Incidental Mutation 'R7583:Kif26b'
| ID |
586846 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Kif26b
|
| Ensembl Gene |
ENSMUSG00000026494 |
| Gene Name |
kinesin family member 26B |
| Synonyms |
D230039L06Rik, N-11 kinesin |
| MMRRC Submission |
045666-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R7583 (G1)
|
| Quality Score |
153.008 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
178356690-178766765 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
G to A
at 178358010 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tryptophan to Stop codon
at position 40
(W40*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000124462
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000161017]
|
| AlphaFold |
Q7TNC6 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000161017
AA Change: W40*
|
| SMART Domains |
Protein: ENSMUSP00000124462
Gene: ENSMUSG00000026494
AA Change: W40*
| 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 |
|
| Meta Mutation Damage Score |
0.9717 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
| Validation Efficiency |
99% (95/96) |
| 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: 98 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4932414N04Rik |
A |
T |
2: 68,569,670 (GRCm39) |
D462V |
probably damaging |
Het |
| Abcc1 |
T |
C |
16: 14,221,902 (GRCm39) |
W222R |
probably damaging |
Het |
| Adamts13 |
A |
G |
2: 26,863,965 (GRCm39) |
K48E |
probably benign |
Het |
| Adgrd1 |
A |
C |
5: 129,256,652 (GRCm39) |
T674P |
probably benign |
Het |
| Agbl4 |
A |
T |
4: 110,976,150 (GRCm39) |
Y169F |
possibly damaging |
Het |
| Ahnak |
T |
A |
19: 8,983,457 (GRCm39) |
N1580K |
possibly damaging |
Het |
| Angptl8 |
A |
C |
9: 21,747,210 (GRCm39) |
|
probably null |
Het |
| Ap3d1 |
G |
A |
10: 80,545,292 (GRCm39) |
T1053I |
probably benign |
Het |
| Atad2 |
T |
C |
15: 57,990,060 (GRCm39) |
T139A |
probably benign |
Het |
| Bdp1 |
T |
A |
13: 100,186,320 (GRCm39) |
T1711S |
probably damaging |
Het |
| Bod1l |
T |
C |
5: 41,991,133 (GRCm39) |
I141V |
probably damaging |
Het |
| Cavin2 |
A |
T |
1: 51,328,777 (GRCm39) |
N78I |
possibly damaging |
Het |
| Ccnb1 |
T |
C |
13: 100,916,262 (GRCm39) |
H406R |
probably benign |
Het |
| Cd200r4 |
A |
G |
16: 44,653,784 (GRCm39) |
T194A |
probably damaging |
Het |
| Cdt1 |
G |
A |
8: 123,296,995 (GRCm39) |
R263H |
probably damaging |
Het |
| Cep85l |
A |
T |
10: 53,157,450 (GRCm39) |
I751N |
probably damaging |
Het |
| Clasp2 |
A |
G |
9: 113,737,755 (GRCm39) |
D1043G |
probably benign |
Het |
| Cmip |
A |
T |
8: 118,181,691 (GRCm39) |
N578I |
probably damaging |
Het |
| Col2a1 |
T |
G |
15: 97,874,065 (GRCm39) |
K1440N |
unknown |
Het |
| Cpne2 |
A |
T |
8: 95,282,209 (GRCm39) |
M252L |
probably benign |
Het |
| Crb2 |
A |
G |
2: 37,680,607 (GRCm39) |
T512A |
probably benign |
Het |
| Csmd1 |
A |
G |
8: 16,048,833 (GRCm39) |
Y2290H |
probably damaging |
Het |
| Ctnnd1 |
A |
T |
2: 84,442,405 (GRCm39) |
D642E |
