Mutagenetix > Incidental Mutations

Incidental Mutation 'R8454:Adgrg7'

654959

Institutional Source

Beutler Lab

Gene Symbol

Adgrg7

Ensembl Gene

ENSMUSG00000022755

Gene Name

adhesion G protein-coupled receptor G7

Synonyms

Gpr128, 9130020O16Rik

MMRRC Submission

Accession Numbers

Is this an essential gene?

Non essential (E-score: 0.000) question?

Stock #

R8454 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

56724609-56795855 bp(-) (GRCm38)

Type of Mutation

start gained

DNA Base Change (assembly)

C to G at 56795682 bp

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000023437 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000023437]

Predicted Effect

probably benign
Transcript: ENSMUST00000023437

SMART Domains

Protein: ENSMUSP00000023437
Gene: ENSMUSG00000022755

Domain	Start	End	E-Value	Type
transmembrane domain	12	34	N/A	INTRINSIC
SCOP:d1edmb_	52	76	1e-3	SMART
GPS	376	424	6.16e-8	SMART
Pfam:7tm_2	428	712	4.5e-40	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.9%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit reduced body weight gain and increased frequency of peristalsis and slow wave potential in the small intestine. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9030624J02Rik	T	A	7: 118,792,572	F493Y	probably benign	Het
Abcc10	C	A	17: 46,324,177	G300V	possibly damaging	Het
Agt	G	A	8: 124,564,103	T155M	probably benign	Het
Atp8b3	A	G	10: 80,525,799	V763A	probably benign	Het
Btn1a1	C	A	13: 23,464,250	V138L	probably benign	Het
Cd163	A	T	6: 124,328,965	N1109I	probably benign	Het
Cideb	T	A	14: 55,755,141	Q106L	possibly damaging	Het
Cntn1	A	G	15: 92,232,249	T126A	probably benign	Het
Dusp27	A	T	1: 166,108,133	N165K	probably damaging	Het
Elfn1	T	C	5: 139,971,471	Y77H	probably damaging	Het
Eml3	A	G	19: 8,934,994	H386R	probably damaging	Het
Fbxo21	A	G	5: 117,995,414	D413G	probably damaging	Het
Fkbp8	T	A	8: 70,531,763		probably null	Het
Fzd1	T	C	5: 4,757,336	Q82R	probably benign	Het
Gast	T	C	11: 100,336,568	L29P	probably benign	Het
Glb1l2	C	A	9: 26,806,417		probably benign	Het
Gm1110	C	G	9: 26,883,280	Q483H	probably benign	Het
Gm1110	T	A	9: 26,883,281	Q483L	probably benign	Het
Gm5737	T	A	7: 120,831,180	V420E	possibly damaging	Het
Gpc6	T	C	14: 116,925,979	L15P	probably damaging	Het
Hagh	C	A	17: 24,857,562	S161*	probably null	Het
Hrh1	A	G	6: 114,480,853	D365G	probably benign	Het
Ighv1-36	A	T	12: 114,879,940	M100K	probably damaging	Het
Itgb8	A	T	12: 119,170,778	V518D	probably benign	Het
Krt82	T	C	15: 101,541,803	Y486C	probably damaging	Het
Lmbr1l	A	G	15: 98,912,476	S85P	probably damaging	Het
Met	A	G	6: 17,491,769	S177G	probably damaging	Het
Myl9	T	A	2: 156,781,128	I162N	possibly damaging	Het
Npat	T	A	9: 53,566,951	N973K	possibly damaging	Het
Olfr493	A	T	7: 108,346,682	C100S	probably damaging	Het
Pcdhga12	A	T	18: 37,768,137	D674V	possibly damaging	Het
Phtf1	T	A	3: 104,004,449	N702K	probably damaging	Het
Plaa	A	T	4: 94,569,477	I752N	probably damaging	Het
Pnpla2	T	C	7: 141,458,098	C194R	probably damaging	Het
Rnaseh2a	T	C	8: 84,965,147	N133S	probably benign	Het
Rps6ka1	T	A	4: 133,848,553	Q685L	probably benign	Het
Ryr1	C	A	7: 29,015,717	G4661C	unknown	Het
Samd13	T	A	3: 146,646,402	M65L	probably benign	Het
Sec22c	A	G	9: 121,695,655	S21P	probably damaging	Het
Sh3d19	C	A	3: 86,107,022	T431K	probably benign	Het
Sin3b	A	G	8: 72,741,480	M277V	probably benign	Het
Sis	T	C	3: 72,947,501	T468A	possibly damaging	Het
Slitrk3	T	C	3: 73,049,180	N753S	probably benign	Het
Slitrk6	C	A	14: 110,752,046	L76F	probably damaging	Het
Stk3	C	T	15: 34,876,724	A478T	probably damaging	Het
Sugp1	C	A	8: 70,071,597	Y617*	probably null	Het
Tinag	T	C	9: 77,031,695	D167G	probably damaging	Het
Tk2	A	G	8: 104,241,114		probably null	Het
Tmem209	A	T	6: 30,489,309	V514D	probably damaging	Het
Tmprss9	A	G	10: 80,887,486	H260R	probably benign	Het
Tnfrsf14	T	A	4: 154,926,655	Y83F	possibly damaging	Het
Tnfrsf8	A	T	4: 145,287,983	D285E	probably benign	Het
Togaram2	C	G	17: 71,697,878	A310G	probably benign	Het
Trpv3	A	G	11: 73,291,622	Y544C	probably damaging	Het
Ttl	T	A	2: 129,066,184	V13D	probably damaging	Het
Usp40	A	T	1: 87,980,972	D602E	probably benign	Het
Vamp5	A	G	6: 72,370,393		probably benign	Het
Vmn2r65	T	A	7: 84,940,194	H838L	possibly damaging	Het
Wdr63	T	C	3: 146,097,227	K70E	probably damaging	Het
Zfp960	T	A	17: 17,088,199	Y392N	probably benign	Het

