Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
G |
A |
11: 58,880,501 (GRCm38) |
G270S |
probably benign |
Het |
Abtb1 |
T |
C |
6: 88,836,554 (GRCm38) |
T401A |
probably benign |
Het |
Adamts14 |
A |
T |
10: 61,270,897 (GRCm38) |
M148K |
probably damaging |
Het |
Adcy5 |
A |
G |
16: 35,268,957 (GRCm38) |
E508G |
probably damaging |
Het |
Ankfy1 |
T |
A |
11: 72,757,318 (GRCm38) |
L875H |
probably damaging |
Het |
Cacng3 |
A |
T |
7: 122,768,401 (GRCm38) |
D168V |
probably damaging |
Het |
Clpb |
G |
A |
7: 101,785,461 (GRCm38) |
R488Q |
probably benign |
Het |
Cpxm2 |
A |
T |
7: 132,062,145 (GRCm38) |
Y350N |
probably damaging |
Het |
D130040H23Rik |
T |
A |
8: 69,303,160 (GRCm38) |
*406R |
probably null |
Het |
Dnah10 |
T |
A |
5: 124,829,614 (GRCm38) |
D4236E |
probably damaging |
Het |
Dpf3 |
T |
A |
12: 83,370,617 (GRCm38) |
Y27F |
probably damaging |
Het |
Esp4 |
T |
C |
17: 40,602,595 (GRCm38) |
*118Q |
probably null |
Het |
Fam222b |
T |
C |
11: 78,154,662 (GRCm38) |
S222P |
possibly damaging |
Het |
Flnc |
T |
C |
6: 29,455,171 (GRCm38) |
V1933A |
probably damaging |
Het |
Gem |
T |
C |
4: 11,713,709 (GRCm38) |
F282L |
possibly damaging |
Het |
Gli2 |
T |
C |
1: 118,841,930 (GRCm38) |
T631A |
possibly damaging |
Het |
Gm13088 |
G |
A |
4: 143,655,617 (GRCm38) |
Q170* |
probably null |
Het |
Gpld1 |
T |
A |
13: 24,956,068 (GRCm38) |
V116E |
probably damaging |
Het |
Gpr176 |
A |
G |
2: 118,280,214 (GRCm38) |
M188T |
probably benign |
Het |
Grk5 |
T |
C |
19: 61,089,972 (GRCm38) |
V489A |
probably damaging |
Het |
H2-Ke6 |
C |
T |
17: 34,027,495 (GRCm38) |
V105I |
possibly damaging |
Het |
Hpdl |
T |
C |
4: 116,820,883 (GRCm38) |
N127S |
probably damaging |
Het |
Id4 |
G |
T |
13: 48,262,294 (GRCm38) |
V151L |
possibly damaging |
Het |
Kcnh8 |
G |
T |
17: 52,956,881 (GRCm38) |
G802V |
probably benign |
Het |
Lamc1 |
C |
A |
1: 153,242,743 (GRCm38) |
S894I |
probably benign |
Het |
Larp1b |
A |
G |
3: 40,972,384 (GRCm38) |
N184S |
probably damaging |
Het |
Lhx1 |
A |
T |
11: 84,519,821 (GRCm38) |
S226T |
probably benign |
Het |
Mog |
G |
C |
17: 37,017,582 (GRCm38) |
N152K |
possibly damaging |
Het |
Mttp |
A |
G |
3: 138,116,405 (GRCm38) |
|
probably null |
Het |
Mycbp2 |
A |
G |
14: 103,252,509 (GRCm38) |
V953A |
possibly damaging |
Het |
Myo3a |
A |
T |
2: 22,340,280 (GRCm38) |
Y509F |
probably damaging |
Het |
Myo9b |
A |
G |
8: 71,315,192 (GRCm38) |
N303S |
possibly damaging |
Het |
Nek3 |
T |
C |
8: 22,132,201 (GRCm38) |
|
probably null |
Het |
Nlrc4 |
A |
T |
17: 74,441,931 (GRCm38) |
D771E |
probably benign |
Het |
Nup160 |
A |
T |
2: 90,722,061 (GRCm38) |
N1127I |
possibly damaging |
Het |
Oas1h |
A |
T |
