Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam11 |
C |
A |
11: 102,662,883 (GRCm39) |
A212D |
probably benign |
Het |
Adamts13 |
C |
A |
2: 26,868,707 (GRCm39) |
H230Q |
probably damaging |
Het |
Adgrl3 |
G |
A |
5: 81,457,874 (GRCm39) |
M1I |
probably null |
Het |
Agap1 |
A |
T |
1: 89,770,821 (GRCm39) |
H657L |
possibly damaging |
Het |
Ano3 |
T |
C |
2: 110,611,768 (GRCm39) |
D238G |
probably damaging |
Het |
Atp8b5 |
A |
T |
4: 43,357,018 (GRCm39) |
I589F |
probably damaging |
Het |
Bmp1 |
C |
T |
14: 70,717,000 (GRCm39) |
A859T |
possibly damaging |
Het |
Cdh20 |
C |
A |
1: 104,921,702 (GRCm39) |
D666E |
probably damaging |
Het |
Cep135 |
T |
G |
5: 76,780,090 (GRCm39) |
D807E |
probably benign |
Het |
Cldn13 |
G |
A |
5: 134,943,766 (GRCm39) |
H140Y |
probably benign |
Het |
Cnksr1 |
G |
T |
4: 133,962,434 (GRCm39) |
Q155K |
possibly damaging |
Het |
Col1a1 |
G |
A |
11: 94,829,352 (GRCm39) |
R121Q |
unknown |
Het |
Coro6 |
G |
A |
11: 77,358,089 (GRCm39) |
A225T |
possibly damaging |
Het |
Ctse |
C |
A |
1: 131,592,112 (GRCm39) |
T146K |
possibly damaging |
Het |
Dhrs7b |
C |
A |
11: 60,746,623 (GRCm39) |
Y237* |
probably null |
Het |
Dnah3 |
A |
G |
7: 119,570,312 (GRCm39) |
F2303L |
probably damaging |
Het |
Dsg2 |
T |
A |
18: 20,734,516 (GRCm39) |
D831E |
probably damaging |
Het |
Dst |
T |
C |
1: 34,202,418 (GRCm39) |
S575P |
probably damaging |
Het |
Epg5 |
T |
C |
18: 77,992,170 (GRCm39) |
L289P |
probably damaging |
Het |
Etl4 |
A |
G |
2: 20,714,387 (GRCm39) |
N162S |
probably damaging |
Het |
Fbf1 |
A |
T |
11: 116,040,300 (GRCm39) |
Y602N |
probably benign |
Het |
Fgd4 |
A |
T |
16: 16,302,420 (GRCm39) |
M45K |
probably benign |
Het |
Fryl |
C |
T |
5: 73,222,438 (GRCm39) |
V2048I |
probably benign |
Het |
Gulp1 |
T |
C |
1: 44,805,292 (GRCm39) |
V127A |
possibly damaging |
Het |
H2-DMb1 |
T |
A |
17: 34,376,490 (GRCm39) |
I203N |
probably damaging |
Het |
Harbi1 |
T |
C |
2: 91,542,790 (GRCm39) |
S84P |
probably damaging |
Het |
Hrh2 |
T |
C |
13: 54,368,266 (GRCm39) |
S81P |
possibly damaging |
Het |
Iars1 |
T |
C |
13: 49,841,791 (GRCm39) |
|
probably null |
Het |
Kcnma1 |
T |
C |
14: 23,359,083 (GRCm39) |
*1087W |
probably null |
Het |
Lama5 |
T |
A |
2: 179,848,877 (GRCm39) |
N241I |
probably damaging |
Het |
Lig4 |
T |
A |
8: 10,022,101 (GRCm39) |
K560* |
probably null |
Het |
Lpin3 |
G |
T |
2: 160,735,923 (GRCm39) |
E68* |
probably null |
Het |
Mrtfb |
A |
T |
16: 13,144,300 (GRCm39) |
I7L |
probably benign |
Het |
Msrb3 |
A |
T |
10: 120,627,305 (GRCm39) |
|
probably null |
Het |
Muc5b |
A |
G |
7: 141,416,602 (GRCm39) |
T3183A |
probably benign |
Het |
Mx1 |
T |
A |
16: 97,253,398 (GRCm39) |
D342V |
probably benign |
Het |
Nrap |
G |
T |
19: 56,333,953 (GRCm39) |
T1003K |
probably damaging |
Het |
Or8u10 |
A |
G |
2: 85,915,159 (GRCm39) |
S321P |
possibly damaging |
Het |
Plxna2 |
C |
T |
1: 194,326,327 (GRCm39) |
P87L |
probably damaging |
Het |
Pms2 |
C |
T |
5: 143,850,452 (GRCm39) |
T89I |
probably damaging |
Het |
Ppp1r12c |
C |
A |
7: 4,492,867 (GRCm39) |
R203L |
probably damaging |
Het |
Pramel31 |
A |
G |
4: 144,088,473 (GRCm39) |
T90A |
probably benign |
Het |
Rab44 |
C |
T |
17: 29,357,013 (GRCm39) |
Q48* |
probably null |
Het |
Rgs14 |
T |
C |
13: 55,531,047 (GRCm39) |
V417A |
probably benign |
Het |
Sgms1 |
T |
A |
19: 32,120,147 (GRCm39) |
K253M |
probably null |
Het |
Sidt2 |
T |
C |
9: 45,856,449 (GRCm39) |
Y492C |
probably damaging |
Het |
Slco1a5 |
G |
T |
6: 142,194,475 (GRCm39) |
Y389* |
probably null |
Het |
Slfn14 |
G |
A |
11: 83,170,214 (GRCm39) |
Q477* |
probably null |
Het |
Sorbs3 |
T |
C |
14: 70,438,934 (GRCm39) |
