Mutagenetix > Incidental Mutation

Incidental Mutation 'R1664:Grip2'

187012

Institutional Source

Beutler Lab

Gene Symbol

Grip2

Ensembl Gene

ENSMUSG00000030098

Gene Name

glutamate receptor interacting protein 2

Synonyms

MMRRC Submission

039700-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1664 (G1)

Quality Score

224

Status

Not validated

Chromosome

Chromosomal Location

91738490-91804231 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 91742233 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Leucine at position 899 (H899L)

Ref Sequence

ENSEMBL: ENSMUSP00000125047 (fasta)

Gene Model

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

AlphaFold

G3XA20

Predicted Effect

probably damaging
Transcript: ENSMUST00000159684
AA Change: H899L

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

SMART Domains

Protein: ENSMUSP00000125047
Gene: ENSMUSG00000030098
AA Change: H899L

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 benign
Transcript: ENSMUST00000162293

SMART Domains

Protein: ENSMUSP00000124717
Gene: ENSMUSG00000030098

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 benign
Transcript: ENSMUST00000162300
AA Change: H940L

PolyPhen 2 Score 0.030 (Sensitivity: 0.95; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000124709
Gene: ENSMUSG00000030098
AA Change: H940L

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

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.5%
20x: 93.0%

Validation Efficiency

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: 81 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930596D02Rik	T	A	14: 35,533,772 (GRCm39)	T45S	probably benign	Het
Ackr1	A	G	1: 173,160,433 (GRCm39)	F29L	probably benign	Het
Adgrf2	T	A	17: 43,025,305 (GRCm39)	S60C	possibly damaging	Het
Alpk2	A	G	18: 65,482,944 (GRCm39)	C355R	probably damaging	Het
Ankmy1	A	C	1: 92,812,913 (GRCm39)	D465E	probably benign	Het
Ankrd27	T	A	7: 35,306,551 (GRCm39)	D310E	probably damaging	Het
Ap3d1	G	A	10: 80,553,571 (GRCm39)	Q559*	probably null	Het
C4b	T	C	17: 34,951,952 (GRCm39)	T1298A	probably damaging	Het
Casr	T	A	16: 36,330,327 (GRCm39)	K336*	probably null	Het
Ccdc116	A	T	16: 16,960,492 (GRCm39)	D108E	probably benign	Het
Ccdc168	T	A	1: 44,098,387 (GRCm39)	I904F	possibly damaging	Het
Ccr7	A	T	11: 99,036,517 (GRCm39)	I135N	possibly damaging	Het
Cd96	A	G	16: 45,938,364 (GRCm39)	Y34H	possibly damaging	Het
Cdan1	T	A	2: 120,550,987 (GRCm39)	D1135V	probably damaging	Het
Cecr2	C	A	6: 120,738,987 (GRCm39)	T1210K	probably damaging	Het
Cep152	C	A	2: 125,408,174 (GRCm39)	A1390S	probably benign	Het
Chd9	T	G	8: 91,749,418 (GRCm39)		probably null	Het
Cntnap5c	G	T	17: 58,600,985 (GRCm39)	W776L	probably benign	Het
Col24a1	G	A	3: 145,095,355 (GRCm39)		probably null	Het
Cpa2	G	T	6: 30,554,314 (GRCm39)	M311I	probably damaging	Het
Cpz	A	G	5: 35,664,087 (GRCm39)	F483L	probably damaging	Het
Ddx19a	A	C	8: 111,716,130 (GRCm39)	V90G	probably damaging	Het
Fabp3	C	T	4: 130,206,180 (GRCm39)	T57I	probably benign	Het
Fbxw7	A	G	3: 84,876,478 (GRCm39)	D213G	possibly damaging	Het
Fgd2	T	C	17: 29,588,273 (GRCm39)	F362L	probably damaging	Het
Fryl	A	G	5: 73,216,778 (GRCm39)	Y2171H	probably damaging	Het
Gba2	T	C	4: 43,578,080 (GRCm39)	R90G	probably benign	Het
Gm10073	T	C	8: 107,299,864 (GRCm39)	E40G	probably damaging	Het
Grhl3	T	C	4: 135,279,861 (GRCm39)	I398V	probably benign	Het
Grk2	T	C	19: 4,337,268 (GRCm39)	K644E	possibly damaging	Het