5: 120,862,600 (GRCm38) |
N91I |
probably damaging |
Het |
Olfr1225 |
A |
T |
2: 89,170,627 (GRCm38) |
V195D |
probably benign |
Het |
Olfr1226 |
G |
T |
2: 89,193,883 (GRCm38) |
S50R |
probably damaging |
Het |
Olfr1342 |
T |
A |
4: 118,690,192 (GRCm38) |
N87Y |
probably damaging |
Het |
Parp4 |
T |
C |
14: 56,589,872 (GRCm38) |
|
probably benign |
Het |
Pi4ka |
G |
A |
16: 17,281,900 (GRCm38) |
C96Y |
probably null |
Het |
Pira2 |
A |
T |
7: 3,844,549 (GRCm38) |
F47Y |
probably damaging |
Het |
Pkhd1 |
C |
A |
1: 20,347,457 (GRCm38) |
G2490V |
probably damaging |
Het |
Plekhg1 |
C |
T |
10: 3,940,526 (GRCm38) |
T394I |
probably damaging |
Het |
Psmd1 |
T |
C |
1: 86,091,997 (GRCm38) |
|
probably benign |
Het |
Rab3ip |
A |
T |
10: 116,939,223 (GRCm38) |
C77S |
probably benign |
Het |
Reln |
A |
T |
5: 21,925,213 (GRCm38) |
M2700K |
probably benign |
Het |
Rfx1 |
A |
G |
8: 84,073,946 (GRCm38) |
T59A |
probably benign |
Het |
Ric8b |
G |
T |
10: 84,980,099 (GRCm38) |
V405L |
probably benign |
Het |
Rufy3 |
G |
T |
5: 88,640,632 (GRCm38) |
A479S |
probably damaging |
Het |
Sardh |
A |
T |
2: 27,242,719 (GRCm38) |
Y166N |
probably damaging |
Het |
Slamf6 |
T |
G |
1: 171,934,408 (GRCm38) |
V132G |
possibly damaging |
Het |
Slc12a3 |
T |
G |
8: 94,345,877 (GRCm38) |
H674Q |
possibly damaging |
Het |
Sned1 |
G |
A |
1: 93,281,654 (GRCm38) |
V830M |
possibly damaging |
Het |
Srsf9 |
A |
G |
5: 115,327,370 (GRCm38) |
N21S |
possibly damaging |
Het |
Stkld1 |
A |
T |
2: 26,950,090 (GRCm38) |
T391S |
probably benign |
Het |
Sumf2 |
C |
A |
5: 129,859,914 (GRCm38) |
N230K |
probably damaging |
Het |
Tbc1d22a |
T |
C |
15: 86,235,569 (GRCm38) |
V22A |
possibly damaging |
Het |
Thsd7b |
T |
A |
1: 129,596,041 (GRCm38) |
S194T |
possibly damaging |
Het |
Tmem27 |
A |
G |
X: 164,118,234 (GRCm38) |
D184G |
possibly damaging |
Het |
Tnn |
T |
A |
1: 160,097,265 (GRCm38) |
Y1173F |
probably damaging |
Het |
Top2a |
A |
G |
11: 99,001,054 (GRCm38) |
F1122L |
probably damaging |
Het |
Trappc9 |
G |
A |
15: 73,025,967 (GRCm38) |
R377W |
probably damaging |
Het |
Trim39 |
G |
A |
17: 36,268,854 (GRCm38) |
R70W |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,794,261 (GRCm38) |
T15289I |
probably damaging |
Het |
Ugt2b38 |
A |
T |
5: 87,411,914 (GRCm38) |
V373E |
probably damaging |
Het |
Usp54 |
A |
G |
14: 20,607,159 (GRCm38) |
S24P |
probably damaging |
Het |
Vmn2r27 |
C |
T |
6: 124,231,634 (GRCm38) |
G51S |
probably benign |
Het |
Xylt2 |
C |
T |
11: 94,667,594 (GRCm38) |
A579T |
probably benign |
Het |
Zbtb21 |
A |
G |
16: 97,952,427 (GRCm38) |
S247P |
probably benign |
Het |
Zc3h7b |
C |
T |
15: 81,777,088 (GRCm38) |
P376L |
probably benign |
Het |