K142R |
probably damaging |
Het |
Sphk1 |
A |
T |
11: 116,426,590 (GRCm39) |
D182V |
probably damaging |
Het |
Srsf9 |
C |
G |
5: 115,465,481 (GRCm39) |
Y38* |
probably null |
Het |
Stk40 |
A |
C |
4: 126,019,547 (GRCm39) |
E107A |
probably damaging |
Het |
Syngr4 |
T |
C |
7: 45,538,101 (GRCm39) |
Y89C |
possibly damaging |
Het |
Tead1 |
G |
A |
7: 112,441,287 (GRCm39) |
R109H |
possibly damaging |
Het |
Thra |
A |
G |
11: 98,651,802 (GRCm39) |
Q108R |
probably damaging |
Het |
Tnni3k |
G |
A |
3: 154,580,782 (GRCm39) |
T621I |
probably damaging |
Het |
Trim3 |
A |
C |
7: 105,262,583 (GRCm39) |
V525G |
possibly damaging |
Het |
Usp49 |
T |
C |
17: 47,989,802 (GRCm39) |
V529A |
probably benign |
Het |
Vill |
A |
T |
9: 118,900,281 (GRCm39) |
Q849L |
possibly damaging |
Het |
Vps36 |
T |
A |
8: 22,701,623 (GRCm39) |
S237T |
probably benign |
Het |
Zar1l |
A |
T |
5: 150,430,558 (GRCm39) |
C284* |
probably null |
Het |
Zfp948 |
T |
C |
17: 21,808,602 (GRCm39) |
V598A |
possibly damaging |
Het |
Zfp952 |
T |
C |
17: 33,222,489 (GRCm39) |
Y323H |
possibly damaging |
Het |
|
Other mutations in A2ml1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00513:A2ml1
|
APN |
6 |
128,555,119 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL00596:A2ml1
|
APN |
6 |
128,547,030 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00912:A2ml1
|
APN |
6 |
128,529,270 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01320:A2ml1
|
APN |
6 |
128,552,551 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01470:A2ml1
|
APN |
6 |
128,557,375 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01576:A2ml1
|
APN |
6 |
128,531,293 (GRCm39) |
splice site |
probably benign |
|
IGL01761:A2ml1
|
APN |
6 |
128,523,300 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL01792:A2ml1
|
APN |
6 |
128,537,642 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01843:A2ml1
|
APN |
6 |
128,530,301 (GRCm39) |
splice site |
probably benign |
|
IGL01946:A2ml1
|
APN |
6 |
128,547,442 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02016:A2ml1
|
APN |
6 |
128,535,298 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02170:A2ml1
|
APN |
6 |
128,524,173 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02269:A2ml1
|
APN |
6 |
128,530,301 (GRCm39) |
splice site |
probably benign |
|
IGL02589:A2ml1
|
APN |
6 |
128,558,463 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02959:A2ml1
|
APN |
6 |
128,544,023 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02970:A2ml1
|
APN |
6 |
128,546,942 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03206:A2ml1
|
APN |
6 |
128,530,239 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL03298:A2ml1
|
APN |
6 |
128,520,923 (GRCm39) |
missense |
probably benign |
0.00 |
1mM(1):A2ml1
|
UTSW |
6 |
128,557,923 (GRCm39) |
missense |
probably benign |
0.02 |
R0055:A2ml1
|
UTSW |
6 |
128,547,057 (GRCm39) |
splice site |
probably benign |
|
R0055:A2ml1
|
UTSW |
6 |
128,547,057 (GRCm39) |
splice site |
probably benign |
|
R0069:A2ml1
|
UTSW |
6 |
128,538,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R0069:A2ml1
|
UTSW |
6 |
128,538,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R0128:A2ml1
|
UTSW |
6 |
128,552,602 (GRCm39) |
splice site |
probably benign |
|
R0299:A2ml1
|
UTSW |
6 |
128,530,195 (GRCm39) |
splice site |
probably benign |
|
R0523:A2ml1
|
UTSW |
6 |
128,535,289 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0565:A2ml1
|
UTSW |
6 |
128,545,706 (GRCm39) |
nonsense |
probably null |
|
R0599:A2ml1
|
UTSW |
6 |
128,529,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:A2ml1
|
UTSW |
6 |
128,527,736 (GRCm39) |
missense |
