Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl4 |
T |
A |
3: 151,203,511 (GRCm39) |
C124S |
probably damaging |
Het |
Aldh1a7 |
T |
C |
19: 20,704,368 (GRCm39) |
N42S |
probably damaging |
Het |
Arhgef1 |
T |
C |
7: 24,623,240 (GRCm39) |
L667P |
probably damaging |
Het |
C1qb |
C |
A |
4: 136,607,811 (GRCm39) |
R184L |
possibly damaging |
Het |
Cacna1s |
A |
G |
1: 136,002,914 (GRCm39) |
|
probably benign |
Het |
Cdk20 |
A |
G |
13: 64,585,734 (GRCm39) |
E244G |
probably benign |
Het |
Copg2 |
C |
A |
6: 30,840,469 (GRCm39) |
|
probably null |
Het |
Cyp2d40 |
A |
T |
15: 82,645,149 (GRCm39) |
|
probably benign |
Het |
Cyp2j6 |
A |
G |
4: 96,414,170 (GRCm39) |
I365T |
probably damaging |
Het |
Dhx29 |
A |
G |
13: 113,064,342 (GRCm39) |
K6E |
probably damaging |
Het |
Dpp10 |
T |
A |
1: 123,295,531 (GRCm39) |
T539S |
probably benign |
Het |
Ehbp1 |
A |
T |
11: 22,046,048 (GRCm39) |
I542K |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,493,593 (GRCm39) |
Y3913C |
probably damaging |
Het |
Flt4 |
C |
T |
11: 49,536,822 (GRCm39) |
T1264I |
probably benign |
Het |
Fmnl1 |
A |
G |
11: 103,070,364 (GRCm39) |
D51G |
probably damaging |
Het |
Gm17093 |
A |
G |
14: 44,755,807 (GRCm39) |
T25A |
unknown |
Het |
Gpatch2 |
A |
G |
1: 186,957,936 (GRCm39) |
E97G |
probably damaging |
Het |
Hcn1 |
T |
C |
13: 118,039,422 (GRCm39) |
L446P |
unknown |
Het |
Hpse2 |
A |
T |
19: 42,920,038 (GRCm39) |
L354I |
probably damaging |
Het |
Hspa4 |
A |
G |
11: 53,190,885 (GRCm39) |
|
probably null |
Het |
Krtap16-1 |
C |
T |
11: 99,877,129 (GRCm39) |
V92M |
probably damaging |
Het |
Med23 |
A |
T |
10: 24,773,239 (GRCm39) |
Q281L |
probably damaging |
Het |
Megf8 |
T |
C |
7: 25,039,873 (GRCm39) |
S963P |
probably benign |
Het |
Mical1 |
G |
A |
10: 41,362,660 (GRCm39) |
E932K |
possibly damaging |
Het |
Mycbp2 |
A |
G |
14: 103,479,643 (GRCm39) |
S1217P |
probably damaging |
Het |
Myocd |
C |
A |
11: 65,069,484 (GRCm39) |
L785F |
probably benign |
Het |
Nell2 |
T |
C |
15: 95,126,982 (GRCm39) |
T798A |
probably damaging |
Het |
Nfat5 |
T |
C |
8: 108,092,808 (GRCm39) |
|
probably benign |
Het |
Olfm5 |
T |
C |
7: 103,803,302 (GRCm39) |
|
probably null |
Het |
Or1e26 |
A |
G |
11: 73,480,081 (GRCm39) |
V161A |
probably benign |
Het |
P2ry1 |
A |
T |
3: 60,911,199 (GRCm39) |
N113Y |
possibly damaging |
Het |
Pan3 |
A |
G |
5: 147,466,933 (GRCm39) |
|
probably null |
Het |
Plcd1 |
A |
G |
9: 118,901,710 (GRCm39) |
F579L |
probably damaging |
Het |
Ptprb |
T |
C |
10: 116,155,238 (GRCm39) |
V664A |
probably benign |
Het |
Slc27a5 |
T |
A |
7: 12,731,487 (GRCm39) |
Q168L |
probably benign |
Het |
Spag8 |
T |
C |
4: 43,651,781 (GRCm39) |
E395G |
probably damaging |
Het |
Stfa2l1 |
T |
C |
16: 35,982,138 (GRCm39) |
Y70H |
probably damaging |
Het |
Taf2 |
T |
C |
15: 54,891,772 (GRCm39) |
N1017S |
probably benign |
Het |
Tnfrsf25 |
C |
A |
4: 152,203,779 (GRCm39) |
Q296K |
probably damaging |
Het |
Trpm3 |
T |
A |
19: 22,676,143 (GRCm39) |
I103N |
probably benign |
Het |
|
Other mutations in Pappa |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01096:Pappa
|
APN |
4 |
65,107,553 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01340:Pappa
|
APN |
4 |
65,242,109 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL01482:Pappa
|
APN |
4 |
65,074,271 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01485:Pappa
|
APN |
4 |
65,107,536 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01759:Pappa
|
APN |
4 |
65,123,395 (GRCm39) |
splice site |
probably null |
|
IGL01860:Pappa
|
APN |
4 |
65,123,329 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01990:Pappa
|
APN |
4 |
65,074,924 (GRCm39) |
splice site |
probably benign |
|
IGL02089:Pappa
|
APN |
4 |
65,074,361 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02153:Pappa
|
APN |
4 |
