Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acoxl |
T |
A |
2: 127,720,701 (GRCm39) |
I188N |
probably damaging |
Het |
Akr1c14 |
T |
C |
13: 4,131,106 (GRCm39) |
V266A |
probably damaging |
Het |
Als2cl |
C |
A |
9: 110,717,810 (GRCm39) |
P301H |
probably damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Catspere2 |
C |
T |
1: 177,843,477 (GRCm39) |
|
probably benign |
Het |
Cpsf1 |
A |
T |
15: 76,487,937 (GRCm39) |
N53K |
possibly damaging |
Het |
Ctsll3 |
C |
T |
13: 60,948,749 (GRCm39) |
G69R |
possibly damaging |
Het |
F2 |
C |
T |
2: 91,458,693 (GRCm39) |
R539Q |
probably damaging |
Het |
Fam78b |
G |
A |
1: 166,906,219 (GRCm39) |
G126D |
probably damaging |
Het |
Fancd2 |
A |
G |
6: 113,568,120 (GRCm39) |
I1332V |
possibly damaging |
Het |
Flg2 |
C |
T |
3: 93,109,244 (GRCm39) |
S424L |
probably damaging |
Het |
Fpr1 |
T |
C |
17: 18,097,471 (GRCm39) |
T173A |
possibly damaging |
Het |
Gas2l3 |
A |
G |
10: 89,249,960 (GRCm39) |
V386A |
probably benign |
Het |
Gdap2 |
A |
C |
3: 100,095,199 (GRCm39) |
E269A |
probably benign |
Het |
Igf2bp2 |
T |
A |
16: 21,898,358 (GRCm39) |
|
probably null |
Het |
Ipo11 |
T |
C |
13: 107,016,118 (GRCm39) |
|
probably null |
Het |
Itpr2 |
G |
T |
6: 146,013,176 (GRCm39) |
P2667Q |
probably benign |
Het |
Itsn2 |
G |
T |
12: 4,683,044 (GRCm39) |
|
probably benign |
Het |
Jakmip2 |
A |
G |
18: 43,698,995 (GRCm39) |
L488P |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 41,265,858 (GRCm39) |
C248S |
probably damaging |
Het |
Lrrc17 |
A |
T |
5: 21,780,046 (GRCm39) |
D340V |
probably damaging |
Het |
Megf9 |
T |
C |
4: 70,351,679 (GRCm39) |
T481A |
probably damaging |
Het |
Mrc1 |
T |
C |
2: 14,249,015 (GRCm39) |
S184P |
possibly damaging |
Het |
Msh4 |
A |
T |
3: 153,573,472 (GRCm39) |
Y533* |
probably null |
Het |
Mug1 |
A |
G |
6: 121,847,458 (GRCm39) |
N612S |
probably benign |
Het |
Nectin2 |
G |
T |
7: 19,464,539 (GRCm39) |
S288R |
probably damaging |
Het |
Neurog2 |
A |
T |
3: 127,427,754 (GRCm39) |
H126L |
probably damaging |
Het |
Nol10 |
A |
T |
12: 17,423,585 (GRCm39) |
E310V |
probably damaging |
Het |
Or1f12 |
T |
G |
13: 21,721,422 (GRCm39) |
K251T |
probably damaging |
Het |
Or4c29 |
A |
G |
2: 88,740,522 (GRCm39) |
S72P |
probably damaging |
Het |
Or51h7 |
A |
T |
7: 102,591,678 (GRCm39) |
F35L |
probably benign |
Het |
Or5h23 |
T |
A |
16: 58,905,949 (GRCm39) |
K299I |
probably benign |
Het |
Pcdhb7 |
T |
A |
18: 37,476,335 (GRCm39) |
F490L |
probably benign |
Het |
Pcsk1 |
T |
A |
13: 75,260,653 (GRCm39) |
|
probably benign |
Het |
Plekhn1 |
T |
A |
4: 156,306,339 (GRCm39) |
D577V |
probably damaging |
Het |
Prrc2c |
C |
A |
1: 162,537,903 (GRCm39) |
|
probably benign |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Pzp |
G |
A |
6: 128,465,010 (GRCm39) |
T1288M |
probably damaging |
Het |
Radil |
A |
C |
5: 142,492,718 (GRCm39) |
H63Q |
probably benign |
Het |
Rai1 |
T |
C |
11: 60,078,422 (GRCm39) |
S829P |
probably benign |
Het |
Rd3 |
A |
G |
1: 191,715,488 (GRCm39) |
I88V |
probably damaging |
Het |
Rfesd |
T |
C |
13: 76,156,244 (GRCm39) |
D54G |
probably damaging |
Het |
Rnf213 |
A |
C |
11: 119,305,896 (GRCm39) |
K568T |
probably damaging |
Het |
Scaper |
T |
A |
9: 55,650,923 (GRCm39) |
K913N |
probably damaging |
Het |
Serpina3c |
T |
C |
12: 104,115,628 (GRCm39) |
|
probably null |
Het |
Serpinb6d |
A |
T |
13: 33,850,357 (GRCm39) |
K61N |
probably benign |
Het |
Skint4 |
A |
T |
4: 111,944,183 (GRCm39) |
|
probably null |
Het |
Sod1 |
T |
C |
16: 90,017,801 (GRCm39) |
I19T |
possibly damaging |
Het |
Stfa3 |
C |
A |
16: 36,271,042 (GRCm39) |
G81* |
probably null |
Het |
Ubr4 |
A |
G |
4: 139,137,960 (GRCm39) |
T1106A |
probably benign |
Het |
Uggt2 |
T |
A |
14: 119,256,917 (GRCm39) |
N1106Y |
probably damaging |
Het |
Vmn1r217 |
G |
A |
13: 23,298,714 (GRCm39) |
Q63* |
probably null |
Het |
Vmn2r129 |
A |
T |
4: 156,690,673 (GRCm39) |
|
noncoding transcript |
Het |
Vps13b |
C |
A |
15: 35,792,334 (GRCm39) |
P2201T |
probably damaging |
Het |
Vps13b |
C |
A |
15: 35,792,335 (GRCm39) |
P2201Q |
probably damaging |
Het |
Vps13d |
G |
T |
4: 144,813,893 (GRCm39) |
|
probably benign |
Het |
Zer1 |
A |
G |
2: 29,994,887 (GRCm39) |
C503R |
probably damaging |
Het |
Zfp369 |
T |
C |
13: 65,444,762 (GRCm39) |
V635A |
probably benign |
Het |
Zfp608 |
A |
T |
18: 55,031,125 (GRCm39) |
Y938* |
probably null |
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 |
IGL02324:Pappa
|
APN |
4 |
65,115,045 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
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 |
|