probably damaging |
0.99 |
R0732:A2ml1
|
UTSW |
6 |
128,523,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R0880:A2ml1
|
UTSW |
6 |
128,537,609 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1070:A2ml1
|
UTSW |
6 |
128,520,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R1166:A2ml1
|
UTSW |
6 |
128,547,880 (GRCm39) |
missense |
probably benign |
0.00 |
R1278:A2ml1
|
UTSW |
6 |
128,535,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R1421:A2ml1
|
UTSW |
6 |
128,520,923 (GRCm39) |
missense |
probably benign |
0.00 |
R1536:A2ml1
|
UTSW |
6 |
128,524,196 (GRCm39) |
nonsense |
probably null |
|
R1786:A2ml1
|
UTSW |
6 |
128,553,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R1808:A2ml1
|
UTSW |
6 |
128,520,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R1813:A2ml1
|
UTSW |
6 |
128,543,236 (GRCm39) |
missense |
probably benign |
0.34 |
R1863:A2ml1
|
UTSW |
6 |
128,527,746 (GRCm39) |
missense |
probably damaging |
0.99 |
R2007:A2ml1
|
UTSW |
6 |
128,519,855 (GRCm39) |
missense |
probably benign |
0.13 |
R2062:A2ml1
|
UTSW |
6 |
128,529,271 (GRCm39) |
missense |
probably benign |
0.08 |
R2127:A2ml1
|
UTSW |
6 |
128,535,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R2130:A2ml1
|
UTSW |
6 |
128,553,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:A2ml1
|
UTSW |
6 |
128,553,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R2201:A2ml1
|
UTSW |
6 |
128,524,268 (GRCm39) |
missense |
probably null |
0.34 |
R2319:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2321:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2322:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2369:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2370:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2371:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2372:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2375:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2893:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2894:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R3438:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R3615:A2ml1
|
UTSW |
6 |
128,535,257 (GRCm39) |
missense |
probably benign |
0.07 |
R3616:A2ml1
|
UTSW |
6 |
128,535,257 (GRCm39) |
missense |
probably benign |
0.07 |
R3773:A2ml1
|
UTSW |
6 |
128,532,046 (GRCm39) |
missense |
probably benign |
0.02 |
R3785:A2ml1
|
UTSW |
6 |
128,521,887 (GRCm39) |
critical splice donor site |
probably null |
|
R3803:A2ml1
|
UTSW |
6 |
128,522,033 (GRCm39) |
missense |
probably benign |
0.17 |
R3824:A2ml1
|
UTSW |
6 |
128,545,726 (GRCm39) |
missense |
probably damaging |
0.99 |
R3878:A2ml1
|
UTSW |
6 |
128,531,324 (GRCm39) |
missense |
probably benign |
0.05 |
R4176:A2ml1
|
UTSW |
6 |
128,522,000 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4229:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4230:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4348:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4351:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4352:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4353:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4427:A2ml1
|
UTSW |
6 |
128,522,009 (GRCm39) |
missense |
probably benign |
0.00 |
R4971:A2ml1
|
UTSW |
6 |
128,524,190 (GRCm39) |
missense |
probably damaging |
0.98 |
R5014:A2ml1
|
UTSW |
6 |
128,520,896 (GRCm39) |
missense |
probably benign |
0.00 |
R5369:A2ml1
|
UTSW |
6 |
128,545,796 (GRCm39) |
missense |
probably damaging |
0.97 |
R5532:A2ml1
|
UTSW |
6 |
128,530,293 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5860:A2ml1
|
UTSW |
6 |
128,518,024 (GRCm39) |
missense |
