Incidental Mutation 'R1961:Kif13a'
ID |
317956 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Kif13a
|
Ensembl Gene |
ENSMUSG00000021375 |
Gene Name |
kinesin family member 13A |
Synonyms |
4930505I07Rik, N-3 kinesin |
MMRRC Submission |
039975-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.264)
|
Stock # |
R1961 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
13 |
Chromosomal Location |
46902563-47083343 bp(-) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
G to A
at 47018314 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000153614
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000056978]
[ENSMUST00000225591]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000056978
|
SMART Domains |
Protein: ENSMUSP00000055304 Gene: ENSMUSG00000021375
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 |
noncoding transcript
Transcript: ENSMUST00000224457
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000225591
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.4%
|
Validation Efficiency |
99% (93/94) |
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: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc1 |
T |
C |
16: 14,214,257 (GRCm39) |
Y191H |
probably damaging |
Het |
Abcc4 |
C |
A |
14: 118,848,871 (GRCm39) |
V494L |
possibly damaging |
Het |
Abcc4 |
C |
A |
14: 118,848,868 (GRCm39) |
G495C |
probably damaging |
Het |
Acsm4 |
T |
C |
7: 119,307,963 (GRCm39) |
Y367H |
probably benign |
Het |
Adam21 |
A |
T |
12: 81,606,282 (GRCm39) |
Y493* |
probably null |
Het |
Add2 |
T |
C |
6: 86,073,738 (GRCm39) |
F209S |
probably damaging |
Het |
Adgre4 |
T |
C |
17: 56,098,497 (GRCm39) |
S136P |
probably benign |
Het |
Aff4 |
T |
G |
11: 53,263,826 (GRCm39) |
L282R |
probably damaging |
Het |
Akt3 |
A |
G |
1: 176,924,561 (GRCm39) |
I178T |
probably damaging |
Het |
Ap3m1 |
T |
C |
14: 21,091,083 (GRCm39) |
Y174C |
probably damaging |
Het |
Arb2a |
C |
A |
13: 78,050,839 (GRCm39) |
H50N |
probably benign |
Het |
Atl1 |
A |
G |
12: 70,000,274 (GRCm39) |
E308G |
probably benign |
Het |
Atp8b5 |
T |
G |
4: 43,369,688 (GRCm39) |
V942G |
probably damaging |
Het |
B3gntl1 |
A |
G |
11: 121,535,351 (GRCm39) |
|
probably null |
Het |
Btrc |
T |
G |
19: 45,515,782 (GRCm39) |
I480S |
probably damaging |
Het |
Cacna1c |
A |
T |
6: 118,607,283 (GRCm39) |
I1366N |
probably benign |
Het |
Ccdc113 |
T |
A |
8: 96,267,459 (GRCm39) |
N141K |
probably benign |
Het |
Ccdc167 |
T |
C |
17: 29,923,405 (GRCm39) |
N77D |
possibly damaging |
Het |
Ccser1 |
T |
C |
6: 61,290,630 (GRCm39) |
|
probably benign |
Het |
Cenpe |
A |
G |
3: 134,948,254 (GRCm39) |
E1230G |
probably damaging |
Het |
Clec12a |
A |
C |
6: 129,327,444 (GRCm39) |
T21P |
possibly damaging |
Het |
Cyp26c1 |
T |
A |
19: 37,675,825 (GRCm39) |
F230I |
