Mutagenetix > Incidental Mutation

Incidental Mutation 'R0833:Tle2'

77655

Institutional Source

Beutler Lab

Gene Symbol

Tle2

Ensembl Gene

ENSMUSG00000034771

Gene Name

transducin-like enhancer of split 2

Synonyms

Grg2

MMRRC Submission

039012-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.355) question?

Stock #

R0833 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

81574561-81590845 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 81588947 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Leucine at position 667 (F667L)

Ref Sequence

ENSEMBL: ENSMUSP00000121173 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000072020] [ENSMUST00000135211] [ENSMUST00000146358] [ENSMUST00000146916] [ENSMUST00000142948]

AlphaFold

Q9WVB2

Predicted Effect

probably benign
Transcript: ENSMUST00000072020

SMART Domains

Protein: ENSMUSP00000071905
Gene: ENSMUSG00000034758

Domain	Start	End	E-Value	Type
WD40	283	320	9.6e-2	SMART
Blast:WD40	334	372	2e-12	BLAST
WD40	377	415	6.16e0	SMART
WD40	418	455	7.43e-1	SMART
Blast:WD40	460	496	4e-13	BLAST
WD40	499	538	1.43e0	SMART
WD40	541	578	2.97e0	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000124854
AA Change: F64L

SMART Domains

Protein: ENSMUSP00000118334
Gene: ENSMUSG00000034771
AA Change: F64L

Domain	Start	End	E-Value	Type
Blast:WD40	6	44	9e-20	BLAST
WD40	46	85	1.2e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000128278

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000129282

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000129798

Predicted Effect

unknown
Transcript: ENSMUST00000131411
AA Change: F54L

SMART Domains

Protein: ENSMUSP00000114400
Gene: ENSMUSG00000034771
AA Change: F54L

Domain	Start	End	E-Value	Type
WD40	36	75	1.2e-2	SMART
WD40	76	116	2.07e-1	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000134457

Predicted Effect

probably damaging
Transcript: ENSMUST00000135211
AA Change: F668L

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000117453
Gene: ENSMUSG00000034771
AA Change: F668L

Domain	Start	End	E-Value	Type
Pfam:TLE_N	1	122	3e-68	PFAM
low complexity region	133	160	N/A	INTRINSIC
low complexity region	172	194	N/A	INTRINSIC
low complexity region	262	277	N/A	INTRINSIC
low complexity region	332	352	N/A	INTRINSIC
WD40	436	473	5.6e-3	SMART
WD40	479	520	9.6e-2	SMART
WD40	525	564	1.88e-4	SMART
WD40	567	606	3.72e-8	SMART
Blast:WD40	609	647	8e-18	BLAST
WD40	649	688	1.2e-2	SMART
WD40	689	729	2.07e-1	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000136254

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000137631

Predicted Effect

probably damaging
Transcript: ENSMUST00000146358
AA Change: F703L

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000121125
Gene: ENSMUSG00000034771
AA Change: F703L

Domain	Start	End	E-Value	Type
Pfam:TLE_N	1	64	2e-31	PFAM
Pfam:TLE_N	81	154	4.3e-34	PFAM
low complexity region	167	194	N/A	INTRINSIC
low complexity region	206	228	N/A	INTRINSIC
low complexity region	296	311	N/A	INTRINSIC
low complexity region	366	386	N/A	INTRINSIC
WD40	471	508	5.6e-3	SMART
WD40	514	555	9.6e-2	SMART
WD40	560	599	1.88e-4	SMART
WD40	602	641	3.72e-8	SMART
Blast:WD40	644	682	9e-18	BLAST
WD40	684	723	1.2e-2	SMART
WD40	724	764	2.07e-1	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000153812

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000139135

Predicted Effect

probably damaging
Transcript: ENSMUST00000146916
AA Change: F667L

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000121173
Gene: ENSMUSG00000034771
AA Change: F667L

