Mutagenetix > Incidental Mutation

Incidental Mutation 'R1908:Tlr11'

210092

Institutional Source

Beutler Lab

Gene Symbol

Tlr11

Ensembl Gene

ENSMUSG00000051969

Gene Name

toll-like receptor 11

Synonyms

LOC239081

MMRRC Submission

039927-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1908 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

50357914-50363663 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 50361207 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Leucine at position 217 (I217L)

Ref Sequence

ENSEMBL: ENSMUSP00000138814 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000063570] [ENSMUST00000185091]

AlphaFold

Q6R5P0

Predicted Effect

probably benign
Transcript: ENSMUST00000063570
AA Change: I212L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000068906
Gene: ENSMUSG00000051969
AA Change: I212L

Domain	Start	End	E-Value	Type
signal peptide	1	30	N/A	INTRINSIC
low complexity region	105	122	N/A	INTRINSIC
low complexity region	153	161	N/A	INTRINSIC
LRR	311	333	3.36e1	SMART
LRR	335	361	4.44e0	SMART
LRR	362	383	2.03e1	SMART
LRR_TYP	384	407	2.57e-3	SMART
LRR_TYP	408	431	2.75e-3	SMART
low complexity region	544	556	N/A	INTRINSIC
LRR	605	628	6.06e1	SMART
transmembrane domain	719	741	N/A	INTRINSIC
Pfam:TIR	773	922	2.1e-9	PFAM
Pfam:TIR_2	776	894	6.6e-13	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000185091
AA Change: I217L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000138814
Gene: ENSMUSG00000051969
AA Change: I217L

Domain	Start	End	E-Value	Type
transmembrane domain	16	38	N/A	INTRINSIC
low complexity region	110	127	N/A	INTRINSIC
low complexity region	158	166	N/A	INTRINSIC
Pfam:LRR_6	221	244	5.3e-2	PFAM
LRR	316	338	3.36e1	SMART
LRR	340	366	4.44e0	SMART
LRR	367	388	2.03e1	SMART
LRR_TYP	389	412	2.57e-3	SMART
LRR_TYP	413	436	2.75e-3	SMART
low complexity region	549	561	N/A	INTRINSIC
LRR	610	633	6.06e1	SMART
transmembrane domain	724	746	N/A	INTRINSIC
Pfam:TIR_2	781	898	1e-12	PFAM
Pfam:TIR	781	922	1.8e-13	PFAM

