Incidental Mutation 'R8850:Bag6'
| ID |
674971 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Bag6
|
| Ensembl Gene |
ENSMUSG00000024392 |
| Gene Name |
BCL2-associated athanogene 6 |
| Synonyms |
2410045D21Rik, G3, D17H6S52E, Bat3, Scythe |
| MMRRC Submission |
068673-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R8850 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
17 |
| Chromosomal Location |
35354154-35366298 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 35361041 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Threonine
at position 440
(M440T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000129324
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000025250]
[ENSMUST00000166426]
[ENSMUST00000172571]
[ENSMUST00000173491]
[ENSMUST00000173535]
[ENSMUST00000173550]
[ENSMUST00000173952]
[ENSMUST00000174281]
[ENSMUST00000174478]
|
| AlphaFold |
Q9Z1R2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000025250
AA Change: M458T
PolyPhen 2
Score 0.190 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000025250
Gene: ENSMUSG00000024392
AA Change: M458T
| Domain | Start | End | E-Value | Type |
|---|
|
UBQ
|
17 |
87 |
5.62e-22 |
SMART |
|
low complexity region
|
96 |
112 |
N/A |
INTRINSIC |
|
low complexity region
|
189 |
206 |
N/A |
INTRINSIC |
|
low complexity region
|
220 |
239 |
N/A |
INTRINSIC |
|
low complexity region
|
246 |
264 |
N/A |
INTRINSIC |
|
Pfam:DUF3538
|
277 |
393 |
1.7e-44 |
PFAM |
|
low complexity region
|
427 |
438 |
N/A |
INTRINSIC |
|
low complexity region
|
557 |
625 |
N/A |
INTRINSIC |
|
low complexity region
|
632 |
648 |
N/A |
INTRINSIC |
|
low complexity region
|
673 |
721 |
N/A |
INTRINSIC |
|
low complexity region
|
725 |
747 |
N/A |
INTRINSIC |
|
low complexity region
|
765 |
780 |
N/A |
INTRINSIC |
|
low complexity region
|
798 |
808 |
N/A |
INTRINSIC |
|
low complexity region
|
1029 |
1042 |
N/A |
INTRINSIC |
|
low complexity region
|
1088 |
1098 |
N/A |
INTRINSIC |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000166426
AA Change: M440T
|
| SMART Domains |
Protein: ENSMUSP00000129324
Gene: ENSMUSG00000024392
AA Change: M440T
| Domain | Start | End | E-Value | Type |
|---|
|
UBQ
|
17 |
87 |
5.62e-22 |
SMART |
|
low complexity region
|
96 |
112 |
N/A |
INTRINSIC |
|
low complexity region
|
171 |
188 |
N/A |
INTRINSIC |
|
low complexity region
|
202 |
221 |
N/A |
INTRINSIC |
|
low complexity region
|
228 |
246 |
N/A |
INTRINSIC |
|
Pfam:DUF3538
|
259 |
375 |
3.7e-53 |
PFAM |
|
low complexity region
|
409 |
420 |
N/A |
INTRINSIC |
|
low complexity region
|
539 |
607 |
N/A |
INTRINSIC |
|
low complexity region
|
614 |
630 |
N/A |
INTRINSIC |
|
low complexity region
|
655 |
703 |
N/A |
INTRINSIC |
|
low complexity region
|
707 |
729 |
N/A |
INTRINSIC |
|
low complexity region
|
747 |
762 |
N/A |
INTRINSIC |
|
low complexity region
|
780 |
790 |
N/A |
INTRINSIC |
|
low complexity region
|
1011 |
1024 |
N/A |
INTRINSIC |
|
low complexity region
|
1070 |
1080 |
N/A |
INTRINSIC |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000172571
