Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsbg1 |
T |
C |
9: 54,529,866 (GRCm39) |
E247G |
possibly damaging |
Het |
Adgra3 |
A |
G |
5: 50,118,096 (GRCm39) |
F1151L |
probably benign |
Het |
Afg3l2 |
G |
T |
18: 67,554,329 (GRCm39) |
L458M |
probably damaging |
Het |
Aldh4a1 |
A |
C |
4: 139,375,612 (GRCm39) |
|
probably benign |
Het |
Anln |
A |
T |
9: 22,264,077 (GRCm39) |
|
probably null |
Het |
Aste1 |
T |
C |
9: 105,282,253 (GRCm39) |
S74P |
probably damaging |
Het |
Atp6v0e2 |
G |
A |
6: 48,517,051 (GRCm39) |
R77H |
probably benign |
Het |
Brpf1 |
A |
G |
6: 113,296,902 (GRCm39) |
D962G |
possibly damaging |
Het |
Btbd2 |
T |
C |
10: 80,482,253 (GRCm39) |
D249G |
probably damaging |
Het |
Catsper3 |
T |
C |
13: 55,955,989 (GRCm39) |
|
probably null |
Het |
Cfap43 |
A |
G |
19: 47,885,811 (GRCm39) |
L268P |
probably damaging |
Het |
Cftr |
T |
C |
6: 18,255,413 (GRCm39) |
V540A |
probably benign |
Het |
Col22a1 |
C |
T |
15: 71,881,255 (GRCm39) |
G32D |
probably damaging |
Het |
Col5a2 |
G |
T |
1: 45,432,241 (GRCm39) |
P804Q |
probably benign |
Het |
Cyp2d41-ps |
A |
G |
15: 82,662,981 (GRCm39) |
|
noncoding transcript |
Het |
Cyp39a1 |
T |
G |
17: 44,057,429 (GRCm39) |
L423V |
possibly damaging |
Het |
Elmo1 |
T |
G |
13: 20,748,607 (GRCm39) |
V484G |
probably benign |
Het |
Eps8 |
C |
A |
6: 137,467,288 (GRCm39) |
Q656H |
probably damaging |
Het |
Eps8 |
T |
C |
6: 137,467,289 (GRCm39) |
Q656R |
possibly damaging |
Het |
Fshb |
T |
C |
2: 106,887,854 (GRCm39) |
D55G |
possibly damaging |
Het |
Garin1a |
G |
T |
6: 29,281,221 (GRCm39) |
|
probably benign |
Het |
H3c4 |
T |
A |
13: 23,760,304 (GRCm39) |
L110Q |
probably damaging |
Het |
Herc1 |
C |
A |
9: 66,355,786 (GRCm39) |
Q2346K |
probably damaging |
Het |
Htr3b |
T |
C |
9: 48,856,815 (GRCm39) |
D221G |
probably benign |
Het |
Ift74 |
T |
A |
4: 94,550,833 (GRCm39) |
D328E |
probably benign |
Het |
Lgr6 |
C |
T |
1: 134,921,748 (GRCm39) |
A199T |
probably damaging |
Het |
Lipc |
T |
A |
9: 70,705,673 (GRCm39) |
E470V |
probably benign |
Het |
Lrrc4 |
G |
T |
6: 28,830,142 (GRCm39) |
T68K |
probably damaging |
Het |
Lrrc63 |
T |
A |
14: 75,322,322 (GRCm39) |
H594L |
possibly damaging |
Het |
Mfsd14a |
A |
T |
3: 116,442,150 (GRCm39) |
|
probably benign |
Het |
Mob2 |
T |
C |
7: 141,563,274 (GRCm39) |
|
probably null |
Het |
Nckap5 |
T |
A |
1: 126,150,410 (GRCm39) |
H105L |
possibly damaging |
Het |
Ngef |
C |
A |
1: 87,437,090 (GRCm39) |
G133* |
probably null |
Het |
Or14j2 |
T |
G |
17: 37,886,111 (GRCm39) |
I68L |
probably benign |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Or2t1 |
T |
A |
14: 14,328,462 (GRCm38) |
M117K |
probably damaging |
Het |
Or52s1 |
G |
A |
7: 102,861,207 (GRCm39) |
V47I |
probably benign |
Het |
Or5b120 |
G |
T |
19: 13,479,748 (GRCm39) |
V14F |
possibly damaging |
Het |
Or5g23 |
T |
C |
2: 85,438,791 (GRCm39) |
I154M |
probably benign |
Het |
Pard3 |
A |
G |
8: 127,800,040 (GRCm39) |
|
probably null |
Het |
Pgm2 |
C |
T |
5: 64,263,175 (GRCm39) |
A274V |
possibly damaging |
Het |
Ppp1r9a |
T |
A |
6: 5,156,177 (GRCm39) |
S1144R |
probably damaging |
Het |
Pramel23 |
A |
C |
4: 143,424,632 (GRCm39) |
C270W |
possibly damaging |
Het |
Prkcq |
C |
T |
2: 11,304,227 (GRCm39) |
P590L |
probably damaging |
Het |
Psmd13 |
T |
A |
7: 140,474,374 (GRCm39) |
|
probably null |
Het |
Rab3gap1 |
T |
A |
1: 127,816,931 (GRCm39) |
