Mutagenetix > Incidental Mutation

Incidental Mutation 'R7011:Gucy1a1'

545004

Institutional Source

Beutler Lab

Gene Symbol

Gucy1a1

Ensembl Gene

ENSMUSG00000033910

Gene Name

guanylate cyclase 1, soluble, alpha 1

Synonyms

sGC-alpha1, alpha 1 sGC, 1200016O07Rik

MMRRC Submission

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.163) question?

Stock #

R7011 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

82092427-82145789 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 82109115 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 189 (S189P)

Ref Sequence

ENSEMBL: ENSMUSP00000142138 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000048976] [ENSMUST00000193924]

AlphaFold

Q9ERL9

Predicted Effect

probably damaging
Transcript: ENSMUST00000048976
AA Change: S189P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000048918
Gene: ENSMUSG00000033910
AA Change: S189P

Domain	Start	End	E-Value	Type
Pfam:HNOB	85	235	2.5e-8	PFAM
PDB:4GJ4\|D	277	403	1e-18	PDB
CYCc	445	636	4.71e-103	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000193924
AA Change: S189P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000142138
Gene: ENSMUSG00000033910
AA Change: S189P

Domain	Start	End	E-Value	Type
Pfam:HNOB	73	237	1.6e-7	PFAM
PDB:4GJ4\|D	277	403	1e-18	PDB
CYCc	445	636	4.71e-103	SMART

