Mutagenetix > Incidental Mutation

Incidental Mutation 'R1703:Grip2'

189881

Institutional Source

Beutler Lab

Gene Symbol

Grip2

Ensembl Gene

ENSMUSG00000030098

Gene Name

glutamate receptor interacting protein 2

Synonyms

MMRRC Submission

039736-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1703 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

91738490-91804231 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 91754379 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 632 (I632N)

Ref Sequence

ENSEMBL: ENSMUSP00000124717 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000159684] [ENSMUST00000162293] [ENSMUST00000162300]

AlphaFold

G3XA20

Predicted Effect

probably damaging
Transcript: ENSMUST00000159684
AA Change: I643N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000125047
Gene: ENSMUSG00000030098
AA Change: I643N

Domain	Start	End	E-Value	Type
low complexity region	25	36	N/A	INTRINSIC
PDZ	62	136	1.12e-12	SMART
PDZ	161	239	3.8e-15	SMART
PDZ	262	337	7.9e-13	SMART
low complexity region	385	390	N/A	INTRINSIC
PDZ	426	506	2.18e-15	SMART
PDZ	527	602	3.86e-16	SMART
PDZ	625	699	1.38e-17	SMART
low complexity region	778	793	N/A	INTRINSIC
low complexity region	867	878	N/A	INTRINSIC
PDZ	910	982	2.95e-12	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000162293
AA Change: I632N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000124717
Gene: ENSMUSG00000030098
AA Change: I632N

Domain	Start	End	E-Value	Type
PDZ	10	84	1.12e-12	SMART
PDZ	109	187	3.8e-15	SMART
PDZ	210	285	7.9e-13	SMART
low complexity region	336	348	N/A	INTRINSIC
low complexity region	374	379	N/A	INTRINSIC
PDZ	415	495	2.18e-15	SMART
PDZ	516	591	3.86e-16	SMART
PDZ	614	688	1.38e-17	SMART
low complexity region	767	782	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000162300
AA Change: I684N

PolyPhen 2 Score 0.969 (Sensitivity: 0.77; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000124709
Gene: ENSMUSG00000030098
AA Change: I684N

Domain	Start	End	E-Value	Type
low complexity region	25	36	N/A	INTRINSIC
PDZ	62	136	1.12e-12	SMART
PDZ	161	239	3.8e-15	SMART
PDZ	262	337	7.9e-13	SMART
low complexity region	388	400	N/A	INTRINSIC
low complexity region	426	431	N/A	INTRINSIC
PDZ	467	547	2.18e-15	SMART
PDZ	568	643	3.86e-16	SMART
PDZ	666	740	1.38e-17	SMART
low complexity region	819	834	N/A	INTRINSIC
low complexity region	908	919	N/A	INTRINSIC
PDZ	951	1023	2.95e-12	SMART

Meta Mutation Damage Score

0.2640

Coding Region Coverage

1x: 99.1%
3x: 98.3%
10x: 96.2%
20x: 92.4%

Validation Efficiency

99% (86/87)

