Mutagenetix > Incidental Mutation

Incidental Mutation 'R0373:Rasip1'

30608

Institutional Source

Beutler Lab

Gene Symbol

Rasip1

Ensembl Gene

ENSMUSG00000044562

Gene Name

Ras interacting protein 1

Synonyms

Rain, 2610025P08Rik

MMRRC Submission

038579-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R0373 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

45276961-45288516 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 45284668 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Lysine at position 678 (N678K)

Ref Sequence

ENSEMBL: ENSMUSP00000062429 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000057927] [ENSMUST00000148532]

AlphaFold

Q3U0S6

Predicted Effect

possibly damaging
Transcript: ENSMUST00000057927
AA Change: N678K

PolyPhen 2 Score 0.505 (Sensitivity: 0.88; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000062429
Gene: ENSMUSG00000044562
AA Change: N678K

Domain	Start	End	E-Value	Type
low complexity region	41	57	N/A	INTRINSIC
low complexity region	59	67	N/A	INTRINSIC
low complexity region	72	90	N/A	INTRINSIC
low complexity region	97	112	N/A	INTRINSIC
RA	141	253	6.94e-8	SMART
low complexity region	284	308	N/A	INTRINSIC
low complexity region	310	326	N/A	INTRINSIC
low complexity region	327	339	N/A	INTRINSIC
SCOP:d1gxca_	391	484	1e-2	SMART
low complexity region	498	509	N/A	INTRINSIC
low complexity region	556	575	N/A	INTRINSIC
low complexity region	679	692	N/A	INTRINSIC
DIL	768	877	4.14e-44	SMART
low complexity region	928	947	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000148532

SMART Domains

Protein: ENSMUSP00000114686
Gene: ENSMUSG00000042918

Domain	Start	End	E-Value	Type
low complexity region	45	56	N/A	INTRINSIC
low complexity region	143	155	N/A	INTRINSIC
SAP	165	199	1.3e-7	SMART
low complexity region	200	213	N/A	INTRINSIC
low complexity region	255	297	N/A	INTRINSIC
low complexity region	320	336	N/A	INTRINSIC
low complexity region	347	372	N/A	INTRINSIC
low complexity region	385	399	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000209998

