Incidental Mutation 'R7644:Kif26b'
| ID |
590393 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Kif26b
|
| Ensembl Gene |
ENSMUSG00000026494 |
| Gene Name |
kinesin family member 26B |
| Synonyms |
D230039L06Rik, N-11 kinesin |
| MMRRC Submission |
045723-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R7644 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
178356690-178766765 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 178506839 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Serine
at position 305
(N305S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000124462
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000161017]
|
| AlphaFold |
Q7TNC6 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000161017
AA Change: N305S
PolyPhen 2
Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)
|
| SMART Domains |
Protein: ENSMUSP00000124462
Gene: ENSMUSG00000026494
AA Change: N305S
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
58 |
123 |
N/A |
INTRINSIC |
|
low complexity region
|
144 |
155 |
N/A |
INTRINSIC |
|
low complexity region
|
220 |
228 |
N/A |
INTRINSIC |
|
Blast:KISc
|
365 |
446 |
4e-8 |
BLAST |
|
KISc
|
448 |
809 |
2.48e-42 |
SMART |
|
low complexity region
|
810 |
822 |
N/A |
INTRINSIC |
|
low complexity region
|
849 |
863 |
N/A |
INTRINSIC |
|
low complexity region
|
907 |
913 |
N/A |
INTRINSIC |
|
low complexity region
|
1007 |
1047 |
N/A |
INTRINSIC |
|
low complexity region
|
1099 |
1109 |
N/A |
INTRINSIC |
|
low complexity region
|
1269 |
1288 |
N/A |
INTRINSIC |
|
low complexity region
|
1485 |
1495 |
N/A |
INTRINSIC |
|
low complexity region
|
1741 |
1769 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.9%
|
| Validation Efficiency |
100% (86/86) |
| MGI Phenotype |
PHENOTYPE: Mice homozygous for a knock-out allele exhibit neonatal lethality with impaired kidney development due to loss of cortical nephrogenic zone mesenchyme and failure of ureteric buds to invade and branch into the mesenchyme. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 86 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700001O22Rik |
C |
T |
2: 30,687,966 (GRCm39) |
R209Q |
possibly damaging |
Het |
| Abl2 |
A |
G |
1: 156,443,563 (GRCm39) |
D24G |
probably benign |
Het |
| Adar |
C |
T |
3: 89,652,826 (GRCm39) |
A754V |
probably benign |
Het |
| Adcy8 |
C |
T |
15: 64,571,218 (GRCm39) |
V1172I |
possibly damaging |
Het |
| Adgrl2 |
C |
T |
3: 148,544,789 (GRCm39) |
V769M |
probably damaging |
Het |
| Akna |
T |
A |
4: 63,313,634 (GRCm39) |
Q163L |
possibly damaging |
Het |
| Alox15 |
C |
T |
11: 70,236,368 (GRCm39) |
A511T |
probably null |
Het |
| Ano8 |
C |
T |
8: 71,937,474 (GRCm39) |
G90D |
probably damaging |
Het |
| Aqp5 |
G |
A |
15: 99,492,107 (GRCm39) |
R235H |
probably damaging |
Het |
| B3galt4 |
A |
T |
17: 34,169,419 (GRCm39) |
V273E |
probably damaging |
Het |
| Ccdc125 |
C |
T |
13: 100,814,884 (GRCm39) |
|
probably null |
Het |
| Ccdc90b |
A |
G |
7: 92,216,868 (GRCm39) |
R47G |
possibly damaging |
Het |
| Celsr2 |
G |
T |
3: 108,320,806 (GRCm39) |
L669I |
probably damaging |
Het |
| Clasp1 |
T |
G |
1: 118,440,480 (GRCm39) |
|
probably null |
Het |
| Clec4a2 |
C |
T |
6: 123,101,974 (GRCm39) |
P43L |
probably benign |
Het |
| Cntn1 |
T |
C |
15: 92,207,890 (GRCm39) |
I827T |
probably benign |
Het |
| Col9a1 |
G |
T |
1: 24,224,243 (GRCm39) |
V142F |
unknown |
Het |
| Cplane1 |
T |
A |
15: 8,252,611 (GRCm39) |
D1944E |
probably benign |
Het |
| Cts7 |
G |
T |
13: 61,504,782 (GRCm39) |
Y23* |
