Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03129:Prkg1'

410245

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Prkg1

Ensembl Gene

ENSMUSG00000052920

Gene Name

protein kinase, cGMP-dependent, type I

Synonyms

Prkgr1b, Prkg1b

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.454) question?

Stock #

IGL03129

Quality Score

Status

Chromosome

Chromosomal Location

30541889-31742433 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

T to A at 30562681 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Stop codon at position 523 (K523*)

Ref Sequence

ENSEMBL: ENSMUSP00000073268 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000065067] [ENSMUST00000073581]

AlphaFold

P0C605

Predicted Effect

probably null
Transcript: ENSMUST00000065067
AA Change: K508*

SMART Domains

Protein: ENSMUSP00000067576
Gene: ENSMUSG00000052920
AA Change: K508*

Domain	Start	End	E-Value	Type
coiled coil region	5	49	N/A	INTRINSIC
cNMP	103	216	6.37e-27	SMART
cNMP	221	343	1.23e-33	SMART
S_TKc	360	619	5.25e-91	SMART
S_TK_X	620	671	1.55e-10	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000073581
AA Change: K523*

SMART Domains

Protein: ENSMUSP00000073268
Gene: ENSMUSG00000052920
AA Change: K523*

Domain	Start	End	E-Value	Type
coiled coil region	10	62	N/A	INTRINSIC
cNMP	118	231	6.37e-27	SMART
cNMP	236	358	1.23e-33	SMART
S_TKc	375	634	5.25e-91	SMART
S_TK_X	635	686	1.55e-10	SMART

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Mammals have three different isoforms of cyclic GMP-dependent protein kinase (Ialpha, Ibeta, and II). These PRKG isoforms act as key mediators of the nitric oxide/cGMP signaling pathway and are important components of many signal transduction processes in diverse cell types. This PRKG1 gene on human chromosome 10 encodes the soluble Ialpha and Ibeta isoforms of PRKG by alternative transcript splicing. A separate gene on human chromosome 4, PRKG2, encodes the membrane-bound PRKG isoform II. The PRKG1 proteins play a central role in regulating cardiovascular and neuronal functions in addition to relaxing smooth muscle tone, preventing platelet aggregation, and modulating cell growth. This gene is most strongly expressed in all types of smooth muscle, platelets, cerebellar Purkinje cells, hippocampal neurons, and the lateral amygdala. Isoforms Ialpha and Ibeta have identical cGMP-binding and catalytic domains but differ in their leucine/isoleucine zipper and autoinhibitory sequences and therefore differ in their dimerization substrates and kinase enzyme activity. [provided by RefSeq, Sep 2011]
PHENOTYPE: Mutant mice exhibit abnormal smooth muscle function and penile erectile deficiency. Conditional disruption in the hippocampus results in impaired LTP. Mice homozygous for a transposon induced allele exhibit postnatal lethality. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 27 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A930011G23Rik	A	G	5: 99,377,238 (GRCm39)	V403A	probably damaging	Het
Adpgk	T	C	9: 59,221,088 (GRCm39)	L298P	probably damaging	Het
Akap6	A	T	12: 53,187,089 (GRCm39)	D1501V	probably damaging	Het
Ank2	C	A	3: 126,749,519 (GRCm39)	E503D	probably damaging	Het
Ankhd1	T	A	18: 36,791,061 (GRCm39)	Y2478*	probably null	Het
Col6a3	A	G	1: 90,749,584 (GRCm39)	Y417H	probably damaging	Het
Csmd1	A	G	8: 16,011,521 (GRCm39)	F2511L	probably damaging	Het
Dzip3	T	C	16: 48,762,446 (GRCm39)	M602V	possibly damaging	Het
Efna2	G	A	10: 80,024,346 (GRCm39)		probably null	Het
Fzd8	T	C	18: 9,214,270 (GRCm39)	S451P	probably damaging	Het
Galntl6	A	T	8: 58,880,750 (GRCm39)	D134E	probably damaging	Het
Grid2	T	C	6: 64,040,888 (GRCm39)	S277P	probably damaging	Het
Lcn2	A	G	2: 32,277,716 (GRCm39)	V91A	possibly damaging	Het
Lrp1b	G	A	2: 41,202,478 (GRCm39)		probably benign	Het
Lrrc7	T	A	3: 157,866,696 (GRCm39)	Y1015F	probably benign	Het
Mdn1	T	A	4: 32,729,994 (GRCm39)	C2779S	possibly damaging	Het
Nlrp10	A	T	7: 108,524,118 (GRCm39)	F454Y	probably damaging	Het
Obox5	T	A	7: 15,492,684 (GRCm39)	L213Q	probably damaging	Het
Or1o2	T	A	17: 37,543,087 (GRCm39)	Y58F	probably damaging	Het
Piezo2	T	C	18: 63,248,043 (GRCm39)	M486V	probably benign	Het
Plcg1	A	C	2: 160,616,446 (GRCm39)		probably null	Het
Polr1b	G	A	2: 128,957,627 (GRCm39)	V561I	probably benign	Het
Polr3c	A	T	3: 96,626,770 (GRCm39)		probably benign	Het
Prss3l	T	C	6: 41,420,432 (GRCm39)	N98S	probably benign	Het
Sema3b	T	A	9: 107,476,995 (GRCm39)		probably benign	Het
Sp9	A	G	2: 73,103,865 (GRCm39)	T140A	probably benign	Het
Zfp507	T	C	7: 35,493,631 (GRCm39)	R471G	probably damaging	Het