probably benign |
0.15 |
R5872:A2ml1
|
UTSW |
6 |
128,538,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5926:A2ml1
|
UTSW |
6 |
128,537,608 (GRCm39) |
missense |
probably benign |
|
R5977:A2ml1
|
UTSW |
6 |
128,558,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R5980:A2ml1
|
UTSW |
6 |
128,544,018 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6014:A2ml1
|
UTSW |
6 |
128,548,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R6032:A2ml1
|
UTSW |
6 |
128,526,799 (GRCm39) |
nonsense |
probably null |
|
R6032:A2ml1
|
UTSW |
6 |
128,526,799 (GRCm39) |
nonsense |
probably null |
|
R6061:A2ml1
|
UTSW |
6 |
128,545,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R6327:A2ml1
|
UTSW |
6 |
128,535,655 (GRCm39) |
splice site |
probably null |
|
R6331:A2ml1
|
UTSW |
6 |
128,529,199 (GRCm39) |
missense |
probably damaging |
0.96 |
R6465:A2ml1
|
UTSW |
6 |
128,518,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R6640:A2ml1
|
UTSW |
6 |
128,530,248 (GRCm39) |
missense |
probably benign |
0.41 |
R6792:A2ml1
|
UTSW |
6 |
128,523,292 (GRCm39) |
nonsense |
probably null |
|
R6793:A2ml1
|
UTSW |
6 |
128,523,292 (GRCm39) |
nonsense |
probably null |
|
R7378:A2ml1
|
UTSW |
6 |
128,523,210 (GRCm39) |
critical splice donor site |
probably null |
|
R7556:A2ml1
|
UTSW |
6 |
128,546,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R8010:A2ml1
|
UTSW |
6 |
128,557,303 (GRCm39) |
missense |
probably benign |
0.08 |
R8017:A2ml1
|
UTSW |
6 |
128,558,410 (GRCm39) |
critical splice donor site |
probably null |
|
R8019:A2ml1
|
UTSW |
6 |
128,558,410 (GRCm39) |
critical splice donor site |
probably null |
|
R8035:A2ml1
|
UTSW |
6 |
128,530,243 (GRCm39) |
missense |
probably damaging |
0.99 |
R8094:A2ml1
|
UTSW |
6 |
128,549,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R8144:A2ml1
|
UTSW |
6 |
128,546,962 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8365:A2ml1
|
UTSW |
6 |
128,557,918 (GRCm39) |
nonsense |
probably null |
|
R8382:A2ml1
|
UTSW |
6 |
128,537,645 (GRCm39) |
missense |
probably benign |
0.01 |
R8388:A2ml1
|
UTSW |
6 |
128,548,937 (GRCm39) |
missense |
probably benign |
0.03 |
R8717:A2ml1
|
UTSW |
6 |
128,543,958 (GRCm39) |
missense |
probably benign |
0.00 |
R8947:A2ml1
|
UTSW |
6 |
128,529,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R8970:A2ml1
|
UTSW |
6 |
128,545,726 (GRCm39) |
missense |
probably damaging |
0.99 |
R9025:A2ml1
|
UTSW |
6 |
128,534,545 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9083:A2ml1
|
UTSW |
6 |
128,534,524 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9129:A2ml1
|
UTSW |
6 |
128,523,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R9145:A2ml1
|
UTSW |
6 |
128,536,032 (GRCm39) |
missense |
probably benign |
|
R9165:A2ml1
|
UTSW |
6 |
128,537,632 (GRCm39) |
missense |
probably benign |
|
R9285:A2ml1
|
UTSW |
6 |
128,526,756 (GRCm39) |
missense |
probably benign |
|
R9408:A2ml1
|
UTSW |
6 |
128,522,030 (GRCm39) |
missense |
probably damaging |
0.98 |
R9486:A2ml1
|
UTSW |
6 |
128,546,942 (GRCm39) |
missense |
probably damaging |
0.99 |
R9781:A2ml1
|
UTSW |
6 |
128,519,860 (GRCm39) |
missense |
probably benign |
0.01 |
RF014:A2ml1
|
UTSW |
6 |
128,547,031 (GRCm39) |
missense |
probably damaging |
0.96 |
X0063:A2ml1
|
UTSW |
6 |
128,548,975 (GRCm39) |
missense |
probably benign |
|
Z1176:A2ml1
|
UTSW |
6 |
128,548,940 (GRCm39) |
missense |
probably benign |
0.09 |
Z1177:A2ml1
|
UTSW |
6 |
128,552,570 (GRCm39) |
missense |
possibly damaging |
0.80 |
Z1177:A2ml1
|
UTSW |
6 |
128,538,579 (GRCm39) |
nonsense |
probably null |
|
Z1177:A2ml1
|
UTSW |
6 |
128,522,039 (GRCm39) |
missense |
probably benign |
|
|