Mutagenetix > Incidental Mutation

Incidental Mutation 'R2357:Gucy1a2'

247442

Institutional Source

Beutler Lab

Gene Symbol

Gucy1a2

Ensembl Gene

ENSMUSG00000041624

Gene Name

guanylate cyclase 1, soluble, alpha 2

Synonyms

6330407I18Rik, A230060L24Rik

MMRRC Submission

040339-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.311) question?

Stock #

R2357 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

3532778-3894736 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 3797299 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Leucine at position 583 (H583L)

Ref Sequence

ENSEMBL: ENSMUSP00000111398 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000115733]

AlphaFold

F8VQK3

Predicted Effect

probably damaging
Transcript: ENSMUST00000115733
AA Change: H583L

PolyPhen 2 Score 0.968 (Sensitivity: 0.77; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000111398
Gene: ENSMUSG00000041624
AA Change: H583L

Domain	Start	End	E-Value	Type
low complexity region	2	22	N/A	INTRINSIC
low complexity region	38	49	N/A	INTRINSIC
low complexity region	51	72	N/A	INTRINSIC
Pfam:HNOB	121	268	3e-19	PFAM
PDB:4GJ4\|D	316	441	1e-17	PDB
CYCc	483	674	6.58e-93	SMART
low complexity region	701	715	N/A	INTRINSIC

Meta Mutation Damage Score

0.9085

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.8%
20x: 93.3%

Validation Efficiency

97% (66/68)

