Mutagenetix > Incidental Mutation

Incidental Mutation 'R6237:Grk5'

505027

Institutional Source

Beutler Lab

Gene Symbol

Grk5

Ensembl Gene

ENSMUSG00000003228

Gene Name

G protein-coupled receptor kinase 5

Synonyms

Gprk5

MMRRC Submission

044362-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6237 (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 61078380 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 479 (D479G)

Ref Sequence

ENSEMBL: ENSMUSP00000003313 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000003313] [ENSMUST00000122927]

AlphaFold

Q8VEB1

Predicted Effect

probably damaging
Transcript: ENSMUST00000003313
AA Change: D479G

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000003313
Gene: ENSMUSG00000003228
AA Change: D479G

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

Predicted Effect

probably benign
Transcript: ENSMUST00000122927

Meta Mutation Damage Score

0.8928

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.4%
20x: 95.4%

Validation Efficiency

100% (53/53)

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: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adad2	G	A	8: 120,342,502 (GRCm39)	R380H	probably damaging	Het
Akr1c12	C	A	13: 4,325,767 (GRCm39)	D109Y	possibly damaging	Het
Cacna1s	A	T	1: 136,033,582 (GRCm39)	M1020L	possibly damaging	Het
Cbx8	C	A	11: 118,931,213 (GRCm39)	R25L	possibly damaging	Het
Ccdc87	A	G	19: 4,891,407 (GRCm39)	Y633C	probably benign	Het
Col4a4	C	T	1: 82,484,752 (GRCm39)	S505N	unknown	Het
Cr2	T	A	1: 194,839,810 (GRCm39)	H539L	probably damaging	Het
Cyp2b9	T	A	7: 25,872,999 (GRCm39)	D47E	probably benign	Het
Dnah3	A	C	7: 119,608,607 (GRCm39)	M1784R	probably damaging	Het
Dnah8	T	A	17: 30,966,828 (GRCm39)	L2520*	probably null	Het
E2f2	A	G	4: 135,905,796 (GRCm39)	E103G	possibly damaging	Het
Eef1akmt3	T	A	10: 126,868,877 (GRCm39)	H199L	possibly damaging	Het
Faxc	A	T	4: 21,993,376 (GRCm39)	N340I	possibly damaging	Het
Fer1l6	A	T	15: 58,497,026 (GRCm39)	R1199*	probably null	Het
Fer1l6	A	G	15: 58,509,855 (GRCm39)	D1439G	probably damaging	Het
Galnt5	G	T	2: 57,925,261 (GRCm39)	W847C	probably damaging	Het
Gbp2	G	A	3: 142,337,793 (GRCm39)	S303N	probably benign	Het
Glipr1l1	A	T	10: 111,896,332 (GRCm39)	K40*	probably null	Het
Gm4353	A	C	7: 115,683,134 (GRCm39)	L149R	possibly damaging	Het
Gzmc	T	A	14: 56,471,486 (GRCm39)		probably null	Het
Hace1	T	C	10: 45,524,986 (GRCm39)	Y251H	probably benign	Het
Hhla1	G	T	15: 65,813,646 (GRCm39)	P229T	probably damaging	Het
Hspa1l	C	T	17: 35,196,428 (GRCm39)	Q156*	probably null	Het
Igkv4-78	A	T	6: 69,036,683 (GRCm39)	Y117N	probably benign	Het
Ikzf3	C	A	11: 98,357,879 (GRCm39)	R486L	probably damaging	Het
Itpr1	C	T	6: 108,355,164 (GRCm39)	T485M	possibly damaging	Het
Kcnab3	T	C	11: 69,219,401 (GRCm39)	Y131H	probably benign	Het
Kcnu1	C	T	8: 26,422,362 (GRCm39)	P209L	probably benign	Het
Klk1b8	T	A	7: 43,448,094 (GRCm39)	C39*	probably null	Het
Mbtps1	A	G	8: 120,255,700 (GRCm39)	L519P	probably damaging	Het
Mgat4a	A	G	1: 37,495,673 (GRCm39)	I287T	probably damaging	Het
Mindy2	T	C	9: 70,512,480 (GRCm39)	E590G	possibly damaging	Het
Mllt11	G	T	3: 95,127,602 (GRCm39)	T56K	probably benign	Het
Myo5b	G	A	18: 74,875,249 (GRCm39)	R1551H	probably damaging	Het
Nmrk2	T	C	10: 81,036,796 (GRCm39)	T16A	possibly damaging	Het
Or2ab1	T	A	11: 58,488,831 (GRCm39)	F203Y	probably damaging	Het
Or7e170	G	T	9: 19,795,365 (GRCm39)	P79T	probably damaging	Het
Osbpl9	T	C	4: 109,013,899 (GRCm39)	D65G	probably damaging	Het
Phf2	T	A	13: 48,957,131 (GRCm39)	K1079*	probably null	Het
Plcb1	A	G	2: 135,212,486 (GRCm39)	S1026G	possibly damaging	Het
Pnrc2	A	T	4: 135,599,397 (GRCm39)	H117Q	probably benign	Het
Ppfia2	A	T	10: 106,749,455 (GRCm39)	I1114F	probably damaging	Het
Rpl12	G	A	2: 32,853,000 (GRCm39)	E72K	probably benign	Het
Sbf1	C	T	15: 89,177,679 (GRCm39)	R1642H	probably benign	Het
Sephs2	G	A	7: 126,873,118 (GRCm39)		probably benign	Het
Slc35c2	A	T	2: 165,122,617 (GRCm39)	L194H	probably damaging	Het
Slfn4	T	A	11: 83,079,938 (GRCm39)	Y150N	probably damaging	Het
Srbd1	T	C	17: 86,292,723 (GRCm39)	R949G	probably damaging	Het
Urah	T	A	7: 140,415,618 (GRCm39)	S28T	probably damaging	Het
Wdr62	A	G	7: 29,941,860 (GRCm39)	S649P	probably damaging	Het
Wnk1	C	A	6: 119,929,728 (GRCm39)	G1263V	probably damaging	Het
Zbtb4	C	A	11: 69,669,069 (GRCm39)	D114E	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
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
R7061:Grk5	UTSW	19	61,034,530 (GRCm39)	missense	probably benign	0.00
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'- ACTAGAACCTGGTCCCTTTTG -3'
(R):5'- ACCCAGTGACCTTCTATGCAC -3'

Sequencing Primer
(F):5'- CCCTTTTGCGGATCTGAGAGAG -3'
(R):5'- ACTTGCACTTCCATTTTCTCTGAAC -3'

Posted On

2018-02-28