probably damaging |
Het |
Exog |
A |
G |
9: 119,281,332 (GRCm39) |
E190G |
possibly damaging |
Het |
Fam162b |
A |
G |
10: 51,466,430 (GRCm39) |
W30R |
probably benign |
Het |
Fndc3b |
G |
A |
3: 27,510,600 (GRCm39) |
Q841* |
probably null |
Het |
Frzb |
T |
A |
2: 80,254,945 (GRCm39) |
Y197F |
probably benign |
Het |
G530012D18Rik |
CAGAGAGA |
CAGAGAGAGA |
1: 85,504,945 (GRCm39) |
|
probably null |
Het |
Gabrb1 |
G |
A |
5: 71,857,679 (GRCm39) |
R43Q |
probably benign |
Het |
Gm21060 |
A |
T |
19: 61,285,445 (GRCm39) |
H21Q |
possibly damaging |
Het |
Gm4825 |
A |
G |
15: 85,395,245 (GRCm39) |
|
noncoding transcript |
Het |
Gm5581 |
A |
C |
6: 131,145,125 (GRCm39) |
|
noncoding transcript |
Het |
Gm9894 |
T |
C |
13: 67,912,034 (GRCm39) |
|
noncoding transcript |
Het |
Gpr15 |
T |
A |
16: 58,538,370 (GRCm39) |
I240L |
probably benign |
Het |
Gria4 |
A |
T |
9: 4,519,546 (GRCm39) |
|
probably benign |
Het |
Grid2 |
T |
C |
6: 63,885,877 (GRCm39) |
L91S |
probably damaging |
Het |
Igsf5 |
A |
C |
16: 96,179,551 (GRCm39) |
T215P |
probably damaging |
Het |
Kif21a |
G |
A |
15: 90,855,051 (GRCm39) |
A703V |
probably damaging |
Het |
Kif27 |
T |
G |
13: 58,440,937 (GRCm39) |
R1159S |
probably benign |
Het |
Kifc2 |
T |
A |
15: 76,547,025 (GRCm39) |
L226H |
probably damaging |
Het |
Klf10 |
T |
C |
15: 38,296,240 (GRCm39) |
H435R |
probably damaging |
Het |
Masp1 |
T |
C |
16: 23,271,682 (GRCm39) |
Y623C |
probably damaging |
Het |
Megf10 |
T |
A |
18: 57,345,426 (GRCm39) |
C118S |
probably damaging |
Het |
Mical3 |
A |
G |
6: 120,959,568 (GRCm39) |
V909A |
possibly damaging |
Het |
Mmrn2 |
A |
G |
14: 34,120,432 (GRCm39) |
|
probably null |
Het |
Mpeg1 |
G |
A |
19: 12,440,275 (GRCm39) |
V578M |
probably damaging |
Het |
Nlrp2 |
T |
C |
7: 5,330,737 (GRCm39) |
E553G |
probably damaging |
Het |
Nmi |
A |
T |
2: 51,838,632 (GRCm39) |
S301T |
probably benign |
Het |
Nr2f2 |
G |
T |
7: 70,007,903 (GRCm39) |
T193K |
possibly damaging |
Het |
Ntng2 |
T |
C |
2: 29,087,110 (GRCm39) |
N404S |
probably damaging |
Het |
Nup50l |
A |
G |
6: 96,142,250 (GRCm39) |
S265P |
possibly damaging |
Het |
Oplah |
G |
A |
15: 76,181,664 (GRCm39) |
T1119I |
probably damaging |
Het |
Or1x2 |
T |
G |
11: 50,918,302 (GRCm39) |
S158A |
probably benign |
Het |
Or52e3 |
T |
C |
7: 102,869,204 (GRCm39) |
V93A |
probably benign |
Het |
Otoa |
T |
A |
7: 120,717,792 (GRCm39) |
D336E |
probably benign |
Het |
Pde4b |
A |
G |
4: 102,454,657 (GRCm39) |
E108G |
probably damaging |
Het |
Pdgfrb |
G |
A |
18: 61,194,577 (GRCm39) |
R118H |
possibly damaging |
Het |
Phactr4 |
G |
A |
4: 132,104,559 (GRCm39) |
T256I |
probably benign |
Het |
Pla2g3 |
C |
T |
11: 3,440,983 (GRCm39) |
T316I |
probably benign |
Het |
Plekhg4 |
A |
G |
8: 106,108,096 (GRCm39) |
E982G |
probably damaging |
Het |