AA Change: M435T
|
| SMART Domains |
Protein: ENSMUSP00000134175
Gene: ENSMUSG00000024392
AA Change: M435T
| Domain | Start | End | E-Value | Type |
|---|
|
UBQ
|
17 |
87 |
5.62e-22 |
SMART |
|
low complexity region
|
96 |
112 |
N/A |
INTRINSIC |
|
low complexity region
|
171 |
188 |
N/A |
INTRINSIC |
|
low complexity region
|
202 |
221 |
N/A |
INTRINSIC |
|
low complexity region
|
228 |
252 |
N/A |
INTRINSIC |
|
Pfam:DUF3538
|
254 |
370 |
3.5e-53 |
PFAM |
|
low complexity region
|
404 |
415 |
N/A |
INTRINSIC |
|
low complexity region
|
534 |
602 |
N/A |
INTRINSIC |
|
low complexity region
|
609 |
625 |
N/A |
INTRINSIC |
|
low complexity region
|
650 |
698 |
N/A |
INTRINSIC |
|
low complexity region
|
702 |
724 |
N/A |
INTRINSIC |
|
low complexity region
|
742 |
757 |
N/A |
INTRINSIC |
|
low complexity region
|
775 |
785 |
N/A |
INTRINSIC |
|
low complexity region
|
1006 |
1019 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000172993
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000173491
|
| SMART Domains |
Protein: ENSMUSP00000134279
Gene: ENSMUSG00000024392
| Domain | Start | End | E-Value | Type |
|---|
|
UBQ
|
17 |
87 |
5.62e-22 |
SMART |
|
low complexity region
|
96 |
112 |
N/A |
INTRINSIC |
|
low complexity region
|
189 |
206 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000173535
AA Change: M499T
PolyPhen 2
Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)
|
| SMART Domains |
Protein: ENSMUSP00000133822
Gene: ENSMUSG00000024392
AA Change: M499T
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
17 |
N/A |
INTRINSIC |
|
low complexity region
|
20 |
29 |
N/A |
INTRINSIC |
|
low complexity region
|
30 |
45 |
N/A |
INTRINSIC |
|
UBQ
|
58 |
128 |
5.62e-22 |
SMART |
|
low complexity region
|
137 |
153 |
N/A |
INTRINSIC |
|
low complexity region
|
230 |
247 |
N/A |
INTRINSIC |
|
low complexity region
|
261 |
280 |
N/A |
INTRINSIC |
|
low complexity region
|
287 |
305 |
N/A |
INTRINSIC |
|
Pfam:DUF3538
|
318 |
434 |
1.3e-53 |
PFAM |
|
low complexity region
|
468 |
479 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000173550
AA Change: M440T
PolyPhen 2
Score 0.655 (Sensitivity: 0.87; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000134628
Gene: ENSMUSG00000024392
AA Change: M440T
| Domain | Start | End | E-Value | Type |
|---|
|
UBQ
|
17 |
87 |
5.62e-22 |
SMART |
|
low complexity region
|
96 |
112 |
N/A |
INTRINSIC |
|
low complexity region
|
171 |
188 |
N/A |
INTRINSIC |
|
low complexity region
|
202 |
221 |
N/A |
INTRINSIC |
|
low complexity region
|
228 |
246 |
N/A |
INTRINSIC |
|
Pfam:DUF3538
|
259 |
375 |
3.7e-53 |
PFAM |
|
low complexity region
|
409 |
420 |
N/A |
INTRINSIC |
|
low complexity region
|
496 |
511 |
N/A |
INTRINSIC |
|
low complexity region
|
574 |
642 |
N/A |
INTRINSIC |
|
low complexity region
|
649 |
665 |
N/A |
INTRINSIC |
|
low complexity region
|
690 |
738 |
N/A |
INTRINSIC |
|
low complexity region
|
742 |
764 |
N/A |
INTRINSIC |
|
low complexity region
|
782 |
797 |
N/A |
INTRINSIC |
|
low complexity region
|
815 |
825 |
N/A |
INTRINSIC |
|
low complexity region
