Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ank2 |
G |
T |
3: 126,804,533 (GRCm39) |
D679E |
probably benign |
Het |
Catsper4 |
A |
T |
4: 133,953,058 (GRCm39) |
Y96N |
probably benign |
Het |
Cnksr3 |
T |
C |
10: 7,110,757 (GRCm39) |
I35V |
probably benign |
Het |
Col16a1 |
A |
G |
4: 129,953,116 (GRCm39) |
E424G |
probably damaging |
Het |
Ctsc |
G |
T |
7: 87,930,666 (GRCm39) |
G82W |
probably damaging |
Het |
Cxcr4 |
T |
C |
1: 128,517,352 (GRCm39) |
D101G |
probably benign |
Het |
Dapk1 |
T |
A |
13: 60,884,138 (GRCm39) |
N635K |
probably benign |
Het |
Dop1a |
T |
C |
9: 86,382,913 (GRCm39) |
M282T |
probably damaging |
Het |
Dpysl4 |
G |
A |
7: 138,671,915 (GRCm39) |
E172K |
probably damaging |
Het |
Efcab3 |
A |
C |
11: 104,799,896 (GRCm39) |
T2931P |
probably damaging |
Het |
Eif2ak3 |
T |
C |
6: 70,855,829 (GRCm39) |
I211T |
probably damaging |
Het |
Fbxw22 |
A |
T |
9: 109,211,144 (GRCm39) |
W386R |
probably benign |
Het |
Garin1b |
T |
A |
6: 29,323,905 (GRCm39) |
I210N |
probably damaging |
Het |
Grm7 |
A |
G |
6: 110,623,265 (GRCm39) |
K146R |
probably benign |
Het |
Grm7 |
C |
A |
6: 111,472,690 (GRCm39) |
P843Q |
probably damaging |
Het |
Gtf2e2 |
A |
G |
8: 34,248,726 (GRCm39) |
D171G |
probably damaging |
Het |
Hyal5 |
T |
C |
6: 24,876,303 (GRCm39) |
S59P |
probably benign |
Het |
Il7r |
T |
A |
15: 9,508,090 (GRCm39) |
T411S |
probably damaging |
Het |
Kcp |
T |
A |
6: 29,484,611 (GRCm39) |
|
probably null |
Het |
Krcc1 |
T |
C |
6: 71,261,135 (GRCm39) |
Y56H |
probably benign |
Het |
Lmo2 |
T |
A |
2: 103,801,018 (GRCm39) |
M1K |
probably null |
Het |
Lrit3 |
G |
A |
3: 129,582,934 (GRCm39) |
T351I |
probably damaging |
Het |
Mcu |
T |
G |
10: 59,292,566 (GRCm39) |
T38P |
possibly damaging |
Het |
Ncoa2 |
A |
T |
1: 13,226,725 (GRCm39) |
C996S |
possibly damaging |
Het |
Npr2 |
A |
G |
4: 43,640,597 (GRCm39) |
E350G |
probably damaging |
Het |
Or5an1b |
T |
C |
19: 12,299,792 (GRCm39) |
Y133C |
probably damaging |
Het |
Pald1 |
T |
C |
10: 61,156,996 (GRCm39) |
E818G |
probably benign |
Het |
Phf19 |
G |
T |
2: 34,794,143 (GRCm39) |
Q210K |
probably damaging |
Het |
Pomgnt1 |
G |
A |
4: 116,011,351 (GRCm39) |
V250M |
probably damaging |
Het |
Ppm1l |
T |
A |
3: 69,456,736 (GRCm39) |
C218S |
possibly damaging |
Het |
Prkdc |
G |
A |
16: 15,617,853 (GRCm39) |
R3228H |
probably benign |
Het |
Pros1 |
A |
T |
16: 62,744,938 (GRCm39) |
T518S |
probably benign |
Het |
Rdh8 |
T |
A |
9: 20,734,003 (GRCm39) |
V63D |
probably benign |
Het |
Rexo1 |
A |
G |
10: 80,386,470 (GRCm39) |
V196A |
possibly damaging |
Het |
Scgb2b20 |
A |
T |
7: 33,065,724 (GRCm39) |
M1K |
probably null |
Het |
Scn11a |
A |
G |
9: 119,594,580 (GRCm39) |
V1271A |
probably benign |
Het |
Serac1 |
C |
A |
17: 6,102,090 (GRCm39) |
D395Y |
probably damaging |
Het |
Syne2 |
A |
G |
12: 76,012,771 (GRCm39) |
D2655G |
probably benign |
Het |
Tm4sf19 |
T |
C |
16: 32,224,676 (GRCm39) |
V8A |
probably benign |
Het |
Usp3 |
A |
T |
9: 66,427,972 (GRCm39) |
D334E |
probably benign |
Het |
Uty |
C |
T |
Y: 1,240,000 (GRCm39) |
|
probably null |
Het |
Vmn2r7 |
T |
C |
3: 64,598,542 (GRCm39) |
N672D |
probably damaging |
Het |
Vmn2r96 |
T |
A |
17: 18,818,100 (GRCm39) |
L751H |
probably damaging |
Het |
Wnk2 |
T |
C |
13: 49,254,616 (GRCm39) |
S300G |
probably damaging |
Het |
Zp3r |
G |
T |