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. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]
PHENOTYPE: Mice homozygous for a null mutation display normal blood vessel and platelet physiology. [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
4932414N04Rik	C	A	2: 68,569,844 (GRCm39)	T520K	possibly damaging	Het
Abca13	T	C	11: 9,247,336 (GRCm39)	L2361P	probably damaging	Het
Acsl6	T	A	11: 54,218,106 (GRCm39)	M248K	probably damaging	Het
Adam11	G	T	11: 102,665,334 (GRCm39)	V467L	probably benign	Het
Afap1	C	T	5: 36,141,618 (GRCm39)	H501Y	probably damaging	Het
Ankrd28	A	T	14: 31,486,251 (GRCm39)	Y22*	probably null	Het
Ccdc124	A	T	8: 71,321,179 (GRCm39)	L187Q	probably damaging	Het
Cdc42bpa	G	A	1: 179,894,792 (GRCm39)	S324N	possibly damaging	Het
Cgnl1	T	A	9: 71,632,950 (GRCm39)	K134*	probably null	Het
Cnpy3	G	T	17: 47,062,909 (GRCm39)	S47R	probably damaging	Het
Cpne8	A	T	15: 90,503,877 (GRCm39)	L96Q	probably damaging	Het
Crisp3	A	T	17: 40,533,396 (GRCm39)	Y212N	probably damaging	Het
Cryba1	A	T	11: 77,613,427 (GRCm39)		probably benign	Het
Cyc1	A	G	15: 76,229,766 (GRCm39)	M288V	possibly damaging	Het
Dnah8	T	A	17: 30,990,846 (GRCm39)	D3296E	probably benign	Het
Dnah8	A	G	17: 31,093,909 (GRCm39)	T4668A	probably benign	Het
Dnajb6	T	A	5: 29,958,638 (GRCm39)	F113I	probably damaging	Het
Dync2h1	A	G	9: 7,081,053 (GRCm39)	I2881T	probably benign	Het
Eps8l1	T	C	7: 4,473,354 (GRCm39)	S179P	probably benign	Het
Esco2	C	A	14: 66,064,000 (GRCm39)	A395S	probably benign	Het
Evi5l	T	C	8: 4,243,113 (GRCm39)		probably benign	Het
Exoc6b	T	C	6: 84,966,321 (GRCm39)	T218A	possibly damaging	Het
Gde1	A	T	7: 118,290,814 (GRCm39)	F170L	probably benign	Het
Ggt5	A	C	10: 75,445,075 (GRCm39)	I361L	probably benign	Het
Golga3	C	T	5: 110,350,514 (GRCm39)	T683M	probably damaging	Het
Golgb1	A	G	16: 36,732,370 (GRCm39)	Q539R	probably damaging	Het
Grm2	A	G	9: 106,524,780 (GRCm39)	V645A	probably damaging	Het
Gtf2h4	A	T	17: 35,978,891 (GRCm39)	V408D	probably damaging	Het
Hivep2	C	T	10: 14,019,043 (GRCm39)	A1938V	probably benign	Het
Iars1	T	C	13: 49,841,679 (GRCm39)	Y56H	probably damaging	Het
Il17re	A	G	6: 113,445,431 (GRCm39)	I381V	possibly damaging	Het
Klrd1	T	A	6: 129,573,872 (GRCm39)	*71K	probably null	Het
Kng1	A	T	16: 22,897,815 (GRCm39)	Y405F	possibly damaging	Het
Kptn	G	T	7: 15,859,709 (GRCm39)	C311F	probably damaging	Het
Lama5	T	C	2: 179,821,890 (GRCm39)	I2982V	probably benign	Het
Mamstr	G	T	7: 45,291,754 (GRCm39)	D35Y	probably damaging	Het
Mdc1	A	G	17: 36,158,337 (GRCm39)	D239G	probably benign	Het
Mindy3	T	G	2: 12,408,987 (GRCm39)		probably benign	Het
Mrpl39	A	T	16: 84,524,452 (GRCm39)	H204Q	probably benign	Het
Myo16	G	A	8: 10,644,905 (GRCm39)	D1746N	possibly damaging	Het
Myo5a	T	A	9: 75,108,647 (GRCm39)	M1476K	probably damaging	Het
Nol4	A	G	18: 23,172,967 (GRCm39)	S45P	probably benign	Het
Nol8	T	C	13: 49,807,980 (GRCm39)		probably null	Het
Or4f61	A	G	2: 111,922,743 (GRCm39)	I101T	possibly damaging	Het
Or5d18	A	T	2: 87,865,028 (GRCm39)	W152R	probably damaging	Het
Or6c207	C	A	10: 129,104,642 (GRCm39)	K183N	probably benign	Het
Or8b56	T	C	9: 38,739,634 (GRCm39)	S216P	probably benign	Het
Plau	T	A	14: 20,888,683 (GRCm39)	V100D	probably damaging	Het
Plpp7	T	C	2: 31,999,654 (GRCm39)	V6A	probably benign	Het
Prr14	T	C	7: 127,074,535 (GRCm39)	S356P	probably benign	Het
Rabl3	A	G	16: 37,362,293 (GRCm39)	D44G	probably null	Het
Rasa4	T	C	5: 136,120,101 (GRCm39)	V59A	probably damaging	Het
Rbm46	A	T	3: 82,771,765 (GRCm39)	D283E	probably benign	Het
Rictor	A	T	15: 6,813,043 (GRCm39)	N932I	probably damaging	Het
Rpl9-ps6	A	G	19: 32,443,743 (GRCm39)	V70A	probably benign	Het
S100a7l2	A	T	3: 90,995,733 (GRCm39)	S56R	probably benign	Het
St3gal1	A	G	15: 66,985,631 (GRCm39)	Y8H	probably benign	Het
Strn	G	A	17: 78,963,028 (GRCm39)	T745I	probably damaging	Het
Tbx15	C	T	3: 99,223,672 (GRCm39)		probably null	Het
Tbx20	T	A	9: 24,681,072 (GRCm39)	D140V	possibly damaging	Het
Ttn	A	C	2: 76,666,923 (GRCm39)	Y42*	probably null	Het
Usp9y	G	A	Y: 1,394,050 (GRCm39)	T560I	possibly damaging	Het
Vmn2r111	A	G	17: 22,778,151 (GRCm39)		probably benign	Het
Vps13d	GG	GGGGGG	4: 144,801,547 (GRCm39)		probably null	Het
Wfdc12	A	T	2: 164,032,170 (GRCm39)	I40N	probably damaging	Het
Zfp78	G	A	7: 6,382,056 (GRCm39)	G369R	probably damaging	Het

