Mutagenetix > Incidental Mutation

Incidental Mutation 'R5604:Ttll11'

439161

Institutional Source

Beutler Lab

Gene Symbol

Ttll11

Ensembl Gene

ENSMUSG00000026885

Gene Name

tubulin tyrosine ligase-like family, member 11

Synonyms

4932702F08Rik, 4933424A20Rik, D2Ertd624e

MMRRC Submission

043156-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5604 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

35641253-35869925 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 35707798 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 503 (I503N)

Ref Sequence

ENSEMBL: ENSMUSP00000028248 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000028248] [ENSMUST00000112976] [ENSMUST00000161970]

AlphaFold

A4Q9F4

Predicted Effect

probably benign
Transcript: ENSMUST00000028248
AA Change: I503N

PolyPhen 2 Score 0.067 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000028248
Gene: ENSMUSG00000026885
AA Change: I503N

Domain	Start	End	E-Value	Type
low complexity region	11	37	N/A	INTRINSIC
low complexity region	79	101	N/A	INTRINSIC
low complexity region	107	122	N/A	INTRINSIC
Pfam:TTL	170	477	9.1e-68	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000112976

SMART Domains

Protein: ENSMUSP00000108600
Gene: ENSMUSG00000026885

Domain	Start	End	E-Value	Type
low complexity region	11	37	N/A	INTRINSIC
low complexity region	79	101	N/A	INTRINSIC
low complexity region	107	122	N/A	INTRINSIC
Pfam:TTL	170	477	5.9e-68	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000139455

Predicted Effect

probably benign
Transcript: ENSMUST00000160906

SMART Domains

Protein: ENSMUSP00000125511
Gene: ENSMUSG00000026885

Domain	Start	End	E-Value	Type
Pfam:TTL	1	304	4.2e-65	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000160939

Predicted Effect

probably benign
Transcript: ENSMUST00000161970

SMART Domains

Protein: ENSMUSP00000125627
Gene: ENSMUSG00000026885

Domain	Start	End	E-Value	Type
SCOP:d1gosa1	33	88	5e-3	SMART
low complexity region	107	122	N/A	INTRINSIC

