Incidental Mutation 'IGL00927:Kif3b'
| ID |
26896 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Kif3b
|
| Ensembl Gene |
ENSMUSG00000027475 |
| Gene Name |
kinesin family member 3B |
| Synonyms |
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL00927
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
153133333-153175310 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 153158381 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Alanine to Threonine
at position 61
(A61T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000028977
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028977]
|
| AlphaFold |
Q61771 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000028977
AA Change: A61T
PolyPhen 2
Score 0.889 (Sensitivity: 0.82; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000028977
Gene: ENSMUSG00000027475
AA Change: A61T
| Domain | Start | End | E-Value | Type |
|---|
|
KISc
|
7 |
348 |
6.36e-186 |
SMART |
|
low complexity region
|
370 |
412 |
N/A |
INTRINSIC |
|
low complexity region
|
437 |
458 |
N/A |
INTRINSIC |
|
Blast:KISc
|
459 |
535 |
3e-10 |
BLAST |
|
low complexity region
|
537 |
548 |
N/A |
INTRINSIC |
|
Blast:KISc
|
549 |
626 |
4e-27 |
BLAST |
|
low complexity region
|
685 |
697 |
N/A |
INTRINSIC |
|
low complexity region
|
714 |
735 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene acts as a heterodimer with kinesin family member 3A to aid in chromosome movement during mitosis and meiosis. The encoded protein is a plus end-directed microtubule motor and can interact with the SMC3 subunit of the cohesin complex. In addition, the encoded protein may be involved in the intracellular movement of membranous organelles. This protein and kinesin family member 3A form the kinesin II subfamily of the kinesin superfamily. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygoous for a targeted null mutation are growth retarded and display neural tube defects, incomplete embryo turning, randomized left-right assymetry, pericardial edema, and die during the midgestational period. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 35 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2310033P09Rik |
A |
G |
11: 59,099,674 (GRCm39) |
T92A |
probably damaging |
Het |
| Ankhd1 |
A |
G |
18: 36,765,125 (GRCm39) |
S1007G |
probably benign |
Het |
| Cabp4 |
A |
T |
19: 4,189,406 (GRCm39) |
S50R |
possibly damaging |
Het |
| Camp |
A |
T |
9: 109,678,336 (GRCm39) |
L56Q |
probably damaging |
Het |
| Cblb |
A |
G |
16: 51,986,461 (GRCm39) |
N568S |
probably benign |
Het |
| Ccr6 |
C |
A |
17: 8,474,825 (GRCm39) |
T10K |
probably benign |
Het |
| Chit1 |
T |
C |
1: 134,072,992 (GRCm39) |
F106S |
probably damaging |
Het |
| Cyb561d1 |
A |
G |
3: 108,106,943 (GRCm39) |
L34P |
probably damaging |
Het |
| Dcun1d1 |
A |
T |
3: 35,975,114 (GRCm39) |
|
probably benign |
Het |
| Deup1 |
A |
G |
9: 15,521,967 (GRCm39) |
|
probably benign |
Het |
| Erich1 |
A |
G |
8: 14,083,518 (GRCm39) |
F184S |
probably damaging |
Het |
| Fmnl3 |
A |
G |
15: 99,235,509 (GRCm39) |
|
probably null |
Het |
| Grk2 |
T |
C |
19: 4,337,982 (GRCm39) |
N508S |
probably benign |
Het |
| Herc4 |
A |
G |
10: 63,109,316 (GRCm39) |
I184V |
probably benign |
Het |
| Hnrnpm |
C |
A |
17: 33,868,876 (GRCm39) |
R517L |
probably damaging |
Het |
| Ift56 |
T |
C |
6: 38,359,155 (GRCm39) |
|
probably benign |
Het |
| Kmt2d |
G |
A |
15: 98,742,890 (GRCm39) |
|
probably benign |
Het |
| Lrrc7 |
C |
A |
3: 157,866,727 (GRCm39) |
V1005L |
possibly damaging |
Het |
| Lrrtm1 |
A |
T |
6: 77,221,046 (GRCm39) |
M168L |
probably benign |
Het |
