Mutagenetix > Incidental Mutation

Incidental Mutation 'R1725:Ttc12'

198079

Institutional Source

Beutler Lab

Gene Symbol

Ttc12

Ensembl Gene

ENSMUSG00000040219

Gene Name

tetratricopeptide repeat domain 12

Synonyms

E330017O07Rik

MMRRC Submission

039757-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.113) question?

Stock #

R1725 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

49348263-49397525 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 49369415 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Alanine at position 235 (D235A)

Ref Sequence

ENSEMBL: ENSMUSP00000056378 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000055096]

AlphaFold

Q8BW49

Predicted Effect

probably benign
Transcript: ENSMUST00000055096
AA Change: D235A

PolyPhen 2 Score 0.076 (Sensitivity: 0.93; Specificity: 0.85)

SMART Domains

Protein: ENSMUSP00000056378
Gene: ENSMUSG00000040219
AA Change: D235A

Domain	Start	End	E-Value	Type
coiled coil region	1	29	N/A	INTRINSIC
low complexity region	88	102	N/A	INTRINSIC
TPR	105	138	9.39e-1	SMART
TPR	139	172	1.97e-3	SMART
TPR	173	206	1.09e-5	SMART
low complexity region	356	368	N/A	INTRINSIC
low complexity region	602	613	N/A	INTRINSIC
Blast:ARM	634	675	1e-7	BLAST

