Mutagenetix > Incidental Mutation

Incidental Mutation 'R0751:Ttll7'

70310

Institutional Source

Beutler Lab

Gene Symbol

Ttll7

Ensembl Gene

ENSMUSG00000036745

Gene Name

tubulin tyrosine ligase-like family, member 7

Synonyms

1110049N09Rik, 4921517B04Rik

MMRRC Submission

038931-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.519) question?

Stock #

R0751 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

146558122-146689764 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 146645746 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Proline to Serine at position 535 (P535S)

Ref Sequence

ENSEMBL: ENSMUSP00000129369 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000037942] [ENSMUST00000106134] [ENSMUST00000170055]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000037942
AA Change: P535S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000038090

SMART Domains

Protein: ENSMUSP00000037875
Gene: ENSMUSG00000036745

Domain	Start	End	E-Value	Type
low complexity region	29	38	N/A	INTRINSIC
Pfam:TTL	84	388	9e-80	PFAM
low complexity region	417	439	N/A	INTRINSIC
low complexity region	501	516	N/A	INTRINSIC
low complexity region	549	563	N/A	INTRINSIC
low complexity region	591	601	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000106134
AA Change: P535S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000101740
Gene: ENSMUSG00000036745
AA Change: P535S

Domain	Start	End	E-Value	Type
low complexity region	29	38	N/A	INTRINSIC
Pfam:TTL	84	388	7.2e-80	PFAM
low complexity region	417	439	N/A	INTRINSIC
low complexity region	501	516	N/A	INTRINSIC
low complexity region	549	563	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000170055
AA Change: P535S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000129369
Gene: ENSMUSG00000036745
AA Change: P535S

Domain	Start	End	E-Value	Type
low complexity region	29	38	N/A	INTRINSIC
Pfam:TTL	84	388	5.9e-80	PFAM
low complexity region	417	439	N/A	INTRINSIC
low complexity region	501	516	N/A	INTRINSIC
low complexity region	549	563	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000197547

Meta Mutation Damage Score

0.1914

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.2%
20x: 94.4%

Validation Efficiency

99% (73/74)

