Other mutations in this stock |
Total: 124 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931428L18Rik |
A |
T |
1: 31,261,580 (GRCm39) |
|
probably benign |
Het |
Acy1 |
T |
A |
9: 106,312,321 (GRCm39) |
I14F |
probably null |
Het |
Ago1 |
T |
C |
4: 126,342,652 (GRCm39) |
D193G |
possibly damaging |
Het |
Arhgap45 |
A |
T |
10: 79,856,791 (GRCm39) |
H201L |
probably damaging |
Het |
Armc9 |
G |
A |
1: 86,140,801 (GRCm39) |
D63N |
probably damaging |
Het |
Asb17 |
A |
T |
3: 153,556,336 (GRCm39) |
I148F |
possibly damaging |
Het |
Atf7ip2 |
A |
G |
16: 10,059,447 (GRCm39) |
E329G |
possibly damaging |
Het |
Atp2a1 |
T |
A |
7: 126,052,600 (GRCm39) |
D373V |
probably benign |
Het |
Cacna1e |
G |
T |
1: 154,357,380 (GRCm39) |
Y603* |
probably null |
Het |
Cbln4 |
G |
A |
2: 171,880,901 (GRCm39) |
T131I |
probably damaging |
Het |
Ccdc126 |
A |
G |
6: 49,311,181 (GRCm39) |
E63G |
probably damaging |
Het |
Ccl4 |
T |
A |
11: 83,553,504 (GRCm39) |
S6T |
unknown |
Het |
Ccnb1 |
A |
T |
13: 100,918,209 (GRCm39) |
I146K |
possibly damaging |
Het |
Ccr8 |
T |
A |
9: 119,923,815 (GRCm39) |
M310K |
probably benign |
Het |
Cd180 |
A |
T |
13: 102,875,672 (GRCm39) |
|
probably null |
Het |
Cd46 |
G |
C |
1: 194,765,107 (GRCm39) |
|
probably benign |
Het |
Cebpb |
A |
G |
2: 167,531,005 (GRCm39) |
M22V |
probably benign |
Het |
Cep152 |
A |
G |
2: 125,453,016 (GRCm39) |
I352T |
possibly damaging |
Het |
Cep295 |
T |
G |
9: 15,244,456 (GRCm39) |
E1333D |
probably damaging |
Het |
Ces4a |
A |
G |
8: 105,864,613 (GRCm39) |
H30R |
probably benign |
Het |
Chrm3 |
A |
G |
13: 9,927,450 (GRCm39) |
Y529H |
probably damaging |
Het |
Chrnb4 |
T |
C |
9: 54,942,101 (GRCm39) |
Y391C |
probably benign |
Het |
Clca3a2 |
A |
G |
3: 144,523,692 (GRCm39) |
Y98H |
probably damaging |
Het |
Clvs1 |
C |
T |
4: 9,424,216 (GRCm39) |
H221Y |
possibly damaging |
Het |
Col3a1 |
G |
A |
1: 45,379,112 (GRCm39) |
|
probably benign |
Het |
Cpn2 |
T |
G |
16: 30,079,344 (GRCm39) |
N119T |
probably damaging |
Het |
Cspg4b |
C |
A |
13: 113,504,882 (GRCm39) |
Q2004K |
probably damaging |
Het |
Cubn |
T |
A |
2: 13,494,721 (GRCm39) |
Q109H |
probably benign |
Het |
Cyp26b1 |
A |
G |
6: 84,553,954 (GRCm39) |
V221A |
possibly damaging |
Het |
Cyp2e1 |
T |
G |
7: 140,350,030 (GRCm39) |
N238K |
probably damaging |
Het |
Dst |
C |
T |
1: 34,247,669 (GRCm39) |
A1693V |
probably damaging |
Het |
Dync2li1 |
A |
G |
17: 84,956,683 (GRCm39) |
Q281R |
probably benign |
Het |
Enpp2 |
C |
T |
15: 54,745,543 (GRCm39) |
G318S |
probably damaging |
Het |
Entrep1 |
T |
C |
19: 23,950,789 (GRCm39) |
*597W |
probably null |
Het |
F13a1 |
G |
T |
13: 37,061,736 (GRCm39) |
P676T |
probably benign |
Het |
Fam227a |
T |
C |
15: 79,521,262 (GRCm39) |
H267R |
possibly damaging |
Het |
Fam78a |
G |
A |
2: 31,959,427 (GRCm39) |
R228C |
probably damaging |
Het |
Fbxw25 |
T |
C |
9: 109,480,705 (GRCm39) |
N325S |
possibly damaging |
Het |
Foxred1 |
T |
C |
9: 35,121,210 (GRCm39) |
|
probably benign |
Het |
Fstl5 |
T |
A |
3: 76,496,272 (GRCm39) |
V345E |
probably damaging |
Het |
Fzd8 |
GAAAAACTCA |
GA |
18: 9,214,492 (GRCm39) |
|
probably null |
Het |
Hand1 |