probably damaging |
Het |
| Ctns |
A |
G |
11: 73,079,296 (GRCm39) |
S141P |
probably benign |
Het |
| Cwh43 |
A |
G |
5: 73,591,632 (GRCm39) |
Q575R |
probably benign |
Het |
| Cyp2b19 |
C |
A |
7: 26,458,489 (GRCm39) |
T68K |
probably damaging |
Het |
| Dcaf6 |
A |
G |
1: 165,160,879 (GRCm39) |
S849P |
probably damaging |
Het |
| Dnm3 |
T |
A |
1: 162,305,343 (GRCm39) |
Q17L |
possibly damaging |
Het |
| Enpp3 |
A |
T |
10: 24,711,990 (GRCm39) |
M1K |
probably null |
Het |
| Fam124a |
T |
A |
14: 62,844,008 (GRCm39) |
C505* |
probably null |
Het |
| Fhip2a |
T |
A |
19: 57,367,034 (GRCm39) |
D192E |
probably benign |
Het |
| Fsip2 |
A |
G |
2: 82,805,585 (GRCm39) |
I635V |
probably benign |
Het |
| Gm5878 |
A |
T |
6: 85,095,682 (GRCm39) |
|
probably null |
Het |
| Gpld1 |
C |
A |
13: 25,159,743 (GRCm39) |
A437D |
probably damaging |
Het |
| Grk5 |
G |
T |
19: 61,071,642 (GRCm39) |
V401L |
possibly damaging |
Het |
| Gucy2g |
A |
T |
19: 55,224,047 (GRCm39) |
L259Q |
probably damaging |
Het |
| Habp2 |
T |
A |
19: 56,300,236 (GRCm39) |
D191E |
probably benign |
Het |
| Helz2 |
T |
A |
2: 180,879,365 (GRCm39) |
H751L |
probably benign |
Het |
| Hgsnat |
A |
G |
8: 26,461,592 (GRCm39) |
|
probably null |
Het |
| Hivep1 |
T |
A |
13: 42,317,716 (GRCm39) |
V2064E |
probably damaging |
Het |
| Ikbke |
C |
T |
1: 131,204,216 (GRCm39) |
A26T |
probably damaging |
Het |
| Ivd |
C |
A |
2: 118,692,612 (GRCm39) |
D37E |
probably damaging |
Het |
| Klrc2 |
A |
G |
6: 129,636,274 (GRCm39) |
S114P |
probably damaging |
Het |
| Lama1 |
A |
T |
17: 68,068,616 (GRCm39) |
T772S |
|
Het |
| Lamc1 |
T |
A |
1: 153,118,978 (GRCm39) |
K880N |
possibly damaging |
Het |
| Lmf1 |
G |
A |
17: 25,874,423 (GRCm39) |
D12N |
|
Het |
| Lpin2 |
G |
T |
17: 71,538,391 (GRCm39) |
E384* |
probably null |
Het |
| Lrrc23 |
T |
C |
6: 124,756,541 (GRCm39) |
|
probably benign |
Het |
| Lrrc31 |
T |
C |
3: 30,745,248 (GRCm39) |
|
probably null |
Het |
| Luc7l2 |
A |
G |
6: 38,528,820 (GRCm39) |
Q13R |
probably damaging |
Het |
| Ly6c1 |
G |
T |
15: 74,920,346 (GRCm39) |
H5Q |
probably damaging |
Het |
| Lyst |
A |
T |
13: 13,810,472 (GRCm39) |
H714L |
probably damaging |
Het |
| Man2a2 |
C |
T |
7: 80,016,692 (GRCm39) |
R374H |
probably damaging |
Het |
| Mchr1 |
A |
T |
15: 81,121,642 (GRCm39) |
T131S |
probably benign |
Het |
| Msto1 |
T |
C |
3: 88,820,236 (GRCm39) |
|
probably null |
Het |
| Myh1 |
C |
T |
11: 67,111,739 (GRCm39) |
T1698I |
probably benign |
Het |
| Ncapd3 |
G |
T |
9: 26,983,144 (GRCm39) |
C964F |
probably damaging |
Het |
| Nefh |
T |
C |
11: 4,891,089 (GRCm39) |
E510G |
probably damaging |
Het |
| Or10g3b |
T |
C |
14: 52,587,360 (GRCm39) |
T48A |
possibly damaging |
Het |
| Or13a24 |
A |
G |
7: 140,154,123 (GRCm39) |
E19G |
probably benign |
Het |
| Or1b1 |
A |
T |
2: 36,995,539 (GRCm39) |
L41* |
probably null |
Het |
| Or1q1 |
A |
C |
2: 36,887,092 (GRCm39) |
K90T |
probably damaging |
Het |
| Or4a73 |
A |
T |
2: 89,421,095 (GRCm39) |
