Incidental Mutation 'R1960:Kif21a'
ID |
318078 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Kif21a
|
Ensembl Gene |
ENSMUSG00000022629 |
Gene Name |
kinesin family member 21A |
Synonyms |
N-5 kinesin |
MMRRC Submission |
039974-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R1960 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
15 |
Chromosomal Location |
90817479-90934151 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 90855051 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Alanine to Valine
at position 703
(A703V)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000104910
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000067205]
[ENSMUST00000088614]
[ENSMUST00000100304]
[ENSMUST00000109287]
[ENSMUST00000109288]
[ENSMUST00000229801]
|
AlphaFold |
Q9QXL2 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000067205
AA Change: A703V
PolyPhen 2
Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
|
SMART Domains |
Protein: ENSMUSP00000066911 Gene: ENSMUSG00000022629 AA Change: A703V
Domain | Start | End | E-Value | Type |
KISc
|
7 |
379 |
8.97e-163 |
SMART |
Blast:KISc
|
469 |
513 |
9e-9 |
BLAST |
low complexity region
|
514 |
525 |
N/A |
INTRINSIC |
low complexity region
|
542 |
557 |
N/A |
INTRINSIC |
low complexity region
|
571 |
585 |
N/A |
INTRINSIC |
low complexity region
|
589 |
628 |
N/A |
INTRINSIC |
low complexity region
|
700 |
713 |
N/A |
INTRINSIC |
coiled coil region
|
924 |
1008 |
N/A |
INTRINSIC |
coiled coil region
|
1043 |
1066 |
N/A |
INTRINSIC |
low complexity region
|
1101 |
1112 |
N/A |
INTRINSIC |
low complexity region
|
1222 |
1234 |
N/A |
INTRINSIC |
low complexity region
|
1251 |
1271 |
N/A |
INTRINSIC |
WD40
|
1290 |
1327 |
1.21e-7 |
SMART |
WD40
|
1330 |
1368 |
7.28e-2 |
SMART |
WD40
|
1394 |
1432 |
3.33e-1 |
SMART |
WD40
|
1435 |
1477 |
7e-4 |
SMART |
WD40
|
1485 |
1523 |
2.4e-1 |
SMART |
WD40
|
1527 |
1566 |
1.48e-2 |
SMART |
WD40
|
1569 |
1606 |
2.07e-6 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000088614
AA Change: A716V
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
SMART Domains |
Protein: ENSMUSP00000085985 Gene: ENSMUSG00000022629 AA Change: A716V
Domain | Start | End | E-Value | Type |
KISc
|
7 |
379 |
8.97e-163 |
SMART |
Blast:KISc
|
469 |
513 |
1e-8 |
BLAST |
low complexity region
|
514 |
525 |
N/A |
INTRINSIC |
low complexity region
|
542 |
564 |
N/A |
INTRINSIC |
low complexity region
|
584 |
598 |
N/A |
INTRINSIC |
low complexity region
|
602 |
641 |
N/A |
INTRINSIC |
low complexity region
|
713 |
726 |
N/A |
INTRINSIC |
coiled coil region
|
937 |
1021 |
N/A |
INTRINSIC |
coiled coil region
|
1056 |
1079 |
N/A |
INTRINSIC |
low complexity region
|
1114 |
1125 |
N/A |
INTRINSIC |
low complexity region
|
1271 |
1283 |
N/A |
INTRINSIC |
low complexity region
|
1300 |
1316 |
N/A |
INTRINSIC |
WD40
|
1334 |
1371 |
1.21e-7 |
SMART |
WD40
|
1374 |
1412 |
7.28e-2 |
SMART |
WD40
|
1438 |
1476 |
3.33e-1 |
SMART |
WD40
|
1479 |
1521 |
7e-4 |
SMART |
WD40
|
1529 |
1567 |
2.4e-1 |
SMART |
WD40
|
1571 |
1610 |
1.48e-2 |
SMART |
WD40
|
1613 |
1650 |
2.07e-6 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000100304
