Mutagenetix > Incidental Mutation

Incidental Mutation 'R4888:Gnas'

377056

Institutional Source

Beutler Lab

Gene Symbol

Gnas

Ensembl Gene

ENSMUSG00000027523

Gene Name

GNAS complex locus

Synonyms

P2, Gnasxl, Gnas1, Nesp, neuroendocrine-specific Golgi protein p55 isoform 1, XLalphas, Gsa, Oedsml, Gs alpha, Nesp55, Galphas, Nespl, SCG6, Gs-alpha, P1, P3, G alpha s

MMRRC Submission

042493-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R4888 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

174126113-174188537 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 174139882 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Arginine at position 17 (K17R)

Ref Sequence

ENSEMBL: ENSMUSP00000139839 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080493] [ENSMUST00000087876] [ENSMUST00000087877] [ENSMUST00000109088] [ENSMUST00000109095] [ENSMUST00000109096] [ENSMUST00000130761] [ENSMUST00000186907] [ENSMUST00000185956] [ENSMUST00000130940] [ENSMUST00000180362]

AlphaFold

Q6R0H7

Predicted Effect

silent
Transcript: ENSMUST00000080493

SMART Domains

Protein: ENSMUSP00000079341
Gene: ENSMUSG00000027523

Domain	Start	End	E-Value	Type
low complexity region	19	48	N/A	INTRINSIC
internal_repeat_1	89	166	3.02e-8	PROSPERO
internal_repeat_1	209	276	3.02e-8	PROSPERO
low complexity region	350	365	N/A	INTRINSIC
low complexity region	391	404	N/A	INTRINSIC
low complexity region	459	477	N/A	INTRINSIC
low complexity region	480	498	N/A	INTRINSIC
low complexity region	515	525	N/A	INTRINSIC
low complexity region	535	570	N/A	INTRINSIC
low complexity region	576	626	N/A	INTRINSIC
low complexity region	633	643	N/A	INTRINSIC
low complexity region	659	678	N/A	INTRINSIC
low complexity region	685	696	N/A	INTRINSIC
G_alpha	759	1132	5.01e-185	SMART

Predicted Effect

silent
Transcript: ENSMUST00000087876

SMART Domains

Protein: ENSMUSP00000085184
Gene: ENSMUSG00000027523

Domain	Start	End	E-Value	Type
low complexity region	19	48	N/A	INTRINSIC
internal_repeat_1	89	166	2.42e-8	PROSPERO
internal_repeat_1	209	276	2.42e-8	PROSPERO
low complexity region	350	365	N/A	INTRINSIC
low complexity region	391	404	N/A	INTRINSIC
low complexity region	459	477	N/A	INTRINSIC
low complexity region	480	498	N/A	INTRINSIC
low complexity region	515	525	N/A	INTRINSIC
low complexity region	535	570	N/A	INTRINSIC
low complexity region	576	626	N/A	INTRINSIC
low complexity region	633	643	N/A	INTRINSIC
low complexity region	659	678	N/A	INTRINSIC
low complexity region	685	696	N/A	INTRINSIC
G_alpha	759	1118	8.32e-191	SMART

Predicted Effect

silent
Transcript: ENSMUST00000087877

SMART Domains

Protein: ENSMUSP00000085185
Gene: ENSMUSG00000027523

Domain	Start	End	E-Value	Type
low complexity region	19	48	N/A	INTRINSIC
internal_repeat_1	89	166	1.1e-8	PROSPERO
internal_repeat_1	209	276	1.1e-8	PROSPERO
low complexity region	350	365	N/A	INTRINSIC
low complexity region	391	404	N/A	INTRINSIC
low complexity region	459	477	N/A	INTRINSIC
low complexity region	480	498	N/A	INTRINSIC
low complexity region	515	525	N/A	INTRINSIC
low complexity region	535	570	N/A	INTRINSIC
low complexity region	576	626	N/A	INTRINSIC
low complexity region	633	643	N/A	INTRINSIC
low complexity region	659	678	N/A	INTRINSIC
low complexity region	685	696	N/A	INTRINSIC
Blast:G_alpha	759	799	2e-14	BLAST
low complexity region	802	816	N/A	INTRINSIC
low complexity region	847	859	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000109088
AA Change: K17R