D63E |
probably benign |
Het |
Rag2 |
C |
A |
2: 101,461,085 (GRCm39) |
T465K |
probably damaging |
Het |
Rnase6 |
A |
G |
14: 51,367,670 (GRCm39) |
M21V |
unknown |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Ryr2 |
A |
T |
13: 11,653,316 (GRCm39) |
|
probably null |
Het |
Sash1 |
T |
G |
10: 8,615,989 (GRCm39) |
R624S |
probably damaging |
Het |
Slc1a2 |
A |
G |
2: 102,586,460 (GRCm39) |
I355V |
probably benign |
Het |
Srrm2 |
T |
C |
17: 24,036,358 (GRCm39) |
S1097P |
probably benign |
Het |
Sugct |
C |
T |
13: 17,497,861 (GRCm39) |
A271T |
probably damaging |
Het |
Tdrd7 |
T |
C |
4: 46,034,350 (GRCm39) |
V1065A |
probably damaging |
Het |
Tmprss6 |
T |
A |
15: 78,338,389 (GRCm39) |
Y307F |
probably damaging |
Het |
Tram1 |
T |
C |
1: 13,642,126 (GRCm39) |
N216S |
probably benign |
Het |
Ttk |
T |
C |
9: 83,721,394 (GRCm39) |
V93A |
probably benign |
Het |
Ubr4 |
A |
G |
4: 139,195,408 (GRCm39) |
Y1210C |
probably damaging |
Het |
Wdr7 |
A |
G |
18: 63,871,937 (GRCm39) |
K364E |
probably benign |
Het |
Xrcc2 |
G |
T |
5: 25,897,656 (GRCm39) |
H98N |
probably benign |
Het |
Zdhhc11 |
A |
G |
13: 74,113,688 (GRCm39) |
I77V |
probably benign |
Het |
Zfp54 |
C |
T |
17: 21,654,442 (GRCm39) |
S312L |
probably benign |
Het |
Zfp647 |
G |
A |
15: 76,796,285 (GRCm39) |
P125L |
probably damaging |
Het |
|
Other mutations in Kif21b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Kif21b
|
APN |
1 |
136,080,080 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01020:Kif21b
|
APN |
1 |
136,081,832 (GRCm39) |
splice site |
probably benign |
|
IGL01288:Kif21b
|
APN |
1 |
136,099,922 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02105:Kif21b
|
APN |
1 |
136,099,041 (GRCm39) |
missense |
probably benign |
|
IGL02264:Kif21b
|
APN |
1 |
136,087,495 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02303:Kif21b
|
APN |
1 |
136,087,495 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02308:Kif21b
|
APN |
1 |
136,087,495 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02310:Kif21b
|
APN |
1 |
136,087,495 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02419:Kif21b
|
APN |
1 |
136,079,005 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02553:Kif21b
|
APN |
1 |
136,081,859 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02568:Kif21b
|
APN |
1 |
136,100,605 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02657:Kif21b
|
APN |
1 |
136,099,968 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03068:Kif21b
|
APN |
1 |
136,086,093 (GRCm39) |
unclassified |
probably benign |
|
IGL03230:Kif21b
|
APN |
1 |
136,090,550 (GRCm39) |
missense |
probably benign |
0.03 |
R0629_Kif21b_729
|
UTSW |
1 |
136,099,895 (GRCm39) |
critical splice acceptor site |
probably null |
|
Schiessen
|
UTSW |
1 |
136,075,607 (GRCm39) |
critical splice donor site |
probably null |
|
wolfen
|
UTSW |
1 |
136,072,496 (GRCm39) |
nonsense |
probably null |
|
R0190:Kif21b
|
UTSW |
1 |
136,098,957 (GRCm39) |
missense |
probably benign |
0.32 |
R0349:Kif21b
|
UTSW |
1 |
136,077,049 (GRCm39) |
missense |
probably damaging |
0.97 |
R0501:Kif21b
|
UTSW |
1 |
136,090,837 (GRCm39) |
missense |
probably benign |
0.44 |
R0620:Kif21b
|
UTSW |
1 |
136,087,166 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0629:Kif21b
|
UTSW |
1 |
136,099,895 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0741:Kif21b
|
UTSW |
1 |