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000210213

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000210648

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000211418

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000211533

Coding Region Coverage

1x: 99.1%
3x: 98.1%
10x: 95.8%
20x: 91.5%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a targeted mutation exhibit complete embryonic lethality during organogenesis associated with a failure in cardiovascular development. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 93 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930579F01Rik	A	T	3: 137,879,343 (GRCm39)	L235Q	probably damaging	Het
Aadacl4fm4	A	T	4: 144,412,790 (GRCm39)	M50K	possibly damaging	Het
Adam6b	T	A	12: 113,454,275 (GRCm39)	V364D	probably benign	Het
Akap13	T	C	7: 75,259,677 (GRCm39)	L767P	probably benign	Het
Akap13	T	A	7: 75,380,248 (GRCm39)	S2193T	probably damaging	Het
Anapc11	T	C	11: 120,496,203 (GRCm39)	V69A	probably benign	Het
Ankmy1	C	T	1: 92,823,912 (GRCm39)	R118Q	probably damaging	Het
Ankrd27	T	C	7: 35,337,478 (GRCm39)	S931P	probably benign	Het
Atp6v1c2	G	A	12: 17,338,169 (GRCm39)	R280C	probably damaging	Het
Bbs10	T	A	10: 111,135,913 (GRCm39)	I342N	probably damaging	Het
Calhm2	T	C	19: 47,121,389 (GRCm39)	D260G	possibly damaging	Het
Camk2a	A	G	18: 61,091,310 (GRCm39)	E264G	probably damaging	Het
Ccdc146	T	A	5: 21,524,543 (GRCm39)	M270L	probably benign	Het
Cdc16	A	G	8: 13,829,264 (GRCm39)	T517A	probably benign	Het
Ces1g	T	C	8: 94,057,821 (GRCm39)	H160R	probably benign	Het
Chst4	T	C	8: 110,757,026 (GRCm39)	N196S	probably damaging	Het
Ciz1	A	T	2: 32,257,479 (GRCm39)	N175Y	probably damaging	Het
Cyb5r4	G	A	9: 86,909,093 (GRCm39)	V57I	probably damaging	Het
Cyth3	A	G	5: 143,670,181 (GRCm39)		probably benign	Het
Def6	A	G	17: 28,439,154 (GRCm39)	E255G	probably damaging	Het
Dhtkd1	T	G	2: 5,916,681 (GRCm39)	Q665P	probably damaging	Het
Dsg3	A	C	18: 20,672,804 (GRCm39)	D825A	probably damaging	Het
Eif3m	T	C	2: 104,835,345 (GRCm39)	T242A	probably benign	Het
Emilin3	A	G	2: 160,751,737 (GRCm39)	F101L	probably benign	Het
Epha7	A	G	4: 28,935,700 (GRCm39)		probably null	Het
Fbxo45	A	T	16: 32,057,223 (GRCm39)	Y224N	probably damaging	Het
Fhod3	A	T	18: 25,223,161 (GRCm39)	M836L	possibly damaging	Het
Fut4	C	A	9: 14,662,506 (GRCm39)	V263F	probably damaging	Het
Ggt1	C	T	10: 75,415,104 (GRCm39)	T206M	probably benign	Het
Gls	T	C	1: 52,227,858 (GRCm39)	R79G	probably damaging	Het
Grhl1	T	C	12: 24,631,514 (GRCm39)	S156P	probably benign	Het
Ipo8	C	T	6: 148,676,540 (GRCm39)	S983N	probably benign	Het
Kcna7	C	T	7: 45,058,868 (GRCm39)	A385V	probably damaging	Het
Kpnb1	A	T	11: 97,075,916 (GRCm39)	L40Q	probably damaging	Het
Matn1	A	T	4: 130,677,417 (GRCm39)	S209C	probably damaging	Het
Mcc	A	G	18: 44,608,289 (GRCm39)	I501T	probably benign	Het
Mdp1	A	T	14: 55,896,832 (GRCm39)	F104L	probably damaging	Het
Mib2	A	T	4: 155,740,745 (GRCm39)	N626K	probably damaging	Het
Mrgprh	T	C	17: 13,095,843 (GRCm39)	S28P	possibly damaging	Het
Mup-ps23	T	A	4: 61,774,386 (GRCm39)		noncoding transcript	Het
Myh15	A	G	16: 49,003,322 (GRCm39)	T1794A	possibly damaging	Het
Myo18a	C	G	11: 77,711,868 (GRCm39)	P680A	probably benign	Het
Myom2	G	T	8: 15,148,419 (GRCm39)	D532Y	possibly damaging	Het
Ndufaf5	A	G	2: 140,012,801 (GRCm39)	N57S	probably benign	Het
Nectin3	C	T	16: 46,278,550 (GRCm39)	V282M	probably damaging	Het
Nup188	G	T	2: 30,221,000 (GRCm39)	D997Y	probably damaging	Het
Olfm3	T	C	3: 114,916,454 (GRCm39)	V462A	probably damaging	Het
Opcml	A	G	9: 28,724,694 (GRCm39)	H164R	possibly damaging	Het
Or14a259	A	T	7: 86,013,013 (GRCm39)	C177*	probably null	Het
Or4c120	A	T	2: 89,000,757 (GRCm39)	F266L	probably benign	Het
Or8u9	A	C	2: 86,002,050 (GRCm39)	F37C	probably damaging	Het
Pacrg	A	G	17: 10,622,347 (GRCm39)	I209T	probably damaging	Het
Pcf11	T	C	7: 92,310,423 (GRCm39)	M522V	probably benign	Het
Pck1	T	A	2: 172,995,183 (GRCm39)	M1K	probably null	Het
Pcm1	G	T	8: 41,729,148 (GRCm39)	E707*	probably null	Het
Pcsk5	G	A	19: 17,632,213 (GRCm39)	R318W	probably damaging	Het
Phf11d	A	T	14: 59,590,793 (GRCm39)	M188K	possibly damaging	Het
Ppip5k2	A	T	1: 97,668,262 (GRCm39)	C615*	probably null	Het
Prkdc	T	A	16: 15,609,791 (GRCm39)	S3132T	probably damaging	Het
Prl2c5	A	T	13: 13,357,609 (GRCm39)		probably benign	Het
Prpsap2	A	G	11: 61,631,826 (GRCm39)	I177T	possibly damaging	Het
Rad50	A	G	11: 53,541,346 (GRCm39)	S1297P	probably damaging	Het
Rubcn	A	G	16: 32,656,350 (GRCm39)	S544P	probably damaging	Het
Rwdd2a	A	T	9: 86,456,453 (GRCm39)	T210S	possibly damaging	Het
Scd2	A	G	19: 44,291,479 (GRCm39)	D306G	probably damaging	Het
Sema3b	T	C	9: 107,480,117 (GRCm39)	N207S	probably benign	Het
Sf3b2	C	T	19: 5,324,852 (GRCm39)	D845N	probably damaging	Het
Sipa1l2	C	A	8: 126,191,149 (GRCm39)	C947F	probably damaging	Het
Slc12a1	A	T	2: 125,067,951 (GRCm39)	T1013S	probably damaging	Het
Slc18a2	A	T	19: 59,275,799 (GRCm39)	I461L	probably benign	Het
Slc1a6	C	A	10: 78,637,756 (GRCm39)	Y427*	probably null	Het
Slc30a4	A	T	2: 122,531,319 (GRCm39)	I231K	probably damaging	Het
Sos1	G	T	17: 80,761,192 (GRCm39)	A168D	probably damaging	Het
Spata31f1a	T	C	4: 42,851,161 (GRCm39)	I332V	probably benign	Het
Sptb	T	C	12: 76,668,145 (GRCm39)	S651G	probably benign	Het
Stk36	T	C	1: 74,672,779 (GRCm39)	L1007P	probably damaging	Het
Tek	A	T	4: 94,692,578 (GRCm39)	N229Y	probably damaging	Het
Tep1	A	G	14: 51,074,225 (GRCm39)	F1887L	possibly damaging	Het
Tet1	A	T	10: 62,713,988 (GRCm39)	C602*	probably null	Het
Tnfrsf19	A	G	14: 61,209,485 (GRCm39)	S262P	possibly damaging	Het
Trim5	T	C	7: 103,914,891 (GRCm39)	I393V	probably benign	Het
Trpm6	A	G	19: 18,830,951 (GRCm39)	E1272G	probably benign	Het
Ttc21b	A	T	2: 66,018,670 (GRCm39)	Y1246N	probably damaging	Het
Ttll3	T	A	6: 113,375,738 (GRCm39)	L151H	probably damaging	Het
U2surp	C	T	9: 95,366,496 (GRCm39)	V470I	probably benign	Het
Ubr1	A	T	2: 120,777,138 (GRCm39)	Y276N	probably benign	Het
Uggt1	A	G	1: 36,218,751 (GRCm39)	S59P	probably benign	Het
Unc45a	T	C	7: 79,976,092 (GRCm39)	T796A	probably damaging	Het
Unc5b	C	A	10: 60,614,719 (GRCm39)	V193F	possibly damaging	Het
Upp1	G	T	11: 9,079,590 (GRCm39)	M50I	probably benign	Het
Vps18	C	T	2: 119,124,386 (GRCm39)	R438C	probably damaging	Het
Zfp715	T	C	7: 42,948,760 (GRCm39)	Y400C	possibly damaging	Het
Zfp955b	T	C	17: 33,521,496 (GRCm39)	Y322H	probably benign	Het

