Other mutations in this stock |
Total: 126 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
7530416G11Rik |
T |
A |
15: 85,378,508 (GRCm39) |
E45V |
unknown |
Homo |
A530064D06Rik |
GTAGGAAGCTTAG |
GTAG |
17: 48,470,549 (GRCm39) |
|
probably benign |
Homo |
Apol6 |
GTTT |
GTTTTTTT |
15: 76,935,638 (GRCm39) |
|
probably null |
Het |
Arrb2 |
C |
T |
11: 70,329,497 (GRCm39) |
T269M |
probably damaging |
Homo |
AY761185 |
CACTGTGGG |
C |
8: 21,433,919 (GRCm39) |
|
probably null |
Het |
Bcas3 |
G |
A |
11: 85,400,323 (GRCm39) |
V431I |
probably benign |
Homo |
Blm |
TACC |
TACCGACC |
7: 80,113,518 (GRCm39) |
|
probably null |
Het |
Btnl10 |
AGA |
AGAGGA |
11: 58,814,755 (GRCm39) |
|
probably benign |
Homo |
Btnl4 |
T |
A |
17: 34,691,610 (GRCm39) |
K293M |
probably benign |
Het |
Catsper2 |
TGTC |
TGTCGTC |
2: 121,228,260 (GRCm39) |
|
probably benign |
Het |
Ccdc121 |
GAGAAG |
GAG |
5: 31,644,717 (GRCm39) |
|
probably benign |
Het |
Cd109 |
ATTTAT |
ATTTATTTATTTCTTTAT |
9: 78,619,811 (GRCm39) |
|
probably benign |
Het |
Cd164 |
G |
T |
10: 41,397,922 (GRCm39) |
A59S |
probably benign |
Homo |
Cd22 |
C |
T |
7: 30,577,507 (GRCm39) |
R2H |
possibly damaging |
Homo |
Chd4 |
C |
T |
6: 125,099,096 (GRCm39) |
P1597L |
probably benign |
Homo |
Chd4 |
CCCCTGCCCCTGCCACTGCCCCTGCC |
CCCCTGCCCCTGCCCCTGCCACTGCCCCTGCC |
6: 125,099,102 (GRCm39) |
|
probably benign |
Homo |
Chga |
AGC |
AGCTGC |
12: 102,527,661 (GRCm39) |
|
probably benign |
Het |
Cluh |
AGCC |
AGCCTGGGCC |
11: 74,560,357 (GRCm39) |
|
probably benign |
Het |
Cnpy3 |
ACCC |
ACCCCCC |
17: 47,047,665 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
CCCAGC |
CCCAGCTCCAGC |
11: 101,080,392 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
AGCCCC |
AGCCCCCGCCCC |
11: 101,080,407 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
CAGCCC |
CAGCCCGAGCCC |
11: 101,080,406 (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 |
Cttnbp2 |
ATT |
ATTTCTGTT |
6: 18,367,457 (GRCm39) |
|
probably benign |
Het |
Dbr1 |
AGGAGG |
AGGAGGGGGAGG |
9: 99,465,730 (GRCm39) |
|
probably benign |
Het |
Dbr1 |
AGGAGG |
AGGAGGGGGAGG |
9: 99,465,733 (GRCm39) |
|
probably benign |
Het |
Dbr1 |
AGGAGG |
AGGAGGCGGAGG |
9: 99,465,736 (GRCm39) |
|
probably benign |
Het |
Dbr1 |
GGAGGA |
GGAGGAAGAGGA |
9: 99,465,749 (GRCm39) |
|
probably benign |
Het |
Dclre1a |
AGGCTTTG |
AG |
19: 56,532,555 (GRCm39) |
|
probably benign |
Het |
Dcpp1 |
A |
C |
17: 24,100,428 (GRCm39) |
K53Q |
probably benign |
Het |
Dhx8 |
CGAGAC |
CGAGACAGAGAC |
11: 101,629,014 (GRCm39) |
|
probably benign |
Homo |
Dnaaf9 |
CC |
CCTGC |
2: 130,612,672 (GRCm39) |
|
probably benign |
Het |
Dnaaf9 |
TCC |
TCCCCC |
