Incidental Mutation 'R1619:Kif26b'
| ID |
174485 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Kif26b
|
| Ensembl Gene |
ENSMUSG00000026494 |
| Gene Name |
kinesin family member 26B |
| Synonyms |
D230039L06Rik, N-11 kinesin |
| MMRRC Submission |
039656-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R1619 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
1 |
| Chromosomal Location |
178356690-178766765 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 178744043 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Glycine
at position 1380
(S1380G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000124462
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000160789]
[ENSMUST00000161017]
|
| AlphaFold |
Q7TNC6 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000160789
AA Change: S933G
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000124608
Gene: ENSMUSG00000026494
AA Change: S933G
| 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 benign
Transcript: ENSMUST00000161017
AA Change: S1380G
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000124462
Gene: ENSMUSG00000026494
AA Change: S1380G
| 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 |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000162545
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.2%
- 10x: 95.8%
- 20x: 91.0%
|
| 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: 85 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca7 |
A |
T |
10: 79,844,889 (GRCm39) |
H1537L |
probably damaging |
Het |
| Actg2 |
T |
A |
6: 83,500,169 (GRCm39) |
N116I |
probably damaging |
Het |
| Actn1 |
G |
A |
12: 80,219,796 (GRCm39) |
H692Y |
probably damaging |
Het |
| Adamts6 |
C |
T |
13: 104,449,285 (GRCm39) |
P36S |
probably benign |
Het |
| Agr3 |
G |
A |
12: 35,997,858 (GRCm39) |
|
probably null |
Het |
| Ank3 |
T |
C |
10: 69,715,805 (GRCm39) |
V500A |
probably damaging |
Het |
| BC051019 |
T |
A |
7: 109,317,269 (GRCm39) |
D141V |
probably damaging |
Het |
| Bco1 |
T |
C |
8: 117,835,454 (GRCm39) |
F135S |
probably damaging |
Het |
| Cacna1c |
C |
T |
6: 118,589,586 (GRCm39) |
R1446H |
probably damaging |
Het |
| Ccdc42 |
A |
G |
11: 68,485,115 (GRCm39) |
K210E |
probably damaging |
Het |
| Cckar |
A |
T |
5: 53,857,409 (GRCm39) |
W263R |
probably damaging |
Het |
| Cela2a |
A |
G |
4: 141,553,252 (GRCm39) |
|
probably null |
Het |
| Cep97 |
A |
T |
16: 55,748,159 (GRCm39) |
N90K |
probably damaging |
Het |
| Ces2g |
A |
T |
8: 105,693,984 (GRCm39) |
Q440L |
probably damaging |
Het |
| Chchd6 |
G |
T |
6: 89,396,736 (GRCm39) |
T225K |
possibly damaging |
Het |
| Chd1l |
C |
T |
3: 97,490,047 (GRCm39) |
E503K |
probably benign |
Het |
| Chrna5 |
A |
G |
9: 54,911,649 (GRCm39) |
T46A |
probably benign |
Het |
| Col16a1 |
