Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam25 |
A |
G |
8: 41,209,141 (GRCm39) |
|
probably benign |
Het |
Adgrb2 |
A |
G |
4: 129,906,302 (GRCm39) |
N910S |
possibly damaging |
Het |
Arhgap24 |
A |
T |
5: 103,040,016 (GRCm39) |
I411F |
probably benign |
Het |
BC030500 |
T |
A |
8: 59,365,911 (GRCm39) |
L15Q |
unknown |
Het |
BC051665 |
A |
G |
13: 60,932,916 (GRCm39) |
V15A |
probably benign |
Het |
Bicc1 |
T |
C |
10: 70,776,862 (GRCm39) |
D732G |
probably damaging |
Het |
Bpifb1 |
A |
G |
2: 154,046,692 (GRCm39) |
I71V |
probably benign |
Het |
Btnl1 |
A |
T |
17: 34,598,681 (GRCm39) |
Q99L |
possibly damaging |
Het |
Castor1 |
T |
A |
11: 4,170,767 (GRCm39) |
V196D |
possibly damaging |
Het |
Col9a2 |
G |
T |
4: 120,900,951 (GRCm39) |
|
probably benign |
Het |
D7Ertd443e |
T |
A |
7: 133,871,986 (GRCm39) |
D625V |
probably damaging |
Het |
Dchs2 |
A |
T |
3: 83,187,535 (GRCm39) |
D1327V |
probably damaging |
Het |
Ddx1 |
A |
G |
12: 13,275,458 (GRCm39) |
V543A |
possibly damaging |
Het |
Dgkz |
G |
T |
2: 91,768,545 (GRCm39) |
D714E |
probably benign |
Het |
Dlk1 |
A |
G |
12: 109,424,051 (GRCm39) |
D105G |
probably benign |
Het |
Fndc3a |
A |
G |
14: 72,802,133 (GRCm39) |
F557L |
probably benign |
Het |
Gm28042 |
C |
T |
2: 119,869,462 (GRCm39) |
L609F |
probably damaging |
Het |
Gsap |
A |
G |
5: 21,458,434 (GRCm39) |
I473V |
probably damaging |
Het |
Jag1 |
A |
T |
2: 136,930,354 (GRCm39) |
M730K |
probably benign |
Het |
Kazald1 |
A |
T |
19: 45,065,211 (GRCm39) |
T31S |
probably benign |
Het |
Ldhb |
A |
G |
6: 142,439,935 (GRCm39) |
W202R |
probably damaging |
Het |
Lrrcc1 |
C |
T |
3: 14,615,489 (GRCm39) |
Q528* |
probably null |
Het |
Magi2 |
A |
T |
5: 20,733,305 (GRCm39) |
K525I |
possibly damaging |
Het |
Mdn1 |
A |
T |
4: 32,701,814 (GRCm39) |
M1516L |
probably damaging |
Het |
Mpzl2 |
T |
A |
9: 44,958,583 (GRCm39) |
S186R |
probably benign |
Het |
Mtif2 |
T |
C |
11: 29,483,951 (GRCm39) |
M208T |
probably benign |
Het |
Myo3a |
T |
C |
2: 22,436,464 (GRCm39) |
V873A |
probably benign |
Het |
Or10ac1 |
A |
C |
6: 42,515,583 (GRCm39) |
Y124* |
probably null |
Het |
Or1j4 |
T |
A |
2: 36,740,143 (GRCm39) |
Y28* |
probably null |
Het |
Or5d38 |
A |
G |
2: 87,955,123 (GRCm39) |
S69P |
probably damaging |
Het |
Or5p6 |
T |
C |
7: 107,630,887 (GRCm39) |
Y221C |
probably damaging |
Het |
Or8g51 |
A |
G |
9: 38,608,735 (GRCm39) |
F309S |
probably benign |
Het |
Pgap4 |
A |
G |
4: 49,587,093 (GRCm39) |
V25A |
probably benign |
Het |
Plod2 |
G |
T |
9: 92,424,380 (GRCm39) |
|
probably benign |
Het |
Rgs14 |
A |
C |
13: 55,528,792 (GRCm39) |
D311A |
probably damaging |
Het |
Rin1 |
C |
A |
19: 5,103,048 (GRCm39) |
P446T |
probably damaging |
Het |
Ripor3 |
T |
C |
2: 167,822,835 (GRCm39) |
K909E |
possibly damaging |
Het |
Rnf139 |
T |
C |
15: 58,771,685 (GRCm39) |
L570P |
probably damaging |
Het |
Snx17 |
A |
G |
5: 31,355,026 (GRCm39) |
E347G |
probably damaging |
Het |
Spaca1 |
A |
G |
4: 34,029,168 (GRCm39) |
S220P |
probably damaging |
Het |
Spen |
G |
T |
4: 141,200,233 (GRCm39) |
T2798K |
|
Het |
Tacc1 |
G |
T |
8: 25,659,255 (GRCm39) |
S570R |
probably damaging |
Het |
Tmem135 |
G |
C |
7: 88,797,186 (GRCm39) |
L357V |
probably benign |
Het |
Trim63 |
G |
A |
4: 134,055,003 (GRCm39) |
|
probably benign |
Het |
Trmt2a |
C |
A |
16: 18,067,722 (GRCm39) |
R132S |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,768,716 (GRCm39) |
E2952G |
unknown |
Het |
Tyw1 |
G |
A |
5: 130,298,065 (GRCm39) |
R202Q |
probably damaging |
Het |
Vmn1r211 |
A |
T |
13: 23,035,936 (GRCm39) |
F244I |
probably damaging |
Het |
Vmn2r86 |
