Incidental Mutation 'R7286:Kif13a'
ID |
566041 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Kif13a
|
Ensembl Gene |
ENSMUSG00000021375 |
Gene Name |
kinesin family member 13A |
Synonyms |
4930505I07Rik, N-3 kinesin |
MMRRC Submission |
045394-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.268)
|
Stock # |
R7286 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
13 |
Chromosomal Location |
46902563-47083343 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 46905931 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Methionine
at position 671
(V671M)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000153657
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000056978]
[ENSMUST00000223881]
|
AlphaFold |
no structure available at present |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000056978
AA Change: V1619M
PolyPhen 2
Score 0.499 (Sensitivity: 0.88; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000055304 Gene: ENSMUSG00000021375 AA Change: V1619M
Domain | Start | End | E-Value | Type |
KISc
|
3 |
360 |
2.69e-175 |
SMART |
low complexity region
|
368 |
381 |
N/A |
INTRINSIC |
low complexity region
|
391 |
406 |
N/A |
INTRINSIC |
FHA
|
469 |
519 |
7.16e-2 |
SMART |
coiled coil region
|
605 |
639 |
N/A |
INTRINSIC |
coiled coil region
|
664 |
704 |
N/A |
INTRINSIC |
Pfam:KIF1B
|
748 |
792 |
1.7e-19 |
PFAM |
low complexity region
|
840 |
854 |
N/A |
INTRINSIC |
low complexity region
|
903 |
915 |
N/A |
INTRINSIC |
Pfam:DUF3694
|
1003 |
1270 |
2.2e-39 |
PFAM |
low complexity region
|
1401 |
1412 |
N/A |
INTRINSIC |
low complexity region
|
1475 |
1492 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000223881
AA Change: V671M
PolyPhen 2
Score 0.949 (Sensitivity: 0.79; Specificity: 0.95)
|
Predicted Effect |
|
Meta Mutation Damage Score |
0.0761 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.6%
|
Validation Efficiency |
|
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 kinesin family of microtubule-based motor proteins that function in the positioning of endosomes. This family member can direct mannose-6-phosphate receptor-containing vesicles from the trans-Golgi network to the plasma membrane, and it is necessary for the steady-state distribution of late endosomes/lysosomes. It is also required for the translocation of FYVE-CENT and TTC19 from the centrosome to the midbody during cytokinesis, and it plays a role in melanosome maturation. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011] PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased anxiety. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
A |
T |
9: 53,334,317 (GRCm39) |
M187L |
possibly damaging |
Het |
9930012K11Rik |
T |
C |
14: 70,394,686 (GRCm39) |
E156G |
possibly damaging |
Het |
Acad9 |
C |
T |
3: 36,130,139 (GRCm39) |
A194V |
probably damaging |
Het |
Agps |
T |
A |
2: 75,683,128 (GRCm39) |
V151E |
probably benign |
Het |
Ak9 |
A |
T |
10: 41,283,367 (GRCm39) |
I1273L |
|
Het |
Akr1c19 |
T |
A |
13: 4,296,818 (GRCm39) |
L288Q |
probably damaging |
Het |
Carmil1 |
T |
G |
13: 24,197,377 (GRCm39) |
D1353A |
probably damaging |
Het |
Ccz1 |
T |
A |
5: 143,949,897 (GRCm39) |
I43F |
probably damaging |
