Mutagenetix > Incidental Mutation

Incidental Mutation 'R7061:Grk5'

548298

Institutional Source

Beutler Lab

Gene Symbol

Grk5

Ensembl Gene

ENSMUSG00000003228

Gene Name

G protein-coupled receptor kinase 5

Synonyms

Gprk5

MMRRC Submission

045384-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7061 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

60878187-61084406 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 61034530 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 93 (T93A)

Ref Sequence

ENSEMBL: ENSMUSP00000003313 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000003313]

AlphaFold

Q8VEB1

Predicted Effect

probably benign
Transcript: ENSMUST00000003313
AA Change: T93A

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000003313
Gene: ENSMUSG00000003228
AA Change: T93A

Domain	Start	End	E-Value	Type
low complexity region	18	31	N/A	INTRINSIC
RGS	52	171	1.21e-35	SMART
S_TKc	186	448	9.44e-84	SMART
S_TK_X	449	528	1.08e-9	SMART
low complexity region	561	590	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

99% (68/69)

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 their deactivation. It has also been shown to play a role in regulating the motility of polymorphonuclear leukocytes (PMNs). [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous mutation of this gene results in a decrease in thermal pain sensation. Mice homozygous for a knock-out allele exhibit decreased response of heart to induced stress. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aard	G	A	15: 51,903,617 (GRCm39)	M13I	probably benign	Het
Abcb5	A	C	12: 118,841,509 (GRCm39)	Y979D	probably damaging	Het
Adgrb1	G	C	15: 74,441,730 (GRCm39)	V4L	probably benign	Het
Ap3b2	C	T	7: 81,110,757 (GRCm39)	R1006Q	unknown	Het
Bpifa6	A	T	2: 153,834,236 (GRCm39)	T343S	probably benign	Het
Celsr3	T	A	9: 108,724,793 (GRCm39)	C2957*	probably null	Het
Chd6	G	A	2: 160,867,885 (GRCm39)	Q428*	probably null	Het
Col5a1	C	A	2: 27,915,690 (GRCm39)	C191*	probably null	Het
Cpox	A	G	16: 58,491,223 (GRCm39)	I145V	possibly damaging	Het
Csnk2a1	C	T	2: 152,116,091 (GRCm39)	R268C	probably benign	Het
Dclk2	A	G	3: 86,739,038 (GRCm39)		probably null	Het
Dennd5a	T	C	7: 109,504,386 (GRCm39)	E909G	probably benign	Het
Depdc1a	T	A	3: 159,228,489 (GRCm39)	S414T	possibly damaging	Het
Dock5	A	G	14: 68,007,703 (GRCm39)	F1502S	probably damaging	Het
Dop1b	G	T	16: 93,558,951 (GRCm39)	A448S	probably benign	Het
Dsg1c	C	A	18: 20,410,066 (GRCm39)	N511K	probably benign	Het
Epc2	G	T	2: 49,425,334 (GRCm39)	R108L	probably damaging	Het
Erp44	T	A	4: 48,219,375 (GRCm39)	I147F	probably benign	Het
Evc	T	C	5: 37,476,446 (GRCm39)	T368A	possibly damaging	Het
Fbxo41	G	T	6: 85,452,448 (GRCm39)	R738S	probably benign	Het
Fli1	T	C	9: 32,335,518 (GRCm39)	T305A	probably damaging	Het
Grm2	A	T	9: 106,528,424 (GRCm39)	N153K	probably damaging	Het
Helz	A	G	11: 107,540,003 (GRCm39)	T1007A	possibly damaging	Het
Helz2	A	G	2: 180,882,307 (GRCm39)	L162P	probably damaging	Het
Hmgcr	T	A	13: 96,802,656 (GRCm39)	Q81L	possibly damaging	Het
Hnrnpu	T	C	1: 178,163,691 (GRCm39)	K218E	unknown	Het
Hydin	A	T	8: 111,329,920 (GRCm39)	I4885F	possibly damaging	Het
Ibsp	A	G	5: 104,457,768 (GRCm39)		probably null	Het
Igfals	T	C	17: 25,099,281 (GRCm39)	L124P	probably damaging	Het
Il24	T	A	1: 130,811,108 (GRCm39)	H142L	possibly damaging	Het
Iqca1l	A	G	5: 24,750,063 (GRCm39)	M660T	probably benign	Het
Kcnh2	A	T	5: 24,536,920 (GRCm39)	H221Q	probably benign	Het
Man1a	A	G	10: 53,796,331 (GRCm39)	S454P	probably damaging	Het
Meiosin	A	T	7: 18,834,053 (GRCm39)		probably benign	Het
Mfsd4b1	C	T	10: 39,879,382 (GRCm39)	V172M	possibly damaging	Het
Mical2	T	A	7: 111,946,008 (GRCm39)	I763K	probably benign	Het
Mybpc3	A	G	2: 90,955,749 (GRCm39)	I594M	possibly damaging	Het
Neo1	T	A	9: 58,897,724 (GRCm39)	R77S	possibly damaging	Het
Nlrp6	A	G	7: 140,502,780 (GRCm39)	I265M	probably benign	Het
Or52n5	T	C	7: 104,587,883 (GRCm39)	L50P	probably damaging	Het
Or5bw2	A	G	7: 6,573,782 (GRCm39)	Y264C	probably damaging	Het
Or8b9	T	A	9: 37,766,942 (GRCm39)	V276D	possibly damaging	Het
Pcdhgb5	C	A	18: 37,864,976 (GRCm39)	P257Q	probably benign	Het
Phactr1	A	G	13: 43,286,457 (GRCm39)	D586G	probably damaging	Het
Pkn3	T	A	2: 29,973,548 (GRCm39)		probably null	Het
Prob1	A	T	18: 35,787,553 (GRCm39)	S234T	probably benign	Het
Rab14	A	T	2: 35,073,429 (GRCm39)	L131*	probably null	Het
Rab5c	G	A	11: 100,610,789 (GRCm39)	R40C	probably damaging	Het
Rhebl1	A	G	15: 98,777,164 (GRCm39)	L103P	probably damaging	Het
Rnf10	G	T	5: 115,395,149 (GRCm39)	F146L	probably damaging	Het
Rrbp1	T	C	2: 143,831,087 (GRCm39)	K360R	possibly damaging	Het
Slc6a9	C	T	4: 117,725,261 (GRCm39)	T575I	probably benign	Het
Smo	A	G	6: 29,760,229 (GRCm39)	H776R	probably damaging	Het
Speer1f	T	C	5: 11,469,071 (GRCm39)	V74A	possibly damaging	Het
Tns2	A	G	15: 102,012,914 (GRCm39)	M1V	probably null	Het
Ttn	C	A	2: 76,725,036 (GRCm39)		probably benign	Het
Ugt3a1	A	T	15: 9,306,240 (GRCm39)	M130L	probably benign	Het
Urb2	C	T	8: 124,755,036 (GRCm39)	H248Y	probably benign	Het
Vit	A	T	17: 78,932,585 (GRCm39)	N564I	probably damaging	Het
Vmn1r60	A	T	7: 5,547,310 (GRCm39)	Y263*	probably null	Het
Vmn2r16	A	T	5: 109,511,620 (GRCm39)	Y609F	probably damaging	Het
Xpo7	T	C	14: 70,908,512 (GRCm39)	I876V	probably benign	Het
Zfp442	A	G	2: 150,249,937 (GRCm39)	I655T	probably benign	Het
Zfp574	T	A	7: 24,779,622 (GRCm39)	C215S	possibly damaging	Het
Zfp608	T	C	18: 55,121,069 (GRCm39)	T173A	probably benign	Het
Zfp69	A	T	4: 120,788,598 (GRCm39)	V239D	possibly damaging	Het

