Incidental Mutation 'IGL00943:Abl1'
| ID |
26930 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Abl1
|
| Ensembl Gene |
ENSMUSG00000026842 |
| Gene Name |
c-abl oncogene 1, non-receptor tyrosine kinase |
| Synonyms |
c-Abl, E430008G22Rik |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.950)
|
| Stock # |
IGL00943
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
31578388-31694239 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 31680824 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Cysteine
at position 372
(Y372C)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000075167
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028190]
[ENSMUST00000075759]
[ENSMUST00000142554]
|
| AlphaFold |
P00520 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000028190
AA Change: Y353C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000028190
Gene: ENSMUSG00000026842
AA Change: Y353C
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
5 |
23 |
N/A |
INTRINSIC |
|
SH3
|
64 |
120 |
6.95e-16 |
SMART |
|
SH2
|
125 |
208 |
6.52e-32 |
SMART |
|
TyrKc
|
242 |
493 |
4.48e-149 |
SMART |
|
low complexity region
|
698 |
703 |
N/A |
INTRINSIC |
|
low complexity region
|
802 |
810 |
N/A |
INTRINSIC |
|
low complexity region
|
883 |
907 |
N/A |
INTRINSIC |
|
low complexity region
|
949 |
960 |
N/A |
INTRINSIC |
|
low complexity region
|
964 |
983 |
N/A |
INTRINSIC |
|
FABD
|
997 |
1123 |
1.36e-63 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000075759
AA Change: Y372C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000075167
Gene: ENSMUSG00000026842
AA Change: Y372C
| Domain | Start | End | E-Value | Type |
|---|
|
SH3
|
83 |
139 |
6.95e-16 |
SMART |
|
SH2
|
144 |
227 |
6.52e-32 |
SMART |
|
TyrKc
|
261 |
512 |
4.48e-149 |
SMART |
|
low complexity region
|
717 |
722 |
N/A |
INTRINSIC |
|
low complexity region
|
821 |
829 |
N/A |
INTRINSIC |
|
low complexity region
|
902 |
926 |
N/A |
INTRINSIC |
|
low complexity region
|
968 |
979 |
N/A |
INTRINSIC |
|
low complexity region
|
983 |
1002 |
N/A |
INTRINSIC |
|
FABD
|
1016 |
1142 |
1.36e-63 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000127714
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000142554
|
| SMART Domains |
Protein: ENSMUSP00000142123
Gene: ENSMUSG00000026842
| Domain | Start | End | E-Value | Type |
|---|
|
PDB:1OPL|B
|
1 |
47 |
2e-27 |
PDB |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a protooncogene that encodes a protein tyrosine kinase involved in a variety of cellular processes, including cell division, adhesion, differentiation, and response to stress. The activity of the protein is negatively regulated by its SH3 domain, whereby deletion of the region encoding this domain results in an oncogene. The ubiquitously expressed protein has DNA-binding activity that is regulated by CDC2-mediated phosphorylation, suggesting a cell cycle function. This gene has been found fused to a variety of translocation partner genes in various leukemias, most notably the t(9;22) translocation that results in a fusion with the 5' end of the breakpoint cluster region gene (BCR; MIM:151410). Alternative splicing of this gene results in two transcript variants, which contain alternative first exons that are spliced to the remaining common exons. [provided by RefSeq, Aug 2014]
PHENOTYPE: Mice homozygous for targeted mutations that inactivate the gene have increased perinatal and postnatal mortality and may display foreshortened crania, abnormal development of spleen, head, heart and eye, reduced B and T cell populations, and osteoporosis. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 33 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Carmil1 |
C |
T |
13: 24,295,869 (GRCm39) |
V382M |
possibly damaging |
Het |
| Chkb |
A |
T |
15: 89,312,951 (GRCm39) |
V138E |
probably damaging |
Het |
| Col7a1 |
G |
T |
9: 108,806,765 (GRCm39) |
G2434* |
probably null |
Het |
| Cpa3 |
A |
G |
3: 20,282,979 (GRCm39) |
V156A |
possibly damaging |
Het |
| Dicer1 |
A |
C |
12: 104,663,031 (GRCm39) |
S1517A |
possibly damaging |
Het |
| Dnajc14 |
T |
G |
10: 128,652,675 (GRCm39) |
S578A |
possibly damaging |
Het |
| Dse |
A |
G |
10: 34,038,801 (GRCm39) |
Y201H |
probably damaging |
Het |
| Fam114a2 |
A |
T |
11: 57,405,099 (GRCm39) |
M1K |
probably null |
Het |
| Gm4847 |
A |
T |
1: 166,469,922 (GRCm39) |
S50R |
probably benign |
Het |
| Gpr156 |
A |
G |
16: 37,808,938 (GRCm39) |
Y220C |
probably damaging |
Het |
| Grxcr1 |
T |
C |
5: 68,189,638 (GRCm39) |
|
probably benign |
Het |
| Hspg2 |
T |
C |
4: 137,289,512 (GRCm39) |
V3824A |
probably benign |
Het |
| Ino80b |
A |
T |
6: 83,101,129 (GRCm39) |
L116Q |
probably damaging |
Het |
| Inpp5e |
A |
G |
2: 26,290,163 (GRCm39) |
|
probably benign |
Het |
| Lrrc8e |
T |
C |
8: 4,285,658 (GRCm39) |
C628R |
probably damaging |
