Mutagenetix > Incidental Mutation

Incidental Mutation 'R1972:Tbc1d30'

221113

Institutional Source

Beutler Lab

Gene Symbol

Tbc1d30

Ensembl Gene

ENSMUSG00000052302

Gene Name

TBC1 domain family, member 30

Synonyms

4930505D03Rik

MMRRC Submission

039985-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1972 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

121099725-121187183 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to T at 121142135 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000151922 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000064107] [ENSMUST00000219179]

AlphaFold

Q69ZT9

Predicted Effect

probably null
Transcript: ENSMUST00000064107

SMART Domains

Protein: ENSMUSP00000070488
Gene: ENSMUSG00000052302

Domain	Start	End	E-Value	Type
low complexity region	11	26	N/A	INTRINSIC
TBC	84	318	2.22e-30	SMART
low complexity region	392	403	N/A	INTRINSIC
Pfam:DUF4682	475	613	4.3e-50	PFAM
low complexity region	623	633	N/A	INTRINSIC
low complexity region	649	657	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000219179

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 96.8%
20x: 94.2%

Validation Efficiency

100% (77/77)

Allele List at MGI

Other mutations in this stock

Total: 75 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adat1	A	G	8: 112,717,050 (GRCm39)		probably benign	Het
Bbs2	A	G	8: 94,807,805 (GRCm39)		probably benign	Het
Bcl9	A	C	3: 97,114,518 (GRCm39)	D1035E	probably damaging	Het
Bmpr2	A	G	1: 59,852,762 (GRCm39)	E31G	possibly damaging	Het
Borcs5	A	G	6: 134,687,137 (GRCm39)	D164G	probably damaging	Het
Cap2	A	G	13: 46,791,375 (GRCm39)	R181G	probably damaging	Het
Ccdc113	A	T	8: 96,264,874 (GRCm39)	H128L	probably benign	Het
Cdh20	G	A	1: 109,988,862 (GRCm39)	V255I	probably benign	Het
Chat	C	T	14: 32,146,148 (GRCm39)	V342I	probably benign	Het
Chrm4	C	T	2: 91,757,838 (GRCm39)	A82V	probably benign	Het
Cyp2d22	A	T	15: 82,260,028 (GRCm39)	M52K	probably benign	Het
Dennd2c	T	C	3: 103,039,014 (GRCm39)	V54A	probably benign	Het
Dgka	C	T	10: 128,556,335 (GRCm39)	G717D	probably damaging	Het
Dnah1	C	T	14: 30,987,348 (GRCm39)	W3550*	probably null	Het
Eif2ak1	A	G	5: 143,821,532 (GRCm39)	T283A	probably benign	Het
Entrep2	A	T	7: 64,425,516 (GRCm39)	I192N	possibly damaging	Het
Fcgbp	A	T	7: 27,793,617 (GRCm39)	Y1173F	probably benign	Het
Flt1	G	A	5: 147,591,903 (GRCm39)		probably benign	Het
Gpr149	T	C	3: 62,438,216 (GRCm39)	K647R	probably benign	Het
Gsdma2	T	C	11: 98,541,744 (GRCm39)	V157A	probably benign	Het
Heatr4	T	A	12: 84,001,794 (GRCm39)	I884F	probably damaging	Het
Ift56	C	A	6: 38,387,738 (GRCm39)	N396K	probably benign	Het
Il17ra	A	G	6: 120,459,177 (GRCm39)	E776G	probably benign	Het
Inpp5d	T	C	1: 87,604,036 (GRCm39)	S235P	probably benign	Het
Iqgap3	T	A	3: 87,991,235 (GRCm39)		probably null	Het
Isoc2a	T	A	7: 4,895,086 (GRCm39)	D171E	probably damaging	Het
Itga10	C	T	3: 96,559,054 (GRCm39)		probably benign	Het
