Incidental Mutation 'R8870:Kif26b'
ID |
676176 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Kif26b
|
Ensembl Gene |
ENSMUSG00000026494 |
Gene Name |
kinesin family member 26B |
Synonyms |
D230039L06Rik, N-11 kinesin |
MMRRC Submission |
068684-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R8870 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
178356690-178766765 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 178692594 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Phenylalanine
at position 512
(V512F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000124462
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000160789]
[ENSMUST00000161017]
|
AlphaFold |
Q7TNC6 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000160789
AA Change: V65F
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000124608 Gene: ENSMUSG00000026494 AA Change: V65F
Domain | Start | End | E-Value | Type |
KISc
|
1 |
362 |
2.48e-42 |
SMART |
low complexity region
|
363 |
375 |
N/A |
INTRINSIC |
low complexity region
|
402 |
416 |
N/A |
INTRINSIC |
low complexity region
|
460 |
466 |
N/A |
INTRINSIC |
low complexity region
|
560 |
600 |
N/A |
INTRINSIC |
low complexity region
|
652 |
662 |
N/A |
INTRINSIC |
low complexity region
|
822 |
841 |
N/A |
INTRINSIC |
low complexity region
|
1038 |
1048 |
N/A |
INTRINSIC |
low complexity region
|
1294 |
1322 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000161017
AA Change: V512F
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000124462 Gene: ENSMUSG00000026494 AA Change: V512F
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: 98.8%
|
Validation Efficiency |
100% (76/76) |
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: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
T |
13: 77,471,840 (GRCm39) |
N1082Y |
possibly damaging |
Het |
4930444P10Rik |
G |
A |
1: 16,136,451 (GRCm39) |
Q122* |
probably null |
Het |
Afg2a |
A |
G |
3: 37,502,661 (GRCm39) |
N607D |
probably benign |
Het |
Ak8 |
C |
T |
2: 28,625,602 (GRCm39) |
T215M |
probably benign |
Het |
Ano3 |
T |
A |
2: 110,614,074 (GRCm39) |
I210F |
probably benign |
Het |
Atg9b |
A |
G |
5: 24,592,032 (GRCm39) |
F656L |
probably damaging |
Het |
Bscl2 |
T |
C |
19: 8,824,793 (GRCm39) |
M292T |
probably benign |
Het |
Cachd1 |
G |
T |
4: 100,754,978 (GRCm39) |
C143F |
probably damaging |
Het |
Calcoco2 |
GGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCC |
GGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCC |
11: 95,990,808 (GRCm39) |
|
probably benign |
Het |
Ccnb1ip1 |
C |
T |
14: 51,029,450 (GRCm39) |
G204E |
probably benign |
Het |
Ccr1 |
T |
A |
9: 123,764,022 (GRCm39) |
L169F |
probably benign |
Het |
Cdc42bpg |
A |
G |
19: 6,364,550 (GRCm39) |
N593D |
possibly damaging |
Het |
Cdh20 |
T |
C |
1: 104,873,048 (GRCm39) |
S265P |
probably damaging |
Het |
Cenpk |
A |
G |
13: 104,367,365 (GRCm39) |
E67G |
probably damaging |
Het |
Cep76 |
A |
T |
18: 67,773,190 (GRCm39) |
I36K |
probably benign |
Het |
Clock |
A |
T |
5: 76,383,632 (GRCm39) |
I507N |
probably benign |
Het |
Cpne1 |
T |
C |
2: 155,920,873 (GRCm39) |
T110A |
probably benign |
Het |
Crybg2 |
A |
T |
4: 133,818,525 (GRCm39) |
E1427V |
possibly damaging |
Het |
Ctu1 |
A |
C |
7: 43,324,746 (GRCm39) |
K62Q |
probably damaging |
Het |
Dnai4 |
C |
T |
4: 102,944,529 (GRCm39) |
|
probably null |
Het |
Drd5 |
C |
A |
5: 38,477,747 (GRCm39) |
Q247K |
possibly damaging |
Het |
Ect2l |
A |
T |
10: 18,014,608 (GRCm39) |
L808* |
probably null |
Het |
Efcab3 |
A |
G |
11: 104,791,500 (GRCm39) |
T2905A |
probably benign |
Het |
Ficd |
A |
T |
5: 113,876,248 (GRCm39) |
D141V |
probably damaging |
Het |
Fnbp1 |
A |
G |
2: 30,938,222 (GRCm39) |
Y148H |
|
Het |
Gm49368 |
A |
G |
7: 127,700,685 (GRCm39) |
K485R |
probably benign |
Het |
Gpr75 |
C |
A |
11: 30,841,860 (GRCm39) |
A255D |
probably benign |
Het |
Hcrtr2 |
G |
T |
9: 76,153,666 (GRCm39) |
A242D |
probably damaging |
Het |
Iapp |
G |
T |
6: 142,244,602 (GRCm39) |
V10F |
probably benign |
Het |
Ikzf2 |
A |
G |
1: 69,722,417 (GRCm39) |
S31P |