2: 130,612,665 (GRCm39) |
|
probably benign |
Het |
Dnah12 |
G |
T |
14: 26,571,342 (GRCm39) |
G2817V |
probably damaging |
Homo |
Dthd1 |
C |
CTT |
5: 63,000,369 (GRCm39) |
|
probably null |
Homo |
Efhd2 |
GCCGCC |
GCCGCCTCCGCC |
4: 141,602,075 (GRCm39) |
|
probably benign |
Het |
Eps8 |
AC |
ACTCGC |
6: 137,494,067 (GRCm39) |
|
probably null |
Het |
Ermn |
TTC |
TTCATC |
2: 57,938,081 (GRCm39) |
|
probably benign |
Het |
Fam81b |
TC |
TCTCC |
13: 76,419,442 (GRCm39) |
|
probably benign |
Het |
Fbrsl1 |
TG |
TGCGTGTGCTGGCG |
5: 110,526,016 (GRCm39) |
|
probably benign |
Het |
Fbxo43 |
CCTGTG |
CCTGTGTCTGTG |
15: 36,152,247 (GRCm39) |
|
probably benign |
Het |
Fbxo43 |
GCCTGT |
GCCTGTTCCTGT |
15: 36,152,246 (GRCm39) |
|
probably benign |
Het |
Fmn1 |
CTCCTC |
CTCCTCTTCCTC |
2: 113,356,118 (GRCm39) |
|
probably benign |
Het |
Fmn1 |
TCCTCC |
TCCTCCCCCTCC |
2: 113,356,119 (GRCm39) |
|
probably benign |
Het |
Frmpd2 |
G |
T |
14: 33,232,978 (GRCm39) |
L399F |
probably damaging |
Homo |
Gabre |
GCTCCGACTCCGACTCCG |
GCTCCGACTCCGACTCCGACTCCG |
X: 71,313,636 (GRCm39) |
|
probably benign |
Homo |
Gabre |
ACTCCGGCTCCGGCTCAGGCTCAGGCTCCGGCTCAGGCTCCGGCTCCGGCTCCGGCTC |
ACTCCGGCTCCGGCTCCGGCTCAGGCTCAGGCTCCGGCTCAGGCTCCGGCTCCGGCTCCGGCTC |
X: 71,313,648 (GRCm39) |
|
probably benign |
Homo |
Gbp2b |
A |
G |
3: 142,309,413 (GRCm39) |
I175V |
probably benign |
Het |
Gm4340 |
AG |
AGCCG |
10: 104,031,961 (GRCm39) |
|
probably benign |
Het |
Gm4340 |
CAG |
CAGTAG |
10: 104,031,939 (GRCm39) |
|
probably null |
Het |
Gm4340 |
AGC |
AGCCGC |
10: 104,031,940 (GRCm39) |
|
probably benign |
Het |
H2-Q4 |
G |
A |
17: 35,599,381 (GRCm39) |
D155N |
probably damaging |
Het |
Ighv5-9 |
C |
T |
12: 113,625,497 (GRCm39) |
S82N |
probably benign |
Homo |
Ipo9 |
TCC |
TCCCCC |
1: 135,314,019 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
CCATC |
CCATCATC |
1: 135,314,004 (GRCm39) |
|
probably benign |
Het |
Isg20l2 |
GAAA |
GAAAAAA |
3: 87,839,024 (GRCm39) |
|
probably benign |
Homo |
Klra9 |
C |
G |
6: 130,159,366 (GRCm39) |
D216H |
probably benign |
Het |
Kmt2b |
TCC |
TCCTCCGCC |
7: 30,285,806 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
CCTCCT |
CCTCCTGCTCCT |
7: 30,285,786 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
CCTCCT |
CCTCCTACTCCT |
7: 30,285,789 (GRCm39) |
|
probably null |
Het |
Krt10 |
TCC |
TCCGCCGCC |
11: 99,280,102 (GRCm39) |
|
probably benign |
Het |
Las1l |
TC |
TCTTCCAC |
X: 94,984,231 (GRCm39) |
|
probably benign |
Het |
Las1l |
TCTTCC |
TCTTCCGCTTCC |
X: 94,984,225 (GRCm39) |
|
probably benign |
Het |
Las1l |
TTCCTCCTCCTC |
TTCCTC |
X: 94,984,227 (GRCm39) |
|
probably benign |
Het |
Lce1m |
TGCTGCCACC |
TGCTGCCACCACGGCTGCCACC |
