Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810004N23Rik |
TT |
TTATGT |
8: 125,566,572 (GRCm39) |
|
probably null |
Homo |
4930433I11Rik |
AACC |
A |
7: 40,642,479 (GRCm39) |
|
probably benign |
Het |
7530416G11Rik |
T |
A |
15: 85,378,508 (GRCm39) |
E45V |
unknown |
Homo |
Ankrd35 |
TCCCC |
TCCC |
3: 96,590,831 (GRCm39) |
|
probably null |
Het |
Anxa2 |
CCC |
CCCACC |
9: 69,387,487 (GRCm39) |
|
probably benign |
Het |
Anxa2 |
C |
CCCA |
9: 69,387,492 (GRCm39) |
|
probably benign |
Het |
Apc |
CAATAAAGC |
CAATAAAGCAAATAAAGC |
18: 34,415,052 (GRCm39) |
|
probably benign |
Homo |
Arrb2 |
C |
T |
11: 70,329,497 (GRCm39) |
T269M |
probably damaging |
Homo |
Bcas3 |
G |
A |
11: 85,400,323 (GRCm39) |
V431I |
probably benign |
Homo |
Begain |
CCCCGCC |
CCCCGCCCCCGCC |
12: 108,999,344 (GRCm39) |
|
probably benign |
Homo |
Catsper2 |
TCA |
TCAACA |
2: 121,228,274 (GRCm39) |
|
probably benign |
Het |
Ccdc121 |
GAGAAG |
GAG |
5: 31,644,717 (GRCm39) |
|
probably benign |
Homo |
Cd164 |
G |
T |
10: 41,397,922 (GRCm39) |
A59S |
probably benign |
Homo |
Cd22 |
C |
T |
7: 30,577,507 (GRCm39) |
R2H |
possibly damaging |
Homo |
Cimip2b |
CAGAG |
CAG |
4: 43,427,384 (GRCm39) |
|
probably null |
Homo |
Cluh |
GAGCCT |
GAGCCTCAGCCT |
11: 74,560,350 (GRCm39) |
|
probably benign |
Het |
Cluh |
GCCTGA |
GCCTGAACCTGA |
11: 74,560,352 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
AGCCCC |
AGCCCCCGCCCC |
11: 101,080,401 (GRCm39) |
|
probably benign |
Het |
Col2a1 |
C |
A |
15: 97,886,862 (GRCm39) |
|
probably null |
Het |
Col6a5 |
A |
T |
9: 105,811,373 (GRCm39) |
N715K |
unknown |
Homo |
Cpeb4 |
T |
TGA |
11: 31,877,638 (GRCm39) |
|
probably benign |
Homo |
Dbr1 |
AGGAGG |
AGGAGGGGGAGG |
9: 99,465,733 (GRCm39) |
|
probably benign |
Het |
Defa29 |
C |
G |
8: 21,816,160 (GRCm39) |
R69P |
probably benign |
Het |
Dhx8 |
CG |
CGAGAACGG |
11: 101,629,032 (GRCm39) |
|
probably null |
Het |
Dnaaf9 |
TCC |
TCCCCC |
2: 130,612,662 (GRCm39) |
|
probably benign |
Het |
Dnah12 |
G |
T |
14: 26,571,342 (GRCm39) |
G2817V |
probably damaging |
Homo |
Dthd1 |
C |
CTTA |
5: 63,000,369 (GRCm39) |
|
probably benign |
Homo |
E4f1 |
GC |
GCCCC |
17: 24,674,171 (GRCm39) |
|
probably benign |
Het |
F830016B08Rik |
A |
ACAG |
18: 60,433,013 (GRCm39) |
|
probably benign |
Homo |
Fbrsl1 |
GTGTGTGTGCTGGTGCGTGTGCTGGTG |
GTGTGTGTGCTGGTGTGTGTGCTGGTGCGTGTGCTGGTG |
5: 110,525,991 (GRCm39) |
|
probably benign |
Het |
Fbxo22 |
A |
C |
9: 55,128,354 (GRCm39) |
|
probably null |
Het |
Flg |
G |
A |
3: 93,197,820 (GRCm39) |
|
probably benign |
Het |
Fmn1 |
TCC |
TCCTCCACC |
2: 113,356,128 (GRCm39) |
|
probably benign |
Homo |
Frmpd2 |
G |
T |
14: 33,232,978 (GRCm39) |
L399F |
probably damaging |
Homo |
Gbp2b |
A |
G |
3: 142,309,413 (GRCm39) |
I175V |
probably benign |
Het |
Gjc2 |
T |
TCCCG |
11: 59,073,569 (GRCm39) |
|
probably benign |
Homo |
Gm14496 |
A |
C |
2: 181,637,699 (GRCm39) |
K258Q |
probably benign |
Het |
Gm4340 |
CAGAAG |
CAGAAGAAG |
10: 104,031,960 (GRCm39) |
|
probably benign |
Het |
Gm4340 |
CAGAAG |
CAGAAGAAG |
10: 104,031,927 (GRCm39) |
|
probably benign |
Het |
Gpatch11 |
AGAGGA |
AGAGGATGAGGA |
17: 79,149,607 (GRCm39) |
|
probably benign |
Het |
H1f6 |
TGTGG |
TG |