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000104716
Gene: ENSMUSG00000027523
AA Change: K17R

Domain	Start	End	E-Value	Type
low complexity region	192	209	N/A	INTRINSIC
low complexity region	336	352	N/A	INTRINSIC
low complexity region	402	415	N/A	INTRINSIC
low complexity region	421	446	N/A	INTRINSIC
low complexity region	459	481	N/A	INTRINSIC
low complexity region	493	510	N/A	INTRINSIC
low complexity region	529	599	N/A	INTRINSIC
low complexity region	643	658	N/A	INTRINSIC
low complexity region	700	716	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000109095

SMART Domains

Protein: ENSMUSP00000104723
Gene: ENSMUSG00000027523

Domain	Start	End	E-Value	Type
Pfam:NESP55	1	253	1.2e-157	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000109096

SMART Domains

Protein: ENSMUSP00000104724
Gene: ENSMUSG00000027523

Domain	Start	End	E-Value	Type
Pfam:NESP55	1	253	1.2e-157	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000130761

Predicted Effect

possibly damaging
Transcript: ENSMUST00000186907
AA Change: K17R

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000139839
Gene: ENSMUSG00000027523
AA Change: K17R

Domain	Start	End	E-Value	Type
low complexity region	192	209	N/A	INTRINSIC
low complexity region	336	352	N/A	INTRINSIC
low complexity region	402	415	N/A	INTRINSIC
low complexity region	421	446	N/A	INTRINSIC
low complexity region	459	481	N/A	INTRINSIC
low complexity region	493	510	N/A	INTRINSIC
low complexity region	529	599	N/A	INTRINSIC
low complexity region	643	658	N/A	INTRINSIC
low complexity region	700	716	N/A	INTRINSIC

Predicted Effect

silent
Transcript: ENSMUST00000185956

SMART Domains

Protein: ENSMUSP00000140174
Gene: ENSMUSG00000027523

Domain	Start	End	E-Value	Type
low complexity region	19	48	N/A	INTRINSIC
internal_repeat_1	89	166	3.02e-8	PROSPERO
internal_repeat_1	209	276	3.02e-8	PROSPERO
low complexity region	350	365	N/A	INTRINSIC
low complexity region	391	404	N/A	INTRINSIC
low complexity region	459	477	N/A	INTRINSIC
low complexity region	480	498	N/A	INTRINSIC
low complexity region	515	525	N/A	INTRINSIC
low complexity region	535	570	N/A	INTRINSIC
low complexity region	576	626	N/A	INTRINSIC
low complexity region	633	643	N/A	INTRINSIC
low complexity region	659	678	N/A	INTRINSIC
low complexity region	685	696	N/A	INTRINSIC
G_alpha	759	1132	5.01e-185	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000154658

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150276

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000184327

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000183673

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000151472

Predicted Effect

probably benign
Transcript: ENSMUST00000130940

SMART Domains

Protein: ENSMUSP00000118210
Gene: ENSMUSG00000027523

Domain	Start	End	E-Value	Type
Pfam:NESP55	1	59	1.6e-30	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000180362

SMART Domains

Protein: ENSMUSP00000136180
Gene: ENSMUSG00000027523

Domain	Start	End	E-Value	Type
Pfam:NESP55	1	253	1.2e-157	PFAM

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 96.8%
20x: 94.1%

Validation Efficiency

99% (150/151)