3: 92,925,575 (GRCm39) |
|
probably benign |
Homo |
Loricrin |
GCCGCCGCC |
GC |
3: 91,989,201 (GRCm39) |
|
probably null |
Het |
Lrit3 |
AC |
ACATCC |
3: 129,597,562 (GRCm39) |
|
probably null |
Het |
Lrrc63 |
CGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGG |
CGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGG |
14: 75,362,622 (GRCm39) |
|
probably benign |
Homo |
Mapk7 |
GG |
GGTGCTAG |
11: 61,381,048 (GRCm39) |
|
probably benign |
Het |
Med12l |
GCAACA |
GCAACAACA |
3: 59,183,377 (GRCm39) |
|
probably benign |
Het |
Nacad |
GGGTCA |
GGGTCATGGTCA |
11: 6,549,753 (GRCm39) |
|
probably benign |
Het |
Ndufc2 |
G |
C |
7: 97,049,497 (GRCm39) |
M34I |
probably benign |
Het |
Nphp3 |
CACG |
C |
9: 103,903,138 (GRCm39) |
|
probably benign |
Het |
Nrg3 |
AG |
AGCCTTTG |
14: 38,119,223 (GRCm39) |
|
probably benign |
Het |
Pdik1l |
TTTTGTTTT |
TTTTGTTTTGTGTTTGTTTT |
4: 134,006,680 (GRCm39) |
|
probably null |
Homo |
Pdik1l |
TTTTTGTTTT |
TTTTTGTTTTGATTTTGTTTT |
4: 134,006,679 (GRCm39) |
|
probably null |
Homo |
Phaf1 |
G |
A |
8: 105,967,730 (GRCm39) |
G207E |
probably benign |
Homo |
Plekhs1 |
AC |
ACCTCCCCCGAGGC |
19: 56,468,295 (GRCm39) |
|
probably benign |
Het |
Prag1 |
CCGC |
CCGCCGC |
8: 36,571,037 (GRCm39) |
|
probably benign |
Homo |
Prtg |
G |
A |
9: 72,764,147 (GRCm39) |
R540Q |
probably damaging |
Het |
Raet1d |
T |
TCCTCTCTGGTAG |
10: 22,246,817 (GRCm39) |
|
probably null |
Homo |
Rhbdf1 |
A |
ATTTT |
11: 32,164,391 (GRCm39) |
|
probably benign |
Het |
Rps19 |
AAAATT |
AAAATTGAAATT |
7: 24,588,607 (GRCm39) |
|
probably benign |
Het |
Rtbdn |
GGCAGC |
GGCAGCCGCAGC |
8: 85,682,800 (GRCm39) |
|
probably benign |
Het |
Scaf4 |
TGCGGC |
TGC |
16: 90,026,742 (GRCm39) |
|
probably benign |
Homo |
Serac1 |
T |
A |
17: 6,121,083 (GRCm39) |
K70N |
probably damaging |
Homo |
Setd1a |
CTGGTGGTGGTGGTGGTGGTAGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGG |
CTGGTGGTGGTGGTGGTGGTGGTGGTGGTAGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGG |
7: 127,384,469 (GRCm39) |
|
probably benign |
Het |
Shf |
TCT |
TCTGCT |
2: 122,184,658 (GRCm39) |
|
probably benign |
Homo |
Shroom4 |
TGCAGCAGCAGCAGCAGCA |
TGCAGCAGCAGCAGCA |
X: 6,536,115 (GRCm39) |
|
probably benign |
Homo |
Six3 |
CGG |
CGGAGG |
17: 85,928,793 (GRCm39) |
|
probably benign |
Het |
Snx1 |
TCT |
TCTCCT |
9: 66,012,208 (GRCm39) |
|
probably benign |
Homo |
Spag17 |
AGG |
AGGGGG |
3: 99,963,561 (GRCm39) |
|
probably benign |
Het |
Spag17 |
GGA |
GGATGA |
3: 99,963,574 (GRCm39) |
|
probably benign |
Het |
Speer4a1 |
C |
A |
5: 26,241,746 (GRCm39) |
E127* |
probably null |
Het |
Sry |
ACTG |
ACTGCTG |
Y: 2,662,818 (GRCm39) |
|
probably benign |