Het |
Cep70 |
G |
A |
9: 99,157,638 (GRCm39) |
C179Y |
probably damaging |
Het |
Comt |
A |
T |
16: 18,229,440 (GRCm39) |
L196H |
probably damaging |
Het |
Cspg5 |
A |
T |
9: 110,076,023 (GRCm39) |
D253V |
probably damaging |
Het |
Dars2 |
A |
G |
1: 160,874,378 (GRCm39) |
V437A |
possibly damaging |
Het |
Dcaf5 |
A |
G |
12: 80,395,164 (GRCm39) |
I335T |
probably damaging |
Het |
Ddn |
T |
C |
15: 98,703,906 (GRCm39) |
K462R |
possibly damaging |
Het |
Dscaml1 |
T |
C |
9: 45,654,044 (GRCm39) |
|
probably null |
Het |
Eef1ece2 |
T |
C |
16: 20,451,341 (GRCm39) |
S325P |
probably benign |
Het |
Ethe1 |
A |
G |
7: 24,307,377 (GRCm39) |
Y197C |
probably damaging |
Het |
Evc |
A |
T |
5: 37,479,527 (GRCm39) |
L269* |
probably null |
Het |
Fam161a |
T |
C |
11: 22,970,001 (GRCm39) |
S60P |
possibly damaging |
Het |
Fam20b |
A |
G |
1: 156,509,012 (GRCm39) |
V400A |
probably benign |
Het |
Fam53b |
T |
A |
7: 132,361,390 (GRCm39) |
S213C |
possibly damaging |
Het |
Flot2 |
A |
G |
11: 77,945,612 (GRCm39) |
I45V |
probably benign |
Het |
Gemin4 |
A |
C |
11: 76,103,579 (GRCm39) |
L394R |
probably damaging |
Het |
Glis2 |
T |
G |
16: 4,429,182 (GRCm39) |
S128R |
possibly damaging |
Het |
Gm3696 |
A |
G |
14: 18,435,009 (GRCm39) |
Y92H |
probably damaging |
Het |
Gpbp1l1 |
T |
C |
4: 116,447,442 (GRCm39) |
V374A |
probably benign |
Het |
Grm1 |
T |
C |
10: 10,565,440 (GRCm39) |
N956S |
probably benign |
Het |
Hbb-bh1 |
T |
C |
7: 103,492,238 (GRCm39) |
E27G |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,458,088 (GRCm39) |
C5233S |
probably damaging |
Het |
Hmgcr |
C |
T |
13: 96,803,105 (GRCm39) |
C30Y |
probably damaging |
Het |
Hoxb6 |
A |
G |
11: 96,183,651 (GRCm39) |
|
probably benign |
Het |
Igf2 |
T |
C |
7: 142,209,555 (GRCm39) |
Q35R |
possibly damaging |
Het |
Ighv1-4 |
C |
T |
12: 114,450,941 (GRCm39) |
V56I |
probably benign |
Het |
Lmtk2 |
C |
T |
5: 144,111,178 (GRCm39) |
Q633* |
probably null |
Het |
Mesd |
T |
C |
7: 83,544,957 (GRCm39) |
Y136H |
probably damaging |
Het |
Mga |
T |
A |
2: 119,795,269 (GRCm39) |
S2984R |
possibly damaging |
Het |
Mkrn3 |
T |
C |
7: 62,068,675 (GRCm39) |
N372S |
probably benign |
Het |
Mtpap |
A |
G |
18: 4,387,068 (GRCm39) |
I373V |
probably benign |
Het |
Mycbp2 |
G |
A |
14: 103,358,027 (GRCm39) |
T4589M |
probably damaging |
Het |
Myh2 |
A |
G |
11: 67,079,195 (GRCm39) |
Q921R |
probably benign |
Het |
Myom1 |
A |
G |
17: 71,352,544 (GRCm39) |
D324G |
possibly damaging |
Het |
Nat10 |
T |
C |
2: 103,584,514 (GRCm39) |
K88E |
probably benign |
Het |
Ncapd3 |
A |
G |
9: 26,981,254 (GRCm39) |
R915G |
probably damaging |
Het |
Nek4 |
T |
C |
14: 30,679,249 (GRCm39) |
Y190H |
probably damaging |
Het |
Nfasc |
A |
C |
1: 132,529,790 (GRCm39) |
Y797D |
probably damaging |
Het |
Ngp |
A |
G |
9: 110,249,978 (GRCm39) |
D92G |
probably benign |
Het |
Nos2 |
A |
C |
11: 78,820,680 (GRCm39) |
H95P |
probably damaging |
Het |
Nr3c1 |
ACGTC |
ACGTCGTC |
18: 39,619,513 (GRCm39) |
|
probably benign |
Het |
Or10ag59 |
C |
T |
2: 87,405,863 (GRCm39) |
T145I |
probably benign |
Het |
Or5bw2 |
C |
A |
7: 6,573,715 (GRCm39) |
H242N |
probably damaging |
Het |
Or5p73 |
T |
C |
7: 108,064,642 (GRCm39) |