T |
G |
10: 130,289,677 (GRCm39) |
S73R |
probably benign |
Het |
Wdr27 |
A |
G |
17: 15,152,846 (GRCm39) |
L87P |
probably damaging |
Het |
Zfp148 |
A |
G |
16: 33,317,596 (GRCm39) |
N756S |
probably benign |
Het |
Zfp57 |
G |
A |
17: 37,320,650 (GRCm39) |
R168H |
probably benign |
Het |
|
Other mutations in Map2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01518:Map2
|
APN |
1 |
66,464,490 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02135:Map2
|
APN |
1 |
66,419,920 (GRCm39) |
nonsense |
probably null |
|
IGL02526:Map2
|
APN |
1 |
66,419,876 (GRCm39) |
missense |
possibly damaging |
0.94 |
Annas
|
UTSW |
1 |
66,472,756 (GRCm39) |
critical splice donor site |
probably null |
|
calliope
|
UTSW |
1 |
66,464,457 (GRCm39) |
missense |
probably damaging |
1.00 |
carthage
|
UTSW |
1 |
66,453,807 (GRCm39) |
missense |
probably damaging |
1.00 |
costas
|
UTSW |
1 |
66,451,812 (GRCm39) |
missense |
possibly damaging |
0.94 |
Jacobin
|
UTSW |
1 |
66,438,578 (GRCm39) |
missense |
probably damaging |
1.00 |
Nectar
|
UTSW |
1 |
66,454,522 (GRCm39) |
nonsense |
probably null |
|
ruby_throat
|
UTSW |
1 |
66,454,043 (GRCm39) |
missense |
possibly damaging |
0.67 |
Rufous
|
UTSW |
1 |
66,419,927 (GRCm39) |
missense |
probably damaging |
1.00 |
Speckled
|
UTSW |
1 |
66,451,886 (GRCm39) |
nonsense |
probably null |
|
Sunbird
|
UTSW |
1 |
66,454,646 (GRCm39) |
missense |
probably benign |
0.01 |
swift
|
UTSW |
1 |
66,455,523 (GRCm39) |
missense |
probably damaging |
1.00 |
E0370:Map2
|
UTSW |
1 |
66,455,883 (GRCm39) |
unclassified |
probably benign |
|
PIT4362001:Map2
|
UTSW |
1 |
66,451,677 (GRCm39) |
missense |
probably benign |
0.05 |
R0067:Map2
|
UTSW |
1 |
66,452,322 (GRCm39) |
missense |
probably benign |
0.04 |
R0238:Map2
|
UTSW |
1 |
66,455,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0238:Map2
|
UTSW |
1 |
66,455,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Map2
|
UTSW |
1 |
66,455,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Map2
|
UTSW |
1 |
66,455,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0268:Map2
|
UTSW |
1 |
66,419,881 (GRCm39) |
nonsense |
probably null |
|
R0302:Map2
|
UTSW |
1 |
66,453,987 (GRCm39) |
missense |
probably benign |
0.15 |
R0305:Map2
|
UTSW |
1 |
66,452,253 (GRCm39) |
missense |
probably benign |
0.00 |
R0409:Map2
|
UTSW |
1 |
66,472,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R0561:Map2
|
UTSW |
1 |
66,464,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R0674:Map2
|
UTSW |
1 |
66,452,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R0738:Map2
|
UTSW |
1 |
66,464,348 (GRCm39) |
splice site |
probably benign |
|
R0893:Map2
|
UTSW |
1 |
66,419,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R1305:Map2
|
UTSW |
1 |
66,464,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R1534:Map2
|
UTSW |
1 |
66,452,339 (GRCm39) |
missense |
probably benign |
0.33 |
R1632:Map2
|
UTSW |
1 |
66,454,245 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1682:Map2
|
UTSW |
1 |
66,454,781 (GRCm39) |
splice site |
probably null |
|
R1774:Map2
|
UTSW |
1 |
66,453,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R2014:Map2
|
UTSW |
1 |
66,455,295 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2017:Map2
|
UTSW |
1 |
66,451,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R2050:Map2
|
UTSW |
1 |
66,453,473 (GRCm39) |
missense |
probably damaging |
0.98 |
R2093:Map2
|
UTSW |
1 |
66,438,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R2214:Map2
|
UTSW |
1 |
66,459,345 (GRCm39) |
missense |
probably damaging |
0.99 |
R2284:Map2
|
UTSW |
1 |
