Incidental Mutation 'R5412:Grk4'
ID |
427526 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Grk4
|
Ensembl Gene |
ENSMUSG00000052783 |
Gene Name |
G protein-coupled receptor kinase 4 |
Synonyms |
Gprk2l, A830025H08Rik |
MMRRC Submission |
042981-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.148)
|
Stock # |
R5412 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
5 |
Chromosomal Location |
34817723-34912649 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 34902612 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Phenylalanine
at position 388
(Y388F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000001112
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000001112]
|
AlphaFold |
O70291 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000001112
AA Change: Y388F
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000001112 Gene: ENSMUSG00000052783 AA Change: Y388F
Domain | Start | End | E-Value | Type |
RGS
|
51 |
171 |
1.61e-31 |
SMART |
S_TKc
|
186 |
448 |
7.78e-85 |
SMART |
S_TK_X
|
449 |
528 |
2.98e-3 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000134217
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000153323
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.5%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor kinase subfamily of the Ser/Thr protein kinase family. The protein phosphorylates the activated forms of G protein-coupled receptors thus initiating its deactivation. This gene has been linked to both genetic and acquired hypertension. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013] PHENOTYPE: Mice heterozygous for a knock-out allele are viable, fertile and overtly normal. [provided by MGI curators]
|
Allele List at MGI |
All alleles(4) : Targeted, knock-out(1) Targeted, other(1) Gene trapped(2)
|
Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563M21Rik |
T |
A |
9: 55,886,036 (GRCm39) |
N36Y |
probably damaging |
Het |
Ankfn1 |
T |
A |
11: 89,396,007 (GRCm39) |
E246D |
probably benign |
Het |
Arid1a |
T |
C |
4: 133,446,913 (GRCm39) |
|
probably benign |
Het |
Bbs7 |
A |
T |
3: 36,653,522 (GRCm39) |
D300E |
probably benign |
Het |
C3 |
T |
C |
17: 57,527,187 (GRCm39) |
D754G |
probably benign |
Het |
Ccpg1 |
A |
T |
9: 72,917,588 (GRCm39) |
Q240L |
probably damaging |
Het |
Cdk13 |
G |
A |
13: 17,941,115 (GRCm39) |
P650S |
probably damaging |
Het |
Celsr2 |
G |
T |
3: 108,307,311 (GRCm39) |
S1933Y |
probably damaging |
Het |
Cep135 |
T |
A |
5: 76,764,709 (GRCm39) |
H562Q |
probably benign |
Het |
Cyp26a1 |
G |
T |
19: 37,689,630 (GRCm39) |
C442F |
probably damaging |
Het |
Dnah7a |
T |
C |
1: 53,674,503 (GRCm39) |
S425G |
probably benign |
Het |
Espn |
C |
T |
4: 152,212,582 (GRCm39) |
V752M |
probably damaging |
Het |
Glyr1 |
A |
G |
16: 4,854,297 (GRCm39) |
S113P |
possibly damaging |
Het |
H2-T15 |
C |
T |
17: 36,366,936 (GRCm39) |
C369Y |
probably benign |
Het |
Heca |
C |
A |
10: 17,778,044 (GRCm39) |
V518F |
probably damaging |
Het |
Hmcn2 |
C |
T |
2: 31,236,629 (GRCm39) |
P391S |
possibly damaging |
Het |
