Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaa1b |
T |
C |
9: 118,983,002 (GRCm39) |
N132S |
probably benign |
Het |
Agpat2 |
A |
G |
2: 26,483,601 (GRCm39) |
*279Q |
probably null |
Het |
Akr1c19 |
C |
A |
13: 4,292,974 (GRCm39) |
D243E |
probably benign |
Het |
Alg2 |
A |
G |
4: 47,474,001 (GRCm39) |
F96L |
probably benign |
Het |
Apob |
C |
T |
12: 8,065,231 (GRCm39) |
Q4067* |
probably null |
Het |
C1ra |
A |
T |
6: 124,489,580 (GRCm39) |
|
probably benign |
Het |
C8a |
T |
C |
4: 104,703,199 (GRCm39) |
Y330C |
probably damaging |
Het |
Ccdc185 |
A |
G |
1: 182,576,221 (GRCm39) |
V156A |
probably benign |
Het |
Ces1g |
A |
G |
8: 94,060,319 (GRCm39) |
L100P |
possibly damaging |
Het |
Cnbd1 |
T |
C |
4: 18,862,113 (GRCm39) |
N359S |
possibly damaging |
Het |
Crybb2 |
C |
T |
5: 113,211,094 (GRCm39) |
A65T |
probably benign |
Het |
Dcaf5 |
T |
C |
12: 80,386,563 (GRCm39) |
D521G |
probably benign |
Het |
Dnmt1 |
A |
G |
9: 20,833,408 (GRCm39) |
F631L |
possibly damaging |
Het |
Dok1 |
T |
A |
6: 83,008,893 (GRCm39) |
D263V |
possibly damaging |
Het |
Ecel1 |
A |
G |
1: 87,081,112 (GRCm39) |
F293L |
probably benign |
Het |
Ehmt1 |
A |
T |
2: 24,738,077 (GRCm39) |
L509Q |
possibly damaging |
Het |
Fbln2 |
T |
A |
6: 91,231,556 (GRCm39) |
V551E |
possibly damaging |
Het |
Fig4 |
C |
T |
10: 41,153,478 (GRCm39) |
V108I |
probably benign |
Het |
Gpa33 |
A |
G |
1: 165,991,396 (GRCm39) |
Y209C |
probably damaging |
Het |
Heatr5a |
T |
C |
12: 51,963,026 (GRCm39) |
H52R |
|
Het |
Heatr9 |
A |
T |
11: 83,409,281 (GRCm39) |
D157E |
possibly damaging |
Het |
Jakmip2 |
A |
C |
18: 43,685,242 (GRCm39) |
M682R |
probably benign |
Het |
Krt1 |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
15: 101,758,813 (GRCm39) |
|
probably benign |
Het |
Layn |
A |
G |
9: 50,968,760 (GRCm39) |
S328P |
possibly damaging |
Het |
Mblac2 |
A |
G |
13: 81,859,769 (GRCm39) |
D41G |
probably damaging |
Het |
Mboat1 |
A |
G |
13: 30,410,392 (GRCm39) |
Y283C |
probably damaging |
Het |
Mdga2 |
A |
G |
12: 66,736,226 (GRCm39) |
V334A |
possibly damaging |
Het |
Mroh4 |
C |
T |
15: 74,485,167 (GRCm39) |
R515H |
possibly damaging |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nos1 |
G |
C |
5: 118,017,402 (GRCm39) |
R255P |
probably benign |
Het |
Nsrp1 |
G |
A |
11: 76,937,036 (GRCm39) |
R387W |
probably benign |
Het |
Or5p59 |
T |
C |
7: 107,703,256 (GRCm39) |
S247P |
probably damaging |
Het |
Or8c16 |
T |
C |
9: 38,130,706 (GRCm39) |
Y193H |
probably benign |
Het |
Ostm1 |
T |
C |
10: 42,574,210 (GRCm39) |
V301A |
probably damaging |
Het |
Pcdhb13 |
A |
T |
18: 37,577,608 (GRCm39) |
D662V |
probably damaging |
Het |
Pfpl |
T |
A |
19: 12,406,374 (GRCm39) |
S208R |
probably damaging |
Het |
Plin5 |
A |
T |
17: 56,419,324 (GRCm39) |
V366E |
probably damaging |
Het |
Rmi1 |
A |
G |
13: 58,556,899 (GRCm39) |
I383V |
probably benign |
Het |
Rnh1 |
T |
C |
7: 140,740,714 (GRCm39) |
T414A |
probably benign |
Het |
Sash1 |
C |
A |
10: 8,617,296 (GRCm39) |
G537W |
probably damaging |