Other mutations in Adgrg7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01783:Adgrg7	APN	16	56747919	critical splice donor site	probably null
IGL03122:Adgrg7	APN	16	56770362	splice site	probably benign
R0632:Adgrg7	UTSW	16	56742589	missense	possibly damaging	0.89
R0673:Adgrg7	UTSW	16	56773486	missense	possibly damaging	0.48
R1690:Adgrg7	UTSW	16	56795630	missense	probably damaging	0.99
R2009:Adgrg7	UTSW	16	56761873	missense	probably benign	0.08
R2017:Adgrg7	UTSW	16	56732806	missense	probably benign	0.02
R2132:Adgrg7	UTSW	16	56767918	missense	probably damaging	1.00
R2153:Adgrg7	UTSW	16	56752428	missense	possibly damaging	0.75
R2229:Adgrg7	UTSW	16	56752403	missense	probably benign
R2436:Adgrg7	UTSW	16	56761945	missense	possibly damaging	0.78
R2878:Adgrg7	UTSW	16	56750454	missense	probably benign	0.14
R2981:Adgrg7	UTSW	16	56750406	critical splice donor site	probably null
R4014:Adgrg7	UTSW	16	56742288	missense	probably damaging	1.00
R4023:Adgrg7	UTSW	16	56730298	missense	probably damaging	1.00
R4024:Adgrg7	UTSW	16	56730298	missense	probably damaging	1.00
R4026:Adgrg7	UTSW	16	56730298	missense	probably damaging	1.00
R4551:Adgrg7	UTSW	16	56748012	missense	probably damaging	1.00
R4834:Adgrg7	UTSW	16	56732869	missense	probably damaging	1.00
R5041:Adgrg7	UTSW	16	56730348	missense	probably benign	0.21
R5145:Adgrg7	UTSW	16	56742319	missense	probably benign	0.04
R5377:Adgrg7	UTSW	16	56730306	missense	possibly damaging	0.68
R5549:Adgrg7	UTSW	16	56750427	missense	probably damaging	1.00
R5915:Adgrg7	UTSW	16	56730385	splice site	probably null
R5957:Adgrg7	UTSW	16	56773427	missense	probably damaging	0.96
R6146:Adgrg7	UTSW	16	56773466	missense	probably benign	0.21
R6198:Adgrg7	UTSW	16	56777193	missense	possibly damaging	0.64
R6233:Adgrg7	UTSW	16	56778642	missense	possibly damaging	0.52
R6337:Adgrg7	UTSW	16	56752425	missense	probably damaging	0.96
R6633:Adgrg7	UTSW	16	56730286	missense	probably benign	0.05
R6693:Adgrg7	UTSW	16	56770224	missense	probably damaging	0.97
R6812:Adgrg7	UTSW	16	56795798	start gained	probably benign
R6841:Adgrg7	UTSW	16	56750424	missense	probably damaging	1.00
R6868:Adgrg7	UTSW	16	56773476	missense	probably benign
R7076:Adgrg7	UTSW	16	56742406	missense	probably damaging	1.00
R7146:Adgrg7	UTSW	16	56730242	missense	probably damaging	1.00
R7232:Adgrg7	UTSW	16	56777152	splice site	probably null
R7266:Adgrg7	UTSW	16	56770311	missense	probably benign	0.00
R7376:Adgrg7	UTSW	16	56724979	missense	probably damaging	1.00
R7390:Adgrg7	UTSW	16	56732844	missense	probably damaging	0.98
R7401:Adgrg7	UTSW	16	56742418	missense	probably benign	0.43
R7496:Adgrg7	UTSW	16	56732857	missense	probably benign
R7540:Adgrg7	UTSW	16	56750429	missense	probably damaging	1.00
R8147:Adgrg7	UTSW	16	56742513	missense	probably damaging	1.00
R8354:Adgrg7	UTSW	16	56795682	start gained	probably benign
R8372:Adgrg7	UTSW	16	56795751	start gained	probably benign
R8393:Adgrg7	UTSW	16	56762114	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CACTTCCCTGGCACTGAAATATC -3'
(R):5'- ATCTCCCTCGGTGAAGAATGAG -3'

Sequencing Primer
(F):5'- GCAGAGTCAGAGAATCAATGCCATC -3'
(R):5'- TCCCTCGGTGAAGAATGAGCATAC -3'

Posted On

2020-10-20