Hnrnpl |
A |
G |
7: 28,510,529 (GRCm39) |
|
probably benign |
Het |
Hsd3b2 |
A |
G |
3: 98,619,208 (GRCm39) |
S246P |
possibly damaging |
Het |
Ifna11 |
C |
T |
4: 88,738,380 (GRCm39) |
P62L |
probably damaging |
Het |
Katnal2 |
A |
T |
18: 77,090,131 (GRCm39) |
V292D |
probably damaging |
Het |
Krt16 |
T |
A |
11: 100,137,593 (GRCm39) |
I371F |
probably damaging |
Het |
Ly6g2 |
A |
T |
15: 75,089,669 (GRCm39) |
E59V |
probably damaging |
Het |
Map10 |
A |
T |
8: 126,397,724 (GRCm39) |
L372F |
probably damaging |
Het |
Megf10 |
A |
T |
18: 57,324,219 (GRCm39) |
M87L |
probably damaging |
Het |
Ncoa6 |
T |
C |
2: 155,249,701 (GRCm39) |
H1201R |
possibly damaging |
Het |
Ndc80 |
C |
A |
17: 71,821,226 (GRCm39) |
D241Y |
probably damaging |
Het |
Ndufs1 |
T |
C |
1: 63,205,508 (GRCm39) |
M94V |
possibly damaging |
Het |
Nkx2-6 |
G |
T |
14: 69,412,195 (GRCm39) |
R121L |
probably damaging |
Het |
Nos1ap |
T |
A |
1: 170,176,968 (GRCm39) |
K145M |
probably damaging |
Het |
Or6a2 |
A |
G |
7: 106,600,842 (GRCm39) |
V75A |
probably damaging |
Het |
Otop1 |
A |
G |
5: 38,455,328 (GRCm39) |
I241V |
probably benign |
Het |
Panx2 |
C |
A |
15: 88,953,135 (GRCm39) |
P542H |
possibly damaging |
Het |
Pcdha5 |
C |
A |
18: 37,095,510 (GRCm39) |
P673Q |
probably benign |
Het |
Pon1 |
A |
G |
6: 5,185,314 (GRCm39) |
L62P |
probably damaging |
Het |
Prdx6 |
A |
T |
1: 161,071,860 (GRCm39) |
I102N |
probably damaging |
Het |
Prkd3 |
T |
A |
17: 79,262,140 (GRCm39) |
I725F |
possibly damaging |
Het |
Selenon |
T |
C |
4: 134,269,749 (GRCm39) |
N395S |
probably benign |
Het |
Serpinb8 |
G |
A |
1: 107,533,616 (GRCm39) |
E224K |
probably benign |
Het |
Serpinb9b |
A |
G |
13: 33,213,496 (GRCm39) |
M18V |
probably benign |
Het |
Smc6 |
A |
G |
12: 11,335,400 (GRCm39) |
E318G |
possibly damaging |
Het |
Srrt |
A |
T |
5: 137,294,549 (GRCm39) |
Y786N |
probably damaging |
Het |
Stk36 |
G |
T |
1: 74,644,615 (GRCm39) |
|
probably null |
Het |
Stpg1 |
T |
A |
4: 135,252,786 (GRCm39) |
L179Q |
possibly damaging |
Het |
Stra8 |
G |
A |
6: 34,907,885 (GRCm39) |
M1I |
probably null |
Het |
Tiam1 |
G |
T |
16: 89,681,753 (GRCm39) |
H408Q |
possibly damaging |
Het |
Tm2d1 |
G |
A |
4: 98,253,855 (GRCm39) |
T106I |
probably damaging |
Het |
Tmem150b |
A |
C |
7: 4,719,368 (GRCm39) |
I184S |
probably null |
Het |
Vmn1r216 |
A |
G |
13: 23,284,081 (GRCm39) |
I255V |
probably benign |
Het |
Vps13b |
G |
A |
15: 35,533,531 (GRCm39) |
A868T |
probably damaging |
Het |
Wdr81 |
C |
T |
11: 75,341,620 (GRCm39) |
D1216N |
probably null |
Het |
Zfp26 |
T |
C |
9: 20,349,535 (GRCm39) |
Y343C |
possibly damaging |
Het |
Zfp276 |
A |
T |
8: 123,982,520 (GRCm39) |
I95F |
probably damaging |
Het |
Zfp330 |
T |
C |
8: 83,490,865 (GRCm39) |
E315G |
probably benign |
Het |
Zfp683 |
C |
A |
4: 133,781,862 (GRCm39) |
P56Q |
probably damaging |
Het |
Zpld1 |
T |
A |
16: 55,052,646 (GRCm39) |
S323C |
possibly damaging |
Het |
|
Other mutations in Grk4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00509:Grk4
|
APN |
5 |