I37T |
possibly damaging |
Het |
Or5t18 |
A |
T |
2: 86,636,967 (GRCm39) |
H125Q |
possibly damaging |
Het |
Otogl |
T |
A |
10: 107,606,471 (GRCm39) |
D2154V |
probably benign |
Het |
Pdss1 |
T |
A |
2: 22,825,653 (GRCm39) |
|
probably null |
Het |
Pex5 |
A |
T |
6: 124,375,022 (GRCm39) |
L609* |
probably null |
Het |
Pglyrp4 |
C |
A |
3: 90,640,281 (GRCm39) |
A177D |
probably damaging |
Het |
Phactr4 |
A |
G |
4: 132,104,489 (GRCm39) |
|
probably null |
Het |
Phf8-ps |
T |
C |
17: 33,284,501 (GRCm39) |
D767G |
probably benign |
Het |
Pik3cd |
G |
C |
4: 149,744,171 (GRCm39) |
N193K |
probably benign |
Het |
Prr36 |
TACCTCTTC |
T |
8: 4,265,163 (GRCm39) |
|
probably benign |
Het |
Prss38 |
A |
T |
11: 59,266,384 (GRCm39) |
W25R |
probably benign |
Het |
Prss8 |
T |
A |
7: 127,526,056 (GRCm39) |
Q189L |
probably damaging |
Het |
Psd |
T |
A |
19: 46,303,240 (GRCm39) |
D713V |
probably damaging |
Het |
Rad51ap2 |
C |
T |
12: 11,507,692 (GRCm39) |
T538I |
probably benign |
Het |
Rarres1 |
T |
C |
3: 67,422,517 (GRCm39) |
T78A |
probably benign |
Het |
Rbl2 |
G |
T |
8: 91,828,922 (GRCm39) |
G651* |
probably null |
Het |
Rev3l |
A |
T |
10: 39,699,601 (GRCm39) |
Q1366L |
probably damaging |
Het |
Rundc1 |
T |
C |
11: 101,320,413 (GRCm39) |
S215P |
probably benign |
Het |
Sanbr |
A |
T |
11: 23,572,479 (GRCm39) |
C130S |
probably benign |
Het |
Scarf2 |
G |
A |
16: 17,620,837 (GRCm39) |
W168* |
probably null |
Het |
Sh2d7 |
A |
G |
9: 54,448,186 (GRCm39) |
D69G |
possibly damaging |
Het |
Slc26a4 |
A |
T |
12: 31,579,527 (GRCm39) |
Y578* |
probably null |
Het |
Slc2a9 |
A |
T |
5: 38,610,538 (GRCm39) |
L87Q |
probably damaging |
Het |
Slc39a10 |
A |
T |
1: 46,849,230 (GRCm39) |
H795Q |
probably damaging |
Het |
Spata13 |
C |
T |
14: 60,993,871 (GRCm39) |
R1108W |
probably damaging |
Het |
Sqle |
T |
C |
15: 59,187,901 (GRCm39) |
S70P |
probably benign |
Het |
Syncrip |
A |
T |
9: 88,346,716 (GRCm39) |
F263I |
probably damaging |
Het |
Synj2 |
T |
C |
17: 6,088,220 (GRCm39) |
S1424P |
possibly damaging |
Het |
Tax1bp3 |
A |
T |
11: 73,071,941 (GRCm39) |
T89S |
possibly damaging |
Het |
Tcaim |
G |
A |
9: 122,648,092 (GRCm39) |
|
probably null |
Het |
Tcp10c |
T |
C |
17: 13,582,438 (GRCm39) |
I240T |
possibly damaging |
Het |
Ttll8 |
G |
T |
15: 88,801,442 (GRCm39) |
N415K |
probably benign |
Het |
Tut7 |
T |
C |
13: 59,969,463 (GRCm39) |
E144G |
probably benign |
Het |
Ugcg |
T |
C |
4: 59,217,111 (GRCm39) |
S212P |
possibly damaging |
Het |
Vmn2r32 |
T |
C |
7: 7,482,807 (GRCm39) |
K56E |
probably benign |
Het |
Vmn2r55 |
T |
C |
7: 12,386,000 (GRCm39) |
E660G |
probably damaging |
Het |
Vmn2r7 |
T |
C |
3: 64,598,301 (GRCm39) |
N752S |
probably benign |
Het |
Vps54 |
T |
A |
11: 21,225,005 (GRCm39) |
M167K |
probably benign |
Het |
Vwa2 |
A |
C |
19: 56,897,791 (GRCm39) |
M699L |
probably benign |
Het |
Wdr59 |
A |
G |
8: 112,192,494 (GRCm39) |
V689A |
|
Het |
Whamm |
T |
G |
7: 81,235,995 (GRCm39) |
N399K |
probably damaging |
Het |
Zfp760 |
A |
G |
17: 21,941,760 (GRCm39) |
K312E |
probably benign |
Het |
Zkscan3 |
C |
A |
13: 21,578,983 (GRCm39) |
V171L |
probably benign |
Het |
|
Other mutations in Kif13a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01084:Kif13a
