Incidental Mutation 'R8746:Rgs8'
| ID |
663529 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Rgs8
|
| Ensembl Gene |
ENSMUSG00000042671 |
| Gene Name |
regulator of G-protein signaling 8 |
| Synonyms |
6530413N01Rik |
| MMRRC Submission |
068590-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.145)
|
| Stock # |
R8746 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
153528612-153573415 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 153547537 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 56
(S56P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000045715
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000041776]
[ENSMUST00000111810]
[ENSMUST00000111812]
[ENSMUST00000111814]
[ENSMUST00000111815]
[ENSMUST00000124500]
[ENSMUST00000147482]
[ENSMUST00000147700]
[ENSMUST00000152114]
|
| AlphaFold |
Q8BXT1 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000041776
AA Change: S56P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000045715
Gene: ENSMUSG00000042671
AA Change: S56P
| Domain | Start | End | E-Value | Type |
|---|
|
RGS
|
56 |
172 |
1.83e-53 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000111810
AA Change: S56P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000107441
Gene: ENSMUSG00000042671
AA Change: S56P
| Domain | Start | End | E-Value | Type |
|---|
|
RGS
|
56 |
172 |
1.83e-53 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000111812
AA Change: S56P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000107443
Gene: ENSMUSG00000042671
AA Change: S56P
| Domain | Start | End | E-Value | Type |
|---|
|
RGS
|
56 |
172 |
1.83e-53 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000111814
AA Change: S54P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000107445
Gene: ENSMUSG00000042671
AA Change: S54P
| Domain | Start | End | E-Value | Type |
|---|
|
RGS
|
54 |
170 |
1.83e-53 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000111815
AA Change: S54P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000107446
Gene: ENSMUSG00000042671
AA Change: S54P
| Domain | Start | End | E-Value | Type |
|---|
|
RGS
|
54 |
170 |
1.83e-53 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000124500
AA Change: S56P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000122518
Gene: ENSMUSG00000042671
AA Change: S56P
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:RGS
|
56 |
99 |
2.3e-14 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000147482
AA Change: S54P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000118365
Gene: ENSMUSG00000042671
AA Change: S54P
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:RGS
|
54 |
115 |
6.5e-19 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000147700
AA Change: S56P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000123565
Gene: ENSMUSG00000042671
AA Change: S56P
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:RGS
|
56 |
115 |
1.1e-18 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000152114
AA Change: S56P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000121910
Gene: ENSMUSG00000042671
AA Change: S56P
| Domain | Start | End | E-Value | Type |
|---|
|
RGS
|
56 |
137 |
1.52e-18 |
SMART |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.5%
|
| Validation Efficiency |
