Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts12 |
G |
T |
15: 11,311,144 (GRCm39) |
D1134Y |
possibly damaging |
Het |
Add3 |
A |
G |
19: 53,225,259 (GRCm39) |
T460A |
probably benign |
Het |
Amer3 |
A |
C |
1: 34,618,381 (GRCm39) |
|
probably benign |
Het |
Arhgap22 |
C |
T |
14: 33,081,065 (GRCm39) |
|
probably benign |
Het |
Arhgap32 |
T |
G |
9: 32,171,056 (GRCm39) |
S1279A |
probably benign |
Het |
Bcas1 |
G |
A |
2: 170,260,601 (GRCm39) |
T26M |
probably damaging |
Het |
Begain |
A |
T |
12: 109,004,860 (GRCm39) |
F256I |
probably damaging |
Het |
Bltp1 |
T |
C |
3: 37,023,301 (GRCm39) |
V2210A |
probably damaging |
Het |
Cabin1 |
A |
T |
10: 75,492,883 (GRCm39) |
I1804N |
probably damaging |
Het |
Cad |
G |
A |
5: 31,231,329 (GRCm39) |
|
probably benign |
Het |
Carmil1 |
G |
A |
13: 24,257,966 (GRCm39) |
S762L |
probably damaging |
Het |
Ccdc93 |
T |
A |
1: 121,420,706 (GRCm39) |
L529Q |
probably damaging |
Het |
Cdh12 |
T |
A |
15: 21,578,635 (GRCm39) |
|
probably null |
Het |
Cep15 |
A |
G |
14: 12,301,266 (GRCm38) |
E124G |
possibly damaging |
Het |
Clip2 |
T |
A |
5: 134,564,069 (GRCm39) |
|
probably benign |
Het |
Cmip |
T |
C |
8: 118,172,105 (GRCm39) |
I480T |
probably damaging |
Het |
Cnot1 |
A |
T |
8: 96,498,628 (GRCm39) |
I203K |
probably benign |
Het |
Col18a1 |
G |
A |
10: 76,895,197 (GRCm39) |
P1155S |
probably damaging |
Het |
Col1a2 |
T |
A |
6: 4,531,956 (GRCm39) |
|
probably benign |
Het |
Crybg3 |
A |
T |
16: 59,364,503 (GRCm39) |
L2373Q |
probably damaging |
Het |
D130043K22Rik |
A |
T |
13: 25,071,860 (GRCm39) |
I935F |
probably damaging |
Het |
Dapl1 |
T |
A |
2: 59,326,938 (GRCm39) |
D61E |
possibly damaging |
Het |
Def6 |
A |
G |
17: 28,447,043 (GRCm39) |
D558G |
possibly damaging |
Het |
Dnah6 |
T |
C |
6: 73,046,382 (GRCm39) |
|
probably benign |
Het |
Dvl2 |
G |
A |
11: 69,891,861 (GRCm39) |
|
probably benign |
Het |
Ecd |
A |
C |
14: 20,370,802 (GRCm39) |
V639G |
probably benign |
Het |
Epg5 |
C |
T |
18: 78,029,687 (GRCm39) |
T1350M |
probably benign |
Het |
Erbb4 |
C |
A |
1: 68,298,418 (GRCm39) |
M657I |
probably benign |
Het |
Evi5 |
T |
C |
5: 107,960,277 (GRCm39) |
R431G |
probably benign |
Het |
Fbxo11 |
G |
A |
17: 88,323,041 (GRCm39) |
A115V |
possibly damaging |
Het |
Fgfr2 |
T |
C |
7: 129,797,979 (GRCm39) |
T192A |
probably benign |
Het |
Gas7 |
C |
T |
11: 67,552,878 (GRCm39) |
A146V |
possibly damaging |
Het |
Gatad2b |
T |
A |
3: 90,263,489 (GRCm39) |
S529T |
probably benign |
Het |
Gm10722 |
G |
T |
9: 3,001,048 (GRCm39) |
Q41H |
probably null |
Het |
Gm10801 |
G |
C |
2: 98,494,352 (GRCm39) |
R143T |
possibly damaging |
Het |
Gm7535 |
A |
G |
17: 18,131,374 (GRCm39) |
|
probably benign |
Het |
Gstm1 |
T |
A |
3: 107,920,012 (GRCm39) |
N193I |
possibly damaging |
Het |
Heatr5b |
G |
A |
17: 79,135,375 (GRCm39) |
P252L |
probably benign |
Het |
Hmgb1 |
A |
G |
5: 148,987,441 (GRCm39) |
V36A |
probably benign |
Het |