Iars1	A	T	13: 49,865,251 (GRCm39)	T576S	probably damaging	Het
Kif26b	G	A	1: 178,759,704 (GRCm39)	V2084M	probably damaging	Het
Kirrel1	C	T	3: 86,996,458 (GRCm39)	M380I	probably null	Het
Lrrc69	G	A	4: 14,775,079 (GRCm39)	T63M	probably damaging	Het
Lrrn4	A	T	2: 132,711,886 (GRCm39)	C646S	probably damaging	Het
Mtf2	C	T	5: 108,252,342 (GRCm39)	T457M	probably damaging	Het
Ncln	A	T	10: 81,323,555 (GRCm39)	C531S	probably benign	Het
Ntn4	C	T	10: 93,543,215 (GRCm39)	R314W	probably damaging	Het
Or14j8	T	C	17: 38,263,784 (GRCm39)	I44V	probably benign	Het
Or5v1	C	T	17: 37,810,316 (GRCm39)	T258M	possibly damaging	Het
Or8c11	A	T	9: 38,289,548 (GRCm39)	M124L	possibly damaging	Het
Otogl	A	G	10: 107,642,437 (GRCm39)	V1331A	probably benign	Het
Palb2	A	G	7: 121,723,615 (GRCm39)		probably benign	Het
Pcdh20	T	C	14: 88,705,758 (GRCm39)	E514G	possibly damaging	Het
Pclaf	A	G	9: 65,797,730 (GRCm39)	N7S	probably benign	Het
Pdrg1	C	T	2: 152,857,248 (GRCm39)		probably benign	Het
Phf8-ps	T	A	17: 33,285,492 (GRCm39)	I437F	probably damaging	Het
Pik3r6	T	A	11: 68,426,932 (GRCm39)	D464E	probably benign	Het
Pkp3	A	G	7: 140,667,560 (GRCm39)	N454D	probably damaging	Het
Plekha7	C	A	7: 115,734,269 (GRCm39)		probably null	Het
Ppip5k1	A	G	2: 121,167,663 (GRCm39)	V784A	probably benign	Het
Ppp1r36	T	A	12: 76,483,028 (GRCm39)	D205E	possibly damaging	Het
Prss35	A	T	9: 86,637,700 (GRCm39)	T157S	probably benign	Het
Ptprn2	T	C	12: 117,125,329 (GRCm39)	L621P	probably damaging	Het
Rasgrp3	A	G	17: 75,831,172 (GRCm39)	K524R	probably damaging	Het
Rasgrp4	T	A	7: 28,839,688 (GRCm39)	H133Q	probably benign	Het
Reln	A	T	5: 22,134,084 (GRCm39)	Y2615N	probably damaging	Het
Rpf1	T	A	3: 146,217,903 (GRCm39)	T204S	probably benign	Het
Scgb2b3	T	A	7: 31,058,464 (GRCm39)	*113L	probably null	Het
Scn5a	A	C	9: 119,350,243 (GRCm39)	L877R	possibly damaging	Het
Sh3pxd2a	A	T	19: 47,256,821 (GRCm39)	D632E	probably benign	Het
Slc39a10	T	C	1: 46,865,269 (GRCm39)	H522R	probably damaging	Het
Spink2	A	T	5: 77,354,855 (GRCm39)	C19S	probably damaging	Het
Spsb4	A	G	9: 96,878,266 (GRCm39)	L19P	possibly damaging	Het
St7l	T	C	3: 104,778,214 (GRCm39)	V117A	probably damaging	Het
Stac2	C	T	11: 97,933,420 (GRCm39)	S174N	probably damaging	Het
Sult4a1	A	G	15: 83,970,818 (GRCm39)	Y196H	probably benign	Het
Tex2	C	T	11: 106,458,608 (GRCm39)		probably benign	Het
Tprg1l	A	T	4: 154,243,862 (GRCm39)	V98D	possibly damaging	Het
Ttn	G	A	2: 76,548,369 (GRCm39)	H31978Y	probably damaging	Het
Ttn	T	C	2: 76,658,853 (GRCm39)		probably benign	Het
Tyk2	C	A	9: 21,031,649 (GRCm39)	R447L	probably damaging	Het
Ucn3	T	C	13: 3,991,634 (GRCm39)	Y6C	possibly damaging	Het
Urb1	A	T	16: 90,584,970 (GRCm39)		probably null	Het
Vmn2r94	G	C	17: 18,464,406 (GRCm39)	A628G	probably damaging	Het
Wdr95	C	A	5: 149,518,752 (GRCm39)	T389K	probably damaging	Het
Wrn	A	T	8: 33,770,794 (GRCm39)		probably null	Het
Xab2	T	A	8: 3,669,068 (GRCm39)		probably null	Het
Zfp458	A	T	13: 67,406,144 (GRCm39)	N95K	possibly damaging	Het
Zfp672	T	C	11: 58,208,138 (GRCm39)	H61R	probably damaging	Het
Zfp942	C	T	17: 22,147,420 (GRCm39)	G403E	possibly damaging	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
R1703:Grip2	UTSW	6	91,754,379 (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'- GCTGAAACCAAAGTCGTTCCTCACC -3'
(R):5'- GACAACTATGTCCCCACAGGCTTC -3'

Sequencing Primer
(F):5'- ATGTGCAGCTTGCAGATCC -3'
(R):5'- CAGGCTTCCATCATGACAGG -3'

Posted On

2014-05-09