Other mutations in Prkg1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00159:Prkg1	APN	19	31,279,740 (GRCm39)	missense	probably benign	0.02
IGL00481:Prkg1	APN	19	30,549,022 (GRCm39)	missense	probably benign	0.28
IGL00517:Prkg1	APN	19	30,872,068 (GRCm39)	missense	probably benign
IGL00782:Prkg1	APN	19	30,556,153 (GRCm39)	splice site	probably benign
IGL01070:Prkg1	APN	19	30,546,743 (GRCm39)	splice site	probably benign
IGL01106:Prkg1	APN	19	30,562,678 (GRCm39)	missense	probably benign	0.05
IGL01783:Prkg1	APN	19	30,602,089 (GRCm39)	missense	probably damaging	1.00
IGL02135:Prkg1	APN	19	30,970,476 (GRCm39)	missense	probably benign	0.13
IGL02492:Prkg1	APN	19	30,701,602 (GRCm39)	missense	probably damaging	1.00
IGL02543:Prkg1	APN	19	30,602,134 (GRCm39)	missense	possibly damaging	0.62
IGL02733:Prkg1	APN	19	31,279,701 (GRCm39)	missense	probably damaging	1.00
IGL03220:Prkg1	APN	19	30,546,637 (GRCm39)	utr 3 prime	probably benign
R0363:Prkg1	UTSW	19	31,641,596 (GRCm39)	missense	probably damaging	1.00
R0693:Prkg1	UTSW	19	30,572,378 (GRCm39)	missense	probably benign
R1099:Prkg1	UTSW	19	30,549,012 (GRCm39)	missense	probably benign
R1464:Prkg1	UTSW	19	30,556,270 (GRCm39)	missense	probably damaging	0.99
R1464:Prkg1	UTSW	19	30,556,270 (GRCm39)	missense	probably damaging	0.99
R1556:Prkg1	UTSW	19	30,602,143 (GRCm39)	missense	probably benign
R1738:Prkg1	UTSW	19	30,764,322 (GRCm39)	missense	possibly damaging	0.48
R1974:Prkg1	UTSW	19	31,563,095 (GRCm39)	missense	probably damaging	1.00
R2011:Prkg1	UTSW	19	31,641,542 (GRCm39)	missense	possibly damaging	0.94
R2207:Prkg1	UTSW	19	30,556,260 (GRCm39)	missense	probably damaging	1.00
R2270:Prkg1	UTSW	19	30,556,031 (GRCm39)	missense	probably benign	0.27
R3009:Prkg1	UTSW	19	31,641,512 (GRCm39)	missense	possibly damaging	0.74
R4078:Prkg1	UTSW	19	31,562,978 (GRCm39)	missense	probably damaging	1.00
R4355:Prkg1	UTSW	19	30,546,629 (GRCm39)	utr 3 prime	probably benign
R4652:Prkg1	UTSW	19	30,572,412 (GRCm39)	missense	probably damaging	1.00
R4669:Prkg1	UTSW	19	31,641,639 (GRCm39)	missense	probably damaging	0.98
R4684:Prkg1	UTSW	19	31,641,579 (GRCm39)	nonsense	probably null