Domain	Start	End	E-Value	Type
Pfam:TLE_N	1	134	1.6e-75	PFAM
low complexity region	144	171	N/A	INTRINSIC
low complexity region	183	205	N/A	INTRINSIC
low complexity region	273	288	N/A	INTRINSIC
low complexity region	343	363	N/A	INTRINSIC
WD40	435	472	5.6e-3	SMART
WD40	478	519	9.6e-2	SMART
WD40	524	563	1.88e-4	SMART
WD40	566	605	3.72e-8	SMART
WD40	648	687	1.2e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000141913

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000146239

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000151470

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000140433

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000145878

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000153379

Predicted Effect

probably benign
Transcript: ENSMUST00000142948

SMART Domains

Protein: ENSMUSP00000117287
Gene: ENSMUSG00000034758

Domain	Start	End	E-Value	Type
WD40	273	310	9.6e-2	SMART
Blast:WD40	324	362	2e-12	BLAST
WD40	367	405	6.16e0	SMART
WD40	408	445	7.43e-1	SMART
Blast:WD40	450	486	4e-13	BLAST
WD40	489	528	1.43e0	SMART
WD40	531	568	2.97e0	SMART

Meta Mutation Damage Score

0.7793

Coding Region Coverage

1x: 99.4%
3x: 98.8%
10x: 97.3%
20x: 94.6%

Validation Efficiency

100% (97/97)