Other mutations in Rasip1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01958:Rasip1	APN	7	45,286,188 (GRCm39)	nonsense	probably null
IGL01995:Rasip1	APN	7	45,286,240 (GRCm39)	missense	probably damaging	0.99
R0208:Rasip1	UTSW	7	45,281,999 (GRCm39)	missense	probably damaging	0.97
R0869:Rasip1	UTSW	7	45,284,452 (GRCm39)	missense	probably damaging	0.99
R0870:Rasip1	UTSW	7	45,284,452 (GRCm39)	missense	probably damaging	0.99
R0871:Rasip1	UTSW	7	45,284,452 (GRCm39)	missense	probably damaging	0.99
R0872:Rasip1	UTSW	7	45,284,452 (GRCm39)	missense	probably damaging	0.99
R1388:Rasip1	UTSW	7	45,279,656 (GRCm39)	missense	probably damaging	0.98
R1780:Rasip1	UTSW	7	45,284,742 (GRCm39)	missense	possibly damaging	0.94
R2348:Rasip1	UTSW	7	45,278,507 (GRCm39)	critical splice donor site	probably null
R2517:Rasip1	UTSW	7	45,284,247 (GRCm39)	missense	probably damaging	1.00
R4587:Rasip1	UTSW	7	45,282,159 (GRCm39)	missense	possibly damaging	0.86
R4678:Rasip1	UTSW	7	45,277,247 (GRCm39)	missense	possibly damaging	0.86
R4679:Rasip1	UTSW	7	45,277,247 (GRCm39)	missense	possibly damaging	0.86
R4714:Rasip1	UTSW	7	45,281,820 (GRCm39)	frame shift	probably null
R5572:Rasip1	UTSW	7	45,286,153 (GRCm39)	missense	probably benign	0.00
R6182:Rasip1	UTSW	7	45,277,879 (GRCm39)	small deletion	probably benign
R7443:Rasip1	UTSW	7	45,288,148 (GRCm39)	missense	probably damaging	1.00
R7769:Rasip1	UTSW	7	45,278,239 (GRCm39)	missense	probably damaging	0.98
R8146:Rasip1	UTSW	7	45,279,704 (GRCm39)	missense	possibly damaging	0.95
R8158:Rasip1	UTSW	7	45,281,943 (GRCm39)	missense	probably damaging	1.00
R8493:Rasip1	UTSW	7	45,284,467 (GRCm39)	missense	possibly damaging	0.89
R9047:Rasip1	UTSW	7	45,282,066 (GRCm39)	missense	possibly damaging	0.52
R9352:Rasip1	UTSW	7	45,278,280 (GRCm39)	missense	possibly damaging	0.69
R9679:Rasip1	UTSW	7	45,277,327 (GRCm39)	missense	possibly damaging	0.85
X0018:Rasip1	UTSW	7	45,288,292 (GRCm39)	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- AAGAAATTGGAGACCGCCAGCC -3'
(R):5'- TCAGAGCAGCACAATGTCAGTTAGG -3'

Sequencing Primer
(F):5'- TGCGACCACTCATACTATGGATG -3'
(R):5'- CACAATGTCAGTTAGGTGGAAAGC -3'

Posted On

2013-04-24