Incidental Mutation 'R9009:Gpr158'
ID |
685483 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Gpr158
|
Ensembl Gene |
ENSMUSG00000045967 |
Gene Name |
G protein-coupled receptor 158 |
Synonyms |
5330427M13Rik |
MMRRC Submission |
068839-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R9009 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
2 |
Chromosomal Location |
21372378-21835355 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 21581760 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Valine
at position 413
(D413V)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000049708
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055946]
|
AlphaFold |
Q8C419 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000055946
AA Change: D413V
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000049708 Gene: ENSMUSG00000045967 AA Change: D413V
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
low complexity region
|
110 |
125 |
N/A |
INTRINSIC |
SCOP:d1edmb_
|
313 |
359 |
5e-4 |
SMART |
Blast:EGF
|
318 |
365 |
2e-27 |
BLAST |
Pfam:7tm_3
|
426 |
669 |
1.2e-35 |
PFAM |
low complexity region
|
840 |
863 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.1599 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
94% (58/62) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430548M08Rik |
T |
A |
8: 120,878,279 (GRCm39) |
|
probably benign |
Het |
Ahctf1 |
C |
T |
1: 179,581,171 (GRCm39) |
S1677N |
probably benign |
Het |
Ank2 |
T |
C |
3: 126,728,025 (GRCm39) |
|
probably benign |
Het |
Arid3c |
A |
T |
4: 41,729,925 (GRCm39) |
I90N |
probably benign |
Het |
Asb1 |
C |
A |
1: 91,480,205 (GRCm39) |
D301E |
unknown |
Het |
Asb1 |
T |
G |
1: 91,480,206 (GRCm39) |
*302G |
probably null |
Het |
Birc2 |
A |
T |
9: 7,833,937 (GRCm39) |
F181L |
probably benign |
Het |
Bnip1 |
T |
A |
17: 27,001,590 (GRCm39) |
|
probably benign |
Het |
Card6 |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
15: 5,128,173 (GRCm39) |
|
probably benign |
Het |
Cd2ap |
T |
C |
17: 43,116,135 (GRCm39) |
D575G |
possibly damaging |
Het |
Cdca7 |
T |
A |
2: 72,314,273 (GRCm39) |
H248Q |
probably damaging |
Het |
Chd2 |
T |
C |
7: 73,143,192 (GRCm39) |
D567G |
probably benign |
Het |
Chd2 |
T |
C |
7: 73,140,402 (GRCm39) |
I609V |
probably benign |
Het |
Cnmd |
T |
A |
14: 79,894,085 (GRCm39) |
T101S |
probably damaging |
Het |
Col6a4 |
T |
C |
9: 105,954,404 (GRCm39) |
T312A |
probably benign |
Het |
Cript |
C |
A |
17: 87,338,475 (GRCm39) |
T41N |
probably damaging |
Het |
Cts6 |
T |
C |
13: 61,344,261 (GRCm39) |
I264V |
probably benign |
Het |
Cyp4a32 |
C |
T |
4: 115,467,802 (GRCm39) |
T262I |
probably null |
Het |
D430041D05Rik |
T |
A |
2: 104,240,521 (GRCm39) |
|
probably benign |
Het |
Dctd |
C |
T |
8: 48,564,712 (GRCm39) |
P5S |
probably benign |
Het |
Det1 |
T |
C |
7: 78,492,984 (GRCm39) |
N340S |
probably benign |
Het |
Dnah7b |
A |
G |
1: 46,262,232 (GRCm39) |
N2032D |
probably benign |
Het |
Dscam |
T |
A |
16: 96,840,116 (GRCm39) |
T164S |
probably benign |
Het |
Emcn |
T |
C |
3: 137,124,775 (GRCm39) |
V196A |
possibly damaging |
Het |
Fbxo32 |
A |
G |
15: 58,046,358 (GRCm39) |
I284T |
possibly damaging |
Het |
Gimap3 |
C |
A |
6: 48,742,094 (GRCm39) |
D279Y |
possibly damaging |
Het |
Gm43302 |
C |
T |
5: 105,427,974 (GRCm39) |
D196N |
probably benign |
Het |
Gpc6 |
C |
A |
14: 117,424,217 (GRCm39) |
H102N |
possibly damaging |
Het |
Ifi207 |
T |
C |
1: 173,555,382 (GRCm39) |