| Ndc1 |
C |
T |
4: 107,241,977 (GRCm39) |
|
probably benign |
Het |
| Nphs1 |
A |
G |
7: 30,160,164 (GRCm39) |
|
probably benign |
Het |
| Or52w1 |
A |
T |
7: 105,018,454 (GRCm39) |
Y298F |
probably damaging |
Het |
| Pbld2 |
T |
C |
10: 62,907,734 (GRCm39) |
V200A |
probably benign |
Het |
| Pcdhb21 |
A |
G |
18: 37,647,606 (GRCm39) |
Y245C |
probably damaging |
Het |
| Pcm1 |
A |
G |
8: 41,740,918 (GRCm39) |
T1055A |
probably damaging |
Het |
| Plcl2 |
C |
T |
17: 50,913,948 (GRCm39) |
S319L |
probably benign |
Het |
| Plekha8 |
C |
A |
6: 54,606,822 (GRCm39) |
Y372* |
probably null |
Het |
| Ralb |
T |
A |
1: 119,399,506 (GRCm39) |
N184I |
probably benign |
Het |
| Robo3 |
C |
T |
9: 37,339,050 (GRCm39) |
|
probably null |
Het |
| Slc41a1 |
T |
A |
1: 131,766,914 (GRCm39) |
L144H |
probably damaging |
Het |
| Smg1 |
C |
T |
7: 117,739,855 (GRCm39) |
G3364D |
probably damaging |
Het |
| Spmap2 |
A |
G |
10: 79,412,433 (GRCm39) |
S329P |
probably damaging |
Het |
| Vmn1r123 |
T |
A |
7: 20,896,216 (GRCm39) |
V36D |
possibly damaging |
Het |
| Zbtb7c |
T |
C |
18: 76,278,921 (GRCm39) |
S460P |
possibly damaging |
Het |
| Zscan30 |
T |
C |
18: 24,104,834 (GRCm39) |
|
noncoding transcript |
Het |
|
| Other mutations in Kif3b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00162:Kif3b
|
APN |
2 |
153,159,051 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02121:Kif3b
|
APN |
2 |
153,159,194 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02302:Kif3b
|
APN |
2 |
153,158,868 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02306:Kif3b
|
APN |
2 |
153,162,572 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02348:Kif3b
|
APN |
2 |
153,158,813 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL03111:Kif3b
|
APN |
2 |
153,171,988 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1463:Kif3b
|
UTSW |
2 |
153,172,073 (GRCm39) |
makesense |
probably null |
|
|
R1474:Kif3b
|
UTSW |
2 |
153,162,235 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1485:Kif3b
|
UTSW |
2 |
153,164,851 (GRCm39) |
splice site |
probably null |
|
|
R1538:Kif3b
|
UTSW |
2 |
153,159,382 (GRCm39) |
small deletion |
probably benign |
|
|
R1834:Kif3b
|
UTSW |
2 |
153,159,405 (GRCm39) |
missense |
probably benign |
0.22 |
|
R2371:Kif3b
|
UTSW |
2 |
153,164,743 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R4051:Kif3b
|
UTSW |
2 |
153,165,477 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4208:Kif3b
|
UTSW |
2 |
153,165,477 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4504:Kif3b
|
UTSW |
2 |
153,165,564 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4619:Kif3b
|
UTSW |
2 |
153,158,594 (GRCm39) |
nonsense |
probably null |
|
|
R4806:Kif3b
|
UTSW |
2 |
153,162,288 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4911:Kif3b
|
UTSW |
2 |
153,159,212 (GRCm39) |
nonsense |
probably null |
|
|
R7017:Kif3b
|
UTSW |
2 |
153,171,644 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R7990:Kif3b
|
UTSW |
2 |
153,159,383 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8056:Kif3b
|
UTSW |
2 |
153,171,979 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R8503:Kif3b
|
UTSW |
2 |
153,162,824 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8515:Kif3b
|
UTSW |
2 |
153,158,427 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9041:Kif3b
|
UTSW |
2 |
153,159,468 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9524:Kif3b
|
UTSW |
2 |
153,159,460 (GRCm39) |
missense |
probably benign |
0.38 |
|
X0026:Kif3b
|
UTSW |
2 |
153,158,241 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-04-17 |
Incidental Mutation