Mutagenetix > Incidental Mutation

Incidental Mutation 'R5322:Gpr157'

404893

Institutional Source

Beutler Lab

Gene Symbol

Gpr157

Ensembl Gene

ENSMUSG00000047875

Gene Name

G protein-coupled receptor 157

Synonyms

F730108M23Rik

MMRRC Submission

042905-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5322 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

150171960-150190457 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 150183309 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Aspartic acid at position 160 (N160D)

Ref Sequence

ENSEMBL: ENSMUSP00000092020 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000094451]

AlphaFold

Q8C206

Predicted Effect

probably benign
Transcript: ENSMUST00000094451
AA Change: N160D

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000092020
Gene: ENSMUSG00000047875
AA Change: N160D

Domain	Start	End	E-Value	Type
Pfam:Dicty_CAR	11	205	4.1e-12	PFAM
Pfam:Frizzled	14	250	2e-8	PFAM
Pfam:7tm_2	14	274	2e-15	PFAM

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.5%
20x: 95.8%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts3	C	T	5: 89,855,159 (GRCm39)		probably null	Het
Ankar	T	C	1: 72,729,545 (GRCm39)		probably null	Het
Ankrd60	T	A	2: 173,410,610 (GRCm39)	K303N	possibly damaging	Het
Appbp2	A	G	11: 85,086,890 (GRCm39)		probably null	Het
Arvcf	T	C	16: 18,215,508 (GRCm39)	M176T	probably benign	Het
Cachd1	T	C	4: 100,809,319 (GRCm39)	I268T	probably damaging	Het
Ccdc66	A	G	14: 27,204,484 (GRCm39)	S933P	probably damaging	Het
Cfi	C	T	3: 129,666,689 (GRCm39)	P471S	probably damaging	Het
Ckmt2	G	T	13: 92,009,891 (GRCm39)	T143K	possibly damaging	Het
Cnksr3	A	T	10: 7,085,078 (GRCm39)	D15E	probably damaging	Het
Copb2	A	T	9: 98,468,029 (GRCm39)	K680N	probably benign	Het
D2hgdh	T	C	1: 93,757,620 (GRCm39)		probably null	Het
Dcn	A	T	10: 97,353,464 (GRCm39)	T338S	probably benign	Het
Dipk2a	A	G	9: 94,402,615 (GRCm39)	I349T	probably benign	Het
Dnah10	G	A	5: 124,850,630 (GRCm39)	G1644D	probably damaging	Het
Dnah5	A	G	15: 28,384,390 (GRCm39)	I3045V	probably benign	Het
Dock3	G	A	9: 106,779,028 (GRCm39)	T307I	probably benign	Het
Dock5	A	T	14: 68,007,715 (GRCm39)	I1498N	probably benign	Het
Emc1	A	T	4: 139,081,557 (GRCm39)	N62Y	probably damaging	Het
Enpp6	C	A	8: 47,521,950 (GRCm39)	H295N	probably benign	Het
Epha10	A	G	4: 124,779,541 (GRCm39)	Y129C	probably damaging	Het
Fbn2	A	T	18: 58,172,387 (GRCm39)	D2139E	probably benign	Het
Fbxl12	A	T	9: 20,550,304 (GRCm39)	V140E	probably damaging	Het
Fignl1	A	T	11: 11,751,571 (GRCm39)	F495I	probably damaging	Het
Gm43302	C	T	5: 105,365,347 (GRCm39)	A554T	probably benign	Het
Il1rn	G	A	2: 24,238,641 (GRCm39)		probably null	Het
Kctd13	T	A	7: 126,528,378 (GRCm39)	L51Q	probably damaging	Het
Kndc1	T	C	7: 139,516,722 (GRCm39)	F1561L	probably damaging	Het
Mast2	A	G	4: 116,190,608 (GRCm39)		probably null	Het
Mib1	A	G	18: 10,792,975 (GRCm39)	H637R	probably damaging	Het
Moxd1	A	T	10: 24,120,151 (GRCm39)	N93I	possibly damaging	Het
Mycbp2	T	C	14: 103,423,119 (GRCm39)		probably null	Het
Myot	T	C	18: 44,487,216 (GRCm39)	F351S	probably benign	Het
N4bp2	T	A	5: 65,947,800 (GRCm39)	N143K	possibly damaging	Het
Or10ac1	T	C	6: 42,515,950 (GRCm39)	D2G	probably benign	Het
Or2ah1	T	A	2: 85,653,531 (GRCm39)	I72N	probably damaging	Het
Or51b6b	T	C	7: 103,309,879 (GRCm39)	I193V	possibly damaging	Het
Or52a20	T	A	7: 103,366,319 (GRCm39)	W173R	probably benign	Het
Or52n2	C	T	7: 104,542,371 (GRCm39)	V155I	probably benign	Het
Or8b3	A	T	9: 38,314,862 (GRCm39)	I228F	probably damaging	Het
Or8b52	T	A	9: 38,576,502 (GRCm39)	I213L	probably benign	Het
Patl1	C	T	19: 11,898,223 (GRCm39)	R134*	probably null	Het
Paxbp1	T	C	16: 90,812,050 (GRCm39)	I887V	probably benign	Het
Pi4kb	G	A	3: 94,901,560 (GRCm39)	R436Q	probably benign	Het
Pla2g3	A	G	11: 3,438,686 (GRCm39)	E112G	probably benign	Het
Ppp2r2a	A	G	14: 67,276,322 (GRCm39)		probably null	Het
Rela	T	A	19: 5,695,408 (GRCm39)	S311R	possibly damaging	Het
Sidt1	T	A	16: 44,101,985 (GRCm39)		probably benign	Het
Smco2	T	C	6: 146,772,785 (GRCm39)	L329P	probably damaging	Het
Speer4f1	A	T	5: 17,682,347 (GRCm39)	I77F	possibly damaging	Het
Tex14	A	G	11: 87,402,298 (GRCm39)	I462V	probably benign	Het
Tmem260	C	T	14: 48,724,306 (GRCm39)	R385W	probably damaging	Het
Trrap	T	C	5: 144,781,034 (GRCm39)	V2974A	probably damaging	Het
Usp47	C	T	7: 111,652,476 (GRCm39)	T31I	probably damaging	Het
Zc2hc1a	A	G	3: 7,616,481 (GRCm39)	N247S	probably benign	Het
Zeb2	A	C	2: 44,887,107 (GRCm39)	M582R	probably damaging	Het