|
1046 |
1059 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000173952
|
| SMART Domains |
Protein: ENSMUSP00000134717
Gene: ENSMUSG00000024392
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
17 |
N/A |
INTRINSIC |
|
low complexity region
|
20 |
29 |
N/A |
INTRINSIC |
|
low complexity region
|
30 |
45 |
N/A |
INTRINSIC |
|
UBQ
|
58 |
128 |
5.62e-22 |
SMART |
|
low complexity region
|
137 |
153 |
N/A |
INTRINSIC |
|
low complexity region
|
212 |
229 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000174281
AA Change: M458T
PolyPhen 2
Score 0.323 (Sensitivity: 0.90; Specificity: 0.89)
|
| SMART Domains |
Protein: ENSMUSP00000134425
Gene: ENSMUSG00000024392
AA Change: M458T
| Domain | Start | End | E-Value | Type |
|---|
|
UBQ
|
17 |
87 |
5.62e-22 |
SMART |
|
low complexity region
|
96 |
112 |
N/A |
INTRINSIC |
|
low complexity region
|
189 |
206 |
N/A |
INTRINSIC |
|
low complexity region
|
220 |
239 |
N/A |
INTRINSIC |
|
low complexity region
|
246 |
264 |
N/A |
INTRINSIC |
|
Pfam:DUF3538
|
277 |
393 |
3.6e-53 |
PFAM |
|
low complexity region
|
427 |
438 |
N/A |
INTRINSIC |
|
low complexity region
|
514 |
529 |
N/A |
INTRINSIC |
|
low complexity region
|
592 |
660 |
N/A |
INTRINSIC |
|
low complexity region
|
667 |
683 |
N/A |
INTRINSIC |
|
low complexity region
|
708 |
756 |
N/A |
INTRINSIC |
|
low complexity region
|
760 |
782 |
N/A |
INTRINSIC |
|
low complexity region
|
800 |
815 |
N/A |
INTRINSIC |
|
low complexity region
|
833 |
843 |
N/A |
INTRINSIC |
|
low complexity region
|
1064 |
1077 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000174478
|
| SMART Domains |
Protein: ENSMUSP00000138117
Gene: ENSMUSG00000024392
| Domain | Start | End | E-Value | Type |
|---|
|
UBQ
|
17 |
87 |
5.62e-22 |
SMART |
|
low complexity region
|
96 |
112 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
| Validation Efficiency |
100% (64/64) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene was first characterized as part of a cluster of genes located within the human major histocompatibility complex class III region. This gene encodes a nuclear protein that is cleaved by caspase 3 and is implicated in the control of apoptosis. In addition, the protein forms a complex with E1A binding protein p300 and is required for the acetylation of p53 in response to DNA damage. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Targeted disruption of this gene results in either embryonic lethality following abnormal brain development or neonatal death associated with severe developmental defects in the lung and kidney. These developmental defects are associated with widespread aberrant apoptosis and proliferation. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 65 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Actr10 |
G |
A |
12: 70,989,032 (GRCm39) |
|
probably null |
Het |
| Adgrd1 |
A |
G |
5: 129,219,574 (GRCm39) |
K465E |
probably benign |
Het |
| Aktip |
A |
T |
8: 91,853,402 (GRCm39) |
V105E |
probably benign |
Het |
| Ankrd7 |
A |
G |
6: 18,870,006 (GRCm39) |
Y253C |
probably damaging |
