Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
T |
A |
16: 4,667,613 (GRCm39) |
S335T |
unknown |
Het |
4933421I07Rik |
T |
A |
7: 42,097,455 (GRCm39) |
H13L |
possibly damaging |
Het |
6030468B19Rik |
A |
G |
11: 117,696,834 (GRCm39) |
T185A |
probably benign |
Het |
Abcc1 |
T |
A |
16: 14,228,635 (GRCm39) |
V294E |
probably benign |
Het |
Abhd16b |
A |
G |
2: 181,135,253 (GRCm39) |
T52A |
possibly damaging |
Het |
Actl7a |
A |
T |
4: 56,743,632 (GRCm39) |
N53I |
probably benign |
Het |
Ankmy1 |
T |
C |
1: 92,814,445 (GRCm39) |
E354G |
probably benign |
Het |
Arap1 |
T |
C |
7: 101,053,574 (GRCm39) |
F1301S |
probably damaging |
Het |
Arfgef1 |
A |
T |
1: 10,223,958 (GRCm39) |
W1447R |
probably damaging |
Het |
Atoh7 |
ATGGCGCT |
AT |
10: 62,936,187 (GRCm39) |
|
probably benign |
Het |
Ccl24 |
T |
A |
5: 135,601,811 (GRCm39) |
T6S |
possibly damaging |
Het |
Cep152 |
G |
T |
2: 125,410,812 (GRCm39) |
P1292Q |
possibly damaging |
Het |
Cfap46 |
T |
C |
7: 139,239,731 (GRCm39) |
|
probably benign |
Het |
Chd6 |
A |
T |
2: 160,791,477 (GRCm39) |
S2627T |
probably damaging |
Het |
Chd8 |
A |
T |
14: 52,468,963 (GRCm39) |
S552T |
probably damaging |
Het |
Ciita |
C |
A |
16: 10,329,230 (GRCm39) |
L502M |
probably damaging |
Het |
Clic1 |
T |
C |
17: 35,271,463 (GRCm39) |
F31S |
probably damaging |
Het |
Cntnap1 |
T |
A |
11: 101,068,898 (GRCm39) |
I147N |
possibly damaging |
Het |
Cplane1 |
T |
C |
15: 8,248,322 (GRCm39) |
S1624P |
probably benign |
Het |
Crispld1 |
T |
A |
1: 17,819,831 (GRCm39) |
D276E |
probably benign |
Het |
Cspg4 |
A |
T |
9: 56,793,092 (GRCm39) |
N276Y |
probably damaging |
Het |
Cspg4b |
A |
T |
13: 113,504,870 (GRCm39) |
N2000Y |
possibly damaging |
Het |
Cwf19l2 |
A |
G |
9: 3,410,035 (GRCm39) |
M55V |
possibly damaging |
Het |
Cyp2c69 |
T |
C |
19: 39,866,038 (GRCm39) |
N185S |
probably benign |
Het |
Dop1b |
T |
C |
16: 93,553,969 (GRCm39) |
I301T |
probably damaging |
Het |
Epg5 |
T |
C |
18: 78,034,580 (GRCm39) |
V1443A |
probably benign |
Het |
Ephb4 |
T |
C |
5: 137,363,964 (GRCm39) |
V612A |
probably benign |
Het |
Fcgbp |
T |
A |
7: 27,794,362 (GRCm39) |
C1189S |
probably damaging |
Het |
Fgfr2 |
T |
G |
7: 129,786,923 (GRCm39) |
|
probably benign |
Het |
Fmn2 |
A |
G |
1: 174,437,461 (GRCm39) |
E1144G |
probably damaging |
Het |
Fmo3 |
T |
C |
1: 162,796,407 (GRCm39) |
Y55C |
probably damaging |
Het |
Frmpd1 |
A |
G |
4: 45,229,865 (GRCm39) |
T11A |
probably damaging |
Het |
Ghdc |
G |
T |
11: 100,660,929 (GRCm39) |
Q79K |
possibly damaging |
Het |
Gm11677 |
C |
T |
11: 111,615,537 (GRCm39) |
|
noncoding transcript |
Het |
Gm5591 |
T |
C |
7: 38,221,680 (GRCm39) |
T130A |
probably damaging |
Het |
Heg1 |
T |
G |
16: 33,540,142 (GRCm39) |
D367E |
probably benign |
Het |
Igkv13-84 |
C |
T |
6: 68,916,894 (GRCm39) |
P64S |
probably damaging |
Het |
Il10rb |
T |
A |
16: 91,211,545 (GRCm39) |
S128T |
possibly damaging |
Het |
Il15ra |
T |
A |
2: 11,723,117 (GRCm39) |
I47N |
probably damaging |
Het |
Il33 |
C |
A |
19: 29,936,311 (GRCm39) |
S207* |
probably null |
Het |
Itgb7 |
A |
G |
15: 102,132,848 (GRCm39) |
Y155H |
possibly damaging |
Het |
Kdm5a |
A |
G |
6: 120,346,060 (GRCm39) |
|
probably benign |
Het |
Kif11 |
G |
A |
19: 37,406,397 (GRCm39) |
V987I |
probably benign |
Het |
Krtap19-2 |
G |
A |
16: 88,670,762 (GRCm39) |
|
probably benign |
Het |
Krtap24-1 |
T |
A |
16: 88,408,417 (GRCm39) |
R236S |
probably damaging |
Het |
L3mbtl2 |
A |
G |
15: 81,566,813 (GRCm39) |
I406V |
probably benign |
Het |
Lrp2 |
A |
T |
2: 69,290,059 (GRCm39) |
H3593Q |
possibly damaging |
Het |
Mavs |
G |
T |
2: 131,082,285 (GRCm39) |
W56C |
probably damaging |
Het |
Mn1 |
C |
T |
5: 111,567,526 (GRCm39) |
P499S |
probably damaging |