100% (52/52) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the regulator of G protein signaling (RGS) family and encodes a protein with a single RGS domain. Regulator of G protein signaling (RGS) proteins are regulatory and structural components of G protein-coupled receptor complexes. They accelerate transit through the cycle of GTP binding and hydrolysis to GDP, thereby terminating signal transduction, but paradoxically, also accelerate receptor-stimulated activation. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit normal fertility and Purkinje cell morphology. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 54 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2210408I21Rik |
T |
A |
13: 77,451,529 (GRCm39) |
M871K |
probably benign |
Het |
| 5530400C23Rik |
A |
C |
6: 133,271,256 (GRCm39) |
E100A |
possibly damaging |
Het |
| Aatf |
A |
T |
11: 84,402,338 (GRCm39) |
I116N |
probably benign |
Het |
| Abcb11 |
G |
T |
2: 69,087,754 (GRCm39) |
|
probably benign |
Het |
| Adarb2 |
G |
T |
13: 8,802,680 (GRCm39) |
A652S |
probably benign |
Het |
| Adgb |
C |
T |
10: 10,281,028 (GRCm39) |
|
probably null |
Het |
| Ankrd34a |
C |
T |
3: 96,504,791 (GRCm39) |
|
probably benign |
Het |
| Ano2 |
A |
G |
6: 125,840,513 (GRCm39) |
I395V |
probably benign |
Het |
| Cadm2 |
C |
A |
16: 66,581,696 (GRCm39) |
R203L |
probably damaging |
Het |
| Ccr2 |
T |
C |
9: 123,906,448 (GRCm39) |
F243L |
probably benign |
Het |
| Ccr4 |
A |
G |
9: 114,321,918 (GRCm39) |
V49A |
probably damaging |
Het |
| Cemip2 |
G |
A |
19: 21,803,465 (GRCm39) |
G833R |
probably damaging |
Het |
| Corin |
T |
C |
5: 72,592,695 (GRCm39) |
D234G |
probably benign |
Het |
| Drd5 |
G |
T |
5: 38,477,433 (GRCm39) |
R142I |
probably benign |
Het |
| Dsg1b |
A |
G |
18: 20,529,056 (GRCm39) |
D264G |
probably damaging |
Het |
| Ezh2 |
T |
C |
6: 47,553,534 (GRCm39) |
K61R |
probably damaging |
Het |
| Frmd4b |
T |
A |
6: 97,269,370 (GRCm39) |
T981S |
probably benign |
Het |
| Gcg |
T |
A |
2: 62,305,325 (GRCm39) |
K180N |
probably damaging |
Het |
| Gm10840 |
G |
A |
11: 106,051,742 (GRCm39) |
E23K |
unknown |
Het |
| Gm2696 |
T |
G |
10: 77,651,037 (GRCm39) |
C174W |
unknown |
Het |
| Grin2b |
T |
C |
6: 135,899,985 (GRCm39) |
I299V |
probably benign |
Het |
| Hepacam |
T |
A |
9: 37,293,030 (GRCm39) |
V207E |
probably damaging |
Het |
| Igf1r |
T |
A |
7: 67,864,745 (GRCm39) |
M1181K |
probably damaging |
Het |
| Lmo2 |
T |
C |
2: 103,806,384 (GRCm39) |
S96P |
possibly damaging |
Het |
| Marf1 |
T |
A |
16: 13,935,168 (GRCm39) |
E1533D |
probably benign |
Het |
| Megf9 |
A |
G |
4: 70,353,511 (GRCm39) |
C432R |
probably damaging |
Het |
| Mpp2 |
A |
G |
11: 101,954,040 (GRCm39) |
Y236H |
probably damaging |
Het |
| Neb |
T |
C |
2: 52,172,613 (GRCm39) |
I1565V |
probably damaging |
Het |
| Or2y1f |
A |
G |
11: 49,183,993 (GRCm39) |
|
probably benign |
Het |
| Or56b2j |
A |
T |
7: 104,353,067 (GRCm39) |
I98F |
probably damaging |
Het |
| Or5ac21 |
T |
A |
16: 59,123,973 (GRCm39) |
F152L |
probably benign |
Het |
| Or5b3 |
A |
G |
19: 13,388,092 (GRCm39) |
D53G |
probably benign |
Het |
| Or5g24-ps1 |
T |
A |
2: 85,464,221 (GRCm39) |
Y149* |
probably null |
Het |
| Or6f1 |
C |
T |
7: 85,970,437 (GRCm39) |
C241Y |
probably damaging |