Het |
| Camk2b |
T |
A |
11: 5,922,838 (GRCm39) |
N426Y |
probably damaging |
Het |
| Ccdc82 |
T |
A |
9: 13,289,706 (GRCm39) |
Y500* |
probably null |
Het |
| Cenpe |
T |
A |
3: 134,930,777 (GRCm39) |
D341E |
probably damaging |
Het |
| Cyp2j13 |
A |
T |
4: 95,956,428 (GRCm39) |
M227K |
probably benign |
Het |
| Dmbt1 |
G |
A |
7: 130,692,134 (GRCm39) |
V967I |
unknown |
Het |
| Dnmt3b |
A |
T |
2: 153,515,933 (GRCm39) |
N447Y |
probably benign |
Het |
| Dtl |
A |
T |
1: 191,285,175 (GRCm39) |
Y320* |
probably null |
Het |
| Dtymk |
A |
C |
1: 93,729,543 (GRCm39) |
S3A |
probably benign |
Het |
| Eefsec |
G |
A |
6: 88,423,253 (GRCm39) |
T70M |
possibly damaging |
Het |
| Fam171a1 |
C |
T |
2: 3,221,344 (GRCm39) |
T270M |
probably damaging |
Het |
| Gm17728 |
T |
C |
17: 9,641,159 (GRCm39) |
S90P |
probably benign |
Het |
| Hdlbp |
A |
G |
1: 93,359,053 (GRCm39) |
L213P |
probably damaging |
Het |
| Heatr5b |
T |
C |
17: 79,109,188 (GRCm39) |
I1024V |
probably benign |
Het |
| Hr |
C |
T |
14: 70,799,305 (GRCm39) |
R597* |
probably null |
Het |
| Ifit3 |
T |
C |
19: 34,564,988 (GRCm39) |
I178T |
probably damaging |
Het |
| Ifna6 |
A |
G |
4: 88,746,222 (GRCm39) |
*190W |
probably null |
Het |
| Igkv4-55 |
A |
T |
6: 69,584,315 (GRCm39) |
M99K |
probably benign |
Het |
| Klk1 |
T |
A |
7: 43,877,056 (GRCm39) |
I53N |
probably damaging |
Het |
| Lpcat2b |
A |
G |
5: 107,580,692 (GRCm39) |
H7R |
probably benign |
Het |
| Lrrc37a |
G |
A |
11: 103,393,481 (GRCm39) |
P648L |
|
Het |
| Mast4 |
G |
T |
13: 102,895,174 (GRCm39) |
P975H |
probably damaging |
Het |
| Mfrp |
C |
T |
9: 44,013,807 (GRCm39) |
L106F |
probably benign |
Het |
| Mllt10 |
T |
A |
2: 18,201,469 (GRCm39) |
S652T |
probably benign |
Het |
| Mroh8 |
C |
A |
2: 157,083,673 (GRCm39) |
G400W |
probably damaging |
Het |
| Neurl4 |
A |
G |
11: 69,794,788 (GRCm39) |
|
probably benign |
Het |
| Nop14 |
A |
C |
5: 34,817,352 (GRCm39) |
V13G |
probably benign |
Het |
| Nup188 |
T |
A |
2: 30,217,576 (GRCm39) |
L837Q |
probably damaging |
Het |
| Or2a54 |
T |
A |
6: 43,092,905 (GRCm39) |
N76K |
possibly damaging |
Het |
| Or2ak5 |
T |
A |
11: 58,611,572 (GRCm39) |
T101S |
probably benign |
Het |
| Or7g30 |
T |
C |
9: 19,352,817 (GRCm39) |
S203P |
probably damaging |
Het |
| Or8k39 |
T |
C |
2: 86,563,302 (GRCm39) |
Y218C |
probably damaging |
Het |
| Pate10 |
A |
G |
9: 35,652,391 (GRCm39) |
Y16C |
probably damaging |
Het |
| Pde8b |
A |
T |
13: 95,226,793 (GRCm39) |
V185E |
probably benign |
Het |
| Pink1 |
G |
T |
4: 138,047,333 (GRCm39) |
A247D |
probably damaging |
Het |
| Pla2g10 |
A |
T |
16: 13,545,914 (GRCm39) |
V40D |
probably damaging |
Het |
| Plce1 |
G |
A |
19: 38,512,811 (GRCm39) |
G37R |
probably benign |
Het |
| Pld1 |
A |
G |
3: 28,166,439 (GRCm39) |
E826G |
possibly damaging |
Het |
| Poc5 |
G |
T |
13: 96,535,228 (GRCm39) |
K164N |
possibly damaging |
Het |
| Polr2b |
A |
T |
5: 77,463,761 (GRCm39) |
M53L |
probably benign |
Het |
| Ppp1r10 |
C |
T |
17: 36,239,690 (GRCm39) |
P470S |
probably damaging |
Het |
| Rasef |
A |
G |
4: 73,645,840 (GRCm39) |
