Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam26a |
A |
T |
8: 44,023,108 (GRCm39) |
N127K |
probably damaging |
Het |
Adgrl3 |
C |
T |
5: 81,457,912 (GRCm39) |
A14V |
probably benign |
Het |
Adra2b |
A |
G |
2: 127,205,858 (GRCm39) |
Y125C |
probably damaging |
Het |
Ahnak |
T |
A |
19: 8,987,711 (GRCm39) |
H2998Q |
probably benign |
Het |
B3galt1 |
C |
A |
2: 67,948,406 (GRCm39) |
H40Q |
probably benign |
Het |
Best3 |
T |
G |
10: 116,860,680 (GRCm39) |
L647V |
probably benign |
Het |
Brip1 |
T |
A |
11: 86,077,897 (GRCm39) |
E177V |
possibly damaging |
Het |
C1qtnf6 |
T |
C |
15: 78,409,109 (GRCm39) |
D246G |
probably benign |
Het |
C4b |
G |
A |
17: 34,948,233 (GRCm39) |
T1622M |
probably benign |
Het |
Catip |
G |
A |
1: 74,401,682 (GRCm39) |
|
probably null |
Het |
Ccdc138 |
T |
C |
10: 58,348,982 (GRCm39) |
V176A |
probably benign |
Het |
Ccdc85a |
T |
C |
11: 28,526,879 (GRCm39) |
H243R |
probably damaging |
Het |
Cep19 |
C |
T |
16: 31,925,883 (GRCm39) |
T97M |
probably damaging |
Het |
Copz2 |
G |
A |
11: 96,747,514 (GRCm39) |
D166N |
possibly damaging |
Het |
Dedd |
C |
T |
1: 171,168,572 (GRCm39) |
L253F |
probably damaging |
Het |
Dennd5a |
A |
G |
7: 109,497,713 (GRCm39) |
|
probably null |
Het |
Dpp10 |
A |
T |
1: 123,339,484 (GRCm39) |
S348T |
probably damaging |
Het |
Eci3 |
A |
G |
13: 35,144,382 (GRCm39) |
|
probably null |
Het |
Egr4 |
A |
G |
6: 85,490,337 (GRCm39) |
S15P |
probably benign |
Het |
Elp6 |
A |
G |
9: 110,134,397 (GRCm39) |
T12A |
probably benign |
Het |
Ewsr1 |
G |
T |
11: 5,041,367 (GRCm39) |
P113T |
unknown |
Het |
Exosc10 |
T |
G |
4: 148,664,859 (GRCm39) |
L789R |
probably benign |
Het |
Flt4 |
A |
G |
11: 49,525,161 (GRCm39) |
Y669C |
probably damaging |
Het |
Frs2 |
G |
T |
10: 116,910,070 (GRCm39) |
H431N |
probably benign |
Het |
Gm10800 |
AAGAAAACTGAAAATCAT |
A |
2: 98,497,379 (GRCm39) |
|
probably benign |
Het |
Gm19410 |
T |
C |
8: 36,247,621 (GRCm39) |
Y478H |
probably damaging |
Het |
Gm3629 |
G |
A |
14: 17,834,542 (GRCm39) |
R150C |
|
Het |
Grik4 |
A |
C |
9: 42,571,168 (GRCm39) |
L179R |
probably damaging |
Het |
Gsdmc3 |
C |
T |
15: 63,730,941 (GRCm39) |
|
probably null |
Het |
Il20ra |
T |
A |
10: 19,635,364 (GRCm39) |
M535K |
probably benign |
Het |
Il9 |
A |
G |
13: 56,628,401 (GRCm39) |
V96A |
possibly damaging |
Het |
Itgal |
A |
G |
7: 126,910,794 (GRCm39) |
D592G |
probably damaging |
Het |
Klk1b11 |
C |
T |
7: 43,427,875 (GRCm39) |
|
probably benign |
Het |
Klk1b27 |
G |
A |
7: 43,705,310 (GRCm39) |
W159* |
probably null |
Het |
Mapk9 |
T |
C |
11: 49,760,000 (GRCm39) |
Y105H |
probably damaging |
Het |
Mmp7 |
A |
G |
9: 7,697,947 (GRCm39) |
|
probably benign |
Het |
Muc2 |
T |
C |
7: 141,286,224 (GRCm39) |
I118T |
probably damaging |
Het |
N4bp2l2 |
T |
C |