Other mutations in Gucy1a2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00549:Gucy1a2	APN	9	3,759,418 (GRCm39)	missense	probably damaging	1.00
IGL00768:Gucy1a2	APN	9	3,635,111 (GRCm39)	missense	possibly damaging	0.65
IGL00928:Gucy1a2	APN	9	3,759,777 (GRCm39)	missense	probably damaging	1.00
IGL01520:Gucy1a2	APN	9	3,759,561 (GRCm39)	missense	probably damaging	0.99
IGL01566:Gucy1a2	APN	9	3,634,661 (GRCm39)	missense	probably damaging	1.00
IGL01819:Gucy1a2	APN	9	3,865,409 (GRCm39)	nonsense	probably null
IGL01874:Gucy1a2	APN	9	3,797,343 (GRCm39)	missense	probably damaging	1.00
IGL02442:Gucy1a2	APN	9	3,865,385 (GRCm39)	missense	probably damaging	1.00
IGL02608:Gucy1a2	APN	9	3,635,113 (GRCm39)	missense	probably damaging	0.99
IGL02612:Gucy1a2	APN	9	3,894,556 (GRCm39)	missense	possibly damaging	0.74
IGL02719:Gucy1a2	APN	9	3,894,719 (GRCm39)	utr 3 prime	probably benign
IGL02823:Gucy1a2	APN	9	3,894,656 (GRCm39)	missense	possibly damaging	0.79
IGL02852:Gucy1a2	APN	9	3,759,691 (GRCm39)	missense	probably benign	0.31
IGL02892:Gucy1a2	APN	9	3,634,471 (GRCm39)	missense	probably damaging	1.00
IGL02964:Gucy1a2	APN	9	3,759,542 (GRCm39)	missense	probably damaging	0.96
Rico	UTSW	9	3,579,513 (GRCm39)	splice site	probably null
R0096:Gucy1a2	UTSW	9	3,758,928 (GRCm39)	intron	probably benign
R0417:Gucy1a2	UTSW	9	3,759,484 (GRCm39)	missense	possibly damaging	0.80
R0920:Gucy1a2	UTSW	9	3,759,472 (GRCm39)	missense	probably damaging	1.00
R1146:Gucy1a2	UTSW	9	3,759,830 (GRCm39)	missense	probably damaging	1.00
R1146:Gucy1a2	UTSW	9	3,759,830 (GRCm39)	missense	probably damaging	1.00
R1384:Gucy1a2	UTSW	9	3,759,620 (GRCm39)	missense	probably damaging	1.00
R1631:Gucy1a2	UTSW	9	3,533,052 (GRCm39)	missense	probably damaging	1.00
R1711:Gucy1a2	UTSW	9	3,759,622 (GRCm39)	missense	probably benign	0.04
R1730:Gucy1a2	UTSW	9	3,634,957 (GRCm39)	missense	probably benign	0.36
R1800:Gucy1a2	UTSW	9	3,582,685 (GRCm39)	missense	possibly damaging	0.62
R2069:Gucy1a2	UTSW	9	3,582,697 (GRCm39)	missense	probably damaging	1.00
R2166:Gucy1a2	UTSW	9	3,579,513 (GRCm39)	splice site	probably null
R3401:Gucy1a2	UTSW	9	3,635,154 (GRCm39)	missense	probably benign	0.00
R3953:Gucy1a2	UTSW	9	3,582,704 (GRCm39)	splice site	probably benign
R4420:Gucy1a2	UTSW	9	3,634,640 (GRCm39)	missense	probably damaging	1.00
R4731:Gucy1a2	UTSW	9	3,759,424 (GRCm39)	missense	probably benign	0.02
R4732:Gucy1a2	UTSW	9	3,759,424 (GRCm39)	missense	probably benign	0.02
R4733:Gucy1a2	UTSW	9	3,759,424 (GRCm39)	missense	probably benign	0.02
R4931:Gucy1a2	UTSW	9	3,759,588 (GRCm39)	missense	probably damaging	1.00
R5094:Gucy1a2	UTSW	9	3,865,443 (GRCm39)	missense	probably damaging	1.00
R5852:Gucy1a2	UTSW	9	3,865,460 (GRCm39)	missense	probably damaging	0.99
R6005:Gucy1a2	UTSW	9	3,865,518 (GRCm39)	splice site	probably null
R7667:Gucy1a2	UTSW	9	3,759,580 (GRCm39)	missense	probably damaging	1.00
R7841:Gucy1a2	UTSW	9	3,634,766 (GRCm39)	missense	probably benign	0.03
R7866:Gucy1a2	UTSW	9	3,532,804 (GRCm39)	start codon destroyed	probably null
R8525:Gucy1a2	UTSW	9	3,865,365 (GRCm39)	missense	probably damaging	1.00
R8802:Gucy1a2	UTSW	9	3,635,050 (GRCm39)	missense	probably benign	0.03
R9098:Gucy1a2	UTSW	9	3,634,489 (GRCm39)	missense	probably benign	0.00
R9127:Gucy1a2	UTSW	9	3,634,553 (GRCm39)	missense	probably damaging	1.00
Z1176:Gucy1a2	UTSW	9	3,635,156 (GRCm39)	missense	probably damaging	1.00
Z1177:Gucy1a2	UTSW	9	3,797,245 (GRCm39)	missense	probably damaging	0.97

Predicted Primers

PCR Primer
(F):5'- GCAAACTCAACTGTGATTACACTC -3'
(R):5'- CCCTGCCCTGTCTAGACTTAATATAG -3'

Sequencing Primer
(F):5'- AACTGTGATTACACTCAGTTGTG -3'
(R):5'- GGAAGTAGAATTCAGAAGGGAATTTC -3'

Posted On

2014-11-11