Kcnk12	T	C	17: 88,104,560 (GRCm39)	D108G	possibly damaging	Het
Klra9	A	T	6: 130,159,345 (GRCm39)		probably null	Het
Lgmn	A	G	12: 102,362,080 (GRCm39)		probably benign	Het
Morf4l1	A	T	9: 89,977,267 (GRCm39)		probably benign	Het
Mthfr	T	C	4: 148,136,384 (GRCm39)	I380T	probably damaging	Het
Mybpc1	T	C	10: 88,387,404 (GRCm39)	I436V	probably benign	Het
Naip5	A	G	13: 100,349,278 (GRCm39)	V1350A	probably damaging	Het
Neil2	A	T	14: 63,423,526 (GRCm39)	C36S	possibly damaging	Het
Nlrx1	A	G	9: 44,164,753 (GRCm39)	V897A	probably benign	Het
Nod2	A	T	8: 89,379,501 (GRCm39)	M8L	probably damaging	Het
Nop2	A	G	6: 125,111,602 (GRCm39)	T112A	probably benign	Het
Nrap	T	A	19: 56,345,785 (GRCm39)	T608S	probably damaging	Het
Nuak2	A	T	1: 132,258,340 (GRCm39)	H257L	probably damaging	Het
Or10x1	T	C	1: 174,197,136 (GRCm39)	F218L	probably benign	Het
Or2ag12	T	C	7: 106,277,426 (GRCm39)	D89G	probably benign	Het
Or4c113	A	T	2: 88,884,891 (GRCm39)	M293K	probably benign	Het
Or52e8	T	C	7: 104,625,106 (GRCm39)	I33V	possibly damaging	Het
Or5ac25	A	T	16: 59,182,476 (GRCm39)	V35D	probably damaging	Het
Or5b119	T	C	19: 13,457,058 (GRCm39)	N168S	probably benign	Het
Or8b40	T	A	9: 38,027,863 (GRCm39)	M257K	possibly damaging	Het
Pde1a	T	C	2: 79,696,065 (GRCm39)	E358G	probably damaging	Het
Pdlim1	A	T	19: 40,211,581 (GRCm39)	S237R	probably damaging	Het
Pithd1	T	C	4: 135,714,340 (GRCm39)	D36G	probably damaging	Het
Ppp2r3d	A	G	9: 101,088,976 (GRCm39)	F449S	probably benign	Het
Prr11	G	A	11: 86,989,580 (GRCm39)	R264C	possibly damaging	Het
Rbm43	A	T	2: 51,815,548 (GRCm39)	H224Q	probably benign	Het
Rfx5	C	T	3: 94,864,603 (GRCm39)	L250F	probably damaging	Het
Rgs22	T	A	15: 36,103,982 (GRCm39)	I160L	probably benign	Het
Rorb	T	A	19: 18,929,567 (GRCm39)	Q393H	probably damaging	Het
Rpl13a	T	A	7: 44,775,419 (GRCm39)	K368*	probably null	Het
Scaf8	T	G	17: 3,219,646 (GRCm39)	S276R	unknown	Het
Scube2	A	T	7: 109,408,421 (GRCm39)	N675K	probably benign	Het
Sec22c	A	T	9: 121,517,320 (GRCm39)	M126K	possibly damaging	Het
Serpinb11	T	C	1: 107,297,210 (GRCm39)	F29L	probably damaging	Het
Sis	A	G	3: 72,828,337 (GRCm39)	F1217S	probably damaging	Het
Slc18a2	A	G	19: 59,263,085 (GRCm39)	D294G	possibly damaging	Het
Slc9c1	A	G	16: 45,413,835 (GRCm39)	T988A	possibly damaging	Het
Smndc1	A	C	19: 53,371,986 (GRCm39)		probably null	Het
Sned1	G	A	1: 93,192,795 (GRCm39)	G361S	probably damaging	Het
Spatc1	A	T	15: 76,169,075 (GRCm39)		probably null	Het
Stab2	A	T	10: 86,796,180 (GRCm39)	C356S	probably damaging	Het
Stk4	C	T	2: 163,942,448 (GRCm39)	T360M	probably benign	Het
Tenm3	T	C	8: 48,681,626 (GRCm39)	E2668G	probably damaging	Het
Tigar	A	G	6: 127,064,889 (GRCm39)	V253A	possibly damaging	Het
Tmc2	T	A	2: 130,056,584 (GRCm39)		probably benign	Het
Ugt1a10	A	T	1: 87,983,769 (GRCm39)	Y189F	probably damaging	Het
Vmn2r82	A	G	10: 79,214,680 (GRCm39)	D221G	probably damaging	Het
Xkr5	C	T	8: 18,991,997 (GRCm39)	V131M	probably damaging	Het

