Mutagenetix > Incidental Mutation

Incidental Mutation 'R8141:Gpr87'

632521

Institutional Source

Beutler Lab

Gene Symbol

Gpr87

Ensembl Gene

ENSMUSG00000051431

Gene Name

G protein-coupled receptor 87

Synonyms

MMRRC Submission

067569-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R8141 (G1)

Quality Score

84.0076

Status

Validated

Chromosome

Chromosomal Location

59086344-59102525 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 59087020 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 162 (S162P)

Ref Sequence

ENSEMBL: ENSMUSP00000143683 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000040325] [ENSMUST00000056898] [ENSMUST00000164225] [ENSMUST00000199659] [ENSMUST00000200095]

AlphaFold

Q99MT7

Predicted Effect

probably benign
Transcript: ENSMUST00000040325

SMART Domains

Protein: ENSMUSP00000042269
Gene: ENSMUSG00000056476

Domain	Start	End	E-Value	Type
Med12	101	161	1.71e-24	SMART
low complexity region	216	224	N/A	INTRINSIC
low complexity region	269	278	N/A	INTRINSIC
Pfam:Med12-LCEWAV	282	730	2.6e-207	PFAM
low complexity region	744	758	N/A	INTRINSIC
low complexity region	853	872	N/A	INTRINSIC
low complexity region	1455	1466	N/A	INTRINSIC
low complexity region	1728	1742	N/A	INTRINSIC
low complexity region	1769	1783	N/A	INTRINSIC
Pfam:Med12-PQL	1803	2029	2.3e-14	PFAM
low complexity region	2055	2076	N/A	INTRINSIC
low complexity region	2083	2101	N/A	INTRINSIC
low complexity region	2116	2136	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000056898
AA Change: S163P

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000059272
Gene: ENSMUSG00000051431
AA Change: S163P

Domain	Start	End	E-Value	Type
Pfam:7tm_1	60	315	1.4e-36	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000164225

SMART Domains

Protein: ENSMUSP00000127038
Gene: ENSMUSG00000056476

Domain	Start	End	E-Value	Type
Med12	101	161	1.71e-24	SMART
low complexity region	216	224	N/A	INTRINSIC
low complexity region	269	278	N/A	INTRINSIC
Pfam:Med12-LCEWAV	283	765	5e-187	PFAM
low complexity region	779	793	N/A	INTRINSIC
low complexity region	888	907	N/A	INTRINSIC
low complexity region	1490	1501	N/A	INTRINSIC
low complexity region	1763	1777	N/A	INTRINSIC
low complexity region	1804	1818	N/A	INTRINSIC
Pfam:Med12-PQL	1840	2063	9.7e-66	PFAM
low complexity region	2090	2111	N/A	INTRINSIC
low complexity region	2118	2136	N/A	INTRINSIC
low complexity region	2151	2171	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000199659

SMART Domains

Protein: ENSMUSP00000142903
Gene: ENSMUSG00000056476

Domain	Start	End	E-Value	Type
Med12	101	161	1.71e-24	SMART
low complexity region	216	224	N/A	INTRINSIC
low complexity region	269	278	N/A	INTRINSIC
Pfam:Med12-LCEWAV	282	765	5.5e-209	PFAM
low complexity region	779	793	N/A	INTRINSIC
low complexity region	888	907	N/A	INTRINSIC
low complexity region	1490	1501	N/A	INTRINSIC
low complexity region	1761	1775	N/A	INTRINSIC
low complexity region	1802	1816	N/A	INTRINSIC
Pfam:Med12-PQL	1836	2062	1.7e-15	PFAM
low complexity region	2088	2130	N/A	INTRINSIC
low complexity region	2144	2164	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000200095
AA Change: S162P

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000143683
Gene: ENSMUSG00000051431
AA Change: S162P