MGI Phenotype

PHENOTYPE: Homozygous null mice are born in numbers expected by the Mendelian ratio and show no overt phenotype. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 78 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310057M21Rik	A	T	7: 130,945,431 (GRCm39)	Y401*	probably null	Het
4932415M13Rik	C	A	17: 54,032,065 (GRCm39)		noncoding transcript	Het
Abtb3	A	G	10: 85,223,248 (GRCm39)	D19G	unknown	Het
Acoxl	T	A	2: 127,820,692 (GRCm39)	S81R	probably damaging	Het
Adamtsl4	A	G	3: 95,584,924 (GRCm39)	C915R	probably damaging	Het
Adgra3	C	T	5: 50,164,117 (GRCm39)	M287I	probably benign	Het
Afg1l	T	G	10: 42,276,395 (GRCm39)	D250A	probably damaging	Het
Akap8l	C	T	17: 32,551,457 (GRCm39)	R511H	probably damaging	Het
Amfr	T	C	8: 94,700,871 (GRCm39)	T530A	probably benign	Het
Ank2	C	T	3: 126,723,415 (GRCm39)	V971M	probably damaging	Het
App	A	G	16: 84,762,656 (GRCm39)	S656P	probably damaging	Het
Arid5a	T	A	1: 36,358,656 (GRCm39)		probably null	Het
Asic5	T	A	3: 81,907,029 (GRCm39)	V60D	possibly damaging	Het
Atm	G	T	9: 53,412,000 (GRCm39)	H1019N	probably benign	Het
Cep250	A	G	2: 155,807,466 (GRCm39)	K277R	probably benign	Het
Chrna7	C	T	7: 62,749,255 (GRCm39)	R409H	probably damaging	Het
Chrng	A	T	1: 87,138,628 (GRCm39)	N419I	possibly damaging	Het
Ciao1	T	C	2: 127,087,739 (GRCm39)	S199G	probably benign	Het
Clstn2	A	T	9: 97,340,290 (GRCm39)	M694K	possibly damaging	Het
Cpeb2	A	G	5: 43,391,181 (GRCm39)		probably benign	Het
Cyp2c69	T	A	19: 39,864,810 (GRCm39)	I223F	probably benign	Het
Dennd1b	A	T	1: 139,097,492 (GRCm39)		probably null	Het
Dnah17	A	T	11: 117,917,575 (GRCm39)	L4162Q	probably damaging	Het
Dnm1	T	C	2: 32,213,463 (GRCm39)	M506V	probably benign	Het
Ecsit	A	G	9: 21,986,107 (GRCm39)	V173A	probably damaging	Het
Fam13b	T	C	18: 34,584,492 (GRCm39)		probably null	Het
Fgl2	T	A	5: 21,577,730 (GRCm39)	W6R	possibly damaging	Het
Galnt9	G	A	5: 110,767,038 (GRCm39)	R503H	probably damaging	Het
Gramd1a	C	T	7: 30,838,959 (GRCm39)	V247M	possibly damaging	Het
Hspg2	T	C	4: 137,286,462 (GRCm39)	V3627A	probably damaging	Het
Ipo8	T	C	6: 148,691,390 (GRCm39)	Y660C	probably benign	Het
Isg15	T	C	4: 156,284,265 (GRCm39)	R88G	possibly damaging	Het
Itgb5	T	A	16: 33,730,870 (GRCm39)	D388E	probably benign	Het
Jhy	T	C	9: 40,856,133 (GRCm39)	Y118C	probably damaging	Het
Kalrn	G	A	16: 34,025,696 (GRCm39)	T931M	probably damaging	Het
Kif21a	A	G	15: 90,833,250 (GRCm39)		probably null	Het
Lama2	A	T	10: 27,142,667 (GRCm39)	Y604N	probably damaging	Het