probably null |
Het |
| Dcdc2a |
T |
A |
13: 25,291,674 (GRCm39) |
Y220N |
probably damaging |
Het |
| Dennd2b |
A |
T |
7: 109,156,000 (GRCm39) |
L250* |
probably null |
Het |
| Dmxl1 |
T |
G |
18: 50,026,619 (GRCm39) |
V1909G |
probably benign |
Het |
| Ehd2 |
G |
A |
7: 15,691,474 (GRCm39) |
P286L |
possibly damaging |
Het |
| Elf3 |
G |
T |
1: 135,184,244 (GRCm39) |
A208E |
possibly damaging |
Het |
| Eml5 |
A |
G |
12: 98,822,203 (GRCm39) |
I775T |
probably benign |
Het |
| Ephb1 |
T |
C |
9: 101,813,393 (GRCm39) |
T791A |
probably damaging |
Het |
| Fanci |
C |
A |
7: 79,094,219 (GRCm39) |
S1105* |
probably null |
Het |
| Fastkd1 |
T |
A |
2: 69,527,184 (GRCm39) |
|
probably null |
Het |
| Fat4 |
A |
G |
3: 39,064,390 (GRCm39) |
E4782G |
possibly damaging |
Het |
| Fnta |
T |
C |
8: 26,503,516 (GRCm39) |
I90V |
probably damaging |
Het |
| Fosl1 |
C |
T |
19: 5,500,332 (GRCm39) |
R84* |
probably null |
Het |
| Gdf2 |
T |
C |
14: 33,666,847 (GRCm39) |
F190L |
probably benign |
Het |
| Gzmn |
T |
A |
14: 56,404,776 (GRCm39) |
Q88L |
probably damaging |
Het |
| Hat1 |
T |
A |
2: 71,240,525 (GRCm39) |
L73Q |
probably damaging |
Het |
| Hdhd2 |
G |
A |
18: 77,031,871 (GRCm39) |
G109E |
possibly damaging |
Het |
| Il22ra1 |
A |
G |
4: 135,460,346 (GRCm39) |
N34S |
probably damaging |
Het |
| Ino80d |
T |
C |
1: 63,097,930 (GRCm39) |
T760A |
probably benign |
Het |
| Itga7 |
A |
G |
10: 128,789,370 (GRCm39) |
D971G |
probably benign |
Het |
| Kdm6b |
T |
C |
11: 69,291,032 (GRCm39) |
N1574S |
unknown |
Het |
| Kel |
T |
C |
6: 41,667,742 (GRCm39) |
E400G |
probably benign |
Het |
| Kif22 |
G |
A |
7: 126,632,134 (GRCm39) |
T350I |
probably damaging |
Het |
| Klk12 |
A |
C |
7: 43,419,134 (GRCm39) |
Q33P |
probably damaging |
Het |
| Klk1b24 |
G |
A |
7: 43,841,304 (GRCm39) |
|
probably null |
Het |
| Krtap31-1 |
T |
A |
11: 99,799,048 (GRCm39) |
C84S |
possibly damaging |
Het |
| Ky |
T |
A |
9: 102,414,972 (GRCm39) |
S295T |
probably benign |
Het |
| Lpin3 |
T |
A |
2: 160,738,690 (GRCm39) |
M214K |
probably benign |
Het |
| Mak |
T |
A |
13: 41,183,586 (GRCm39) |
N565Y |
probably benign |
Het |
| Mphosph6 |
T |
C |
8: 118,528,623 (GRCm39) |
T7A |
probably benign |
Het |
| Muc6 |
G |
C |
7: 141,217,659 (GRCm39) |
P2338R |
probably damaging |
Het |
| Myh11 |
T |
C |
16: 14,039,688 (GRCm39) |
T814A |
|
Het |
| Nmbr |
T |
C |
10: 14,636,433 (GRCm39) |
L134P |
probably damaging |
Het |
| Nup107 |
C |
T |
10: 117,606,375 (GRCm39) |
V456M |
probably damaging |
Het |
| Or56b1b |
A |
G |
7: 108,164,649 (GRCm39) |
S118P |
possibly damaging |
Het |
| Or8g22 |
C |
A |
9: 38,958,638 (GRCm39) |
D26Y |
probably damaging |
Het |
| Pink1 |
A |
T |
4: 138,044,683 (GRCm39) |
H351Q |
probably damaging |
Het |
| Piwil4 |
A |
T |
9: 14,645,711 (GRCm39) |
|
probably null |
Het |
| Pkd1l1 |
C |
A |
11: 8,825,758 (GRCm39) |
V1498F |
|
Het |
| Polb |
A |
G |
8: 23,130,443 (GRCm39) |
I161T |
probably benign |
Het |
| Polg |
A |
T |
7: 79,101,416 (GRCm39) |
L1097Q |
probably damaging |
Het |
| Prelp |
T |
C |
1: 133,842,356 (GRCm39) |
N263S |
probably benign |
Het |
| Pten |
T |
C |
19: 32,789,234 (GRCm39) |
C211R |
probably damaging |
Het |
| Ptprc |
G |
A |
1: 137,995,645 (GRCm39) |
A1012V |
probably benign |
Het |
| Ptprr |
T |
A |
10: 115,884,133 (GRCm39) |
H63Q |
probably benign |
Het |
| Rapsn |
A |
T |
2: 90,872,299 (GRCm39) |
H211L |
possibly damaging |
Het |
| Reln |
T |
C |
5: 22,183,929 (GRCm39) |
N1690S |
probably benign |
Het |
| Rpap2 |
A |
G |
5: 107,768,167 (GRCm39) |