Other mutations in Gpr157

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01611:Gpr157	APN	4	150,186,094 (GRCm39)	missense	possibly damaging	0.59
IGL02233:Gpr157	APN	4	150,186,184 (GRCm39)	missense	possibly damaging	0.63
R2912:Gpr157	UTSW	4	150,183,222 (GRCm39)	missense	probably benign	0.08
R2913:Gpr157	UTSW	4	150,183,222 (GRCm39)	missense	probably benign	0.08
R4721:Gpr157	UTSW	4	150,183,420 (GRCm39)	missense	probably benign	0.01
R4840:Gpr157	UTSW	4	150,186,823 (GRCm39)	missense	probably benign	0.00
R5089:Gpr157	UTSW	4	150,186,750 (GRCm39)	missense	possibly damaging	0.89
R5445:Gpr157	UTSW	4	150,186,825 (GRCm39)	missense	probably benign	0.00
R6210:Gpr157	UTSW	4	150,186,055 (GRCm39)	missense	probably damaging	1.00
R7252:Gpr157	UTSW	4	150,183,331 (GRCm39)	missense	probably benign	0.01
R8246:Gpr157	UTSW	4	150,186,753 (GRCm39)	missense	possibly damaging	0.80
R8274:Gpr157	UTSW	4	150,172,500 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CTCCCTTGTTTTGTAGGAGCAC -3'
(R):5'- GGGTCTTCAGAGATACAGCCTG -3'

Sequencing Primer
(F):5'- CTGAGAGAACCCCAGTCAGTTTTG -3'
(R):5'- GAGATACAGCCTGTCCCCTAAGG -3'

Posted On

2016-07-22