Domain	Start	End	E-Value	Type
Pfam:7tm_1	59	314	3.5e-37	PFAM

Coding Region Coverage

1x: 99.8%
3x: 99.6%
10x: 98.3%
20x: 90.7%

Validation Efficiency

100% (59/59)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a G protein-coupled receptor and is located in a cluster of G protein-couple receptor genes on chromosome 3. The encoded protein has been shown to be overexpressed in lung squamous cell carcinoma (PMID:18057535) and regulated by p53 (PMID:19602589). [provided by RefSeq, Nov 2011]
PHENOTYPE: Mice homozygous for a null allele exhibit decreased mean vertebral and femoral bone measurements. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 51 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700017B05Rik	T	C	9: 57,165,688 (GRCm39)	T229A	probably benign	Het
4930438A08Rik	A	G	11: 58,177,411 (GRCm39)	E40G		Het
Actn2	T	C	13: 12,303,516 (GRCm39)	D428G	probably damaging	Het
Arl14epl	C	A	18: 47,059,410 (GRCm39)	N8K	probably benign	Het
Bend7	T	C	2: 4,757,636 (GRCm39)	V226A	probably benign	Het
C1s1	A	T	6: 124,508,321 (GRCm39)	L556Q	probably damaging	Het
Casr	T	C	16: 36,315,173 (GRCm39)	K966E	probably damaging	Het
Ccm2l	T	C	2: 152,912,791 (GRCm39)	L110P	probably damaging	Het
Cdhr4	G	A	9: 107,873,991 (GRCm39)	R59H		Het
Celf3	C	A	3: 94,395,850 (GRCm39)	N410K	probably damaging	Het
Cfap251	T	G	5: 123,424,493 (GRCm39)	V726G	possibly damaging	Het
Cpne6	T	C	14: 55,750,066 (GRCm39)	C66R	possibly damaging	Het
Cyp2f2	G	A	7: 26,828,678 (GRCm39)	V183I	probably benign	Het
Eln	CTCCAGCTCCGAT	C	5: 134,758,003 (GRCm39)		probably benign	Het
Fam53b	A	C	7: 132,361,758 (GRCm39)	V90G	probably damaging	Het
Fat3	T	A	9: 15,908,362 (GRCm39)	I2547F	possibly damaging	Het
Foxk1	A	G	5: 142,439,716 (GRCm39)	Y524C	probably damaging	Het
Ifi204	A	G	1: 173,583,189 (GRCm39)	V343A	possibly damaging	Het
Igsf10	A	G	3: 59,237,949 (GRCm39)	L744P	probably damaging	Het
Iqub	T	A	6: 24,491,608 (GRCm39)	K359N	probably benign	Het
Kdm3b	A	T	18: 34,961,599 (GRCm39)	K1459*	probably null	Het
Kirrel1	C	T	3: 86,993,735 (GRCm39)	W507*	probably null	Het
Klra17	T	C	6: 129,849,292 (GRCm39)	D94G	probably damaging	Het
Llgl1	G	C	11: 60,601,142 (GRCm39)	E693D	probably benign	Het
Lrrc37	T	C	11: 103,511,855 (GRCm39)	T38A	unknown	Het
Lypd4	A	T	7: 24,564,254 (GRCm39)	D201E	possibly damaging	Het
Nin	A	G	12: 70,076,795 (GRCm39)	S1794P		Het
Oog2	T	C	4: 143,920,777 (GRCm39)	L70P	probably damaging	Het
Or6n2	T	C	1: 173,897,488 (GRCm39)	L208P	probably damaging	Het
Pacsin1	G	T	17: 27,926,034 (GRCm39)	R282S	possibly damaging	Het
Pcdhb9	T	A	18: 37,535,361 (GRCm39)	Y452N	probably damaging	Het
Pdgfra	T	C	5: 75,338,387 (GRCm39)	V547A	possibly damaging	Het
Plcb4	T	C	2: 135,781,169 (GRCm39)	F209L	probably damaging	Het
Pnpla6	T	C	8: 3,571,384 (GRCm39)	S158P	probably benign	Het
Prlhr	C	G	19: 60,455,747 (GRCm39)	R273P	probably damaging	Het
Prss41	G	A	17: 24,056,607 (GRCm39)	P196L	probably damaging	Het
Ptgr3	T	C	18: 84,112,651 (GRCm39)	L109P	probably benign	Het
Ptpn22	A	G	3: 103,793,643 (GRCm39)	E598G	possibly damaging	Het
Rasal2	T	C	1: 156,992,240 (GRCm39)	D569G	possibly damaging	Het
Sf3b3	A	C	8: 111,547,483 (GRCm39)	M715R	possibly damaging	Het
Ska1	T	C	18: 74,339,907 (GRCm39)	N13S	probably benign	Het
Spocd1	A	C	4: 129,823,497 (GRCm39)	E98A		Het
Sycp1	G	T	3: 102,842,885 (GRCm39)	A28E	possibly damaging	Het
Syf2	C	T	4: 134,664,182 (GRCm39)	R199C	probably damaging	Het
Syne2	A	G	12: 76,108,442 (GRCm39)	D942G	possibly damaging	Het
Tamalin	T	A	15: 101,129,790 (GRCm39)	C358S	possibly damaging	Het
Tmem63a	A	G	1: 180,801,776 (GRCm39)	T764A	probably benign	Het
Ttf1	C	T	2: 28,957,238 (GRCm39)	Q503*	probably null	Het
Usp13	T	C	3: 32,949,025 (GRCm39)	V454A	possibly damaging	Het
Usp47	A	G	7: 111,652,472 (GRCm39)	T50A	possibly damaging	Het
Zfyve26	A	T	12: 79,315,331 (GRCm39)	C1382S	possibly damaging	Het

