Mutagenetix > Incidental Mutation

Incidental Mutation 'R8115:S1pr1'

631122

Institutional Source

Beutler Lab

Gene Symbol

S1pr1

Ensembl Gene

ENSMUSG00000045092

Gene Name

sphingosine-1-phosphate receptor 1

Synonyms

S1P1, Edg1, S1P

MMRRC Submission

067544-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R8115 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

115504082-115508704 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 115506298 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Serine at position 99 (T99S)

Ref Sequence

ENSEMBL: ENSMUSP00000050897 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000055676]

AlphaFold

O08530

Predicted Effect

probably benign
Transcript: ENSMUST00000055676
AA Change: T99S

PolyPhen 2 Score 0.025 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000050897
Gene: ENSMUSG00000045092
AA Change: T99S

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srsx	56	326	1.6e-9	PFAM
Pfam:7tm_1	62	311	1.7e-43	PFAM

Meta Mutation Damage Score

0.0802

Coding Region Coverage

1x: 99.7%
3x: 99.5%
10x: 98.4%
20x: 94.2%

Validation Efficiency

100% (68/68)

MGI Phenotype

FUNCTION: This gene encodes a G-protein-coupled receptor bound by the lysophospholipid, sphingosine 1-phosphate. The gene product functions in endothelial cells and is involved in vascular and heart development. This receptor is highly expressed in T and B lymphocytes, and it plays a role in T cell and B cell export from peripheral lymphoid organs. This protein is bound and downregulated by FTY720, an exogenous immunosuppressant drug studied in mouse disease models for multiple sclerosis in humans. [provided by RefSeq, Jan 2010]
PHENOTYPE: Homozygotes for targeted mutations exhibit vascular defects resulting in embryonic hemorrhaging and lethality by embryonic day 14.5. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A1bg	T	G	15: 60,791,996 (GRCm39)	I211L	probably benign	Het
Abhd16b	G	A	2: 181,135,527 (GRCm39)	R143H	possibly damaging	Het
Abt1	T	C	13: 23,606,402 (GRCm39)	E184G	probably damaging	Het
Aqp1	AGG	AGGG	6: 55,322,498 (GRCm39)		probably null	Het
Asxl3	G	A	18: 22,650,642 (GRCm39)	R877Q	probably damaging	Het
B3galt1	A	G	2: 67,948,320 (GRCm39)	T12A	possibly damaging	Het
Bcat1	G	A	6: 144,955,819 (GRCm39)	P354L	probably damaging	Het
C9orf72	T	C	4: 35,218,763 (GRCm39)	Y32C		Het
Cad	T	C	5: 31,218,271 (GRCm39)	F452L	possibly damaging	Het
Cadps2	T	A	6: 23,328,897 (GRCm39)	I973F	probably benign	Het
Cenpq	T	C	17: 41,243,720 (GRCm39)	N43D	probably damaging	Het
Chd9	G	T	8: 91,762,960 (GRCm39)	V2262L	probably damaging	Het
Cttnbp2nl	G	T	3: 104,913,402 (GRCm39)	Q161K	probably damaging	Het
D630003M21Rik	A	T	2: 158,058,510 (GRCm39)	H463Q	probably benign	Het
Defb1	C	T	8: 22,284,500 (GRCm39)	H40Y	probably benign	Het
Dmrtb1	A	T	4: 107,534,256 (GRCm39)	D186E	probably benign	Het
Dsc2	C	T	18: 20,165,331 (GRCm39)	G881R	possibly damaging	Het
Efr3a	T	A	15: 65,738,644 (GRCm39)	F758I	probably damaging	Het
Fap	A	G	2: 62,349,385 (GRCm39)	I501T	probably benign	Het
Galr3	C	T	15: 78,927,524 (GRCm39)	R322*	probably null	Het
Hrnr	C	A	3: 93,231,039 (GRCm39)	R426S	unknown	Het
Hsp90ab1	A	T	17: 45,880,201 (GRCm39)	M476K	possibly damaging	Het
Igsf3	G	T	3: 101,362,595 (GRCm39)	R872L	probably benign	Het
Ippk	C	T	13: 49,599,818 (GRCm39)	P226S		Het
Iqsec3	T	G	6: 121,449,989 (GRCm39)	R178S	unknown	Het
Itgbl1	T	C	14: 124,094,955 (GRCm39)	C327R	probably damaging	Het
Itsn2	A	T	12: 4,723,602 (GRCm39)	Q1179L	possibly damaging	Het
Kcnb2	T	C	1: 15,781,851 (GRCm39)	*908R	probably null	Het
Kdm5b	G	T	1: 134,547,411 (GRCm39)	W1020L	possibly damaging	Het
Kpna3	C	A	14: 61,608,367 (GRCm39)	V364L	probably damaging	Het
Lsm14a	T	C	7: 34,074,662 (GRCm39)	I93V	probably benign	Het
Mast2	A	G	4: 116,292,644 (GRCm39)	S109P	probably benign	Het
Muc4	G	A	16: 32,575,678 (GRCm39)	S1726N	unknown	Het
Myo7a	T	C	7: 97,715,653 (GRCm39)	D1477G	probably damaging	Het
Nostrin	G	A	2: 69,011,264 (GRCm39)		probably null	Het
Oasl1	T	A	5: 115,074,996 (GRCm39)	V352E	probably damaging	Het
Or9a2	T	A	6: 41,748,472 (GRCm39)	T254S	probably benign	Het
Pafah1b1	A	G	11: 74,575,319 (GRCm39)	V195A	probably damaging	Het
Pcdhb4	G	A	18: 37,442,453 (GRCm39)	V588M	probably damaging	Het
Pcsk5	A	G	19: 17,487,530 (GRCm39)		probably null	Het
Peg10	A	G	6: 4,756,707 (GRCm39)	I428V	unknown	Het
Pmfbp1	G	A	8: 110,263,669 (GRCm39)	V824M	probably damaging	Het
Prkag3	T	C	1: 74,787,118 (GRCm39)	R47G	possibly damaging	Het
Prl8a1	T	A	13: 27,758,028 (GRCm39)	H227L	probably benign	Het
Prune2	A	G	19: 17,101,288 (GRCm39)	D2264G	probably benign	Het
Psg28	A	G	7: 18,164,311 (GRCm39)	Y134H	probably benign	Het
Rab3gap2	T	A	1: 184,999,447 (GRCm39)	Y1019N	possibly damaging	Het
Rbm15	A	T	3: 107,238,966 (GRCm39)	F477L	probably damaging	Het
Ric1	A	T	19: 29,563,973 (GRCm39)	N576Y	probably damaging	Het
Serpinb9b	G	T	13: 33,219,531 (GRCm39)	V153F	probably null	Het
Sh2d3c	A	G	2: 32,615,276 (GRCm39)	E122G	probably benign	Het
Slc6a11	T	A	6: 114,108,442 (GRCm39)	W69R	probably damaging	Het
Slco6c1	T	A	1: 97,000,686 (GRCm39)	I539F	probably damaging	Het
Smgc	G	T	15: 91,733,322 (GRCm39)		probably null	Het
Spata17	T	C	1: 186,849,653 (GRCm39)	Y194C	probably damaging	Het
Tap1	A	T	17: 34,412,293 (GRCm39)		probably null	Het
Topbp1	T	C	9: 103,197,740 (GRCm39)	S440P	probably benign	Het
Trpc6	T	C	9: 8,609,982 (GRCm39)	L150P	probably damaging	Het
Ttll4	C	T	1: 74,726,489 (GRCm39)	Q696*	probably null	Het
Ubash3b	C	T	9: 40,937,624 (GRCm39)	E447K	probably damaging	Het
Unc5cl	T	C	17: 48,774,438 (GRCm39)	S477P	possibly damaging	Het
Unc80	A	G	1: 66,688,072 (GRCm39)	T2357A	probably benign	Het
Vmn1r58	A	T	7: 5,413,341 (GRCm39)	S296R	probably benign	Het
Vmn2r85	G	T	10: 130,261,820 (GRCm39)	N172K	probably benign	Het
Wdfy4	G	A	14: 32,826,072 (GRCm39)	P1193L		Het
Yipf7	T	A	5: 69,684,570 (GRCm39)	T82S	probably benign	Het
Zap70	A	G	1: 36,820,287 (GRCm39)	S523G	probably damaging	Het
Zfp354a	A	G	11: 50,960,490 (GRCm39)	T233A	probably benign	Het