T |
C |
11: 57,722,078 (GRCm39) |
R179G |
possibly damaging |
Het |
Hk1 |
G |
T |
10: 62,194,165 (GRCm39) |
|
probably benign |
Het |
Hmcn1 |
A |
C |
1: 150,598,286 (GRCm39) |
L1672R |
probably damaging |
Het |
Hps5 |
G |
A |
7: 46,418,775 (GRCm39) |
Q297* |
probably null |
Het |
Iars1 |
T |
A |
13: 49,871,460 (GRCm39) |
F699I |
probably benign |
Het |
Ift140 |
G |
A |
17: 25,267,462 (GRCm39) |
G620E |
probably benign |
Het |
Igkv4-80 |
A |
C |
6: 68,993,649 (GRCm39) |
S81A |
probably benign |
Het |
Inpp4a |
T |
G |
1: 37,426,922 (GRCm39) |
Y628D |
possibly damaging |
Het |
Itk |
C |
T |
11: 46,280,152 (GRCm39) |
R29H |
probably damaging |
Het |
Kcnv1 |
A |
G |
15: 44,972,644 (GRCm39) |
F413S |
probably damaging |
Het |
Klhl3 |
A |
T |
13: 58,250,231 (GRCm39) |
Y4* |
probably null |
Het |
Lonrf1 |
C |
A |
8: 36,701,103 (GRCm39) |
C369F |
probably damaging |
Het |
Magohb |
A |
T |
6: 131,261,558 (GRCm39) |
|
probably benign |
Het |
Map3k4 |
G |
A |
17: 12,490,787 (GRCm39) |
R215C |
probably damaging |
Het |
Map3k8 |
A |
T |
18: 4,339,548 (GRCm39) |
S274R |
possibly damaging |
Het |
Masp1 |
T |
G |
16: 23,283,826 (GRCm39) |
M470L |
probably damaging |
Het |
Mfng |
C |
T |
15: 78,648,588 (GRCm39) |
R163H |
probably benign |
Het |
Muc4 |
A |
T |
16: 32,576,472 (GRCm39) |
|
probably benign |
Het |
Myo1c |
T |
A |
11: 75,562,676 (GRCm39) |
V981E |
probably damaging |
Het |
Nedd9 |
A |
T |
13: 41,492,411 (GRCm39) |
I27K |
probably damaging |
Het |
Nkd2 |
C |
A |
13: 73,970,841 (GRCm39) |
G247V |
probably damaging |
Het |
Nucb2 |
A |
C |
7: 116,139,199 (GRCm39) |
Q398P |
possibly damaging |
Het |
Numa1 |
T |
A |
7: 101,660,064 (GRCm39) |
D376E |
probably benign |
Het |
Or2w1 |
G |
A |
13: 21,317,241 (GRCm39) |
V99I |
probably benign |
Het |
Or4c101 |
C |
T |
2: 88,389,930 (GRCm39) |
T39I |
probably benign |
Het |
Or4n5 |
T |
C |
14: 50,133,206 (GRCm39) |
T18A |
probably benign |
Het |
Or4p23 |
A |
T |
2: 88,576,398 (GRCm39) |
L278* |
probably null |
Het |
Or4q3 |
C |
T |
14: 50,583,345 (GRCm39) |
V185M |
probably damaging |
Het |
Or5b119 |
G |
A |
19: 13,456,956 (GRCm39) |
T202I |
possibly damaging |
Het |
Or6c76b |
A |
T |
10: 129,692,896 (GRCm39) |
N170Y |
possibly damaging |
Het |
Or8d23 |
A |
T |
9: 38,842,129 (GRCm39) |
I221F |
probably damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pamr1 |
C |
T |
2: 102,472,549 (GRCm39) |
T616I |
probably benign |
Het |
Pcnx1 |
G |
A |
12: 82,038,599 (GRCm39) |
V1955I |
possibly damaging |
Het |
Pira13 |
A |
G |
7: 3,825,676 (GRCm39) |
Y398H |
probably damaging |
Het |
Plekha3 |
T |
A |
2: 76,510,571 (GRCm39) |
D35E |
possibly damaging |
Het |
Pnpla2 |
T |
G |
7: 141,038,085 (GRCm39) |
N184K |
probably damaging |
Het |
Polr3a |
C |
T |
14: 24,502,692 (GRCm39) |
E1216K |
probably benign |
Het |
Prdm13 |
G |
T |
4: 21,678,223 (GRCm39) |
|
probably benign |
Het |
Prss53 |
T |
C |
7: 127,487,879 (GRCm39) |
N201S |
probably benign |
Het |
Rab11fip2 |
A |
G |
19: 59,924,290 (GRCm39) |
L338S |
probably damaging |
Het |
Rad50 |
T |
C |
11: 53,575,102 (GRCm39) |
N546S |
probably benign |
Het |
Ralgapa1 |
T |
C |
12: 55,809,359 (GRCm39) |
D472G |