Lrp3	T	G	7: 34,912,586 (GRCm39)	S34R	possibly damaging	Het
Lrrc37	C	T	11: 103,431,700 (GRCm39)	V1372I	probably benign	Het
Lyn	T	C	4: 3,738,867 (GRCm39)		probably null	Het
Mroh8	C	T	2: 157,113,896 (GRCm39)	V132I	probably benign	Het
Mthfd1l	T	C	10: 4,098,093 (GRCm39)	F977L	probably damaging	Het
Nol8	C	T	13: 49,820,933 (GRCm39)	T912M	possibly damaging	Het
Nrxn1	A	T	17: 90,515,845 (GRCm39)	N169K	probably damaging	Het
Oplah	A	G	15: 76,180,867 (GRCm39)	Y1279H	probably benign	Het
Or10ag56	T	C	2: 87,139,754 (GRCm39)	V207A	probably benign	Het
Or4c101	T	A	2: 88,390,599 (GRCm39)	M262K	possibly damaging	Het
Pcsk5	T	C	19: 17,729,458 (GRCm39)	N129S	probably benign	Het
Pcyt2	G	T	11: 120,503,894 (GRCm39)	P185T	probably benign	Het
Pdlim2	A	G	14: 70,411,784 (GRCm39)		probably null	Het
Pgs1	T	C	11: 117,905,554 (GRCm39)		probably benign	Het
Qprt	A	G	7: 126,707,343 (GRCm39)	V251A	probably benign	Het
Rasal2	A	C	1: 156,985,170 (GRCm39)	L834R	probably damaging	Het
Reg1	T	C	6: 78,405,432 (GRCm39)	C161R	probably damaging	Het
Rp1	T	A	1: 4,415,392 (GRCm39)	I1907F	probably damaging	Het
S1pr5	T	C	9: 21,155,346 (GRCm39)	D360G	possibly damaging	Het
Sart3	C	A	5: 113,890,280 (GRCm39)	V482F	probably benign	Het
Scarf2	A	G	16: 17,620,713 (GRCm39)	E127G	probably damaging	Het
Serinc5	T	C	13: 92,825,305 (GRCm39)	S245P	probably damaging	Het
Serpinc1	G	T	1: 160,821,087 (GRCm39)	R57L	probably damaging	Het
Setd2	A	G	9: 110,378,932 (GRCm39)	S632G	probably benign	Het
Sgca	A	T	11: 94,860,217 (GRCm39)	L307M	probably damaging	Het
Slc7a9	C	A	7: 35,154,000 (GRCm39)	Q208K	probably benign	Het
Slfn10-ps	C	T	11: 82,920,869 (GRCm39)		noncoding transcript	Het
Spam1	A	T	6: 24,796,256 (GRCm39)	D69V	probably damaging	Het
Tanc1	A	G	2: 59,673,365 (GRCm39)	E1490G	probably benign	Het
Tbc1d22a	G	T	15: 86,123,416 (GRCm39)	D150Y	probably benign	Het
Tex10	C	T	4: 48,456,800 (GRCm39)	R637Q	probably benign	Het
Tlx1	A	G	19: 45,144,443 (GRCm39)	D55G	possibly damaging	Het
Tram2	G	T	1: 21,074,458 (GRCm39)	N241K	probably damaging	Het
Ttc23l	T	C	15: 10,523,744 (GRCm39)	Y325C	probably damaging	Het
Ubac2	T	A	14: 122,142,582 (GRCm39)	S27T	probably benign	Het
Utrn	G	A	10: 12,603,473 (GRCm39)		probably benign	Het
Vnn3	A	T	10: 23,741,828 (GRCm39)	M378L	probably benign	Het
Vps18	T	A	2: 119,119,538 (GRCm39)	D6E	probably benign	Het
Xkr5	T	A	8: 18,989,134 (GRCm39)	I253F	probably benign	Het
Yeats4	A	T	10: 117,051,628 (GRCm39)	C210S	probably benign	Het
Zdhhc20	A	G	14: 58,076,545 (GRCm39)		probably null	Het

