Incidental Mutation 'R3980:Bean1'
| ID |
311257 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Bean1
|
| Ensembl Gene |
ENSMUSG00000031872 |
| Gene Name |
brain expressed, associated with Nedd4, 1 |
| Synonyms |
|
| MMRRC Submission |
040843-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R3980 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
8 |
| Chromosomal Location |
104897110-104945730 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 104937730 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamine to Leucine
at position 103
(Q103L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148571
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000093245]
[ENSMUST00000164076]
[ENSMUST00000167633]
[ENSMUST00000171018]
[ENSMUST00000212979]
[ENSMUST00000213077]
|
| AlphaFold |
Q9EQG5 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000093245
AA Change: Q69L
PolyPhen 2
Score 0.810 (Sensitivity: 0.84; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000090931
Gene: ENSMUSG00000031872
AA Change: Q69L
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
38 |
60 |
N/A |
INTRINSIC |
|
low complexity region
|
70 |
90 |
N/A |
INTRINSIC |
|
low complexity region
|
217 |
232 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000164076
|
| SMART Domains |
Protein: ENSMUSP00000132056
Gene: ENSMUSG00000031872
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
156 |
171 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000167633
AA Change: Q69L
PolyPhen 2
Score 0.810 (Sensitivity: 0.84; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000131530
Gene: ENSMUSG00000031872
AA Change: Q69L
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
38 |
60 |
N/A |
INTRINSIC |
|
low complexity region
|
70 |
90 |
N/A |
INTRINSIC |
|
low complexity region
|
217 |
232 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000171018
AA Change: Q103L
PolyPhen 2
Score 0.924 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000129403
Gene: ENSMUSG00000031872
AA Change: Q103L
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
72 |
94 |
N/A |
INTRINSIC |
|
low complexity region
|
104 |
124 |
N/A |
INTRINSIC |
|
low complexity region
|
288 |
303 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000212979
AA Change: Q103L
PolyPhen 2
Score 0.924 (Sensitivity: 0.81; Specificity: 0.94)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213077
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 97.2%
- 20x: 94.8%
|
| 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 is one of several proteins that interact with NEDD4, a member of a family of ubiquitin-protein ligases. These proteins have PY motifs in common that bind to the WW domains of NEDD4. NEDD4 is developmentally regulated, and is highly expressed in embryonic tissues. Mutations in this gene (i.e., intronic insertions of >100 copies of pentanucleotide repeats including a (TGGAA)n sequence) are associated with spinocerebellar ataxia type 31. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]
PHENOTYPE: Mice homozygous for a null targeted allele are viable and fertile and exhibit no apparent abnormalities. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 66 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgrb1 |
G |
A |
15: 74,454,792 (GRCm39) |
G268R |
probably damaging |
Het |
| Amacr |
T |
A |
15: 10,989,015 (GRCm39) |
Y240* |
probably null |
Het |
| Ankhd1 |
A |
T |
18: 36,780,666 (GRCm39) |
H1906L |
probably damaging |
Het |
| Arhgef25 |
C |
A |
10: 127,023,089 (GRCm39) |
C106F |
probably damaging |
Het |
| Ccr9 |
A |
T |
9: 123,608,441 (GRCm39) |
N41I |
probably benign |
Het |
| Ceacam16 |
A |
G |
7: 19,592,558 (GRCm39) |
F117L |
probably benign |
Het |
| Col4a1 |
T |
C |
8: 11,289,155 (GRCm39) |
|
probably benign |
Het |
| Csk |
A |
G |
9: 57,538,063 (GRCm39) |
Y48H |
probably damaging |
Het |
| Csmd1 |
T |
A |
8: 15,956,056 (GRCm39) |
K3384* |
probably null |
Het |
| Ctnnd2 |
