Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abi1 |
T |
C |
2: 22,843,555 (GRCm39) |
T297A |
probably benign |
Het |
Acadl |
G |
T |
1: 66,892,337 (GRCm39) |
T162K |
probably benign |
Het |
Aldoart2 |
A |
T |
12: 55,612,536 (GRCm39) |
I154F |
probably damaging |
Het |
Alkbh8 |
G |
A |
9: 3,385,478 (GRCm39) |
R625H |
probably damaging |
Het |
Ankrd31 |
T |
A |
13: 96,969,036 (GRCm39) |
V891E |
probably benign |
Het |
Aopep |
G |
A |
13: 63,216,065 (GRCm39) |
V446I |
probably damaging |
Het |
Atp8b5 |
C |
T |
4: 43,356,982 (GRCm39) |
R577* |
probably null |
Het |
Capn3 |
G |
T |
2: 120,316,867 (GRCm39) |
E285D |
probably benign |
Het |
Cd79b |
G |
T |
11: 106,204,526 (GRCm39) |
P87T |
probably damaging |
Het |
Celsr2 |
T |
G |
3: 108,319,971 (GRCm39) |
D947A |
probably damaging |
Het |
Csmd3 |
A |
C |
15: 47,569,783 (GRCm39) |
S1213R |
|
Het |
Cyp2j5 |
T |
C |
4: 96,552,241 (GRCm39) |
M3V |
probably benign |
Het |
Ddi1 |
C |
T |
9: 6,265,787 (GRCm39) |
R194K |
probably benign |
Het |
Decr1 |
T |
C |
4: 15,933,019 (GRCm39) |
K49R |
probably benign |
Het |
Dnah10 |
A |
C |
5: 124,905,575 (GRCm39) |
E4130A |
probably benign |
Het |
Dst |
A |
G |
1: 34,323,444 (GRCm39) |
D4648G |
probably damaging |
Het |
Ecd |
A |
G |
14: 20,380,020 (GRCm39) |
|
probably null |
Het |
Erbin |
A |
T |
13: 103,970,864 (GRCm39) |
Y917* |
probably null |
Het |
Evpl |
T |
C |
11: 116,113,989 (GRCm39) |
K1234E |
probably benign |
Het |
F11r |
T |
A |
1: 171,289,191 (GRCm39) |
Y218N |
possibly damaging |
Het |
Fam43a |
C |
G |
16: 30,420,622 (GRCm39) |
T402S |
probably benign |
Het |
Frem2 |
T |
C |
3: 53,457,064 (GRCm39) |
N2096S |
probably benign |
Het |
Gpd2 |
T |
A |
2: 57,196,962 (GRCm39) |
Y172* |
probably null |
Het |
Hscb |
A |
G |
5: 110,983,844 (GRCm39) |
V90A |
probably benign |
Het |
Iqgap2 |
T |
C |
13: 95,794,387 (GRCm39) |
D1195G |
probably damaging |
Het |
Map2k2 |
T |
C |
10: 80,950,900 (GRCm39) |
I115T |
probably damaging |
Het |
Mast2 |
C |
T |
4: 116,170,172 (GRCm39) |
R707H |
probably damaging |
Het |
Mindy4 |
A |
G |
6: 55,277,977 (GRCm39) |
N607S |
probably damaging |
Het |
Mrpl9 |
T |
A |
3: 94,351,050 (GRCm39) |
Y77N |
probably damaging |
Het |
Muc16 |
G |
A |
9: 18,570,347 (GRCm39) |
T724I |
unknown |
Het |
Nat3 |
A |
T |
8: 68,000,478 (GRCm39) |
Y119F |
possibly damaging |
Het |
Nol7 |
T |
C |
13: 43,554,990 (GRCm39) |
S208P |
probably damaging |
Het |
Notch3 |
A |
T |
17: 32,365,545 (GRCm39) |
C1056S |
probably damaging |
Het |
Nup50l |
TCC |
TCCGCC |
6: 96,142,078 (GRCm39) |
|
probably benign |
Het |
Nup50l |
TCC |
TCCCCC |
6: 96,142,084 (GRCm39) |
|
probably benign |
Het |
Or13j1 |
A |
T |
4: 43,705,884 (GRCm39) |
V228E |
probably damaging |
Het |
Or3a4 |
T |
A |
11: 73,945,301 (GRCm39) |
I95F |
probably benign |
Het |
Or5al5 |
A |
T |
2: 85,961,721 (GRCm39) |
Y95* |
probably null |
Het |
Or8g17 |
G |
T |
9: 38,930,783 (GRCm39) |
T18K |
probably damaging |
Het |
Osbpl3 |
A |
C |
6: 50,322,995 (GRCm39) |
L288R |
probably damaging |
Het |
Oscp1 |
A |
C |
4: 125,982,116 (GRCm39) |
D352A |
possibly damaging |
Het |
Pcdh9 |
G |
A |
14: 94,123,222 (GRCm39) |
R983C |
probably benign |
Het |
Pcdhgb8 |
T |
C |
18: 37,896,555 (GRCm39) |
S542P |
probably benign |
Het |
Pi4ka |
T |
C |
16: 17,174,030 (GRCm39) |
T490A |
|
Het |
Pkd1l1 |
A |
T |
11: 8,897,315 (GRCm39) |
D531E |
|
Het |
Potefam3d |
A |
T |
8: 69,975,404 (GRCm39) |
Y21N |
possibly damaging |
Het |
Prr3 |
G |
T |
17: 36,290,053 (GRCm39) |
D26E |
possibly damaging |
Het |
Psmd8 |
T |
C |
7: 28,880,001 (GRCm39) |
K24E |
probably benign |
Het |
Rasgrp4 |
G |
A |
7: 28,849,362 (GRCm39) |
C583Y |
probably damaging |
Het |
Rest |
A |
G |
5: 77,416,171 (GRCm39) |
I128M |
probably benign |
Het |
Rusc2 |
T |
C |
4: 43,421,851 (GRCm39) |
F757S |
probably benign |
Het |
Ryr1 |
A |
G |
7: 28,782,810 (GRCm39) |
S1942P |
probably benign |
Het |
Sdk2 |
C |
T |
11: 113,745,177 (GRCm39) |
R706Q |
probably damaging |
Het |
Sergef |
G |
T |
7: 46,264,062 (GRCm39) |
T275K |
probably damaging |
Het |
Serpina10 |
T |
C |
12: 103,594,569 (GRCm39) |
T217A |
probably damaging |
Het |
Shd |
G |
C |
17: 56,283,235 (GRCm39) |
S288T |
probably damaging |
Het |
Siglec15 |
C |
A |
18: 78,091,803 (GRCm39) |
A133S |
possibly damaging |
Het |
Stat4 |
C |
T |
1: 52,118,932 (GRCm39) |
P325L |
probably damaging |
Het |
Syt8 |
G |
A |
7: 141,993,881 (GRCm39) |
G344D |
probably damaging |
Het |
Tes |
A |
G |
6: 17,097,291 (GRCm39) |
E133G |
probably benign |
Het |
Tmprss2 |
T |
C |
16: 97,369,616 (GRCm39) |
Y386C |
probably damaging |
Het |
Tnfrsf11b |
A |
T |
15: 54,115,502 (GRCm39) |
L365Q |
probably damaging |
Het |
Tns1 |
T |
A |