Other mutations in Grip2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01141:Grip2	APN	6	91,759,878 (GRCm39)	missense	probably benign	0.00
IGL01748:Grip2	APN	6	91,741,724 (GRCm39)	missense	probably damaging	1.00
IGL01838:Grip2	APN	6	91,741,744 (GRCm39)	missense	possibly damaging	0.92
IGL02392:Grip2	APN	6	91,764,276 (GRCm39)	missense	probably damaging	1.00
IGL02620:Grip2	APN	6	91,755,587 (GRCm39)	missense	possibly damaging	0.93
IGL02862:Grip2	APN	6	91,765,085 (GRCm39)	missense	probably damaging	0.98
IGL03027:Grip2	APN	6	91,755,852 (GRCm39)	missense	probably benign	0.02
IGL03180:Grip2	APN	6	91,762,742 (GRCm39)	splice site	probably benign
R0265:Grip2	UTSW	6	91,750,773 (GRCm39)	critical splice donor site	probably null
R0448:Grip2	UTSW	6	91,756,194 (GRCm39)	missense	probably damaging	1.00
R0597:Grip2	UTSW	6	91,773,178 (GRCm39)	intron	probably benign
R1405:Grip2	UTSW	6	91,765,133 (GRCm39)	splice site	probably null
R1405:Grip2	UTSW	6	91,765,133 (GRCm39)	splice site	probably null
R1466:Grip2	UTSW	6	91,765,424 (GRCm39)	missense	probably damaging	0.98
R1466:Grip2	UTSW	6	91,765,424 (GRCm39)	missense	probably damaging	0.98
R1664:Grip2	UTSW	6	91,742,233 (GRCm39)	missense	probably damaging	1.00
R1793:Grip2	UTSW	6	91,760,623 (GRCm39)	missense	probably benign	0.03
R1951:Grip2	UTSW	6	91,760,829 (GRCm39)	missense	probably damaging	1.00
R2001:Grip2	UTSW	6	91,756,831 (GRCm39)	missense	probably benign	0.00
R4730:Grip2	UTSW	6	91,762,693 (GRCm39)	makesense	probably null
R4754:Grip2	UTSW	6	91,756,173 (GRCm39)	missense	probably damaging	0.97
R4754:Grip2	UTSW	6	91,756,163 (GRCm39)	missense	probably damaging	1.00
R4773:Grip2	UTSW	6	91,759,413 (GRCm39)	missense	possibly damaging	0.80
R5135:Grip2	UTSW	6	91,750,897 (GRCm39)	missense	possibly damaging	0.89
R5213:Grip2	UTSW	6	91,756,812 (GRCm39)	missense	probably benign	0.04
R5972:Grip2	UTSW	6	91,784,262 (GRCm39)	missense	probably benign	0.01
R6176:Grip2	UTSW	6	91,756,832 (GRCm39)	missense	probably benign	0.00
R6188:Grip2	UTSW	6	91,740,514 (GRCm39)	missense	probably damaging	1.00
R6289:Grip2	UTSW	6	91,755,852 (GRCm39)	missense	probably benign	0.02
R6345:Grip2	UTSW	6	91,742,369 (GRCm39)	missense	possibly damaging	0.91
R6348:Grip2	UTSW	6	91,757,419 (GRCm39)	missense	probably damaging	0.99
R6394:Grip2	UTSW	6	91,764,182 (GRCm39)	missense	probably damaging	1.00
R6658:Grip2	UTSW	6	91,763,472 (GRCm39)	missense	probably damaging	1.00
R7065:Grip2	UTSW	6	91,760,550 (GRCm39)	critical splice donor site	probably null
R7074:Grip2	UTSW	6	91,761,689 (GRCm39)	missense	probably benign	0.24
R7308:Grip2	UTSW	6	91,755,669 (GRCm39)	missense	possibly damaging	0.74
R7607:Grip2	UTSW	6	91,765,393 (GRCm39)	missense	probably benign
R7617:Grip2	UTSW	6	91,742,031 (GRCm39)	splice site	probably null
R7970:Grip2	UTSW	6	91,763,513 (GRCm39)	missense	probably benign	0.07
R8221:Grip2	UTSW	6	91,762,665 (GRCm39)	missense	possibly damaging	0.90
R8549:Grip2	UTSW	6	91,750,769 (GRCm39)	splice site	probably null
R8838:Grip2	UTSW	6	91,762,721 (GRCm39)	utr 3 prime	probably benign
R8962:Grip2	UTSW	6	91,754,391 (GRCm39)	missense	probably damaging	1.00
R9430:Grip2	UTSW	6	91,784,265 (GRCm39)	missense	probably benign	0.05
R9699:Grip2	UTSW	6	91,742,318 (GRCm39)	missense	probably benign
R9732:Grip2	UTSW	6	91,761,686 (GRCm39)	missense	probably damaging	0.99
RF003:Grip2	UTSW	6	91,760,574 (GRCm39)	missense	probably benign	0.02
Z1176:Grip2	UTSW	6	91,740,491 (GRCm39)	missense	possibly damaging	0.55

Predicted Primers

PCR Primer
(F):5'- AGCTGAAGGTGAGCTATCCTGCCC -3'
(R):5'- AGGTCCCCAGGTTGTACCCCGAAAG -3'

Sequencing Primer
(F):5'- CTGGGCTGGACCAAAATTCATTC -3'
(R):5'- GAGGGTTCGATGAGGTCAC -3'

Posted On

2014-05-14