AA Change: A716V
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
SMART Domains |
Protein: ENSMUSP00000097877 Gene: ENSMUSG00000022629 AA Change: A716V
Domain | Start | End | E-Value | Type |
KISc
|
7 |
379 |
8.97e-163 |
SMART |
Blast:KISc
|
469 |
513 |
1e-8 |
BLAST |
low complexity region
|
514 |
525 |
N/A |
INTRINSIC |
low complexity region
|
542 |
564 |
N/A |
INTRINSIC |
low complexity region
|
584 |
598 |
N/A |
INTRINSIC |
low complexity region
|
602 |
641 |
N/A |
INTRINSIC |
low complexity region
|
713 |
726 |
N/A |
INTRINSIC |
coiled coil region
|
937 |
1021 |
N/A |
INTRINSIC |
coiled coil region
|
1056 |
1079 |
N/A |
INTRINSIC |
low complexity region
|
1271 |
1283 |
N/A |
INTRINSIC |
low complexity region
|
1300 |
1316 |
N/A |
INTRINSIC |
WD40
|
1334 |
1371 |
1.21e-7 |
SMART |
WD40
|
1374 |
1412 |
7.28e-2 |
SMART |
WD40
|
1438 |
1476 |
3.33e-1 |
SMART |
WD40
|
1479 |
1521 |
7e-4 |
SMART |
WD40
|
1529 |
1567 |
2.4e-1 |
SMART |
WD40
|
1571 |
1610 |
1.48e-2 |
SMART |
WD40
|
1613 |
1650 |
2.07e-6 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000109287
AA Change: A703V
PolyPhen 2
Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000104910 Gene: ENSMUSG00000022629 AA Change: A703V
Domain | Start | End | E-Value | Type |
KISc
|
7 |
379 |
8.97e-163 |
SMART |
Blast:KISc
|
469 |
513 |
9e-9 |
BLAST |
low complexity region
|
514 |
525 |
N/A |
INTRINSIC |
low complexity region
|
542 |
557 |
N/A |
INTRINSIC |
low complexity region
|
571 |
585 |
N/A |
INTRINSIC |
low complexity region
|
589 |
628 |
N/A |
INTRINSIC |
low complexity region
|
700 |
713 |
N/A |
INTRINSIC |
coiled coil region
|
924 |
1008 |
N/A |
INTRINSIC |
coiled coil region
|
1043 |
1066 |
N/A |
INTRINSIC |
low complexity region
|
1101 |
1112 |
N/A |
INTRINSIC |
WD40
|
1229 |
1266 |
1.21e-7 |
SMART |
WD40
|
1269 |
1307 |
7.28e-2 |
SMART |
WD40
|
1333 |
1371 |
3.33e-1 |
SMART |
WD40
|
1374 |
1416 |
7e-4 |
SMART |
WD40
|
1424 |
1462 |
2.4e-1 |
SMART |
WD40
|
1466 |
1505 |
1.48e-2 |
SMART |
WD40
|
1508 |
1545 |
2.07e-6 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000109288
AA Change: A703V
PolyPhen 2
Score 0.045 (Sensitivity: 0.94; Specificity: 0.83)
|
SMART Domains |
Protein: ENSMUSP00000104911 Gene: ENSMUSG00000022629 AA Change: A703V
Domain | Start | End | E-Value | Type |
KISc
|
7 |
379 |
8.97e-163 |
SMART |
Blast:KISc
|
469 |
513 |
9e-9 |
BLAST |
low complexity region
|
514 |
525 |
N/A |
INTRINSIC |
low complexity region
|
542 |
557 |
N/A |
INTRINSIC |
low complexity region
|
571 |
585 |
N/A |
INTRINSIC |
low complexity region
|
589 |
628 |
N/A |
INTRINSIC |
low complexity region
|
700 |
713 |
N/A |
INTRINSIC |
coiled coil region
|
924 |
1008 |
N/A |
INTRINSIC |
coiled coil region
|
1043 |
1066 |
N/A |
INTRINSIC |
low complexity region
|
1205 |
1216 |
N/A |
INTRINSIC |
WD40
|
1235 |
1272 |
1.21e-7 |
SMART |
WD40
|
1275 |
1313 |
7.28e-2 |
SMART |
WD40
|
1339 |
1377 |
3.33e-1 |
SMART |
WD40
|
1380 |
1422 |
7e-4 |
SMART |
WD40
|
1430 |
1468 |
2.4e-1 |
SMART |
WD40
|
1472 |
1511 |
1.48e-2 |
SMART |
WD40
|
1514 |
1551 |
2.07e-6 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000229801