Allele List at MGI

Other mutations in this stock

Total: 75 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ahdc1	T	A	4: 132,792,707 (GRCm39)	M1316K	probably benign	Het
Alox12	T	C	11: 70,137,776 (GRCm39)	I455V	probably benign	Het
Ankrd28	A	G	14: 31,486,225 (GRCm39)	L89P	probably damaging	Het
Aqp9	A	T	9: 71,045,487 (GRCm39)	C41S	probably damaging	Het
Arhgap17	T	C	7: 122,913,913 (GRCm39)	Y199C	probably damaging	Het
Aspm	A	T	1: 139,384,636 (GRCm39)		probably benign	Het
Cacfd1	T	C	2: 26,908,993 (GRCm39)		probably null	Het
Cd33	T	C	7: 43,181,545 (GRCm39)	D205G	probably damaging	Het
Chadl	T	C	15: 81,577,258 (GRCm39)	S198G	probably benign	Het
Chtf8	A	G	8: 107,613,109 (GRCm39)		probably null	Het
Clec4a4	G	T	6: 122,989,671 (GRCm39)	W104L	probably benign	Het
Clock	A	T	5: 76,377,208 (GRCm39)	I696K	possibly damaging	Het
Crtc2	T	A	3: 90,169,940 (GRCm39)	Y445*	probably null	Het
Dapk1	A	T	13: 60,844,112 (GRCm39)	I44F	probably damaging	Het
Dcbld2	T	A	16: 58,270,204 (GRCm39)		probably null	Het
Derl2	T	C	11: 70,905,373 (GRCm39)		probably null	Het
Dnah7c	A	G	1: 46,505,065 (GRCm39)	T154A	probably benign	Het
Dnmt3b	T	A	2: 153,516,762 (GRCm39)		probably null	Het
Dusp3	A	T	11: 101,872,554 (GRCm39)	S106T	probably benign	Het
Eftud2	A	G	11: 102,730,079 (GRCm39)	V897A	probably damaging	Het
Eif3l	T	A	15: 78,959,966 (GRCm39)		probably null	Het
Fbxo33	A	C	12: 59,265,878 (GRCm39)	F130V	probably damaging	Het
Ffar3	T	A	7: 30,554,529 (GRCm39)	N264Y	probably damaging	Het
Fig4	T	C	10: 41,148,978 (GRCm39)	D158G	probably damaging	Het
Fyco1	A	G	9: 123,648,218 (GRCm39)	F1239L	probably damaging	Het
Gabra2	A	G	5: 71,249,442 (GRCm39)		probably benign	Het
Gabra6	C	A	11: 42,205,844 (GRCm39)	R336S	probably benign	Het
Hkdc1	T	C	10: 62,234,452 (GRCm39)	D581G	probably damaging	Het
Ift70a2	C	T	2: 75,808,375 (GRCm39)	A46T	probably damaging	Het
Iqgap1	A	G	7: 80,375,321 (GRCm39)		probably benign	Het
Larp4b	T	C	13: 9,216,345 (GRCm39)		probably benign	Het
Lcp1	A	T	14: 75,436,827 (GRCm39)	M58L	probably benign	Het
Lrrc8a	T	C	2: 30,146,362 (GRCm39)	V392A	possibly damaging	Het
Mavs	A	T	2: 131,088,684 (GRCm39)	Y496F	probably damaging	Het
Mpi	A	T	9: 57,457,897 (GRCm39)	S102T	probably damaging	Het
Mroh9	G	A	1: 162,893,693 (GRCm39)	R161W	possibly damaging	Het
Myo1h	A	T	5: 114,458,747 (GRCm39)	S161C	probably damaging	Het
Napg	T	G	18: 63,127,409 (GRCm39)	H204Q	probably benign	Het
Nelfcd	C	A	2: 174,264,807 (GRCm39)	A182D	probably benign	Het
Ntsr2	G	T	12: 16,704,031 (GRCm39)	K91N	probably damaging	Het
Obscn	A	G	11: 58,972,645 (GRCm39)	S2134P	probably damaging	Het
Ogfod2	G	A	5: 124,251,539 (GRCm39)		probably benign	Het
Or13a19	G	A	7: 139,903,238 (GRCm39)	V209I	probably benign	Het
Or1e26	G	T	11: 73,479,970 (GRCm39)	T198K	probably benign	Het
Pcdha8	T	C	18: 37,127,123 (GRCm39)	V535A	probably damaging	Het
Pdlim2	C	T	14: 70,402,228 (GRCm39)	R296H	probably damaging	Het
Pik3r1	T	C	13: 101,822,866 (GRCm39)		probably null	Het
Pimreg	C	A	11: 71,933,939 (GRCm39)	Q22K	probably benign	Het
Pld5	A	G	1: 175,872,462 (GRCm39)	I225T	probably damaging	Het
Plxnc1	T	C	10: 94,667,195 (GRCm39)		probably benign	Het
Ppip5k2	A	T	1: 97,677,377 (GRCm39)	C306*	probably null	Het
Ptprc	A	G	1: 138,020,668 (GRCm39)	Y588H	probably damaging	Het
Rac2	T	G	15: 78,450,145 (GRCm39)	D65A	possibly damaging	Het
Rgl3	A	G	9: 21,888,676 (GRCm39)		probably null	Het
Serpinb1a	T	C	13: 33,027,199 (GRCm39)	K248E	probably benign	Het
Serpinb9e	A	C	13: 33,443,757 (GRCm39)	E259A	probably benign	Het
Slc12a4	A	T	8: 106,678,532 (GRCm39)	V266E	probably damaging	Het
Slc8b1	A	G	5: 120,662,260 (GRCm39)		probably benign	Het
Spink6	T	C	18: 44,204,605 (GRCm39)		probably benign	Het
Spta1	G	A	1: 174,012,256 (GRCm39)	R354H	probably damaging	Het
Ssb	T	A	2: 69,700,909 (GRCm39)	S330T	probably benign	Het
Stard9	G	T	2: 120,527,966 (GRCm39)	V1408F	probably benign	Het
Sumf2	A	T	5: 129,878,846 (GRCm39)	T61S	probably benign	Het
Sypl2	T	C	3: 108,124,072 (GRCm39)	T157A	probably damaging	Het
Tgfbr3	A	T	5: 107,287,749 (GRCm39)	D483E	probably damaging	Het
Tnrc6a	A	G	7: 122,769,563 (GRCm39)	N451S	possibly damaging	Het
Tradd	T	C	8: 105,986,403 (GRCm39)	E123G	probably damaging	Het
Trim36	T	C	18: 46,329,318 (GRCm39)	T41A	probably damaging	Het
Ubr4	C	T	4: 139,164,509 (GRCm39)		probably benign	Het
Uqcc5	G	T	14: 30,810,953 (GRCm39)		probably benign	Het
Vmn1r195	A	G	13: 22,463,181 (GRCm39)	Y217C	probably damaging	Het
Vmn2r63	A	C	7: 42,577,459 (GRCm39)	F360V	probably damaging	Het
Vmn2r78	G	A	7: 86,603,588 (GRCm39)	V589M	possibly damaging	Het
Vmn2r-ps158	A	G	7: 42,696,833 (GRCm39)	Y630C	probably damaging	Het
Vrk2	A	G	11: 26,433,331 (GRCm39)		probably benign	Het