MGI Phenotype

FUNCTION: This locus has a highly complex imprinted expression pattern. It gives rise to maternally, paternally, and biallelically expressed transcripts that are derived from four alternative promoters and 5' exons. Some transcripts contain a differentially methylated region (DMR) at their 5' exons, which is commonly found in imprinted genes and correlates with transcript expression. This gene has an antisense transcript. One of the transcripts produced from this locus, and the antisense transcript, are both paternally expressed noncoding RNAs, and may regulate imprinting in this region. In addition, one of the transcripts contains a second overlapping ORF, which encodes a structurally unrelated protein - Alex. Alternative splicing of downstream exons is also observed, which results in different forms of the stimulatory G-protein alpha subunit, a key element of the classical signal transduction pathway linking receptor-ligand interactions with the activation of adenylyl cyclase and a variety of cellular reponses. Additional transcript variants have been found for this gene, but the full-length nature and/or biological validity of some variants have not been determined. [provided by RefSeq, Jun 2015]
PHENOTYPE: Mutant homozygotes stop developing normally by embryonic day 10.5 and die prenatally. On some backgrounds heterozygotes show imprinted phenotypes, including differences in body shape/weight, locomotor activity, metabolism, and developmental anomalies. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 139 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4931403M11Rik	C	A	14: 24,671,419 (GRCm39)		noncoding transcript	Het
Abca7	A	G	10: 79,838,562 (GRCm39)	K612R	probably damaging	Het
Adamtsl3	T	C	7: 82,223,822 (GRCm39)	V275A	possibly damaging	Het
Afg3l1	G	A	8: 124,215,065 (GRCm39)		probably null	Het
Ajm1	G	A	2: 25,469,759 (GRCm39)	R51C	possibly damaging	Het
Alcam	T	A	16: 52,089,176 (GRCm39)	H508L	probably benign	Het
Ankrd45	G	A	1: 160,982,942 (GRCm39)	R151H	probably damaging	Het
Aqr	G	A	2: 113,980,990 (GRCm39)	L264F	probably damaging	Het
Arfgef2	G	A	2: 166,677,533 (GRCm39)	A53T	probably damaging	Het
Arhgap30	A	G	1: 171,236,880 (GRCm39)	T1085A	probably benign	Het
Atp10a	T	C	7: 58,435,055 (GRCm39)	V314A	probably damaging	Het
Bdp1	T	C	13: 100,187,627 (GRCm39)	D1580G	probably benign	Het
Btbd17	T	A	11: 114,684,917 (GRCm39)	T41S	possibly damaging	Het
Cacna1c	T	C	6: 118,728,400 (GRCm39)	N378S	probably damaging	Het
