Mutagenetix > Incidental Mutation

Incidental Mutation 'R0481:Prkg2'

43358

Institutional Source

Beutler Lab

Gene Symbol

Prkg2

Ensembl Gene

ENSMUSG00000029334

Gene Name

protein kinase, cGMP-dependent, type II

Synonyms

cGK-II, Prkgr2

MMRRC Submission

038681-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.232) question?

Stock #

R0481 (G1)

Quality Score

205

Status

Validated

Chromosome

Chromosomal Location

99077632-99185042 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to T at 99142514 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000124963 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000031277] [ENSMUST00000031277] [ENSMUST00000161490] [ENSMUST00000161490]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000031277

SMART Domains

Protein: ENSMUSP00000031277
Gene: ENSMUSG00000029334

Domain	Start	End	E-Value	Type
coiled coil region	19	85	N/A	INTRINSIC
cNMP	168	284	2.82e-19	SMART
cNMP	286	409	3.02e-28	SMART
S_TKc	424	682	9.46e-75	SMART
S_TK_X	683	733	9.83e-4	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000031277

SMART Domains

Protein: ENSMUSP00000031277
Gene: ENSMUSG00000029334

Domain	Start	End	E-Value	Type
coiled coil region	19	85	N/A	INTRINSIC
cNMP	168	284	2.82e-19	SMART
cNMP	286	409	3.02e-28	SMART
S_TKc	424	682	9.46e-75	SMART
S_TK_X	683	733	9.83e-4	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000161490

SMART Domains

Protein: ENSMUSP00000124963
Gene: ENSMUSG00000029334

Domain	Start	End	E-Value	Type
coiled coil region	19	85	N/A	INTRINSIC
cNMP	168	284	2.82e-19	SMART
cNMP	286	409	3.02e-28	SMART
S_TKc	453	711	1.19e-89	SMART
S_TK_X	712	762	9.83e-4	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000161490

SMART Domains

Protein: ENSMUSP00000124963
Gene: ENSMUSG00000029334

Domain	Start	End	E-Value	Type
coiled coil region	19	85	N/A	INTRINSIC
cNMP	168	284	2.82e-19	SMART
cNMP	286	409	3.02e-28	SMART
S_TKc	453	711	1.19e-89	SMART
S_TK_X	712	762	9.83e-4	SMART

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.1%
3x: 98.3%
10x: 96.5%
20x: 93.3%

Validation Efficiency

95% (89/94)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that belongs to the serine/threonine protein kinase family of proteins. The encoded protein plays a role in the regulation of fluid balance in the intestine. A similar protein in mouse is thought to regulate differentiation and proliferation of cells in the colon. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]
PHENOTYPE: Homozygous null mice exhibit dwarfism, with abnormal skull morphology and short limbs and vertebrae. Defects in axial organization of the growth plates was evident as mice aged. Digestive secretion in response to enterotoxin was reduced. [provided by MGI curators]

Allele List at MGI

All alleles(4) : Targeted(3) Gene trapped(1)