1: 130,505,632 (GRCm39) |
S508R |
probably benign |
Het |
|
Other mutations in Mylk |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01384:Mylk
|
APN |
16 |
34,759,322 (GRCm39) |
missense |
probably benign |
0.36 |
IGL01386:Mylk
|
APN |
16 |
34,791,610 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01684:Mylk
|
APN |
16 |
34,792,310 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL01884:Mylk
|
APN |
16 |
34,809,247 (GRCm39) |
splice site |
probably benign |
|
IGL02079:Mylk
|
APN |
16 |
34,681,001 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02104:Mylk
|
APN |
16 |
34,635,805 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02624:Mylk
|
APN |
16 |
34,750,266 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02756:Mylk
|
APN |
16 |
34,784,016 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02794:Mylk
|
APN |
16 |
34,806,911 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02833:Mylk
|
APN |
16 |
34,735,270 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02946:Mylk
|
APN |
16 |
34,742,158 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03012:Mylk
|
APN |
16 |
34,773,151 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03093:Mylk
|
APN |
16 |
34,732,562 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL03272:Mylk
|
APN |
16 |
34,799,559 (GRCm39) |
missense |
probably benign |
0.09 |
billy
|
UTSW |
16 |
34,695,990 (GRCm39) |
missense |
probably damaging |
0.97 |
brutus
|
UTSW |
16 |
34,774,065 (GRCm39) |
missense |
probably benign |
0.12 |
Club
|
UTSW |
16 |
34,732,645 (GRCm39) |
nonsense |
probably null |
|
popeye
|
UTSW |
16 |
34,783,947 (GRCm39) |
missense |
probably benign |
0.29 |
F5770:Mylk
|
UTSW |
16 |
34,815,574 (GRCm39) |
critical splice donor site |
probably null |
|
P4717OSA:Mylk
|
UTSW |
16 |
34,797,483 (GRCm39) |
splice site |
probably benign |
|
PIT4382001:Mylk
|
UTSW |
16 |
34,696,012 (GRCm39) |
missense |
probably damaging |
0.99 |
R0131:Mylk
|
UTSW |
16 |
34,695,874 (GRCm39) |
missense |
probably benign |
0.03 |
R0309:Mylk
|
UTSW |
16 |
34,732,667 (GRCm39) |
splice site |
probably benign |
|
R0358:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0381:Mylk
|
UTSW |
16 |
34,605,344 (GRCm39) |
splice site |
probably null |
|
R0390:Mylk
|
UTSW |
16 |
34,695,990 (GRCm39) |
missense |
probably damaging |
0.97 |
R0413:Mylk
|
UTSW |
16 |
34,742,314 (GRCm39) |
missense |
probably benign |
0.01 |
R0536:Mylk
|
UTSW |
16 |
34,820,757 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0544:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0545:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0546:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0547:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0548:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0627:Mylk
|
UTSW |
16 |
34,820,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R0726:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0755:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0782:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0783:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0784:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1136:Mylk
|
UTSW |
16 |
34,820,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R1170:Mylk
|
UTSW |
16 |
34,694,409 (GRCm39) |
missense |
probably benign |
0.20 |
R1222:Mylk
|
UTSW |