R4789:Prkg1	UTSW	19	31,563,045 (GRCm39)	missense	probably damaging	0.97
R4826:Prkg1	UTSW	19	31,742,006 (GRCm39)	missense	possibly damaging	0.93
R4936:Prkg1	UTSW	19	30,563,775 (GRCm39)	missense	probably benign	0.37
R5625:Prkg1	UTSW	19	31,742,162 (GRCm39)	missense	possibly damaging	0.95
R5819:Prkg1	UTSW	19	31,563,072 (GRCm39)	missense	probably benign	0.02
R5855:Prkg1	UTSW	19	30,872,094 (GRCm39)	missense	possibly damaging	0.93
R5882:Prkg1	UTSW	19	31,563,097 (GRCm39)	missense	probably damaging	1.00
R5965:Prkg1	UTSW	19	30,701,556 (GRCm39)	splice site	probably null
R5968:Prkg1	UTSW	19	30,570,324 (GRCm39)	missense	probably damaging	1.00
R6310:Prkg1	UTSW	19	30,546,651 (GRCm39)	missense	probably damaging	1.00
R6433:Prkg1	UTSW	19	30,758,746 (GRCm39)	missense	probably benign	0.21
R6702:Prkg1	UTSW	19	30,970,484 (GRCm39)	missense	probably benign	0.00
R6750:Prkg1	UTSW	19	31,741,961 (GRCm39)	missense	probably benign	0.41
R6894:Prkg1	UTSW	19	30,602,174 (GRCm39)	nonsense	probably null
R7155:Prkg1	UTSW	19	31,279,701 (GRCm39)	missense	probably damaging	1.00
R7165:Prkg1	UTSW	19	30,562,599 (GRCm39)	missense	probably damaging	1.00
R7238:Prkg1	UTSW	19	30,602,090 (GRCm39)	missense	probably damaging	1.00
R7428:Prkg1	UTSW	19	30,556,235 (GRCm39)	missense	probably damaging	1.00
R7748:Prkg1	UTSW	19	30,970,491 (GRCm39)	missense	possibly damaging	0.90
R7804:Prkg1	UTSW	19	30,602,170 (GRCm39)	missense	possibly damaging	0.92
R7804:Prkg1	UTSW	19	30,556,032 (GRCm39)	missense	probably benign	0.00
R7893:Prkg1	UTSW	19	30,563,767 (GRCm39)	missense	probably damaging	0.99
R8304:Prkg1	UTSW	19	30,701,584 (GRCm39)	missense	possibly damaging	0.75
R8497:Prkg1	UTSW	19	31,279,709 (GRCm39)	missense	probably damaging	1.00
R8676:Prkg1	UTSW	19	31,742,146 (GRCm39)	missense	probably damaging	0.98
R9318:Prkg1	UTSW	19	30,549,038 (GRCm39)	missense	probably benign	0.09
R9694:Prkg1	UTSW	19	30,764,371 (GRCm39)	missense	possibly damaging	0.84
X0011:Prkg1	UTSW	19	30,970,521 (GRCm39)	missense	probably damaging	1.00
Z1177:Prkg1	UTSW	19	31,279,773 (GRCm39)	missense	probably damaging	0.97

Posted On

2016-08-02