Mutagenetix > Incidental Mutation

Incidental Mutation 'R7121:Ttc27'

552040

Institutional Source

Beutler Lab

Gene Symbol

Ttc27

Ensembl Gene

ENSMUSG00000024078

Gene Name

tetratricopeptide repeat domain 27

Synonyms

2610511O17Rik

MMRRC Submission

045210-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.957) question?

Stock #

R7121 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

75024730-75170565 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 75054710 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Lysine at position 339 (Q339K)

Ref Sequence

ENSEMBL: ENSMUSP00000024882 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000024882]

AlphaFold

Q8CD92

Predicted Effect

probably benign
Transcript: ENSMUST00000024882
AA Change: Q339K

PolyPhen 2 Score 0.035 (Sensitivity: 0.94; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000024882
Gene: ENSMUSG00000024078
AA Change: Q339K

Domain	Start	End	E-Value	Type
TPR	531	564	7.34e-3	SMART
TPR	565	598	5.56e-3	SMART
TPR	599	632	3.81e-1	SMART
Blast:TPR	633	666	7e-15	BLAST
coiled coil region	817	847	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.9%

Validation Efficiency

99% (71/72)

Allele List at MGI

Other mutations in this stock

Total: 70 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933411K16Rik	C	T	19: 42,041,112 (GRCm39)	A81V	probably benign	Het
Abcc9	A	T	6: 142,634,853 (GRCm39)	L137*	probably null	Het
Akap10	A	G	11: 61,777,524 (GRCm39)		probably null	Het
Alms1	T	A	6: 85,601,604 (GRCm39)	Y1683N	probably damaging	Het
Atl1	A	G	12: 69,978,408 (GRCm39)	S127G	probably damaging	Het
Cadm1	G	A	9: 47,710,708 (GRCm39)	V204M	probably damaging	Het
Cbr3	T	A	16: 93,487,438 (GRCm39)	I207N	probably damaging	Het
Ccdc148	A	T	2: 58,717,579 (GRCm39)	Y475N	probably damaging	Het
Ccdc33	A	T	9: 57,988,167 (GRCm39)	S144T	probably benign	Het
Ceacam5	C	A	7: 17,479,462 (GRCm39)	A193E	probably benign	Het
Chd2	T	C	7: 73,119,418 (GRCm39)	D1042G	probably benign	Het
Chmp5	A	T	4: 40,952,217 (GRCm39)		probably null	Het
Clca3a1	T	A	3: 144,717,567 (GRCm39)	N467I	probably damaging	Het
D130040H23Rik	T	C	8: 69,754,931 (GRCm39)	V112A	probably damaging	Het
Dbh	A	T	2: 27,058,318 (GRCm39)	D162V	probably damaging	Het
Dnah12	G	A	14: 26,500,869 (GRCm39)		probably null	Het
Dnm2	C	T	9: 21,385,862 (GRCm39)	T295I	probably benign	Het
Faiml	A	C	9: 99,116,446 (GRCm39)	D81E	probably benign	Het
Fer1l4	T	A	2: 155,886,477 (GRCm39)	Y720F	probably benign	Het
Fn1	A	C	1: 71,639,697 (GRCm39)		probably benign	Het
Ftsj3	T	C	11: 106,143,123 (GRCm39)	E397G	probably damaging	Het
Gm16506	T	C	14: 43,964,817 (GRCm39)	K42E		Het
Gpr179	A	G	11: 97,225,556 (GRCm39)	S2200P	probably benign	Het
Gusb	T	C	5: 130,028,884 (GRCm39)	D202G	probably benign	Het