Hrh1 |
G |
T |
6: 114,457,193 (GRCm39) |
W158L |
probably damaging |
Het |
Ighv6-4 |
T |
C |
12: 114,370,294 (GRCm39) |
M53V |
probably benign |
Het |
Iqgap2 |
T |
A |
13: 95,772,141 (GRCm39) |
D1346V |
probably damaging |
Het |
Kcng3 |
A |
T |
17: 83,895,166 (GRCm39) |
N433K |
possibly damaging |
Het |
Kif1a |
T |
A |
1: 92,980,288 (GRCm39) |
|
probably benign |
Het |
Lctl |
C |
A |
9: 64,026,169 (GRCm39) |
Q75K |
probably benign |
Het |
Ldb3 |
T |
A |
14: 34,300,608 (GRCm39) |
I89F |
possibly damaging |
Het |
Lrrc49 |
A |
T |
9: 60,584,378 (GRCm39) |
L156Q |
probably damaging |
Het |
Mark2 |
G |
T |
19: 7,259,193 (GRCm39) |
T83K |
probably benign |
Het |
Ms4a15 |
A |
T |
19: 10,957,574 (GRCm39) |
D170E |
probably damaging |
Het |
Msantd2 |
A |
G |
9: 37,434,056 (GRCm39) |
S99G |
possibly damaging |
Het |
Nemf |
G |
T |
12: 69,400,577 (GRCm39) |
T124N |
probably benign |
Het |
Nlrp9c |
A |
T |
7: 26,093,561 (GRCm39) |
F35I |
possibly damaging |
Het |
Nwd2 |
A |
G |
5: 63,962,116 (GRCm39) |
I567V |
probably benign |
Het |
Optn |
C |
T |
2: 5,028,926 (GRCm39) |
G526R |
probably damaging |
Het |
Or11l3 |
T |
C |
11: 58,516,566 (GRCm39) |
Y102C |
probably damaging |
Het |
Or13p8 |
A |
G |
4: 118,584,367 (GRCm39) |
I308V |
probably null |
Het |
Or5v1b |
A |
C |
17: 37,841,533 (GRCm39) |
I222L |
probably benign |
Het |
Or7g16 |
T |
A |
9: 18,727,290 (GRCm39) |
Q100L |
probably damaging |
Het |
Pdk4 |
T |
C |
6: 5,491,138 (GRCm39) |
E209G |
probably benign |
Het |
Plch1 |
T |
C |
3: 63,618,399 (GRCm39) |
Q712R |
probably damaging |
Het |
Pnpla1 |
T |
A |
17: 29,105,852 (GRCm39) |
V569E |
possibly damaging |
Het |
Prkar2a |
A |
T |
9: 108,596,457 (GRCm39) |
D134V |
probably damaging |
Het |
Ptov1 |
T |
A |
7: 44,514,046 (GRCm39) |
Q40L |
possibly damaging |
Het |
Ptprq |
T |
C |
10: 107,544,589 (GRCm39) |
I314V |
probably benign |
Het |
Rabl2 |
T |
C |
15: 89,468,169 (GRCm39) |
K66E |
probably damaging |
Het |
Rnf38 |
A |
G |
4: 44,152,507 (GRCm39) |
V19A |
possibly damaging |
Het |
Scn2a |
T |
A |
2: 65,512,435 (GRCm39) |
W191R |
probably damaging |
Het |
Sec22b |
T |
A |
3: 97,828,572 (GRCm39) |
F212I |
possibly damaging |
Het |
Sec24c |
T |
A |
14: 20,738,783 (GRCm39) |
|
probably null |
Het |
Septin2 |
T |
C |
1: 93,423,321 (GRCm39) |
S51P |
probably damaging |
Het |
Slc1a2 |
C |
T |
2: 102,574,208 (GRCm39) |
T206I |
probably benign |
Het |
Slc25a19 |
C |
A |
11: 115,515,032 (GRCm39) |
R42L |
probably damaging |
Het |
St14 |
G |
A |
9: 31,002,620 (GRCm39) |
|
probably benign |
Het |
Stxbp1 |
C |
T |
2: 32,692,917 (GRCm39) |
|
probably benign |
Het |
Tas2r131 |
C |
T |
6: 132,934,792 (GRCm39) |
V6I |
probably benign |
Het |
Tdo2 |
T |
A |
3: 81,871,307 (GRCm39) |
M235L |
probably benign |
Het |
Tenm3 |
T |
G |
8: 48,685,140 (GRCm39) |
H2432P |
probably damaging |
Het |
Tmprss15 |
C |
T |
16: 78,821,630 (GRCm39) |
|
probably benign |
Het |
Tmx1 |
A |
G |
12: 70,500,030 (GRCm39) |