Zfp251 |
C |
T |
15: 76,853,039 (GRCm38) |
R613K |
possibly damaging |
Het |
Zfp251 |
T |
A |
15: 76,853,038 (GRCm38) |
R613S |
probably damaging |
Het |
Zfp91 |
T |
C |
19: 12,779,075 (GRCm38) |
D135G |
probably benign |
Het |
|
Other mutations in Lmo7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00569:Lmo7
|
APN |
14 |
101,887,051 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL00733:Lmo7
|
APN |
14 |
101,915,702 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00778:Lmo7
|
APN |
14 |
101,910,885 (GRCm38) |
splice site |
probably benign |
|
IGL01014:Lmo7
|
APN |
14 |
101,920,557 (GRCm38) |
splice site |
probably benign |
|
IGL01401:Lmo7
|
APN |
14 |
101,794,277 (GRCm38) |
nonsense |
probably null |
|
IGL01550:Lmo7
|
APN |
14 |
101,926,140 (GRCm38) |
utr 3 prime |
probably benign |
|
IGL01570:Lmo7
|
APN |
14 |
101,902,371 (GRCm38) |
critical splice donor site |
probably null |
|
IGL01602:Lmo7
|
APN |
14 |
101,910,756 (GRCm38) |
splice site |
probably benign |
|
IGL01605:Lmo7
|
APN |
14 |
101,910,756 (GRCm38) |
splice site |
probably benign |
|
IGL02012:Lmo7
|
APN |
14 |
101,888,716 (GRCm38) |
intron |
probably benign |
|
IGL02145:Lmo7
|
APN |
14 |
101,902,223 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02236:Lmo7
|
APN |
14 |
101,926,088 (GRCm38) |
splice site |
probably benign |
|
IGL02318:Lmo7
|
APN |
14 |
101,900,066 (GRCm38) |
splice site |
probably benign |
|
IGL02345:Lmo7
|
APN |
14 |
101,887,473 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02498:Lmo7
|
APN |
14 |
101,807,482 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02583:Lmo7
|
APN |
14 |
101,933,924 (GRCm38) |
utr 3 prime |
probably benign |
|
IGL02670:Lmo7
|
APN |
14 |
101,880,980 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02694:Lmo7
|
APN |
14 |
101,887,170 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03026:Lmo7
|
APN |
14 |
101,929,333 (GRCm38) |
utr 3 prime |
probably benign |
|
IGL03062:Lmo7
|
APN |
14 |
101,912,079 (GRCm38) |
missense |
possibly damaging |
0.66 |
IGL03068:Lmo7
|
APN |
14 |
101,875,492 (GRCm38) |
unclassified |
probably benign |
|
IGL03178:Lmo7
|
APN |
14 |
101,929,260 (GRCm38) |
nonsense |
probably null |
|
IGL03279:Lmo7
|
APN |
14 |
101,900,508 (GRCm38) |
missense |
probably benign |
0.30 |
PIT4458001:Lmo7
|
UTSW |
14 |
101,887,487 (GRCm38) |
nonsense |
probably null |
|
R0029:Lmo7
|
UTSW |
14 |
101,933,921 (GRCm38) |
utr 3 prime |
probably benign |
|
R0112:Lmo7
|
UTSW |
14 |
101,887,193 (GRCm38) |
nonsense |
probably null |
|
R0345:Lmo7
|
UTSW |
14 |
101,876,877 (GRCm38) |
missense |
probably damaging |
1.00 |
R0372:Lmo7
|
UTSW |
14 |
101,918,053 (GRCm38) |
splice site |
probably benign |
|