16 |
34,681,022 (GRCm39) |
missense |
probably benign |
0.12 |
R1445:Mylk
|
UTSW |
16 |
34,635,835 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1583:Mylk
|
UTSW |
16 |
34,695,956 (GRCm39) |
missense |
probably benign |
0.29 |
R1618:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1643:Mylk
|
UTSW |
16 |
34,696,005 (GRCm39) |
missense |
probably benign |
0.03 |
R1702:Mylk
|
UTSW |
16 |
34,742,314 (GRCm39) |
missense |
probably benign |
0.00 |
R1776:Mylk
|
UTSW |
16 |
34,773,152 (GRCm39) |
missense |
probably benign |
0.16 |
R1865:Mylk
|
UTSW |
16 |
34,732,600 (GRCm39) |
missense |
probably benign |
0.03 |
R1975:Mylk
|
UTSW |
16 |
34,700,673 (GRCm39) |
splice site |
probably null |
|
R2016:Mylk
|
UTSW |
16 |
34,817,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R2045:Mylk
|
UTSW |
16 |
34,774,023 (GRCm39) |
missense |
probably benign |
0.29 |
R2134:Mylk
|
UTSW |
16 |
34,806,846 (GRCm39) |
missense |
probably benign |
0.13 |
R3547:Mylk
|
UTSW |
16 |
34,700,538 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3844:Mylk
|
UTSW |
16 |
34,742,247 (GRCm39) |
missense |
probably benign |
0.01 |
R4003:Mylk
|
UTSW |
16 |
34,783,947 (GRCm39) |
missense |
probably benign |
0.29 |
R4396:Mylk
|
UTSW |
16 |
34,732,645 (GRCm39) |
nonsense |
probably null |
|
R4470:Mylk
|
UTSW |
16 |
34,732,522 (GRCm39) |
missense |
probably benign |
0.09 |
R4507:Mylk
|
UTSW |
16 |
34,774,065 (GRCm39) |
missense |
probably benign |
0.12 |
R4700:Mylk
|
UTSW |
16 |
34,742,805 (GRCm39) |
missense |
probably benign |
0.16 |
R4751:Mylk
|
UTSW |
16 |
34,699,539 (GRCm39) |
missense |
probably benign |
0.29 |
R4815:Mylk
|
UTSW |
16 |
34,715,295 (GRCm39) |
missense |
probably damaging |
0.97 |
R4832:Mylk
|
UTSW |
16 |
34,742,737 (GRCm39) |
missense |
probably benign |
0.36 |
R4872:Mylk
|
UTSW |
16 |
34,735,360 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4953:Mylk
|
UTSW |
16 |
34,809,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R4969:Mylk
|
UTSW |
16 |
34,791,810 (GRCm39) |
missense |
probably damaging |
0.96 |
R5009:Mylk
|
UTSW |
16 |
34,719,877 (GRCm39) |
missense |
probably benign |
0.39 |
R5130:Mylk
|
UTSW |
16 |
34,809,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R5173:Mylk
|
UTSW |
16 |
34,797,383 (GRCm39) |
missense |
probably benign |
0.40 |
R5195:Mylk
|
UTSW |
16 |
34,799,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R5209:Mylk
|
UTSW |
16 |
34,742,995 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5311:Mylk
|
UTSW |
16 |
34,742,127 (GRCm39) |
missense |
probably benign |
0.01 |
R5418:Mylk
|
UTSW |
16 |
34,732,600 (GRCm39) |
missense |
probably benign |
0.02 |
R5481:Mylk
|
UTSW |
16 |
34,741,974 (GRCm39) |
missense |
probably benign |
0.09 |
R5590:Mylk
|
UTSW |
16 |
34,699,722 (GRCm39) |
missense |
probably benign |
0.29 |
R5603:Mylk
|
UTSW |
16 |
34,776,862 (GRCm39) |
missense |
probably benign |
0.06 |
R5823:Mylk
|
UTSW |
16 |
34,715,317 (GRCm39) |
critical splice donor site |
probably null |
|
R6290:Mylk
|
UTSW |
16 |
34,715,213 (GRCm39) |
missense |
probably benign |
0.39 |
R6351:Mylk
|
UTSW |
16 |
34,742,341 (GRCm39) |
missense |
probably benign |
0.01 |
R6365:Mylk
|
UTSW |
16 |
34,680,961 (GRCm39) |
missense |
probably benign |
0.12 |
R6490:Mylk
|
UTSW |
16 |
34,750,237 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6723:Mylk
|
UTSW |
16 |