E335G |
probably benign |
Het |
| Rspry1 |
T |
A |
8: 95,385,396 (GRCm39) |
S567T |
probably benign |
Het |
| Sf3b1 |
G |
A |
1: 55,036,302 (GRCm39) |
R924* |
probably null |
Het |
| Sftpb |
G |
A |
6: 72,286,818 (GRCm39) |
E241K |
probably benign |
Het |
| Smarca4 |
G |
T |
9: 21,566,950 (GRCm39) |
A677S |
probably benign |
Het |
| Srrm2 |
G |
A |
17: 24,038,294 (GRCm39) |
R1646Q |
unknown |
Het |
| Tex15 |
T |
A |
8: 34,064,445 (GRCm39) |
C1292S |
probably benign |
Het |
| Tmem140 |
A |
G |
6: 34,849,708 (GRCm39) |
I75V |
probably benign |
Het |
| Trhr2 |
T |
A |
8: 123,084,061 (GRCm39) |
Q313L |
possibly damaging |
Het |
| Trim35 |
A |
G |
14: 66,534,546 (GRCm39) |
T10A |
unknown |
Het |
| Ttn |
T |
C |
2: 76,750,124 (GRCm39) |
I3642V |
probably benign |
Het |
| Ugt1a2 |
T |
C |
1: 88,128,507 (GRCm39) |
L50P |
probably damaging |
Het |
| Unc13a |
C |
A |
8: 72,087,182 (GRCm39) |
V1522L |
probably benign |
Het |
| Usp33 |
A |
G |
3: 152,063,589 (GRCm39) |
D21G |
possibly damaging |
Het |
| Vmn1r90 |
G |
A |
7: 14,295,616 (GRCm39) |
Q161* |
probably null |
Het |
| Vmn2r117 |
A |
T |
17: 23,696,265 (GRCm39) |
W381R |
probably damaging |
Het |
| Vmn2r16 |
G |
C |
5: 109,487,837 (GRCm39) |
A237P |
probably damaging |
Het |
| Vmn2r74 |
A |
G |
7: 85,606,746 (GRCm39) |
V200A |
probably benign |
Het |
| Yjefn3 |
C |
T |
8: 70,340,544 (GRCm39) |
V227M |
probably damaging |
Het |
| Zfp652 |
T |
C |
11: 95,640,914 (GRCm39) |
F280L |
probably damaging |
Het |
| Zfp748 |
G |
A |
13: 67,689,568 (GRCm39) |
T564I |
probably damaging |
Het |
|
| Other mutations in Kif26b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00337:Kif26b
|
APN |
1 |
178,743,213 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00425:Kif26b
|
APN |
1 |
178,743,866 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL00952:Kif26b
|
APN |
1 |
178,759,770 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01100:Kif26b
|
APN |
1 |
178,744,809 (GRCm39) |
missense |
probably benign |
|
|
IGL01347:Kif26b
|
APN |
1 |
178,698,240 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01543:Kif26b
|
APN |
1 |
178,506,526 (GRCm39) |
missense |
probably benign |
0.41 |
|
IGL01938:Kif26b
|
APN |
1 |
178,743,603 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02100:Kif26b
|
APN |
1 |
178,743,512 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02262:Kif26b
|
APN |
1 |
178,743,633 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL02576:Kif26b
|
APN |
1 |
178,743,912 (GRCm39) |
missense |
probably benign |
|
|
IGL02673:Kif26b
|
APN |
1 |
178,649,170 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03078:Kif26b
|
APN |
1 |
178,698,291 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03155:Kif26b
|
APN |
1 |
178,701,693 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03157:Kif26b
|
APN |
1 |
178,743,930 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03162:Kif26b
|
APN |
1 |
178,744,497 (GRCm39) |
missense |
probably benign |
|
|
IGL03220:Kif26b
|
APN |
1 |
178,692,434 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03299:Kif26b
|
APN |
1 |
178,649,125 (GRCm39) |
missense |
probably benign |
0.09 |
|
IGL03368:Kif26b
|
APN |
1 |
178,743,773 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03370:Kif26b
|
APN |
1 |
178,742,946 (GRCm39) |
missense |
probably benign |
0.39 |
|
PIT4449001:Kif26b
|
UTSW |
1 |
178,745,651 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0142:Kif26b
|
UTSW |
1 |
178,742,954 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0621:Kif26b