Camsap1	G	T	2: 25,825,562 (GRCm39)	Q1375K	probably benign	Het
Catsper2	G	T	2: 121,227,604 (GRCm39)		probably null	Het
Cblif	A	G	19: 11,729,583 (GRCm39)	T181A	probably benign	Het
Ccar1	A	G	10: 62,588,997 (GRCm39)	S829P	unknown	Het
Ccdc180	T	C	4: 45,909,308 (GRCm39)	L492P	probably damaging	Het
Ccser2	A	T	14: 36,662,343 (GRCm39)	N280K	probably damaging	Het
Cd37	T	C	7: 44,883,359 (GRCm39)	D271G	probably damaging	Het
Cdcp1	G	A	9: 123,011,194 (GRCm39)		probably benign	Het
Cemip2	T	C	19: 21,833,528 (GRCm39)	V1322A	probably benign	Het
Cep85	T	A	4: 133,892,062 (GRCm39)		probably benign	Het
Cfi	C	T	3: 129,666,726 (GRCm39)	P483L	probably damaging	Het
Csmd1	A	G	8: 15,945,674 (GRCm39)		probably benign	Het
Cytl1	G	T	5: 37,892,918 (GRCm39)	L9F	unknown	Het
Defb26	T	C	2: 152,350,085 (GRCm39)	E65G	possibly damaging	Het
Degs1	G	A	1: 182,104,370 (GRCm39)	T305I	probably damaging	Het
Dnttip2	T	G	3: 122,070,241 (GRCm39)	C485W	probably damaging	Het
Ecel1	G	A	1: 87,076,449 (GRCm39)		probably benign	Het
Edrf1	G	T	7: 133,260,339 (GRCm39)	M83I	probably damaging	Het
Elmo2	A	T	2: 165,137,209 (GRCm39)	C562S	probably benign	Het
Etl4	T	A	2: 20,344,922 (GRCm39)		probably null	Het
F2r	A	C	13: 95,740,905 (GRCm39)	V210G	probably damaging	Het
Fam171a1	T	A	2: 3,224,546 (GRCm39)	V179E	probably damaging	Het
Fmod	G	T	1: 133,967,977 (GRCm39)	V6F	possibly damaging	Het
Foxr2	A	G	X: 151,913,312 (GRCm39)	Q61R	probably damaging	Het
Gabra4	G	A	5: 71,729,546 (GRCm39)	H76Y	probably benign	Het
Gck	A	T	11: 5,859,150 (GRCm39)	M139K	possibly damaging	Het
Gm10192	C	G	4: 97,071,345 (GRCm39)	S20T	probably null	Het
Gm44501	T	C	17: 40,887,515 (GRCm39)	L11P	unknown	Het
Gm572	T	C	4: 148,751,302 (GRCm39)		probably null	Het
Grm2	T	A	9: 106,527,865 (GRCm39)	S340C	probably damaging	Het
Gsc	T	A	12: 104,438,274 (GRCm39)	H198L	probably damaging	Het
H2-Q3	A	T	17: 35,578,424 (GRCm39)		noncoding transcript	Het
H4c1	T	C	13: 23,944,935 (GRCm39)	D69G	probably damaging	Het
Hivep3	A	G	4: 119,980,131 (GRCm39)	E1723G	probably damaging	Het
Hk3	A	T	13: 55,154,405 (GRCm39)	L757Q	probably damaging	Het
Homer2	A	T	7: 81,299,311 (GRCm39)	D51E	probably benign	Het
Ier3ip1	T	A	18: 77,027,227 (GRCm39)		probably benign	Het
Itch	T	A	2: 155,059,897 (GRCm39)		probably null	Het
Kalrn	T	A	16: 33,991,700 (GRCm39)	Q974L	probably damaging	Het
Kirrel3	G	T	9: 34,924,601 (GRCm39)	G296W	probably damaging	Het
Klhl17	A	G	4: 156,315,082 (GRCm39)	V525A	probably benign	Het
Klhl9	T	C	4: 88,640,182 (GRCm39)	K20E	probably benign	Het
