTSW |
18 |
89,113,772 (GRCm39) |
critical splice donor site |
probably null |
|
R2201:Rttn
|
UTSW |
18 |
89,029,067 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2266:Rttn
|
UTSW |
18 |
89,082,295 (GRCm39) |
missense |
probably benign |
0.05 |
R3014:Rttn
|
UTSW |
18 |
89,032,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R3052:Rttn
|
UTSW |
18 |
89,033,370 (GRCm39) |
splice site |
probably benign |
|
R3427:Rttn
|
UTSW |
18 |
89,113,775 (GRCm39) |
splice site |
probably null |
|
R3431:Rttn
|
UTSW |
18 |
89,113,695 (GRCm39) |
missense |
probably benign |
0.04 |
R3786:Rttn
|
UTSW |
18 |
89,056,018 (GRCm39) |
missense |
probably benign |
0.00 |
R3803:Rttn
|
UTSW |
18 |
88,995,831 (GRCm39) |
missense |
probably damaging |
0.96 |
R3980:Rttn
|
UTSW |
18 |
89,035,399 (GRCm39) |
missense |
probably benign |
0.12 |
R4035:Rttn
|
UTSW |
18 |
89,013,777 (GRCm39) |
missense |
probably benign |
0.03 |
R4170:Rttn
|
UTSW |
18 |
88,993,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R4223:Rttn
|
UTSW |
18 |
89,113,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R4273:Rttn
|
UTSW |
18 |
89,110,020 (GRCm39) |
missense |
probably benign |
|
R4517:Rttn
|
UTSW |
18 |
89,047,097 (GRCm39) |
missense |
probably damaging |
0.99 |
R4674:Rttn
|
UTSW |
18 |
89,029,135 (GRCm39) |
splice site |
probably null |
|
R4837:Rttn
|
UTSW |
18 |
89,108,539 (GRCm39) |
splice site |
probably null |
|
R4869:Rttn
|
UTSW |
18 |
89,061,138 (GRCm39) |
nonsense |
probably null |
|
R4881:Rttn
|
UTSW |
18 |
89,119,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R4959:Rttn
|
UTSW |
18 |
89,060,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R4973:Rttn
|
UTSW |
18 |
89,060,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R4975:Rttn
|
UTSW |
18 |
89,082,209 (GRCm39) |
splice site |
probably null |
|
R5166:Rttn
|
UTSW |
18 |
89,031,218 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5243:Rttn
|
UTSW |
18 |
89,126,187 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5594:Rttn
|
UTSW |
18 |
89,108,560 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5654:Rttn
|
UTSW |
18 |
89,066,556 (GRCm39) |
missense |
probably benign |
|
R5794:Rttn
|
UTSW |
18 |
89,013,693 (GRCm39) |
missense |
probably benign |
0.18 |
R5799:Rttn
|
UTSW |
18 |
89,056,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R5955:Rttn
|
UTSW |
18 |
89,139,133 (GRCm39) |
missense |
probably damaging |
0.99 |
R5963:Rttn
|
UTSW |
18 |
89,091,819 (GRCm39) |
missense |
probably benign |
0.01 |
R5989:Rttn
|
UTSW |
18 |
88,991,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R6004:Rttn
|
UTSW |
18 |
89,039,816 (GRCm39) |
missense |
probably damaging |
0.96 |
R6132:Rttn
|
UTSW |
18 |
89,133,770 (GRCm39) |
critical splice donor site |
probably null |
|
R6430:Rttn
|
UTSW |
18 |
89,039,809 (GRCm39) |
missense |
probably null |
0.18 |
R6436:Rttn
|
UTSW |
18 |
89,128,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R6681:Rttn
|
UTSW |
18 |
89,032,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R6994:Rttn
|
UTSW |
18 |
89,047,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R7049:Rttn
|
UTSW |
18 |
89,082,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R7078:Rttn
|
UTSW |
18 |
89,027,546 (GRCm39) |
missense |
probably benign |
0.03 |
R7083:Rttn
|
UTSW |
18 |
89,108,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R7250:Rttn
|
UTSW |
18 |
89,007,647 (GRCm39) |
missense |
probably benign |
0.03 |
R7402:Rttn
|
UTSW |
18 |
89,004,035 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7565:Rttn
|
UTSW |
18 |
89,078,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R7588:Rttn
|
UTSW |
18 |
89,082,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R8029:Rttn
|
UTSW |
18 |
89,108,598 (GRCm39) |
missense |
not run |
|
R8085:Rttn
|
UTSW |
18 |
89,071,672 (GRCm39) |
nonsense |
probably null |
|
R8113:Rttn
|
UTSW |
18 |
89,029,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R8355:Rttn
|
UTSW |
18 |
89,047,016 (GRCm39) |
missense |
probably benign |
0.05 |
R8531:Rttn
|
UTSW |
18 |
89,131,467 (GRCm39) |
missense |
probably benign |
0.00 |
R8992:Rttn
|
UTSW |
18 |
88,995,832 (GRCm39) |
missense |
probably benign |
0.24 |
R9008:Rttn
|
UTSW |
18 |
89,027,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R9139:Rttn
|
UTSW |
18 |
89,038,261 (GRCm39) |
missense |
probably benign |
0.30 |
R9210:Rttn
|
UTSW |
18 |
89,064,286 (GRCm39) |
critical splice donor site |
probably null |
|
R9212:Rttn
|
UTSW |
18 |
89,064,286 (GRCm39) |
critical splice donor site |
probably null |
|
R9286:Rttn
|
UTSW |
18 |
88,995,849 (GRCm39) |
missense |
probably benign |
0.06 |
R9632:Rttn
|
UTSW |
18 |
89,035,334 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9710:Rttn
|
UTSW |
18 |
89,035,334 (GRCm39) |
missense |
possibly damaging |
0.82 |
X0017:Rttn
|
UTSW |
18 |
89,131,526 (GRCm39) |
missense |
probably benign |
0.01 |
X0022:Rttn
|
UTSW |
18 |
88,991,791 (GRCm39) |
nonsense |
probably null |
|
|