Coding Region Coverage

1x: 97.3%
3x: 96.8%
10x: 95.4%
20x: 93.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 83 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700011H14Rik	G	T	14: 49,226,575 (GRCm38)	D292E	probably damaging	Het
4931406P16Rik	T	A	7: 34,258,036 (GRCm38)	I59L	probably benign	Het
Abca8b	C	A	11: 109,957,098 (GRCm38)	L852F	possibly damaging	Het
Abcc6	T	C	7: 46,020,134 (GRCm38)		probably null	Het
Alg11	T	G	8: 22,065,568 (GRCm38)	C240G	probably damaging	Het
Aox1	A	G	1: 58,102,624 (GRCm38)	I1190V	probably damaging	Het
Apc2	T	G	10: 80,314,844 (GRCm38)	S1911A	probably benign	Het
Arfgef3	T	C	10: 18,652,763 (GRCm38)	D292G	possibly damaging	Het
Arhgef4	C	A	1: 34,724,259 (GRCm38)	S865R	probably benign	Het
Ass1	T	A	2: 31,493,148 (GRCm38)	Y190*	probably null	Het
B4galnt3	A	T	6: 120,210,090 (GRCm38)		probably null	Het
Btnl10	C	A	11: 58,920,541 (GRCm38)	P230Q	possibly damaging	Het
C3	A	G	17: 57,209,489 (GRCm38)	Y1348H	probably damaging	Het
Cebpz	A	T	17: 78,934,907 (GRCm38)	Y439*	probably null	Het
Cic	C	A	7: 25,286,840 (GRCm38)	T1229K	probably damaging	Het
Clip4	T	C	17: 71,837,749 (GRCm38)	S524P	probably damaging	Het
Col6a3	A	C	1: 90,811,699 (GRCm38)	I269R	probably damaging	Het
Dbh	C	T	2: 27,181,494 (GRCm38)	T533I	possibly damaging	Het
Dcaf17	A	T	2: 71,060,369 (GRCm38)	R83*	probably null	Het
Dnah1	A	G	14: 31,262,558 (GRCm38)	L3923P	probably damaging	Het
Dnah7a	A	T	1: 53,631,562 (GRCm38)	D510E	probably benign	Het
Dock6	A	G	9: 21,841,629 (GRCm38)	F296S	probably damaging	Het
Eif4enif1	T	C	11: 3,227,455 (GRCm38)	S341P	probably damaging	Het
Epb41l1	G	T	2: 156,510,817 (GRCm38)	G461V	possibly damaging	Het
Epg5	T	A	18: 77,959,032 (GRCm38)	D555E	probably benign	Het
Fes	T	C	7: 80,386,861 (GRCm38)	R113G	probably damaging	Het
Gm10684	A	G	9: 45,110,213 (GRCm38)		probably benign	Het
Gm12185	T	C	11: 48,915,404 (GRCm38)	E320G	probably benign	Het
Gm14412	A	C	2: 177,315,837 (GRCm38)	S88R	probably benign	Het
Gm14412	G	T	2: 177,315,476 (GRCm38)	H209N	probably damaging	Het
Grhl1	T	A	12: 24,608,556 (GRCm38)	L400Q	probably damaging	Het
Havcr1	T	A	11: 46,773,684 (GRCm38)	Y216*	probably null	Het
Hephl1	A	C	9: 15,074,124 (GRCm38)	Y745*	probably null	Het
Hmcn2	T	G	2: 31,411,910 (GRCm38)		probably null	Het
Hs3st6	A	G	17: 24,758,136 (GRCm38)	K197E	possibly damaging	Het
Ifi214	C	T	1: 173,529,511 (GRCm38)	V9I	probably benign	Het
Jakmip2	T	C	18: 43,567,144 (GRCm38)	T450A	probably benign	Het
Lrp4	T	A	2: 91,498,408 (GRCm38)	V1551D	possibly damaging	Het
Macf1	A	T	4: 123,457,841 (GRCm38)	H1634Q	possibly damaging	Het
Mcpt8	T	A	14: 56,083,834 (GRCm38)	I58F	probably benign	Het