Other mutations in Gpr87

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00496:Gpr87	APN	3	59,087,211 (GRCm39)	missense	probably damaging	1.00
IGL02309:Gpr87	APN	3	59,086,975 (GRCm39)	missense	possibly damaging	0.74
IGL02614:Gpr87	APN	3	59,086,738 (GRCm39)	missense	probably damaging	1.00
R0097:Gpr87	UTSW	3	59,086,506 (GRCm39)	missense	probably damaging	1.00
R0097:Gpr87	UTSW	3	59,086,506 (GRCm39)	missense	probably damaging	1.00
R0113:Gpr87	UTSW	3	59,086,932 (GRCm39)	missense	possibly damaging	0.86
R1801:Gpr87	UTSW	3	59,086,813 (GRCm39)	missense	possibly damaging	0.92
R2213:Gpr87	UTSW	3	59,086,465 (GRCm39)	missense	probably damaging	0.99
R2698:Gpr87	UTSW	3	59,086,587 (GRCm39)	missense	probably damaging	1.00
R5459:Gpr87	UTSW	3	59,087,148 (GRCm39)	missense	possibly damaging	0.89
R5490:Gpr87	UTSW	3	59,086,747 (GRCm39)	missense	probably damaging	0.99
R5963:Gpr87	UTSW	3	59,086,690 (GRCm39)	nonsense	probably null
R6189:Gpr87	UTSW	3	59,086,650 (GRCm39)	missense	probably damaging	1.00
R6251:Gpr87	UTSW	3	59,086,528 (GRCm39)	missense	probably damaging	0.99
R7863:Gpr87	UTSW	3	59,087,317 (GRCm39)	missense	probably damaging	1.00
R8008:Gpr87	UTSW	3	59,087,466 (GRCm39)	missense	probably benign
R8065:Gpr87	UTSW	3	59,087,308 (GRCm39)	missense	probably damaging	1.00
R8067:Gpr87	UTSW	3	59,087,308 (GRCm39)	missense	probably damaging	1.00
R8096:Gpr87	UTSW	3	59,087,229 (GRCm39)	missense	possibly damaging	0.70
R8326:Gpr87	UTSW	3	59,102,395 (GRCm39)	start gained	probably benign
R9326:Gpr87	UTSW	3	59,086,609 (GRCm39)	missense	probably damaging	1.00
R9485:Gpr87	UTSW	3	59,087,005 (GRCm39)	missense	possibly damaging	0.85
Z1177:Gpr87	UTSW	3	59,087,491 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- GCTTATGAATTGCCTGCTGG -3'
(R):5'- TTCGGACCTTGGTACTTCGAG -3'

Sequencing Primer
(F):5'- TATCTGGAGATGGCTATGTAGCATCC -3'
(R):5'- CGAGTTTATCCTCTGCAGATACAC -3'

Posted On

2020-06-30