1: 73,992,596 (GRCm39) |
D67V |
probably damaging |
Het |
Tns2 |
T |
C |
15: 102,021,280 (GRCm39) |
S982P |
probably damaging |
Het |
Tpcn2 |
A |
T |
7: 144,814,683 (GRCm39) |
F473I |
probably benign |
Het |
Tsg101 |
A |
T |
7: 46,542,257 (GRCm39) |
I232N |
probably damaging |
Het |
Ttc3 |
T |
C |
16: 94,268,848 (GRCm39) |
S1977P |
probably benign |
Het |
Ttll11 |
T |
A |
2: 35,869,527 (GRCm39) |
E37V |
unknown |
Het |
Ttn |
A |
T |
2: 76,649,160 (GRCm39) |
V12716E |
possibly damaging |
Het |
Vmn2r70 |
A |
C |
7: 85,212,923 (GRCm39) |
S495A |
probably benign |
Het |
Zfp974 |
A |
G |
7: 27,610,697 (GRCm39) |
C343R |
probably damaging |
Het |
Zfy1 |
A |
T |
Y: 726,004 (GRCm39) |
I587N |
possibly damaging |
Het |
|
Other mutations in Rftn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00552:Rftn1
|
APN |
17 |
50,362,405 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02318:Rftn1
|
APN |
17 |
50,343,998 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02568:Rftn1
|
APN |
17 |
50,344,027 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02873:Rftn1
|
APN |
17 |
50,476,180 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02965:Rftn1
|
APN |
17 |
50,362,280 (GRCm39) |
missense |
probably benign |
0.32 |
BB001:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
BB003:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
BB004:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
BB005:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
BB011:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
BB013:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
BB014:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
BB015:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R0544:Rftn1
|
UTSW |
17 |
50,301,289 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2219:Rftn1
|
UTSW |
17 |
50,476,173 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R4542:Rftn1
|
UTSW |
17 |
50,362,259 (GRCm39) |
splice site |
probably null |
|
R5318:Rftn1
|
UTSW |
17 |
50,301,486 (GRCm39) |
missense |
probably benign |
0.09 |
R5605:Rftn1
|
UTSW |
17 |
50,354,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R5700:Rftn1
|
UTSW |
17 |
50,309,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R5853:Rftn1
|
UTSW |
17 |
50,354,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R6459:Rftn1
|
UTSW |
17 |
50,354,334 (GRCm39) |
missense |
probably benign |
0.02 |
R6994:Rftn1
|
UTSW |
17 |
50,344,019 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7210:Rftn1
|
UTSW |
17 |
50,301,335 (GRCm39) |
nonsense |
probably null |
|
R7283:Rftn1
|
UTSW |
17 |
50,354,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R7348:Rftn1
|
UTSW |
17 |
50,311,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R7444:Rftn1
|
UTSW |
17 |
50,354,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R7684:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R7685:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R7686:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R7881:Rftn1
|
UTSW |
17 |
50,354,463 (GRCm39) |
missense |
probably benign |
0.08 |
R7924:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R7926:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R7927:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R7928:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R7943:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8162:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8164:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8248:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8249:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8250:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8271:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8272:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8273:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8296:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8297:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8300:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8315:Rftn1
|
UTSW |
17 |
50,309,665 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8551:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8552:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8554:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8555:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8736:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8739:Rftn1
|
UTSW |
17 |
50,354,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R9526:Rftn1
|
UTSW |
17 |
50,301,237 (GRCm39) |
missense |
probably benign |
0.31 |
Z1176:Rftn1
|
UTSW |
17 |
50,476,031 (GRCm39) |
missense |
probably damaging |
1.00 |
|