65,215,674 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02184:Pappa
|
APN |
4 |
65,258,928 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02542:Pappa
|
APN |
4 |
65,094,518 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02556:Pappa
|
APN |
4 |
65,074,863 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02698:Pappa
|
APN |
4 |
65,099,257 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02903:Pappa
|
APN |
4 |
65,180,217 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02974:Pappa
|
APN |
4 |
65,123,172 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03107:Pappa
|
APN |
4 |
65,122,940 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03376:Pappa
|
APN |
4 |
65,115,071 (GRCm39) |
missense |
probably benign |
0.01 |
caer
|
UTSW |
4 |
65,043,128 (GRCm39) |
missense |
probably damaging |
0.98 |
Maennel
|
UTSW |
4 |
65,232,824 (GRCm39) |
missense |
probably benign |
0.05 |
maennelein
|
UTSW |
4 |
65,233,033 (GRCm39) |
splice site |
probably null |
|
mama
|
UTSW |
4 |
65,123,104 (GRCm39) |
missense |
possibly damaging |
0.94 |
Revisitation
|
UTSW |
4 |
65,212,705 (GRCm39) |
missense |
probably damaging |
0.96 |
Sesquester
|
UTSW |
4 |
65,074,612 (GRCm39) |
missense |
possibly damaging |
0.66 |
untersuchen
|
UTSW |
4 |
65,215,494 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02980:Pappa
|
UTSW |
4 |
65,226,011 (GRCm39) |
missense |
probably benign |
0.25 |
PIT4498001:Pappa
|
UTSW |
4 |
65,234,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R0077:Pappa
|
UTSW |
4 |
65,226,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R0390:Pappa
|
UTSW |
4 |
65,269,850 (GRCm39) |
splice site |
probably null |
|
R0458:Pappa
|
UTSW |
4 |
65,074,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R0883:Pappa
|
UTSW |
4 |
65,107,552 (GRCm39) |
nonsense |
probably null |
|
R0946:Pappa
|
UTSW |
4 |
65,233,029 (GRCm39) |
critical splice donor site |
probably null |
|
R1228:Pappa
|
UTSW |
4 |
65,258,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R1327:Pappa
|
UTSW |
4 |
65,269,840 (GRCm39) |
splice site |
probably benign |
|
R1489:Pappa
|
UTSW |
4 |
65,099,185 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1619:Pappa
|
UTSW |
4 |
65,094,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R1856:Pappa
|
UTSW |
4 |
65,258,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R2047:Pappa
|
UTSW |
4 |
65,149,378 (GRCm39) |
splice site |
probably benign |
|
R2102:Pappa
|
UTSW |
4 |
65,234,465 (GRCm39) |
nonsense |
probably null |
|
R2127:Pappa
|
UTSW |
4 |
65,215,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R2143:Pappa
|
UTSW |
4 |
65,099,186 (GRCm39) |
nonsense |
probably null |
|
R2144:Pappa
|
UTSW |
4 |
65,099,186 (GRCm39) |
nonsense |
probably null |
|
R2166:Pappa
|
UTSW |
4 |
65,074,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R2167:Pappa
|
UTSW |
4 |
65,074,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R2168:Pappa
|
UTSW |
4 |
65,074,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R2178:Pappa
|
UTSW |
4 |
65,269,924 (GRCm39) |
missense |
probably benign |
0.00 |
R2504:Pappa
|
UTSW |
4 |
65,099,126 (GRCm39) |
nonsense |
probably null |
|
R4043:Pappa
|
UTSW |
4 |
65,232,824 (GRCm39) |
missense |
probably benign |
0.05 |
R4289:Pappa
|
UTSW |
4 |
65,074,100 (GRCm39) |
missense |
probably benign |
0.19 |
R4415:Pappa
|
UTSW |
4 |
65,223,532 (GRCm39) |
missense |
probably benign |
0.00 |
R4529:Pappa
|
UTSW |
4 |
65,149,419 (GRCm39) |
missense |
probably benign |
|
R4620:Pappa
|
UTSW |
4 |
65,245,265 (GRCm39) |
missense |
probably benign |
0.43 |
R4657:Pappa
|
UTSW |
4 |
65,233,033 (GRCm39) |
splice site |
probably null |
|
R4658:Pappa
|
UTSW |
4 |
65,233,033 (GRCm39) |
splice site |
probably null |
|
R5074:Pappa
|
UTSW |
4 |
65,123,365 (GRCm39) |
missense |
probably benign |
0.15 |