R0393:Lmo7
|
UTSW |
14 |
101,900,456 (GRCm38) |
missense |
probably benign |
|
R0514:Lmo7
|
UTSW |
14 |
101,896,559 (GRCm38) |
missense |
probably damaging |
1.00 |
R0514:Lmo7
|
UTSW |
14 |
101,887,173 (GRCm38) |
missense |
probably damaging |
1.00 |
R0526:Lmo7
|
UTSW |
14 |
101,900,560 (GRCm38) |
missense |
probably damaging |
1.00 |
R0615:Lmo7
|
UTSW |
14 |
101,876,859 (GRCm38) |
nonsense |
probably null |
|
R0900:Lmo7
|
UTSW |
14 |
101,887,188 (GRCm38) |
missense |
probably damaging |
1.00 |
R0961:Lmo7
|
UTSW |
14 |
101,794,269 (GRCm38) |
missense |
probably benign |
0.00 |
R0964:Lmo7
|
UTSW |
14 |
101,920,567 (GRCm38) |
splice site |
probably benign |
|
R1078:Lmo7
|
UTSW |
14 |
101,920,474 (GRCm38) |
splice site |
probably benign |
|
R1252:Lmo7
|
UTSW |
14 |
101,900,583 (GRCm38) |
missense |
probably damaging |
1.00 |
R1527:Lmo7
|
UTSW |
14 |
101,876,828 (GRCm38) |
missense |
probably damaging |
1.00 |
R1537:Lmo7
|
UTSW |
14 |
101,929,264 (GRCm38) |
utr 3 prime |
probably benign |
|
R1637:Lmo7
|
UTSW |
14 |
101,880,832 (GRCm38) |
missense |
probably damaging |
1.00 |
R1943:Lmo7
|
UTSW |
14 |
101,902,302 (GRCm38) |
missense |
probably damaging |
1.00 |
R1967:Lmo7
|
UTSW |
14 |
101,900,215 (GRCm38) |
missense |
probably benign |
0.36 |
R2002:Lmo7
|
UTSW |
14 |
101,887,061 (GRCm38) |
missense |
probably benign |
0.13 |
R2057:Lmo7
|
UTSW |
14 |
101,887,178 (GRCm38) |
missense |
probably damaging |
1.00 |
R2131:Lmo7
|
UTSW |
14 |
101,900,238 (GRCm38) |
missense |
probably damaging |
0.99 |
R2153:Lmo7
|
UTSW |
14 |
101,920,515 (GRCm38) |
utr 3 prime |
probably benign |
|
R2257:Lmo7
|
UTSW |
14 |
101,900,130 (GRCm38) |
missense |
probably damaging |
1.00 |
R2355:Lmo7
|
UTSW |
14 |
101,888,685 (GRCm38) |
missense |
probably damaging |
1.00 |
R2356:Lmo7
|
UTSW |
14 |
101,886,945 (GRCm38) |
missense |
probably damaging |
1.00 |
R2898:Lmo7
|
UTSW |
14 |
101,876,914 (GRCm38) |
missense |
possibly damaging |
0.93 |
R3847:Lmo7
|
UTSW |
14 |
101,922,095 (GRCm38) |
critical splice acceptor site |
probably null |
|
R3848:Lmo7
|
UTSW |
14 |
101,922,095 (GRCm38) |
critical splice acceptor site |
probably null |
|
R3849:Lmo7
|
UTSW |
14 |
101,922,095 (GRCm38) |
critical splice acceptor site |
probably null |
|
R3916:Lmo7
|
UTSW |
14 |
101,929,342 (GRCm38) |
utr 3 prime |
probably benign |
|
R4050:Lmo7
|
UTSW |
14 |
101,902,277 (GRCm38) |
nonsense |
probably null |
|
R4326:Lmo7
|
UTSW |
14 |
101,900,074 (GRCm38) |
missense |
possibly damaging |
0.93 |
R4357:Lmo7
|
UTSW |
14 |
101,887,655 (GRCm38) |
missense |
probably null |
1.00 |
R4571:Lmo7
|
UTSW |
14 |
101,887,594 (GRCm38) |
missense |
probably damaging |
0.96 |
R4658:Lmo7
|
UTSW |
14 |
101,886,957 (GRCm38) |