5: 150,566,724 (GRCm39) |
N131D |
unknown |
Het |
Nbea |
A |
C |
3: 55,862,809 (GRCm39) |
S1814R |
probably benign |
Het |
Nlrp9c |
G |
T |
7: 26,081,837 (GRCm39) |
L630I |
probably benign |
Het |
Or1j8 |
T |
C |
2: 36,191,956 (GRCm39) |
V135A |
|
Het |
Or6c76 |
T |
C |
10: 129,612,521 (GRCm39) |
V261A |
probably damaging |
Het |
Or8g27 |
G |
A |
9: 39,128,831 (GRCm39) |
M59I |
probably damaging |
Het |
Pbx3 |
C |
A |
2: 34,114,629 (GRCm39) |
D102Y |
probably damaging |
Het |
Pdia6 |
G |
A |
12: 17,320,492 (GRCm39) |
V44I |
probably benign |
Het |
Pkdcc |
G |
A |
17: 83,528,471 (GRCm39) |
R280H |
probably damaging |
Het |
Ppm1h |
A |
G |
10: 122,638,264 (GRCm39) |
E178G |
probably benign |
Het |
Prom1 |
C |
T |
5: 44,172,161 (GRCm39) |
S619N |
probably benign |
Het |
Prtg |
A |
C |
9: 72,755,607 (GRCm39) |
I270L |
probably damaging |
Het |
Rfx6 |
A |
T |
10: 51,599,106 (GRCm39) |
H487L |
probably damaging |
Het |
Rpl18a |
A |
C |
8: 71,348,788 (GRCm39) |
Y63D |
probably benign |
Het |
Rtl1 |
T |
A |
12: 109,560,718 (GRCm39) |
M374L |
probably benign |
Het |
Scaper |
A |
G |
9: 55,819,400 (GRCm39) |
L105P |
unknown |
Het |
Slc16a13 |
T |
A |
11: 70,111,530 (GRCm39) |
|
probably benign |
Het |
Slc6a13 |
A |
G |
6: 121,313,044 (GRCm39) |
K487R |
probably benign |
Het |
Slc7a11 |
T |
A |
3: 50,332,082 (GRCm39) |
T459S |
probably benign |
Het |
Smarcad1 |
A |
G |
6: 65,075,649 (GRCm39) |
Q708R |
probably benign |
Het |
Stat2 |
T |
C |
10: 128,117,111 (GRCm39) |
|
probably null |
Het |
Syde1 |
T |
C |
10: 78,421,670 (GRCm39) |
H627R |
probably benign |
Het |
Tas2r113 |
G |
A |
6: 132,870,116 (GRCm39) |
R48H |
probably benign |
Het |
Tbc1d16 |
T |
C |
11: 119,038,626 (GRCm39) |
Y690C |
probably damaging |
Het |
Tchh |
A |
T |
3: 93,354,610 (GRCm39) |
H1350L |
unknown |
Het |
Tex15 |
T |
A |
8: 34,060,950 (GRCm39) |
Y127N |
possibly damaging |
Het |
Thsd4 |
T |
C |
9: 59,964,179 (GRCm39) |
T438A |
possibly damaging |
Het |
Tubg1 |
A |
G |
11: 101,015,099 (GRCm39) |
D216G |
probably benign |
Het |
Tyk2 |
T |
C |
9: 21,026,762 (GRCm39) |
D642G |
possibly damaging |
Het |
Uqcc1 |
C |
T |
2: 155,743,217 (GRCm39) |
|
probably null |
Het |
Uvssa |
A |
C |
5: 33,571,404 (GRCm39) |
K683Q |
probably damaging |
Het |
Vmn1r59 |
A |
T |
7: 5,457,166 (GRCm39) |
M198K |
probably benign |
Het |
Zfp772 |
T |
A |
7: 7,207,190 (GRCm39) |
H167L |
possibly damaging |
Het |
|
Other mutations in Foxred2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01394:Foxred2
|
APN |
15 |
77,839,820 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01479:Foxred2
|
APN |
15 |
77,836,489 (GRCm39) |
splice site |
probably null |
|
IGL01748:Foxred2
|
APN |
15 |
77,836,546 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02160:Foxred2
|
APN |
15 |
