Incidental Mutation 'IGL03068:Irs2'
| ID |
409766 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Irs2
|
| Ensembl Gene |
ENSMUSG00000038894 |
| Gene Name |
insulin receptor substrate 2 |
| Synonyms |
Irs-2 |
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.579)
|
| Stock # |
IGL03068
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
8 |
| Chromosomal Location |
11034681-11058458 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 11054974 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 1153
(S1153P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000038514
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000040514]
|
| AlphaFold |
P81122 |
| PDB Structure |
Crystal structure of the insulin receptor kinase in complex with IRS2 KRLB peptide [X-RAY DIFFRACTION]
Crystal structure of the insulin receptor kinase in complex with IRS2 KRLB peptide and ATP [X-RAY DIFFRACTION]
Crystal structure of the insulin receptor kinase in complex with IRS2 KRLB phosphopeptide [X-RAY DIFFRACTION]
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000040514
AA Change: S1153P
PolyPhen 2
Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000038514
Gene: ENSMUSG00000038894
AA Change: S1153P
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
18 |
N/A |
INTRINSIC |
|
low complexity region
|
19 |
28 |
N/A |
INTRINSIC |
|
PH
|
31 |
146 |
2.83e-13 |
SMART |
|
IRS
|
191 |
293 |
4.98e-38 |
SMART |
|
PTBI
|
191 |
293 |
2.24e-51 |
SMART |
|
low complexity region
|
301 |
309 |
N/A |
INTRINSIC |
|
low complexity region
|
364 |
377 |
N/A |
INTRINSIC |
|
low complexity region
|
435 |
473 |
N/A |
INTRINSIC |
|
low complexity region
|
478 |
490 |
N/A |
INTRINSIC |
|
low complexity region
|
688 |
710 |
N/A |
INTRINSIC |
|
low complexity region
|
721 |
730 |
N/A |
INTRINSIC |
|
low complexity region
|
834 |
846 |
N/A |
INTRINSIC |
|
low complexity region
|
923 |
959 |
N/A |
INTRINSIC |
|
low complexity region
|
976 |
984 |
N/A |
INTRINSIC |
|
low complexity region
|
997 |
1028 |
N/A |
INTRINSIC |
|
low complexity region
|
1137 |
1154 |
N/A |
INTRINSIC |
|
low complexity region
|
1191 |
1208 |
N/A |
INTRINSIC |
|
low complexity region
|
1274 |
1296 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000180750
|
| 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 encodes the insulin receptor substrate 2, a cytoplasmic signaling molecule that mediates effects of insulin, insulin-like growth factor 1, and other cytokines by acting as a molecular adaptor between diverse receptor tyrosine kinases and downstream effectors. The product of this gene is phosphorylated by the insulin receptor tyrosine kinase upon receptor stimulation, as well as by an interleukin 4 receptor-associated kinase in response to IL4 treatment. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous disruption of this gene results in type 2 diabetes due to insulin resistance and pancreatic beta cell dysfunction, causes defects in leptin action, energy balance, lipid homeostasis and vascular wound healing, and leads to female infertility due to hypothalamic and ovarian dysfunction. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 45 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Ago3 |
A |
G |
4: 126,311,171 (GRCm39) |
L14P |
probably damaging |
Het |
| Ak2 |
G |
T |
4: 128,901,819 (GRCm39) |
|
probably benign |
Het |
| Appbp2 |
T |
C |
11: 85,092,246 (GRCm39) |
Y311C |
probably damaging |
Het |
| Arl9 |
C |
A |
5: 77,155,225 (GRCm39) |
L119I |
possibly damaging |
Het |
| Atp1a1 |
T |
C |
3: 101,491,175 (GRCm39) |
H620R |
probably benign |
Het |
| Cfap52 |
T |
