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 |
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 |
Tshz3 |
T |
C |
7: 36,468,397 (GRCm39) |
S129P |
probably damaging |
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 Mn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01019:Mn1
|
APN |
5 |
111,569,413 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01139:Mn1
|
APN |
5 |
111,569,315 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01546:Mn1
|
APN |
5 |
111,569,114 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02252:Mn1
|
APN |
5 |
111,569,107 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02821:Mn1
|
APN |
5 |
111,569,717 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03203:Mn1
|
APN |
5 |
111,569,269 (GRCm39) |
missense |
probably benign |
|
Uebermus
|
UTSW |
5 |
111,569,752 (GRCm39) |
splice site |
probably null |
|
FR4342:Mn1
|
UTSW |
5 |
111,567,572 (GRCm39) |
small insertion |
probably benign |
|
FR4449:Mn1
|
UTSW |
5 |
111,567,576 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Mn1
|
UTSW |
5 |
111,567,564 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Mn1
|
UTSW |
5 |
111,567,568 (GRCm39) |
small insertion |
probably benign |
|
R0639:Mn1
|
UTSW |
5 |
111,567,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R0676:Mn1
|
UTSW |
5 |
111,568,900 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1537:Mn1
|
UTSW |
5 |
111,602,646 (GRCm39) |
missense |
probably damaging |
0.96 |
R1638:Mn1
|
UTSW |
5 |
111,569,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Mn1
|
UTSW |
5 |
111,567,880 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1922:Mn1
|
UTSW |
5 |
111,566,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R2008:Mn1
|
UTSW |
5 |
111,566,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R2104:Mn1
|
UTSW |
5 |
111,602,617 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2519:Mn1
|
UTSW |
5 |
111,566,418 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3980:Mn1
|
UTSW |
5 |
111,569,636 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4008:Mn1
|
UTSW |
5 |
111,568,035 (GRCm39) |
missense |
probably benign |
|
R4564:Mn1
|
UTSW |
5 |
111,568,533 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4647:Mn1
|
UTSW |
5 |
111,567,949 (GRCm39) |
missense |
probably benign |
|
R4819:Mn1
|
UTSW |
5 |
111,567,803 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4962:Mn1
|
UTSW |
5 |
111,602,652 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5373:Mn1
|
UTSW |
5 |
111,569,752 (GRCm39) |
splice site |
probably null |
|
R5374:Mn1
|
UTSW |
5 |
111,569,752 (GRCm39) |
splice site |
probably null |
|
R5521:Mn1
|
UTSW |
5 |
111,569,635 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5633:Mn1
|
UTSW |
5 |
111,568,192 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5744:Mn1
|
UTSW |
5 |
111,568,402 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6050:Mn1
|
UTSW |
5 |
111,567,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R6552:Mn1
|
UTSW |
5 |
111,568,753 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7206:Mn1
|
UTSW |
5 |
111,568,378 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7244:Mn1
|
UTSW |
5 |
111,566,699 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8207:Mn1
|
UTSW |
5 |
111,569,651 (GRCm39) |
missense |
probably damaging |
0.99 |
R8222:Mn1
|
UTSW |
5 |
111,566,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R8353:Mn1
|
UTSW |
5 |
111,568,505 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8677:Mn1
|
UTSW |
5 |
111,566,885 (GRCm39) |
nonsense |
probably null |
|
R8990:Mn1
|
UTSW |
5 |
111,566,381 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9602:Mn1
|
UTSW |
5 |
111,565,449 (GRCm39) |
start gained |
probably benign |
|
R9603:Mn1
|
UTSW |
5 |
111,566,393 (GRCm39) |
missense |
probably damaging |
1.00 |
RF025:Mn1
|
UTSW |
5 |
111,567,571 (GRCm39) |
nonsense |
probably null |
|
RF027:Mn1
|
UTSW |
5 |
111,567,571 (GRCm39) |
small insertion |
probably benign |
|
RF028:Mn1
|
UTSW |
5 |
111,567,577 (GRCm39) |
small insertion |
probably benign |
|
RF032:Mn1
|
UTSW |
5 |
111,567,577 (GRCm39) |
small insertion |
probably benign |
|
RF040:Mn1
|
UTSW |
5 |
111,567,571 (GRCm39) |
small insertion |
probably benign |
|
Z1088:Mn1
|
UTSW |
5 |
111,566,146 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1176:Mn1
|
UTSW |
5 |
111,602,572 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1176:Mn1
|
UTSW |
5 |
111,568,245 (GRCm39) |
missense |
probably benign |
0.08 |
Z1177:Mn1
|
UTSW |
5 |
111,567,934 (GRCm39) |
missense |
probably damaging |
1.00 |
|