R5200:Pappa
|
UTSW |
4 |
65,074,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R5420:Pappa
|
UTSW |
4 |
65,254,017 (GRCm39) |
critical splice donor site |
probably null |
|
R5469:Pappa
|
UTSW |
4 |
65,123,389 (GRCm39) |
missense |
probably benign |
0.01 |
R5651:Pappa
|
UTSW |
4 |
65,074,589 (GRCm39) |
missense |
probably damaging |
0.99 |
R5725:Pappa
|
UTSW |
4 |
65,107,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5941:Pappa
|
UTSW |
4 |
65,232,830 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6002:Pappa
|
UTSW |
4 |
65,215,645 (GRCm39) |
missense |
probably damaging |
0.99 |
R6252:Pappa
|
UTSW |
4 |
65,107,649 (GRCm39) |
missense |
probably benign |
0.02 |
R6303:Pappa
|
UTSW |
4 |
65,122,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R6322:Pappa
|
UTSW |
4 |
65,232,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R6431:Pappa
|
UTSW |
4 |
65,074,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R6462:Pappa
|
UTSW |
4 |
65,043,128 (GRCm39) |
missense |
probably damaging |
0.98 |
R6484:Pappa
|
UTSW |
4 |
65,232,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R6537:Pappa
|
UTSW |
4 |
65,215,519 (GRCm39) |
missense |
probably damaging |
0.99 |
R6578:Pappa
|
UTSW |
4 |
65,074,374 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6704:Pappa
|
UTSW |
4 |
65,123,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R6789:Pappa
|
UTSW |
4 |
65,099,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R7023:Pappa
|
UTSW |
4 |
65,269,955 (GRCm39) |
missense |
probably benign |
0.00 |
R7139:Pappa
|
UTSW |
4 |
65,107,687 (GRCm39) |
missense |
probably benign |
0.30 |
R7158:Pappa
|
UTSW |
4 |
65,123,104 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7165:Pappa
|
UTSW |
4 |
65,180,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R7196:Pappa
|
UTSW |
4 |
65,242,128 (GRCm39) |
splice site |
probably null |
|
R7410:Pappa
|
UTSW |
4 |
65,253,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R7457:Pappa
|
UTSW |
4 |
65,107,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R7506:Pappa
|
UTSW |
4 |
65,149,419 (GRCm39) |
missense |
probably benign |
0.00 |
R7546:Pappa
|
UTSW |
4 |
65,074,352 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7975:Pappa
|
UTSW |
4 |
65,212,705 (GRCm39) |
missense |
probably damaging |
0.96 |
R8111:Pappa
|
UTSW |
4 |
65,180,229 (GRCm39) |
missense |
probably damaging |
0.99 |
R8260:Pappa
|
UTSW |
4 |
65,234,419 (GRCm39) |
missense |
probably damaging |
0.99 |
R8347:Pappa
|
UTSW |
4 |
65,245,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R8520:Pappa
|
UTSW |
4 |
65,254,001 (GRCm39) |
missense |
probably benign |
0.01 |
R8812:Pappa
|
UTSW |
4 |
65,123,166 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8815:Pappa
|
UTSW |
4 |
65,099,347 (GRCm39) |
missense |
probably benign |
0.00 |
R9008:Pappa
|
UTSW |
4 |
65,074,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R9162:Pappa
|
UTSW |
4 |
65,123,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R9170:Pappa
|
UTSW |
4 |
65,258,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R9205:Pappa
|
UTSW |
4 |
65,074,612 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9336:Pappa
|
UTSW |
4 |
65,042,918 (GRCm39) |
missense |
unknown |
|
R9389:Pappa
|
UTSW |
4 |
65,099,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R9781:Pappa
|
UTSW |
4 |
65,043,104 (GRCm39) |
missense |
possibly damaging |
0.89 |
RF006:Pappa
|
UTSW |
4 |
65,242,110 (GRCm39) |
missense |
probably benign |
0.00 |
RF020:Pappa
|
UTSW |
4 |
65,123,282 (GRCm39) |
missense |
possibly damaging |
0.77 |
X0058:Pappa
|
UTSW |
4 |
65,074,469 (GRCm39) |
missense |
probably damaging |
1.00 |
X0060:Pappa
|
UTSW |
4 |
65,043,178 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Pappa
|
UTSW |
4 |
65,225,995 (GRCm39) |
missense |
probably damaging |
1.00 |
|