Het |
Supt20 |
A |
AGCAGCT |
3: 54,635,092 (GRCm39) |
|
probably benign |
Het |
Supt20 |
GCAGCA |
GCAGCATCAGCA |
3: 54,635,072 (GRCm39) |
|
probably benign |
Het |
Supt20 |
CAGCAG |
CAGCAGGAGCAG |
3: 54,635,076 (GRCm39) |
|
probably benign |
Het |
Tcof1 |
GGGTA |
G |
18: 60,961,722 (GRCm39) |
|
probably benign |
Homo |
Tert |
C |
CAAGGGTGCG |
13: 73,796,423 (GRCm39) |
|
probably benign |
Het |
Tmbim7 |
C |
T |
5: 3,720,064 (GRCm39) |
R100C |
possibly damaging |
Het |
Tmed6 |
C |
CTAGA |
8: 107,788,230 (GRCm39) |
|
probably null |
Homo |
Tob1 |
CACA |
CACAACA |
11: 94,105,277 (GRCm39) |
|
probably benign |
Het |
Tob1 |
CA |
CAGCAA |
11: 94,105,303 (GRCm39) |
|
probably null |
Het |
Trcg1 |
AGCTCCTGTGTCTGT |
A |
9: 57,149,485 (GRCm39) |
|
probably null |
Homo |
Trim16 |
A |
AAGC |
11: 62,711,521 (GRCm39) |
|
probably benign |
Homo |
Tsbp1 |
GCA |
GCACCA |
17: 34,679,027 (GRCm39) |
|
probably benign |
Het |
Tsbp1 |
AGC |
AGCCGC |
17: 34,679,047 (GRCm39) |
|
probably benign |
Het |
Tubgcp4 |
GTGA |
G |
2: 121,005,944 (GRCm39) |
|
probably benign |
Het |
Tusc1 |
ACCGCC |
ACCGCCCCCGCC |
4: 93,223,544 (GRCm39) |
|
probably benign |
Het |
Ubtf |
CTTC |
CTTCTTC |
11: 102,197,771 (GRCm39) |
|
probably benign |
Het |
Ubtf |
CTCTTC |
CTCTTCTTC |
11: 102,197,769 (GRCm39) |
|
probably benign |
Het |
Vars1 |
GTGG |
GTGGAGTCCTGGTTGG |
17: 35,234,964 (GRCm39) |
|
probably benign |
Homo |
Vmn2r52 |
C |
T |
7: 9,892,947 (GRCm39) |
E731K |
probably damaging |
Het |
Vmn2r87 |
C |
T |
10: 130,314,583 (GRCm39) |
M334I |
probably benign |
Homo |
Zc3h13 |
GTGCGAGAT |
GTGCGAGATTTGCGAGAT |
14: 75,561,038 (GRCm39) |
|
probably benign |
Het |
Zc3h13 |
CGGGATGTGCG |
CGGGATGTGCGGGATGTGCG |
14: 75,561,032 (GRCm39) |
|
probably benign |
Homo |
Zc3h13 |
TGTGCGAG |
TGTGCGAGGAGTGCGAG |
14: 75,561,037 (GRCm39) |
|
probably benign |
Het |
Zfhx3 |
CAGCA |
CAGCAACAGAAGCA |
8: 109,682,733 (GRCm39) |
|
probably benign |
Het |
Zfp282 |
GGC |
GGCAGC |
6: 47,881,725 (GRCm39) |
|
probably benign |
Het |
Zfp459 |
GA |
GAGTTA |
13: 67,556,394 (GRCm39) |
|
probably null |
Homo |
Zfp598 |
ACCACC |
ACCACCCCCACC |
17: 24,899,753 (GRCm39) |
|
probably benign |
Het |
Zfp831 |
TCC |
TCCCCC |
2: 174,487,261 (GRCm39) |
|
probably benign |
Het |
Zfp997 |
G |
A |
13: 66,270,022 (GRCm39) |
S396N |
probably benign |
Het |
|
Other mutations in Anxa2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01375:Anxa2
|
APN |
9 |
69,390,301 (GRCm39) |
nonsense |
probably null |
|
IGL02550:Anxa2
|
APN |
9 |
69,374,588 (GRCm39) |
missense |
probably benign |
0.00 |
FR4342:Anxa2
|
UTSW |
9 |
69,387,492 (GRCm39) |
small insertion |
probably benign |
|
FR4342:Anxa2
|
UTSW |
9 |