Hspe1	A	G	1: 55,128,310 (GRCm39)	E35G	probably damaging	Het
Kptn	T	A	7: 15,857,023 (GRCm39)	H170Q	probably damaging	Het
Lama3	G	A	18: 12,595,839 (GRCm39)	A923T	probably benign	Het
Lmo7	T	A	14: 102,124,471 (GRCm39)	I432K	probably damaging	Het
Maneal	G	A	4: 124,750,905 (GRCm39)	P284S	probably benign	Het
Mrgbp	A	G	2: 180,224,682 (GRCm39)	T28A	probably benign	Het
Myo1h	T	C	5: 114,476,290 (GRCm39)	V493A		Het
Naxd	T	C	8: 11,556,745 (GRCm39)	L122P	probably damaging	Het
Neto2	T	C	8: 86,397,020 (GRCm39)		probably null	Het
Obscn	T	A	11: 58,904,078 (GRCm39)	R7299*	probably null	Het
Odf2l	G	A	3: 144,845,581 (GRCm39)	V363I	possibly damaging	Het
Or2g25	T	C	17: 37,970,699 (GRCm39)	H175R	probably damaging	Het
Or2t35	A	G	14: 14,407,998 (GRCm38)	T257A	possibly damaging	Het
Or4c100	A	T	2: 88,356,170 (GRCm39)	D81V	probably damaging	Het
Or52a5b	A	T	7: 103,416,940 (GRCm39)	Y221*	probably null	Het
Or5b105	T	A	19: 13,080,537 (GRCm39)	I44F	probably benign	Het
Otud3	G	A	4: 138,624,067 (GRCm39)	P325L	probably benign	Het
Palb2	T	C	7: 121,724,057 (GRCm39)	N564S	probably benign	Het
Pcnt	A	G	10: 76,263,761 (GRCm39)	V401A	possibly damaging	Het
Plcd4	G	A	1: 74,604,524 (GRCm39)	E767K	probably benign	Het
Ppp3ca	T	C	3: 136,574,387 (GRCm39)	F95S	probably damaging	Het
Prkar2a	A	G	9: 108,569,821 (GRCm39)	T56A	probably benign	Het
Psma2	T	A	13: 14,799,815 (GRCm39)	D186E	probably benign	Het
Psmd11	T	A	11: 80,329,099 (GRCm39)	Y72*	probably null	Het
Ror1	G	A	4: 100,160,142 (GRCm39)	D53N	probably benign	Het
Rubcn	C	T	16: 32,656,839 (GRCm39)	R527Q	probably damaging	Het
Sgca	G	A	11: 94,860,373 (GRCm39)	P255S	possibly damaging	Het
Skint11	A	T	4: 114,084,993 (GRCm39)	R167S	probably benign	Het
Slco5a1	A	G	1: 13,060,661 (GRCm39)	V20A	probably benign	Het
Snai2	T	C	16: 14,524,970 (GRCm39)	S159P	probably benign	Het
Taar2	T	G	10: 23,816,725 (GRCm39)	S88R	probably damaging	Het
Tacc3	T	A	5: 33,824,509 (GRCm39)	N378K	possibly damaging	Het
Tek	A	G	4: 94,699,647 (GRCm39)	K342E	probably benign	Het
Tm9sf3	G	T	19: 41,233,944 (GRCm39)	S198*	probably null	Het
Tmbim4	T	A	10: 120,051,514 (GRCm39)	F56I	possibly damaging	Het
Tsen34	T	A	7: 3,697,986 (GRCm39)	S85T	probably benign	Het
Ubap2	G	T	4: 41,205,550 (GRCm39)	P636T	probably benign	Het
Ubr1	G	A	2: 120,705,979 (GRCm39)	L1495F	probably benign	Het
Vsig10	T	C	5: 117,481,967 (GRCm39)	S386P	probably damaging	Het
Wnk2	C	A	13: 49,300,653 (GRCm39)	R19L	probably benign	Het
Wsb2	T	C	5: 117,508,944 (GRCm39)	L126P	probably damaging	Het
Xylb	A	G	9: 119,211,358 (GRCm39)	I402V	probably benign	Het
Yrdc	A	G	4: 124,744,748 (GRCm39)	S61G	probably benign	Het
Zbtb3	A	G	19: 8,780,771 (GRCm39)	D128G	probably damaging	Het
Zfp423	C	T	8: 88,507,489 (GRCm39)	G952R	probably damaging	Het
Zfp646	A	G	7: 127,478,944 (GRCm39)	T374A	possibly damaging	Het

