Mutagenetix > Incidental Mutation

Incidental Mutation 'R2261:Tuba1c'

243824

Institutional Source

Beutler Lab

Gene Symbol

Tuba1c

Ensembl Gene

ENSMUSG00000043091

Gene Name

tubulin, alpha 1C

Synonyms

M[a]6, Tuba6

MMRRC Submission

040261-MU

Accession Numbers

Essential gene?

Not available question?

Stock #

R2261 (G1)

Quality Score

Status

Not validated

Chromosome

Chromosomal Location

98927772-98935986 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 98935757 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Arginine at position 406 (H406R)

Ref Sequence

ENSEMBL: ENSMUSP00000051033 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000058914]

AlphaFold

P68373

Predicted Effect

probably damaging
Transcript: ENSMUST00000058914
AA Change: H406R

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

SMART Domains

Protein: ENSMUSP00000051033
Gene: ENSMUSG00000043091
AA Change: H406R

Domain	Start	End	E-Value	Type
Tubulin	49	246	6.98e-83	SMART
Tubulin_C	248	393	9.05e-59	SMART
low complexity region	433	448	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000230447

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 97.2%
20x: 94.7%

Validation Efficiency

98% (60/61)

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca13	A	T	11: 9,242,288 (GRCm39)	M1384L	probably benign	Het
Ahdc1	A	G	4: 132,790,474 (GRCm39)	T572A	unknown	Het
Arhgap31	T	A	16: 38,429,639 (GRCm39)	Q412L	probably damaging	Het
Arsi	T	C	18: 61,049,737 (GRCm39)	Y207H	probably damaging	Het
Bco1	T	C	8: 117,859,764 (GRCm39)	L489S	probably damaging	Het
Cacna1g	T	A	11: 94,347,961 (GRCm39)	H709L	probably benign	Het
Cacna1h	T	C	17: 25,652,139 (GRCm39)	T2A	possibly damaging	Het
Casz1	G	T	4: 149,013,556 (GRCm39)	R40L	probably damaging	Het
Cdh23	A	G	10: 60,152,907 (GRCm39)	V2372A	probably damaging	Het
Cdk17	T	A	10: 93,047,820 (GRCm39)	S56T	possibly damaging	Het
Ces2h	T	A	8: 105,743,191 (GRCm39)	M142K	probably damaging	Het
Cfap69	C	A	5: 5,646,018 (GRCm39)	V561F	probably damaging	Het
Col1a2	G	A	6: 4,518,822 (GRCm39)		probably benign	Het
Dnah11	T	A	12: 117,843,760 (GRCm39)	M4362L	probably benign	Het
Dnah11	T	C	12: 117,930,374 (GRCm39)	T3324A	probably damaging	Het
Dnajc3	A	G	14: 119,198,232 (GRCm39)	Q118R	probably damaging	Het
Dok4	A	T	8: 95,593,140 (GRCm39)	C182S	probably damaging	Het
Fam184a	A	G	10: 53,523,666 (GRCm39)		probably null	Het
Fanca	A	G	8: 124,016,098 (GRCm39)		probably null	Het
Flt3	G	A	5: 147,284,873 (GRCm39)	P748L	probably benign	Het
Gbp2b	G	A	3: 142,312,496 (GRCm39)	S293N	probably benign	Het
Gbp8	T	C	5: 105,163,999 (GRCm39)	Q433R	possibly damaging	Het
Gm12874	G	A	4: 122,487,533 (GRCm39)		noncoding transcript	Het
Golgb1	T	A	16: 36,713,722 (GRCm39)	F234L	probably damaging	Het
Gpr65	A	T	12: 98,241,494 (GRCm39)	N49I	probably damaging	Het
Grip1	G	A	10: 119,821,489 (GRCm39)	V385M	probably benign	Het
Ltbp3	G	A	19: 5,804,050 (GRCm39)	R854Q	probably benign	Het
Mast4	A	G	13: 102,934,715 (GRCm39)		probably benign	Het
Mia3	A	G	1: 183,115,647 (GRCm39)	Y295H	probably benign	Het
Morc3	T	A	16: 93,650,109 (GRCm39)		probably benign	Het
Muc6	G	A	7: 141,218,313 (GRCm39)	S2120F	possibly damaging	Het
Nell1	C	T	7: 50,210,569 (GRCm39)	T494I	possibly damaging	Het
Npy2r	A	G	3: 82,448,346 (GRCm39)	V30A	possibly damaging	Het
Nsd2	A	T	5: 34,042,871 (GRCm39)	Q1045L	probably damaging	Het
Or51t4	T	C	7: 102,598,464 (GRCm39)	F254S	probably damaging	Het
Or5d40	T	A	2: 88,015,965 (GRCm39)	I248N	probably damaging	Het
Otub1	T	A	19: 7,176,861 (GRCm39)		probably null	Het
Pcdh1	A	T	18: 38,331,710 (GRCm39)	L431H	probably benign	Het
Pdgfra	T	C	5: 75,346,184 (GRCm39)	V778A	probably benign	Het
Plekhm2	C	T	4: 141,370,043 (GRCm39)	E29K	probably damaging	Het
Ralgapa2	T	C	2: 146,184,603 (GRCm39)	N1468S	probably damaging	Het
Rnf111	T	C	9: 70,383,673 (GRCm39)	S87G	probably benign	Het
Ryr3	C	G	2: 112,506,218 (GRCm39)	R3443P	probably damaging	Het
Saxo1	C	T	4: 86,397,212 (GRCm39)	D109N	probably damaging	Het
Slc19a3	A	T	1: 83,000,678 (GRCm39)	F113Y	probably damaging	Het
Slc20a1	A	G	2: 129,048,394 (GRCm39)	R260G	possibly damaging	Het
Slk	T	C	19: 47,625,791 (GRCm39)	I1090T	probably damaging	Het
Spr-ps1	G	T	6: 85,132,945 (GRCm39)		noncoding transcript	Het
Ssh1	T	C	5: 114,080,764 (GRCm39)	S867G	possibly damaging	Het
St18	T	A	1: 6,915,796 (GRCm39)	C814S	probably damaging	Het
Stmn2	T	C	3: 8,606,955 (GRCm39)	F25S	probably damaging	Het
Taar3	A	G	10: 23,826,053 (GRCm39)	I200V	probably benign	Het
Tmem184c	A	G	8: 78,323,672 (GRCm39)	Y397H	probably damaging	Het
Tmem184c	T	C	8: 78,323,804 (GRCm39)	T353A	probably damaging	Het
Ubr4	T	C	4: 139,140,773 (GRCm39)	S1231P	probably damaging	Het
Ubr5	A	T	15: 37,988,528 (GRCm39)	D2143E	probably damaging	Het
Vmn2r6	T	C	3: 64,464,090 (GRCm39)	N248S	probably benign	Het
Vmn2r63	G	T	7: 42,578,031 (GRCm39)	T169N	probably benign	Het
Zfp37	A	T	4: 62,109,873 (GRCm39)	L397Q	probably damaging	Het
Zmym2	G	A	14: 57,165,719 (GRCm39)	E681K	probably damaging	Het

