Mutagenetix > Incidental Mutation

Incidental Mutation 'R0189:Ripk2'

258006

Institutional Source

Beutler Lab

Gene Symbol

Ripk2

Ensembl Gene

ENSMUSG00000041135

Gene Name

receptor (TNFRSF)-interacting serine-threonine kinase 2

Synonyms

2210420D18Rik, D4Bwg0615e, CARDIAK, RICK, CCK, CARD3, RIP2

MMRRC Submission

038450-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.301) question?

Stock #

R0189 (G1)

Quality Score

177

Status

Not validated

Chromosome

Chromosomal Location

16122733-16163647 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to T at 16129125 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000038833 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000037035] [ENSMUST00000183871]

AlphaFold

P58801

Predicted Effect

probably null
Transcript: ENSMUST00000037035

SMART Domains

Protein: ENSMUSP00000038833
Gene: ENSMUSG00000041135

Domain	Start	End	E-Value	Type
Pfam:Pkinase	18	289	2.1e-43	PFAM
Pfam:Pkinase_Tyr	18	290	1.1e-45	PFAM
CARD	434	522	2.34e-1	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000175054

Predicted Effect

probably benign
Transcript: ENSMUST00000183871

SMART Domains

Protein: ENSMUSP00000139381
Gene: ENSMUSG00000041135

Domain	Start	End	E-Value	Type
Pfam:Pkinase	18	290	5.6e-46	PFAM
Pfam:Pkinase_Tyr	18	290	1.2e-44	PFAM

Coding Region Coverage

1x: 99.1%
3x: 98.3%
10x: 96.3%
20x: 92.1%

Validation Efficiency

98% (96/98)

MGI Phenotype

FUNCTION: This gene encodes a member of the receptor-interacting protein family of serine/threonine protein kinases. The encoded protein contains a C-terminal caspase activation and recruitment domain, and is a component of signaling complexes in both the innate and adaptive immune pathways. It is a potent activator of nuclear factor kappa B and inducer of apoptosis in response to various stimuli. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]
PHENOTYPE: Homozygous inactivation of this gene leads to impaired cytokine production in response to LPS treatment, and may result in resistance to LPS-induced septic shock and defects in Toll-like receptor and T-cell receptor signaling. Macrophages homozygous for a knock-in allele show normal LPS signaling. [provided by MGI curators]

Allele List at MGI

All alleles(7) : Targeted(5) Gene trapped(2)