C |
11: 67,826,682 (GRCm39) |
D381G |
probably benign |
Het |
| Cngb3 |
T |
C |
4: 19,375,246 (GRCm39) |
F292S |
possibly damaging |
Het |
| Comtd1 |
G |
A |
14: 21,897,711 (GRCm39) |
R203C |
probably damaging |
Het |
| Crmp1 |
G |
T |
5: 37,422,633 (GRCm39) |
A147S |
possibly damaging |
Het |
| Csmd3 |
T |
A |
15: 47,710,517 (GRCm39) |
H1586L |
possibly damaging |
Het |
| Ctnna1 |
G |
A |
18: 35,382,785 (GRCm39) |
E644K |
possibly damaging |
Het |
| Dock3 |
T |
C |
9: 106,841,958 (GRCm39) |
D957G |
possibly damaging |
Het |
| Ear1 |
G |
T |
14: 44,056,502 (GRCm39) |
S122* |
probably null |
Het |
| Eefsec |
G |
T |
6: 88,235,209 (GRCm39) |
Q576K |
probably benign |
Het |
| Efcab5 |
T |
A |
11: 76,994,927 (GRCm39) |
I1215L |
probably benign |
Het |
| Etfa |
A |
T |
9: 55,394,766 (GRCm39) |
D160E |
probably benign |
Het |
| Exoc7 |
G |
A |
11: 116,191,960 (GRCm39) |
R197C |
possibly damaging |
Het |
| G6pc1 |
A |
G |
11: 101,261,576 (GRCm39) |
D92G |
probably benign |
Het |
| Gm3182 |
T |
A |
14: 4,483,921 (GRCm38) |
|
probably null |
Het |
| Gm4952 |
A |
G |
19: 12,601,068 (GRCm39) |
N96S |
probably damaging |
Het |
| Gpr156 |
G |
A |
16: 37,812,491 (GRCm39) |
V276M |
probably damaging |
Het |
| Kif21b |
T |
C |
1: 136,086,093 (GRCm39) |
|
probably benign |
Het |
| Lmo7 |
A |
T |
14: 102,112,928 (GRCm39) |
|
probably benign |
Het |
| Mapk4 |
G |
T |
18: 74,103,415 (GRCm39) |
N31K |
probably damaging |
Het |
| Mccc2 |
T |
C |
13: 100,100,319 (GRCm39) |
T357A |
probably damaging |
Het |
| Mpeg1 |
A |
G |
19: 12,439,570 (GRCm39) |
T343A |
probably benign |
Het |
| Myo3b |
G |
T |
2: 70,257,160 (GRCm39) |
|
probably benign |
Het |
| Pald1 |
T |
C |
10: 61,156,963 (GRCm39) |
E829G |
possibly damaging |
Het |
| Pde11a |
A |
G |
2: 75,848,208 (GRCm39) |
I873T |
probably damaging |
Het |
| Samd9l |
T |
A |
6: 3,375,348 (GRCm39) |
K638* |
probably null |
Het |
| Sema4d |
A |
G |
13: 51,862,922 (GRCm39) |
S479P |
probably damaging |
Het |
| Slc12a2 |
T |
C |
18: 58,037,407 (GRCm39) |
|
probably benign |
Het |
| Slc47a2 |
T |
C |
11: 61,194,769 (GRCm39) |
N470S |
probably damaging |
Het |
| Spag17 |
C |
T |
3: 99,987,521 (GRCm39) |
P1604S |
probably benign |
Het |
| Taf8 |
C |
A |
17: 47,812,290 (GRCm39) |
V39L |
probably damaging |
Het |
| Tlr11 |
A |
G |
14: 50,598,941 (GRCm39) |
E309G |
probably benign |
Het |
| Tmem260 |
A |
G |
14: 48,724,371 (GRCm39) |
|
probably benign |
Het |
| Tsc1 |
A |
T |
2: 28,571,270 (GRCm39) |
K816M |
probably damaging |
Het |
| Ttc29 |
A |
G |
8: 79,052,180 (GRCm39) |
I354V |
probably benign |
Het |
| Ttll3 |
A |
T |
6: 113,386,158 (GRCm39) |
N665Y |
probably damaging |
Het |
| Ubr4 |
A |
G |
4: 139,137,041 (GRCm39) |
T971A |
probably benign |
Het |
| Vmn2r96 |
T |
A |
17: 18,803,137 (GRCm39) |
I349N |
probably benign |
Het |
| Vwa5a |
A |
G |
9: 38,646,143 (GRCm39) |
T504A |
probably benign |
Het |
| Ythdf3 |
T |
A |
3: 16,258,882 (GRCm39) |
V354E |
possibly damaging |
Het |
| Zan |
C |
A |
5: 137,474,677 (GRCm39) |
G13V |
probably damaging |
Het |
|
| Other mutations in Irs2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00963:Irs2
|
APN |
8 |
11,055,867 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01328:Irs2
|
APN |
8 |
11,054,792 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01875:Irs2
|
APN |
8 |
11,056,221 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02444:Irs2
|
APN |
8 |
11,056,306 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL02448:Irs2
|
APN |
8 |
11,057,862 (GRCm39) |
missense |
probably benign |
0.21 |
|
IGL02945:Irs2
|
APN |
8 |
11,057,781 (GRCm39) |
missense |
