Incidental Mutation 'IGL03076:Bcl2'
| ID |
417698 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Bcl2
|
| Ensembl Gene |
ENSMUSG00000057329 |
| Gene Name |
B cell leukemia/lymphoma 2 |
| Synonyms |
Bcl-2, C430015F12Rik, D830018M01Rik |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.910)
|
| Stock # |
IGL03076
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
1 |
| Chromosomal Location |
106465908-106642004 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 106471037 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 223
(V223A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000108371
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000112751]
|
| AlphaFold |
P10417 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000112751
AA Change: V223A
PolyPhen 2
Score 0.236 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000108371
Gene: ENSMUSG00000057329
AA Change: V223A
| Domain | Start | End | E-Value | Type |
|---|
|
BH4
|
7 |
33 |
1.13e-12 |
SMART |
|
BCL
|
94 |
192 |
4.43e-48 |
SMART |
|
transmembrane domain
|
211 |
233 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000144260
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000149909
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000183743
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: This gene encodes a member of the B cell lymphoma 2 protein family. Members of this family regulate cell death in multiple cell types and can have either proapoptotic or antiapoptotic activities. The protein encoded by this gene inhibits mitochondrial-mediated apoptosis. This protein is an integral outer mitochondrial membrane protein that functions as part of signaling pathway that controls mitochondrial permeability in response to apoptotic stimuli. This protein may also play a role in neuron cell survival and autophagy. Abnormal expression and chromosomal translocations of this gene are associated with cancer progression in numerous tissues. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]
PHENOTYPE: Homozygous null mutants show pleiotropic abnormalities including small size, increased postnatal mortality, polycystic kidneys, apoptotic involution of thymus and spleen, graying in the second hair follicle cycle, and reduced numbers of motor, sympathetic and sensory neurons. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(11) : Targeted(8) Gene trapped(2) Chemically induced(1)
|
| Other mutations in this stock |
Total: 37 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Ankmy2 |
T |
C |
12: 36,215,917 (GRCm39) |
V39A |
probably damaging |
Het |
| Bsn |
T |
A |
9: 107,982,581 (GRCm39) |
Y3724F |
unknown |
Het |
| Chd8 |
T |
C |
14: 52,463,619 (GRCm39) |
|
probably benign |
Het |
| Cyp2a5 |
T |
C |
7: 26,535,299 (GRCm39) |
V87A |
probably damaging |
Het |
| Dnah10 |
T |
C |
5: 124,807,226 (GRCm39) |
|
probably null |
Het |
| Dync1h1 |
C |
T |
12: 110,624,327 (GRCm39) |
R3652W |
probably damaging |
Het |
| Epha5 |
T |
A |
5: 84,479,549 (GRCm39) |
T152S |
probably damaging |
Het |
| Flnb |
T |
G |
14: 7,901,988 (GRCm38) |
N950K |
probably benign |
Het |
| Fmn1 |
A |
G |
2: 113,414,437 (GRCm39) |
D1128G |
probably damaging |
Het |
| Fndc3a |
T |
A |
14: 72,793,908 (GRCm39) |
T922S |
possibly damaging |
Het |
| Fsip2 |
A |
T |
2: 82,812,482 (GRCm39) |
N2934Y |
possibly damaging |
Het |
| Gnptab |
T |
C |
10: 88,276,151 (GRCm39) |
V1146A |
possibly damaging |
Het |
| Gsg1l |
A |
G |
7: 125,522,665 (GRCm39) |
F188L |
probably benign |
Het |
| Kmt2c |
C |
A |
5: 25,504,149 (GRCm39) |
E309* |
probably null |
Het |
| Krt71 |
C |
T |
15: 101,643,032 (GRCm39) |
R492H |
probably benign |
Het |
| Lama1 |
T |
A |
17: 68,023,794 (GRCm39) |
V63E |
possibly damaging |
Het |
| Lrch3 |
T |
C |
16: 32,802,223 (GRCm39) |
V58A |
possibly damaging |
Het |
| Lrrc8b |
T |
A |
