Incidental Mutation 'IGL00861:Fut10'
ID |
278033 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Fut10
|
Ensembl Gene |
ENSMUSG00000046152 |
Gene Name |
fucosyltransferase 10 |
Synonyms |
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.074)
|
Stock # |
IGL00861
|
Quality Score |
|
Status
|
|
Chromosome |
8 |
Chromosomal Location |
31677359-31751766 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 31725733 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Phenylalanine
at position 163
(V163F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000124437
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000066173]
[ENSMUST00000110527]
[ENSMUST00000161502]
[ENSMUST00000161788]
|
AlphaFold |
Q5F2L2 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000066173
AA Change: V163F
PolyPhen 2
Score 0.968 (Sensitivity: 0.77; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000069816 Gene: ENSMUSG00000046152 AA Change: V163F
Domain | Start | End | E-Value | Type |
transmembrane domain
|
9 |
31 |
N/A |
INTRINSIC |
Pfam:Glyco_tran_10_N
|
79 |
184 |
5e-13 |
PFAM |
Pfam:Glyco_transf_10
|
209 |
410 |
7.9e-38 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000110527
|
SMART Domains |
Protein: ENSMUSP00000106156 Gene: ENSMUSG00000046152
Domain | Start | End | E-Value | Type |
Pfam:Glyco_transf_10
|
7 |
134 |
3e-9 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000161502
AA Change: V163F
PolyPhen 2
Score 0.968 (Sensitivity: 0.77; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000125265 Gene: ENSMUSG00000046152 AA Change: V163F
Domain | Start | End | E-Value | Type |
Pfam:Glyco_transf_10
|
7 |
412 |
4.1e-92 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000161788
AA Change: V163F
PolyPhen 2
Score 0.968 (Sensitivity: 0.77; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000124437 Gene: ENSMUSG00000046152 AA Change: V163F
Domain | Start | End | E-Value | Type |
Pfam:Glyco_transf_10
|
7 |
411 |
1.3e-92 |
PFAM |
low complexity region
|
418 |
429 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000162162
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 22 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adm2 |
G |
A |
15: 89,207,488 (GRCm39) |
|
probably benign |
Het |
Ambra1 |
T |
A |
2: 91,601,271 (GRCm39) |
D189E |
possibly damaging |
Het |
Atg16l1 |
G |
A |
1: 87,702,560 (GRCm39) |
G274S |
probably damaging |
Het |
Cdh20 |
C |
A |
1: 109,988,718 (GRCm39) |
|
probably benign |
Het |
Chat |
T |
C |
14: 32,170,980 (GRCm39) |
Y173C |
probably damaging |
Het |
Crygd |
C |
T |
1: 65,101,250 (GRCm39) |
R115Q |
probably benign |
Het |
Ctnnd1 |
T |
C |
2: 84,434,096 (GRCm39) |
D874G |
probably damaging |
Het |
Dbt |
G |
A |
3: 116,339,763 (GRCm39) |
G384S |
probably benign |
Het |
Depdc5 |
T |
C |
5: 33,125,158 (GRCm39) |
|
probably null |
Het |
Eef1b2 |
G |
A |
1: 63,217,665 (GRCm39) |
G91R |
probably damaging |
Het |
Glmn |
A |
T |
5: 107,718,005 (GRCm39) |
M304K |
possibly damaging |
Het |
Klra6 |
A |
G |
6: 130,000,663 (GRCm39) |
V47A |
possibly damaging |
Het |
Lgi2 |
T |
C |
5: 52,695,463 (GRCm39) |
K491E |
probably benign |
Het |
Lrrc72 |
T |
A |
12: 36,271,507 (GRCm39) |
Q138L |
probably benign |
Het |
Nherf4 |
A |
G |
9: 44,160,933 (GRCm39) |
L211P |
possibly damaging |
Het |
Nxph2 |
T |
A |
2: 23,289,974 (GRCm39) |
F109I |
probably damaging |
Het |
Oosp3 |
A |
G |
19: 11,689,004 (GRCm39) |
D84G |
probably benign |
Het |
Poc1b |
C |
T |
10: 98,965,514 (GRCm39) |
R106C |
probably benign |
Het |
Ptk2 |
A |
G |
15: 73,134,396 (GRCm39) |
S568P |
probably damaging |
Het |
Slc4a5 |
A |
G |
6: 83,276,453 (GRCm39) |
I1093V |
probably benign |
Het |
Snx2 |
G |
A |
18: 53,343,869 (GRCm39) |
|
probably null |
Het |
Washc5 |
G |
T |
15: 59,209,125 (GRCm39) |
T1033K |
probably damaging |
Het |
|
Other mutations in Fut10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Fut10
|
APN |
8 |
31,685,319 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00566:Fut10
|
APN |
8 |
31,725,712 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00858:Fut10
|
APN |
8 |
31,725,733 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00862:Fut10
|
APN |
8 |
31,725,733 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01916:Fut10
|
APN |
8 |
31,725,734 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02030:Fut10
|
APN |
8 |
31,726,006 (GRCm39) |
nonsense |
probably null |
|
IGL02318:Fut10
|
APN |
8 |
31,726,286 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02354:Fut10
|
APN |
8 |
31,691,398 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02361:Fut10
|
APN |
8 |
31,691,398 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02932:Fut10
|
APN |
8 |
31,749,965 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03345:Fut10
|
APN |
8 |
31,750,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R0234:Fut10
|
UTSW |
8 |
31,726,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R0234:Fut10
|
UTSW |
8 |
31,726,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Fut10
|
UTSW |
8 |
31,691,418 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Fut10
|
UTSW |
8 |
31,691,418 (GRCm39) |
missense |
probably benign |
0.00 |
R1845:Fut10
|
UTSW |
8 |
31,726,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R2173:Fut10
|
UTSW |
8 |
31,726,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R2518:Fut10
|
UTSW |
8 |
31,726,495 (GRCm39) |
missense |
probably benign |
0.19 |
R3692:Fut10
|
UTSW |
8 |
31,726,048 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4449:Fut10
|
UTSW |
8 |
31,726,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R5015:Fut10
|
UTSW |
8 |
31,726,148 (GRCm39) |
missense |
probably damaging |
0.96 |
R5942:Fut10
|
UTSW |
8 |
31,691,485 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6497:Fut10
|
UTSW |
8 |
31,726,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R7566:Fut10
|
UTSW |
8 |
31,749,950 (GRCm39) |
missense |
probably benign |
0.00 |
R7645:Fut10
|
UTSW |
8 |
31,726,232 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8127:Fut10
|
UTSW |
8 |
31,684,999 (GRCm39) |
start gained |
probably benign |
|
R8241:Fut10
|
UTSW |
8 |
31,750,034 (GRCm39) |
nonsense |
probably null |
|
R8899:Fut10
|
UTSW |
8 |
31,726,514 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9314:Fut10
|
UTSW |
8 |
31,691,504 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Posted On |
2015-04-16 |