Y121* |
probably null |
Het |
| P4ha1 |
T |
A |
10: 59,205,462 (GRCm39) |
S497R |
probably benign |
Het |
| Palb2 |
T |
C |
7: 121,726,565 (GRCm39) |
D435G |
probably benign |
Het |
| Papola |
C |
T |
12: 105,777,304 (GRCm39) |
P282L |
probably damaging |
Het |
| Pcdhgb1 |
A |
G |
18: 37,815,377 (GRCm39) |
R623G |
probably damaging |
Het |
| Pcolce |
T |
G |
5: 137,605,707 (GRCm39) |
K229Q |
probably benign |
Het |
| Pkhd1l1 |
T |
C |
15: 44,431,760 (GRCm39) |
|
probably null |
Het |
| Ppp6r3 |
T |
A |
19: 3,540,790 (GRCm39) |
T443S |
probably benign |
Het |
| Pramel58 |
A |
T |
5: 94,830,753 (GRCm39) |
T84S |
possibly damaging |
Het |
| Psg20 |
T |
A |
7: 18,416,408 (GRCm39) |
D236V |
probably damaging |
Het |
| Ptgr2 |
T |
G |
12: 84,355,179 (GRCm39) |
S304R |
probably damaging |
Het |
| Ptpn22 |
A |
T |
3: 103,809,430 (GRCm39) |
D681V |
probably benign |
Het |
| Rab3gap1 |
T |
C |
1: 127,858,612 (GRCm39) |
S574P |
probably benign |
Het |
| Slc36a1 |
A |
G |
11: 55,104,754 (GRCm39) |
|
probably null |
Het |
| Slc9a5 |
A |
G |
8: 106,089,904 (GRCm39) |
S621G |
possibly damaging |
Het |
| Sntg1 |
A |
G |
1: 8,515,249 (GRCm39) |
|
probably null |
Het |
| Snx17 |
A |
G |
5: 31,353,877 (GRCm39) |
N222D |
possibly damaging |
Het |
| Spata19 |
G |
T |
9: 27,311,729 (GRCm39) |
S116I |
possibly damaging |
Het |
| Spn |
G |
A |
7: 126,736,234 (GRCm39) |
A91V |
probably damaging |
Het |
| Srrm3 |
T |
C |
5: 135,881,135 (GRCm39) |
V145A |
probably benign |
Het |
| St7 |
A |
T |
6: 17,942,753 (GRCm39) |
T575S |
possibly damaging |
Het |
| Taf2 |
A |
T |
15: 54,928,072 (GRCm39) |
Y110* |
probably null |
Het |
| Tcf20 |
T |
C |
15: 82,739,477 (GRCm39) |
E658G |
possibly damaging |
Het |
| Tdrd6 |
G |
T |
17: 43,935,129 (GRCm39) |
A1973E |
probably benign |
Het |
| Tg |
T |
G |
15: 66,636,267 (GRCm39) |
L2237W |
probably damaging |
Het |
| Ticrr |
C |
A |
7: 79,346,487 (GRCm39) |
Y1882* |
probably null |
Het |
| Trim45 |
T |
A |
3: 100,832,339 (GRCm39) |
C191S |
probably damaging |
Het |
| Upf3a |
G |
A |
8: 13,835,889 (GRCm39) |
|
probably null |
Het |
| Vmn2r42 |
A |
T |
7: 8,197,740 (GRCm39) |
L293* |
probably null |
Het |
| Vmn2r62 |
T |
A |
7: 42,437,466 (GRCm39) |
Q339H |
possibly damaging |
Het |
| Wdr24 |
A |
T |
17: 26,044,804 (GRCm39) |
R220W |
probably null |
Het |
| Wdr5 |
T |
A |
2: 27,408,787 (GRCm39) |
S22T |
probably benign |
Het |
| Zfp37 |
G |
A |
4: 62,110,253 (GRCm39) |
|
probably benign |
Het |
| Zfp735 |
A |
T |
11: 73,601,933 (GRCm39) |
L292F |
possibly damaging |
Het |
| Zfp985 |
T |
A |
4: 147,667,946 (GRCm39) |
C271* |
probably null |
Het |
| Zranb1 |
G |
A |
7: 132,585,625 (GRCm39) |
R691Q |
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 |
|
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'- TTGGTCACTTGAAGGATGGAGATAG -3'
(R):5'- CGTTACAGTTCTCGCACCAGAC -3'
Sequencing Primer
(F):5'- GATAGATGGAGGGCAGGTTTG -3'
(R):5'- GTGAGCCGCCCAGAGAG -3'
|
| Posted On |
2019-10-24 |
Incidental Mutation