Het |
| Or9k2b |
T |
C |
10: 130,016,086 (GRCm39) |
Y221C |
probably damaging |
Het |
| Patj |
T |
A |
4: 98,394,067 (GRCm39) |
|
probably benign |
Het |
| Pknox1 |
A |
T |
17: 31,809,624 (GRCm39) |
Q76L |
possibly damaging |
Het |
| Plekhg1 |
C |
A |
10: 3,907,777 (GRCm39) |
T953K |
|
Het |
| Plekhn1 |
C |
A |
4: 156,316,682 (GRCm39) |
R333L |
probably damaging |
Het |
| Plk5 |
T |
A |
10: 80,194,610 (GRCm39) |
V111D |
probably benign |
Het |
| Polr1b |
A |
G |
2: 128,954,597 (GRCm39) |
I398M |
possibly damaging |
Het |
| Ranbp3 |
T |
C |
17: 57,009,826 (GRCm39) |
V137A |
probably benign |
Het |
| Rc3h1 |
T |
A |
1: 160,757,744 (GRCm39) |
F21I |
probably damaging |
Het |
| Rhpn1 |
G |
A |
15: 75,585,425 (GRCm39) |
V593M |
probably damaging |
Het |
| Sdad1 |
A |
G |
5: 92,437,784 (GRCm39) |
S589P |
probably benign |
Het |
| Skp1 |
A |
G |
11: 52,136,843 (GRCm39) |
K163R |
probably damaging |
Het |
| Slf2 |
A |
G |
19: 44,962,063 (GRCm39) |
Y1080C |
probably damaging |
Het |
| Tcf4 |
C |
T |
18: 69,654,572 (GRCm39) |
|
probably benign |
Het |
| Tmem144 |
C |
T |
3: 79,732,655 (GRCm39) |
V208M |
probably damaging |
Het |
| Tomm34 |
A |
T |
2: 163,902,884 (GRCm39) |
L142Q |
probably benign |
Het |
| Unc13b |
T |
A |
4: 43,176,120 (GRCm39) |
V2316D |
unknown |
Het |
| Yme1l1 |
T |
A |
2: 23,052,543 (GRCm39) |
S66T |
probably benign |
Het |
| Zfc3h1 |
T |
C |
10: 115,243,885 (GRCm39) |
S739P |
probably damaging |
Het |
| Zscan25 |
T |
A |
5: 145,224,157 (GRCm39) |
V209E |
possibly damaging |
Het |
|
| Other mutations in Rgs8 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02100:Rgs8
|
APN |
1 |
153,568,469 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL02163:Rgs8
|
APN |
1 |
153,547,511 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
IGL02826:Rgs8
|
APN |
1 |
153,546,545 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03345:Rgs8
|
APN |
1 |
153,568,556 (GRCm39) |
missense |
probably benign |
0.34 |
|
R0561:Rgs8
|
UTSW |
1 |
153,541,668 (GRCm39) |
splice site |
probably null |
|
|
R0801:Rgs8
|
UTSW |
1 |
153,546,557 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3618:Rgs8
|
UTSW |
1 |
153,566,742 (GRCm39) |
missense |
probably null |
0.35 |
|
R4058:Rgs8
|
UTSW |
1 |
153,566,742 (GRCm39) |
missense |
probably null |
0.35 |
|
R4059:Rgs8
|
UTSW |
1 |
153,566,742 (GRCm39) |
missense |
probably null |
0.35 |
|
R4877:Rgs8
|
UTSW |
1 |
153,568,633 (GRCm39) |
unclassified |
probably benign |
|
|
R5070:Rgs8
|
UTSW |
1 |
153,541,650 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5841:Rgs8
|
UTSW |
1 |
153,568,574 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6028:Rgs8
|
UTSW |
1 |
153,566,734 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6413:Rgs8
|
UTSW |
1 |
153,568,619 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7682:Rgs8
|
UTSW |
1 |
153,566,668 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8951:Rgs8
|
UTSW |
1 |
153,546,567 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0028:Rgs8
|
UTSW |
1 |
153,546,592 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATCTGTAAGCTGTAGCCCCAC -3'
(R):5'- ACCAGTTTTCTCAGCAATCTGC -3'
Sequencing Primer
(F):5'- ACTTAGAGGTTTCCCCAGCTGTG -3'
(R):5'- AATCTGCTCCCCTTGCTGTG -3'
|
| Posted On |
2021-03-08 |
Incidental Mutation