13: 23,879,896 (GRCm39) |
|
probably benign |
Homo |
H2-Q4 |
G |
A |
17: 35,599,381 (GRCm39) |
D155N |
probably damaging |
Homo |
Hoxa3 |
G |
GCTT |
6: 52,147,110 (GRCm39) |
|
probably benign |
Homo |
Ifi208 |
ATGGTG |
ATG |
1: 173,505,264 (GRCm39) |
|
probably benign |
Homo |
Ighv5-9 |
C |
T |
12: 113,625,497 (GRCm39) |
S82N |
probably benign |
Homo |
Klra10 |
G |
A |
6: 130,249,710 (GRCm39) |
R192C |
probably benign |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,800 (GRCm39) |
|
probably benign |
Het |
Krt10 |
CGCC |
CGCCGCC |
11: 99,277,025 (GRCm39) |
|
probably benign |
Het |
Krt10 |
ACC |
ACCCCC |
11: 99,277,029 (GRCm39) |
|
probably benign |
Homo |
Lce1m |
CGCTGCTGCTGCCACAGCA |
C |
3: 92,925,554 (GRCm39) |
|
probably benign |
Het |
Mak16 |
T |
G,A |
8: 31,651,777 (GRCm39) |
E203D |
probably benign |
Homo |
Med12l |
AGC |
AGCGGC |
3: 59,183,409 (GRCm39) |
|
probably benign |
Het |
Med12l |
AGCGGC |
AGCGGCGGC |
3: 59,183,415 (GRCm39) |
|
probably benign |
Het |
Nacad |
TC |
TCAGGGGC |
11: 6,549,762 (GRCm39) |
|
probably benign |
Het |
Naip1 |
C |
T |
13: 100,561,979 (GRCm39) |
R1062K |
probably benign |
Het |
Ndel1 |
G |
A |
11: 68,724,235 (GRCm39) |
P246L |
probably damaging |
Het |
Nelfe |
AC |
ACAAAGAGCGGGATCGAGACAGAGCC |
17: 35,073,065 (GRCm39) |
|
probably benign |
Het |
Or51q1 |
TCC |
TCCC |
7: 103,629,110 (GRCm39) |
|
probably null |
Het |
Or5p70 |
A |
G |
7: 107,995,100 (GRCm39) |
T258A |
probably benign |
Het |
Or5p70 |
G |
A |
7: 107,995,105 (GRCm39) |
M259I |
probably benign |
Het |
P4ha2 |
GTGTTGCTG |
GTG |
11: 54,001,077 (GRCm39) |
|
probably benign |
Homo |
Pde3b |
GGTGGTGGTG |
GGTGGTGGTGGTG |
7: 114,134,010 (GRCm39) |
|
probably benign |
Homo |
Pdik1l |
ACCACC |
ACCACCCCCACC |
4: 134,006,820 (GRCm39) |
|
probably benign |
Homo |
Phaf1 |
G |
A |
8: 105,967,730 (GRCm39) |
G207E |
probably benign |
Homo |
Plekhs1 |
AGAC |
AGACCTCCCCCGCGAC |
19: 56,468,293 (GRCm39) |
|
probably benign |
Homo |
Plekhs1 |
TCCAGAC |
TCCAGACCTCCCCCCAGAC |
19: 56,468,290 (GRCm39) |
|
probably benign |
Homo |
Pramel16 |
AAGAG |
AAG |
4: 143,676,327 (GRCm39) |
|
probably null |
Het |
Pramel16 |
G |
A |
4: 143,676,312 (GRCm39) |
T264M |
probably damaging |
Het |
Pramel27 |
AA |
AATA |
4: 143,578,213 (GRCm39) |
|
probably null |
Homo |
Prkn |
G |
A |
17: 12,073,650 (GRCm39) |
V323M |
probably damaging |
Homo |
Ptms |
TCT |
TCTCCT |
6: 124,891,417 (GRCm39) |
|
probably benign |
Homo |
Raet1d |
A |
G |
10: 22,247,458 (GRCm39) |
Q178R |
probably benign |
Het |
Rtbdn |
AGCG |
AGCGCCGGCG |
8: 85,682,797 (GRCm39) |
|
probably benign |
Het |
Rtbdn |
GC |
GCAGCGCC |
8: 85,682,807 (GRCm39) |
|
probably benign |
Het |
Semp2l2a |
G |
C |
8: 13,887,613 (GRCm39) |
H159Q |
probably benign |
Het |
Serac1 |
T |
A |
17: 6,121,083 (GRCm39) |
K70N |
probably damaging |
Homo |
Sfswap |
CCCACTC |
CCCACTCAGACCACTC |
5: 129,646,821 (GRCm39) |
|
probably benign |
Homo |
Sp110 |
ACT |
ACTGCT |
1: 85,515,209 (GRCm39) |
|
probably benign |
Het |
Spaca1 |
GCTCTC |
GCTCTCACTCTC |
4: 34,049,838 (GRCm39) |
|
probably benign |
Het |
Spag17 |
GGA |
GGATGA |
3: 99,963,565 (GRCm39) |
|
probably benign |
Het |
Spag17 |
GGAGGAGGA |
GGAGGAGGAGGA |
3: 99,963,568 (GRCm39) |
|