|
APN |
13 |
46,904,110 (GRCm39) |
splice site |
probably benign |
|
IGL01433:Kif13a
|
APN |
13 |
46,926,384 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01528:Kif13a
|
APN |
13 |
47,018,313 (GRCm39) |
splice site |
probably benign |
|
IGL01536:Kif13a
|
APN |
13 |
46,905,765 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01620:Kif13a
|
APN |
13 |
47,018,296 (GRCm39) |
missense |
probably benign |
|
IGL02020:Kif13a
|
APN |
13 |
46,947,495 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02142:Kif13a
|
APN |
13 |
46,925,011 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02375:Kif13a
|
APN |
13 |
46,978,698 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02407:Kif13a
|
APN |
13 |
46,938,769 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02476:Kif13a
|
APN |
13 |
46,938,772 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03038:Kif13a
|
APN |
13 |
46,926,314 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03053:Kif13a
|
APN |
13 |
46,905,564 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03366:Kif13a
|
APN |
13 |
46,918,099 (GRCm39) |
missense |
probably benign |
0.00 |
R0025:Kif13a
|
UTSW |
13 |
46,939,987 (GRCm39) |
critical splice donor site |
probably null |
|
R0106:Kif13a
|
UTSW |
13 |
46,978,823 (GRCm39) |
splice site |
probably benign |
|
R0106:Kif13a
|
UTSW |
13 |
46,978,823 (GRCm39) |
splice site |
probably benign |
|
R0135:Kif13a
|
UTSW |
13 |
46,947,419 (GRCm39) |
missense |
probably damaging |
0.99 |
R0137:Kif13a
|
UTSW |
13 |
46,918,079 (GRCm39) |
missense |
probably benign |
0.38 |
R0243:Kif13a
|
UTSW |
13 |
46,944,827 (GRCm39) |
missense |
probably benign |
0.24 |
R0346:Kif13a
|
UTSW |
13 |
46,967,695 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0403:Kif13a
|
UTSW |
13 |
46,944,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R0492:Kif13a
|
UTSW |
13 |
46,966,218 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0607:Kif13a
|
UTSW |
13 |
46,956,187 (GRCm39) |
missense |
probably damaging |
0.96 |
R0631:Kif13a
|
UTSW |
13 |
46,932,364 (GRCm39) |
unclassified |
probably benign |
|
R0654:Kif13a
|
UTSW |
13 |
46,966,218 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0697:Kif13a
|
UTSW |
13 |
47,001,813 (GRCm39) |
missense |
probably benign |
0.19 |
R0699:Kif13a
|
UTSW |
13 |
46,952,689 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0715:Kif13a
|
UTSW |
13 |
46,966,299 (GRCm39) |
missense |
probably damaging |
0.98 |
R0834:Kif13a
|
UTSW |
13 |
46,967,712 (GRCm39) |
missense |
probably damaging |
0.96 |
R0903:Kif13a
|
UTSW |
13 |
47,082,735 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1419:Kif13a
|
UTSW |
13 |
46,978,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R1428:Kif13a
|
UTSW |
13 |
46,944,987 (GRCm39) |
splice site |
probably benign |
|
R1449:Kif13a
|
UTSW |
13 |
46,966,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R1463:Kif13a
|
UTSW |
13 |
47,083,088 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1541:Kif13a
|
UTSW |
13 |
46,962,689 (GRCm39) |
missense |
probably benign |
|
R1579:Kif13a
|
UTSW |
13 |
46,906,332 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1582:Kif13a
|
