Mutagenetix > Incidental Mutation

Incidental Mutation 'R2116:Rgs7'

233101

Institutional Source

Beutler Lab

Gene Symbol

Rgs7

Ensembl Gene

ENSMUSG00000026527

Gene Name

regulator of G protein signaling 7

Synonyms

MMRRC Submission

040120-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.672) question?

Stock #

R2116 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

174886653-175320066 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 174918639 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Isoleucine at position 235 (N235I)

Ref Sequence

ENSEMBL: ENSMUSP00000141380 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000027812] [ENSMUST00000192227] [ENSMUST00000194288] [ENSMUST00000194555] [ENSMUST00000195324] [ENSMUST00000195477]

AlphaFold

O54829

Predicted Effect

probably damaging
Transcript: ENSMUST00000027812
AA Change: N235I

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000027812
Gene: ENSMUSG00000026527
AA Change: N235I

Domain	Start	End	E-Value	Type
DEP	37	112	1.69e-26	SMART
G_gamma	252	316	4.56e-20	SMART
GGL	255	316	2.75e-27	SMART
RGS	333	448	9.08e-49	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000192227
AA Change: N235I

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000142278
Gene: ENSMUSG00000026527
AA Change: N235I

Domain	Start	End	E-Value	Type
DEP	37	112	1.69e-26	SMART
G_gamma	252	316	4.56e-20	SMART
GGL	255	316	2.75e-27	SMART
RGS	333	448	9.08e-49	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000194288

SMART Domains

Protein: ENSMUSP00000141855
Gene: ENSMUSG00000026527

Domain	Start	End	E-Value	Type
RGS	16	131	9.08e-49	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000194555
AA Change: N235I

PolyPhen 2 Score 0.198 (Sensitivity: 0.92; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000142180
Gene: ENSMUSG00000026527
AA Change: N235I

Domain	Start	End	E-Value	Type
DEP	37	112	1.69e-26	SMART
G_gamma	252	316	4.56e-20	SMART
GGL	255	316	2.75e-27	SMART
RGS	333	448	9.08e-49	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000195324
AA Change: N235I

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000141380
Gene: ENSMUSG00000026527
AA Change: N235I

Domain	Start	End	E-Value	Type
DEP	37	112	7.7e-29	SMART
G_gamma	252	316	2.1e-24	SMART
GGL	255	316	1.8e-29	SMART
RGS	333	448	3.4e-51	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000195477