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000146666

Coding Region Coverage

1x: 97.5%
3x: 96.9%
10x: 95.3%
20x: 92.5%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 74 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310079G19Rik	A	T	16: 88,424,163 (GRCm39)	F109L	probably benign	Het
Aacs	T	C	5: 125,559,999 (GRCm39)		probably null	Het
Abcc6	C	A	7: 45,641,781 (GRCm39)	D866Y	possibly damaging	Het
Acox3	T	C	5: 35,749,516 (GRCm39)	Y214H	probably benign	Het
Acss2	A	G	2: 155,398,764 (GRCm39)	T404A	possibly damaging	Het
Adgrb3	T	A	1: 25,865,381 (GRCm39)	E154V	probably damaging	Het
Akap12	G	A	10: 4,303,942 (GRCm39)	V251M	probably damaging	Het
Ambp	A	T	4: 63,062,513 (GRCm39)	M242K	possibly damaging	Het
Angptl7	T	G	4: 148,584,469 (GRCm39)	Y93S	probably damaging	Het
Apof	A	G	10: 128,105,680 (GRCm39)		probably benign	Het
Arv1	T	C	8: 125,455,191 (GRCm39)	F135L	probably damaging	Het
Auh	G	A	13: 52,989,532 (GRCm39)	P308L	probably benign	Het
Cacna1s	C	T	1: 136,026,361 (GRCm39)	T1116I	probably damaging	Het
Ccdc91	A	G	6: 147,493,541 (GRCm39)	E311G	unknown	Het
Cenpf	T	C	1: 189,412,676 (GRCm39)	T196A	probably damaging	Het
Chd8	A	T	14: 52,470,030 (GRCm39)	S527T	probably benign	Het
Csmd3	A	C	15: 47,460,203 (GRCm39)	N3529K	probably damaging	Het
Csnk2a1	T	C	2: 152,099,892 (GRCm39)	V116A	probably damaging	Het
Dhx36	T	G	3: 62,414,360 (GRCm39)	M1L	probably benign	Het
Diaph3	A	G	14: 87,203,759 (GRCm39)		probably null	Het
Ephb2	G	A	4: 136,387,089 (GRCm39)	Q714*	probably null	Het
Eprs1	T	A	1: 185,139,189 (GRCm39)	L858Q	probably damaging	Het
Espl1	G	T	15: 102,221,656 (GRCm39)	V982L	probably benign	Het
Eya2	A	G	2: 165,566,605 (GRCm39)	T219A	probably benign	Het
Fam83f	T	G	15: 80,576,468 (GRCm39)	V373G	possibly damaging	Het
Fbxl18	C	T	5: 142,872,458 (GRCm39)	R259H	probably damaging	Het
Gcc2	G	A	10: 58,139,937 (GRCm39)	R1629H	possibly damaging	Het
Gje1	G	A	10: 14,592,168 (GRCm39)	R205*	probably null	Het
Gm10277	TC	T	11: 77,676,828 (GRCm39)		probably null	Het
Kmt2d	T	C	15: 98,743,115 (GRCm39)		probably benign	Het
Krt6a	A	T	15: 101,600,992 (GRCm39)	M268K	probably damaging	Het
Loxhd1	T	A	18: 77,380,937 (GRCm39)	S85T	probably benign	Het
Loxl3	G	A	6: 83,012,574 (GRCm39)	V38I	probably benign	Het
Mill2	A	G	7: 18,573,993 (GRCm39)	D26G	probably benign	Het
Muc15	T	C	2: 110,561,591 (GRCm39)	L9S	probably damaging	Het
Nat8f4	G	A	6: 85,878,080 (GRCm39)	R148*	probably null	Het
Nav3	A	T	10: 109,659,451 (GRCm39)	V722E	probably damaging	Het
Nfkb1	C	A	3: 135,373,519 (GRCm39)	G10W	probably damaging	Het
Or10j5	C	T	1: 172,784,908 (GRCm39)	P182L	possibly damaging	Het
Or2ag1	A	T	7: 106,313,265 (GRCm39)	F208I	probably benign	Het
Or2t1	T	G	14: 14,328,977 (GRCm38)	Y289D	probably damaging	Het
Or5b120	T	C	19: 13,479,883 (GRCm39)	Y59H	probably damaging	Het
Pcdhb22	T	A	18: 37,653,241 (GRCm39)	C313S	probably benign	Het
Plin4	A	G	17: 56,413,473 (GRCm39)	L384P	probably damaging	Het
Pm20d1	T	C	1: 131,743,796 (GRCm39)	I487T	probably damaging	Het
Prex1	A	T	2: 166,443,656 (GRCm39)	D334E	probably damaging	Het
Psg28	A	T	7: 18,161,936 (GRCm39)	I189N	possibly damaging	Het
Ptk2	A	G	15: 73,114,255 (GRCm39)	V701A	possibly damaging	Het
Rae1	A	G	2: 172,848,754 (GRCm39)	I123M	possibly damaging	Het
Sh3glb2	C	A	2: 30,240,679 (GRCm39)	E129*	probably null	Het
Simc1	T	C	13: 54,674,219 (GRCm39)	S856P	probably damaging	Het
Slc19a1	T	A	10: 76,877,672 (GRCm39)	M69K	probably benign	Het
Slc30a8	A	T	15: 52,197,000 (GRCm39)	I304F	possibly damaging	Het
Snx1	A	G	9: 66,005,611 (GRCm39)		probably null	Het
Spmip5	T	G	19: 58,781,194 (GRCm39)	K10T	probably benign	Het
Stx18	G	A	5: 38,292,599 (GRCm39)	V234M	probably damaging	Het
Sulf2	T	C	2: 165,923,281 (GRCm39)	T615A	probably damaging	Het
Sult3a2	T	A	10: 33,655,705 (GRCm39)	K91N	probably benign	Het
Tet1	A	G	10: 62,650,256 (GRCm39)	S22P	probably damaging	Het
Tmc3	T	C	7: 83,253,940 (GRCm39)	V362A	probably damaging	Het
Trim16	A	C	11: 62,711,331 (GRCm39)	M1L	possibly damaging	Het
Trp53bp1	C	T	2: 121,082,481 (GRCm39)	V10I	possibly damaging	Het
Ttn	T	C	2: 76,692,727 (GRCm39)	R452G	possibly damaging	Het
Ugt2b38	A	T	5: 87,559,730 (GRCm39)	H387Q	probably damaging	Het
Usp48	T	A	4: 137,360,733 (GRCm39)	L20*	probably null	Het
Utrn	T	C	10: 12,539,263 (GRCm39)	D1918G	probably damaging	Het
Vmn1r158	A	G	7: 22,490,072 (GRCm39)	S46P	probably benign	Het
Vmn2r97	T	A	17: 19,149,397 (GRCm39)	W262R	probably benign	Het
Vps13d	A	T	4: 144,869,830 (GRCm39)	S1917T	possibly damaging	Het
Vsx1	T	C	2: 150,528,120 (GRCm39)	N158D	probably benign	Het
Vwf	G	A	6: 125,623,245 (GRCm39)	V1781I	probably benign	Het
Wrap73	T	C	4: 154,233,209 (GRCm39)	Y128H	possibly damaging	Het
Zfp472	A	G	17: 33,196,311 (GRCm39)	K129E	possibly damaging	Het
Zscan18	A	T	7: 12,504,784 (GRCm39)	L611Q	probably damaging	Het