UTSW |
13 |
46,947,398 (GRCm39) |
missense |
probably benign |
0.03 |
R1644:Kif13a
|
UTSW |
13 |
46,947,398 (GRCm39) |
missense |
probably benign |
0.31 |
R1752:Kif13a
|
UTSW |
13 |
46,951,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R1755:Kif13a
|
UTSW |
13 |
46,927,154 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1755:Kif13a
|
UTSW |
13 |
46,906,089 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1858:Kif13a
|
UTSW |
13 |
47,018,314 (GRCm39) |
splice site |
probably benign |
|
R1891:Kif13a
|
UTSW |
13 |
47,082,695 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1902:Kif13a
|
UTSW |
13 |
46,941,638 (GRCm39) |
missense |
probably benign |
0.00 |
R1928:Kif13a
|
UTSW |
13 |
46,966,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R1960:Kif13a
|
UTSW |
13 |
47,018,314 (GRCm39) |
splice site |
probably benign |
|
R1961:Kif13a
|
UTSW |
13 |
47,018,314 (GRCm39) |
splice site |
probably benign |
|
R2016:Kif13a
|
UTSW |
13 |
46,964,275 (GRCm39) |
missense |
probably benign |
0.13 |
R2139:Kif13a
|
UTSW |
13 |
46,905,945 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2174:Kif13a
|
UTSW |
13 |
46,922,652 (GRCm39) |
missense |
probably damaging |
0.99 |
R2407:Kif13a
|
UTSW |
13 |
46,930,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Kif13a
|
UTSW |
13 |
46,967,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R3122:Kif13a
|
UTSW |
13 |
46,918,072 (GRCm39) |
splice site |
probably benign |
|
R3499:Kif13a
|
UTSW |
13 |
46,978,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R3905:Kif13a
|
UTSW |
13 |
46,956,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R4474:Kif13a
|
UTSW |
13 |
46,967,631 (GRCm39) |
splice site |
probably null |
|
R4771:Kif13a
|
UTSW |
13 |
46,978,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R4838:Kif13a
|
UTSW |
13 |
46,980,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R4924:Kif13a
|
UTSW |
13 |
47,083,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R4931:Kif13a
|
UTSW |
13 |
46,962,531 (GRCm39) |
missense |
probably damaging |
0.96 |
R4980:Kif13a
|
UTSW |
13 |
46,906,222 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4992:Kif13a
|
UTSW |
13 |
46,930,639 (GRCm39) |
missense |
probably damaging |
0.96 |
R5047:Kif13a
|
UTSW |
13 |
46,941,561 (GRCm39) |
missense |
probably benign |
0.00 |
R5054:Kif13a
|
UTSW |
13 |
46,956,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R5141:Kif13a
|
UTSW |
13 |
46,906,197 (GRCm39) |
missense |
probably benign |
|
R5329:Kif13a
|
UTSW |
13 |
46,928,877 (GRCm39) |
critical splice donor site |
probably null |
|
R5429:Kif13a
|
UTSW |
13 |
46,926,245 (GRCm39) |
critical splice donor site |
probably null |
|
R5499:Kif13a
|
UTSW |
13 |
46,986,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R5509:Kif13a
|
UTSW |
13 |
46,905,591 (GRCm39) |
missense |
probably benign |
0.13 |
R5594:Kif13a
|
UTSW |
13 |
46,906,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R5921:Kif13a
|
UTSW |
13 |
46,978,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R5964:Kif13a
|
UTSW |
13 |
46,925,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R6115:Kif13a
|
UTSW |
13 |
46,954,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R6317:Kif13a