Other mutations in S1pr1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02635:S1pr1	APN	3	115,505,739 (GRCm39)	missense	probably benign
IGL02698:S1pr1	APN	3	115,505,746 (GRCm39)	nonsense	probably null
IGL03038:S1pr1	APN	3	115,506,343 (GRCm39)	missense	possibly damaging	0.74
Compatriot	UTSW	3	115,505,683 (GRCm39)	missense	probably damaging	1.00
Jammed	UTSW	3	115,505,452 (GRCm39)	missense	possibly damaging	0.83
sardines	UTSW	3	115,505,628 (GRCm39)	missense	probably damaging	1.00
Stau	UTSW	3	115,505,710 (GRCm39)	missense	probably damaging	1.00
Stuffed	UTSW	3	115,505,922 (GRCm39)	missense	probably damaging	1.00
R1753:S1pr1	UTSW	3	115,505,587 (GRCm39)	missense	probably benign
R2002:S1pr1	UTSW	3	115,506,544 (GRCm39)	missense	probably benign	0.00
R5819:S1pr1	UTSW	3	115,505,789 (GRCm39)	nonsense	probably null
R6571:S1pr1	UTSW	3	115,505,452 (GRCm39)	missense	possibly damaging	0.83
R6784:S1pr1	UTSW	3	115,505,710 (GRCm39)	missense	probably damaging	1.00
R7348:S1pr1	UTSW	3	115,505,710 (GRCm39)	missense	probably damaging	1.00
R7493:S1pr1	UTSW	3	115,505,922 (GRCm39)	missense	probably damaging	1.00
R7816:S1pr1	UTSW	3	115,505,947 (GRCm39)	missense	possibly damaging	0.49
R8088:S1pr1	UTSW	3	115,505,683 (GRCm39)	missense	probably damaging	1.00
R8714:S1pr1	UTSW	3	115,505,470 (GRCm39)	missense	probably benign	0.02
R8871:S1pr1	UTSW	3	115,505,628 (GRCm39)	missense	probably damaging	1.00
R8962:S1pr1	UTSW	3	115,505,569 (GRCm39)	missense
RF004:S1pr1	UTSW	3	115,506,536 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- TGCAGTTCCAGCCCATGATG -3'
(R):5'- GGACCATGGCATTAAACTGACTTC -3'

Sequencing Primer
(F):5'- AGATGACCCAGCAGGCG -3'
(R):5'- CTGACTTCAGTGGTGTTCATTC -3'

Posted On

2020-06-30