5: 105,629,415 (GRCm39) |
L587Q |
probably damaging |
Het |
| Lrrtm1 |
T |
C |
6: 77,221,568 (GRCm39) |
C342R |
probably damaging |
Het |
| Mdm1 |
T |
C |
10: 117,995,588 (GRCm39) |
S541P |
possibly damaging |
Het |
| Mdn1 |
T |
A |
4: 32,735,564 (GRCm39) |
V3410D |
probably damaging |
Het |
| Neb |
G |
A |
2: 52,059,100 (GRCm39) |
H213Y |
probably damaging |
Het |
| Or52p2 |
A |
T |
7: 102,237,679 (GRCm39) |
N90K |
probably benign |
Het |
| Or7e175 |
T |
C |
9: 20,049,023 (GRCm39) |
S204P |
probably benign |
Het |
| Pigt |
A |
G |
2: 164,339,585 (GRCm39) |
E36G |
probably damaging |
Het |
| Plxnb1 |
T |
A |
9: 108,935,970 (GRCm39) |
V1120D |
probably damaging |
Het |
| Rapgef6 |
T |
C |
11: 54,516,793 (GRCm39) |
L350P |
probably damaging |
Het |
| Rasgef1c |
C |
A |
11: 49,861,073 (GRCm39) |
T302K |
probably damaging |
Het |
| Riox2 |
C |
A |
16: 59,311,575 (GRCm39) |
A386D |
possibly damaging |
Het |
| Semp2l1 |
A |
G |
1: 32,584,626 (GRCm39) |
I428T |
probably damaging |
Het |
| Slc12a2 |
T |
C |
18: 58,059,469 (GRCm39) |
|
probably benign |
Het |
| Trim24 |
T |
A |
6: 37,942,567 (GRCm39) |
S992R |
probably damaging |
Het |
| Trpc3 |
T |
C |
3: 36,694,804 (GRCm39) |
N717D |
probably damaging |
Het |
| Vwa5b1 |
T |
C |
4: 138,327,499 (GRCm39) |
D359G |
probably damaging |
Het |
| Wapl |
A |
G |
14: 34,414,046 (GRCm39) |
T303A |
probably benign |
Het |
| Zfp128 |
A |
G |
7: 12,618,636 (GRCm39) |
T45A |
possibly damaging |
Het |
| Zfp280d |
T |
C |
9: 72,219,944 (GRCm39) |
S240P |
probably damaging |
Het |
|
| Other mutations in Bcl2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00570:Bcl2
|
APN |
1 |
106,640,088 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
Croce
|
UTSW |
1 |
106,471,011 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0002:Bcl2
|
UTSW |
1 |
106,640,241 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0002:Bcl2
|
UTSW |
1 |
106,640,241 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0083:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0086:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0107:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0183:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0217:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0219:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0346:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0347:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0348:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0361:Bcl2
|
UTSW |
1 |
106,640,424 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0470:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0471:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0601:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0609:Bcl2
|
UTSW |
1 |
106,640,292 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0965:Bcl2
|
UTSW |
1 |
106,640,021 (GRCm39) |
missense |
probably benign |
0.13 |
|
R1756:Bcl2
|
UTSW |
1 |
106,640,122 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2764:Bcl2
|
UTSW |
1 |
106,640,166 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4798:Bcl2
|
UTSW |
1 |
106,640,338 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R4922:Bcl2
|
UTSW |
1 |
106,640,376 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6864:Bcl2
|
UTSW |
1 |
106,471,011 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7576:Bcl2
|
UTSW |
1 |
106,640,153 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R7837:Bcl2
|
UTSW |
1 |
106,471,086 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R8176:Bcl2
|
UTSW |
1 |
106,640,528 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9486:Bcl2
|
UTSW |
1 |
106,471,109 (GRCm39) |
missense |
probably benign |
0.40 |
|
R9548:Bcl2
|
UTSW |
1 |
106,640,508 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Posted On |
2016-08-02 |
Incidental Mutation