Other mutations in this stock

Total: 87 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcg4	T	A	9: 44,190,666 (GRCm39)	N39Y	probably benign	Het
Adamts10	C	T	17: 33,768,347 (GRCm39)	Q840*	probably null	Het
Aff2	C	T	X: 68,878,248 (GRCm39)	T678I	probably damaging	Het
Ahctf1	A	G	1: 179,587,836 (GRCm39)	V1418A	probably benign	Het
Ankrd11	G	A	8: 123,626,775 (GRCm39)	R136C	probably damaging	Het
Arf5	A	G	6: 28,426,075 (GRCm39)	Y154C	probably damaging	Het
AW551984	A	G	9: 39,511,912 (GRCm39)	V33A	probably null	Het
B4galt5	A	G	2: 167,151,154 (GRCm39)	L118P	probably damaging	Het
Bcl9l	A	G	9: 44,417,979 (GRCm39)	I606V	probably benign	Het
Bdp1	A	G	13: 100,177,962 (GRCm39)	I1969T	probably benign	Het
Bicd1	A	T	6: 149,413,389 (GRCm39)	D260V	possibly damaging	Het
Cap1	A	T	4: 122,756,868 (GRCm39)	H272Q	possibly damaging	Het
Ccnk	A	G	12: 108,165,568 (GRCm39)		probably benign	Het
Cd209f	A	T	8: 4,155,558 (GRCm39)		probably null	Het
Cdk13	C	A	13: 17,894,079 (GRCm39)	A1123S	probably damaging	Het
Cdx1	C	T	18: 61,153,564 (GRCm39)	R158H	probably damaging	Het
Chd8	A	G	14: 52,474,663 (GRCm39)	S123P	probably benign	Het
Cwc22	G	A	2: 77,738,455 (GRCm39)	A497V	probably damaging	Het
Cwh43	T	C	5: 73,575,370 (GRCm39)	S296P	probably damaging	Het
Dhx38	A	T	8: 110,282,848 (GRCm39)		probably benign	Het
Dnah5	T	A	15: 28,383,745 (GRCm39)	M2989K	probably benign	Het
Dpy19l4	A	C	4: 11,272,993 (GRCm39)		probably benign	Het
F11r	A	T	1: 171,288,847 (GRCm39)	H155L	probably benign	Het
Fcgbpl1	A	T	7: 27,853,174 (GRCm39)	D1487V	probably damaging	Het
Fitm2	A	G	2: 163,311,634 (GRCm39)	V193A	probably benign	Het
Foxk1	T	A	5: 142,434,578 (GRCm39)	S281T	probably benign	Het
Furin	A	G	7: 80,043,297 (GRCm39)	C305R	probably damaging	Het
Fut8	T	A	12: 77,495,334 (GRCm39)	V308D	probably damaging	Het
Gjb3	T	A	4: 127,220,125 (GRCm39)	I136F	probably benign	Het
Glmn	A	T	5: 107,708,800 (GRCm39)	S385T	probably benign	Het
Glp1r	T	A	17: 31,150,191 (GRCm39)	M371K	probably benign	Het
Gpr179	T	C	11: 97,240,544 (GRCm39)	H293R	probably damaging	Het
H2-M11	A	T	17: 36,859,846 (GRCm39)	R280*	probably null	Het
Hadhb	T	A	5: 30,373,543 (GRCm39)	H78Q	probably damaging	Het
Hectd4	A	G	5: 121,433,569 (GRCm39)		probably benign	Het
Hexa	A	G	9: 59,462,693 (GRCm39)		probably benign	Het
Hsh2d	G	A	8: 72,954,304 (GRCm39)	D229N	probably benign	Het
Hyal6	G	A	6: 24,743,417 (GRCm39)	C371Y	probably damaging	Het
Il1rap	T	C	16: 26,511,585 (GRCm39)	Y210H	probably damaging	Het
Ino80	A	T	2: 119,261,497 (GRCm39)	H722Q	probably damaging	Het
Kcnt1	A	G	2: 25,782,508 (GRCm39)	N200S	probably damaging	Het
Kif27	T	A	13: 58,459,078 (GRCm39)		probably benign	Het