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 98.9%

Validation Efficiency

96% (66/69)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Soluble guanylate cyclases are heterodimeric proteins that catalyze the conversion of GTP to 3',5'-cyclic GMP and pyrophosphate. The protein encoded by this gene is an alpha subunit of this complex and it interacts with a beta subunit to form the guanylate cyclase enzyme, which is activated by nitric oxide. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]
PHENOTYPE: Mice homozygous for a null mutation display mild elevation of systolic blood pressure, and abnormal blood vessel and platelet responses to NO. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam19	C	T	11: 46,143,018	P886S	probably benign	Het
Anapc1	C	T	2: 128,648,681		probably null	Het
Ankrd34c	C	A	9: 89,728,948	G447*	probably null	Het
Apbb1ip	A	T	2: 22,835,931	E238D	probably damaging	Het
Arfgap1	T	C	2: 180,972,142	L110P	probably damaging	Het
Arhgap21	G	A	2: 20,848,878	T1901I	possibly damaging	Het
Brpf1	C	A	6: 113,318,466	Q679K	probably benign	Het
Btnl2	A	G	17: 34,363,513	E351G	probably damaging	Het
Cd209f	T	A	8: 4,104,859	T80S	probably benign	Het
Cdc16	A	G	8: 13,769,451	E349G	probably damaging	Het
Cfap53	A	T	18: 74,329,493	D436V	probably benign	Het
Crhr2	A	T	6: 55,099,210		probably null	Het
Cux1	T	C	5: 136,360,033	K226E	probably damaging	Het
Ddr2	A	T	1: 169,982,103	D768E	probably damaging	Het
Dhx8	T	C	11: 101,741,520	L435P	probably damaging	Het
Dnah11	AGGCC	AGGCCGGCC	12: 117,922,018		probably null	Het
Eif4ebp1	G	A	8: 27,273,344	R55Q	probably damaging	Het
Fbxo18	T	A	2: 11,762,963	D358V	probably damaging	Het
Fra10ac1	T	A	19: 38,188,794	E304D	probably benign	Het
Gabrb2	T	C	11: 42,626,661	S399P	possibly damaging	Het
Gpatch2l	G	A	12: 86,244,184	R47H	probably damaging	Het
Gprin2	G	T	14: 34,195,436	H126N	probably null	Het
Htr1d	T	C	4: 136,443,006	M182T	probably benign	Het
Lipc	A	G	9: 70,818,954	F73L	probably benign	Het
Liph	A	G	16: 21,984,097	I74T	probably damaging	Het
Lrif1	T	G	3: 106,732,285	Y229D	probably damaging	Het
Magel2	C	T	7: 62,378,533	T395I	possibly damaging	Het
Magi3	T	C	3: 104,105,754	N139S	probably damaging	Het
Man2c1	T	A	9: 57,137,833	V336E	probably damaging	Het
Mapk12	A	T	15: 89,135,600	Y135N	probably damaging	Het
Mapkapk3	C	T	9: 107,289,396		probably benign	Het
Mast1	A	T	8: 84,911,945	Y653*	probably null	Het
Muc16	T	A	9: 18,637,451	I5849F	probably benign	Het
Muc16	T	A	9: 18,637,543	H5818L	probably benign	Het
Ndufa10	A	G	1: 92,470,859	S68P	probably damaging	Het
Nedd1	C	A	10: 92,690,773	L503F	probably benign	Het
Nr1i3	A	G	1: 171,214,358	M4V	probably benign	Het
Olfr1121	G	A	2: 87,372,260	A243T	possibly damaging	Het
Olfr1307	A	T	2: 111,944,686	F257I	probably benign	Het
Olfr1501	T	C	19: 13,839,039	I45V	probably benign	Het
Olfr332	T	A	11: 58,490,144	I204F	possibly damaging	Het
Papd7	C	T	13: 69,500,080	G489S	probably damaging	Het
Pcdh18	A	T	3: 49,754,782	S695T	probably benign	Het
Pcdha1	T	C	18: 36,930,535	I84T	probably damaging	Het
Plek	T	A	11: 16,994,760	D90V	possibly damaging	Het
Ppp6r1	A	G	7: 4,646,826	C47R	probably damaging	Het
Psg27	G	C	7: 18,556,873	N468K	probably benign	Het
Ptchd4	G	A	17: 42,503,868	E887K	probably benign	Het
Rabgap1	C	T	2: 37,540,480	L678F	probably damaging	Het
Rmdn3	T	C	2: 119,138,423	Y429C	probably damaging	Het
Ros1	A	T	10: 52,180,176	C73S	probably damaging	Het
Rtkn2	G	A	10: 67,979,665		probably benign	Het
Slc25a42	A	G	8: 70,186,702	S242P	probably damaging	Het
Smtnl1	T	A	2: 84,818,409	D167V	probably benign	Het
Smurf2	A	G	11: 106,833,784	L511P	probably benign	Het
Stbd1	A	T	5: 92,605,118	K156*	probably null	Het
Tenm4	G	T	7: 96,896,135	G2453*	probably null	Het
Tpr	A	G	1: 150,433,772	K1760E	probably damaging	Het
Triobp	T	A	15: 78,978,723	L1427Q	probably damaging	Het
Uaca	A	G	9: 60,870,368	E679G	probably damaging	Het
Ucn3	T	G	13: 3,941,421	H77P	possibly damaging	Het
Wnk2	T	A	13: 49,071,091	D998V	probably damaging	Het
Xrcc3	A	G	12: 111,804,535	V320A	probably damaging	Het
Zdbf2	A	G	1: 63,306,766	T1435A	possibly damaging	Het
Zfp36l2	G	T	17: 84,186,433	H259N	possibly damaging	Het
Zfp619	A	T	7: 39,537,762	H1072L	probably damaging	Het
Zfy2	T	A	Y: 2,107,127	E502D	possibly damaging	Het
Zfyve16	G	A	13: 92,521,987	P472L	probably benign	Het