Allele List at MGI

Other mutations in this stock

Total: 93 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700113H08Rik	T	C	10: 87,165,069	L41P	probably damaging	Het
3110082I17Rik	A	G	5: 139,364,120	V58A	possibly damaging	Het
4932415M13Rik	A	T	17: 53,724,346		noncoding transcript	Het
Aldh1a7	C	T	19: 20,702,243	V390M	probably damaging	Het
Alg14	A	G	3: 121,298,610	H34R	probably damaging	Het
Ankrd27	A	G	7: 35,608,347	N337S	probably damaging	Het
Apoa2	T	A	1: 171,225,379		probably benign	Het
Arl2	T	G	19: 6,136,022	K126T	probably damaging	Het
Ascc3	T	C	10: 50,845,666	W2072R	probably benign	Het
Astl	T	C	2: 127,342,419	F21L	probably benign	Het
Asxl3	A	G	18: 22,516,040	D362G	probably damaging	Het
Bdp1	A	T	13: 100,035,825	H2094Q	probably benign	Het
Cacna2d4	C	T	6: 119,307,286	R745W	probably damaging	Het
Cbwd1	A	G	19: 24,940,839		probably benign	Het
Ccdc144b	A	G	3: 36,020,213		probably benign	Het
Ccdc85a	T	A	11: 28,583,296	I83F	probably damaging	Het
Ccnt2	T	A	1: 127,802,394	M336K	probably benign	Het
Cd226	A	C	18: 89,207,020		probably benign	Het
Ces1f	A	T	8: 93,270,024	S214T	probably damaging	Het
Clip1	T	C	5: 123,630,721	D605G	probably benign	Het
Col26a1	A	G	5: 136,765,300		probably null	Het
Crtc1	A	G	8: 70,393,013	V306A	probably benign	Het
D130043K22Rik	G	A	13: 24,863,580		probably benign	Het
D17H6S53E	A	T	17: 35,127,409		probably null	Het
D17Wsu92e	A	T	17: 27,786,138	S148R	probably damaging	Het
Dnah11	G	A	12: 118,196,662	A111V	probably benign	Het
Dyrk2	T	C	10: 118,861,122	H77R	probably benign	Het
E330017A01Rik	G	A	16: 58,635,523	S129L	probably damaging	Het
Epha3	A	G	16: 63,603,519		probably benign	Het
Epn2	T	C	11: 61,519,491	N611S	probably benign	Het
Erich6	A	C	3: 58,618,944		probably benign	Het
Fam217b	T	C	2: 178,420,989	S249P	probably benign	Het
Fam219b	A	G	9: 57,538,016		probably benign	Het
Fryl	A	T	5: 73,089,081		probably benign	Het
Gm12800	G	A	4: 101,910,097	C181Y	probably damaging	Het
Gm13089	A	T	4: 143,698,486	M129K	probably benign	Het
Gm14496	T	C	2: 181,996,266	W378R	probably damaging	Het
Gm5155	C	A	7: 17,904,981	A301E	possibly damaging	Het
Gm8674	A	T	13: 49,904,575		noncoding transcript	Het
Grap	T	A	11: 61,660,239	D32E	possibly damaging	Het
Grk2	C	A	19: 4,289,357	L428F	probably damaging	Het
Grm8	T	A	6: 27,363,179	E779V	probably damaging	Het
Hipk1	A	G	3: 103,754,296	S670P	probably damaging	Het
Itgae	A	T	11: 73,129,206	M845L	probably benign	Het
Itih1	A	T	14: 30,941,555	V164E	probably damaging	Het
Itpka	T	A	2: 119,750,831	N448K	probably damaging	Het
Jak3	A	C	8: 71,683,978	N643T	probably damaging	Het
Lrfn5	A	C	12: 61,839,668	T81P	probably damaging	Het
Lrrc45	T	A	11: 120,718,193		probably null	Het
March6	T	C	15: 31,480,291	Y562C	probably benign	Het
Mcrs1	T	C	15: 99,243,449		probably benign	Het
Meis1	G	A	11: 18,881,767	H424Y	possibly damaging	Het
Mst1r	G	A	9: 107,913,167	V660I	probably benign	Het
Mst1r	A	G	9: 107,914,776	N837S	probably benign	Het
Mthfd2l	T	C	5: 90,946,942	V90A	probably damaging	Het
Mtnr1a	A	T	8: 45,087,937	I312F	probably benign	Het
Olfr1513	T	C	14: 52,349,378	I223V	probably benign	Het
Olfr578	C	A	7: 102,984,836	L109F	possibly damaging	Het
Olfr875	T	C	9: 37,773,076	V139A	probably benign	Het
Otog	C	T	7: 46,269,362	T954I	possibly damaging	Het
Pdcd6	A	G	13: 74,316,324		probably benign	Het
Phlpp2	A	G	8: 109,937,106	T926A	probably damaging	Het
Plec	GGCAGCAG	GGCAGCAGCAG	15: 76,181,907		probably benign	Het
Plekha5	T	A	6: 140,589,634		probably benign	Het
Ppp1r16a	C	T	15: 76,693,669	Q328*	probably null	Het
Rab27b	T	C	18: 69,987,041		probably benign	Het
Rapsn	T	C	2: 91,036,808	Y152H	probably damaging	Het
Rasd1	A	T	11: 59,964,553	F85I	probably damaging	Het
Rgs1	A	T	1: 144,247,933	S85T	probably damaging	Het
Samd9l	T	C	6: 3,372,725	E1512G	possibly damaging	Het
Sgsm1	C	T	5: 113,279,184	A127T	probably benign	Het
Shc1	A	G	3: 89,422,969	D70G	probably damaging	Het
Slc26a1	T	A	5: 108,673,523	T167S	probably benign	Het
Slc26a7	A	T	4: 14,593,873	Y81N	probably damaging	Het
Slc2a12	T	C	10: 22,702,016		probably benign	Het
Slc30a7	T	A	3: 115,990,140		probably null	Het
Slc44a5	T	C	3: 154,265,474	S654P	probably damaging	Het
Stard9	T	G	2: 120,696,999	S1246A	possibly damaging	Het
Stxbp5	A	T	10: 9,865,099	S116R	probably damaging	Het
Syvn1	C	T	19: 6,052,453	P517L	probably benign	Het
Tas2r105	T	C	6: 131,687,430	I12V	probably benign	Het
Tas2r121	A	G	6: 132,700,362	S216P	probably damaging	Het
Tcof1	T	C	18: 60,845,832	D48G	probably damaging	Het
Tgm3	C	T	2: 130,026,682		probably benign	Het
Tnfaip3	C	A	10: 19,002,949	A704S	probably benign	Het
Trabd2b	A	G	4: 114,580,322	Q232R	probably benign	Het
Ttc28	T	A	5: 111,231,081	I1144N	probably damaging	Het
Ucp3	T	A	7: 100,479,541	C25*	probably null	Het
Ugt3a2	A	G	15: 9,370,150	D460G	probably damaging	Het
Urb1	T	C	16: 90,795,448	D308G	possibly damaging	Het
Ush1g	G	T	11: 115,318,868	R167S	possibly damaging	Het
Vav3	A	G	3: 109,647,679	N81S	possibly damaging	Het
Vmn2r108	A	T	17: 20,471,459	D267E	probably benign	Het

