Incidental Mutation 'IGL02373:Vwa5b2'
| ID |
291003 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Vwa5b2
|
| Ensembl Gene |
ENSMUSG00000046613 |
| Gene Name |
von Willebrand factor A domain containing 5B2 |
| Synonyms |
EG328644 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.131)
|
| Stock # |
IGL02373
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
16 |
| Chromosomal Location |
20408221-20424127 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 20423594 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Histidine
at position 1169
(R1169H)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000123727
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000045918]
[ENSMUST00000096197]
[ENSMUST00000123774]
[ENSMUST00000147867]
[ENSMUST00000159780]
[ENSMUST00000232451]
[ENSMUST00000231386]
[ENSMUST00000231387]
[ENSMUST00000231471]
[ENSMUST00000231531]
[ENSMUST00000232319]
[ENSMUST00000231904]
[ENSMUST00000232458]
[ENSMUST00000231749]
[ENSMUST00000231362]
|
| AlphaFold |
Q3UR50 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000045918
|
| SMART Domains |
Protein: ENSMUSP00000045272
Gene: ENSMUSG00000033809
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ALG3
|
47 |
406 |
2.5e-145 |
PFAM |
|
low complexity region
|
407 |
420 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000046188
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000096197
AA Change: R1169H
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000093911
Gene: ENSMUSG00000046613
AA Change: R1169H
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:VIT_2
|
2 |
79 |
7.3e-31 |
PFAM |
|
VWA
|
352 |
521 |
3.16e-1 |
SMART |
|
low complexity region
|
684 |
706 |
N/A |
INTRINSIC |
|
low complexity region
|
725 |
733 |
N/A |
INTRINSIC |
|
low complexity region
|
744 |
764 |
N/A |
INTRINSIC |
|
low complexity region
|
780 |
797 |
N/A |
INTRINSIC |
|
low complexity region
|
823 |
833 |
N/A |
INTRINSIC |
|
low complexity region
|
1032 |
1046 |
N/A |
INTRINSIC |
|
low complexity region
|
1127 |
1145 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000117019
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000123774
|
| SMART Domains |
Protein: ENSMUSP00000123378
Gene: ENSMUSG00000033809
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
42 |
61 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000127454
|
| SMART Domains |
Protein: ENSMUSP00000120559
Gene: ENSMUSG00000033809
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
25 |
47 |
N/A |
INTRINSIC |
|
Pfam:ALG3
|
51 |
118 |
2.1e-17 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000147867
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000159780
AA Change: R1169H
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000123727
Gene: ENSMUSG00000046613
AA Change: R1169H
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:VIT_2
|
2 |
79 |
5.5e-31 |
PFAM |
|
VWA
|
352 |
521 |
3.16e-1 |
SMART |
|
low complexity region
|
684 |
706 |
N/A |
INTRINSIC |
|
low complexity region
|
725 |
733 |
N/A |
INTRINSIC |
|
low complexity region
|
744 |
764 |
N/A |
INTRINSIC |
|
low complexity region
|
780 |
797 |
N/A |
INTRINSIC |
|
low complexity region
|
823 |
833 |
N/A |
INTRINSIC |
|
low complexity region
|
1032 |
1046 |
N/A |
INTRINSIC |
|
low complexity region
|
1127 |
1145 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000232451
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000231386
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000231387
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000231471
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000231531
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000232319