S510P |
probably damaging |
Het |
| Rnf17 |
T |
A |
14: 56,722,658 (GRCm39) |
L1073Q |
probably damaging |
Het |
| Rpl13a-ps1 |
C |
T |
19: 50,018,739 (GRCm39) |
G146R |
probably damaging |
Het |
| Scn2a |
A |
G |
2: 65,518,730 (GRCm39) |
D368G |
probably damaging |
Het |
| Shc3 |
T |
A |
13: 51,634,248 (GRCm39) |
S86C |
probably benign |
Het |
| Sos1 |
T |
C |
17: 80,741,405 (GRCm39) |
H460R |
probably damaging |
Het |
| Steap1 |
T |
A |
5: 5,790,838 (GRCm39) |
M37L |
probably benign |
Het |
| Themis |
G |
T |
10: 28,673,492 (GRCm39) |
C593F |
possibly damaging |
Het |
| Tnn |
A |
G |
1: 159,937,814 (GRCm39) |
|
probably null |
Het |
| Trabd |
G |
T |
15: 88,969,667 (GRCm39) |
|
probably benign |
Het |
| Trim42 |
T |
A |
9: 97,248,047 (GRCm39) |
K216N |
probably damaging |
Het |
| Trmt44 |
G |
A |
5: 35,721,673 (GRCm39) |
P497S |
probably benign |
Het |
| Trp53bp2 |
A |
G |
1: 182,256,475 (GRCm39) |
Y15C |
probably damaging |
Het |
| Trpm7 |
T |
A |
2: 126,652,100 (GRCm39) |
I1458L |
probably benign |
Het |
| Ttc17 |
G |
T |
2: 94,237,003 (GRCm39) |
A3E |
possibly damaging |
Het |
| Ttn |
C |
A |
2: 76,704,208 (GRCm39) |
V9274L |
unknown |
Het |
| Tut7 |
T |
A |
13: 59,937,011 (GRCm39) |
Q1212L |
possibly damaging |
Het |
| Vmn2r105 |
T |
A |
17: 20,428,872 (GRCm39) |
I735F |
probably damaging |
Het |
| Vmn2r22 |
A |
G |
6: 123,614,454 (GRCm39) |
C379R |
probably damaging |
Het |
| Vmn2r97 |
G |
A |
17: 19,149,607 (GRCm39) |
E332K |
probably benign |
Het |
| Xrn1 |
A |
G |
9: 95,920,732 (GRCm39) |
T1331A |
probably benign |
Het |
|
| Other mutations in Bag6 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00333:Bag6
|
APN |
17 |
35,363,627 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00489:Bag6
|
APN |
17 |
35,363,627 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01613:Bag6
|
APN |
17 |
35,361,992 (GRCm39) |
unclassified |
probably benign |
|
|
IGL01735:Bag6
|
APN |
17 |
35,364,737 (GRCm39) |
unclassified |
probably benign |
|
|
IGL02146:Bag6
|
APN |
17 |
35,355,191 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03092:Bag6
|
APN |
17 |
35,364,603 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03377:Bag6
|
APN |
17 |
35,363,958 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Hobbit
|
UTSW |
17 |
35,364,898 (GRCm39) |
critical splice donor site |
probably null |
|
|
Hunter
|
UTSW |
17 |
35,364,214 (GRCm39) |
splice site |
probably null |
|
|
R0196:Bag6
|
UTSW |
17 |
35,363,239 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0449:Bag6
|
UTSW |
17 |
35,360,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1228:Bag6
|
UTSW |
17 |
35,364,309 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1450:Bag6
|
UTSW |
17 |
35,360,934 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1686:Bag6
|
UTSW |
17 |
35,363,928 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R1869:Bag6
|
UTSW |
17 |
35,361,802 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2034:Bag6
|
UTSW |
17 |
35,363,668 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2205:Bag6
|
UTSW |
17 |
