Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700013D24Rik |
A |
T |
6: 124,324,803 (GRCm39) |
|
probably null |
Het |
9530002B09Rik |
T |
A |
4: 122,583,198 (GRCm39) |
C13* |
probably null |
Het |
Abca12 |
C |
A |
1: 71,302,647 (GRCm39) |
V2191L |
probably benign |
Het |
Adamts18 |
G |
C |
8: 114,571,635 (GRCm39) |
A116G |
possibly damaging |
Het |
Anxa2 |
TCCC |
TCC |
9: 69,397,036 (GRCm39) |
|
probably null |
Het |
Arfgef1 |
C |
T |
1: 10,270,103 (GRCm39) |
A349T |
probably benign |
Het |
Arhgap6 |
A |
G |
X: 167,579,496 (GRCm39) |
T94A |
probably benign |
Het |
Arhgef5 |
T |
C |
6: 43,260,252 (GRCm39) |
S1413P |
probably damaging |
Het |
Atg4c |
C |
A |
4: 99,109,463 (GRCm39) |
N143K |
possibly damaging |
Het |
C1qtnf12 |
A |
G |
4: 156,050,922 (GRCm39) |
N297S |
probably benign |
Het |
Cadps2 |
G |
T |
6: 23,838,998 (GRCm39) |
|
probably benign |
Het |
Ccdc185 |
G |
T |
1: 182,575,085 (GRCm39) |
H535N |
possibly damaging |
Het |
Ccdc57 |
A |
G |
11: 120,776,051 (GRCm39) |
|
probably benign |
Het |
Cd163 |
A |
G |
6: 124,286,167 (GRCm39) |
H239R |
probably damaging |
Het |
Ceacam2 |
G |
T |
7: 25,227,368 (GRCm39) |
C166* |
probably null |
Het |
Ces5a |
T |
A |
8: 94,261,327 (GRCm39) |
E33D |
probably benign |
Het |
Chl1 |
T |
C |
6: 103,692,362 (GRCm39) |
|
probably null |
Het |
Chsy3 |
G |
A |
18: 59,309,544 (GRCm39) |
V266I |
probably benign |
Het |
Cpa5 |
G |
T |
6: 30,626,821 (GRCm39) |
R251L |
probably damaging |
Het |
Cps1 |
A |
C |
1: 67,191,538 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
CCTTTGCGCTT |
CCTT |
15: 47,604,632 (GRCm39) |
|
probably null |
Het |
Cstf1 |
T |
C |
2: 172,217,683 (GRCm39) |
Y99H |
probably damaging |
Het |
Cyp2j11 |
G |
A |
4: 96,204,595 (GRCm39) |
T317I |
probably damaging |
Het |
Dcaf8l |
T |
C |
X: 88,449,883 (GRCm39) |
D82G |
possibly damaging |
Het |
Dennd3 |
C |
T |
15: 73,395,345 (GRCm39) |
T146M |
probably damaging |
Het |
Dennd3 |
A |
T |
15: 73,426,909 (GRCm39) |
H762L |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,406,587 (GRCm39) |
M552V |
probably benign |
Het |
Dnajc22 |
T |
C |
15: 99,002,264 (GRCm39) |
V303A |
probably benign |
Het |
Dtx2 |
T |
G |
5: 136,059,464 (GRCm39) |
L458R |
probably benign |
Het |
Fat3 |
A |
T |
9: 15,901,808 (GRCm39) |
F3072L |
probably benign |
Het |
Fgf5 |
T |
C |
5: 98,423,409 (GRCm39) |
*265R |
probably null |
Het |
Fndc11 |
A |
G |
2: 180,863,918 (GRCm39) |
E241G |
probably damaging |
Het |
Glb1 |
T |
C |
9: 114,279,716 (GRCm39) |
Y375H |
probably damaging |
Het |
Gm4922 |
T |
G |
10: 18,659,264 (GRCm39) |
Q486P |
probably benign |
Het |
Gm5786 |
A |
T |
12: 59,128,084 (GRCm39) |
|
noncoding transcript |
Het |
Hepacam2 |
A |
T |
6: 3,463,378 (GRCm39) |
|
probably benign |
Het |
Ints9 |
G |
A |
14: 65,223,792 (GRCm39) |
G89R |
possibly damaging |
Het |
Iqcm |
T |
A |
8: 76,615,241 (GRCm39) |
W441R |
probably damaging |
Het |
Itga10 |
T |
C |