136,087,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R1087:Kif21b
|
UTSW |
1 |
136,090,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R1217:Kif21b
|
UTSW |
1 |
136,080,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Kif21b
|
UTSW |
1 |
136,083,891 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1464:Kif21b
|
UTSW |
1 |
136,083,891 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1511:Kif21b
|
UTSW |
1 |
136,097,062 (GRCm39) |
critical splice donor site |
probably null |
|
R1512:Kif21b
|
UTSW |
1 |
136,080,543 (GRCm39) |
missense |
probably benign |
0.01 |
R1513:Kif21b
|
UTSW |
1 |
136,083,849 (GRCm39) |
missense |
probably damaging |
0.98 |
R1591:Kif21b
|
UTSW |
1 |
136,077,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R1616:Kif21b
|
UTSW |
1 |
136,099,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R1628:Kif21b
|
UTSW |
1 |
136,098,958 (GRCm39) |
missense |
probably benign |
0.01 |
R1658:Kif21b
|
UTSW |
1 |
136,099,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Kif21b
|
UTSW |
1 |
136,087,859 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1741:Kif21b
|
UTSW |
1 |
136,083,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Kif21b
|
UTSW |
1 |
136,087,859 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1807:Kif21b
|
UTSW |
1 |
136,075,531 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1896:Kif21b
|
UTSW |
1 |
136,075,583 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1970:Kif21b
|
UTSW |
1 |
136,098,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R1984:Kif21b
|
UTSW |
1 |
136,075,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R1985:Kif21b
|
UTSW |
1 |
136,075,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R1986:Kif21b
|
UTSW |
1 |
136,075,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R1988:Kif21b
|
UTSW |
1 |
136,080,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R1990:Kif21b
|
UTSW |
1 |
136,089,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R2014:Kif21b
|
UTSW |
1 |
136,076,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R2045:Kif21b
|
UTSW |
1 |
136,088,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Kif21b
|
UTSW |
1 |
136,080,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R2248:Kif21b
|
UTSW |
1 |
136,100,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R2886:Kif21b
|
UTSW |
1 |
136,075,612 (GRCm39) |
splice site |
probably benign |
|
R2896:Kif21b
|
UTSW |
1 |
136,081,955 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3706:Kif21b
|
UTSW |
1 |
136,087,148 (GRCm39) |
missense |
probably benign |
0.06 |
R3780:Kif21b
|
UTSW |
1 |
136,083,964 (GRCm39) |
missense |
probably damaging |
0.99 |
R3827:Kif21b
|
UTSW |
1 |
136,090,732 (GRCm39) |
critical splice donor site |
probably null |
|
R4227:Kif21b
|
UTSW |
1 |
136,081,831 (GRCm39) |
splice site |
probably null |
|
R4600:Kif21b
|
UTSW |
1 |
136,075,602 (GRCm39) |
missense |
probably benign |
0.39 |
R4608:Kif21b
|
UTSW |
1 |
136,075,924 (GRCm39) |
intron |
probably benign |
|
R4749:Kif21b
|
UTSW |
1 |
136,072,487 (GRCm39) |
nonsense |
probably null |
|
R4841:Kif21b
|
UTSW |
1 |
136,072,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R4842:Kif21b
|
UTSW |
1 |
136,072,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R4933:Kif21b
|
UTSW |
1 |
136,079,063 (GRCm39) |
splice site |
probably null |
|
R4959:Kif21b
|
UTSW |
1 |
136,076,108 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5018:Kif21b