|
Meta Mutation Damage Score |
0.1955 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 94.9%
|
Validation Efficiency |
100% (95/95) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the KIF4 subfamily of kinesin-like motor proteins. The encoded protein is characterized by an N-terminal motor domain a coiled-coil stalk domain and a C-terminal WD-40 repeat domain. This protein may be involved in microtubule dependent transport. Mutations in this gene are the cause of congenital fibrosis of extraocular muscles-1. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410004B18Rik |
C |
T |
3: 145,643,976 (GRCm39) |
P55S |
probably damaging |
Het |
Adgre4 |
T |
C |
17: 56,098,497 (GRCm39) |
S136P |
probably benign |
Het |
Aoc1l1 |
C |
T |
6: 48,952,687 (GRCm39) |
T204I |
probably damaging |
Het |
Arap1 |
C |
A |
7: 101,022,222 (GRCm39) |
A8E |
probably damaging |
Het |
Arid1a |
A |
T |
4: 133,480,401 (GRCm39) |
H174Q |
possibly damaging |
Het |
Btbd2 |
A |
G |
10: 80,480,539 (GRCm39) |
I358T |
probably benign |
Het |
Camkk2 |
G |
A |
5: 122,875,575 (GRCm39) |
R492* |
probably null |
Het |
Capn3 |
T |
C |
2: 120,294,421 (GRCm39) |
V23A |
probably benign |
Het |
Carm1 |
T |
G |
9: 21,491,606 (GRCm39) |
V225G |
probably benign |
Het |
Ccdc113 |
T |
A |
8: 96,267,459 (GRCm39) |
N141K |
probably benign |
Het |
Ccdc60 |
C |
A |
5: 116,284,243 (GRCm39) |
M298I |
probably benign |
Het |
Celsr3 |
C |
T |
9: 108,723,016 (GRCm39) |
P2801L |
probably benign |
Het |
Clec4n |
T |
A |
6: 123,207,505 (GRCm39) |
V23E |
probably damaging |
Het |
Cmtr2 |
T |
G |
8: 110,948,382 (GRCm39) |
L231V |
probably damaging |
Het |
Csrnp3 |
T |
G |
2: 65,853,363 (GRCm39) |
V585G |
probably null |
Het |
Ctnnd2 |
T |
C |
15: 30,647,257 (GRCm39) |
S318P |
probably damaging |
Het |
Cubn |
A |
T |
2: 13,344,828 (GRCm39) |
|
probably null |
Het |
Dgkd |
C |
A |
1: 87,857,549 (GRCm39) |
P754T |
possibly damaging |
Het |
Dnah7a |
A |
G |
1: 53,724,142 (GRCm39) |
S108P |
probably benign |
Het |
Dnajc24 |
A |
G |
2: 105,832,268 (GRCm39) |
|
probably benign |
Het |
Dner |
A |
T |
1: 84,423,177 (GRCm39) |
S475R |
probably damaging |
Het |
Dtnb |
T |
C |
12: 3,831,190 (GRCm39) |
L630P |
probably benign |
Het |
Dysf |
T |
C |
6: 84,050,885 (GRCm39) |
F411L |
probably benign |
Het |
Fbh1 |
G |
A |
2: 11,762,339 (GRCm39) |
A566V |
probably damaging |
Het |
Fbxw19 |
G |
T |
9: 109,315,004 (GRCm39) |
T186K |
probably benign |
Het |
Flacc1 |
A |
T |
1: 58,698,437 (GRCm39) |
V327D |
possibly damaging |
Het |
Gm4825 |
A |
G |
15: 85,395,245 (GRCm39) |
|
noncoding transcript |
Het |
Grhl2 |
T |
A |
15: 37,336,558 (GRCm39) |
V54D |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,551,742 (GRCm39) |
I2621V |
probably benign |
Het |
Hmcn1 |
T |
A |
1: 150,553,127 (GRCm39) |
E2521V |
possibly damaging |
Het |
Kcng1 |
A |
G |
2: 168,104,904 (GRCm39) |
V314A |
probably benign |
Het |
Kif13a |
G |
A |
13: 47,018,314 (GRCm39) |
|
probably benign |
Het |
Kifc1 |
A |
G |
17: 34,103,561 (GRCm39) |
|
probably null |
Het |
Klk13 |
T |
A |
7: 43,370,431 (GRCm39) |
N31K |
possibly damaging |
Het |
Klri1 |
T |
A |