Het |
Slc9c1 |
A |
G |
16: 45,370,551 (GRCm39) |
N264S |
probably benign |
Het |
Speg |
A |
C |
1: 75,398,420 (GRCm39) |
T1956P |
probably damaging |
Het |
St14 |
T |
C |
9: 31,002,905 (GRCm39) |
Y666C |
probably damaging |
Het |
Stab2 |
T |
A |
10: 86,727,481 (GRCm39) |
H1448L |
probably damaging |
Het |
Syne2 |
C |
T |
12: 76,154,230 (GRCm39) |
|
probably benign |
Het |
Taf9 |
T |
A |
13: 100,790,860 (GRCm39) |
|
probably benign |
Het |
Thumpd2 |
G |
A |
17: 81,334,040 (GRCm39) |
A516V |
possibly damaging |
Het |
Tmem132e |
A |
G |
11: 82,335,308 (GRCm39) |
K797E |
probably damaging |
Het |
Tpte |
A |
G |
8: 22,841,489 (GRCm39) |
T494A |
possibly damaging |
Het |
Ttc41 |
T |
A |
10: 86,567,113 (GRCm39) |
L593Q |
probably benign |
Het |
Uggt1 |
A |
C |
1: 36,249,103 (GRCm39) |
I279S |
possibly damaging |
Het |
Uxs1 |
A |
G |
1: 43,804,084 (GRCm39) |
F277S |
probably damaging |
Het |
Vat1 |
A |
T |
11: 101,351,380 (GRCm39) |
N320K |
possibly damaging |
Het |
Wdr81 |
G |
T |
11: 75,336,256 (GRCm39) |
A592E |
|
Het |
Zfp780b |
C |
T |
7: 27,673,143 (GRCm39) |
|
probably null |
Het |
Zfp944 |
A |
T |
17: 22,562,619 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Zfp956 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01110:Zfp956
|
APN |
6 |
47,940,346 (GRCm39) |
missense |
probably benign |
0.28 |
ANU74:Zfp956
|
UTSW |
6 |
47,940,507 (GRCm39) |
missense |
probably benign |
0.00 |
R0603:Zfp956
|
UTSW |
6 |
47,932,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R1243:Zfp956
|
UTSW |
6 |
47,932,985 (GRCm39) |
missense |
probably damaging |
0.98 |
R1879:Zfp956
|
UTSW |
6 |
47,940,678 (GRCm39) |
missense |
probably benign |
0.19 |
R1999:Zfp956
|
UTSW |
6 |
47,940,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R2106:Zfp956
|
UTSW |
6 |
47,941,359 (GRCm39) |
makesense |
probably null |
|
R2150:Zfp956
|
UTSW |
6 |
47,940,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R4737:Zfp956
|
UTSW |
6 |
47,939,476 (GRCm39) |
missense |
probably damaging |
0.99 |
R4740:Zfp956
|
UTSW |
6 |
47,939,476 (GRCm39) |
missense |
probably damaging |
0.99 |
R4751:Zfp956
|
UTSW |
6 |
47,940,510 (GRCm39) |
missense |
probably benign |
0.00 |
R4832:Zfp956
|
UTSW |
6 |
47,928,987 (GRCm39) |
unclassified |
probably benign |
|
R5325:Zfp956
|
UTSW |
6 |
47,928,012 (GRCm39) |
unclassified |
probably benign |
|
R5523:Zfp956
|
UTSW |
6 |
47,930,455 (GRCm39) |
start gained |
probably benign |
|
R6842:Zfp956
|
UTSW |
6 |
47,940,763 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7131:Zfp956
|
UTSW |
6 |
47,932,781 (GRCm39) |
missense |
probably benign |
0.00 |
R7367:Zfp956
|
UTSW |
6 |
47,940,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R8806:Zfp956
|
UTSW |
6 |
47,933,042 (GRCm39) |
missense |
probably benign |
0.00 |
R9074:Zfp956
|
UTSW |
6 |
47,939,462 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9452:Zfp956
|
UTSW |
6 |
47,940,370 (GRCm39) |
missense |
probably benign |
|
R9464:Zfp956
|
UTSW |
6 |
47,941,041 (GRCm39) |
missense |
probably damaging |
1.00 |
|