77,839,850 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02328:Foxred2
|
APN |
15 |
77,840,032 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02630:Foxred2
|
APN |
15 |
77,831,362 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02672:Foxred2
|
APN |
15 |
77,829,777 (GRCm39) |
critical splice donor site |
probably null |
|
soma
|
UTSW |
15 |
77,837,558 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0271:Foxred2
|
UTSW |
15 |
77,827,590 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1386:Foxred2
|
UTSW |
15 |
77,832,721 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1581:Foxred2
|
UTSW |
15 |
77,839,961 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4399:Foxred2
|
UTSW |
15 |
77,839,880 (GRCm39) |
missense |
probably benign |
0.06 |
R4399:Foxred2
|
UTSW |
15 |
77,837,558 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4528:Foxred2
|
UTSW |
15 |
77,827,449 (GRCm39) |
missense |
probably benign |
0.01 |
R4937:Foxred2
|
UTSW |
15 |
77,840,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R5165:Foxred2
|
UTSW |
15 |
77,840,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R5318:Foxred2
|
UTSW |
15 |
77,836,598 (GRCm39) |
missense |
probably benign |
0.00 |
R5893:Foxred2
|
UTSW |
15 |
77,831,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R6336:Foxred2
|
UTSW |
15 |
77,839,964 (GRCm39) |
missense |
probably damaging |
0.99 |
R6370:Foxred2
|
UTSW |
15 |
77,827,506 (GRCm39) |
missense |
probably benign |
0.01 |
R6426:Foxred2
|
UTSW |
15 |
77,837,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R6826:Foxred2
|
UTSW |
15 |
77,831,285 (GRCm39) |
missense |
probably benign |
0.01 |
R6891:Foxred2
|
UTSW |
15 |
77,839,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R6934:Foxred2
|
UTSW |
15 |
77,836,530 (GRCm39) |
nonsense |
probably null |
|
R7193:Foxred2
|
UTSW |
15 |
77,836,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R7821:Foxred2
|
UTSW |
15 |
77,827,550 (GRCm39) |
missense |
probably benign |
0.01 |
R8401:Foxred2
|
UTSW |
15 |
77,836,191 (GRCm39) |
missense |
probably damaging |
0.98 |
R8540:Foxred2
|
UTSW |
15 |
77,836,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R8844:Foxred2
|
UTSW |
15 |
77,832,677 (GRCm39) |
missense |
probably benign |
0.00 |
R8916:Foxred2
|
UTSW |
15 |
77,837,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R8963:Foxred2
|
UTSW |
15 |
77,829,805 (GRCm39) |
missense |
probably benign |
0.20 |
R9153:Foxred2
|
UTSW |
15 |
77,839,787 (GRCm39) |
critical splice donor site |
probably null |
|
R9205:Foxred2
|
UTSW |
15 |
77,836,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R9612:Foxred2
|
UTSW |
15 |
77,836,206 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Foxred2
|
UTSW |
15 |
77,836,203 (GRCm39) |
missense |
probably damaging |
1.00 |
|