Mutagenetix > Incidental Mutation

Incidental Mutation 'R7830:Gpr146'

602368

Institutional Source

Beutler Lab

Gene Symbol

Gpr146

Ensembl Gene

ENSMUSG00000044197

Gene Name

G protein-coupled receptor 146

Synonyms

PGR8

MMRRC Submission

045884-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7830 (G1)

Quality Score

220.009

Status

Not validated

Chromosome

Chromosomal Location

139363452-139382170 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 139378357 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Valine at position 53 (A53V)

Ref Sequence

ENSEMBL: ENSMUSP00000119464 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000051293] [ENSMUST00000066052] [ENSMUST00000100514] [ENSMUST00000138631] [ENSMUST00000198474]

AlphaFold

Q99LE2

Predicted Effect

probably benign
Transcript: ENSMUST00000051293
AA Change: A53V

PolyPhen 2 Score 0.023 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000049707
Gene: ENSMUSG00000044197
AA Change: A53V

Domain	Start	End	E-Value	Type
low complexity region	21	36	N/A	INTRINSIC
Pfam:7tm_1	43	294	2e-16	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000066052

SMART Domains

Protein: ENSMUSP00000069230
Gene: ENSMUSG00000053553

Domain	Start	End	E-Value	Type
low complexity region	54	77	N/A	INTRINSIC
Pfam:DUF2373	103	165	3e-26	PFAM
low complexity region	184	194	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000100514
AA Change: A53V

PolyPhen 2 Score 0.023 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000098083
Gene: ENSMUSG00000044197
AA Change: A53V

Domain	Start	End	E-Value	Type
low complexity region	21	36	N/A	INTRINSIC
Pfam:7tm_1	43	294	1.6e-13	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000138631
AA Change: A53V

PolyPhen 2 Score 0.023 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000119464
Gene: ENSMUSG00000044197
AA Change: A53V

Domain	Start	End	E-Value	Type
SCOP:d1l9ha_	26	80	3e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000198474

SMART Domains

Protein: ENSMUSP00000142949
Gene: ENSMUSG00000053553

Domain	Start	End	E-Value	Type
low complexity region	54	77	N/A	INTRINSIC
Pfam:DUF2373	102	141	9e-12	PFAM

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adat3	T	C	10: 80,442,654 (GRCm39)	L164P	probably damaging	Het
Aldh16a1	A	T	7: 44,795,649 (GRCm39)	L388Q	probably damaging	Het
Angpt1	T	C	15: 42,539,664 (GRCm39)	N65S	probably damaging	Het
Ankrd54	G	A	15: 78,938,250 (GRCm39)	T287I	probably damaging	Het
Bltp1	CCAGATTCATGTAGCA	CCA	3: 37,019,081 (GRCm39)		probably null	Het
Cc2d2b	T	A	19: 40,753,801 (GRCm39)	V108E	possibly damaging	Het
Cd200l1	A	T	16: 45,262,917 (GRCm39)	I187N	probably damaging	Het
Cntnap5c	A	T	17: 58,469,245 (GRCm39)	D609V	probably damaging	Het
Col6a4	G	T	9: 105,952,589 (GRCm39)	D436E	probably damaging	Het
Cul9	A	T	17: 46,851,237 (GRCm39)	D394E	probably benign	Het
Cyfip1	A	G	7: 55,523,210 (GRCm39)	E75G	probably damaging	Het
Efr3a	G	A	15: 65,701,679 (GRCm39)	V198I	probably benign	Het
Eif2ak2	C	T	17: 79,173,832 (GRCm39)	G249S	probably damaging	Het
Erich4	A	T	7: 25,315,149 (GRCm39)	M42K	probably benign	Het
Fig4	A	C	10: 41,132,462 (GRCm39)	V448G	probably benign	Het
Gas1	T	C	13: 60,323,848 (GRCm39)	D303G	probably damaging	Het
Golgb1	T	G	16: 36,719,083 (GRCm39)	Y330D	possibly damaging	Het
Klk1b27	A	C	7: 43,705,150 (GRCm39)	M106L	probably benign	Het
Lipc	T	C	9: 70,720,183 (GRCm39)	T190A	probably damaging	Het
Lrrc4b	A	G	7: 44,111,231 (GRCm39)	I368V	possibly damaging	Het
Mmp10	A	T	9: 7,507,284 (GRCm39)	Q368L	probably benign	Het
Myo10	T	A	15: 25,738,057 (GRCm39)	Y501*	probably null	Het
Neb	T	A	2: 52,055,201 (GRCm39)	H6445L	probably benign	Het
Numa1	T	A	7: 101,648,492 (GRCm39)	M741K	probably benign	Het
Nxn	T	A	11: 76,164,819 (GRCm39)	I231F	probably damaging	Het
Or1j13	A	G	2: 36,369,392 (GRCm39)	L250P	probably damaging	Het
Or5b116	T	C	19: 13,422,985 (GRCm39)	L203S	probably benign	Het
Osbp2	A	G	11: 3,813,414 (GRCm39)	S152P	probably benign	Het
P3h4	T	C	11: 100,304,869 (GRCm39)	T173A	probably damaging	Het
Pcdh15	C	A	10: 74,221,733 (GRCm39)	R678S	probably damaging	Het
Pcdhb6	C	A	18: 37,469,365 (GRCm39)	T762K	probably benign	Het
Pnrc1	G	A	4: 33,248,057 (GRCm39)	P114L	probably damaging	Het
Ppp3ca	T	A	3: 136,574,481 (GRCm39)	S126R	probably damaging	Het
Prl3d2	C	T	13: 27,310,000 (GRCm39)	T155I	probably benign	Het
Prune2	C	A	19: 17,100,038 (GRCm39)	N1847K	probably benign	Het
Psg21	A	T	7: 18,381,223 (GRCm39)	V440E	probably damaging	Het
Rag1	A	G	2: 101,472,404 (GRCm39)	S913P	probably damaging	Het
Rmc1	A	G	18: 12,301,928 (GRCm39)	N24S	probably benign	Het
Ros1	T	A	10: 52,031,030 (GRCm39)	H525L	probably damaging	Het
Scarb1	T	C	5: 125,364,447 (GRCm39)	Y94C	probably damaging	Het
Serpinb6a	T	G	13: 34,114,030 (GRCm39)	D120A	probably benign	Het
Sik3	ACAGCAGCAGCAGCAGCAGCAGCAGCA	ACAGCAGCAGCAGCAGCAGCAGCA	9: 46,123,355 (GRCm39)		probably benign	Het
Slc39a14	T	C	14: 70,547,566 (GRCm39)	D299G	probably benign	Het
Sox1	G	A	8: 12,446,955 (GRCm39)	A199T	probably damaging	Het
Strc	T	A	2: 121,205,530 (GRCm39)	I867F	probably damaging	Het
Tfrc	A	G	16: 32,437,985 (GRCm39)	K346R	probably benign	Het
Usf3	C	T	16: 44,040,142 (GRCm39)	Q1541*	probably null	Het
Wrn	G	A	8: 33,759,082 (GRCm39)	L716F	probably damaging	Het
Zfp141	G	A	7: 42,124,612 (GRCm39)	T620I	probably benign	Het
Zfp354b	A	T	11: 50,814,136 (GRCm39)	I263K	probably benign	Het
Zfp804b	T	A	5: 6,821,124 (GRCm39)	E646D	probably benign	Het
Zfp970	G	T	2: 177,167,338 (GRCm39)	C304F	probably damaging	Het