Other mutations in Tle2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00691:Tle2	APN	10	81581739	missense	probably benign	0.12
IGL02651:Tle2	APN	10	81586889	missense	probably damaging	1.00
IGL02809:Tle2	APN	10	81586362	splice site	probably null
IGL03235:Tle2	APN	10	81586251	missense	probably benign	0.22
IGL03307:Tle2	APN	10	81590240	missense	probably damaging	1.00
foxbat	UTSW	10	81586313	nonsense	probably null
Illyushin	UTSW	10	81588872	missense	probably damaging	1.00
R5011_Tle2_517	UTSW	10	81584697	missense	probably damaging	1.00
PIT4515001:Tle2	UTSW	10	81587130	missense	possibly damaging	0.72
R0394:Tle2	UTSW	10	81577648	missense	probably damaging	1.00
R0744:Tle2	UTSW	10	81588947	missense	probably damaging	1.00
R0826:Tle2	UTSW	10	81586314	missense	possibly damaging	0.95
R1796:Tle2	UTSW	10	81589497	critical splice donor site	probably null
R2067:Tle2	UTSW	10	81580551	missense	probably damaging	1.00
R2184:Tle2	UTSW	10	81590277	missense	probably damaging	1.00
R2198:Tle2	UTSW	10	81590313	missense	probably damaging	1.00
R4439:Tle2	UTSW	10	81581682	missense	possibly damaging	0.62
R4440:Tle2	UTSW	10	81581682	missense	possibly damaging	0.62
R4441:Tle2	UTSW	10	81581682	missense	possibly damaging	0.62
R4513:Tle2	UTSW	10	81587560	missense	probably damaging	1.00
R4839:Tle2	UTSW	10	81577684	missense	probably damaging	1.00
R4863:Tle2	UTSW	10	81588891	missense	possibly damaging	0.88
R5011:Tle2	UTSW	10	81584697	missense	probably damaging	1.00
R5505:Tle2	UTSW	10	81581740	missense	probably benign	0.00
R5538:Tle2	UTSW	10	81580584	missense	probably damaging	1.00
R5790:Tle2	UTSW	10	81590315	missense	probably damaging	1.00
R5917:Tle2	UTSW	10	81580916	critical splice donor site	probably null
R6176:Tle2	UTSW	10	81587334	missense	probably damaging	0.99
R6200:Tle2	UTSW	10	81588872	missense	probably damaging	1.00
R6914:Tle2	UTSW	10	81586356	missense	probably damaging	1.00
R7367:Tle2	UTSW	10	81580318	missense	probably damaging	0.99
R7600:Tle2	UTSW	10	81586313	nonsense	probably null
R7729:Tle2	UTSW	10	81587147	missense	probably damaging	0.99
R8333:Tle2	UTSW	10	81577684	missense	probably damaging	1.00
R8511:Tle2	UTSW	10	81587996	missense	probably damaging	1.00
R9562:Tle2	UTSW	10	81581733	missense	probably benign	0.11
R9565:Tle2	UTSW	10	81581733	missense	probably benign	0.11
T0970:Tle2	UTSW	10	81580285	missense	possibly damaging	0.71
Z1177:Tle2	UTSW	10	81582446	missense	possibly damaging	0.95

Predicted Primers

PCR Primer
(F):5'- CTCAAGGTGCTGTGTTCCTCTGATG -3'
(R):5'- AGAAATTCACTCCTTCCTGAAGCCG -3'

Sequencing Primer
(F):5'- CTCTGATGAATGCTAAGGTGTGAC -3'
(R):5'- ACCTGAATAAGCAGCTGGGT -3'

Posted On

2013-10-16