Other mutations in this stock

Total: 83 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca9	A	T	11: 109,999,479 (GRCm39)	W1459R	probably damaging	Het
Abca9	A	T	11: 110,032,488 (GRCm39)		probably benign	Het
Adam25	T	A	8: 41,208,467 (GRCm39)	C578S	probably damaging	Het
Adam32	T	A	8: 25,412,353 (GRCm39)		probably null	Het
Add1	T	C	5: 34,773,992 (GRCm39)	V67A	probably benign	Het
Aggf1	A	T	13: 95,492,988 (GRCm39)		probably benign	Het
Ahcyl2	A	T	6: 29,891,242 (GRCm39)	I449F	probably benign	Het
Ak6	A	G	13: 100,791,650 (GRCm39)	Y31C	probably damaging	Het
Akap6	T	C	12: 53,188,037 (GRCm39)	V1817A	probably benign	Het
Arhgef17	G	T	7: 100,578,057 (GRCm39)	P964T	probably damaging	Het
Atxn7l3b	A	T	10: 112,764,485 (GRCm39)	L48Q	possibly damaging	Het
Bbs10	T	G	10: 111,136,926 (GRCm39)	S680A	probably damaging	Het
Bcl7c	G	A	7: 127,304,936 (GRCm39)	T164I	probably damaging	Het
Btbd9	C	T	17: 30,493,916 (GRCm39)	D492N	possibly damaging	Het
Ccdc110	T	A	8: 46,388,119 (GRCm39)	D25E	probably damaging	Het
Ccdc83	T	A	7: 89,875,891 (GRCm39)	T327S	possibly damaging	Het
Coro1b	T	C	19: 4,203,250 (GRCm39)	Y364H	probably damaging	Het
Cstf3	A	G	2: 104,482,791 (GRCm39)	D313G	probably damaging	Het
Dlgap5	T	A	14: 47,650,432 (GRCm39)		probably null	Het
Dusp3	A	T	11: 101,872,547 (GRCm39)	I83N	probably damaging	Het
Eea1	A	T	10: 95,831,444 (GRCm39)	K178N	possibly damaging	Het
Efr3b	T	A	12: 4,032,925 (GRCm39)	D144V	probably damaging	Het
Gfus	C	A	15: 75,798,827 (GRCm39)	D127Y	probably damaging	Het
Gm1110	T	A	9: 26,794,514 (GRCm39)	E504V	probably null	Het
Got2	T	C	8: 96,614,881 (GRCm39)	H18R	probably benign	Het
Gprc5b	T	C	7: 118,582,856 (GRCm39)	M338V	probably benign	Het
Has2	A	T	15: 56,531,831 (GRCm39)	F295I	probably damaging	Het
Hcn3	T	C	3: 89,056,107 (GRCm39)	D519G	probably damaging	Het
Ino80	T	A	2: 119,210,160 (GRCm39)	D1377V	probably benign	Het
Iqsec3	A	T	6: 121,390,521 (GRCm39)		probably benign	Het
Kif3c	T	A	12: 3,415,989 (GRCm39)	S3R	probably benign	Het
Krt17	A	G	11: 100,151,445 (GRCm39)	I116T	possibly damaging	Het
Lrba	T	C	3: 86,275,816 (GRCm39)	V1728A	probably damaging	Het
Map3k6	G	T	4: 132,974,252 (GRCm39)	V550L	possibly damaging	Het
Mcph1	T	C	8: 18,838,487 (GRCm39)	V803A	probably damaging	Het
Med13	A	G	11: 86,210,702 (GRCm39)	V480A	probably benign	Het
Ms4a20	A	G	19: 11,074,311 (GRCm39)	V207A	possibly damaging	Het
Msh5	T	C	17: 35,248,630 (GRCm39)	E772G	probably null	Het
Nanos3	C	T	8: 84,902,763 (GRCm39)	R133Q	probably damaging	Het
Ndfip2	T	C	14: 105,542,174 (GRCm39)	L308P	probably damaging	Het
Ndufb10	T	C	17: 24,943,209 (GRCm39)	T34A	probably benign	Het
Nipal3	A	T	4: 135,195,829 (GRCm39)	I258N	possibly damaging	Het
Nup54	A	G	5: 92,570,423 (GRCm39)	V328A	probably damaging	Het
Oprm1	T	C	10: 6,739,071 (GRCm39)	V66A	possibly damaging	Het
Or10p21	T	A	10: 128,847,191 (GRCm39)	F12L	possibly damaging	Het
Or51ah3	G	T	7: 103,210,289 (GRCm39)	V202F	probably benign	Het
Or5b105	G	A	19: 13,080,642 (GRCm39)	R3C	possibly damaging	Het
Or8b56	T	A	9: 38,739,111 (GRCm39)	Y41*	probably null	Het
Or9s14	T	C	1: 92,535,615 (GRCm39)	F19L	probably damaging	Het
Peg12	G	A	7: 62,113,296 (GRCm39)	T267I	unknown	Het
Phf20	A	G	2: 156,145,061 (GRCm39)	S890G	probably benign	Het
Plk2	C	T	13: 110,535,997 (GRCm39)	T567M	probably damaging	Het
Pola2	A	T	19: 5,992,370 (GRCm39)		probably benign	Het
Ppp1r12b	A	G	1: 134,793,514 (GRCm39)		probably null	Het
Prickle1	A	T	15: 93,400,900 (GRCm39)	L528*	probably null	Het
Prpf6	T	A	2: 181,297,250 (GRCm39)	N903K	probably benign	Het
Ptprc	G	A	1: 138,010,453 (GRCm39)	A601V	probably benign	Het
Ranbp1	A	T	16: 18,059,607 (GRCm39)		probably null	Het
Rapgef6	C	T	11: 54,582,075 (GRCm39)	S1334L	probably benign	Het
Rgs2	T	C	1: 143,878,022 (GRCm39)		probably null	Het
Rnf17	A	G	14: 56,719,650 (GRCm39)	S967G	probably null	Het
Rock2	T	A	12: 17,009,517 (GRCm39)		probably benign	Het
Rpusd3	C	T	6: 113,392,514 (GRCm39)		probably null	Het
Scgb1b20	G	T	7: 33,072,935 (GRCm39)	V48L	probably benign	Het
Sec16a	T	A	2: 26,314,426 (GRCm39)		probably null	Het
Serpina5	T	A	12: 104,069,589 (GRCm39)	L267H	probably damaging	Het
Slc12a3	C	T	8: 95,082,986 (GRCm39)	H875Y	probably benign	Het
Slc45a4	A	G	15: 73,453,763 (GRCm39)	S745P	probably benign	Het
Sucla2	T	C	14: 73,830,088 (GRCm39)	V375A	probably damaging	Het
Sun2	C	A	15: 79,621,277 (GRCm39)	V213F	probably damaging	Het
Taar2	G	A	10: 23,817,393 (GRCm39)	R311H	probably benign	Het
Tac1	C	T	6: 7,562,424 (GRCm39)	R129C	probably damaging	Het
Taf6	T	C	5: 138,180,975 (GRCm39)	E202G	probably benign	Het
Tex21	T	A	12: 76,286,307 (GRCm39)	H64L	probably benign	Het
Tgs1	A	G	4: 3,593,620 (GRCm39)	S503G	probably benign	Het
Tmem184c	C	T	8: 78,324,441 (GRCm39)	V350I	possibly damaging	Het
Tnks1bp1	A	G	2: 84,901,273 (GRCm39)	S960G	possibly damaging	Het
Trbc2	T	C	6: 41,525,083 (GRCm39)		probably benign	Het
Tubgcp2	A	T	7: 139,581,518 (GRCm39)		probably benign	Het
Vmn1r39	T	A	6: 66,782,181 (GRCm39)	T46S	probably benign	Het
Vmn1r61	T	C	7: 5,613,699 (GRCm39)	H205R	probably benign	Het
Zdhhc14	T	C	17: 5,775,539 (GRCm39)	S264P	possibly damaging	Het
Zfp101	T	A	17: 33,601,213 (GRCm39)	H181L	possibly damaging	Het