Kmt2a	G	T	9: 44,732,977 (GRCm39)		probably benign	Het
Krt17	C	A	11: 100,147,305 (GRCm39)	V409L	probably benign	Het
Lmx1b	T	C	2: 33,454,802 (GRCm39)	N322S	probably benign	Het
Lrrc63	G	C	14: 75,363,406 (GRCm39)	P242A	probably benign	Het
Ltk	T	C	2: 119,583,708 (GRCm39)	N256D	probably damaging	Het
Map3k19	T	A	1: 127,745,470 (GRCm39)	E1328V	probably damaging	Het
Map4k2	C	T	19: 6,394,033 (GRCm39)	A280V	probably benign	Het
Micall1	C	T	15: 79,016,048 (GRCm39)	R802*	probably null	Het
Mmp14	A	G	14: 54,673,662 (GRCm39)	R109G	probably damaging	Het
Mmp27	A	T	9: 7,581,369 (GRCm39)	H544L	probably benign	Het
Mpeg1	A	G	19: 12,440,434 (GRCm39)	T631A	probably damaging	Het
Mpnd	A	G	17: 56,318,641 (GRCm39)	M217V	probably benign	Het
Mrc2	T	C	11: 105,232,034 (GRCm39)	V862A	probably damaging	Het
Mug2	T	A	6: 122,058,154 (GRCm39)	S1239T	probably damaging	Het
Myb	T	A	10: 21,002,137 (GRCm39)	M616L	probably benign	Het
Myo18b	A	T	5: 113,022,346 (GRCm39)		probably benign	Het
Myo1c	C	A	11: 75,560,053 (GRCm39)	T703N	probably damaging	Het
Myt1l	T	G	12: 29,936,138 (GRCm39)	C909G	unknown	Het
Nbea	T	C	3: 55,912,776 (GRCm39)	S1004G	possibly damaging	Het
Neb	T	C	2: 52,186,319 (GRCm39)	N918D	probably benign	Het
Nrtn	T	C	17: 57,058,636 (GRCm39)	T122A	probably damaging	Het
Nsd3	A	T	8: 26,188,939 (GRCm39)	S1042C	probably damaging	Het
Ntmt2	A	T	1: 163,530,633 (GRCm39)	C269S	probably benign	Het
Nvl	A	G	1: 180,945,191 (GRCm39)	L461S	probably damaging	Het
Onecut2	A	T	18: 64,473,998 (GRCm39)	H183L	possibly damaging	Het
Or13p5	A	C	4: 118,591,885 (GRCm39)	H53P	probably benign	Het
Or2h2	G	A	17: 37,396,343 (GRCm39)	T238I	probably damaging	Het
Or4d10	C	G	19: 12,051,679 (GRCm39)	G106R	probably damaging	Het
Or52e4	A	G	7: 104,705,689 (GRCm39)	T79A	possibly damaging	Het
Or5c1	T	G	2: 37,222,601 (GRCm39)	F281V	probably damaging	Het
Or6c1b	A	C	10: 129,273,248 (GRCm39)	D189A	possibly damaging	Het
Or6z5	A	T	7: 6,477,612 (GRCm39)	I168F	probably damaging	Het
Pcdhb21	G	T	18: 37,648,130 (GRCm39)	V420F	possibly damaging	Het
Pcdhb9	G	A	18: 37,536,286 (GRCm39)	G760D	probably benign	Het
Pglyrp2	G	A	17: 32,637,771 (GRCm39)	P86S	probably benign	Het
Phyhip	T	A	14: 70,704,765 (GRCm39)	V328E	probably damaging	Het
Pitpnb	A	T	5: 111,530,862 (GRCm39)	K218N	possibly damaging	Het
Pitrm1	A	G	13: 6,628,596 (GRCm39)	D963G	probably damaging	Het
Pmfbp1	A	G	8: 110,258,792 (GRCm39)	Y699C	probably damaging	Het
Pmpcb	T	A	5: 21,945,660 (GRCm39)		probably benign	Het
Polg	A	T	7: 79,114,353 (GRCm39)	W203R	probably damaging	Het