SMART Domains

Protein: ENSMUSP00000142181
Gene: ENSMUSG00000026527

Domain	Start	End	E-Value	Type
RGS	36	151	9.08e-49	SMART

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.5%
20x: 95.9%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a hypomorphic allele exhibit reduced exploration in a new environment, impaired glucose tolerance in males, and abnormal rod b-wave electrophysiology. Mice homozygous for a knock-out allele exhibit runting, delayed eye opening, and transient prolonged b-wave implicit time. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 96 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts20	A	G	15: 94,253,243 (GRCm39)	C377R	probably damaging	Het
Adgrv1	T	C	13: 81,677,132 (GRCm39)	K1180E	probably benign	Het
Ankle1	A	G	8: 71,860,562 (GRCm39)	T340A	probably benign	Het
Armc2	A	T	10: 41,839,663 (GRCm39)	L434Q	probably damaging	Het
Ash1l	C	T	3: 88,890,571 (GRCm39)	L817F	probably benign	Het
Atm	C	T	9: 53,412,269 (GRCm39)	E960K	probably benign	Het
Bend5	G	T	4: 111,272,436 (GRCm39)	R22L	probably benign	Het
Cacng6	C	T	7: 3,479,020 (GRCm39)	T133I	probably damaging	Het
Cep120	G	A	18: 53,873,208 (GRCm39)	T41I	probably damaging	Het
Ciz1	T	C	2: 32,257,477 (GRCm39)	L174P	probably damaging	Het
Cmah	G	A	13: 24,612,880 (GRCm39)	D26N	probably benign	Het
Cnot1	A	C	8: 96,452,781 (GRCm39)	D2098E	probably damaging	Het
Cnot10	A	C	9: 114,455,504 (GRCm39)	S207R	probably damaging	Het
Col14a1	A	G	15: 55,271,160 (GRCm39)	T638A	unknown	Het
Coro1a	T	C	7: 126,301,194 (GRCm39)	E102G	probably damaging	Het
Ddx27	A	C	2: 166,869,684 (GRCm39)	D373A	probably benign	Het
Defb38	A	T	8: 19,073,483 (GRCm39)	Y63*	probably null	Het
Dhx37	A	G	5: 125,498,166 (GRCm39)	V681A	probably damaging	Het
Dmxl1	T	A	18: 50,011,884 (GRCm39)	L1347H	probably damaging	Het
Dnmt3l	C	A	10: 77,899,130 (GRCm39)	L110I	probably damaging	Het
Gcn1	A	T	5: 115,736,884 (GRCm39)	M1276L	probably benign	Het
Gfus	A	G	15: 75,797,991 (GRCm39)	F223S	probably damaging	Het
Gm10277	TC	T	11: 77,676,828 (GRCm39)		probably null	Het
Gm12790	G	A	4: 101,824,848 (GRCm39)	T140I	possibly damaging	Het
Golga3	A	T	5: 110,335,261 (GRCm39)	M192L	probably damaging	Het
H2-T22	A	T	17: 36,349,949 (GRCm39)		probably null	Het
Hectd2	C	A	19: 36,591,824 (GRCm39)	T675K	probably damaging	Het
Hinfp	T	C	9: 44,210,912 (GRCm39)	N116S	probably damaging	Het
Hoatz	A	G	9: 51,012,384 (GRCm39)	S79P	possibly damaging	Het
Hs6st3	T	A	14: 120,106,699 (GRCm39)	L369Q	probably damaging	Het
Ift74	A	G	4: 94,515,496 (GRCm39)	T138A	probably benign	Het
Ipo7	T	A	7: 109,650,325 (GRCm39)	Y792N	probably damaging	Het
Jak1	A	T	4: 101,036,872 (GRCm39)	I256N	probably damaging	Het
Kcnd2	T	A	6: 21,216,431 (GRCm39)	L45Q	probably damaging	Het
Klhl3	A	T	13: 58,166,805 (GRCm39)	V342E	probably damaging	Het
Krt28	A	C	11: 99,255,943 (GRCm39)	S439A	probably benign	Het
L3mbtl1	T	A	2: 162,801,990 (GRCm39)		probably null	Het
Lrch1	G	A	14: 75,022,971 (GRCm39)	P634L	probably damaging	Het
Lrp1	C	T	10: 127,412,362 (GRCm39)	W1314*	probably null	Het
Lrwd1	T	A	5: 136,159,332 (GRCm39)	Y431F	probably damaging	Het
Lyst	A	G	13: 13,810,286 (GRCm39)	E652G	probably damaging	Het
Mageb3	A	G	2: 121,785,033 (GRCm39)	V223A	probably damaging	Het
Map1b	G	T	13: 99,567,152 (GRCm39)	S1856R	unknown	Het
Mecom	T	A	3: 30,019,607 (GRCm39)	Q759L	probably damaging	Het
Mfsd6	T	A	1: 52,700,134 (GRCm39)	R671S	probably benign	Het
Mllt10	A	G	2: 18,167,380 (GRCm39)	N435S	probably benign	Het
Mta2	T	C	19: 8,920,880 (GRCm39)	I27T	probably damaging	Het
Ndufab1	A	G	7: 121,700,987 (GRCm39)	L20P	probably benign	Het
Nfatc2ip	T	A	7: 125,984,280 (GRCm39)	Y371F	probably damaging	Het
Nhlrc1	A	C	13: 47,167,661 (GRCm39)	S199A	probably benign	Het
Nipa1	G	T	7: 55,635,273 (GRCm39)	N113K	possibly damaging	Het
Nlgn1	T	A	3: 26,187,414 (GRCm39)	N157I	probably damaging	Het
Nlrp1a	T	A	11: 71,005,326 (GRCm39)	K630*	probably null	Het
Nmi	T	C	2: 51,838,719 (GRCm39)	T272A	probably benign	Het
Nr1i3	T	A	1: 171,046,163 (GRCm39)	L181Q	probably damaging	Het
Nrxn1	A	T	17: 91,011,705 (GRCm39)	I308K	probably damaging	Het
Nup50l	A	T	6: 96,141,841 (GRCm39)	V401E	probably damaging	Het
Or14a256	T	C	7: 86,265,286 (GRCm39)	D189G	probably benign	Het
Or52z15	T	C	7: 103,332,519 (GRCm39)	I188T	probably damaging	Het
Or5al7	A	T	2: 85,993,073 (GRCm39)	Y73*	probably null	Het
Or8g50	T	A	9: 39,648,600 (GRCm39)	M163K	probably damaging	Het
Osgin2	G	A	4: 16,008,648 (GRCm39)	T51M	probably damaging	Het
Pkd1l2	T	A	8: 117,757,461 (GRCm39)	T1526S	possibly damaging	Het
Pkhd1l1	G	T	15: 44,432,878 (GRCm39)	A3378S	probably damaging	Het
Plg	A	T	17: 12,603,364 (GRCm39)	D90V	probably damaging	Het
Plppr3	A	T	10: 79,701,572 (GRCm39)	D423E	probably benign	Het
Prpf8	T	C	11: 75,378,547 (GRCm39)	V66A	possibly damaging	Het
Psg19	A	T	7: 18,528,180 (GRCm39)	Y188N	probably damaging	Het
Ptgs1	C	A	2: 36,127,708 (GRCm39)	S89*	probably null	Het
Ptx3	T	A	3: 66,132,187 (GRCm39)	I236N	probably damaging	Het
Pygm	A	G	19: 6,436,438 (GRCm39)	N100S	probably damaging	Het
Reps1	A	G	10: 18,000,668 (GRCm39)	E760G	probably damaging	Het
Rgsl1	T	A	1: 153,693,295 (GRCm39)	M629L	probably benign	Het
Rrh	T	C	3: 129,604,336 (GRCm39)	I288M	probably damaging	Het
Sctr	A	T	1: 119,959,312 (GRCm39)	D70V	probably damaging	Het
Sec11c	A	T	18: 65,933,720 (GRCm39)	T9S	probably benign	Het
Spty2d1	C	T	7: 46,645,933 (GRCm39)	G570D	probably damaging	Het
Stx1b	T	C	7: 127,410,077 (GRCm39)	E153G	probably damaging	Het
Synm	G	A	7: 67,383,343 (GRCm39)	R1440W	probably benign	Het
Tcof1	T	C	18: 60,965,857 (GRCm39)	E415G	possibly damaging	Het
Tgfb1i1	G	A	7: 127,851,977 (GRCm39)	R353H	probably damaging	Het
Thbs3	T	C	3: 89,126,699 (GRCm39)	F271S	probably damaging	Het
Tlr5	T	C	1: 182,803,194 (GRCm39)	W833R	probably damaging	Het
Tmem132b	A	G	5: 125,699,615 (GRCm39)	E92G	probably damaging	Het
Tmem221	T	C	8: 72,010,472 (GRCm39)	Y133C	probably damaging	Het
Tmem229b-ps	A	G	10: 53,351,552 (GRCm39)		noncoding transcript	Het
Tnxb	T	C	17: 34,891,201 (GRCm39)	C515R	probably damaging	Het
Trp53rka	T	A	2: 165,333,415 (GRCm39)	N158I	probably damaging	Het
Usp20	T	A	2: 30,906,317 (GRCm39)	C562S	probably damaging	Het
Usp31	C	T	7: 121,247,919 (GRCm39)	V1175M	probably benign	Het
Veph1	G	T	3: 65,964,610 (GRCm39)	N806K	probably benign	Het
Vmn1r223	G	T	13: 23,433,832 (GRCm39)	C142F	probably damaging	Het
Vmn2r80	A	T	10: 79,030,558 (GRCm39)	S795C	probably benign	Het
Wdr41	A	G	13: 95,151,537 (GRCm39)		probably null	Het
Zfp617	A	T	8: 72,686,009 (GRCm39)	H113L	probably benign	Het
Zfp715	T	A	7: 42,947,370 (GRCm39)	R863S	possibly damaging	Het