69,387,487 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Anxa2
|
UTSW |
9 |
69,387,485 (GRCm39) |
small insertion |
probably benign |
|
R1480:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R1482:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R1519:Anxa2
|
UTSW |
9 |
69,392,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R1609:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R1610:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R1624:Anxa2
|
UTSW |
9 |
69,386,990 (GRCm39) |
missense |
probably benign |
0.10 |
R1672:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R1696:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R1760:Anxa2
|
UTSW |
9 |
69,397,049 (GRCm39) |
missense |
probably benign |
0.00 |
R1775:Anxa2
|
UTSW |
9 |
69,395,363 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1828:Anxa2
|
UTSW |
9 |
69,390,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R1884:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R1991:Anxa2
|
UTSW |
9 |
69,391,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R2020:Anxa2
|
UTSW |
9 |
69,391,099 (GRCm39) |
missense |
probably damaging |
0.99 |
R2029:Anxa2
|
UTSW |
9 |
69,371,762 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2103:Anxa2
|
UTSW |
9 |
69,391,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R2129:Anxa2
|
UTSW |
9 |
69,383,410 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2146:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R2148:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R2149:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R2150:Anxa2
|
UTSW |
9 |
69,397,036 (GRCm39) |
frame shift |
probably null |
|
R2437:Anxa2
|
UTSW |
9 |
69,397,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R3848:Anxa2
|
UTSW |
9 |
69,374,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R4036:Anxa2
|
UTSW |
9 |
69,395,352 (GRCm39) |
missense |
probably damaging |
0.99 |
R4565:Anxa2
|
UTSW |
9 |
69,397,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R4731:Anxa2
|
UTSW |
9 |
69,393,812 (GRCm39) |
missense |
probably benign |
0.41 |
R5172:Anxa2
|
UTSW |
9 |
69,392,533 (GRCm39) |
missense |
probably damaging |
0.99 |
R5181:Anxa2
|
UTSW |
9 |
69,383,347 (GRCm39) |
missense |
probably benign |
0.00 |
R6427:Anxa2
|
UTSW |
9 |
69,383,431 (GRCm39) |
critical splice donor site |
probably null |
|
R6759:Anxa2
|
UTSW |
9 |
69,391,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R7725:Anxa2
|
UTSW |
9 |
69,387,410 (GRCm39) |
missense |
unknown |
|
R7734:Anxa2
|
UTSW |
9 |
69,398,764 (GRCm39) |
missense |
probably benign |
0.41 |
R8532:Anxa2
|
UTSW |
9 |
69,374,594 (GRCm39) |
missense |
probably benign |
0.02 |
|