Incidental Mutation 'R1664:Kif26b'
ID |
186982 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Kif26b
|
Ensembl Gene |
ENSMUSG00000026494 |
Gene Name |
kinesin family member 26B |
Synonyms |
D230039L06Rik, N-11 kinesin |
MMRRC Submission |
039700-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R1664 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
178356690-178766765 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 178759704 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Methionine
at position 2084
(V2084M)
|
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: V1637M
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000124608 Gene: ENSMUSG00000026494 AA Change: V1637M
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: V2084M
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000124462 Gene: ENSMUSG00000026494 AA Change: V2084M
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: 99.1%
- 3x: 98.4%
- 10x: 96.5%
- 20x: 93.0%
|
Validation Efficiency |
|
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: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930596D02Rik |
T |
A |
14: 35,533,772 (GRCm39) |
T45S |
probably benign |
Het |
Ackr1 |
A |
G |
1: 173,160,433 (GRCm39) |
F29L |
probably benign |
Het |
Adgrf2 |
T |
A |
17: 43,025,305 (GRCm39) |
S60C |
possibly damaging |
Het |
Alpk2 |
A |
G |
18: 65,482,944 (GRCm39) |
C355R |
probably damaging |
Het |
Ankmy1 |
A |
C |
1: 92,812,913 (GRCm39) |
D465E |
probably benign |
Het |
Ankrd27 |
T |
A |
7: 35,306,551 (GRCm39) |
D310E |
probably damaging |
Het |
Ap3d1 |
G |
A |
10: 80,553,571 (GRCm39) |
Q559* |
probably null |
Het |
C4b |
T |
C |
17: 34,951,952 (GRCm39) |
T1298A |
probably damaging |
Het |
Casr |
T |
A |
16: 36,330,327 (GRCm39) |
K336* |
probably null |
Het |
Ccdc116 |
A |
T |
16: 16,960,492 (GRCm39) |
D108E |
probably benign |
Het |
Ccdc168 |
T |
A |
1: 44,098,387 (GRCm39) |
I904F |
possibly damaging |
Het |
Ccr7 |
A |
T |
11: 99,036,517 (GRCm39) |
I135N |
possibly damaging |
Het |
Cd96 |
A |
G |
16: 45,938,364 (GRCm39) |
Y34H |
possibly damaging |
Het |
Cdan1 |
T |
A |
2: 120,550,987 (GRCm39) |
D1135V |
probably damaging |
Het |
Cecr2 |
C |
A |
6: 120,738,987 (GRCm39) |
T1210K |
probably damaging |
Het |
Cep152 |
C |
A |
2: 125,408,174 (GRCm39) |
A1390S |
probably benign |
Het |
Chd9 |
T |
G |
8: 91,749,418 (GRCm39) |
|
probably null |
Het |
Cntnap5c |
G |
T |
17: 58,600,985 (GRCm39) |
W776L |
probably benign |
Het |
Col24a1 |
G |
A |
3: 145,095,355 (GRCm39) |
|
probably null |
Het |
Cpa2 |
G |
T |
6: 30,554,314 (GRCm39) |
M311I |
probably damaging |
Het |
Cpz |
A |
G |
5: 35,664,087 (GRCm39) |
F483L |
probably damaging |
Het |
Ddx19a |
A |
C |
8: 111,716,130 (GRCm39) |
V90G |
probably damaging |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fbxw7 |
A |
G |
3: 84,876,478 (GRCm39) |
D213G |
possibly damaging |
Het |
Fgd2 |
T |
C |
17: 29,588,273 (GRCm39) |
F362L |
probably damaging |
Het |
Fryl |
A |
G |
5: 73,216,778 (GRCm39) |
Y2171H |
probably damaging |
Het |
Gba2 |
T |
C |
4: 43,578,080 (GRCm39) |
R90G |
probably benign |
Het |
Gm10073 |
T |
C |
8: 107,299,864 (GRCm39) |
E40G |
probably damaging |
Het |
Grhl3 |
T |
C |
4: 135,279,861 (GRCm39) |
I398V |
probably benign |
Het |
Grip2 |
T |
A |
6: 91,742,233 (GRCm39) |
H899L |
probably damaging |
Het |
Grk2 |
T |
C |
19: 4,337,268 (GRCm39) |
K644E |
possibly damaging |
Het |
Iars1 |
A |
T |
13: 49,865,251 (GRCm39) |
T576S |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lrrc69 |
G |
A |
4: 14,775,079 (GRCm39) |
T63M |
probably damaging |
Het |
Lrrn4 |
A |
T |
2: 132,711,886 (GRCm39) |
C646S |
probably damaging |
Het |
Mtf2 |
C |
T |
5: 108,252,342 (GRCm39) |