missense |
probably damaging |
1.00 |
R4857:Lmo7
|
UTSW |
14 |
101,887,348 (GRCm38) |
splice site |
probably null |
|
R5006:Lmo7
|
UTSW |
14 |
101,926,237 (GRCm38) |
utr 3 prime |
probably benign |
|
R5528:Lmo7
|
UTSW |
14 |
101,902,086 (GRCm38) |
missense |
probably damaging |
1.00 |
R5588:Lmo7
|
UTSW |
14 |
101,896,590 (GRCm38) |
splice site |
probably null |
|
R5643:Lmo7
|
UTSW |
14 |
101,929,336 (GRCm38) |
utr 3 prime |
probably benign |
|
R5644:Lmo7
|
UTSW |
14 |
101,929,336 (GRCm38) |
utr 3 prime |
probably benign |
|
R5650:Lmo7
|
UTSW |
14 |
101,898,674 (GRCm38) |
missense |
probably damaging |
1.00 |
R5737:Lmo7
|
UTSW |
14 |
101,887,236 (GRCm38) |
missense |
probably damaging |
1.00 |
R5832:Lmo7
|
UTSW |
14 |
101,884,213 (GRCm38) |
missense |
probably damaging |
1.00 |
R5966:Lmo7
|
UTSW |
14 |
101,900,502 (GRCm38) |
missense |
possibly damaging |
0.92 |
R6026:Lmo7
|
UTSW |
14 |
101,880,990 (GRCm38) |
missense |
probably benign |
0.04 |
R6072:Lmo7
|
UTSW |
14 |
101,929,336 (GRCm38) |
utr 3 prime |
probably benign |
|
R6158:Lmo7
|
UTSW |
14 |
101,900,137 (GRCm38) |
missense |
probably benign |
0.03 |
R6246:Lmo7
|
UTSW |
14 |
101,918,700 (GRCm38) |
missense |
probably damaging |
1.00 |
R6335:Lmo7
|
UTSW |
14 |
101,900,636 (GRCm38) |
missense |
probably damaging |
1.00 |
R6620:Lmo7
|
UTSW |
14 |
101,875,452 (GRCm38) |
missense |
probably benign |
0.29 |
R6658:Lmo7
|
UTSW |
14 |
101,910,845 (GRCm38) |
missense |
possibly damaging |
0.84 |
R6917:Lmo7
|
UTSW |
14 |
101,918,010 (GRCm38) |
missense |
probably damaging |
1.00 |
R7064:Lmo7
|
UTSW |
14 |
101,884,179 (GRCm38) |
missense |
probably damaging |
1.00 |
R7072:Lmo7
|
UTSW |
14 |
101,898,700 (GRCm38) |
critical splice donor site |
probably null |
|
R7121:Lmo7
|
UTSW |
14 |
101,887,035 (GRCm38) |
missense |
probably damaging |
1.00 |
R7136:Lmo7
|
UTSW |
14 |
101,920,539 (GRCm38) |
missense |
unknown |
|
R7196:Lmo7
|
UTSW |
14 |
101,896,500 (GRCm38) |
missense |
possibly damaging |
0.75 |
R7228:Lmo7
|
UTSW |
14 |
101,896,535 (GRCm38) |
missense |
probably damaging |
0.99 |
R7337:Lmo7
|
UTSW |
14 |
101,884,204 (GRCm38) |
missense |
probably damaging |
0.98 |
R7341:Lmo7
|
UTSW |
14 |
101,885,512 (GRCm38) |
missense |
probably benign |
0.30 |
R7408:Lmo7
|
UTSW |
14 |
101,880,953 (GRCm38) |
missense |
probably damaging |
1.00 |
R7432:Lmo7
|
UTSW |
14 |
101,902,115 (GRCm38) |
missense |
probably benign |
0.42 |
R7470:Lmo7
|
UTSW |
14 |
101,900,604 (GRCm38) |
missense |
possibly damaging |
0.83 |
R7506:Lmo7
|
UTSW |
14 |
101,919,609 (GRCm38) |
missense |
unknown |
|
R7559:Lmo7
|
UTSW |
14 |
101,887,226 (GRCm38) |
nonsense |
probably null |
|
R7565:Lmo7
|
UTSW |
14 |
101,885,301 (GRCm38) |