6: 129,674,347 (GRCm39) |
H221L |
probably benign |
Het |
Ltbp4 |
G |
A |
7: 27,028,443 (GRCm39) |
P273L |
unknown |
Het |
Med16 |
T |
C |
10: 79,742,929 (GRCm39) |
H14R |
possibly damaging |
Het |
Mpeg1 |
G |
A |
19: 12,440,275 (GRCm39) |
V578M |
probably damaging |
Het |
Mrgpra2a |
T |
A |
7: 47,076,983 (GRCm39) |
I92F |
probably benign |
Het |
Muc5b |
T |
C |
7: 141,416,374 (GRCm39) |
C3107R |
possibly damaging |
Het |
Myo5a |
T |
A |
9: 75,055,139 (GRCm39) |
F441I |
probably damaging |
Het |
Ndst4 |
T |
A |
3: 125,232,331 (GRCm39) |
L300* |
probably null |
Het |
Nlgn2 |
G |
T |
11: 69,718,136 (GRCm39) |
D356E |
probably damaging |
Het |
Nlrp2 |
T |
C |
7: 5,330,737 (GRCm39) |
E553G |
probably damaging |
Het |
Oas1f |
G |
A |
5: 120,994,502 (GRCm39) |
C341Y |
possibly damaging |
Het |
Olfm5 |
A |
T |
7: 103,809,619 (GRCm39) |
C111S |
possibly damaging |
Het |
Oplah |
G |
A |
15: 76,181,664 (GRCm39) |
T1119I |
probably damaging |
Het |
Or2ag15 |
T |
C |
7: 106,340,601 (GRCm39) |
E180G |
probably damaging |
Het |
Or5d46 |
T |
C |
2: 88,170,545 (GRCm39) |
L212P |
probably damaging |
Het |
Or6c74 |
C |
T |
10: 129,870,187 (GRCm39) |
Q231* |
probably null |
Het |
Or6f2 |
A |
T |
7: 139,756,596 (GRCm39) |
I188L |
probably benign |
Het |
Or8b12c |
A |
G |
9: 37,715,242 (GRCm39) |
I12V |
probably benign |
Het |
Or8g51 |
T |
A |
9: 38,609,500 (GRCm39) |
H58L |
probably benign |
Het |
Pde10a |
T |
C |
17: 9,161,750 (GRCm39) |
I477T |
possibly damaging |
Het |
Pde4b |
A |
G |
4: 102,454,657 (GRCm39) |
E108G |
probably damaging |
Het |
Pdgfrb |
A |
T |
18: 61,198,855 (GRCm39) |
T338S |
probably benign |
Het |
Pgghg |
A |
G |
7: 140,523,260 (GRCm39) |
M180V |
probably benign |
Het |
Phactr4 |
G |
A |
4: 132,104,559 (GRCm39) |
T256I |
probably benign |
Het |
Pot1b |
A |
T |
17: 55,969,531 (GRCm39) |
Y546N |
probably damaging |
Het |
Rangap1 |
T |
C |
15: 81,590,704 (GRCm39) |
T463A |
probably benign |
Het |
Rap1gds1 |
T |
C |
3: 138,756,317 (GRCm39) |
I13V |
probably null |
Het |
Rbak |
A |
T |
5: 143,160,437 (GRCm39) |
Y205* |
probably null |
Het |
Reg3b |
A |
T |
6: 78,348,797 (GRCm39) |
K31M |
probably damaging |
Het |
Rfpl4 |
A |
T |
7: 5,118,533 (GRCm39) |
Y12* |
probably null |
Het |
Rnase6 |
A |
G |
14: 51,367,889 (GRCm39) |
N94D |
possibly damaging |
Het |
Rtn4 |
T |
C |
11: 29,686,464 (GRCm39) |
L273P |
probably damaging |
Het |
Ryr3 |
A |
C |
2: 112,624,812 (GRCm39) |
F2203V |
probably damaging |
Het |
Sae1 |
A |
T |
7: 16,102,490 (GRCm39) |
D161E |
possibly damaging |
Het |
Sema5a |
T |
C |
15: 32,562,877 (GRCm39) |
F296S |
possibly damaging |
Het |
Sh3rf1 |
C |
A |
8: 61,837,897 (GRCm39) |
P814Q |
probably damaging |
Het |
Slc22a29 |
C |
A |
19: 8,146,557 (GRCm39) |
R415M |
probably benign |
Het |
Slc25a25 |
C |
T |
2: 32,310,663 (GRCm39) |
|
probably null |
Het |
Slco4c1 |
T |
A |
1: 96,795,654 (GRCm39) |
M135L |
probably benign |
Het |
Slfn1 |
A |
G |
11: 83,012,579 (GRCm39) |
I232V |
possibly damaging |
Het |
Slitrk1 |
T |
A |
14: 109,149,622 (GRCm39) |
N363I |
probably damaging |
Het |
Srr |
A |
G |
11: 74,799,542 (GRCm39) |
V311A |
probably damaging |
Het |
Tasor |