Pramel22	A	G	4: 143,380,971 (GRCm39)	S351P	probably benign	Het
Prss41	A	T	17: 24,055,977 (GRCm39)	M252K	probably benign	Het
Prss46	A	T	9: 110,673,618 (GRCm39)	M1L	possibly damaging	Het
Rimklb	T	C	6: 122,441,051 (GRCm39)		probably null	Het
Rngtt	T	C	4: 33,500,335 (GRCm39)	I556T	unknown	Het
Rock1	A	C	18: 10,122,698 (GRCm39)	D374E	probably benign	Het
Rspry1	C	A	8: 95,385,417 (GRCm39)	H450N	probably benign	Het
Rusc2	T	C	4: 43,423,942 (GRCm39)	V1032A	probably damaging	Het
Sacs	A	G	14: 61,449,647 (GRCm39)	R3898G	probably damaging	Het
Scnn1b	A	T	7: 121,502,110 (GRCm39)	H256L	probably benign	Het
Sh3gl2	T	A	4: 85,297,494 (GRCm39)	H157Q	probably benign	Het
Sipa1l1	C	A	12: 82,389,107 (GRCm39)	S444R	probably damaging	Het
Sntg1	T	A	1: 8,433,818 (GRCm39)	I478F	probably damaging	Het
Spata31e2	A	G	1: 26,722,628 (GRCm39)	Y851H	probably benign	Het
Sptb	G	T	12: 76,655,811 (GRCm39)	L1424M	probably benign	Het
Sry	T	A	Y: 2,663,105 (GRCm39)	H185L	unknown	Het
Stox2	T	G	8: 47,656,198 (GRCm39)	T93P	probably damaging	Het
Tatdn2	T	A	6: 113,681,566 (GRCm39)	F472Y	possibly damaging	Het
Tefm	A	T	11: 80,031,185 (GRCm39)	V17D	possibly damaging	Het
Tekt2	G	T	4: 126,218,460 (GRCm39)	T70N	probably benign	Het
Ticam1	T	C	17: 56,578,642 (GRCm39)	D151G	probably damaging	Het
Tmem63c	A	G	12: 87,136,139 (GRCm39)	E785G	probably damaging	Het
Tnmd	A	T	X: 132,765,551 (GRCm39)	N219I	probably benign	Het
Ttc14	T	A	3: 33,861,024 (GRCm39)	L407*	probably null	Het
Ttll7	T	C	3: 146,599,932 (GRCm39)	M1T	probably null	Het
Ttn	T	A	2: 76,746,835 (GRCm39)		probably null	Het
Uchl1	T	C	5: 66,833,780 (GRCm39)	M12T	probably benign	Het
Uggt2	A	T	14: 119,315,062 (GRCm39)		probably null	Het
Uggt2	T	C	14: 119,286,665 (GRCm39)	T224A	probably damaging	Het
Umodl1	A	G	17: 31,218,175 (GRCm39)	E1254G	probably damaging	Het
Unc5d	A	G	8: 29,156,927 (GRCm39)	F773L	probably benign	Het
Unc80	C	A	1: 66,683,606 (GRCm39)	P2216Q	probably damaging	Het
Usp40	T	A	1: 87,913,923 (GRCm39)		probably null	Het
Vmn1r117	A	T	7: 20,617,421 (GRCm39)	M209K	probably damaging	Het
Vmn2r44	A	T	7: 8,380,985 (GRCm39)	W303R	probably benign	Het
Wnk2	G	A	13: 49,224,478 (GRCm39)	R268C	probably damaging	Het
Wnt2	T	C	6: 18,023,125 (GRCm39)	K175E	possibly damaging	Het
Xkr6	T	C	14: 64,056,953 (GRCm39)	V288A	unknown	Het
Zfp125	A	G	12: 20,950,459 (GRCm39)		noncoding transcript	Het
Zfp512b	A	C	2: 181,228,856 (GRCm39)	V703G	probably damaging	Het
Zglp1	A	T	9: 20,973,957 (GRCm39)	I243N	probably benign	Het
Zgpat	T	C	2: 181,020,651 (GRCm39)	S275P	probably benign	Het

