Mutagenetix > Incidental Mutation

Incidental Mutation 'R1780:Rasip1'

197449

Institutional Source

Beutler Lab

Gene Symbol

Rasip1

Ensembl Gene

ENSMUSG00000044562

Gene Name

Ras interacting protein 1

Synonyms

Rain, 2610025P08Rik

MMRRC Submission

039811-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R1780 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

45627488-45639093 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 45635318 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 703 (Y703C)

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: Y703C

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000062429
Gene: ENSMUSG00000044562
AA Change: Y703C

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

Meta Mutation Damage Score

0.4107

Coding Region Coverage

1x: 97.4%
3x: 96.8%
10x: 95.2%
20x: 92.3%

Validation Efficiency

98% (80/82)

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: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrl2	T	C	3: 148,852,593	E493G	probably damaging	Het
Aff3	A	T	1: 38,535,702	S66T	probably damaging	Het
Ankrd17	T	A	5: 90,232,415	K2470N	probably damaging	Het
Ap3m1	T	C	14: 21,041,070	T156A	probably benign	Het
Arhgef4	T	A	1: 34,724,160	S832R	possibly damaging	Het
Asb10	T	C	5: 24,533,676	D423G	possibly damaging	Het
Ash1l	A	G	3: 88,965,984	T25A	probably benign	Het
Atp13a2	T	A	4: 141,002,460	L663I	possibly damaging	Het
Atp9b	A	T	18: 80,776,897	Y174*	probably null	Het
Bche	A	G	3: 73,700,620	I491T	probably benign	Het
Bckdhb	T	C	9: 83,953,783		probably null	Het
Cadps2	C	T	6: 23,320,932		probably null	Het
Cdc42bpb	A	T	12: 111,322,907	V468E	probably damaging	Het
Chrnd	T	C	1: 87,192,548	V33A	possibly damaging	Het
Col6a5	A	T	9: 105,936,878	V645D	unknown	Het
Cpa1	C	T	6: 30,643,008	L312F	probably damaging	Het
Cyp2a5	A	G	7: 26,841,876		probably benign	Het
Cyp2c39	C	A	19: 39,538,851		probably benign	Het
Cyp2d26	T	C	15: 82,794,007	N56S	probably damaging	Het
Ddx21	A	G	10: 62,594,147		probably benign	Het
Dnah11	A	T	12: 118,027,558	C2358S	probably damaging	Het
Entpd8	T	C	2: 25,084,306	S368P	probably benign	Het
Epg5	A	T	18: 78,023,990	Q2222L	probably damaging	Het
Ercc5	T	A	1: 44,167,796	V623E	probably benign	Het
Flg2	A	G	3: 93,202,999	E778G	unknown	Het
Gbe1	C	T	16: 70,495,324	R515*	probably null	Het
Hsd17b6	A	G	10: 127,994,327		probably null	Het
Hyal6	C	T	6: 24,734,032		probably benign	Het
Ifi27l2b	A	G	12: 103,451,319	I203T	probably damaging	Het
Kcnk9	A	C	15: 72,512,401	D309E	unknown	Het
Lrp6	C	T	6: 134,464,451	R1184Q	probably damaging	Het
Mdn1	T	C	4: 32,700,103	F1399L	probably damaging	Het
Mroh2a	C	T	1: 88,230,680	R150*	probably null	Het
Mx1	T	C	16: 97,451,512	*289W	probably null	Het
Myo7b	T	C	18: 31,961,185	E1970G	probably damaging	Het
Mypn	T	C	10: 63,121,964	Y24C	probably damaging	Het
Naxe	G	C	3: 88,057,133	P167A	probably benign	Het
Nmnat2	A	T	1: 153,112,440	K272*	probably null	Het
Nmnat3	C	T	9: 98,354,111	T19M	probably damaging	Het
Olfr1275	T	C	2: 111,231,698	I32V	probably benign	Het
Olfr1412	G	A	1: 92,588,389	V20M	probably benign	Het
Olfr1474	A	G	19: 13,471,362	T131A	probably benign	Het
Olfr64	A	T	7: 103,893,555	F60Y	probably damaging	Het
Olfr66	A	G	7: 103,881,592	V217A	probably benign	Het
Pgm3	T	G	9: 86,556,204	E509D	probably damaging	Het
Phf3	A	T	1: 30,811,942	D1110E	probably damaging	Het
Pkd1	T	G	17: 24,581,569	S3062A	probably benign	Het
Pogz	A	T	3: 94,870,126	K372N	possibly damaging	Het
Pou1f1	A	G	16: 65,523,470	Y15C	probably benign	Het
Ppfia2	A	G	10: 106,896,507	T972A	possibly damaging	Het
Recql	T	A	6: 142,364,598	Q502L	probably benign	Het
Rgs9	A	T	11: 109,239,499	Y383*	probably null	Het
Rimbp3	T	C	16: 17,212,632	S1307P	probably benign	Het
Rspo1	A	G	4: 125,007,745	T200A	probably damaging	Het
Ryr3	C	T	2: 112,867,292	M922I	probably damaging	Het
Samm50	C	T	15: 84,211,127	A438V	probably damaging	Het
Sec1	A	C	7: 45,678,832	S264A	probably benign	Het
Sec31a	A	T	5: 100,381,336		probably null	Het
Slc13a3	T	C	2: 165,406,699	N553S	unknown	Het
Smg6	T	A	11: 74,946,116	L852Q	probably damaging	Het
Spata13	A	G	14: 60,691,725	N244S	probably damaging	Het
Srbd1	T	C	17: 86,057,685	R648G	probably damaging	Het
Sugct	T	G	13: 17,452,454		probably null	Het
Tmed10	A	G	12: 85,354,879	Y85H	probably damaging	Het
Trim68	A	G	7: 102,684,073	I134T	possibly damaging	Het
Trio	A	G	15: 27,744,038	C2603R	possibly damaging	Het
Tspyl3	G	A	2: 153,225,256	R21W	probably damaging	Het
Ttn	T	C	2: 76,810,699	I11863V	probably null	Het
Ubp1	G	A	9: 113,964,579	A283T	possibly damaging	Het
Ubtf	A	T	11: 102,314,918	F60L	probably damaging	Het
Vmn1r235	T	C	17: 21,261,737	I108T	probably benign	Het
Vmn2r125	T	C	4: 156,351,373	S349P	probably damaging	Het
Vmn2r25	A	G	6: 123,828,465	S478P	probably damaging	Het
Vmn2r88	T	A	14: 51,418,572	V746D	probably damaging	Het
Zcwpw1	A	G	5: 137,796,652	K37E	probably damaging	Het
Zdhhc24	T	C	19: 4,883,766	S284P	probably damaging	Het
Zswim8	C	A	14: 20,716,327	H841N	probably damaging	Het