R767G |
probably damaging |
Het |
Kcnip2 |
T |
C |
19: 45,800,634 (GRCm39) |
|
probably benign |
Het |
Kifap3 |
A |
C |
1: 163,696,291 (GRCm39) |
D640A |
probably damaging |
Het |
Lmbrd2 |
A |
T |
15: 9,157,311 (GRCm39) |
Q183L |
possibly damaging |
Het |
Malt1 |
A |
G |
18: 65,577,911 (GRCm39) |
I135V |
probably benign |
Het |
Mfhas1 |
T |
C |
8: 36,057,109 (GRCm39) |
V528A |
probably damaging |
Het |
Mllt10 |
T |
C |
2: 18,167,163 (GRCm39) |
S363P |
probably damaging |
Het |
Mrnip |
A |
G |
11: 50,073,323 (GRCm39) |
Y44C |
probably damaging |
Het |
Mstn |
C |
T |
1: 53,103,131 (GRCm39) |
Q156* |
probably null |
Het |
Mtmr7 |
T |
C |
8: 41,008,904 (GRCm39) |
D469G |
possibly damaging |
Het |
Muc6 |
A |
G |
7: 141,217,018 (GRCm39) |
S2552P |
possibly damaging |
Het |
Myo1f |
C |
A |
17: 33,823,662 (GRCm39) |
N1063K |
probably benign |
Het |
Or52k2 |
T |
A |
7: 102,253,642 (GRCm39) |
I27N |
probably benign |
Het |
Or5af1 |
A |
T |
11: 58,722,280 (GRCm39) |
Y100F |
probably benign |
Het |
Or6z5 |
G |
A |
7: 6,477,399 (GRCm39) |
V97M |
probably benign |
Het |
Orai2 |
A |
G |
5: 136,179,430 (GRCm39) |
V201A |
possibly damaging |
Het |
Pcdhga6 |
A |
T |
18: 37,841,878 (GRCm39) |
T533S |
possibly damaging |
Het |
Pkd1l1 |
T |
A |
11: 8,881,552 (GRCm39) |
K907N |
|
Het |
Plaat5 |
G |
T |
19: 7,614,823 (GRCm39) |
M228I |
probably benign |
Het |
Ppp1r15a |
A |
T |
7: 45,174,049 (GRCm39) |
V253E |
probably benign |
Het |
Ppp1r9b |
A |
G |
11: 94,887,467 (GRCm39) |
E493G |
probably benign |
Het |
Prdm1 |
T |
C |
10: 44,322,997 (GRCm39) |
N151S |
probably benign |
Het |
Prkcd |
C |
T |
14: 30,329,297 (GRCm39) |
A163T |
probably damaging |
Het |
Prl7a2 |
T |
A |
13: 27,849,994 (GRCm39) |
E26V |
probably damaging |
Het |
Ptprm |
A |
T |
17: 66,996,354 (GRCm39) |
N1278K |
probably damaging |
Het |
Ptprz1 |
T |
A |
6: 23,001,653 (GRCm39) |
S1248T |
possibly damaging |
Het |
Scn9a |
T |
C |
2: 66,338,927 (GRCm39) |
I1186M |
probably damaging |
Het |
Sv2a |
T |
C |
3: 96,094,409 (GRCm39) |
F248S |
probably benign |
Het |
Tas2r116 |
T |
A |
6: 132,832,963 (GRCm39) |
I188K |
probably damaging |
Het |
Tcf21 |
T |
C |
10: 22,693,671 (GRCm39) |
T169A |
probably benign |
Het |
Tecrl |
C |
A |
5: 83,432,121 (GRCm39) |
C258F |
probably damaging |
Het |
Tet2 |
T |
A |
3: 133,193,360 (GRCm39) |
E358V |
possibly damaging |
Het |
Thada |
A |
T |
17: 84,759,203 (GRCm39) |
S219T |
possibly damaging |
Het |
Tpgs2 |
T |
A |
18: 25,301,777 (GRCm39) |
|
probably benign |
Het |
Ttc6 |
A |
T |
12: 57,744,219 (GRCm39) |
I1284F |
probably damaging |
Het |
Vmn1r160 |
T |
C |
7: 22,571,127 (GRCm39) |
V160A |
possibly damaging |
Het |
Vmn1r44 |
T |
C |
6: 89,870,671 (GRCm39) |
L139P |
probably damaging |
Het |
|
Other mutations in Gpr158 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00340:Gpr158
|
APN |
2 |
21,373,494 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00469:Gpr158
|
APN |
2 |
21,751,606 (GRCm39) |
splice site |
probably benign |
|
IGL00706:Gpr158
|
APN |
2 |
21,751,584 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00780:Gpr158
|
APN |
2 |
21,831,629 (GRCm39) |
nonsense |
probably null |
|
IGL00885:Gpr158
|
APN |
2 |
21,653,832 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01339:Gpr158
|
APN |
2 |
21,373,842 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01368:Gpr158
|
APN |
2 |
21,831,909 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02141:Gpr158
|
APN |
2 |