Other mutations in Tuba1c

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02190:Tuba1c	APN	15	98,935,870 (GRCm39)	missense	unknown
R2262:Tuba1c	UTSW	15	98,935,757 (GRCm39)	missense	probably damaging	1.00
R4939:Tuba1c	UTSW	15	98,935,835 (GRCm39)	missense	probably damaging	1.00
R6367:Tuba1c	UTSW	15	98,935,334 (GRCm39)	missense	probably damaging	1.00
R6397:Tuba1c	UTSW	15	98,935,738 (GRCm39)	missense	probably benign	0.29
R6999:Tuba1c	UTSW	15	98,935,193 (GRCm39)	missense	probably benign	0.00
R8146:Tuba1c	UTSW	15	98,935,496 (GRCm39)	missense	probably damaging	1.00
R8186:Tuba1c	UTSW	15	98,935,396 (GRCm39)	missense	probably benign
R8403:Tuba1c	UTSW	15	98,931,985 (GRCm39)	missense	probably damaging	0.98
R9192:Tuba1c	UTSW	15	98,935,737 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- AGCGTACCATCCAGTTTGTG -3'
(R):5'- TAGGACAGTTAGAGCACACAC -3'

Sequencing Primer
(F):5'- TTTGTGGACTGGTGCCCCAC -3'
(R):5'- GGACAGTTAGAGCACACACAAAGAC -3'

Posted On

2014-10-16