Other mutations in Rasip1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01958:Rasip1	APN	7	45636764	nonsense	probably null
IGL01995:Rasip1	APN	7	45636816	missense	probably damaging	0.99
R0208:Rasip1	UTSW	7	45632575	missense	probably damaging	0.97
R0373:Rasip1	UTSW	7	45635244	missense	possibly damaging	0.50
R0869:Rasip1	UTSW	7	45635028	missense	probably damaging	0.99
R0870:Rasip1	UTSW	7	45635028	missense	probably damaging	0.99
R0871:Rasip1	UTSW	7	45635028	missense	probably damaging	0.99
R0872:Rasip1	UTSW	7	45635028	missense	probably damaging	0.99
R1388:Rasip1	UTSW	7	45630232	missense	probably damaging	0.98
R2348:Rasip1	UTSW	7	45629083	critical splice donor site	probably null
R2517:Rasip1	UTSW	7	45634823	missense	probably damaging	1.00
R4587:Rasip1	UTSW	7	45632735	missense	possibly damaging	0.86
R4678:Rasip1	UTSW	7	45627823	missense	possibly damaging	0.86
R4679:Rasip1	UTSW	7	45627823	missense	possibly damaging	0.86
R4714:Rasip1	UTSW	7	45632396	frame shift	probably null
R5572:Rasip1	UTSW	7	45636729	missense	probably benign	0.00
R6182:Rasip1	UTSW	7	45628455	small deletion	probably benign
R7443:Rasip1	UTSW	7	45638724	missense	probably damaging	1.00
R7769:Rasip1	UTSW	7	45628815	missense	probably damaging	0.98
R8146:Rasip1	UTSW	7	45630280	missense	possibly damaging	0.95
R8158:Rasip1	UTSW	7	45632519	missense	probably damaging	1.00
R8493:Rasip1	UTSW	7	45635043	missense	possibly damaging	0.89
R9047:Rasip1	UTSW	7	45632642	missense	possibly damaging	0.52
R9352:Rasip1	UTSW	7	45628856	missense	possibly damaging	0.69
R9679:Rasip1	UTSW	7	45627903	missense	possibly damaging	0.85
X0018:Rasip1	UTSW	7	45638868	missense	probably damaging	0.98

Predicted Primers

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

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

Posted On

2014-05-23