|
UTSW |
1 |
178,743,218 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0987:Kif26b
|
UTSW |
1 |
178,649,185 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1107:Kif26b
|
UTSW |
1 |
178,745,238 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1367:Kif26b
|
UTSW |
1 |
178,744,028 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1386:Kif26b
|
UTSW |
1 |
178,743,209 (GRCm39) |
missense |
probably benign |
|
|
R1619:Kif26b
|
UTSW |
1 |
178,744,043 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1664:Kif26b
|
UTSW |
1 |
178,759,704 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2240:Kif26b
|
UTSW |
1 |
178,543,488 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2264:Kif26b
|
UTSW |
1 |
178,756,407 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R2443:Kif26b
|
UTSW |
1 |
178,742,579 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3023:Kif26b
|
UTSW |
1 |
178,692,433 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3744:Kif26b
|
UTSW |
1 |
178,506,595 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3831:Kif26b
|
UTSW |
1 |
178,744,181 (GRCm39) |
frame shift |
probably null |
|
|
R3832:Kif26b
|
UTSW |
1 |
178,744,181 (GRCm39) |
frame shift |
probably null |
|
|
R3833:Kif26b
|
UTSW |
1 |
178,744,181 (GRCm39) |
frame shift |
probably null |
|
|
R3843:Kif26b
|
UTSW |
1 |
178,755,742 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4108:Kif26b
|
UTSW |
1 |
178,744,530 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R4181:Kif26b
|
UTSW |
1 |
178,742,991 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4551:Kif26b
|
UTSW |
1 |
178,711,600 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4552:Kif26b
|
UTSW |
1 |
178,711,600 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4597:Kif26b
|
UTSW |
1 |
178,744,358 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4599:Kif26b
|
UTSW |
1 |
178,358,024 (GRCm39) |
missense |
unknown |
|
|
R4610:Kif26b
|
UTSW |
1 |
178,506,920 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4746:Kif26b
|
UTSW |
1 |
178,701,546 (GRCm39) |
nonsense |
probably null |
|
|
R4873:Kif26b
|
UTSW |
1 |
178,742,892 (GRCm39) |
missense |
probably benign |
0.38 |
|
R4875:Kif26b
|
UTSW |
1 |
178,742,892 (GRCm39) |
missense |
probably benign |
0.38 |
|
R5015:Kif26b
|
UTSW |
1 |
178,755,895 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5060:Kif26b
|
UTSW |
1 |
178,358,195 (GRCm39) |
missense |
unknown |
|
|
R5301:Kif26b
|
UTSW |
1 |
178,358,233 (GRCm39) |
missense |
unknown |
|
|
R5368:Kif26b
|
UTSW |
1 |
178,743,449 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5387:Kif26b
|
UTSW |
1 |
178,742,441 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5589:Kif26b
|
UTSW |
1 |
178,743,864 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6150:Kif26b
|
UTSW |
1 |
178,743,111 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6259:Kif26b
|
UTSW |
1 |
178,744,970 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6355:Kif26b
|
UTSW |
1 |
178,743,743 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6408:Kif26b
|
UTSW |
1 |
178,745,133 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6488:Kif26b
|
UTSW |
1 |
178,357,138 (GRCm39) |
missense |
unknown |
|
|
R6546:Kif26b
|
UTSW |
1 |
178,755,871 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6702:Kif26b
|
UTSW |
1 |
178,744,852 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R6886:Kif26b
|
UTSW |
1 |
178,701,703 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6953:Kif26b
|
UTSW |
1 |