21,788,101 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02455:Gpr158
|
APN |
2 |
21,373,511 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02554:Gpr158
|
APN |
2 |
21,831,407 (GRCm39) |
missense |
probably benign |
|
IGL02681:Gpr158
|
APN |
2 |
21,820,441 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02752:Gpr158
|
APN |
2 |
21,831,638 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02756:Gpr158
|
APN |
2 |
21,831,890 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03181:Gpr158
|
APN |
2 |
21,787,972 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03258:Gpr158
|
APN |
2 |
21,830,085 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03386:Gpr158
|
APN |
2 |
21,831,057 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4810001:Gpr158
|
UTSW |
2 |
21,831,682 (GRCm39) |
missense |
probably benign |
0.01 |
R0071:Gpr158
|
UTSW |
2 |
21,815,479 (GRCm39) |
missense |
probably benign |
0.08 |
R0081:Gpr158
|
UTSW |
2 |
21,831,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R0528:Gpr158
|
UTSW |
2 |
21,830,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R0560:Gpr158
|
UTSW |
2 |
21,830,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R0603:Gpr158
|
UTSW |
2 |
21,820,480 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1560:Gpr158
|
UTSW |
2 |
21,831,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R1561:Gpr158
|
UTSW |
2 |
21,820,505 (GRCm39) |
splice site |
probably null |
|
R1609:Gpr158
|
UTSW |
2 |
21,788,104 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1741:Gpr158
|
UTSW |
2 |
21,832,359 (GRCm39) |
missense |
probably benign |
0.00 |
R1827:Gpr158
|
UTSW |
2 |
21,832,129 (GRCm39) |
missense |
probably benign |
|
R1854:Gpr158
|
UTSW |
2 |
21,373,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R1871:Gpr158
|
UTSW |
2 |
21,820,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Gpr158
|
UTSW |
2 |
21,832,325 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2273:Gpr158
|
UTSW |
2 |
21,831,674 (GRCm39) |
missense |
probably benign |
|
R2275:Gpr158
|
UTSW |
2 |
21,831,674 (GRCm39) |
missense |
probably benign |
|
R3004:Gpr158
|
UTSW |
2 |
21,831,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R3151:Gpr158
|
UTSW |
2 |
21,581,771 (GRCm39) |
missense |
possibly damaging |
0.68 |
R3943:Gpr158
|
UTSW |
2 |
21,373,370 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4238:Gpr158
|
UTSW |
2 |
21,373,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R4379:Gpr158
|
UTSW |
2 |
21,830,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R4381:Gpr158
|
UTSW |
2 |
21,832,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R4464:Gpr158
|
UTSW |
2 |
21,831,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R4467:Gpr158
|
UTSW |
2 |
21,831,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R4496:Gpr158
|
UTSW |
2 |
21,831,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R4506:Gpr158
|
UTSW |
2 |
21,831,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R4530:Gpr158
|
UTSW |
2 |
21,373,811 (GRCm39) |
missense |
probably benign |
0.03 |
R4646:Gpr158
|
UTSW |
2 |
21,831,864 (GRCm39) |
missense |
probably benign |
|
R4798:Gpr158
|
UTSW |
2 |
21,787,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R4882:Gpr158
|
UTSW |
2 |
21,830,059 (GRCm39) |
missense |
probably damaging |
0.98 |
R4943:Gpr158
|
UTSW |
2 |
21,831,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R5334:Gpr158
|
UTSW |
2 |
21,832,316 (GRCm39) |
missense |
probably benign |
0.01 |