possibly damaging |
Het |
Il18rap |
G |
A |
1: 40,564,280 (GRCm39) |
|
probably benign |
Het |
Irak2 |
A |
T |
6: 113,663,902 (GRCm39) |
N423Y |
probably damaging |
Het |
Itpkb |
A |
G |
1: 180,159,744 (GRCm39) |
|
probably benign |
Het |
Itpr1 |
A |
G |
6: 108,365,172 (GRCm39) |
I874M |
probably damaging |
Het |
Lhx6 |
G |
A |
2: 35,995,232 (GRCm39) |
|
probably benign |
Het |
Lrfn1 |
A |
G |
7: 28,158,918 (GRCm39) |
E279G |
possibly damaging |
Het |
Masp1 |
A |
C |
16: 23,314,882 (GRCm39) |
D126E |
probably damaging |
Het |
Mef2a |
T |
C |
7: 66,890,176 (GRCm39) |
I299V |
probably benign |
Het |
Midn |
A |
G |
10: 79,985,939 (GRCm39) |
S10G |
probably damaging |
Het |
Mrps12 |
A |
T |
7: 28,439,361 (GRCm39) |
L118Q |
probably damaging |
Het |
Mxi1 |
G |
A |
19: 53,360,126 (GRCm39) |
G283S |
probably damaging |
Het |
Mzf1 |
A |
G |
7: 12,786,836 (GRCm39) |
V78A |
probably benign |
Het |
Ncoa6 |
A |
G |
2: 155,263,078 (GRCm39) |
V452A |
probably damaging |
Het |
Neb |
A |
G |
2: 52,051,481 (GRCm39) |
Y6600H |
probably damaging |
Het |
Nlgn2 |
A |
G |
11: 69,716,297 (GRCm39) |
L748P |
possibly damaging |
Het |
Nnmt |
A |
T |
9: 48,514,801 (GRCm39) |
L72H |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 90,171,560 (GRCm39) |
T964A |
probably benign |
Het |
Or12k7 |
A |
G |
2: 36,958,982 (GRCm39) |
I222V |
probably benign |
Het |
Or1e35 |
T |
G |
11: 73,797,725 (GRCm39) |
M198L |
probably benign |
Het |
Or2y16 |
T |
A |
11: 49,335,350 (GRCm39) |
V224E |
probably damaging |
Het |
Or4k35 |
T |
A |
2: 111,100,464 (GRCm39) |
I83F |
possibly damaging |
Het |
Or5h27 |
G |
A |
16: 59,006,130 (GRCm39) |
P239S |
unknown |
Het |
Or8c11 |
A |
G |
9: 38,289,720 (GRCm39) |
N175S |
probably benign |
Het |
Or8g33 |
A |
G |
9: 39,337,548 (GRCm39) |
V273A |
probably damaging |
Het |
Osbpl11 |
A |
G |
16: 33,034,850 (GRCm39) |
N280D |
probably benign |
Het |
Peg10 |
A |
T |
6: 4,754,825 (GRCm39) |
Y202F |
probably damaging |
Het |
Pick1 |
A |
G |
15: 79,140,107 (GRCm39) |
R469G |
unknown |
Het |
Rev3l |
A |
G |
10: 39,738,786 (GRCm39) |
I2847V |
probably damaging |
Het |
Rmc1 |
A |
G |
18: 12,321,618 (GRCm39) |
E473G |
probably benign |
Het |
Rnaseh2b |
T |
A |
14: 62,569,617 (GRCm39) |
L18Q |
probably damaging |
Het |
Rpl19 |
A |
G |
11: 97,920,615 (GRCm39) |
Y122C |
probably benign |
Het |
Selp |
A |
G |
1: 163,964,787 (GRCm39) |
Y483C |
probably damaging |
Het |
Setd2 |
T |
A |
9: 110,423,321 (GRCm39) |
F347L |
|
Het |
Snx14 |
A |
G |
9: 88,295,541 (GRCm39) |
I208T |
probably benign |
Het |
Spag16 |
T |
A |
1: 70,036,017 (GRCm39) |
F348L |
probably benign |
Het |
Spata22 |
A |
T |
11: 73,231,091 (GRCm39) |
N115I |
probably damaging |
Het |
Spata31 |
T |
C |
13: 65,068,818 (GRCm39) |
V322A |
probably benign |
Het |
Stc1 |
A |
T |
14: 69,275,825 (GRCm39) |
H206L |
probably benign |
Het |
Tas2r129 |
A |
G |
6: 132,928,522 (GRCm39) |
D153G |
probably damaging |
Het |
Tmem196 |
T |
A |
12: 119,982,268 (GRCm39) |
N167K |
possibly damaging |
Het |
Tmpo |
T |
C |
10: 90,987,581 (GRCm39) |
T356A |
probably damaging |
Het |
Tnks |
A |
G |
8: 35,314,433 (GRCm39) |
|
probably null |
Het |
Ttbk1 |
A |
C |
17: 46,781,661 (GRCm39) |
L364R |
probably damaging |
Het |
Vmn1r176 |
A |
T |
7: 23,534,480 (GRCm39) |
N224K |
probably damaging |
Het |
Vmn1r36 |
T |
A |
6: 66,693,720 (GRCm39) |
M52L |
probably benign |
Het |
Vmn2r93 |
A |
T |
17: 18,525,320 (GRCm39) |
H326L |
possibly damaging |
Het |
Wrn |
A |
T |
8: 33,819,220 (GRCm39) |
M244K |
probably benign |
Het |
Zcchc24 |
C |
T |
14: 25,757,578 (GRCm39) |
A102T |
probably benign |
Het |
Zfp1010 |
T |
A |
2: 176,957,312 (GRCm39) |
Q62L |
probably benign |
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 |
R7644:Kif26b
|
UTSW |
1 |
178,506,839 (GRCm39) |
missense |
probably benign |
0.04 |
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 |
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'- GTAGCCCGCTCTTTAATCCG -3'
(R):5'- ACTTGGAAGAGCTGGGGTATTC -3'
Sequencing Primer
(F):5'- CAGGTGAAAGTCATGCTGCGTATC -3'
(R):5'- ATTCCGTGGAGCTCAGAATGACTTC -3'
|
Posted On |
2021-07-15 |