T |
C |
14: 27,160,621 (GRCm39) |
S128P |
probably damaging |
Het |
Tasor |
C |
T |
14: 27,201,746 (GRCm39) |
H1419Y |
possibly damaging |
Het |
Tenm1 |
T |
C |
X: 41,916,078 (GRCm39) |
D402G |
probably benign |
Het |
Topors |
T |
C |
4: 40,261,044 (GRCm39) |
R747G |
unknown |
Het |
Trank1 |
A |
T |
9: 111,220,696 (GRCm39) |
I2478F |
probably damaging |
Het |
Trim69 |
A |
G |
2: 121,998,165 (GRCm39) |
N46D |
probably benign |
Het |
Trpm1 |
T |
A |
7: 63,879,978 (GRCm39) |
L661Q |
probably damaging |
Het |
Ttbk1 |
A |
C |
17: 46,791,150 (GRCm39) |
F45V |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,644,649 (GRCm39) |
K4708R |
probably damaging |
Het |
Unkl |
A |
G |
17: 25,428,619 (GRCm39) |
|
probably benign |
Het |
Uros |
A |
T |
7: 133,288,735 (GRCm39) |
N257K |
probably benign |
Het |
Usp25 |
A |
G |
16: 76,873,259 (GRCm39) |
Y439C |
probably damaging |
Het |
Vgf |
A |
G |
5: 137,061,029 (GRCm39) |
|
probably benign |
Het |
Vmn2r8 |
A |
T |
5: 108,947,152 (GRCm39) |
D533E |
probably damaging |
Het |
Vps13a |
A |
T |
19: 16,702,995 (GRCm39) |
Y653N |
probably damaging |
Het |
Zfp358 |
T |
C |
8: 3,545,742 (GRCm39) |
V135A |
possibly damaging |
Het |
|
Other mutations in Kif21a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00539:Kif21a
|
APN |
15 |
90,821,504 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01476:Kif21a
|
APN |
15 |
90,828,067 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01617:Kif21a
|
APN |
15 |
90,879,840 (GRCm39) |
splice site |
probably benign |
|
IGL01736:Kif21a
|
APN |
15 |
90,843,948 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL01923:Kif21a
|
APN |
15 |
90,840,633 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01985:Kif21a
|
APN |
15 |
90,875,970 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02304:Kif21a
|
APN |
15 |
90,849,738 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02589:Kif21a
|
APN |
15 |
90,869,489 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03115:Kif21a
|
APN |
15 |
90,869,598 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03211:Kif21a
|
APN |
15 |
90,882,166 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL03372:Kif21a
|
APN |
15 |
90,840,579 (GRCm39) |
missense |
probably benign |
0.38 |
reflex
|
UTSW |
15 |
90,852,561 (GRCm39) |
missense |
probably null |
1.00 |
R0052:Kif21a
|
UTSW |
15 |
90,855,060 (GRCm39) |
missense |
probably damaging |
0.98 |
R0052:Kif21a
|
UTSW |
15 |
90,855,060 (GRCm39) |
missense |
probably damaging |
0.98 |
R0304:Kif21a
|
UTSW |
15 |
90,860,724 (GRCm39) |
splice site |
probably null |
|
R0378:Kif21a
|
UTSW |
15 |
90,853,977 (GRCm39) |
splice site |
probably null |
|
R0420:Kif21a
|
UTSW |
15 |
90,852,257 (GRCm39) |
unclassified |
probably benign |
|
R0536:Kif21a
|
UTSW |
15 |
90,843,886 (GRCm39) |
splice site |
probably benign |
|
R0826:Kif21a
|
UTSW |
15 |
90,881,744 (GRCm39) |
critical splice donor site |
probably null |
|
R0971:Kif21a
|
UTSW |
15 |
90,824,784 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1052:Kif21a
|
UTSW |
15 |
90,819,853 (GRCm39) |
missense |
probably benign |
0.17 |
R1168:Kif21a
|
UTSW |
15 |