Other mutations in Tbc1d30

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00818:Tbc1d30	APN	10	121,102,729 (GRCm39)	utr 3 prime	probably benign
IGL00837:Tbc1d30	APN	10	121,132,750 (GRCm39)	missense	probably damaging	1.00
IGL01081:Tbc1d30	APN	10	121,103,319 (GRCm39)	missense	probably damaging	1.00
IGL01813:Tbc1d30	APN	10	121,102,956 (GRCm39)	missense	probably benign
IGL01844:Tbc1d30	APN	10	121,103,084 (GRCm39)	missense	probably benign	0.01
R1782:Tbc1d30	UTSW	10	121,103,525 (GRCm39)	missense	probably damaging	1.00
R2025:Tbc1d30	UTSW	10	121,115,051 (GRCm39)	missense	probably benign	0.18
R2197:Tbc1d30	UTSW	10	121,140,312 (GRCm39)	missense	probably damaging	1.00
R3752:Tbc1d30	UTSW	10	121,108,073 (GRCm39)	missense	probably damaging	1.00
R4374:Tbc1d30	UTSW	10	121,130,617 (GRCm39)	missense	probably damaging	1.00
R4540:Tbc1d30	UTSW	10	121,115,063 (GRCm39)	missense	probably damaging	0.99
R4624:Tbc1d30	UTSW	10	121,132,691 (GRCm39)	missense	probably damaging	0.99
R4960:Tbc1d30	UTSW	10	121,103,121 (GRCm39)	missense	probably benign	0.04
R5170:Tbc1d30	UTSW	10	121,142,743 (GRCm39)	missense	possibly damaging	0.49
R5566:Tbc1d30	UTSW	10	121,138,015 (GRCm39)	missense	probably damaging	1.00
R5642:Tbc1d30	UTSW	10	121,132,692 (GRCm39)	missense	probably damaging	1.00
R5726:Tbc1d30	UTSW	10	121,103,479 (GRCm39)	missense	probably damaging	1.00
R6051:Tbc1d30	UTSW	10	121,132,750 (GRCm39)	missense	probably damaging	1.00
R6364:Tbc1d30	UTSW	10	121,130,630 (GRCm39)	missense	possibly damaging	0.95
R7106:Tbc1d30	UTSW	10	121,137,897 (GRCm39)	missense	possibly damaging	0.94
R7233:Tbc1d30	UTSW	10	121,107,962 (GRCm39)	missense	probably benign	0.35
R7256:Tbc1d30	UTSW	10	121,124,870 (GRCm39)	missense	probably damaging	1.00
R7826:Tbc1d30	UTSW	10	121,132,710 (GRCm39)	missense	probably damaging	1.00
R7910:Tbc1d30	UTSW	10	121,183,061 (GRCm39)	nonsense	probably null
R7958:Tbc1d30	UTSW	10	121,107,962 (GRCm39)	missense	probably benign	0.35
R7978:Tbc1d30	UTSW	10	121,142,104 (GRCm39)	missense	probably damaging	1.00
R8021:Tbc1d30	UTSW	10	121,103,448 (GRCm39)	missense	probably benign	0.09
R8394:Tbc1d30	UTSW	10	121,183,013 (GRCm39)	nonsense	probably null
R8472:Tbc1d30	UTSW	10	121,187,009 (GRCm39)	missense	probably benign	0.00
R8532:Tbc1d30	UTSW	10	121,103,335 (GRCm39)	missense	probably damaging	1.00
R8887:Tbc1d30	UTSW	10	121,187,059 (GRCm39)	missense	possibly damaging	0.45
R9124:Tbc1d30	UTSW	10	121,132,716 (GRCm39)	missense	probably damaging	0.99
R9186:Tbc1d30	UTSW	10	121,111,639 (GRCm39)	missense	probably benign
R9282:Tbc1d30	UTSW	10	121,142,128 (GRCm39)	critical splice acceptor site	probably null
R9342:Tbc1d30	UTSW	10	121,103,366 (GRCm39)	nonsense	probably null
R9531:Tbc1d30	UTSW	10	121,183,105 (GRCm39)	missense	probably damaging	1.00
R9665:Tbc1d30	UTSW	10	121,102,886 (GRCm39)	missense	possibly damaging	0.83
R9799:Tbc1d30	UTSW	10	121,142,074 (GRCm39)	missense	possibly damaging	0.55
R9803:Tbc1d30	UTSW	10	121,107,980 (GRCm39)	missense	probably damaging	1.00
Z1176:Tbc1d30	UTSW	10	121,138,018 (GRCm39)	missense	probably damaging	1.00
Z1177:Tbc1d30	UTSW	10	121,186,969 (GRCm39)	missense	probably benign	0.09

Predicted Primers

PCR Primer
(F):5'- GCATGATTAAGGACGCATACAC -3'
(R):5'- AACTTTCTCACGTTCTATGGATGC -3'

Sequencing Primer
(F):5'- GACGCATACACTTTTAGATTTCCCAG -3'
(R):5'- AGCACTGTTCATCGCTGAAG -3'

Posted On

2014-08-25