Other mutations in Gucy1a1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00951:Gucy1a1	APN	3	82111191	missense	probably benign	0.00
IGL01626:Gucy1a1	APN	3	82108619	missense	probably damaging	1.00
IGL01662:Gucy1a1	APN	3	82109253	missense	possibly damaging	0.63
IGL02480:Gucy1a1	APN	3	82097733	missense	probably damaging	1.00
IGL02902:Gucy1a1	APN	3	82118917	missense	possibly damaging	0.87
IGL03022:Gucy1a1	APN	3	82109097	missense	probably benign	0.30
IGL03056:Gucy1a1	APN	3	82113287	missense	probably benign	0.00
IGL03089:Gucy1a1	APN	3	82097681	missense	probably damaging	1.00
IGL03226:Gucy1a1	APN	3	82119024	missense	probably benign	0.00
IGL03377:Gucy1a1	APN	3	82106015	missense	probably damaging	1.00
R0245:Gucy1a1	UTSW	3	82108787	missense	possibly damaging	0.67
R0762:Gucy1a1	UTSW	3	82094896	missense	unknown
R0907:Gucy1a1	UTSW	3	82111191	missense	probably benign	0.00
R1242:Gucy1a1	UTSW	3	82105953	splice site	probably null
R1625:Gucy1a1	UTSW	3	82102055	missense	probably benign	0.02
R1671:Gucy1a1	UTSW	3	82106222	missense	probably damaging	1.00
R2056:Gucy1a1	UTSW	3	82109285	missense	possibly damaging	0.89
R2094:Gucy1a1	UTSW	3	82113332	missense	probably benign
R2140:Gucy1a1	UTSW	3	82118886	splice site	probably null
R2154:Gucy1a1	UTSW	3	82111151	critical splice donor site	probably null
R3418:Gucy1a1	UTSW	3	82106133	missense	probably damaging	1.00
R3419:Gucy1a1	UTSW	3	82106133	missense	probably damaging	1.00
R4290:Gucy1a1	UTSW	3	82094759	missense	possibly damaging	0.95
R4291:Gucy1a1	UTSW	3	82094759	missense	possibly damaging	0.95
R4292:Gucy1a1	UTSW	3	82094759	missense	possibly damaging	0.95
R4294:Gucy1a1	UTSW	3	82094759	missense	possibly damaging	0.95
R4573:Gucy1a1	UTSW	3	82108922	missense	possibly damaging	0.95
R4629:Gucy1a1	UTSW	3	82097624	missense	probably damaging	1.00
R4755:Gucy1a1	UTSW	3	82094795	missense	probably benign	0.40
R4865:Gucy1a1	UTSW	3	82119162	utr 5 prime	probably benign
R5528:Gucy1a1	UTSW	3	82109073	missense	probably damaging	1.00
R5933:Gucy1a1	UTSW	3	82094807	missense	probably damaging	0.96
R6278:Gucy1a1	UTSW	3	82097634	missense	probably damaging	1.00
R6385:Gucy1a1	UTSW	3	82109006	missense	probably benign
R7361:Gucy1a1	UTSW	3	82097720	missense	probably damaging	1.00
R7648:Gucy1a1	UTSW	3	82108707	missense	possibly damaging	0.63
R7709:Gucy1a1	UTSW	3	82094789	missense	unknown
R7770:Gucy1a1	UTSW	3	82108805	missense	possibly damaging	0.95
R8443:Gucy1a1	UTSW	3	82097693	missense	probably damaging	1.00
R8531:Gucy1a1	UTSW	3	82111161	missense	probably benign
R8872:Gucy1a1	UTSW	3	82108742	missense	probably damaging	0.99
R9055:Gucy1a1	UTSW	3	82109126	missense	possibly damaging	0.73
R9168:Gucy1a1	UTSW	3	82102046	missense	probably damaging	0.97
R9231:Gucy1a1	UTSW	3	82106001	missense	probably damaging	1.00
R9316:Gucy1a1	UTSW	3	82108943	missense	possibly damaging	0.50

Predicted Primers

PCR Primer
(F):5'- GTACAGTCACTTCGGAAGCAGG -3'
(R):5'- CTGAGCTGACCCACTTGATG -3'

Sequencing Primer
(F):5'- GGAGGCATCAGGGACACCTC -3'
(R):5'- ACTTGATGGCCGACTGTGC -3'

Posted On

2019-05-13