Mga	T	A	2: 119,926,594 (GRCm38)	H1018Q	possibly damaging	Het
Myo10	T	A	15: 25,801,222 (GRCm38)	V1499E	probably damaging	Het
Myom2	G	T	8: 15,081,023 (GRCm38)	D320Y	probably damaging	Het
Olfr1220	G	A	2: 89,097,544 (GRCm38)	P128S	probably damaging	Het
Olfr1395	A	C	11: 49,148,274 (GRCm38)	N6H	possibly damaging	Het
Olfr458	C	T	6: 42,460,426 (GRCm38)	V198M	probably benign	Het
Olfr60	T	C	7: 140,345,465 (GRCm38)	I175V	probably benign	Het
Olfr74	A	T	2: 87,974,059 (GRCm38)	V202D	possibly damaging	Het
Olfr740	T	A	14: 50,453,838 (GRCm38)	M262K	probably damaging	Het
Pabpc4	G	T	4: 123,289,068 (GRCm38)	R166L	possibly damaging	Het
Pcdhb8	A	G	18: 37,355,962 (GRCm38)	E231G	possibly damaging	Het
Pomgnt2	A	T	9: 121,982,191 (GRCm38)	I508N	possibly damaging	Het
Ppp2r5e	C	G	12: 75,469,567 (GRCm38)	A239P	probably damaging	Het
Prdm15	G	T	16: 97,837,685 (GRCm38)	D58E	probably benign	Het
Rgl2	A	G	17: 33,932,148 (GRCm38)	T117A	probably benign	Het
Rp1	A	G	1: 4,348,720 (GRCm38)	I723T	probably damaging	Het
Serpina3g	A	G	12: 104,241,277 (GRCm38)	E233G	probably damaging	Het
Skint6	T	A	4: 112,891,990 (GRCm38)	S798C	probably benign	Het
Slc35f1	T	C	10: 53,021,904 (GRCm38)	L137P	possibly damaging	Het
Slc6a20a	T	C	9: 123,656,308 (GRCm38)	N246S	probably damaging	Het
Slc7a2	T	C	8: 40,916,497 (GRCm38)	L663S	probably benign	Het
Slco1a4	A	G	6: 141,815,447 (GRCm38)		probably null	Het
Slit2	A	G	5: 48,281,988 (GRCm38)	T41A	probably damaging	Het
Smc2	T	C	4: 52,450,863 (GRCm38)	I227T	probably damaging	Het
Smg1	A	G	7: 118,154,199 (GRCm38)		probably benign	Het
Ssu2	A	T	6: 112,384,427 (GRCm38)	L23M	probably benign	Het
St5	G	A	7: 109,525,326 (GRCm38)	Q686*	probably null	Het
Syne2	A	G	12: 76,094,279 (GRCm38)		probably null	Het
Tekt1	T	C	11: 72,351,935 (GRCm38)	T249A	probably benign	Het
Tfr2	T	C	5: 137,571,692 (GRCm38)	V120A	probably benign	Het
Thsd7b	C	T	1: 129,678,109 (GRCm38)	P529L	probably damaging	Het
Tll1	C	T	8: 64,025,107 (GRCm38)	D871N	probably damaging	Het
Tmem87b	T	A	2: 128,831,559 (GRCm38)	V241D	probably damaging	Het
Tshz2	T	A	2: 169,885,545 (GRCm38)	I218N	possibly damaging	Het
Vmn1r18	A	T	6: 57,390,041 (GRCm38)	I176N	possibly damaging	Het
Vmn2r68	T	A	7: 85,234,052 (GRCm38)	H164L	probably benign	Het
Vmn2r74	T	C	7: 85,952,442 (GRCm38)	T663A	probably benign	Het
Vmn2r8	T	C	5: 108,797,570 (GRCm38)	T724A	probably benign	Het
Wdr11	T	C	7: 129,605,230 (GRCm38)	V289A	possibly damaging	Het
Zfp62	T	A	11: 49,216,220 (GRCm38)	D379E	probably damaging	Het
Zfp78	C	T	7: 6,378,898 (GRCm38)	P316S	probably damaging	Het
Zfyve27	T	G	19: 42,171,548 (GRCm38)	M1R	probably null	Het
Zkscan8	G	A	13: 21,525,155 (GRCm38)	P191L	probably damaging	Het