probably benign |
Homo |
Speer4a1 |
C |
A |
5: 26,241,746 (GRCm39) |
E127* |
probably null |
Het |
Sry |
GGT |
GGTTGT |
Y: 2,662,836 (GRCm39) |
|
probably benign |
Het |
Sry |
TGG |
TGGGGG |
Y: 2,662,835 (GRCm39) |
|
probably benign |
Het |
Sry |
CTGCTGGTG |
CTG |
Y: 2,663,146 (GRCm39) |
|
probably benign |
Het |
Sry |
GGT |
GGTAGT |
Y: 2,662,839 (GRCm39) |
|
probably benign |
Homo |
Tdpoz3 |
C |
T |
3: 93,733,819 (GRCm39) |
P165S |
probably benign |
Het |
Tdpoz4 |
GAA |
GA |
3: 93,704,187 (GRCm39) |
|
probably null |
Het |
Tert |
AGGCC |
AGGCCAAGGGGGCC |
13: 73,796,419 (GRCm39) |
|
probably benign |
Homo |
Tmbim7 |
C |
T |
5: 3,720,064 (GRCm39) |
R100C |
possibly damaging |
Homo |
Tnfrsf9 |
CT |
CTGAT |
4: 151,018,851 (GRCm39) |
|
probably benign |
Homo |
Tob1 |
AGC |
AGCCGC |
11: 94,105,298 (GRCm39) |
|
probably benign |
Het |
Trav6n-5 |
GCTT |
G |
14: 53,342,369 (GRCm39) |
|
probably benign |
Homo |
Triobp |
G |
GTCA |
15: 78,877,592 (GRCm39) |
|
probably benign |
Homo |
Tsen2 |
AGG |
AGGTGG |
6: 115,537,033 (GRCm39) |
|
probably benign |
Het |
Ubtf |
TCC |
TCCGCC |
11: 102,197,782 (GRCm39) |
|
probably benign |
Het |
Ubtf |
TC |
TCCCC |
11: 102,197,785 (GRCm39) |
|
probably benign |
Het |
Vmn2r125 |
G |
A |
4: 156,703,260 (GRCm39) |
V213I |
probably benign |
Het |
Vmn2r87 |
C |
T |
10: 130,314,583 (GRCm39) |
M334I |
probably benign |
Homo |
Zdhhc16 |
G |
A |
19: 41,930,588 (GRCm39) |
|
probably benign |
Het |
Zfp28 |
G |
A |
7: 6,397,862 (GRCm39) |
G766R |
probably damaging |
Het |
Zfp335 |
GTCGTC |
GTCGTCGTC |
2: 164,749,385 (GRCm39) |
|
probably benign |
Het |
Zfp335 |
C |
CCCC |
2: 164,749,397 (GRCm39) |
|
probably benign |
Het |
Zfp428 |
G |
A |
7: 24,214,506 (GRCm39) |
D41N |
probably damaging |
Homo |
Zfp429 |
A |
T |
13: 67,544,769 (GRCm39) |
F48Y |
probably benign |
Het |
Zfp598 |
CCACC |
CCACCCACACC |
17: 24,899,754 (GRCm39) |
|
probably benign |
Het |
Zfp93 |
G |
A |
7: 23,975,011 (GRCm39) |
R332H |
possibly damaging |
Het |
Zpld2 |
G |
GCTC |
4: 133,929,942 (GRCm39) |
|
probably benign |
Homo |
|
Other mutations in Mn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01019:Mn1
|
APN |
5 |
111,569,413 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01139:Mn1
|
APN |
5 |
111,569,315 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01546:Mn1
|
APN |
5 |
111,569,114 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02252:Mn1
|
APN |
5 |
111,569,107 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02821:Mn1
|
APN |
5 |
111,569,717 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03203:Mn1
|
APN |
5 |
111,569,269 (GRCm39) |
missense |
probably benign |
|
Uebermus
|
UTSW |
5 |
111,569,752 (GRCm39) |
splice site |
probably null |
|
FR4449:Mn1
|
UTSW |
5 |
111,567,576 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Mn1
|
UTSW |
5 |
111,567,564 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Mn1
|
UTSW |
5 |
111,567,568 (GRCm39) |
small insertion |
probably benign |
|
R0639:Mn1
|
UTSW |
5 |
111,567,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R0676:Mn1
|
UTSW |
5 |
111,568,900 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1537:Mn1
|
UTSW |
5 |
111,602,646 (GRCm39) |
missense |
probably damaging |
