Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930003A15Rik |
T |
C |
16: 19,702,518 (GRCm39) |
|
noncoding transcript |
Het |
Angpt4 |
A |
G |
2: 151,785,342 (GRCm39) |
M453V |
probably benign |
Het |
Atr |
T |
A |
9: 95,779,783 (GRCm39) |
D1380E |
probably benign |
Het |
Carmil1 |
A |
T |
13: 24,278,438 (GRCm39) |
M177K |
probably damaging |
Het |
Cenpk |
T |
A |
13: 104,379,280 (GRCm39) |
I203N |
probably damaging |
Het |
Cerk |
A |
T |
15: 86,027,014 (GRCm39) |
N165K |
probably benign |
Het |
Col27a1 |
G |
A |
4: 63,242,869 (GRCm39) |
|
probably benign |
Het |
Crb2 |
A |
T |
2: 37,681,428 (GRCm39) |
D757V |
probably benign |
Het |
Csnk1a1 |
A |
G |
18: 61,701,376 (GRCm39) |
D91G |
probably damaging |
Het |
Dnajc6 |
G |
T |
4: 101,474,057 (GRCm39) |
W486L |
probably damaging |
Het |
Elmod1 |
C |
T |
9: 53,841,507 (GRCm39) |
|
probably benign |
Het |
Ercc3 |
G |
T |
18: 32,381,360 (GRCm39) |
R392L |
possibly damaging |
Het |
Fam135b |
C |
T |
15: 71,335,410 (GRCm39) |
V595I |
probably benign |
Het |
Fem1al |
T |
A |
11: 29,774,360 (GRCm39) |
I366F |
probably damaging |
Het |
Fermt1 |
A |
T |
2: 132,775,059 (GRCm39) |
S256T |
probably damaging |
Het |
Fstl5 |
G |
T |
3: 76,443,618 (GRCm39) |
C321F |
probably damaging |
Het |
Gpatch1 |
T |
G |
7: 35,002,742 (GRCm39) |
N256T |
probably benign |
Het |
Gpd2 |
T |
A |
2: 57,245,581 (GRCm39) |
S425R |
probably damaging |
Het |
Igkv4-57-1 |
T |
G |
6: 69,521,574 (GRCm39) |
M43L |
probably benign |
Het |
Itgae |
A |
G |
11: 73,004,427 (GRCm39) |
Q238R |
probably damaging |
Het |
Lats1 |
T |
A |
10: 7,588,510 (GRCm39) |
D1042E |
probably benign |
Het |
Lcn8 |
G |
A |
2: 25,545,377 (GRCm39) |
G156D |
probably damaging |
Het |
Loxl4 |
A |
C |
19: 42,593,718 (GRCm39) |
V224G |
probably benign |
Het |
Lrp2 |
T |
A |
2: 69,285,177 (GRCm39) |
D3827V |
probably damaging |
Het |
Neb |
C |
A |
2: 52,073,837 (GRCm39) |
R231S |
probably benign |
Het |
Or2g1 |
G |
A |
17: 38,106,679 (GRCm39) |
V115I |
probably benign |
Het |
Or5b105 |
A |
T |
19: 13,080,401 (GRCm39) |
M89K |
probably benign |
Het |
Or6c211 |
A |
G |
10: 129,505,809 (GRCm39) |
M193T |
probably benign |
Het |
Or6d13 |
T |
G |
6: 116,517,900 (GRCm39) |
M162R |
possibly damaging |
Het |
Or8g54 |
T |
G |
9: 39,707,475 (GRCm39) |
M268R |
probably benign |
Het |
Pced1a |
G |
A |
2: 130,264,755 (GRCm39) |
T61I |
possibly damaging |
Het |
Pik3cg |
T |
C |
12: 32,250,594 (GRCm39) |
D731G |
probably damaging |
Het |
Plxnb1 |
G |
A |
9: 108,934,054 (GRCm39) |
D761N |
probably benign |
Het |
Pmp22 |
T |
C |
11: 63,049,135 (GRCm39) |
V126A |
probably benign |
Het |
Ppp6r2 |
G |
T |
15: 89,152,748 (GRCm39) |
R296S |
probably damaging |
Het |
Prkcq |
A |
C |
2: 11,265,597 (GRCm39) |
H438P |
probably damaging |
Het |
Ryr1 |
T |
A |
7: 28,774,624 (GRCm39) |
Y2339F |
probably damaging |
Het |
Scaper |
T |
C |
9: 55,765,686 (GRCm39) |
|
probably benign |
Het |
Scp2 |
T |
A |
4: 107,955,312 (GRCm39) |
I144F |
probably benign |
Het |
Secisbp2 |
T |
C |
13: 51,806,793 (GRCm39) |
|
probably null |
Het |
Sema5a |
T |
A |
15: 32,669,554 (GRCm39) |
Y693N |
probably damaging |
Het |
Sin3b |
T |
A |
8: 73,480,213 (GRCm39) |
I905K |
probably damaging |
Het |
Slc13a3 |
T |
A |
2: 165,279,227 (GRCm39) |
M195L |
probably benign |
Het |
Strada |
A |
G |
11: 106,054,863 (GRCm39) |
|
probably benign |
Het |
Stx18 |
G |
A |
5: 38,293,655 (GRCm39) |
V294M |
probably damaging |
Het |
Tbpl2 |
A |
T |
2: 23,983,845 (GRCm39) |
N197K |
probably benign |
Het |
Tdrd9 |
A |
T |
12: 112,009,274 (GRCm39) |
H1060L |
probably damaging |
Het |
Tm4sf5 |
G |
A |
11: 70,396,223 (GRCm39) |
V23M |
possibly damaging |
Het |
Tmem54 |
C |
A |
4: 129,004,705 (GRCm39) |
L187I |
probably damaging |
Het |
Tmprss5 |
A |
G |
9: 49,024,528 (GRCm39) |
H281R |
possibly damaging |
Het |
Trim30c |
A |
G |
7: 104,031,820 (GRCm39) |
Y332H |
possibly damaging |
Het |
Uba6 |
T |
A |
5: 86,275,633 (GRCm39) |
|
probably benign |
Het |
Unc80 |
C |
A |
1: 66,670,613 (GRCm39) |
P1912Q |
probably damaging |
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 |
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 |
|