possibly damaging |
Het |
Rexo4 |
A |
G |
2: 26,850,346 (GRCm39) |
I277T |
probably damaging |
Het |
Rimbp2 |
C |
T |
5: 128,865,579 (GRCm39) |
V590I |
probably benign |
Het |
Ripor3 |
A |
G |
2: 167,824,736 (GRCm39) |
V864A |
probably benign |
Het |
Rnpc3 |
G |
A |
3: 113,418,628 (GRCm39) |
H107Y |
possibly damaging |
Het |
Ryr1 |
A |
T |
7: 28,767,520 (GRCm39) |
D2927E |
probably damaging |
Het |
Samd9l |
G |
A |
6: 3,375,621 (GRCm39) |
Q547* |
probably null |
Het |
Scaper |
T |
C |
9: 55,716,459 (GRCm39) |
E724G |
probably damaging |
Het |
Secisbp2l |
C |
T |
2: 125,582,409 (GRCm39) |
V1016I |
probably damaging |
Het |
Selenoo |
T |
A |
15: 88,982,970 (GRCm39) |
M499K |
probably damaging |
Het |
Sema4a |
T |
A |
3: 88,345,568 (GRCm39) |
D505V |
probably damaging |
Het |
Sema5a |
T |
C |
15: 32,679,310 (GRCm39) |
M863T |
probably damaging |
Het |
Slc24a5 |
T |
C |
2: 124,929,940 (GRCm39) |
C414R |
probably damaging |
Het |
Slc34a2 |
A |
G |
5: 53,224,942 (GRCm39) |
D361G |
probably damaging |
Het |
Slc5a1 |
T |
C |
5: 33,261,858 (GRCm39) |
Y20H |
probably benign |
Het |
Slx4ip |
A |
T |
2: 136,910,267 (GRCm39) |
|
probably benign |
Het |
Snx14 |
T |
A |
9: 88,280,341 (GRCm39) |
E538V |
probably damaging |
Het |
Sspo |
C |
A |
6: 48,442,486 (GRCm39) |
L1994I |
probably damaging |
Het |
St13 |
G |
C |
15: 81,283,786 (GRCm39) |
R4G |
probably benign |
Het |
Stap2 |
A |
G |
17: 56,304,901 (GRCm39) |
S294P |
possibly damaging |
Het |
Stat1 |
C |
A |
1: 52,193,082 (GRCm39) |
Y651* |
probably null |
Het |
Syne2 |
A |
G |
12: 75,946,046 (GRCm39) |
T373A |
probably benign |
Het |
Tacc2 |
A |
G |
7: 130,330,318 (GRCm39) |
S201G |
probably damaging |
Het |
Tdpoz3 |
G |
A |
3: 93,734,287 (GRCm39) |
E321K |
probably benign |
Het |
Thumpd1 |
T |
C |
7: 119,316,002 (GRCm39) |
T316A |
probably benign |
Het |
Tlr3 |
A |
T |
8: 45,850,072 (GRCm39) |
C866S |
probably benign |
Het |
Tmprss11g |
T |
A |
5: 86,644,401 (GRCm39) |
I148F |
probably benign |
Het |
Topbp1 |
T |
A |
9: 103,205,568 (GRCm39) |
|
probably benign |
Het |
Tpm1 |
T |
C |
9: 66,935,331 (GRCm39) |
|
probably null |
Het |
Traf3ip2 |
T |
A |
10: 39,502,096 (GRCm39) |
S81R |
probably damaging |
Het |
Trim29 |
T |
A |
9: 43,222,265 (GRCm39) |
N31K |
probably benign |
Het |
Ubn2 |
C |
T |
6: 38,467,433 (GRCm39) |
P563S |
probably benign |
Het |
Usp24 |
T |
C |
4: 106,283,743 (GRCm39) |
Y2418H |
probably benign |
Het |
Vmn2r6 |
T |
A |
3: 64,463,766 (GRCm39) |
D267V |
probably damaging |
Het |
Wapl |
T |
A |
14: 34,414,052 (GRCm39) |
C305S |
probably benign |
Het |
Yme1l1 |
C |
A |
2: 23,058,333 (GRCm39) |
S155* |
probably null |
Het |
Ythdf3 |
T |
A |
3: 16,258,220 (GRCm39) |
H126Q |
probably damaging |
Het |
Zbtb32 |
A |
T |
7: 30,290,678 (GRCm39) |
C206S |
possibly damaging |
Het |
Zbtb47 |
T |
C |
9: 121,593,045 (GRCm39) |
V455A |
probably damaging |
Het |
Zfp518a |
A |
T |
19: 40,902,707 (GRCm39) |
I879F |
probably benign |
Het |
Zfp938 |
A |
T |
10: 82,062,012 (GRCm39) |
Y203N |
possibly damaging |
Het |
|
Other mutations in Ppp1r21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01753:Ppp1r21
|
APN |
17 |
88,869,530 (GRCm39) |
splice site |