35,363,583 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2428:Bag6
|
UTSW |
17 |
35,366,151 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2987:Bag6
|
UTSW |
17 |
35,364,661 (GRCm39) |
nonsense |
probably null |
|
|
R4691:Bag6
|
UTSW |
17 |
35,358,224 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4705:Bag6
|
UTSW |
17 |
35,361,319 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4905:Bag6
|
UTSW |
17 |
35,364,162 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5001:Bag6
|
UTSW |
17 |
35,364,152 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5168:Bag6
|
UTSW |
17 |
35,363,671 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5808:Bag6
|
UTSW |
17 |
35,365,298 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6118:Bag6
|
UTSW |
17 |
35,362,600 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6212:Bag6
|
UTSW |
17 |
35,359,278 (GRCm39) |
missense |
probably benign |
0.17 |
|
R6279:Bag6
|
UTSW |
17 |
35,357,577 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6300:Bag6
|
UTSW |
17 |
35,357,577 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6564:Bag6
|
UTSW |
17 |
35,359,347 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6783:Bag6
|
UTSW |
17 |
35,363,211 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6927:Bag6
|
UTSW |
17 |
35,364,898 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7226:Bag6
|
UTSW |
17 |
35,361,921 (GRCm39) |
missense |
unknown |
|
|
R7490:Bag6
|
UTSW |
17 |
35,359,818 (GRCm39) |
missense |
unknown |
|
|
R7499:Bag6
|
UTSW |
17 |
35,363,368 (GRCm39) |
missense |
probably benign |
0.29 |
|
R7688:Bag6
|
UTSW |
17 |
35,365,868 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8016:Bag6
|
UTSW |
17 |
35,357,733 (GRCm39) |
missense |
unknown |
|
|
R8066:Bag6
|
UTSW |
17 |
35,361,283 (GRCm39) |
missense |
unknown |
|
|
R8189:Bag6
|
UTSW |
17 |
35,364,214 (GRCm39) |
splice site |
probably null |
|
|
R8424:Bag6
|
UTSW |
17 |
35,365,830 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8542:Bag6
|
UTSW |
17 |
35,363,334 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8838:Bag6
|
UTSW |
17 |
35,363,367 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9022:Bag6
|
UTSW |
17 |
35,363,641 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9028:Bag6
|
UTSW |
17 |
35,363,130 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9128:Bag6
|
UTSW |
17 |
35,363,688 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9135:Bag6
|
UTSW |
17 |
35,362,437 (GRCm39) |
missense |
unknown |
|
|
R9186:Bag6
|
UTSW |
17 |
35,363,667 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0025:Bag6
|
UTSW |
17 |
35,365,053 (GRCm39) |
nonsense |
probably null |
|
|
Z1176:Bag6
|
UTSW |
17 |
35,358,286 (GRCm39) |
critical splice donor site |
probably null |
|
|
Z1177:Bag6
|
UTSW |
17 |
35,361,900 (GRCm39) |
missense |
unknown |
|
|
| Predicted Primers |
PCR Primer
(F):5'- GGGACTACTGTGACCATGACAG -3'
(R):5'- GTCATGCCTCCAAAACCCTG -3'
Sequencing Primer
(F):5'- CTACTGTGACCATGACAGGCAATG -3'
(R):5'- TCCAAAACCCTGCCCTGTC -3'
|
| Posted On |
2021-07-15 |
Incidental Mutation