Pmfbp1 |
T |
G |
8: 110,256,776 (GRCm39) |
|
probably benign |
Het |
Pot1b |
A |
T |
17: 55,969,531 (GRCm39) |
Y546N |
probably damaging |
Het |
Pphln1-ps1 |
T |
A |
16: 13,495,592 (GRCm39) |
H230Q |
probably benign |
Het |
Rab11fip5 |
C |
A |
6: 85,325,973 (GRCm39) |
Q144H |
possibly damaging |
Het |
Reep3 |
A |
T |
10: 66,875,278 (GRCm39) |
|
probably null |
Het |
Rgl2 |
T |
C |
17: 34,152,589 (GRCm39) |
L400P |
probably damaging |
Het |
Rnf122 |
A |
G |
8: 31,614,874 (GRCm39) |
|
probably benign |
Het |
Scgb1b21 |
G |
T |
7: 33,226,803 (GRCm39) |
|
noncoding transcript |
Het |
Sec63 |
A |
T |
10: 42,699,882 (GRCm39) |
K647N |
probably damaging |
Het |
Sema4a |
C |
T |
3: 88,345,483 (GRCm39) |
|
probably benign |
Het |
Serpinf1 |
C |
T |
11: 75,307,245 (GRCm39) |
V31I |
probably benign |
Het |
Sez6l |
C |
T |
5: 112,572,481 (GRCm39) |
|
probably benign |
Het |
Shank3 |
T |
C |
15: 89,442,167 (GRCm39) |
S1612P |
possibly damaging |
Het |
Slc19a3 |
G |
A |
1: 83,000,519 (GRCm39) |
T166M |
probably benign |
Het |
Slc22a29 |
C |
A |
19: 8,146,557 (GRCm39) |
R415M |
probably benign |
Het |
Slc38a11 |
A |
T |
2: 65,160,683 (GRCm39) |
F304I |
possibly damaging |
Het |
Slitrk1 |
T |
A |
14: 109,149,622 (GRCm39) |
N363I |
probably damaging |
Het |
Slx4ip |
A |
G |
2: 136,909,601 (GRCm39) |
T129A |
probably benign |
Het |
Spop |
T |
C |
11: 95,382,537 (GRCm39) |
V332A |
possibly damaging |
Het |
Sptlc1 |
A |
C |
13: 53,512,916 (GRCm39) |
D147E |
probably benign |
Het |
Tnpo1 |
T |
C |
13: 98,989,440 (GRCm39) |
Y754C |
probably damaging |
Het |
Tox |
C |
A |
4: 6,688,886 (GRCm39) |
V493L |
probably damaging |
Het |
Ttbk1 |
A |
C |
17: 46,791,150 (GRCm39) |
F45V |
probably damaging |
Het |
Ttc27 |
T |
A |
17: 75,087,851 (GRCm39) |
M472K |
probably damaging |
Het |
Ttll7 |
A |
G |
3: 146,621,550 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,552,104 (GRCm39) |
C22851S |
probably benign |
Het |
Ttn |
T |
A |
2: 76,628,556 (GRCm39) |
M14535L |
possibly damaging |
Het |
Txlna |
T |
C |
4: 129,534,055 (GRCm39) |
T54A |
probably benign |
Het |
Usp33 |
T |
C |
3: 152,086,265 (GRCm39) |
V668A |
probably damaging |
Het |
Vmn2r28 |
C |
A |
7: 5,484,070 (GRCm39) |
C710F |
possibly damaging |
Het |
Vmn2r8 |
T |
A |
5: 108,945,961 (GRCm39) |
M549L |
probably benign |
Het |
Vwa5b2 |
T |
C |
16: 20,420,941 (GRCm39) |
|
probably null |
Het |
Wnk1 |
T |
C |
6: 119,946,208 (GRCm39) |
I648M |
probably damaging |
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 |
|
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 |
R7286: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'- CAGAGGGTAAGTAACATGCTGATC -3'
(R):5'- CCCTGTGCATGTCTACATCG -3'
Sequencing Primer
(F):5'- GGGTAAGTAACATGCTGATCTTCCAG -3'
(R):5'- CCTGTGCATGTCTACATCGAGAGG -3'
|
Posted On |
2015-05-19 |