0.96 |
R1638:Mn1
|
UTSW |
5 |
111,569,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Mn1
|
UTSW |
5 |
111,567,880 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1922:Mn1
|
UTSW |
5 |
111,566,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R2008:Mn1
|
UTSW |
5 |
111,566,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R2104:Mn1
|
UTSW |
5 |
111,602,617 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2519:Mn1
|
UTSW |
5 |
111,566,418 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3980:Mn1
|
UTSW |
5 |
111,569,636 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4008:Mn1
|
UTSW |
5 |
111,568,035 (GRCm39) |
missense |
probably benign |
|
R4564:Mn1
|
UTSW |
5 |
111,568,533 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4647:Mn1
|
UTSW |
5 |
111,567,949 (GRCm39) |
missense |
probably benign |
|
R4779:Mn1
|
UTSW |
5 |
111,567,526 (GRCm39) |
missense |
probably damaging |
0.99 |
R4819:Mn1
|
UTSW |
5 |
111,567,803 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4962:Mn1
|
UTSW |
5 |
111,602,652 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5373:Mn1
|
UTSW |
5 |
111,569,752 (GRCm39) |
splice site |
probably null |
|
R5374:Mn1
|
UTSW |
5 |
111,569,752 (GRCm39) |
splice site |
probably null |
|
R5521:Mn1
|
UTSW |
5 |
111,569,635 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5633:Mn1
|
UTSW |
5 |
111,568,192 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5744:Mn1
|
UTSW |
5 |
111,568,402 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6050:Mn1
|
UTSW |
5 |
111,567,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R6552:Mn1
|
UTSW |
5 |
111,568,753 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7206:Mn1
|
UTSW |
5 |
111,568,378 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7244:Mn1
|
UTSW |
5 |
111,566,699 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8207:Mn1
|
UTSW |
5 |
111,569,651 (GRCm39) |
missense |
probably damaging |
0.99 |
R8222:Mn1
|
UTSW |
5 |
111,566,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R8353:Mn1
|
UTSW |
5 |
111,568,505 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8677:Mn1
|
UTSW |
5 |
111,566,885 (GRCm39) |
nonsense |
probably null |
|
R8990:Mn1
|
UTSW |
5 |
111,566,381 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9602:Mn1
|
UTSW |
5 |
111,565,449 (GRCm39) |
start gained |
probably benign |
|
R9603:Mn1
|
UTSW |
5 |
111,566,393 (GRCm39) |
missense |
probably damaging |
1.00 |
RF025:Mn1
|
UTSW |
5 |
111,567,571 (GRCm39) |
nonsense |
probably null |
|
RF027:Mn1
|
UTSW |
5 |
111,567,571 (GRCm39) |
small insertion |
probably benign |
|
RF028:Mn1
|
UTSW |
5 |
111,567,577 (GRCm39) |
small insertion |
probably benign |
|
RF032:Mn1
|
UTSW |
5 |
111,567,577 (GRCm39) |
small insertion |
probably benign |
|
RF040:Mn1
|
UTSW |
5 |
111,567,571 (GRCm39) |
small insertion |
probably benign |
|
Z1088:Mn1
|
UTSW |
5 |
111,566,146 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1176:Mn1
|
UTSW |
5 |
111,602,572 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1176:Mn1
|
UTSW |
5 |
111,568,245 (GRCm39) |
missense |
probably benign |
0.08 |
Z1177:Mn1
|
UTSW |
5 |
111,567,934 (GRCm39) |
missense |
probably damaging |
1.00 |
|