Lyst	T	C	13: 13,852,537 (GRCm39)	V2179A	probably benign	Het
Macf1	C	A	4: 123,377,815 (GRCm39)		probably null	Het
Mamdc4	A	G	2: 25,461,228 (GRCm39)	M1T	probably null	Het
Mansc4	A	G	6: 146,976,725 (GRCm39)	I297T	possibly damaging	Het
Mdn1	G	A	4: 32,767,182 (GRCm39)		probably benign	Het
Mib2	A	G	4: 155,740,519 (GRCm39)		probably benign	Het
Mon2	A	G	10: 122,849,301 (GRCm39)	V1333A	possibly damaging	Het
Ndst2	T	C	14: 20,774,536 (GRCm39)	D840G	possibly damaging	Het
Nell2	A	T	15: 95,330,563 (GRCm39)		probably null	Het
Or4c102	A	T	2: 88,422,999 (GRCm39)	I284F	probably damaging	Het
Or4k51	T	A	2: 111,584,930 (GRCm39)	M112K	probably damaging	Het
Or5g29	C	A	2: 85,421,448 (GRCm39)	A188E	possibly damaging	Het
Pde5a	C	T	3: 122,611,726 (GRCm39)		probably benign	Het
Phip	A	G	9: 82,758,769 (GRCm39)		probably benign	Het
Polr2b	A	G	5: 77,479,929 (GRCm39)	I561V	possibly damaging	Het
Ppp4r3c2	T	C	X: 88,796,299 (GRCm39)	S44P	probably damaging	Het
Prl8a6	T	C	13: 27,617,084 (GRCm39)	D201G	probably benign	Het
Ptk6	G	A	2: 180,844,320 (GRCm39)		probably benign	Het
Ptprn2	T	C	12: 117,175,466 (GRCm39)		probably benign	Het
Rdh1	G	T	10: 127,598,993 (GRCm39)	R158L	probably damaging	Het
Rhbdl3	T	C	11: 80,214,175 (GRCm39)		probably benign	Het
Rims4	A	T	2: 163,706,040 (GRCm39)	V198E	probably damaging	Het
Ripk1	T	C	13: 34,193,733 (GRCm39)	S32P	probably damaging	Het
Rnf13	T	A	3: 57,686,872 (GRCm39)	N88K	probably damaging	Het
Rnf13	C	A	3: 57,714,474 (GRCm39)	L178I	probably damaging	Het
Slc17a5	G	T	9: 78,445,584 (GRCm39)		probably null	Het
Sorcs1	A	G	19: 50,624,891 (GRCm39)		probably benign	Het
Spata31e3	T	A	13: 50,401,000 (GRCm39)	Q442L	probably benign	Het
Srpk1	G	A	17: 28,809,218 (GRCm39)		probably benign	Het
Stk10	A	G	11: 32,564,708 (GRCm39)	K840E	probably damaging	Het
Suco	A	G	1: 161,689,882 (GRCm39)		probably benign	Het
T2	G	A	17: 8,636,007 (GRCm39)		probably null	Het
Tbc1d5	A	G	17: 51,226,079 (GRCm39)	S255P	probably damaging	Het
Tenm1	T	C	X: 41,625,058 (GRCm39)	Y2254C	probably damaging	Het
Tex9	T	A	9: 72,385,678 (GRCm39)	K11*	probably null	Het
Tlr4	A	G	4: 66,746,153 (GRCm39)	I29V	probably benign	Het
Tmem255a	A	T	X: 37,288,523 (GRCm39)	V278D	probably damaging	Het
Trpc3	T	C	3: 36,678,566 (GRCm39)	I840V	probably benign	Het
Trpm3	G	A	19: 22,878,435 (GRCm39)	R622Q	possibly damaging	Het
Vmn1r214	T	A	13: 23,219,464 (GRCm39)	Y319*	probably null	Het
Vmn1r53	A	T	6: 90,200,700 (GRCm39)	V208E	probably damaging	Het
Vmn2r89	T	C	14: 51,693,577 (GRCm39)	F309S	probably damaging	Het
Xirp2	T	A	2: 67,340,253 (GRCm39)	F831L	possibly damaging	Het
Yes1	G	T	5: 32,797,749 (GRCm39)	E23*	probably null	Het
Zfp292	A	T	4: 34,810,059 (GRCm39)	M995K	probably benign	Het