90,877,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R1324:Kif21a
|
UTSW |
15 |
90,832,525 (GRCm39) |
critical splice donor site |
probably null |
|
R1471:Kif21a
|
UTSW |
15 |
90,840,622 (GRCm39) |
missense |
probably benign |
0.04 |
R1625:Kif21a
|
UTSW |
15 |
90,826,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R1636:Kif21a
|
UTSW |
15 |
90,869,008 (GRCm39) |
splice site |
probably benign |
|
R1647:Kif21a
|
UTSW |
15 |
90,878,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R1648:Kif21a
|
UTSW |
15 |
90,878,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R1699:Kif21a
|
UTSW |
15 |
90,843,946 (GRCm39) |
missense |
probably damaging |
0.99 |
R1703:Kif21a
|
UTSW |
15 |
90,833,250 (GRCm39) |
splice site |
probably null |
|
R1795:Kif21a
|
UTSW |
15 |
90,856,930 (GRCm39) |
splice site |
probably null |
|
R1812:Kif21a
|
UTSW |
15 |
90,855,969 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1959:Kif21a
|
UTSW |
15 |
90,855,051 (GRCm39) |
missense |
probably damaging |
0.99 |
R1961:Kif21a
|
UTSW |
15 |
90,855,051 (GRCm39) |
missense |
probably damaging |
0.99 |
R1996:Kif21a
|
UTSW |
15 |
90,878,574 (GRCm39) |
nonsense |
probably null |
|
R2230:Kif21a
|
UTSW |
15 |
90,869,565 (GRCm39) |
nonsense |
probably null |
|
R2231:Kif21a
|
UTSW |
15 |
90,869,565 (GRCm39) |
nonsense |
probably null |
|
R2232:Kif21a
|
UTSW |
15 |
90,869,565 (GRCm39) |
nonsense |
probably null |
|
R2424:Kif21a
|
UTSW |
15 |
90,855,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R2429:Kif21a
|
UTSW |
15 |
90,882,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R2513:Kif21a
|
UTSW |
15 |
90,878,594 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2846:Kif21a
|
UTSW |
15 |
90,818,667 (GRCm39) |
missense |
probably benign |
|
R3027:Kif21a
|
UTSW |
15 |
90,856,845 (GRCm39) |
missense |
probably damaging |
0.99 |
R3624:Kif21a
|
UTSW |
15 |
90,849,798 (GRCm39) |
missense |
probably damaging |
0.99 |
R3820:Kif21a
|
UTSW |
15 |
90,852,277 (GRCm39) |
missense |
probably benign |
0.17 |
R3923:Kif21a
|
UTSW |
15 |
90,821,497 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3962:Kif21a
|
UTSW |
15 |
90,869,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R4355:Kif21a
|
UTSW |
15 |
90,855,036 (GRCm39) |
missense |
probably benign |
0.17 |
R4516:Kif21a
|
UTSW |
15 |
90,855,345 (GRCm39) |
missense |
probably benign |
0.38 |
R4530:Kif21a
|
UTSW |
15 |
90,852,292 (GRCm39) |
splice site |
probably null |
|
R4612:Kif21a
|
UTSW |
15 |
90,852,426 (GRCm39) |
splice site |
probably null |
|
R4674:Kif21a
|
UTSW |
15 |
90,824,748 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4675:Kif21a
|
UTSW |
15 |
90,824,748 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4698:Kif21a
|
UTSW |
15 |
90,840,508 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4712:Kif21a
|
UTSW |
15 |
90,868,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R4955:Kif21a
|
UTSW |
15 |
90,821,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R4974:Kif21a
|
UTSW |
15 |
90,833,213 (GRCm39) |
missense |
probably benign |
0.16 |
R5034:Kif21a
|
UTSW |
15 |
90,852,561 (GRCm39) |
missense |
probably null |
1.00 |
R5165:Kif21a