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.6%
20x: 96.3%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310034C09Rik	A	T	16: 88,556,278 (GRCm39)	N164I	possibly damaging	Het
4933402J07Rik	C	A	8: 88,295,125 (GRCm39)	R88S	possibly damaging	Het
Abca1	A	T	4: 53,067,168 (GRCm39)		probably null	Het
Abca13	T	A	11: 9,516,279 (GRCm39)	I4406K	probably damaging	Het
Adam6b	T	A	12: 113,454,420 (GRCm39)	Y412*	probably null	Het
Ahcyl2	C	T	6: 29,908,366 (GRCm39)	H370Y	probably damaging	Het
Ahi1	A	G	10: 20,862,904 (GRCm39)	Y693C	probably damaging	Het
Anapc4	T	A	5: 52,999,076 (GRCm39)	Y129*	probably null	Het
Ankrd35	A	G	3: 96,592,215 (GRCm39)	T834A	probably benign	Het
Antxr2	T	C	5: 98,096,169 (GRCm39)	K372E	probably damaging	Het
Arhgef1	C	T	7: 24,612,210 (GRCm39)	H198Y	probably benign	Het
Barhl2	T	C	5: 106,603,412 (GRCm39)	E249G	probably benign	Het
C2cd5	T	C	6: 142,957,747 (GRCm39)	E987G	probably benign	Het
C87436	T	C	6: 86,424,337 (GRCm39)	S290P	probably benign	Het
Ccser1	C	T	6: 61,290,788 (GRCm39)	T490M	probably damaging	Het
Cd8b1	T	C	6: 71,303,159 (GRCm39)	V78A	probably benign	Het
Cdc25c	A	G	18: 34,866,701 (GRCm39)	Y374H	probably damaging	Het
Cmya5	C	T	13: 93,229,271 (GRCm39)	R1939H	probably benign	Het
Cyp2d40	A	G	15: 82,648,256 (GRCm39)	F19S	probably damaging	Het
Dll3	A	G	7: 27,994,057 (GRCm39)	V460A	probably benign	Het
Dnajb12	GC	G	10: 59,728,574 (GRCm39)		probably null	Het
E4f1	A	G	17: 24,663,118 (GRCm39)	I729T	probably damaging	Het
Endou	A	C	15: 97,618,800 (GRCm39)	S75A	probably benign	Het
Epas1	C	T	17: 87,113,200 (GRCm39)	H129Y	probably damaging	Het
Grm1	T	A	10: 10,622,479 (GRCm39)	N415Y	probably damaging	Het
Hdc	A	T	2: 126,436,583 (GRCm39)	S429R	probably benign	Het
Hnf4g	C	T	3: 3,722,186 (GRCm39)	Q447*	probably null	Het
Htr6	C	T	4: 138,788,814 (GRCm39)	A414T	probably benign	Het
Insig1	T	C	5: 28,280,080 (GRCm39)	L224P	probably damaging	Het
Ipo9	G	A	1: 135,329,983 (GRCm39)	L486F	probably damaging	Het
Irak2	T	A	6: 113,667,792 (GRCm39)	S458T	possibly damaging	Het
Irs2	A	G	8: 11,055,007 (GRCm39)	S1142P	possibly damaging	Het
Kirrel1	T	A	3: 86,996,462 (GRCm39)	N379I	possibly damaging	Het
L3mbtl4	T	A	17: 69,084,917 (GRCm39)	D609E	probably benign	Het
Lama3	A	G	18: 12,572,405 (GRCm39)	T537A	probably benign	Het
Lce1i	A	T	3: 92,685,056 (GRCm39)	V40E	unknown	Het
Mprip	T	A	11: 59,649,293 (GRCm39)	V999D	probably benign	Het
Myd88	G	T	9: 119,168,829 (GRCm39)	T85K	possibly damaging	Het
Or1e35	T	A	11: 73,797,853 (GRCm39)	H155L	probably benign	Het
Padi6	A	T	4: 140,458,473 (GRCm39)	M473K	probably damaging	Het
Pcdh12	T	A	18: 38,401,935 (GRCm39)	S97C	probably damaging	Het
Pkd1l1	T	A	11: 8,783,877 (GRCm39)	D2026V	probably damaging	Het
Plcxd1	T	C	5: 110,250,451 (GRCm39)	V264A	probably benign	Het
Plekha4	T	C	7: 45,198,580 (GRCm39)	S558P	probably damaging	Het
Ppm1a	T	A	12: 72,837,455 (GRCm39)	M334K	probably benign	Het
Ppp1r13l	T	C	7: 19,109,524 (GRCm39)	S684P	possibly damaging	Het
Prdm4	TCTCCTCCT	TCTCCT	10: 85,728,987 (GRCm39)		probably null	Het
Prl2a1	T	C	13: 27,990,369 (GRCm39)		probably benign	Het
Ptch1	T	C	13: 63,672,936 (GRCm39)	K753E	probably benign	Het
Qrich1	A	G	9: 108,436,502 (GRCm39)		probably benign	Het
Ror2	G	A	13: 53,271,201 (GRCm39)	R373C	probably benign	Het
Rtn4	C	A	11: 29,658,140 (GRCm39)	L765I	probably damaging	Het
Sema3a	T	C	5: 13,523,487 (GRCm39)		probably null	Het
Setd2	T	A	9: 110,433,284 (GRCm39)	D62E	probably damaging	Het
Ss18	A	T	18: 14,769,577 (GRCm39)	Y327N	unknown	Het
Ticam1	G	A	17: 56,578,756 (GRCm39)	T113I	probably benign	Het
Tnrc6a	A	G	7: 122,773,459 (GRCm39)	I1134V	probably damaging	Het
Top3b	T	G	16: 16,707,399 (GRCm39)	Y526*	probably null	Het
Tph2	T	C	10: 114,926,614 (GRCm39)	E384G	probably damaging	Het
Zfp87	T	G	13: 67,665,945 (GRCm39)	K172N	probably damaging	Het