Other mutations in Prkg2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00420:Prkg2	APN	5	99,172,400 (GRCm39)	missense	probably benign	0.00
IGL01063:Prkg2	APN	5	99,117,795 (GRCm39)	critical splice donor site	probably null
IGL02060:Prkg2	APN	5	99,172,374 (GRCm39)	missense	probably benign	0.32
IGL02666:Prkg2	APN	5	99,145,378 (GRCm39)	splice site	probably benign
IGL02992:Prkg2	APN	5	99,172,365 (GRCm39)	missense	probably benign
IGL03040:Prkg2	APN	5	99,120,966 (GRCm39)	critical splice donor site	probably null
devito	UTSW	5	99,114,369 (GRCm39)	critical splice donor site	probably null
Goldwyn	UTSW	5	99,090,067 (GRCm39)	missense	possibly damaging	0.86
kilmer	UTSW	5	99,095,333 (GRCm39)	missense	probably damaging	1.00
Pulp	UTSW	5	99,124,321 (GRCm39)	missense	possibly damaging	0.92
travolta	UTSW	5	99,117,839 (GRCm39)	missense	probably damaging	1.00
P0005:Prkg2	UTSW	5	99,117,806 (GRCm39)	missense	probably damaging	1.00
R0044:Prkg2	UTSW	5	99,120,989 (GRCm39)	missense	probably damaging	0.98
R0044:Prkg2	UTSW	5	99,120,989 (GRCm39)	missense	probably damaging	0.98
R0115:Prkg2	UTSW	5	99,142,514 (GRCm39)	splice site	probably null
R0403:Prkg2	UTSW	5	99,142,504 (GRCm39)	missense	possibly damaging	0.95
R0452:Prkg2	UTSW	5	99,145,379 (GRCm39)	splice site	probably benign
R1194:Prkg2	UTSW	5	99,119,785 (GRCm39)	missense	probably benign	0.00
R1534:Prkg2	UTSW	5	99,142,420 (GRCm39)	missense	probably damaging	1.00
R1861:Prkg2	UTSW	5	99,095,275 (GRCm39)	missense	probably damaging	1.00
R2010:Prkg2	UTSW	5	99,172,664 (GRCm39)	missense	probably benign
R2031:Prkg2	UTSW	5	99,172,310 (GRCm39)	missense	possibly damaging	0.85
R2176:Prkg2	UTSW	5	99,114,368 (GRCm39)	splice site	probably benign
R3607:Prkg2	UTSW	5	99,095,236 (GRCm39)	missense	probably damaging	1.00
R3958:Prkg2	UTSW	5	99,145,354 (GRCm39)	missense	possibly damaging	0.84
R3960:Prkg2	UTSW	5	99,145,354 (GRCm39)	missense	possibly damaging	0.84
R4012:Prkg2	UTSW	5	99,127,674 (GRCm39)	missense	possibly damaging	0.93
R4794:Prkg2	UTSW	5	99,114,492 (GRCm39)	missense	probably damaging	1.00
R4840:Prkg2	UTSW	5	99,129,002 (GRCm39)	missense	probably benign	0.03
R4867:Prkg2	UTSW	5	99,172,568 (GRCm39)	missense	probably benign	0.21
R5182:Prkg2	UTSW	5	99,172,568 (GRCm39)	missense	probably benign	0.21
R5226:Prkg2	UTSW	5	99,124,321 (GRCm39)	missense	possibly damaging	0.92
R5274:Prkg2	UTSW	5	99,117,850 (GRCm39)	missense	probably damaging	1.00
R5416:Prkg2	UTSW	5	99,091,326 (GRCm39)	missense	probably benign	0.05
R5531:Prkg2	UTSW	5	99,115,593 (GRCm39)	missense	probably damaging	1.00
R5619:Prkg2	UTSW	5	99,136,156 (GRCm39)	missense	probably damaging	1.00
R6264:Prkg2	UTSW	5	99,082,223 (GRCm39)	missense	probably benign	0.22
R6925:Prkg2	UTSW	5	99,114,369 (GRCm39)	critical splice donor site	probably null
R7971:Prkg2	UTSW	5	99,079,873 (GRCm39)	missense	probably damaging	1.00
R8210:Prkg2	UTSW	5	99,114,393 (GRCm39)	missense	probably damaging	1.00
R8788:Prkg2	UTSW	5	99,117,839 (GRCm39)	missense	probably damaging	1.00
R8824:Prkg2	UTSW	5	99,090,067 (GRCm39)	missense	possibly damaging	0.86
R8825:Prkg2	UTSW	5	99,090,043 (GRCm39)	missense	probably benign	0.02
R8932:Prkg2	UTSW	5	99,095,299 (GRCm39)	missense	possibly damaging	0.80
R8950:Prkg2	UTSW	5	99,119,815 (GRCm39)	missense	possibly damaging	0.54
R9026:Prkg2	UTSW	5	99,114,386 (GRCm39)	missense	probably benign
R9210:Prkg2	UTSW	5	99,095,333 (GRCm39)	missense	probably damaging	1.00
R9363:Prkg2	UTSW	5	99,172,257 (GRCm39)	missense	probably benign	0.30
R9627:Prkg2	UTSW	5	99,079,869 (GRCm39)	makesense	probably null
Z1088:Prkg2	UTSW	5	99,172,663 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- TGCAGTGGTGATTCTTAGCAGCTTC -3'
(R):5'- CCTCATGGCAAGAGCTATGCAGTG -3'

Sequencing Primer
(F):5'- GTGATTCTTAGCAGCTTCTCTCC -3'
(R):5'- ccaaagtttacatagcatctagcc -3'

Posted On

2013-05-23