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000231904
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000232458
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000231608
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000231749
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000231362
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 27 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adamtsl1 |
C |
T |
4: 86,168,042 (GRCm39) |
L462F |
probably damaging |
Het |
| Adgrv1 |
T |
C |
13: 81,607,832 (GRCm39) |
D4080G |
possibly damaging |
Het |
| Apc |
A |
C |
18: 34,449,212 (GRCm39) |
D2002A |
probably damaging |
Het |
| Apobr |
T |
A |
7: 126,184,563 (GRCm39) |
F25I |
probably damaging |
Het |
| Cyp4a10 |
T |
A |
4: 115,378,274 (GRCm39) |
L120* |
probably null |
Het |
| Daam2 |
A |
G |
17: 49,780,408 (GRCm39) |
S704P |
probably damaging |
Het |
| Dcst1 |
G |
T |
3: 89,265,198 (GRCm39) |
N217K |
probably damaging |
Het |
| Efr3b |
C |
T |
12: 4,033,391 (GRCm39) |
V139I |
probably benign |
Het |
| Fmn1 |
C |
A |
2: 113,194,471 (GRCm39) |
P57Q |
unknown |
Het |
| Galnt1 |
G |
A |
18: 24,413,092 (GRCm39) |
G464D |
possibly damaging |
Het |
| Ggcx |
T |
A |
6: 72,404,902 (GRCm39) |
W437R |
probably damaging |
Het |
| Igkv13-54-1 |
T |
C |
6: 69,594,304 (GRCm39) |
|
noncoding transcript |
Het |
| Iglon5 |
T |
C |
7: 43,128,643 (GRCm39) |
E58G |
probably benign |
Het |
| Met |
C |
T |
6: 17,491,528 (GRCm39) |
P97S |
probably damaging |
Het |
| Msantd5f6 |
T |
C |
4: 73,321,880 (GRCm39) |
M52V |
probably benign |
Het |
| Myg1 |
T |
A |
15: 102,245,268 (GRCm39) |
M158K |
probably damaging |
Het |
| Ncald |
T |
A |
15: 37,372,453 (GRCm39) |
M131L |
probably benign |
Het |
| Nipa2 |
T |
C |
7: 55,582,876 (GRCm39) |
I290V |
probably benign |
Het |
| Or4f14b |
C |
A |
2: 111,775,178 (GRCm39) |
V208L |
probably benign |
Het |
| Or5p79 |
A |
T |
7: 108,221,310 (GRCm39) |
Y97F |
probably benign |
Het |
| Or6c219 |
A |
G |
10: 129,781,334 (GRCm39) |
L84S |
probably benign |
Het |
| Ppfia3 |
C |
T |
7: 45,008,273 (GRCm39) |
R48Q |
probably damaging |
Het |
| Rab12 |
A |
G |
17: 66,805,060 (GRCm39) |
L156P |
probably damaging |
Het |
| Slc28a3 |
C |
T |
13: 58,726,218 (GRCm39) |
|
probably null |
Het |
| Slc4a11 |
T |
C |
2: 130,526,818 (GRCm39) |
N770S |
probably benign |
Het |
| Tanc1 |
T |
C |
2: 59,626,372 (GRCm39) |
|
probably null |
Het |
| Vmn2r130 |
A |
T |
17: 23,295,866 (GRCm39) |
R679* |
probably null |
Het |
|
| Other mutations in Vwa5b2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01307:Vwa5b2
|
APN |
16 |
20,423,020 (GRCm39) |
missense |
probably benign |
|
|
IGL01543:Vwa5b2
|
APN |
16 |
20,414,466 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL01719:Vwa5b2
|
APN |
16 |
20,416,183 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02006:Vwa5b2
|
APN |
16 |
20,415,843 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL02150:Vwa5b2
|
APN |
16 |
20,423,576 (GRCm39) |
missense |
probably benign |
|
|
IGL02301:Vwa5b2
|
APN |
16 |
20,423,540 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02413:Vwa5b2
|
APN |
16 |
20,416,851 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02664:Vwa5b2
|
APN |
16 |
20,414,063 (GRCm39) |
unclassified |
probably benign |
|
|
R1171:Vwa5b2
|
UTSW |
16 |
20,423,734 (GRCm39) |
missense |
probably benign |
|
|
R1405:Vwa5b2
|
UTSW |
16 |
20,423,066 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1405:Vwa5b2
|
UTSW |
16 |
20,423,066 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1464:Vwa5b2
|
UTSW |
16 |
20,415,019 (GRCm39) |
missense |
probably benign |
0.08 |
|