Other mutations in Gnas

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00565:Gnas	APN	2	174,183,504 (GRCm39)	splice site	probably benign
IGL00928:Gnas	APN	2	174,139,746 (GRCm39)	nonsense	probably null
IGL01014:Gnas	APN	2	174,139,767 (GRCm39)	utr 5 prime	probably benign
IGL01743:Gnas	APN	2	174,140,125 (GRCm39)	nonsense	probably null
IGL01808:Gnas	APN	2	174,140,490 (GRCm39)	missense	probably damaging	0.96
IGL02559:Gnas	APN	2	174,183,729 (GRCm39)	splice site	probably benign
R0555:Gnas	UTSW	2	174,140,304 (GRCm39)	missense	possibly damaging	0.78
R0627:Gnas	UTSW	2	174,139,928 (GRCm39)	intron	probably benign
R1418:Gnas	UTSW	2	174,187,007 (GRCm39)	splice site	probably benign
R1706:Gnas	UTSW	2	174,141,768 (GRCm39)	missense	possibly damaging	0.90
R1751:Gnas	UTSW	2	174,139,687 (GRCm39)	utr 5 prime	probably benign
R1968:Gnas	UTSW	2	174,140,526 (GRCm39)	missense	probably damaging	0.96
R2290:Gnas	UTSW	2	174,141,803 (GRCm39)	missense	probably benign	0.09
R4125:Gnas	UTSW	2	174,141,958 (GRCm39)	missense	possibly damaging	0.94
R4128:Gnas	UTSW	2	174,141,958 (GRCm39)	missense	possibly damaging	0.94
R4697:Gnas	UTSW	2	174,139,873 (GRCm39)	missense	probably damaging	1.00
R5458:Gnas	UTSW	2	174,140,124 (GRCm39)	missense	probably benign	0.41
R5640:Gnas	UTSW	2	174,126,764 (GRCm39)	missense	probably benign	0.44
R5696:Gnas	UTSW	2	174,141,468 (GRCm39)	intron	probably benign
R5757:Gnas	UTSW	2	174,187,040 (GRCm39)	missense	probably damaging	1.00
R6053:Gnas	UTSW	2	174,141,645 (GRCm39)	missense	possibly damaging	0.89
R6083:Gnas	UTSW	2	174,139,655 (GRCm39)	start codon destroyed	probably null
R6736:Gnas	UTSW	2	174,176,044 (GRCm39)	missense	probably damaging	0.98
R7074:Gnas	UTSW	2	174,126,842 (GRCm39)	missense	probably damaging	1.00
R7239:Gnas	UTSW	2	174,140,408 (GRCm39)	missense	unknown
R7541:Gnas	UTSW	2	174,139,892 (GRCm39)	missense	unknown
R7679:Gnas	UTSW	2	174,126,624 (GRCm39)	missense	probably damaging	0.99
R7694:Gnas	UTSW	2	174,142,005 (GRCm39)	missense	probably damaging	1.00
R7713:Gnas	UTSW	2	174,140,820 (GRCm39)	missense	unknown
R7834:Gnas	UTSW	2	174,140,783 (GRCm39)	nonsense	probably null
R8138:Gnas	UTSW	2	174,140,179 (GRCm39)	missense	probably benign	0.06
R8459:Gnas	UTSW	2	174,126,732 (GRCm39)	missense	probably benign	0.05
R8537:Gnas	UTSW	2	174,140,394 (GRCm39)	missense	possibly damaging	0.83
R8731:Gnas	UTSW	2	174,126,699 (GRCm39)	missense	probably benign	0.01
R8924:Gnas	UTSW	2	174,141,277 (GRCm39)	missense	unknown
R9431:Gnas	UTSW	2	174,139,826 (GRCm39)	missense	unknown
R9513:Gnas	UTSW	2	174,185,089 (GRCm39)	missense	probably damaging	0.98
R9617:Gnas	UTSW	2	174,141,988 (GRCm39)	missense	possibly damaging	0.90
R9710:Gnas	UTSW	2	174,141,132 (GRCm39)	missense	unknown
R9711:Gnas	UTSW	2	174,141,392 (GRCm39)	missense	unknown
R9762:Gnas	UTSW	2	174,140,639 (GRCm39)	nonsense	probably null
X0022:Gnas	UTSW	2	174,141,537 (GRCm39)	missense	probably benign	0.33
Z1088:Gnas	UTSW	2	174,140,166 (GRCm39)	missense	probably benign	0.27
Z1176:Gnas	UTSW	2	174,140,399 (GRCm39)	missense	unknown
Z1177:Gnas	UTSW	2	174,126,680 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- GGCAATAATATGTCAGGACAACAC -3'
(R):5'- CCAAAATCGCTGGGTTGAAGG -3'

Sequencing Primer
(F):5'- TATGTCAGGACAACACGATATCC -3'
(R):5'- GCTTGGAGGCCTGATGG -3'

Posted On

2016-03-17