|
UTSW |
1 |
136,099,972 (GRCm39) |
missense |
probably benign |
0.30 |
R5116:Kif21b
|
UTSW |
1 |
136,080,521 (GRCm39) |
missense |
probably damaging |
0.99 |
R5119:Kif21b
|
UTSW |
1 |
136,090,838 (GRCm39) |
missense |
probably benign |
|
R5230:Kif21b
|
UTSW |
1 |
136,099,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R5249:Kif21b
|
UTSW |
1 |
136,096,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R5337:Kif21b
|
UTSW |
1 |
136,098,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R5358:Kif21b
|
UTSW |
1 |
136,100,030 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5466:Kif21b
|
UTSW |
1 |
136,075,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R5557:Kif21b
|
UTSW |
1 |
136,097,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R5727:Kif21b
|
UTSW |
1 |
136,097,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R5865:Kif21b
|
UTSW |
1 |
136,078,875 (GRCm39) |
nonsense |
probably null |
|
R5929:Kif21b
|
UTSW |
1 |
136,078,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R6274:Kif21b
|
UTSW |
1 |
136,077,156 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6349:Kif21b
|
UTSW |
1 |
136,086,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R6648:Kif21b
|
UTSW |
1 |
136,080,135 (GRCm39) |
missense |
probably benign |
0.00 |
R6831:Kif21b
|
UTSW |
1 |
136,072,496 (GRCm39) |
nonsense |
probably null |
|
R7156:Kif21b
|
UTSW |
1 |
136,075,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R7165:Kif21b
|
UTSW |
1 |
136,077,186 (GRCm39) |
missense |
probably damaging |
0.98 |
R7327:Kif21b
|
UTSW |
1 |
136,087,387 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7680:Kif21b
|
UTSW |
1 |
136,075,607 (GRCm39) |
critical splice donor site |
probably null |
|
R7975:Kif21b
|
UTSW |
1 |
136,098,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R8356:Kif21b
|
UTSW |
1 |
136,100,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R8467:Kif21b
|
UTSW |
1 |
136,100,021 (GRCm39) |
missense |
probably damaging |
0.98 |
R9031:Kif21b
|
UTSW |
1 |
136,073,042 (GRCm39) |
missense |
probably damaging |
0.99 |
R9101:Kif21b
|
UTSW |
1 |
136,078,893 (GRCm39) |
missense |
probably damaging |
0.96 |
R9191:Kif21b
|
UTSW |
1 |
136,100,559 (GRCm39) |
nonsense |
probably null |
|
R9261:Kif21b
|
UTSW |
1 |
136,077,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R9280:Kif21b
|
UTSW |
1 |
136,099,445 (GRCm39) |
critical splice donor site |
probably null |
|
R9307:Kif21b
|
UTSW |
1 |
136,101,800 (GRCm39) |
missense |
probably benign |
|
R9562:Kif21b
|
UTSW |
1 |
136,077,090 (GRCm39) |
missense |
probably damaging |
0.99 |
R9563:Kif21b
|
UTSW |
1 |
136,077,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Kif21b
|
UTSW |
1 |
136,077,090 (GRCm39) |
missense |
probably damaging |
0.99 |
R9758:Kif21b
|
UTSW |
1 |
136,080,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R9760:Kif21b
|
UTSW |
1 |
136,076,421 (GRCm39) |
missense |
probably damaging |
1.00 |
RF024:Kif21b
|
UTSW |
1 |
136,086,079 (GRCm39) |
missense |
probably damaging |
1.00 |
X0053:Kif21b
|
UTSW |
1 |
136,077,054 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Kif21b
|
UTSW |
1 |
136,100,683 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Kif21b
|
UTSW |
1 |
136,081,875 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Kif21b
|
UTSW |
1 |
136,076,050 (GRCm39) |
missense |
probably damaging |
1.00 |
|