missense |
probably damaging |
0.98 |
R7788:Lmo7
|
UTSW |
14 |
101,898,576 (GRCm38) |
missense |
possibly damaging |
0.64 |
R8095:Lmo7
|
UTSW |
14 |
101,887,419 (GRCm38) |
missense |
possibly damaging |
0.88 |
R8100:Lmo7
|
UTSW |
14 |
101,900,463 (GRCm38) |
missense |
probably benign |
0.33 |
R8121:Lmo7
|
UTSW |
14 |
101,926,300 (GRCm38) |
missense |
unknown |
|
R8308:Lmo7
|
UTSW |
14 |
101,902,371 (GRCm38) |
critical splice donor site |
probably null |
|
R8371:Lmo7
|
UTSW |
14 |
101,887,008 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8403:Lmo7
|
UTSW |
14 |
101,902,364 (GRCm38) |
missense |
probably benign |
0.03 |
R8690:Lmo7
|
UTSW |
14 |
101,931,208 (GRCm38) |
missense |
unknown |
|
R8778:Lmo7
|
UTSW |
14 |
101,919,219 (GRCm38) |
missense |
probably benign |
0.24 |
R8778:Lmo7
|
UTSW |
14 |
101,912,067 (GRCm38) |
missense |
probably damaging |
0.98 |
R8822:Lmo7
|
UTSW |
14 |
101,884,174 (GRCm38) |
missense |
probably damaging |
1.00 |
R8849:Lmo7
|
UTSW |
14 |
101,926,107 (GRCm38) |
missense |
unknown |
|
R8923:Lmo7
|
UTSW |
14 |
101,900,243 (GRCm38) |
missense |
probably benign |
0.31 |
R9006:Lmo7
|
UTSW |
14 |
101,917,636 (GRCm38) |
small deletion |
probably benign |
|
R9135:Lmo7
|
UTSW |
14 |
101,880,861 (GRCm38) |
missense |
probably damaging |
1.00 |
R9154:Lmo7
|
UTSW |
14 |
101,885,307 (GRCm38) |
missense |
probably damaging |
0.99 |
R9178:Lmo7
|
UTSW |
14 |
101,807,470 (GRCm38) |
nonsense |
probably null |
|
R9375:Lmo7
|
UTSW |
14 |
101,898,687 (GRCm38) |
missense |
probably damaging |
0.99 |
R9428:Lmo7
|
UTSW |
14 |
101,917,640 (GRCm38) |
missense |
probably damaging |
0.99 |
R9488:Lmo7
|
UTSW |
14 |
101,885,347 (GRCm38) |
missense |
possibly damaging |
0.85 |
R9493:Lmo7
|
UTSW |
14 |
101,900,471 (GRCm38) |
missense |
probably benign |
0.01 |
R9594:Lmo7
|
UTSW |
14 |
101,918,700 (GRCm38) |
missense |
probably null |
0.98 |
R9674:Lmo7
|
UTSW |
14 |
101,840,904 (GRCm38) |
missense |
probably damaging |
1.00 |
R9736:Lmo7
|
UTSW |
14 |
101,920,493 (GRCm38) |
missense |
unknown |
|
X0066:Lmo7
|
UTSW |
14 |
101,887,461 (GRCm38) |
missense |
probably damaging |
1.00 |
X0067:Lmo7
|
UTSW |
14 |
101,886,933 (GRCm38) |
splice site |
probably null |
|
Z1176:Lmo7
|
UTSW |
14 |
101,919,281 (GRCm38) |
missense |
probably benign |
0.00 |
Z1176:Lmo7
|
UTSW |
14 |
101,884,306 (GRCm38) |
missense |
probably damaging |
0.99 |
Z1176:Lmo7
|
UTSW |
14 |
101,929,228 (GRCm38) |
missense |
unknown |
|
Z1176:Lmo7
|
UTSW |
14 |
101,919,443 (GRCm38) |
missense |
unknown |
|
Z1177:Lmo7
|
UTSW |
14 |
101,898,557 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Lmo7
|
UTSW |
14 |
101,896,518 (GRCm38) |
missense |
possibly damaging |
0.96 |
|