probably benign |
|
IGL02366:Ppp1r21
|
APN |
17 |
88,855,090 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02604:Ppp1r21
|
APN |
17 |
88,880,171 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02680:Ppp1r21
|
APN |
17 |
88,891,290 (GRCm39) |
missense |
probably benign |
0.00 |
R0266:Ppp1r21
|
UTSW |
17 |
88,876,500 (GRCm39) |
splice site |
probably benign |
|
R0436:Ppp1r21
|
UTSW |
17 |
88,873,117 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1398:Ppp1r21
|
UTSW |
17 |
88,850,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R1472:Ppp1r21
|
UTSW |
17 |
88,866,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R1599:Ppp1r21
|
UTSW |
17 |
88,880,055 (GRCm39) |
missense |
probably benign |
0.00 |
R1677:Ppp1r21
|
UTSW |
17 |
88,858,097 (GRCm39) |
missense |
probably benign |
0.04 |
R1760:Ppp1r21
|
UTSW |
17 |
88,869,653 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2571:Ppp1r21
|
UTSW |
17 |
88,852,810 (GRCm39) |
missense |
probably benign |
0.06 |
R3700:Ppp1r21
|
UTSW |
17 |
88,889,882 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3786:Ppp1r21
|
UTSW |
17 |
88,884,555 (GRCm39) |
splice site |
probably null |
|
R3959:Ppp1r21
|
UTSW |
17 |
88,857,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R4649:Ppp1r21
|
UTSW |
17 |
88,856,941 (GRCm39) |
missense |
probably benign |
|
R4654:Ppp1r21
|
UTSW |
17 |
88,866,227 (GRCm39) |
missense |
probably benign |
0.01 |
R4724:Ppp1r21
|
UTSW |
17 |
88,863,019 (GRCm39) |
nonsense |
probably null |
|
R4766:Ppp1r21
|
UTSW |
17 |
88,880,043 (GRCm39) |
missense |
probably benign |
0.00 |
R4933:Ppp1r21
|
UTSW |
17 |
88,855,049 (GRCm39) |
missense |
probably benign |
0.07 |
R4934:Ppp1r21
|
UTSW |
17 |
88,852,804 (GRCm39) |
missense |
probably damaging |
0.98 |
R4992:Ppp1r21
|
UTSW |
17 |
88,876,508 (GRCm39) |
missense |
probably benign |
0.44 |
R5109:Ppp1r21
|
UTSW |
17 |
88,866,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R5372:Ppp1r21
|
UTSW |
17 |
88,858,103 (GRCm39) |
missense |
probably benign |
0.21 |
R5861:Ppp1r21
|
UTSW |
17 |
88,889,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R6200:Ppp1r21
|
UTSW |
17 |
88,876,613 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6369:Ppp1r21
|
UTSW |
17 |
88,889,840 (GRCm39) |
splice site |
probably null |
|
R7060:Ppp1r21
|
UTSW |
17 |
88,887,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R7154:Ppp1r21
|
UTSW |
17 |
88,862,314 (GRCm39) |
missense |
probably damaging |
0.99 |
R7390:Ppp1r21
|
UTSW |
17 |
88,856,958 (GRCm39) |
missense |
probably benign |
0.26 |
R7470:Ppp1r21
|
UTSW |
17 |
88,869,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R7475:Ppp1r21
|
UTSW |
17 |
88,863,031 (GRCm39) |
missense |
probably benign |
0.07 |
R7657:Ppp1r21
|
UTSW |
17 |
88,863,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R8021:Ppp1r21
|
UTSW |
17 |
88,856,935 (GRCm39) |
missense |
probably benign |
0.00 |
R8081:Ppp1r21
|
UTSW |
17 |
88,866,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R9272:Ppp1r21
|
UTSW |
17 |
88,866,086 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9377:Ppp1r21
|
UTSW |
17 |
88,852,815 (GRCm39) |
nonsense |
probably null |
|
|