probably damaging |
1.00 |
|
beefed
|
UTSW |
8 |
11,056,522 (GRCm39) |
nonsense |
probably null |
|
|
Dum_dum
|
UTSW |
8 |
11,037,012 (GRCm39) |
makesense |
probably null |
|
|
Lush
|
UTSW |
8 |
11,056,678 (GRCm39) |
nonsense |
probably null |
|
|
muscular
|
UTSW |
8 |
11,054,659 (GRCm39) |
nonsense |
probably null |
|
|
Plink
|
UTSW |
8 |
11,055,121 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0062:Irs2
|
UTSW |
8 |
11,055,723 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R0062:Irs2
|
UTSW |
8 |
11,055,723 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R0107:Irs2
|
UTSW |
8 |
11,054,691 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0147:Irs2
|
UTSW |
8 |
11,057,568 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0501:Irs2
|
UTSW |
8 |
11,056,396 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0565:Irs2
|
UTSW |
8 |
11,054,592 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2042:Irs2
|
UTSW |
8 |
11,057,580 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2268:Irs2
|
UTSW |
8 |
11,057,586 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2518:Irs2
|
UTSW |
8 |
11,055,352 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2762:Irs2
|
UTSW |
8 |
11,056,408 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3623:Irs2
|
UTSW |
8 |
11,057,643 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3624:Irs2
|
UTSW |
8 |
11,057,643 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5022:Irs2
|
UTSW |
8 |
11,037,012 (GRCm39) |
makesense |
probably null |
|
|
R5270:Irs2
|
UTSW |
8 |
11,056,678 (GRCm39) |
nonsense |
probably null |
|
|
R5377:Irs2
|
UTSW |
8 |
11,055,277 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5604:Irs2
|
UTSW |
8 |
11,055,007 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R6049:Irs2
|
UTSW |
8 |
11,056,805 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6219:Irs2
|
UTSW |
8 |
11,055,121 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6654:Irs2
|
UTSW |
8 |
11,056,486 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6726:Irs2
|
UTSW |
8 |
11,054,961 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R6813:Irs2
|
UTSW |
8 |
11,054,659 (GRCm39) |
nonsense |
probably null |
|
|
R6934:Irs2
|
UTSW |
8 |
11,054,697 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7261:Irs2
|
UTSW |
8 |
11,057,018 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7285:Irs2
|
UTSW |
8 |
11,056,797 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7458:Irs2
|
UTSW |
8 |
11,057,739 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7757:Irs2
|
UTSW |
8 |
11,056,522 (GRCm39) |
nonsense |
probably null |
|
|
R8347:Irs2
|
UTSW |
8 |
11,058,000 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R8348:Irs2
|
UTSW |
8 |
11,054,974 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8377:Irs2
|
UTSW |
8 |
11,054,848 (GRCm39) |
nonsense |
probably null |
|
|
R8444:Irs2
|
UTSW |
8 |
11,056,683 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8912:Irs2
|
UTSW |
8 |
11,056,655 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9229:Irs2
|
UTSW |
8 |
11,057,400 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9344:Irs2
|
UTSW |
8 |
11,057,289 (GRCm39) |
nonsense |
probably null |
|
|
R9405:Irs2
|
UTSW |
8 |
11,055,061 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9484:Irs2
|
UTSW |
8 |
11,057,334 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9736:Irs2
|
UTSW |
8 |
11,058,217 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Irs2
|
UTSW |
8 |
11,056,185 (GRCm39) |
missense |
probably damaging |
0.97 |
|
| Posted On |
2016-08-02 |
Incidental Mutation