Other mutations in Grk5

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02565:Grk5	APN	19	61,057,809 (GRCm39)	missense	probably damaging	0.99
IGL03183:Grk5	APN	19	61,057,774 (GRCm39)	missense	probably damaging	0.99
R0257:Grk5	UTSW	19	61,065,068 (GRCm39)	intron	probably benign
R1565:Grk5	UTSW	19	61,078,410 (GRCm39)	missense	probably damaging	0.99
R1603:Grk5	UTSW	19	61,057,800 (GRCm39)	missense	probably benign	0.06
R1672:Grk5	UTSW	19	61,074,653 (GRCm39)	splice site	probably null
R1687:Grk5	UTSW	19	61,065,221 (GRCm39)	missense	probably damaging	1.00
R1793:Grk5	UTSW	19	61,065,200 (GRCm39)	missense	probably damaging	1.00
R1822:Grk5	UTSW	19	61,078,410 (GRCm39)	missense	probably damaging	0.99
R1824:Grk5	UTSW	19	61,078,410 (GRCm39)	missense	probably damaging	0.99
R1876:Grk5	UTSW	19	61,071,663 (GRCm39)	missense	probably damaging	1.00
R4320:Grk5	UTSW	19	61,080,383 (GRCm39)	nonsense	probably null
R4828:Grk5	UTSW	19	60,976,213 (GRCm39)	nonsense	probably null
R5085:Grk5	UTSW	19	61,065,122 (GRCm39)	missense	probably damaging	1.00
R6237:Grk5	UTSW	19	61,078,380 (GRCm39)	missense	probably damaging	1.00
R6310:Grk5	UTSW	19	61,069,349 (GRCm39)	missense	probably damaging	0.96
R6736:Grk5	UTSW	19	60,879,064 (GRCm39)	missense	probably damaging	0.99
R7248:Grk5	UTSW	19	60,879,045 (GRCm39)	missense	probably benign	0.05
R7583:Grk5	UTSW	19	61,071,642 (GRCm39)	missense	possibly damaging	0.85
R7852:Grk5	UTSW	19	61,069,383 (GRCm39)	critical splice donor site	probably null
R8810:Grk5	UTSW	19	61,078,432 (GRCm39)	missense	possibly damaging	0.69
R9082:Grk5	UTSW	19	61,034,567 (GRCm39)	missense	possibly damaging	0.95
R9729:Grk5	UTSW	19	61,078,467 (GRCm39)	missense	possibly damaging	0.90

Predicted Primers

PCR Primer
(F):5'- TCACGGTTTCAGAGGTTTCAG -3'
(R):5'- CTATGGCACTCTGGAAACCAC -3'

Sequencing Primer
(F):5'- CATGTGTGGGTGAATCCATTCC -3'
(R):5'- TCTGGAAACCACAGGAAGC -3'

Posted On

2019-05-13