N30D |
probably benign |
Het |
Tom1 |
A |
G |
8: 75,791,020 (GRCm39) |
|
probably null |
Het |
Top2a |
T |
C |
11: 98,913,781 (GRCm39) |
N20S |
probably benign |
Het |
Ttc23l |
T |
A |
15: 10,540,049 (GRCm39) |
T145S |
probably benign |
Het |
Unc13b |
T |
A |
4: 43,236,983 (GRCm39) |
M3351K |
possibly damaging |
Het |
Vmn1r47 |
T |
C |
6: 89,999,641 (GRCm39) |
S258P |
probably damaging |
Het |
Vmn2r8 |
T |
G |
5: 108,945,317 (GRCm39) |
|
probably null |
Het |
Vps11 |
T |
C |
9: 44,265,135 (GRCm39) |
Q641R |
probably null |
Het |
Wapl |
T |
A |
14: 34,414,281 (GRCm39) |
I381N |
probably damaging |
Het |
Zmym6 |
G |
A |
4: 127,016,601 (GRCm39) |
G794E |
probably damaging |
Het |
|
Other mutations in Serpinb1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01391:Serpinb1a
|
APN |
13 |
33,029,398 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02470:Serpinb1a
|
APN |
13 |
33,034,376 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03215:Serpinb1a
|
APN |
13 |
33,034,352 (GRCm39) |
missense |
probably damaging |
0.99 |
R0047:Serpinb1a
|
UTSW |
13 |
33,034,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R0047:Serpinb1a
|
UTSW |
13 |
33,034,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R0121:Serpinb1a
|
UTSW |
13 |
33,032,754 (GRCm39) |
splice site |
probably benign |
|
R0387:Serpinb1a
|
UTSW |
13 |
33,032,721 (GRCm39) |
missense |
probably benign |
0.03 |
R0751:Serpinb1a
|
UTSW |
13 |
33,027,199 (GRCm39) |
missense |
probably benign |
|
R1184:Serpinb1a
|
UTSW |
13 |
33,027,199 (GRCm39) |
missense |
probably benign |
|
R2096:Serpinb1a
|
UTSW |
13 |
33,031,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R2165:Serpinb1a
|
UTSW |
13 |
33,034,397 (GRCm39) |
splice site |
probably benign |
|
R3432:Serpinb1a
|
UTSW |
13 |
33,026,842 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5247:Serpinb1a
|
UTSW |
13 |
33,034,389 (GRCm39) |
start codon destroyed |
probably damaging |
1.00 |
R5669:Serpinb1a
|
UTSW |
13 |
33,029,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R6274:Serpinb1a
|
UTSW |
13 |
33,026,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R7133:Serpinb1a
|
UTSW |
13 |
33,034,308 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7358:Serpinb1a
|
UTSW |
13 |
33,026,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R7944:Serpinb1a
|
UTSW |
13 |
33,034,239 (GRCm39) |
missense |
probably benign |
0.34 |
R7994:Serpinb1a
|
UTSW |
13 |
33,027,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R8213:Serpinb1a
|
UTSW |
13 |
33,026,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R8272:Serpinb1a
|
UTSW |
13 |
33,029,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R9023:Serpinb1a
|
UTSW |
13 |
33,029,763 (GRCm39) |
missense |
probably damaging |
0.99 |
R9287:Serpinb1a
|
UTSW |
13 |
33,026,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R9423:Serpinb1a
|
UTSW |
13 |
33,026,910 (GRCm39) |
missense |
probably benign |
0.44 |
|