Het |
| Maml1 |
A |
G |
11: 50,149,541 (GRCm39) |
V733A |
probably damaging |
Het |
| Mcm9 |
A |
G |
10: 53,424,685 (GRCm39) |
L635P |
probably damaging |
Het |
| Myh15 |
A |
T |
16: 48,986,176 (GRCm39) |
I1549F |
probably damaging |
Het |
| Myo1b |
T |
A |
1: 51,823,646 (GRCm39) |
I414F |
probably damaging |
Het |
| Nlrc3 |
T |
A |
16: 3,782,981 (GRCm39) |
I159F |
possibly damaging |
Het |
| Nvl |
A |
T |
1: 180,929,199 (GRCm39) |
D727E |
possibly damaging |
Het |
| Or1l4 |
T |
C |
2: 37,092,183 (GRCm39) |
V310A |
probably benign |
Het |
| Pgs1 |
A |
G |
11: 117,896,366 (GRCm39) |
I348V |
probably benign |
Het |
| Pkp1 |
A |
T |
1: 135,805,922 (GRCm39) |
V592E |
probably damaging |
Het |
| Setd7 |
T |
A |
3: 51,440,459 (GRCm39) |
D194V |
probably damaging |
Het |
| Slc26a7 |
T |
C |
4: 14,506,477 (GRCm39) |
D624G |
probably benign |
Het |
| Slc39a6 |
A |
G |
18: 24,722,802 (GRCm39) |
|
probably null |
Het |
| Sorbs1 |
T |
C |
19: 40,283,484 (GRCm39) |
|
probably benign |
Het |
| Tnfrsf19 |
A |
T |
14: 61,261,631 (GRCm39) |
M56K |
possibly damaging |
Het |
| Togaram2 |
C |
T |
17: 72,031,999 (GRCm39) |
R873C |
probably damaging |
Het |
| Tubgcp6 |
G |
A |
15: 89,006,600 (GRCm39) |
R141* |
probably null |
Het |
| Vill |
A |
G |
9: 118,892,380 (GRCm39) |
E337G |
probably damaging |
Het |
| Vmn1r17 |
A |
G |
6: 57,338,185 (GRCm39) |
L11S |
possibly damaging |
Het |
|
| Other mutations in Abl1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01453:Abl1
|
APN |
2 |
31,668,989 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02079:Abl1
|
APN |
2 |
31,579,960 (GRCm39) |
splice site |
probably benign |
|
|
IGL02179:Abl1
|
APN |
2 |
31,682,261 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02424:Abl1
|
APN |
2 |
31,691,144 (GRCm39) |
missense |
probably benign |
|
|
IGL02824:Abl1
|
APN |
2 |
31,690,831 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Hourglass
|
UTSW |
2 |
31,684,586 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Sands
|
UTSW |
2 |
31,669,022 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0733:Abl1
|
UTSW |
2 |
31,668,957 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1222:Abl1
|
UTSW |
2 |
31,691,006 (GRCm39) |
missense |
probably benign |
|
|
R1428:Abl1
|
UTSW |
2 |
31,691,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1582:Abl1
|
UTSW |
2 |
31,690,371 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1596:Abl1
|
UTSW |
2 |
31,680,350 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1824:Abl1
|
UTSW |
2 |
31,690,656 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2240:Abl1
|
UTSW |
2 |
31,690,517 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2251:Abl1
|
UTSW |
2 |
31,669,131 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2405:Abl1
|
UTSW |
2 |
31,690,986 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R2893:Abl1
|
UTSW |
2 |
31,687,624 (GRCm39) |
missense |
probably benign |
0.22 |
|
R3952:Abl1
|
UTSW |
2 |
31,674,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4119:Abl1
|
UTSW |
2 |
31,691,739 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4210:Abl1
|
UTSW |
2 |
31,691,708 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4809:Abl1
|
UTSW |
2 |
31,690,254 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4854:Abl1
|
UTSW |
2 |
31,669,022 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5345:Abl1
|
UTSW |
2 |
31,687,059 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5518:Abl1
|
UTSW |
2 |
31,680,754 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5551:Abl1
|
UTSW |
2 |
31,691,682 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5568:Abl1
|
UTSW |
2 |
31,669,086 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5627:Abl1
|
UTSW |
2 |
31,690,595 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6435:Abl1
|
UTSW |
2 |
31,691,561 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6492:Abl1
|
UTSW |
2 |
31,691,667 (GRCm39) |
missense |
probably benign |
0.38 |
|
R6738:Abl1
|
UTSW |
2 |
31,684,586 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7310:Abl1
|
UTSW |
2 |
31,690,604 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7398:Abl1
|
UTSW |
2 |
31,680,811 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7639:Abl1
|
UTSW |
2 |
31,669,173 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7674:Abl1
|
UTSW |
2 |
31,579,841 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R7781:Abl1
|
UTSW |
2 |
31,680,709 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7802:Abl1
|
UTSW |
2 |
31,650,438 (GRCm39) |
missense |
probably benign |
|
|
R7941:Abl1
|
UTSW |
2 |
31,579,691 (GRCm39) |
start gained |
probably benign |
|
|
R9743:Abl1
|
UTSW |
2 |
31,687,716 (GRCm39) |
missense |
probably benign |
0.34 |
|
Z1176:Abl1
|
UTSW |
2 |
31,579,839 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-04-17 |
Incidental Mutation