Het |
Ntn5 |
T |
A |
7: 45,340,895 (GRCm39) |
C178S |
probably damaging |
Het |
Nufip2 |
A |
G |
11: 77,577,154 (GRCm39) |
H34R |
unknown |
Het |
Or5p51 |
T |
A |
7: 107,444,755 (GRCm39) |
M62L |
possibly damaging |
Het |
Or6f2 |
T |
A |
7: 139,756,363 (GRCm39) |
L110Q |
probably damaging |
Het |
Osbpl10 |
C |
T |
9: 114,938,598 (GRCm39) |
S86L |
probably damaging |
Het |
Pitpna |
T |
A |
11: 75,511,153 (GRCm39) |
M242K |
possibly damaging |
Het |
Pnpla6 |
T |
C |
8: 3,572,838 (GRCm39) |
V345A |
probably benign |
Het |
Polk |
A |
G |
13: 96,632,999 (GRCm39) |
|
probably null |
Het |
Polr3k |
A |
G |
2: 181,506,340 (GRCm39) |
Y30C |
probably damaging |
Het |
Pramel6 |
A |
G |
2: 87,339,941 (GRCm39) |
H235R |
probably benign |
Het |
Ptpra |
G |
A |
2: 130,379,537 (GRCm39) |
V364I |
probably damaging |
Het |
Recql |
A |
G |
6: 142,309,426 (GRCm39) |
|
probably benign |
Het |
Ring1 |
T |
C |
17: 34,241,263 (GRCm39) |
|
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Samsn1 |
C |
A |
16: 75,744,177 (GRCm39) |
|
noncoding transcript |
Het |
Scara5 |
A |
G |
14: 65,968,198 (GRCm39) |
H157R |
probably benign |
Het |
Sdc3 |
C |
T |
4: 130,546,376 (GRCm39) |
P245L |
probably damaging |
Het |
Slc18b1 |
T |
A |
10: 23,696,767 (GRCm39) |
M318K |
possibly damaging |
Het |
Slc26a10 |
C |
T |
10: 127,009,224 (GRCm39) |
A638T |
possibly damaging |
Het |
Slc35f2 |
T |
A |
9: 53,717,013 (GRCm39) |
W259R |
possibly damaging |
Het |
Spata13 |
G |
A |
14: 60,991,356 (GRCm39) |
W366* |
probably null |
Het |
Sptlc3 |
A |
G |
2: 139,431,509 (GRCm39) |
T344A |
probably benign |
Het |
Tap1 |
T |
C |
17: 34,412,865 (GRCm39) |
V560A |
probably damaging |
Het |
Tbc1d1 |
T |
C |
5: 64,435,389 (GRCm39) |
|
probably null |
Het |
Tlr11 |
A |
G |
14: 50,598,707 (GRCm39) |
Y231C |
possibly damaging |
Het |
Tmem245 |
A |
T |
4: 56,936,468 (GRCm39) |
S230T |
possibly damaging |
Het |
Tnnt3 |
C |
T |
7: 142,068,020 (GRCm39) |
|
probably benign |
Het |
Traf7 |
C |
G |
17: 24,729,412 (GRCm39) |
|
probably benign |
Het |
Tshz2 |
A |
G |
2: 169,804,601 (GRCm39) |
|
probably benign |
Het |
Ttc6 |
A |
T |
12: 57,776,237 (GRCm39) |
N1727I |
probably damaging |
Het |
Ttc7b |
A |
G |
12: 100,369,621 (GRCm39) |
S383P |
probably damaging |
Het |
Tulp3 |
T |
A |
6: 128,300,083 (GRCm39) |
I448F |
probably damaging |
Het |
Ube3b |
T |
C |
5: 114,542,778 (GRCm39) |
|
probably null |
Het |
Vav1 |
G |
A |
17: 57,603,552 (GRCm39) |
V84I |
probably damaging |
Het |
Vav3 |
A |
T |
3: 109,416,110 (GRCm39) |
K243I |
possibly damaging |
Het |
Vmn1r25 |
T |
A |
6: 57,956,011 (GRCm39) |
I93F |
probably damaging |
Het |
Vmn2r73 |
C |
T |
7: 85,520,923 (GRCm39) |
W348* |
probably null |
Het |
Zdbf2 |
A |
G |
1: 63,342,397 (GRCm39) |
R259G |
possibly damaging |
Het |
|
Other mutations in Tshz3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01875:Tshz3
|
APN |
7 |
36,469,385 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01922:Tshz3
|
APN |
7 |
36,469,030 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02047:Tshz3
|
APN |
7 |
36,469,893 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02166:Tshz3
|
APN |
7 |
36,468,346 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02405:Tshz3
|
APN |
7 |
36,469,075 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02658:Tshz3
|
APN |
7 |
36,468,583 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02968:Tshz3
|
APN |
7 |
36,469,249 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03073:Tshz3
|
APN |
7 |
36,470,170 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03233:Tshz3
|
APN |
7 |
36,469,504 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03296:Tshz3
|
APN |
7 |
36,470,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Tshz3
|
UTSW |