R1464:Vwa5b2
|
UTSW |
16 |
20,415,019 (GRCm39) |
missense |
probably benign |
0.08 |
|
R1730:Vwa5b2
|
UTSW |
16 |
20,419,675 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1901:Vwa5b2
|
UTSW |
16 |
20,423,582 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R1902:Vwa5b2
|
UTSW |
16 |
20,423,582 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R1903:Vwa5b2
|
UTSW |
16 |
20,423,582 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R1959:Vwa5b2
|
UTSW |
16 |
20,420,941 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1961:Vwa5b2
|
UTSW |
16 |
20,420,941 (GRCm39) |
critical splice donor site |
probably null |
|
|
R3522:Vwa5b2
|
UTSW |
16 |
20,420,358 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3687:Vwa5b2
|
UTSW |
16 |
20,410,308 (GRCm39) |
unclassified |
probably benign |
|
|
R3746:Vwa5b2
|
UTSW |
16 |
20,417,076 (GRCm39) |
intron |
probably benign |
|
|
R3747:Vwa5b2
|
UTSW |
16 |
20,417,076 (GRCm39) |
intron |
probably benign |
|
|
R3749:Vwa5b2
|
UTSW |
16 |
20,417,076 (GRCm39) |
intron |
probably benign |
|
|
R3952:Vwa5b2
|
UTSW |
16 |
20,417,111 (GRCm39) |
makesense |
probably null |
|
|
R4641:Vwa5b2
|
UTSW |
16 |
20,423,393 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4646:Vwa5b2
|
UTSW |
16 |
20,415,079 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4772:Vwa5b2
|
UTSW |
16 |
20,419,553 (GRCm39) |
splice site |
probably null |
|
|
R5032:Vwa5b2
|
UTSW |
16 |
20,419,459 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5286:Vwa5b2
|
UTSW |
16 |
20,415,058 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5569:Vwa5b2
|
UTSW |
16 |
20,414,089 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5585:Vwa5b2
|
UTSW |
16 |
20,413,428 (GRCm39) |
nonsense |
probably null |
|
|
R5640:Vwa5b2
|
UTSW |
16 |
20,416,292 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6330:Vwa5b2
|
UTSW |
16 |
20,420,727 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6459:Vwa5b2
|
UTSW |
16 |
20,413,429 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6992:Vwa5b2
|
UTSW |
16 |
20,416,952 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7102:Vwa5b2
|
UTSW |
16 |
20,422,984 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7231:Vwa5b2
|
UTSW |
16 |
20,422,878 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7591:Vwa5b2
|
UTSW |
16 |
20,420,317 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7765:Vwa5b2
|
UTSW |
16 |
20,413,361 (GRCm39) |
missense |
probably benign |
|
|
R8269:Vwa5b2
|
UTSW |
16 |
20,423,188 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8311:Vwa5b2
|
UTSW |
16 |
20,409,972 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8707:Vwa5b2
|
UTSW |
16 |
20,412,965 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8716:Vwa5b2
|
UTSW |
16 |
20,415,026 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8815:Vwa5b2
|
UTSW |
16 |
20,419,516 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8965:Vwa5b2
|
UTSW |
16 |
20,415,076 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R9245:Vwa5b2
|
UTSW |
16 |
20,416,890 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9431:Vwa5b2
|
UTSW |
16 |
20,423,046 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9536:Vwa5b2
|
UTSW |
16 |
20,414,449 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9695:Vwa5b2
|
UTSW |
16 |
20,422,975 (GRCm39) |
missense |
probably benign |
|
|
R9727:Vwa5b2
|
UTSW |
16 |
20,423,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Vwa5b2
|
UTSW |
16 |
20,410,003 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Z1177:Vwa5b2
|
UTSW |
16 |
20,419,401 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2015-04-16 |
Incidental Mutation