3: 96,558,808 (GRCm39) |
L382P |
possibly damaging |
Het |
Itga10 |
G |
T |
3: 96,561,039 (GRCm39) |
G635W |
probably damaging |
Het |
Kbtbd2 |
A |
G |
6: 56,756,075 (GRCm39) |
Y554H |
probably damaging |
Het |
Kif1b |
T |
C |
4: 149,268,766 (GRCm39) |
K1649R |
probably damaging |
Het |
L1cam |
A |
T |
X: 72,904,747 (GRCm39) |
F536Y |
probably damaging |
Het |
Magee1 |
A |
T |
X: 104,166,564 (GRCm39) |
D783V |
probably damaging |
Het |
Marveld3 |
A |
T |
8: 110,686,434 (GRCm39) |
V144E |
probably benign |
Het |
Mcam |
T |
C |
9: 44,047,932 (GRCm39) |
V59A |
probably damaging |
Het |
Mdga2 |
C |
T |
12: 66,915,515 (GRCm39) |
E47K |
probably damaging |
Het |
Metrn |
T |
A |
17: 26,015,601 (GRCm39) |
E38V |
probably damaging |
Het |
Mfrp |
T |
C |
9: 44,015,015 (GRCm39) |
L314P |
probably benign |
Het |
Mgat4f |
T |
A |
1: 134,318,251 (GRCm39) |
M341K |
probably damaging |
Het |
Mideas |
G |
T |
12: 84,219,809 (GRCm39) |
P382T |
probably damaging |
Het |
Mospd2 |
A |
G |
X: 163,739,473 (GRCm39) |
|
probably null |
Het |
Mycbp2 |
G |
A |
14: 103,393,358 (GRCm39) |
H3068Y |
probably damaging |
Het |
Myh6 |
C |
T |
14: 55,191,228 (GRCm39) |
R871H |
probably damaging |
Het |
Nup214 |
C |
T |
2: 31,924,478 (GRCm39) |
S1669F |
probably damaging |
Het |
Or13c7b |
A |
G |
4: 43,821,178 (GRCm39) |
F61S |
probably damaging |
Het |
Or5b111 |
T |
C |
19: 13,291,485 (GRCm39) |
T55A |
probably benign |
Het |
Or8i2 |
T |
A |
2: 86,852,009 (GRCm39) |
N293I |
probably damaging |
Het |
Parvb |
A |
G |
15: 84,116,369 (GRCm39) |
K33E |
possibly damaging |
Het |
Pdcd11 |
A |
G |
19: 47,093,191 (GRCm39) |
M490V |
probably benign |
Het |
Pkd2 |
A |
C |
5: 104,603,456 (GRCm39) |
|
probably benign |
Het |
Reps1 |
T |
A |
10: 17,969,061 (GRCm39) |
D206E |
probably benign |
Het |
Rimkla |
T |
A |
4: 119,331,779 (GRCm39) |
M140L |
possibly damaging |
Het |
Rnf13 |
T |
G |
3: 57,709,907 (GRCm39) |
I150S |
probably null |
Het |
Rxfp4 |
C |
T |
3: 88,560,200 (GRCm39) |
A84T |
probably damaging |
Het |
Serpinb8 |
T |
A |
1: 107,533,657 (GRCm39) |
D237E |
probably benign |
Het |
Sgo2b |
T |
G |
8: 64,381,057 (GRCm39) |
T592P |
probably benign |
Het |
Slc35d1 |
A |
T |
4: 103,062,349 (GRCm39) |
I228N |
probably damaging |
Het |
Slc39a1 |
T |
G |
3: 90,156,757 (GRCm39) |
H104Q |
probably benign |
Het |
Slc6a6 |
T |
C |
6: 91,712,161 (GRCm39) |
V230A |
probably benign |
Het |
Slc9a3 |
A |
G |
13: 74,269,722 (GRCm39) |
E30G |
probably benign |
Het |
Slc9c1 |
A |
G |
16: 45,413,827 (GRCm39) |
Y985C |
probably benign |
Het |
Supt6 |
A |
G |
11: 78,121,758 (GRCm39) |
F298S |
probably damaging |
Het |
Tada2a |
T |
C |
11: 83,970,455 (GRCm39) |
D432G |
probably damaging |
Het |
Thoc2l |
T |
C |
5: 104,666,857 (GRCm39) |
F460L |
probably benign |
Het |
Tmem131 |
C |
A |
1: 36,851,690 (GRCm39) |
V938L |
probably benign |
Het |
Tnpo3 |
A |
G |
6: 29,589,035 (GRCm39) |
V105A |
probably benign |
Het |
Ttc7 |
T |
C |