66,453,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R3011:Map2
|
UTSW |
1 |
66,453,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R3105:Map2
|
UTSW |
1 |
66,472,756 (GRCm39) |
critical splice donor site |
probably null |
|
R3708:Map2
|
UTSW |
1 |
66,455,714 (GRCm39) |
unclassified |
probably benign |
|
R3709:Map2
|
UTSW |
1 |
66,455,015 (GRCm39) |
nonsense |
probably null |
|
R3729:Map2
|
UTSW |
1 |
66,451,605 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3760:Map2
|
UTSW |
1 |
66,478,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R3788:Map2
|
UTSW |
1 |
66,456,022 (GRCm39) |
missense |
probably damaging |
0.99 |
R3789:Map2
|
UTSW |
1 |
66,456,022 (GRCm39) |
missense |
probably damaging |
0.99 |
R4003:Map2
|
UTSW |
1 |
66,454,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R4120:Map2
|
UTSW |
1 |
66,455,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R4172:Map2
|
UTSW |
1 |
66,452,759 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4198:Map2
|
UTSW |
1 |
66,464,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R4200:Map2
|
UTSW |
1 |
66,464,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R4205:Map2
|
UTSW |
1 |
66,464,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R4613:Map2
|
UTSW |
1 |
66,464,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R4700:Map2
|
UTSW |
1 |
66,449,796 (GRCm39) |
missense |
probably damaging |
0.96 |
R4974:Map2
|
UTSW |
1 |
66,452,664 (GRCm39) |
missense |
probably benign |
0.15 |
R5007:Map2
|
UTSW |
1 |
66,452,448 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5039:Map2
|
UTSW |
1 |
66,477,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R5237:Map2
|
UTSW |
1 |
66,478,169 (GRCm39) |
unclassified |
probably benign |
|
R5313:Map2
|
UTSW |
1 |
66,464,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R5455:Map2
|
UTSW |
1 |
66,438,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R5490:Map2
|
UTSW |
1 |
66,452,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R5517:Map2
|
UTSW |
1 |
66,454,415 (GRCm39) |
missense |
probably benign |
0.00 |
R5532:Map2
|
UTSW |
1 |
66,453,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R5583:Map2
|
UTSW |
1 |
66,455,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R5764:Map2
|
UTSW |
1 |
66,454,034 (GRCm39) |
missense |
probably damaging |
0.99 |
R5996:Map2
|
UTSW |
1 |
66,454,043 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6058:Map2
|
UTSW |
1 |
66,454,573 (GRCm39) |
missense |
probably benign |
0.05 |
R6199:Map2
|
UTSW |
1 |
66,464,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R6208:Map2
|
UTSW |
1 |
66,470,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R6276:Map2
|
UTSW |
1 |
66,438,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R6378:Map2
|
UTSW |
1 |
66,454,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R6424:Map2
|
UTSW |
1 |
66,453,946 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6743:Map2
|
UTSW |
1 |
66,454,766 (GRCm39) |
missense |
probably benign |
0.04 |
R6837:Map2
|
UTSW |
1 |
66,453,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R6901:Map2
|
UTSW |
1 |
66,460,932 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6984:Map2
|
UTSW |
1 |
66,454,395 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6989:Map2
|
UTSW |
1 |
66,454,065 (GRCm39) |
missense |
probably benign |
0.00 |
R7001:Map2
|
UTSW |
1 |
66,454,646 (GRCm39) |
missense |
probably benign |
0.01 |
R7055:Map2
|
UTSW |
1 |
66,455,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R7094:Map2
|
UTSW |
1 |
66,451,886 (GRCm39) |
nonsense |
probably null |
|
R7106:Map2
|
UTSW |
1 |