Other mutations in Ttc27

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00422:Ttc27	APN	17	75,087,811 (GRCm39)	missense	probably damaging	1.00
IGL01508:Ttc27	APN	17	75,142,352 (GRCm39)	missense	probably damaging	0.98
IGL02010:Ttc27	APN	17	75,087,906 (GRCm39)	splice site	probably benign
IGL02189:Ttc27	APN	17	75,036,894 (GRCm39)	missense	probably damaging	0.99
IGL02487:Ttc27	APN	17	75,163,549 (GRCm39)	missense	probably damaging	1.00
IGL02745:Ttc27	APN	17	75,046,728 (GRCm39)	missense	probably benign	0.37
IGL02816:Ttc27	APN	17	75,054,769 (GRCm39)	splice site	probably benign
IGL03389:Ttc27	APN	17	75,165,028 (GRCm39)	missense	probably benign	0.00
R0024:Ttc27	UTSW	17	75,077,259 (GRCm39)	missense	possibly damaging	0.79
R0511:Ttc27	UTSW	17	75,025,710 (GRCm39)	missense	probably benign	0.22
R0518:Ttc27	UTSW	17	75,163,544 (GRCm39)	missense	possibly damaging	0.80
R0521:Ttc27	UTSW	17	75,163,544 (GRCm39)	missense	possibly damaging	0.80
R0633:Ttc27	UTSW	17	75,036,972 (GRCm39)	missense	probably benign	0.02
R1415:Ttc27	UTSW	17	75,046,667 (GRCm39)	missense	probably benign
R1597:Ttc27	UTSW	17	75,170,402 (GRCm39)	missense	possibly damaging	0.95
R1961:Ttc27	UTSW	17	75,087,851 (GRCm39)	missense	probably damaging	0.99
R2038:Ttc27	UTSW	17	75,163,497 (GRCm39)	missense	probably benign	0.00
R3012:Ttc27	UTSW	17	75,147,454 (GRCm39)	missense	probably benign	0.17
R3619:Ttc27	UTSW	17	75,058,123 (GRCm39)	splice site	probably null
R4155:Ttc27	UTSW	17	75,147,455 (GRCm39)	missense	probably benign	0.09
R4272:Ttc27	UTSW	17	75,147,355 (GRCm39)	missense	probably damaging	1.00
R4291:Ttc27	UTSW	17	75,163,474 (GRCm39)	missense	probably damaging	1.00
R4557:Ttc27	UTSW	17	75,136,544 (GRCm39)	missense	probably benign	0.00
R5068:Ttc27	UTSW	17	75,106,337 (GRCm39)	missense	probably damaging	1.00
R5069:Ttc27	UTSW	17	75,106,337 (GRCm39)	missense	probably damaging	1.00
R5070:Ttc27	UTSW	17	75,106,337 (GRCm39)	missense	probably damaging	1.00
R5074:Ttc27	UTSW	17	75,054,750 (GRCm39)	missense	probably damaging	1.00
R5169:Ttc27	UTSW	17	75,054,690 (GRCm39)	nonsense	probably null
R5203:Ttc27	UTSW	17	75,084,649 (GRCm39)	missense	probably damaging	1.00
R5272:Ttc27	UTSW	17	75,049,972 (GRCm39)	missense	probably damaging	1.00
R6260:Ttc27	UTSW	17	75,165,086 (GRCm39)	missense	probably damaging	0.99
R6797:Ttc27	UTSW	17	75,036,883 (GRCm39)	missense	probably benign	0.28
R6830:Ttc27	UTSW	17	75,163,550 (GRCm39)	nonsense	probably null
R6987:Ttc27	UTSW	17	75,084,736 (GRCm39)	critical splice donor site	probably null
R7393:Ttc27	UTSW	17	75,077,259 (GRCm39)	missense	possibly damaging	0.79
R7543:Ttc27	UTSW	17	75,024,745 (GRCm39)	start gained	probably benign
R7635:Ttc27	UTSW	17	75,025,710 (GRCm39)	missense	probably benign	0.22
R8231:Ttc27	UTSW	17	75,024,959 (GRCm39)	missense	probably benign	0.19
R8365:Ttc27	UTSW	17	75,054,669 (GRCm39)	missense	probably damaging	1.00
R8464:Ttc27	UTSW	17	75,024,925 (GRCm39)	missense	probably benign
R8493:Ttc27	UTSW	17	75,050,047 (GRCm39)	critical splice donor site	probably null
R8687:Ttc27	UTSW	17	75,046,679 (GRCm39)	missense	probably benign	0.00
X0026:Ttc27	UTSW	17	75,163,432 (GRCm39)	missense	probably benign	0.19

Predicted Primers

PCR Primer
(F):5'- GCATGCTGACCACATTTAGGC -3'
(R):5'- TCGTTGCCCAAGAAGTCTCC -3'

Sequencing Primer
(F):5'- TACACAGGTATGGTGCTACAGTCC -3'
(R):5'- TGCCCAAGAAGTCTCCACCTTC -3'

Posted On

2019-05-15