Other mutations in Rgs7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01450:Rgs7	APN	1	174,913,746 (GRCm39)	missense	probably benign	0.04
IGL02334:Rgs7	APN	1	175,016,788 (GRCm39)	missense	probably damaging	0.96
IGL02805:Rgs7	APN	1	174,977,262 (GRCm39)	missense	probably damaging	1.00
IGL03169:Rgs7	APN	1	175,098,401 (GRCm39)	missense	possibly damaging	0.75
R0269:Rgs7	UTSW	1	175,098,386 (GRCm39)	missense	possibly damaging	0.81
R1161:Rgs7	UTSW	1	174,907,021 (GRCm39)	missense	probably damaging	1.00
R1658:Rgs7	UTSW	1	174,907,120 (GRCm39)	missense	probably benign	0.02
R1840:Rgs7	UTSW	1	174,980,714 (GRCm39)	missense	probably damaging	0.99
R1944:Rgs7	UTSW	1	174,980,769 (GRCm39)	missense	possibly damaging	0.88
R2064:Rgs7	UTSW	1	174,949,508 (GRCm39)	missense	probably damaging	0.98
R2114:Rgs7	UTSW	1	174,918,639 (GRCm39)	missense	probably damaging	1.00
R3803:Rgs7	UTSW	1	175,016,785 (GRCm39)	missense	probably benign	0.39
R5106:Rgs7	UTSW	1	174,904,416 (GRCm39)	missense	possibly damaging	0.87
R6042:Rgs7	UTSW	1	174,977,226 (GRCm39)	missense	probably damaging	0.99
R7652:Rgs7	UTSW	1	174,921,396 (GRCm39)	missense	probably benign
R7689:Rgs7	UTSW	1	174,949,296 (GRCm39)	missense	probably benign	0.33
R7814:Rgs7	UTSW	1	174,903,635 (GRCm39)	missense	probably benign
R7884:Rgs7	UTSW	1	174,977,216 (GRCm39)	critical splice donor site	probably null
R8884:Rgs7	UTSW	1	174,980,730 (GRCm39)	missense	probably benign	0.06
Z1088:Rgs7	UTSW	1	174,911,586 (GRCm39)	missense	possibly damaging	0.92

Predicted Primers

PCR Primer
(F):5'- GCAGTTGACCATACAAATAACCTTC -3'
(R):5'- TAGCACACAGTTGGGAGTGG -3'

Sequencing Primer
(F):5'- AATAACCTTCTAAAACACCCGTATG -3'
(R):5'- GGAGTGGCAGACATTATTATCCC -3'

Posted On

2014-09-18