R5560:Gpr158
|
UTSW |
2 |
21,831,101 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5600:Gpr158
|
UTSW |
2 |
21,832,046 (GRCm39) |
missense |
probably benign |
|
R5637:Gpr158
|
UTSW |
2 |
21,788,083 (GRCm39) |
missense |
probably benign |
0.00 |
R5701:Gpr158
|
UTSW |
2 |
21,751,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R5744:Gpr158
|
UTSW |
2 |
21,373,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R5911:Gpr158
|
UTSW |
2 |
21,373,932 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5991:Gpr158
|
UTSW |
2 |
21,373,319 (GRCm39) |
missense |
probably damaging |
0.99 |
R6200:Gpr158
|
UTSW |
2 |
21,404,227 (GRCm39) |
missense |
probably damaging |
0.97 |
R6306:Gpr158
|
UTSW |
2 |
21,820,422 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6324:Gpr158
|
UTSW |
2 |
21,815,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R6384:Gpr158
|
UTSW |
2 |
21,831,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R6698:Gpr158
|
UTSW |
2 |
21,831,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R6997:Gpr158
|
UTSW |
2 |
21,653,802 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7086:Gpr158
|
UTSW |
2 |
21,831,386 (GRCm39) |
missense |
probably benign |
0.01 |
R7175:Gpr158
|
UTSW |
2 |
21,373,113 (GRCm39) |
missense |
probably benign |
0.13 |
R7197:Gpr158
|
UTSW |
2 |
21,815,412 (GRCm39) |
missense |
probably damaging |
0.99 |
R7293:Gpr158
|
UTSW |
2 |
21,581,750 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7427:Gpr158
|
UTSW |
2 |
21,832,129 (GRCm39) |
missense |
probably benign |
|
R7515:Gpr158
|
UTSW |
2 |
21,373,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R7730:Gpr158
|
UTSW |
2 |
21,831,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R8122:Gpr158
|
UTSW |
2 |
21,831,674 (GRCm39) |
missense |
probably benign |
|
R8311:Gpr158
|
UTSW |
2 |
21,373,701 (GRCm39) |
missense |
probably benign |
0.00 |
R8754:Gpr158
|
UTSW |
2 |
21,581,693 (GRCm39) |
missense |
probably benign |
0.00 |
R8782:Gpr158
|
UTSW |
2 |
21,404,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R8792:Gpr158
|
UTSW |
2 |
21,558,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R8842:Gpr158
|
UTSW |
2 |
21,581,751 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9102:Gpr158
|
UTSW |
2 |
21,830,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R9150:Gpr158
|
UTSW |
2 |
21,831,251 (GRCm39) |
missense |
probably benign |
0.17 |
R9254:Gpr158
|
UTSW |
2 |
21,373,042 (GRCm39) |
start gained |
probably benign |
|
R9317:Gpr158
|
UTSW |
2 |
21,832,037 (GRCm39) |
missense |
probably benign |
|
R9379:Gpr158
|
UTSW |
2 |
21,373,042 (GRCm39) |
start gained |
probably benign |
|
R9428:Gpr158
|
UTSW |
2 |
21,787,972 (GRCm39) |
missense |
probably benign |
|
R9497:Gpr158
|
UTSW |
2 |
21,831,825 (GRCm39) |
missense |
probably benign |
0.00 |
R9667:Gpr158
|
UTSW |
2 |
21,830,054 (GRCm39) |
missense |
probably damaging |
0.99 |
R9681:Gpr158
|
UTSW |
2 |
21,831,315 (GRCm39) |
missense |
probably damaging |
0.99 |
X0062:Gpr158
|
UTSW |
2 |
21,831,180 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Gpr158
|
UTSW |
2 |
21,815,501 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Gpr158
|
UTSW |
2 |
21,832,083 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
Predicted Primers |
PCR Primer
(F):5'- GGTGAAGGTCTAACTCTCTTCTCTC -3'
(R):5'- CTCAACCAATCACATTGTAGGATG -3'
Sequencing Primer
(F):5'- TCTCTTCTCTCTCACTTACTTTAGAG -3'
(R):5'- GTATGTTTACTAGAACAGTAATGGGG -3'
|
Posted On |
2021-10-11 |