|
UTSW |
13 |
46,980,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R6318:Kif13a
|
UTSW |
13 |
46,968,683 (GRCm39) |
splice site |
probably null |
|
R6393:Kif13a
|
UTSW |
13 |
46,905,931 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6394:Kif13a
|
UTSW |
13 |
46,905,931 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6395:Kif13a
|
UTSW |
13 |
46,905,931 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6735:Kif13a
|
UTSW |
13 |
46,906,222 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7037:Kif13a
|
UTSW |
13 |
46,905,931 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7038:Kif13a
|
UTSW |
13 |
46,905,931 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7039:Kif13a
|
UTSW |
13 |
46,905,931 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7237:Kif13a
|
UTSW |
13 |
46,962,632 (GRCm39) |
critical splice donor site |
probably null |
|
R7285:Kif13a
|
UTSW |
13 |
46,905,931 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7287:Kif13a
|
UTSW |
13 |
46,905,931 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7341:Kif13a
|
UTSW |
13 |
46,980,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R7693:Kif13a
|
UTSW |
13 |
46,904,089 (GRCm39) |
missense |
probably benign |
0.01 |
R7761:Kif13a
|
UTSW |
13 |
46,951,955 (GRCm39) |
missense |
probably benign |
|
R8098:Kif13a
|
UTSW |
13 |
46,968,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Kif13a
|
UTSW |
13 |
46,932,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R8271:Kif13a
|
UTSW |
13 |
46,906,057 (GRCm39) |
missense |
probably benign |
0.01 |
R8806:Kif13a
|
UTSW |
13 |
46,914,813 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8871:Kif13a
|
UTSW |
13 |
46,984,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R8877:Kif13a
|
UTSW |
13 |
46,954,921 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8906:Kif13a
|
UTSW |
13 |
46,927,154 (GRCm39) |
missense |
probably benign |
0.17 |
R9028:Kif13a
|
UTSW |
13 |
46,951,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R9058:Kif13a
|
UTSW |
13 |
46,944,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R9062:Kif13a
|
UTSW |
13 |
46,941,536 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9070:Kif13a
|
UTSW |
13 |
46,905,934 (GRCm39) |
missense |
probably benign |
0.00 |
R9083:Kif13a
|
UTSW |
13 |
46,966,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R9250:Kif13a
|
UTSW |
13 |
46,928,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R9328:Kif13a
|
UTSW |
13 |
46,951,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R9360:Kif13a
|
UTSW |
13 |
46,962,472 (GRCm39) |
missense |
probably benign |
0.01 |
R9369:Kif13a
|
UTSW |
13 |
46,940,099 (GRCm39) |
missense |
probably damaging |
0.99 |
R9589:Kif13a
|
UTSW |
13 |
46,956,020 (GRCm39) |
missense |
probably benign |
0.01 |
R9749:Kif13a
|
UTSW |
13 |
46,914,227 (GRCm39) |
missense |
probably damaging |
0.96 |
X0013:Kif13a
|
UTSW |
13 |
47,082,746 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
Predicted Primers |
PCR Primer
(F):5'- TGAACTCTGTGAAGGAATGGTCC -3'
(R):5'- AATGCCACTCTGTCTGACATG -3'
Sequencing Primer
(F):5'- CCTCCAAAATGTTTGTAGTGTGTTC -3'
(R):5'- ACTCTGTCTGACATGGCAGTC -3'
|
Posted On |
2019-06-26 |