Other mutations in Tlr11

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00590:Tlr11	APN	14	50,360,916 (GRCm38)	missense	probably benign
IGL02090:Tlr11	APN	14	50,363,032 (GRCm38)	missense	probably damaging	0.99
IGL02286:Tlr11	APN	14	50,360,871 (GRCm38)	missense	possibly damaging	0.91
IGL02671:Tlr11	APN	14	50,360,692 (GRCm38)	missense	probably damaging	1.00
IGL03064:Tlr11	APN	14	50,361,100 (GRCm38)	missense	probably damaging	1.00
IGL03068:Tlr11	APN	14	50,361,484 (GRCm38)	missense	probably benign
R0099:Tlr11	UTSW	14	50,360,818 (GRCm38)	missense	probably benign	0.14
R0727:Tlr11	UTSW	14	50,361,469 (GRCm38)	missense	possibly damaging	0.67
R0944:Tlr11	UTSW	14	50,362,336 (GRCm38)	missense	probably benign	0.12
R1490:Tlr11	UTSW	14	50,363,176 (GRCm38)	missense	probably benign	0.00
R1726:Tlr11	UTSW	14	50,361,541 (GRCm38)	missense	probably benign	0.00
R1803:Tlr11	UTSW	14	50,360,647 (GRCm38)	missense	probably benign	0.00
R1971:Tlr11	UTSW	14	50,361,234 (GRCm38)	missense	probably benign
R1981:Tlr11	UTSW	14	50,361,988 (GRCm38)	missense	possibly damaging	0.95
R2023:Tlr11	UTSW	14	50,362,569 (GRCm38)	missense	probably damaging	0.96
R2079:Tlr11	UTSW	14	50,360,980 (GRCm38)	missense	probably damaging	0.99
R2155:Tlr11	UTSW	14	50,360,682 (GRCm38)	missense	probably benign	0.01
R2251:Tlr11	UTSW	14	50,360,792 (GRCm38)	missense	probably benign	0.02
R3017:Tlr11	UTSW	14	50,362,721 (GRCm38)	nonsense	probably null
R3760:Tlr11	UTSW	14	50,362,243 (GRCm38)	missense	probably damaging	1.00
R3876:Tlr11	UTSW	14	50,363,154 (GRCm38)	missense	probably benign
R3936:Tlr11	UTSW	14	50,362,735 (GRCm38)	missense	possibly damaging	0.78
R4002:Tlr11	UTSW	14	50,362,527 (GRCm38)	missense	probably benign
R4024:Tlr11	UTSW	14	50,362,846 (GRCm38)	missense	probably benign	0.02
R4118:Tlr11	UTSW	14	50,363,227 (GRCm38)	missense	probably damaging	1.00
R4222:Tlr11	UTSW	14	50,361,849 (GRCm38)	missense	probably damaging	0.99
R4365:Tlr11	UTSW	14	50,361,469 (GRCm38)	missense	probably damaging	0.98
R4678:Tlr11	UTSW	14	50,360,982 (GRCm38)	missense	possibly damaging	0.85
R4779:Tlr11	UTSW	14	50,361,250 (GRCm38)	missense	possibly damaging	0.76
R4910:Tlr11	UTSW	14	50,362,889 (GRCm38)	missense	probably benign	0.45
R4921:Tlr11	UTSW	14	50,362,885 (GRCm38)	missense	possibly damaging	0.48
R5114:Tlr11	UTSW	14	50,363,121 (GRCm38)	missense	possibly damaging	0.81
R5126:Tlr11	UTSW	14	50,360,830 (GRCm38)	missense	probably damaging	1.00
R5349:Tlr11	UTSW	14	50,360,880 (GRCm38)	missense	probably benign	0.45
R5606:Tlr11	UTSW	14	50,362,260 (GRCm38)	missense	probably benign	0.08
R5650:Tlr11	UTSW	14	50,361,201 (GRCm38)	missense	probably benign	0.03
R5958:Tlr11	UTSW	14	50,360,777 (GRCm38)	missense	probably damaging	0.99
R5966:Tlr11	UTSW	14	50,362,255 (GRCm38)	missense	probably benign	0.02
R6480:Tlr11	UTSW	14	50,363,055 (GRCm38)	missense	possibly damaging	0.62
R6484:Tlr11	UTSW	14	50,362,678 (GRCm38)	missense	probably damaging	0.99
R6679:Tlr11	UTSW	14	50,362,854 (GRCm38)	missense	probably benign	0.00
R6717:Tlr11	UTSW	14	50,362,104 (GRCm38)	missense	probably benign
R7085:Tlr11	UTSW	14	50,362,656 (GRCm38)	missense	probably damaging	0.99
R7241:Tlr11	UTSW	14	50,362,141 (GRCm38)	missense	possibly damaging	0.95
R7440:Tlr11	UTSW	14	50,361,344 (GRCm38)	missense	probably benign	0.00
R7482:Tlr11	UTSW	14	50,362,999 (GRCm38)	missense	probably damaging	0.99
R7582:Tlr11	UTSW	14	50,361,729 (GRCm38)	nonsense	probably null
R7790:Tlr11	UTSW	14	50,361,925 (GRCm38)	missense	probably benign
R7818:Tlr11	UTSW	14	50,361,828 (GRCm38)	missense	probably damaging	1.00
R7827:Tlr11	UTSW	14	50,361,154 (GRCm38)	missense	probably benign	0.00
R8144:Tlr11	UTSW	14	50,362,488 (GRCm38)	missense	probably damaging	0.99
R8847:Tlr11	UTSW	14	50,362,725 (GRCm38)	missense	possibly damaging	0.85
R9027:Tlr11	UTSW	14	50,361,292 (GRCm38)	missense	probably damaging	1.00
R9035:Tlr11	UTSW	14	50,360,977 (GRCm38)	missense	probably benign	0.00
R9393:Tlr11	UTSW	14	50,362,090 (GRCm38)	missense	probably benign	0.03
RF002:Tlr11	UTSW	14	50,361,225 (GRCm38)	missense	possibly damaging	0.63
Z1088:Tlr11	UTSW	14	50,362,338 (GRCm38)	missense	possibly damaging	0.48
Z1176:Tlr11	UTSW	14	50,362,336 (GRCm38)	missense	probably benign	0.40
Z1176:Tlr11	UTSW	14	50,360,662 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTCAAGGACTGGACCAGCTAC -3'
(R):5'- ATGCAAGTGGAGCAGTCCTG -3'

Sequencing Primer
(F):5'- TGAGTCTCTTAGATCCCTTAGTAGTC -3'
(R):5'- CAGTCCTGAGTCTGTGAGATCAAG -3'

Posted On

2014-06-30