Other mutations in Gpr146

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01355:Gpr146	APN	5	139,364,659 (GRCm39)	intron	probably benign
IGL02152:Gpr146	APN	5	139,378,467 (GRCm39)	missense	probably damaging	1.00
IGL02369:Gpr146	APN	5	139,378,443 (GRCm39)	missense	probably benign	0.00
IGL02392:Gpr146	APN	5	139,378,533 (GRCm39)	missense	probably damaging	0.99
IGL02828:Gpr146	APN	5	139,378,576 (GRCm39)	missense	probably damaging	0.97
IGL03095:Gpr146	APN	5	139,378,705 (GRCm39)	missense	probably benign	0.11
R0360:Gpr146	UTSW	5	139,364,933 (GRCm39)	intron	probably benign
R0364:Gpr146	UTSW	5	139,364,933 (GRCm39)	intron	probably benign
R0746:Gpr146	UTSW	5	139,378,977 (GRCm39)	missense	probably damaging	1.00
R1446:Gpr146	UTSW	5	139,379,177 (GRCm39)	missense	probably benign	0.00
R1507:Gpr146	UTSW	5	139,379,124 (GRCm39)	missense	probably benign
R1758:Gpr146	UTSW	5	139,379,137 (GRCm39)	missense	probably benign	0.34
R2032:Gpr146	UTSW	5	139,364,902 (GRCm39)	intron	probably benign
R6513:Gpr146	UTSW	5	139,378,573 (GRCm39)	missense	probably damaging	1.00
R6797:Gpr146	UTSW	5	139,378,795 (GRCm39)	missense	possibly damaging	0.79
R7977:Gpr146	UTSW	5	139,378,440 (GRCm39)	missense	possibly damaging	0.53
R7987:Gpr146	UTSW	5	139,378,440 (GRCm39)	missense	possibly damaging	0.53
R8225:Gpr146	UTSW	5	139,378,371 (GRCm39)	missense	probably benign	0.03
R8792:Gpr146	UTSW	5	139,378,549 (GRCm39)	missense	probably damaging	1.00
R9354:Gpr146	UTSW	5	139,378,366 (GRCm39)	missense	probably benign	0.00
X0064:Gpr146	UTSW	5	139,364,664 (GRCm39)	intron	probably benign

Predicted Primers

PCR Primer
(F):5'- AGTGGTGACTAACTCTGTCCC -3'
(R):5'- TACATGGTCACCAGGGAAGC -3'

Sequencing Primer
(F):5'- TCTCTCTCAACAGCTGCGAAG -3'
(R):5'- CCACGTTGAACAGGATGAGC -3'

Posted On

2019-12-03