34,873,634 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00574:Grk4
|
APN |
5 |
34,852,162 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02127:Grk4
|
APN |
5 |
34,867,530 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02191:Grk4
|
APN |
5 |
34,912,533 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02227:Grk4
|
APN |
5 |
34,852,126 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03152:Grk4
|
APN |
5 |
34,902,701 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03214:Grk4
|
APN |
5 |
34,909,553 (GRCm39) |
missense |
probably benign |
|
F5426:Grk4
|
UTSW |
5 |
34,902,503 (GRCm39) |
splice site |
probably benign |
|
R0110:Grk4
|
UTSW |
5 |
34,873,557 (GRCm39) |
missense |
probably damaging |
0.97 |
R0469:Grk4
|
UTSW |
5 |
34,873,557 (GRCm39) |
missense |
probably damaging |
0.97 |
R0671:Grk4
|
UTSW |
5 |
34,905,611 (GRCm39) |
missense |
probably benign |
0.04 |
R1466:Grk4
|
UTSW |
5 |
34,852,094 (GRCm39) |
missense |
probably benign |
0.02 |
R1466:Grk4
|
UTSW |
5 |
34,852,094 (GRCm39) |
missense |
probably benign |
0.02 |
R1584:Grk4
|
UTSW |
5 |
34,852,094 (GRCm39) |
missense |
probably benign |
0.02 |
R1605:Grk4
|
UTSW |
5 |
34,831,901 (GRCm39) |
missense |
probably damaging |
0.98 |
R1607:Grk4
|
UTSW |
5 |
34,888,882 (GRCm39) |
missense |
probably benign |
0.01 |
R1903:Grk4
|
UTSW |
5 |
34,833,531 (GRCm39) |
splice site |
probably null |
|
R2352:Grk4
|
UTSW |
5 |
34,826,520 (GRCm39) |
missense |
probably benign |
0.04 |
R4561:Grk4
|
UTSW |
5 |
34,852,157 (GRCm39) |
missense |
probably benign |
0.00 |
R4580:Grk4
|
UTSW |
5 |
34,818,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R4807:Grk4
|
UTSW |
5 |
34,909,552 (GRCm39) |
missense |
probably benign |
|
R5905:Grk4
|
UTSW |
5 |
34,869,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R6360:Grk4
|
UTSW |
5 |
34,831,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R6604:Grk4
|
UTSW |
5 |
34,877,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R6865:Grk4
|
UTSW |
5 |
34,888,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R7265:Grk4
|
UTSW |
5 |
34,873,608 (GRCm39) |
missense |
probably damaging |
0.96 |
R7394:Grk4
|
UTSW |
5 |
34,908,962 (GRCm39) |
missense |
probably benign |
|
R7718:Grk4
|
UTSW |
5 |
34,852,160 (GRCm39) |
missense |
probably benign |
|
R7821:Grk4
|
UTSW |
5 |
34,867,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R8074:Grk4
|
UTSW |
5 |
34,833,482 (GRCm39) |
missense |
probably benign |
0.30 |
R8218:Grk4
|
UTSW |
5 |
34,826,540 (GRCm39) |
missense |
probably benign |
0.01 |
R8499:Grk4
|
UTSW |
5 |
34,902,690 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9026:Grk4
|
UTSW |
5 |
34,877,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R9068:Grk4
|
UTSW |
5 |
34,905,653 (GRCm39) |
missense |
|
|
X0064:Grk4
|
UTSW |
5 |
34,877,228 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
Predicted Primers |
PCR Primer
(F):5'- TGCATCATTACTGCCTGGCTG -3'
(R):5'- CTTCTGAACCATCAAAAGAGAGG -3'
Sequencing Primer
(F):5'- CTGCCTGGCTGTGATTTTTAAAAAC -3'
(R):5'- GAGGTGAATTAAATGCTTCCCTGCC -3'
|
Posted On |
2016-09-01 |