7 |
36,469,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Tshz3
|
UTSW |
7 |
36,469,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R0090:Tshz3
|
UTSW |
7 |
36,468,317 (GRCm39) |
missense |
probably benign |
|
R0329:Tshz3
|
UTSW |
7 |
36,469,458 (GRCm39) |
missense |
probably benign |
|
R0330:Tshz3
|
UTSW |
7 |
36,469,458 (GRCm39) |
missense |
probably benign |
|
R0360:Tshz3
|
UTSW |
7 |
36,469,958 (GRCm39) |
missense |
probably benign |
|
R0364:Tshz3
|
UTSW |
7 |
36,469,958 (GRCm39) |
missense |
probably benign |
|
R0380:Tshz3
|
UTSW |
7 |
36,470,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R0547:Tshz3
|
UTSW |
7 |
36,470,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R1061:Tshz3
|
UTSW |
7 |
36,468,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R1618:Tshz3
|
UTSW |
7 |
36,471,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R1704:Tshz3
|
UTSW |
7 |
36,470,785 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1881:Tshz3
|
UTSW |
7 |
36,471,079 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1926:Tshz3
|
UTSW |
7 |
36,468,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R1994:Tshz3
|
UTSW |
7 |
36,469,247 (GRCm39) |
missense |
probably damaging |
0.99 |
R2404:Tshz3
|
UTSW |
7 |
36,469,805 (GRCm39) |
missense |
probably damaging |
0.99 |
R2447:Tshz3
|
UTSW |
7 |
36,468,178 (GRCm39) |
missense |
probably benign |
0.00 |
R2930:Tshz3
|
UTSW |
7 |
36,471,017 (GRCm39) |
missense |
possibly damaging |
0.74 |
R3879:Tshz3
|
UTSW |
7 |
36,470,962 (GRCm39) |
nonsense |
probably null |
|
R4033:Tshz3
|
UTSW |
7 |
36,470,009 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4212:Tshz3
|
UTSW |
7 |
36,469,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R4394:Tshz3
|
UTSW |
7 |
36,469,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R4977:Tshz3
|
UTSW |
7 |
36,470,615 (GRCm39) |
missense |
probably benign |
0.31 |
R5139:Tshz3
|
UTSW |
7 |
36,470,450 (GRCm39) |
missense |
probably benign |
0.23 |
R5448:Tshz3
|
UTSW |
7 |
36,470,654 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5516:Tshz3
|
UTSW |
7 |
36,469,775 (GRCm39) |
missense |
probably benign |
0.03 |
R5760:Tshz3
|
UTSW |
7 |
36,470,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R6360:Tshz3
|
UTSW |
7 |
36,468,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R6481:Tshz3
|
UTSW |
7 |
36,451,764 (GRCm39) |
splice site |
probably null |
|
R6535:Tshz3
|
UTSW |
7 |
36,468,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R7105:Tshz3
|
UTSW |
7 |
36,469,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R7133:Tshz3
|
UTSW |
7 |
36,469,994 (GRCm39) |
missense |
probably benign |
0.12 |
R7225:Tshz3
|
UTSW |
7 |
36,469,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R7238:Tshz3
|
UTSW |
7 |
36,469,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R7851:Tshz3
|
UTSW |
7 |
36,471,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R7938:Tshz3
|
UTSW |
7 |
36,468,583 (GRCm39) |
missense |
probably damaging |
0.99 |
R8344:Tshz3
|
UTSW |
7 |
36,470,962 (GRCm39) |
missense |
probably damaging |
0.98 |
R9501:Tshz3
|
UTSW |
7 |
36,470,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R9583:Tshz3
|
UTSW |
7 |
36,470,492 (GRCm39) |
missense |
possibly damaging |
0.71 |
X0067:Tshz3
|
UTSW |
7 |
36,468,746 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Tshz3
|
UTSW |
7 |
36,468,221 (GRCm39) |
missense |
probably benign |
0.19 |
Z1186:Tshz3
|
UTSW |
7 |
36,469,999 (GRCm39) |
missense |
probably benign |
|
Z1186:Tshz3
|
UTSW |
7 |
36,468,341 (GRCm39) |
missense |
probably benign |
|
Z1191:Tshz3
|
UTSW |
7 |
36,469,999 (GRCm39) |
missense |
probably benign |
|
Z1191:Tshz3
|
UTSW |
7 |
36,468,341 (GRCm39) |
missense |
probably benign |
|
|