T457M |
probably damaging |
Het |
Ncln |
A |
T |
10: 81,323,555 (GRCm39) |
C531S |
probably benign |
Het |
Ntn4 |
C |
T |
10: 93,543,215 (GRCm39) |
R314W |
probably damaging |
Het |
Or14j8 |
T |
C |
17: 38,263,784 (GRCm39) |
I44V |
probably benign |
Het |
Or5v1 |
C |
T |
17: 37,810,316 (GRCm39) |
T258M |
possibly damaging |
Het |
Or8c11 |
A |
T |
9: 38,289,548 (GRCm39) |
M124L |
possibly damaging |
Het |
Otogl |
A |
G |
10: 107,642,437 (GRCm39) |
V1331A |
probably benign |
Het |
Palb2 |
A |
G |
7: 121,723,615 (GRCm39) |
|
probably benign |
Het |
Pcdh20 |
T |
C |
14: 88,705,758 (GRCm39) |
E514G |
possibly damaging |
Het |
Pclaf |
A |
G |
9: 65,797,730 (GRCm39) |
N7S |
probably benign |
Het |
Pdrg1 |
C |
T |
2: 152,857,248 (GRCm39) |
|
probably benign |
Het |
Phf8-ps |
T |
A |
17: 33,285,492 (GRCm39) |
I437F |
probably damaging |
Het |
Pik3r6 |
T |
A |
11: 68,426,932 (GRCm39) |
D464E |
probably benign |
Het |
Pkp3 |
A |
G |
7: 140,667,560 (GRCm39) |
N454D |
probably damaging |
Het |
Plekha7 |
C |
A |
7: 115,734,269 (GRCm39) |
|
probably null |
Het |
Ppip5k1 |
A |
G |
2: 121,167,663 (GRCm39) |
V784A |
probably benign |
Het |
Ppp1r36 |
T |
A |
12: 76,483,028 (GRCm39) |
D205E |
possibly damaging |
Het |
Prss35 |
A |
T |
9: 86,637,700 (GRCm39) |
T157S |
probably benign |
Het |
Ptprn2 |
T |
C |
12: 117,125,329 (GRCm39) |
L621P |
probably damaging |
Het |
Rasgrp3 |
A |
G |
17: 75,831,172 (GRCm39) |
K524R |
probably damaging |
Het |
Rasgrp4 |
T |
A |
7: 28,839,688 (GRCm39) |
H133Q |
probably benign |
Het |
Reln |
A |
T |
5: 22,134,084 (GRCm39) |
Y2615N |
probably damaging |
Het |
Rpf1 |
T |
A |
3: 146,217,903 (GRCm39) |
T204S |
probably benign |
Het |
Scgb2b3 |
T |
A |
7: 31,058,464 (GRCm39) |
*113L |
probably null |
Het |
Scn5a |
A |
C |
9: 119,350,243 (GRCm39) |
L877R |
possibly damaging |
Het |
Sh3pxd2a |
A |
T |
19: 47,256,821 (GRCm39) |
D632E |
probably benign |
Het |
Slc39a10 |
T |
C |
1: 46,865,269 (GRCm39) |
H522R |
probably damaging |
Het |
Spink2 |
A |
T |
5: 77,354,855 (GRCm39) |
C19S |
probably damaging |
Het |
Spsb4 |
A |
G |
9: 96,878,266 (GRCm39) |
L19P |
possibly damaging |
Het |
St7l |
T |
C |
3: 104,778,214 (GRCm39) |
V117A |
probably damaging |
Het |
Stac2 |
C |
T |
11: 97,933,420 (GRCm39) |
S174N |
probably damaging |
Het |
Sult4a1 |
A |
G |
15: 83,970,818 (GRCm39) |
Y196H |
probably benign |
Het |
Tex2 |
C |
T |
11: 106,458,608 (GRCm39) |
|
probably benign |
Het |
Tprg1l |
A |
T |
4: 154,243,862 (GRCm39) |
V98D |
possibly damaging |
Het |
Ttn |
G |
A |
2: 76,548,369 (GRCm39) |
H31978Y |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,658,853 (GRCm39) |
|
probably benign |
Het |
Tyk2 |
C |
A |
9: 21,031,649 (GRCm39) |
R447L |
probably damaging |
Het |
Ucn3 |
T |
C |
13: 3,991,634 (GRCm39) |
Y6C |
possibly damaging |
Het |
Urb1 |
A |
T |
16: 90,584,970 (GRCm39) |
|
probably null |
Het |
Vmn2r94 |
G |
C |
17: 18,464,406 (GRCm39) |
A628G |
probably damaging |
Het |
Wdr95 |
C |
A |
5: 149,518,752 (GRCm39) |
T389K |
probably damaging |
Het |
Wrn |
A |
T |
8: 33,770,794 (GRCm39) |
|
probably null |
Het |
Xab2 |
T |
A |
8: 3,669,068 (GRCm39) |
|
probably null |
Het |
Zfp458 |
A |
T |
13: 67,406,144 (GRCm39) |
N95K |
possibly damaging |
Het |
Zfp672 |
T |
C |
11: 58,208,138 (GRCm39) |
H61R |
probably damaging |
Het |
Zfp942 |
C |
T |
17: 22,147,420 (GRCm39) |
G403E |
possibly 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 |
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 |
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'- ACAACTCAGTTGCCCTTAGCCCAG -3'
(R):5'- AGGAAACATCGCCTTTCGCTCCAC -3'
Sequencing Primer
(F):5'- CCTTAGCCCAGAGGAGGTG -3'
(R):5'- CACGCTCACTCCAGACTTG -3'
|
Posted On |
2014-05-09 |