17: 87,654,135 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
C |
2: 76,727,532 (GRCm39) |
|
probably benign |
Het |
Usp16 |
T |
C |
16: 87,270,075 (GRCm39) |
|
probably null |
Het |
Usp36 |
A |
G |
11: 118,159,491 (GRCm39) |
L486S |
probably benign |
Het |
Uty |
T |
C |
Y: 1,239,816 (GRCm39) |
I72V |
probably benign |
Het |
Vps51 |
A |
G |
19: 6,118,164 (GRCm39) |
V777A |
probably benign |
Het |
Zfp160 |
A |
G |
17: 21,247,244 (GRCm39) |
K598R |
probably benign |
Het |
Zfp39 |
T |
C |
11: 58,781,158 (GRCm39) |
N535D |
probably benign |
Het |
|
Other mutations in Zfp804a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00466:Zfp804a
|
APN |
2 |
81,884,219 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02011:Zfp804a
|
APN |
2 |
82,087,035 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02218:Zfp804a
|
APN |
2 |
82,089,546 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02645:Zfp804a
|
APN |
2 |
81,884,220 (GRCm39) |
missense |
possibly damaging |
0.94 |
PIT4431001:Zfp804a
|
UTSW |
2 |
82,089,536 (GRCm39) |
missense |
probably benign |
0.04 |
R0027:Zfp804a
|
UTSW |
2 |
82,087,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R0167:Zfp804a
|
UTSW |
2 |
82,086,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R0437:Zfp804a
|
UTSW |
2 |
81,884,135 (GRCm39) |
start codon destroyed |
probably null |
0.08 |
R0521:Zfp804a
|
UTSW |
2 |
82,089,761 (GRCm39) |
nonsense |
probably null |
|
R0546:Zfp804a
|
UTSW |
2 |
82,089,264 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0609:Zfp804a
|
UTSW |
2 |
82,087,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R0694:Zfp804a
|
UTSW |
2 |
81,884,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R0837:Zfp804a
|
UTSW |
2 |
82,089,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R0947:Zfp804a
|
UTSW |
2 |
82,089,062 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1103:Zfp804a
|
UTSW |
2 |
82,087,844 (GRCm39) |
missense |
probably damaging |
0.99 |
R1168:Zfp804a
|
UTSW |
2 |
82,087,041 (GRCm39) |
missense |
probably benign |
0.43 |
R1365:Zfp804a
|
UTSW |
2 |
82,087,590 (GRCm39) |
missense |
probably benign |
0.00 |
R1377:Zfp804a
|
UTSW |
2 |
82,088,841 (GRCm39) |
missense |
probably benign |
0.39 |
R1501:Zfp804a
|
UTSW |
2 |
82,066,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R1526:Zfp804a
|
UTSW |
2 |
82,088,532 (GRCm39) |
missense |
probably benign |
|
R1585:Zfp804a
|
UTSW |
2 |
81,884,095 (GRCm39) |
start gained |
probably benign |
|
R1674:Zfp804a
|
UTSW |
2 |
82,089,168 (GRCm39) |
missense |
probably benign |
0.35 |
R2058:Zfp804a
|
UTSW |
2 |
82,087,710 (GRCm39) |
missense |
probably benign |
0.00 |
R2149:Zfp804a
|
UTSW |
2 |
82,089,008 (GRCm39) |
missense |
probably benign |
0.02 |
R2171:Zfp804a
|
UTSW |
2 |
82,087,527 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2307:Zfp804a
|
UTSW |
2 |
82,087,201 (GRCm39) |
missense |
probably benign |
0.04 |
R2398:Zfp804a
|