66,449,903 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7182:Map2
|
UTSW |
1 |
66,451,812 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7235:Map2
|
UTSW |
1 |
66,453,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R7424:Map2
|
UTSW |
1 |
66,453,983 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7473:Map2
|
UTSW |
1 |
66,454,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R7642:Map2
|
UTSW |
1 |
66,452,466 (GRCm39) |
missense |
probably benign |
0.01 |
R7660:Map2
|
UTSW |
1 |
66,453,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R7673:Map2
|
UTSW |
1 |
66,452,933 (GRCm39) |
missense |
probably benign |
0.03 |
R7768:Map2
|
UTSW |
1 |
66,453,642 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7796:Map2
|
UTSW |
1 |
66,455,654 (GRCm39) |
splice site |
probably null |
|
R7834:Map2
|
UTSW |
1 |
66,455,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Map2
|
UTSW |
1 |
66,455,570 (GRCm39) |
missense |
probably benign |
|
R7955:Map2
|
UTSW |
1 |
66,452,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R8056:Map2
|
UTSW |
1 |
66,454,779 (GRCm39) |
missense |
probably damaging |
0.99 |
R8118:Map2
|
UTSW |
1 |
66,464,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R8135:Map2
|
UTSW |
1 |
66,452,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R8152:Map2
|
UTSW |
1 |
66,453,902 (GRCm39) |
missense |
probably benign |
0.00 |
R8223:Map2
|
UTSW |
1 |
66,464,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R8329:Map2
|
UTSW |
1 |
66,454,272 (GRCm39) |
missense |
probably benign |
0.01 |
R8344:Map2
|
UTSW |
1 |
66,460,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R8475:Map2
|
UTSW |
1 |
66,453,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R8548:Map2
|
UTSW |
1 |
66,452,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Map2
|
UTSW |
1 |
66,460,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R8713:Map2
|
UTSW |
1 |
66,453,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R8745:Map2
|
UTSW |
1 |
66,452,556 (GRCm39) |
missense |
probably benign |
0.00 |
R8786:Map2
|
UTSW |
1 |
66,472,755 (GRCm39) |
critical splice donor site |
probably benign |
|
R8790:Map2
|
UTSW |
1 |
66,477,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R8874:Map2
|
UTSW |
1 |
66,455,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R8887:Map2
|
UTSW |
1 |
66,454,758 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8948:Map2
|
UTSW |
1 |
66,419,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R8950:Map2
|
UTSW |
1 |
66,419,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R8998:Map2
|
UTSW |
1 |
66,452,473 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8999:Map2
|
UTSW |
1 |
66,452,473 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9072:Map2
|
UTSW |
1 |
66,453,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R9088:Map2
|
UTSW |
1 |
66,453,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R9089:Map2
|
UTSW |
1 |
66,452,098 (GRCm39) |
missense |
probably benign |
0.09 |
R9106:Map2
|
UTSW |
1 |
66,454,522 (GRCm39) |
nonsense |
probably null |
|
R9112:Map2
|
UTSW |
1 |
66,472,723 (GRCm39) |
nonsense |
probably null |
|
R9161:Map2
|
UTSW |
1 |
66,477,503 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9464:Map2
|
UTSW |
1 |
66,454,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R9589:Map2
|
UTSW |
1 |
66,449,753 (GRCm39) |
missense |
probably benign |
|
V8831:Map2
|
UTSW |
1 |
66,455,004 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Map2
|
UTSW |
1 |
66,477,520 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Map2
|
UTSW |
1 |
66,419,839 (GRCm39) |
missense |
probably benign |
0.01 |
|