34,750,258 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6864:Mylk
|
UTSW |
16 |
34,694,520 (GRCm39) |
missense |
probably benign |
0.03 |
R6908:Mylk
|
UTSW |
16 |
34,700,643 (GRCm39) |
missense |
probably benign |
0.18 |
R7018:Mylk
|
UTSW |
16 |
34,820,796 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7035:Mylk
|
UTSW |
16 |
34,797,352 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7162:Mylk
|
UTSW |
16 |
34,742,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R7236:Mylk
|
UTSW |
16 |
34,742,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R7269:Mylk
|
UTSW |
16 |
34,605,381 (GRCm39) |
missense |
probably damaging |
0.96 |
R7475:Mylk
|
UTSW |
16 |
34,734,446 (GRCm39) |
splice site |
probably null |
|
R7525:Mylk
|
UTSW |
16 |
34,809,357 (GRCm39) |
missense |
probably benign |
0.06 |
R7587:Mylk
|
UTSW |
16 |
34,742,887 (GRCm39) |
missense |
probably benign |
0.29 |
R7607:Mylk
|
UTSW |
16 |
34,715,184 (GRCm39) |
missense |
probably benign |
0.09 |
R7616:Mylk
|
UTSW |
16 |
34,699,927 (GRCm39) |
missense |
probably damaging |
0.97 |
R7647:Mylk
|
UTSW |
16 |
34,699,894 (GRCm39) |
missense |
probably benign |
0.29 |
R7648:Mylk
|
UTSW |
16 |
34,699,894 (GRCm39) |
missense |
probably benign |
0.29 |
R7764:Mylk
|
UTSW |
16 |
34,742,553 (GRCm39) |
missense |
probably benign |
0.16 |
R7890:Mylk
|
UTSW |
16 |
34,784,018 (GRCm39) |
nonsense |
probably null |
|
R7892:Mylk
|
UTSW |
16 |
34,699,894 (GRCm39) |
missense |
probably benign |
0.29 |
R7893:Mylk
|
UTSW |
16 |
34,699,894 (GRCm39) |
missense |
probably benign |
0.29 |
R8065:Mylk
|
UTSW |
16 |
34,792,389 (GRCm39) |
missense |
probably benign |
0.08 |
R8067:Mylk
|
UTSW |
16 |
34,792,389 (GRCm39) |
missense |
probably benign |
0.08 |
R8143:Mylk
|
UTSW |
16 |
34,734,525 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8210:Mylk
|
UTSW |
16 |
34,820,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R8271:Mylk
|
UTSW |
16 |
34,742,949 (GRCm39) |
missense |
probably damaging |
0.97 |
R8540:Mylk
|
UTSW |
16 |
34,750,257 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8721:Mylk
|
UTSW |
16 |
34,817,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R8743:Mylk
|
UTSW |
16 |
34,741,427 (GRCm39) |
missense |
probably benign |
0.03 |
R8798:Mylk
|
UTSW |
16 |
34,719,772 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8956:Mylk
|
UTSW |
16 |
34,791,779 (GRCm39) |
missense |
probably benign |
0.01 |
R9131:Mylk
|
UTSW |
16 |
34,776,835 (GRCm39) |
missense |
probably benign |
0.29 |
R9403:Mylk
|
UTSW |
16 |
34,696,012 (GRCm39) |
nonsense |
probably null |
|
R9624:Mylk
|
UTSW |
16 |
34,699,677 (GRCm39) |
missense |
probably benign |
0.29 |
R9735:Mylk
|
UTSW |
16 |
34,735,179 (GRCm39) |
missense |
probably benign |
0.09 |
R9756:Mylk
|
UTSW |
16 |
34,734,387 (GRCm39) |
missense |
probably damaging |
0.96 |
R9763:Mylk
|
UTSW |
16 |
34,699,482 (GRCm39) |
nonsense |
probably null |
|
RF001:Mylk
|
UTSW |
16 |
34,699,741 (GRCm39) |
missense |
probably benign |
0.03 |
V7580:Mylk
|
UTSW |
16 |
34,815,574 (GRCm39) |
critical splice donor site |
probably null |
|
V7583:Mylk
|
UTSW |
16 |
34,815,574 (GRCm39) |
critical splice donor site |
probably null |
|
X0065:Mylk
|
UTSW |
16 |
34,820,811 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Mylk
|
UTSW |
16 |
34,743,021 (GRCm39) |
missense |
possibly damaging |
0.74 |
|