Other mutations in Ttll11

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00815:Ttll11	APN	2	35,792,732 (GRCm39)	nonsense	probably null
IGL01148:Ttll11	APN	2	35,674,205 (GRCm39)	missense	probably damaging	0.96
IGL02933:Ttll11	APN	2	35,869,422 (GRCm39)	missense	probably benign
e-suppressor	UTSW	2	35,642,418 (GRCm39)	missense	probably damaging	1.00
R0356:Ttll11	UTSW	2	35,792,688 (GRCm39)	missense	possibly damaging	0.66
R0494:Ttll11	UTSW	2	35,834,886 (GRCm39)	missense	probably damaging	1.00
R1494:Ttll11	UTSW	2	35,685,391 (GRCm39)	missense	probably damaging	1.00
R1630:Ttll11	UTSW	2	35,779,337 (GRCm39)	missense	probably damaging	0.96
R1688:Ttll11	UTSW	2	35,685,391 (GRCm39)	missense	probably damaging	1.00
R1939:Ttll11	UTSW	2	35,830,765 (GRCm39)	missense	probably null
R2414:Ttll11	UTSW	2	35,869,546 (GRCm39)	missense	unknown
R2986:Ttll11	UTSW	2	35,707,750 (GRCm39)	missense	probably benign	0.00
R4295:Ttll11	UTSW	2	35,869,564 (GRCm39)	small deletion	probably benign
R4346:Ttll11	UTSW	2	35,674,130 (GRCm39)	missense	probably benign	0.22
R5234:Ttll11	UTSW	2	35,830,745 (GRCm39)	missense	probably damaging	1.00
R5340:Ttll11	UTSW	2	35,792,801 (GRCm39)	missense	probably damaging	0.99
R5442:Ttll11	UTSW	2	35,793,135 (GRCm39)	makesense	probably null
R5482:Ttll11	UTSW	2	35,642,418 (GRCm39)	missense	probably damaging	1.00
R6219:Ttll11	UTSW	2	35,642,511 (GRCm39)	splice site	probably null
R6481:Ttll11	UTSW	2	35,792,766 (GRCm39)	missense	probably damaging	1.00
R6764:Ttll11	UTSW	2	35,780,460 (GRCm39)	splice site	probably null
R6944:Ttll11	UTSW	2	35,642,306 (GRCm39)	missense	probably benign	0.05
R7224:Ttll11	UTSW	2	35,792,685 (GRCm39)	missense	probably damaging	1.00
R7511:Ttll11	UTSW	2	35,793,046 (GRCm39)	missense	probably damaging	1.00
R8030:Ttll11	UTSW	2	35,792,685 (GRCm39)	missense	probably damaging	1.00
R8052:Ttll11	UTSW	2	35,869,527 (GRCm39)	missense	unknown
R8200:Ttll11	UTSW	2	35,834,940 (GRCm39)	missense	probably damaging	1.00
R8332:Ttll11	UTSW	2	35,830,721 (GRCm39)	missense	possibly damaging	0.85
R8691:Ttll11	UTSW	2	35,674,161 (GRCm39)	missense	probably damaging	1.00
R8801:Ttll11	UTSW	2	35,792,985 (GRCm39)	missense	probably damaging	1.00
R8993:Ttll11	UTSW	2	35,707,813 (GRCm39)	missense	possibly damaging	0.92
R9054:Ttll11	UTSW	2	35,869,392 (GRCm39)	missense	probably benign	0.23
X0026:Ttll11	UTSW	2	35,685,364 (GRCm39)	splice site	probably null

Predicted Primers

PCR Primer
(F):5'- AAGCCTGAGGATCCACAGTC -3'
(R):5'- ACATTTGGCAGGAAGGTCCC -3'

Sequencing Primer
(F):5'- ATAGTCTTGATACGTAGCCCAGGC -3'
(R):5'- GAAGGTCCCACCCCAGTC -3'

Posted On

2016-10-26