178,701,637 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R7262:Kif26b
|
UTSW |
1 |
178,745,219 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R7291:Kif26b
|
UTSW |
1 |
178,506,611 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R7346:Kif26b
|
UTSW |
1 |
178,358,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7383:Kif26b
|
UTSW |
1 |
178,358,275 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7448:Kif26b
|
UTSW |
1 |
178,742,339 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7506:Kif26b
|
UTSW |
1 |
178,357,064 (GRCm39) |
start gained |
probably benign |
|
|
R7562:Kif26b
|
UTSW |
1 |
178,742,541 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7583:Kif26b
|
UTSW |
1 |
178,358,010 (GRCm39) |
nonsense |
probably null |
|
|
R7585:Kif26b
|
UTSW |
1 |
178,744,061 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7759:Kif26b
|
UTSW |
1 |
178,506,509 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7775:Kif26b
|
UTSW |
1 |
178,692,441 (GRCm39) |
missense |
probably benign |
0.15 |
|
R7954:Kif26b
|
UTSW |
1 |
178,696,944 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7960:Kif26b
|
UTSW |
1 |
178,506,484 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8012:Kif26b
|
UTSW |
1 |
178,743,815 (GRCm39) |
missense |
probably benign |
0.20 |
|
R8152:Kif26b
|
UTSW |
1 |
178,506,794 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R8320:Kif26b
|
UTSW |
1 |
178,711,641 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8360:Kif26b
|
UTSW |
1 |
178,743,938 (GRCm39) |
missense |
probably benign |
0.18 |
|
R8428:Kif26b
|
UTSW |
1 |
178,744,923 (GRCm39) |
missense |
probably benign |
0.09 |
|
R8670:Kif26b
|
UTSW |
1 |
178,741,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8737:Kif26b
|
UTSW |
1 |
178,692,430 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8788:Kif26b
|
UTSW |
1 |
178,357,090 (GRCm39) |
start gained |
probably benign |
|
|
R8854:Kif26b
|
UTSW |
1 |
178,743,948 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R8870:Kif26b
|
UTSW |
1 |
178,692,594 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8963:Kif26b
|
UTSW |
1 |
178,743,714 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9232:Kif26b
|
UTSW |
1 |
178,742,511 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9297:Kif26b
|
UTSW |
1 |
178,543,374 (GRCm39) |
nonsense |
probably null |
|
|
R9338:Kif26b
|
UTSW |
1 |
178,744,058 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9572:Kif26b
|
UTSW |
1 |
178,745,042 (GRCm39) |
missense |
probably benign |
|
|
R9580:Kif26b
|
UTSW |
1 |
178,506,643 (GRCm39) |
nonsense |
probably null |
|
|
R9694:Kif26b
|
UTSW |
1 |
178,743,815 (GRCm39) |
missense |
probably benign |
0.20 |
|
X0021:Kif26b
|
UTSW |
1 |
178,755,724 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0024:Kif26b
|
UTSW |
1 |
178,506,647 (GRCm39) |
missense |
probably benign |
0.14 |
|
X0025:Kif26b
|
UTSW |
1 |
178,742,948 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
X0025:Kif26b
|
UTSW |
1 |
178,742,831 (GRCm39) |
nonsense |
probably null |
|
|
Z1177:Kif26b
|
UTSW |
1 |
178,742,970 (GRCm39) |
nonsense |
probably null |
|
|
Z1177:Kif26b
|
UTSW |
1 |
178,649,115 (GRCm39) |
nonsense |
probably null |
|
|
Z1177:Kif26b
|
UTSW |
1 |
178,649,113 (GRCm39) |
missense |
probably benign |
0.11 |
|
| Predicted Primers |
PCR Primer
(F):5'- GATCTCCAGCATTCCCACACTG -3'
(R):5'- GCCTCGACTCTGACTTGTAG -3'
Sequencing Primer
(F):5'- ACATGGGTGGGCTCCAG -3'
(R):5'- CGACTCTGACTTGTAGAGGGAGATC -3'
|
| Posted On |
2019-10-24 |
Incidental Mutation