T |
A |
15: 30,669,589 (GRCm39) |
H399Q |
probably benign |
Het |
| Cutal |
T |
C |
2: 34,772,325 (GRCm39) |
Y30H |
possibly damaging |
Het |
| Cybb |
T |
C |
X: 9,310,827 (GRCm39) |
Y425C |
probably damaging |
Het |
| Dab2 |
A |
G |
15: 6,464,644 (GRCm39) |
|
probably null |
Het |
| Defb30 |
C |
A |
14: 63,273,421 (GRCm39) |
C64F |
probably damaging |
Het |
| Eif2a |
T |
C |
3: 58,446,960 (GRCm39) |
I45T |
probably benign |
Het |
| Esyt1 |
T |
A |
10: 128,347,393 (GRCm39) |
D1044V |
probably damaging |
Het |
| Gabpb2 |
A |
T |
3: 95,096,081 (GRCm39) |
V382E |
probably damaging |
Het |
| Glb1 |
T |
A |
9: 114,246,132 (GRCm39) |
I61K |
probably damaging |
Het |
| Insyn2b |
G |
A |
11: 34,352,678 (GRCm39) |
C240Y |
probably benign |
Het |
| Kcnt1 |
T |
C |
2: 25,783,226 (GRCm39) |
V263A |
possibly damaging |
Het |
| Kdm5b |
A |
G |
1: 134,547,408 (GRCm39) |
D1019G |
probably benign |
Het |
| Klhl2 |
A |
T |
8: 65,196,109 (GRCm39) |
L545M |
probably damaging |
Het |
| Klhl2 |
C |
A |
8: 65,196,115 (GRCm39) |
G543C |
probably damaging |
Het |
| Krt31 |
G |
T |
11: 99,939,030 (GRCm39) |
Q264K |
probably damaging |
Het |
| Lmnb1 |
A |
G |
18: 56,864,091 (GRCm39) |
D232G |
probably damaging |
Het |
| Loxhd1 |
T |
C |
18: 77,501,855 (GRCm39) |
F859L |
probably damaging |
Het |
| Map7 |
C |
A |
10: 20,143,099 (GRCm39) |
T416K |
unknown |
Het |
| Med18 |
T |
A |
4: 132,190,251 (GRCm39) |
I45F |
probably benign |
Het |
| Mn1 |
A |
T |
5: 111,569,636 (GRCm39) |
H1202L |
possibly damaging |
Het |
| Mpp7 |
T |
C |
18: 7,444,062 (GRCm39) |
D120G |
probably benign |
Het |
| Nlrp1b |
A |
T |
11: 71,072,437 (GRCm39) |
F469I |
possibly damaging |
Het |
| Nos3 |
T |
A |
5: 24,582,929 (GRCm39) |
D685E |
probably damaging |
Het |
| Nrap |
G |
A |
19: 56,369,984 (GRCm39) |
A206V |
probably benign |
Het |
| Nuggc |
T |
C |
14: 65,856,542 (GRCm39) |
|
probably null |
Het |
| Oasl1 |
C |
T |
5: 115,070,957 (GRCm39) |
T274I |
probably damaging |
Het |
| Or10ak12 |
T |
A |
4: 118,666,500 (GRCm39) |
Y187F |
probably benign |
Het |
| Or51a25 |
T |
C |
7: 102,372,959 (GRCm39) |
N246S |
probably damaging |
Het |
| Parp3 |
T |
C |
9: 106,351,267 (GRCm39) |
D278G |
probably damaging |
Het |
| Phc3 |
T |
A |
3: 30,991,080 (GRCm39) |
Q346L |
probably damaging |
Het |
| Pigo |
A |
G |
4: 43,019,231 (GRCm39) |
L1029P |
probably damaging |
Het |
| Plcb3 |
A |
G |
19: 6,943,803 (GRCm39) |
I66T |
probably damaging |
Het |
| Plch2 |
T |
C |
4: 155,069,255 (GRCm39) |
S1019G |
probably benign |
Het |
| Plekhg6 |
C |
A |
6: 125,350,146 (GRCm39) |
C264F |
probably damaging |
Het |
| Plxna2 |
C |
T |
1: 194,431,625 (GRCm39) |
S538F |
probably damaging |
Het |
| Pou4f2 |
G |
T |
8: 79,162,067 (GRCm39) |
H179N |
possibly damaging |
Het |
| Prpf39 |
T |
C |
12: 65,108,231 (GRCm39) |
|
probably benign |
Het |
| Rapgef1 |
G |
A |
2: 29,609,662 (GRCm39) |
V700I |
probably benign |
Het |
| Rdh14 |
A |
G |
12: 10,444,703 (GRCm39) |
I185V |
probably benign |
Het |
| Rnf111 |
A |
T |
9: 70,349,607 (GRCm39) |
H785Q |
probably damaging |
Het |
| Rttn |
C |
T |
18: 89,035,399 (GRCm39) |
R758W |
probably benign |
Het |
| Sik3 |
G |
A |
9: 46,113,361 (GRCm39) |
V601M |
probably damaging |
Het |
| Slc22a14 |
T |
C |
9: 119,007,552 (GRCm39) |
T286A |
probably benign |
Het |
| Slc36a3 |
G |
A |
11: 55,026,209 (GRCm39) |
T203I |
probably benign |
Het |
| Spata31 |
A |
T |
13: 65,070,468 (GRCm39) |
Q872L |
probably benign |
Het |
| Spata31d1c |
A |
G |
13: 65,182,974 (GRCm39) |
D172G |
possibly damaging |
Het |
| Sphkap |
A |
T |
1: 83,245,215 (GRCm39) |
|
probably null |
Het |
| Stat6 |
T |
C |
10: 127,491,248 (GRCm39) |
V463A |
probably damaging |
Het |
| Stx7 |
T |
C |
10: 24,060,947 (GRCm39) |
S225P |
probably damaging |
Het |
| Sult2a7 |
A |
T |
7: 14,207,334 (GRCm39) |
|
probably benign |
Het |
| Tada2a |
A |
T |
11: 83,993,946 (GRCm39) |
F179L |
probably benign |
Het |
| Tas2r103 |
A |
G |
6: 133,013,280 (GRCm39) |
L262P |