Other mutations in Ttc12

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00326:Ttc12	APN	9	49,382,506 (GRCm39)	splice site	probably null
IGL01300:Ttc12	APN	9	49,359,222 (GRCm39)	splice site	probably benign
IGL02100:Ttc12	APN	9	49,351,482 (GRCm39)	missense	probably damaging	1.00
IGL03106:Ttc12	APN	9	49,369,362 (GRCm39)	missense	possibly damaging	0.75
I2288:Ttc12	UTSW	9	49,381,558 (GRCm39)	missense	possibly damaging	0.62
R1238:Ttc12	UTSW	9	49,369,487 (GRCm39)	splice site	probably benign
R1712:Ttc12	UTSW	9	49,356,499 (GRCm39)	missense	probably benign
R1824:Ttc12	UTSW	9	49,368,184 (GRCm39)	missense	probably damaging	1.00
R1916:Ttc12	UTSW	9	49,371,698 (GRCm39)	missense	probably damaging	1.00
R2226:Ttc12	UTSW	9	49,353,135 (GRCm39)	critical splice donor site	probably null
R4498:Ttc12	UTSW	9	49,383,705 (GRCm39)	missense	probably damaging	1.00
R5920:Ttc12	UTSW	9	49,364,633 (GRCm39)	missense	possibly damaging	0.48
R6020:Ttc12	UTSW	9	49,354,422 (GRCm39)	missense	probably damaging	0.96
R6687:Ttc12	UTSW	9	49,349,718 (GRCm39)	missense	probably benign	0.08
R6755:Ttc12	UTSW	9	49,364,646 (GRCm39)	missense	probably benign	0.00
R6975:Ttc12	UTSW	9	49,349,718 (GRCm39)	missense	probably benign	0.08
R7349:Ttc12	UTSW	9	49,359,267 (GRCm39)	missense	possibly damaging	0.94
R7357:Ttc12	UTSW	9	49,349,687 (GRCm39)	missense	probably benign	0.02
R7451:Ttc12	UTSW	9	49,383,179 (GRCm39)	missense	probably benign	0.00
R7725:Ttc12	UTSW	9	49,351,602 (GRCm39)	missense	probably benign	0.00
R7842:Ttc12	UTSW	9	49,349,724 (GRCm39)	missense	possibly damaging	0.80
R7943:Ttc12	UTSW	9	49,381,620 (GRCm39)	missense	possibly damaging	0.53
R8029:Ttc12	UTSW	9	49,381,551 (GRCm39)	missense	possibly damaging	0.83
R8862:Ttc12	UTSW	9	49,351,515 (GRCm39)	missense	probably benign	0.10
R8965:Ttc12	UTSW	9	49,349,718 (GRCm39)	missense	probably benign	0.08
R9116:Ttc12	UTSW	9	49,364,757 (GRCm39)	missense	probably benign
R9342:Ttc12	UTSW	9	49,351,680 (GRCm39)	missense	probably benign	0.00
R9762:Ttc12	UTSW	9	49,368,166 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- TCGTTTCACGAAGCCAGATCCC -3'
(R):5'- TGCTGCTAAGCTGCATCTGAACC -3'

Sequencing Primer
(F):5'- GATCCCCAGCCCCATGC -3'
(R):5'- TGTATTCCTAGAATGCCCCAAG -3'

Posted On

2014-05-23