G |
A |
4: 129,992,733 (GRCm39) |
G1531S |
probably damaging |
Het |
| Col19a1 |
A |
T |
1: 24,573,172 (GRCm39) |
V200E |
unknown |
Het |
| Csf2rb |
A |
G |
15: 78,219,411 (GRCm39) |
D2G |
probably damaging |
Het |
| Csmd3 |
G |
A |
15: 47,813,346 (GRCm39) |
S1062L |
probably damaging |
Het |
| Cul5 |
G |
T |
9: 53,569,893 (GRCm39) |
Q113K |
probably benign |
Het |
| Dmwd |
TAGCCTGGGAA |
TAGCCTGGGAAGCCTGGGAA |
7: 18,814,959 (GRCm39) |
|
probably benign |
Het |
| Dse |
T |
C |
10: 34,029,230 (GRCm39) |
D620G |
probably damaging |
Het |
| Dsg1c |
A |
G |
18: 20,397,899 (GRCm39) |
N33S |
probably benign |
Het |
| Epc2 |
G |
A |
2: 49,439,990 (GRCm39) |
V803I |
probably damaging |
Het |
| Erap1 |
T |
A |
13: 74,819,500 (GRCm39) |
H171Q |
probably damaging |
Het |
| Esrrb |
T |
C |
12: 86,561,274 (GRCm39) |
V336A |
possibly damaging |
Het |
| Fech |
A |
T |
18: 64,595,189 (GRCm39) |
W300R |
probably damaging |
Het |
| Fgd4 |
T |
C |
16: 16,241,920 (GRCm39) |
I635V |
possibly damaging |
Het |
| Galc |
A |
T |
12: 98,200,563 (GRCm39) |
N282K |
probably benign |
Het |
| Gpat2 |
A |
G |
2: 127,270,637 (GRCm39) |
Y95C |
probably benign |
Het |
| Grm2 |
T |
A |
9: 106,524,670 (GRCm39) |
I682F |
probably damaging |
Het |
| Hdac10 |
G |
T |
15: 89,010,878 (GRCm39) |
A241D |
probably damaging |
Het |
| Helz |
T |
A |
11: 107,527,105 (GRCm39) |
C182* |
probably null |
Het |
| Ift140 |
A |
G |
17: 25,307,839 (GRCm39) |
Y978C |
probably damaging |
Het |
| Intu |
T |
A |
3: 40,652,061 (GRCm39) |
C839* |
probably null |
Het |
| Jmjd1c |
T |
C |
10: 67,055,654 (GRCm39) |
V358A |
probably benign |
Het |
| Lrp1b |
A |
G |
2: 40,587,601 (GRCm39) |
S116P |
unknown |
Het |
| Lrrc2 |
T |
A |
9: 110,790,041 (GRCm39) |
S99R |
probably benign |
Het |
| Mrpl48 |
G |
A |
7: 100,195,482 (GRCm39) |
|
probably benign |
Het |
| Mup9 |
A |
G |
4: 60,377,878 (GRCm39) |
|
probably benign |
Het |
| Nap1l1 |
G |
A |
10: 111,329,240 (GRCm39) |
V285I |
possibly damaging |
Het |
| Nepro |
A |
G |
16: 44,547,391 (GRCm39) |
D36G |
probably benign |
Het |
| Nkain4 |
A |
G |
2: 180,577,794 (GRCm39) |
F187L |
probably damaging |
Het |
| Nobox |
A |
T |
6: 43,284,401 (GRCm39) |
C82S |
possibly damaging |
Het |
| Ntn4 |
C |
A |
10: 93,480,596 (GRCm39) |
Q70K |
probably damaging |
Het |
| Or13j1 |
A |
G |
4: 43,706,292 (GRCm39) |
I92T |
probably damaging |
Het |
| Or1e26 |
A |
T |
11: 73,480,118 (GRCm39) |
W149R |
probably damaging |
Het |
| Or4k37 |
A |
G |
2: 111,159,306 (GRCm39) |
I181V |
probably benign |
Het |
| Or51a43 |
T |
C |
7: 103,717,738 (GRCm39) |
R167G |
probably damaging |
Het |
| Or5b122 |
T |
A |
19: 13,562,978 (GRCm39) |
F103L |
probably benign |
Het |
| Or9r3 |
A |
G |
10: 129,948,548 (GRCm39) |
I37T |
possibly damaging |
Het |
| Pappa |
A |
G |
4: 65,094,466 (GRCm39) |