|
UTSW |
15 |
90,840,579 (GRCm39) |
missense |
probably benign |
0.38 |
R5464:Kif21a
|
UTSW |
15 |
90,878,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R5541:Kif21a
|
UTSW |
15 |
90,852,316 (GRCm39) |
missense |
probably damaging |
0.99 |
R5757:Kif21a
|
UTSW |
15 |
90,835,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R5936:Kif21a
|
UTSW |
15 |
90,819,850 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5976:Kif21a
|
UTSW |
15 |
90,820,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R6074:Kif21a
|
UTSW |
15 |
90,865,095 (GRCm39) |
missense |
probably benign |
|
R6638:Kif21a
|
UTSW |
15 |
90,850,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R6723:Kif21a
|
UTSW |
15 |
90,824,649 (GRCm39) |
missense |
probably damaging |
0.97 |
R6785:Kif21a
|
UTSW |
15 |
90,819,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R6977:Kif21a
|
UTSW |
15 |
90,865,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R7058:Kif21a
|
UTSW |
15 |
90,833,106 (GRCm39) |
splice site |
probably null |
|
R7147:Kif21a
|
UTSW |
15 |
90,865,086 (GRCm39) |
missense |
probably benign |
0.13 |
R7290:Kif21a
|
UTSW |
15 |
90,851,432 (GRCm39) |
nonsense |
probably null |
|
R7438:Kif21a
|
UTSW |
15 |
90,877,999 (GRCm39) |
missense |
probably benign |
0.37 |
R7593:Kif21a
|
UTSW |
15 |
90,828,064 (GRCm39) |
missense |
probably benign |
0.03 |
R7661:Kif21a
|
UTSW |
15 |
90,865,122 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7891:Kif21a
|
UTSW |
15 |
90,840,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R8137:Kif21a
|
UTSW |
15 |
90,852,645 (GRCm39) |
missense |
probably benign |
|
R8182:Kif21a
|
UTSW |
15 |
90,819,964 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8303:Kif21a
|
UTSW |
15 |
90,855,399 (GRCm39) |
missense |
probably damaging |
0.99 |
R8388:Kif21a
|
UTSW |
15 |
90,843,327 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8867:Kif21a
|
UTSW |
15 |
90,852,382 (GRCm39) |
missense |
probably damaging |
0.96 |
R8921:Kif21a
|
UTSW |
15 |
90,855,930 (GRCm39) |
missense |
probably benign |
0.04 |
R8984:Kif21a
|
UTSW |
15 |
90,840,559 (GRCm39) |
missense |
probably benign |
0.00 |
R9024:Kif21a
|
UTSW |
15 |
90,821,399 (GRCm39) |
nonsense |
probably null |
|
R9254:Kif21a
|
UTSW |
15 |
90,854,030 (GRCm39) |
missense |
probably damaging |
0.99 |
R9366:Kif21a
|
UTSW |
15 |
90,843,951 (GRCm39) |
missense |
probably damaging |
0.99 |
R9379:Kif21a
|
UTSW |
15 |
90,854,030 (GRCm39) |
missense |
probably damaging |
0.99 |
R9393:Kif21a
|
UTSW |
15 |
90,853,981 (GRCm39) |
missense |
probably benign |
0.00 |
R9518:Kif21a
|
UTSW |
15 |
90,840,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R9712:Kif21a
|
UTSW |
15 |
90,879,715 (GRCm39) |
missense |
probably benign |
0.13 |
R9712:Kif21a
|
UTSW |
15 |
90,869,528 (GRCm39) |
missense |
probably damaging |
0.98 |
R9721:Kif21a
|
UTSW |
15 |
90,855,330 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Predicted Primers |
PCR Primer
(F):5'- CAGGAGTAGTCGAGGTACCTTG -3'
(R):5'- AGTCTCCATCCTTACTCAGGGC -3'
Sequencing Primer
(F):5'- AGTCGAGGTACCTTGGTTTTC -3'
(R):5'- TGGAGCCCAAAACCTTAGTCATTAG -3'
|
Posted On |
2015-05-19 |