UTSW |
2 |
82,089,013 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2496:Zfp804a
|
UTSW |
2 |
82,066,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Zfp804a
|
UTSW |
2 |
82,087,863 (GRCm39) |
missense |
probably benign |
0.00 |
R2919:Zfp804a
|
UTSW |
2 |
82,066,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R2943:Zfp804a
|
UTSW |
2 |
82,066,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R3116:Zfp804a
|
UTSW |
2 |
82,089,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R4170:Zfp804a
|
UTSW |
2 |
82,083,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R4393:Zfp804a
|
UTSW |
2 |
82,087,265 (GRCm39) |
missense |
probably benign |
0.43 |
R4701:Zfp804a
|
UTSW |
2 |
82,086,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R4771:Zfp804a
|
UTSW |
2 |
82,088,286 (GRCm39) |
missense |
probably benign |
0.01 |
R4793:Zfp804a
|
UTSW |
2 |
82,066,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R5523:Zfp804a
|
UTSW |
2 |
82,089,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R5526:Zfp804a
|
UTSW |
2 |
82,088,934 (GRCm39) |
missense |
probably benign |
0.00 |
R5961:Zfp804a
|
UTSW |
2 |
82,088,346 (GRCm39) |
missense |
probably benign |
|
R6181:Zfp804a
|
UTSW |
2 |
82,087,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R6209:Zfp804a
|
UTSW |
2 |
82,088,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R6325:Zfp804a
|
UTSW |
2 |
82,087,382 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7147:Zfp804a
|
UTSW |
2 |
82,088,531 (GRCm39) |
missense |
probably benign |
0.00 |
R7229:Zfp804a
|
UTSW |
2 |
82,088,969 (GRCm39) |
missense |
probably benign |
0.04 |
R7666:Zfp804a
|
UTSW |
2 |
82,089,404 (GRCm39) |
nonsense |
probably null |
|
R7910:Zfp804a
|
UTSW |
2 |
82,086,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R8256:Zfp804a
|
UTSW |
2 |
81,884,193 (GRCm39) |
missense |
probably damaging |
0.99 |
R8669:Zfp804a
|
UTSW |
2 |
82,088,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R8738:Zfp804a
|
UTSW |
2 |
82,089,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R8749:Zfp804a
|
UTSW |
2 |
82,087,919 (GRCm39) |
missense |
probably benign |
0.18 |
R8751:Zfp804a
|
UTSW |
2 |
82,066,190 (GRCm39) |
missense |
probably damaging |
0.96 |
R8828:Zfp804a
|
UTSW |
2 |
82,089,459 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8834:Zfp804a
|
UTSW |
2 |
82,089,441 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8924:Zfp804a
|
UTSW |
2 |
82,088,747 (GRCm39) |
missense |
probably benign |
0.03 |
R8982:Zfp804a
|
UTSW |
2 |
82,066,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R9459:Zfp804a
|
UTSW |
2 |
82,089,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R9570:Zfp804a
|
UTSW |
2 |
82,088,844 (GRCm39) |
missense |
probably benign |
0.22 |
X0064:Zfp804a
|
UTSW |
2 |
82,066,167 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Zfp804a
|
UTSW |
2 |
82,088,907 (GRCm39) |
missense |
probably benign |
0.25 |
|