Other mutations in Ripk2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01290:Ripk2	APN	4	16,139,198 (GRCm39)	splice site	probably benign
IGL01346:Ripk2	APN	4	16,132,775 (GRCm39)	critical splice donor site	probably null
IGL01631:Ripk2	APN	4	16,163,342 (GRCm39)	missense	possibly damaging	0.83
IGL02151:Ripk2	APN	4	16,139,240 (GRCm39)	missense	possibly damaging	0.83
IGL03093:Ripk2	APN	4	16,152,056 (GRCm39)	missense	probably damaging	1.00
R0066:Ripk2	UTSW	4	16,123,868 (GRCm39)	nonsense	probably null
R0066:Ripk2	UTSW	4	16,123,868 (GRCm39)	nonsense	probably null
R1454:Ripk2	UTSW	4	16,163,239 (GRCm39)	missense	probably damaging	0.96
R1715:Ripk2	UTSW	4	16,155,192 (GRCm39)	critical splice acceptor site	probably null
R2153:Ripk2	UTSW	4	16,132,775 (GRCm39)	critical splice donor site	probably null
R2266:Ripk2	UTSW	4	16,152,011 (GRCm39)	missense	possibly damaging	0.91
R2394:Ripk2	UTSW	4	16,132,774 (GRCm39)	splice site	probably benign
R3693:Ripk2	UTSW	4	16,127,695 (GRCm39)	missense	probably benign
R4412:Ripk2	UTSW	4	16,124,511 (GRCm39)	missense	probably benign
R4463:Ripk2	UTSW	4	16,151,968 (GRCm39)	missense	possibly damaging	0.70
R4843:Ripk2	UTSW	4	16,155,073 (GRCm39)	missense	probably damaging	0.99
R5085:Ripk2	UTSW	4	16,127,663 (GRCm39)	missense	possibly damaging	0.78
R5453:Ripk2	UTSW	4	16,151,989 (GRCm39)	missense	probably damaging	1.00
R6197:Ripk2	UTSW	4	16,163,330 (GRCm39)	missense	probably damaging	1.00
R6576:Ripk2	UTSW	4	16,131,558 (GRCm39)	splice site	probably null
R6967:Ripk2	UTSW	4	16,158,275 (GRCm39)	critical splice donor site	probably null
R7351:Ripk2	UTSW	4	16,155,048 (GRCm39)	missense	probably damaging	1.00
R7479:Ripk2	UTSW	4	16,155,154 (GRCm39)	missense	probably benign	0.02
R7718:Ripk2	UTSW	4	16,151,968 (GRCm39)	missense	possibly damaging	0.70
R8188:Ripk2	UTSW	4	16,139,218 (GRCm39)	missense	probably damaging	1.00
R8242:Ripk2	UTSW	4	16,124,430 (GRCm39)	missense	probably benign	0.00
R8509:Ripk2	UTSW	4	16,124,436 (GRCm39)	missense	probably benign
R8700:Ripk2	UTSW	4	16,158,422 (GRCm39)	missense	possibly damaging	0.91
R8987:Ripk2	UTSW	4	16,123,699 (GRCm39)	missense	possibly damaging	0.72
R9084:Ripk2	UTSW	4	16,123,795 (GRCm39)	missense	probably damaging	1.00
R9202:Ripk2	UTSW	4	16,124,502 (GRCm39)	missense	probably benign
R9369:Ripk2	UTSW	4	16,127,651 (GRCm39)	missense	probably benign	0.01
R9469:Ripk2	UTSW	4	16,138,181 (GRCm39)	missense	possibly damaging	0.73
Z1176:Ripk2	UTSW	4	16,151,943 (GRCm39)	missense	probably damaging	1.00
Z1177:Ripk2	UTSW	4	16,163,331 (GRCm39)	missense	probably benign	0.21

Predicted Primers

Posted On

2015-01-14