E497G |
probably damaging |
Het |
| Pard3 |
C |
A |
8: 128,106,983 (GRCm39) |
T569K |
probably benign |
Het |
| Parp14 |
G |
A |
16: 35,677,130 (GRCm39) |
A946V |
probably benign |
Het |
| Pcdh10 |
A |
G |
3: 45,334,747 (GRCm39) |
N354D |
possibly damaging |
Het |
| Pdgfc |
T |
C |
3: 81,082,194 (GRCm39) |
V129A |
probably benign |
Het |
| Pdia3 |
G |
A |
2: 121,262,858 (GRCm39) |
G275S |
probably damaging |
Het |
| Phf20l1 |
A |
T |
15: 66,487,108 (GRCm39) |
H407L |
possibly damaging |
Het |
| Phip |
A |
T |
9: 82,753,502 (GRCm39) |
D1747E |
probably benign |
Het |
| Pkd1l1 |
A |
G |
11: 8,900,413 (GRCm39) |
S43P |
probably damaging |
Het |
| Plekhg2 |
T |
C |
7: 28,067,846 (GRCm39) |
E202G |
probably damaging |
Het |
| Rapsn |
A |
G |
2: 90,873,504 (GRCm39) |
D270G |
possibly damaging |
Het |
| Rims2 |
A |
C |
15: 39,370,382 (GRCm39) |
S939R |
probably damaging |
Het |
| Ripor3 |
T |
C |
2: 167,822,765 (GRCm39) |
D932G |
probably damaging |
Het |
| Rtp2 |
A |
T |
16: 23,749,421 (GRCm39) |
W30R |
probably damaging |
Het |
| Scgb2b27 |
A |
T |
7: 33,711,557 (GRCm39) |
D97E |
probably benign |
Het |
| Slc25a46 |
T |
C |
18: 31,716,542 (GRCm39) |
N320S |
probably benign |
Het |
| Slc9b1 |
A |
G |
3: 135,060,765 (GRCm39) |
|
probably null |
Het |
| Socs4 |
T |
A |
14: 47,527,740 (GRCm39) |
M225K |
possibly damaging |
Het |
| Spata31d1a |
A |
T |
13: 59,850,247 (GRCm39) |
L627* |
probably null |
Het |
| Srcin1 |
A |
G |
11: 97,416,307 (GRCm39) |
L975P |
probably damaging |
Het |
| Stard3 |
T |
A |
11: 98,267,435 (GRCm39) |
|
probably null |
Het |
| Susd2 |
G |
T |
10: 75,473,878 (GRCm39) |
S572R |
possibly damaging |
Het |
| Tll1 |
C |
A |
8: 64,509,307 (GRCm39) |
A568S |
probably benign |
Het |
| Tmem132a |
C |
G |
19: 10,839,062 (GRCm39) |
G460A |
probably damaging |
Het |
| Trim62 |
A |
G |
4: 128,803,281 (GRCm39) |
K444E |
probably damaging |
Het |
| Trpm3 |
A |
G |
19: 22,689,271 (GRCm39) |
T67A |
probably damaging |
Het |
| Ttc6 |
T |
C |
12: 57,784,454 (GRCm39) |
M1841T |
possibly damaging |
Het |
| Ulk2 |
A |
T |
11: 61,672,572 (GRCm39) |
V922D |
probably damaging |
Het |
| Vmn2r38 |
C |
A |
7: 9,078,532 (GRCm39) |
V617L |
probably damaging |
Het |
| Xkr6 |
G |
A |
14: 64,056,766 (GRCm39) |
V226M |
probably benign |
Het |
| Zfp940 |
G |
A |
7: 29,544,962 (GRCm39) |
A315V |
possibly damaging |
Het |
| Zfr |
C |
A |
15: 12,150,473 (GRCm39) |
T480K |
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 |
|
|
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 |
|
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'- GTTTGTCAGCAGCATCCAGAACAC -3'
(R):5'- TGGAGTAAGCGTTCTCCCTTTTCAC -3'
Sequencing Primer
(F):5'- TCCAGAACACGGCAGTG -3'
(R):5'- GATCCTCAAATTTCATCTCTCTCC -3'
|
| Posted On |
2014-04-24 |
Incidental Mutation