Other mutations in Ttll7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01060:Ttll7	APN	3	146,615,337 (GRCm39)	missense	possibly damaging	0.72
IGL01353:Ttll7	APN	3	146,667,474 (GRCm39)	missense	probably damaging	1.00
IGL01415:Ttll7	APN	3	146,615,354 (GRCm39)	missense	possibly damaging	0.90
IGL01843:Ttll7	APN	3	146,645,776 (GRCm39)	missense	possibly damaging	0.93
IGL03101:Ttll7	APN	3	146,602,445 (GRCm39)	missense	possibly damaging	0.82
IGL03378:Ttll7	APN	3	146,615,408 (GRCm39)	missense	probably benign	0.06
P0038:Ttll7	UTSW	3	146,650,939 (GRCm39)	missense	possibly damaging	0.80
R0265:Ttll7	UTSW	3	146,649,915 (GRCm39)	nonsense	probably null
R0358:Ttll7	UTSW	3	146,649,871 (GRCm39)	missense	probably benign
R0363:Ttll7	UTSW	3	146,649,970 (GRCm39)	missense	probably benign	0.00
R0364:Ttll7	UTSW	3	146,650,936 (GRCm39)	missense	possibly damaging	0.82
R1184:Ttll7	UTSW	3	146,645,746 (GRCm39)	missense	probably damaging	1.00
R1533:Ttll7	UTSW	3	146,602,422 (GRCm39)	missense	probably damaging	1.00
R1771:Ttll7	UTSW	3	146,600,160 (GRCm39)	missense	probably benign	0.02
R1789:Ttll7	UTSW	3	146,621,535 (GRCm39)	missense	probably damaging	1.00
R1961:Ttll7	UTSW	3	146,621,550 (GRCm39)	splice site	probably benign
R1995:Ttll7	UTSW	3	146,667,510 (GRCm39)	missense	possibly damaging	0.95
R2083:Ttll7	UTSW	3	146,635,859 (GRCm39)	missense	possibly damaging	0.77
R2152:Ttll7	UTSW	3	146,635,944 (GRCm39)	missense	probably damaging	1.00
R2655:Ttll7	UTSW	3	146,653,376 (GRCm39)	missense	probably damaging	1.00
R2926:Ttll7	UTSW	3	146,636,170 (GRCm39)	nonsense	probably null
R4888:Ttll7	UTSW	3	146,599,932 (GRCm39)	start codon destroyed	probably null	0.99
R4999:Ttll7	UTSW	3	146,600,224 (GRCm39)	missense	probably damaging	1.00
R5648:Ttll7	UTSW	3	146,667,465 (GRCm39)	missense	probably damaging	1.00
R5937:Ttll7	UTSW	3	146,649,847 (GRCm39)	nonsense	probably null
R6009:Ttll7	UTSW	3	146,640,290 (GRCm39)	missense	probably damaging	0.99
R6036:Ttll7	UTSW	3	146,645,917 (GRCm39)	missense	probably benign
R6036:Ttll7	UTSW	3	146,645,917 (GRCm39)	missense	probably benign
R6463:Ttll7	UTSW	3	146,637,337 (GRCm39)	missense	possibly damaging	0.86
R6747:Ttll7	UTSW	3	146,649,811 (GRCm39)	missense	probably benign	0.02
R6922:Ttll7	UTSW	3	146,615,369 (GRCm39)	missense	possibly damaging	0.92
R7123:Ttll7	UTSW	3	146,619,051 (GRCm39)	missense	possibly damaging	0.95
R7211:Ttll7	UTSW	3	146,619,031 (GRCm39)	missense	probably damaging	0.97
R8229:Ttll7	UTSW	3	146,607,204 (GRCm39)	missense	probably damaging	0.99
R8406:Ttll7	UTSW	3	146,645,779 (GRCm39)	missense	probably benign
R9343:Ttll7	UTSW	3	146,667,497 (GRCm39)	missense	probably damaging	1.00
R9348:Ttll7	UTSW	3	146,673,768 (GRCm39)	missense	probably benign	0.31
R9629:Ttll7	UTSW	3	146,621,487 (GRCm39)	missense	probably damaging	1.00
RF015:Ttll7	UTSW	3	146,685,413 (GRCm39)	missense	probably benign	0.00
X0024:Ttll7	UTSW	3	146,615,308 (GRCm39)	missense	probably damaging	1.00
X0026:Ttll7	UTSW	3	146,667,450 (GRCm39)	missense	probably damaging	1.00
X0027:Ttll7	UTSW	3	146,653,408 (GRCm39)	missense	probably damaging	1.00
Z1176:Ttll7	UTSW	3	146,653,390 (GRCm39)	missense	probably damaging	1.00
Z1176:Ttll7	UTSW	3	146,635,933 (GRCm39)	missense	probably benign	0.01
Z1176:Ttll7	UTSW	3	146,621,526 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TAAGCCAGATTCACAGCTAGGGCG -3'
(R):5'- ACAGGTTTCCTCACACAGGACAATG -3'

Sequencing Primer
(F):5'- GAGAGGGCTTTCCATCATCACTA -3'
(R):5'- CACAGGACAATGCTTCTTTTGG -3'

Posted On

2013-09-30