probably benign |
Het |
| Tfap2d |
A |
G |
1: 19,236,187 (GRCm39) |
I382V |
possibly damaging |
Het |
| Tshr |
C |
A |
12: 91,504,517 (GRCm39) |
A485D |
probably damaging |
Het |
| Vmn1r32 |
T |
A |
6: 66,530,698 (GRCm39) |
Y26F |
probably damaging |
Het |
| Vmn1r5 |
A |
G |
6: 56,962,636 (GRCm39) |
T104A |
probably damaging |
Het |
| Wbp1l |
T |
A |
19: 46,642,396 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Bean1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02016:Bean1
|
APN |
8 |
104,937,550 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R0135:Bean1
|
UTSW |
8 |
104,943,807 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0490:Bean1
|
UTSW |
8 |
104,941,660 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R1319:Bean1
|
UTSW |
8 |
104,943,856 (GRCm39) |
missense |
probably benign |
|
|
R1920:Bean1
|
UTSW |
8 |
104,937,742 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R2513:Bean1
|
UTSW |
8 |
104,908,643 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4209:Bean1
|
UTSW |
8 |
104,940,566 (GRCm39) |
start codon destroyed |
probably null |
0.04 |
|
R4369:Bean1
|
UTSW |
8 |
104,943,742 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4516:Bean1
|
UTSW |
8 |
104,941,786 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4542:Bean1
|
UTSW |
8 |
104,937,591 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4663:Bean1
|
UTSW |
8 |
104,937,799 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4962:Bean1
|
UTSW |
8 |
104,943,606 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5221:Bean1
|
UTSW |
8 |
104,941,784 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6288:Bean1
|
UTSW |
8 |
104,937,622 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6588:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R6615:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R6994:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R7359:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R7451:Bean1
|
UTSW |
8 |
104,940,628 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7454:Bean1
|
UTSW |
8 |
104,937,658 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7473:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R7537:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R7826:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R8034:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R8418:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R8789:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R8885:Bean1
|
UTSW |
8 |
104,908,752 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8888:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R8892:Bean1
|
UTSW |
8 |
104,943,610 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8896:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R8992:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R9015:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R9113:Bean1
|
UTSW |
8 |
104,940,557 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9122:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R9135:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R9151:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R9255:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R9340:Bean1
|
UTSW |
8 |
104,908,739 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9363:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R9417:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R9537:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R9566:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
R9731:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
RF054:Bean1
|
UTSW |
8 |
104,908,664 (GRCm39) |
frame shift |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- ACCCAGCTGAGTGTCCTTTC -3'
(R):5'- GACACCTGTGCACTCTTCCTATAG -3'
Sequencing Primer
(F):5'- TGTGTCCACAGTAGCACGATAC -3'
(R):5'- GTGCACTCTTCCTATAGACCAAG -3'
|
| Posted On |
2015-04-29 |
Incidental Mutation