Mutagenetix > Incidental Mutation

Incidental Mutation 'R7240:Trbv21'

563136

Institutional Source

Beutler Lab

Gene Symbol

Trbv21

Ensembl Gene

ENSMUSG00000076477

Gene Name

T cell receptor beta, variable 21

Synonyms

Tcrb-V19, Gm16778

MMRRC Submission

045347-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.072) question?

Stock #

R7240 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

41179521-41179978 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 41179892 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Asparagine at position 69 (K69N)

Ref Sequence

ENSEMBL: ENSMUSP00000141778 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000103278] [ENSMUST00000195087]

AlphaFold

A0A075B5I8

Predicted Effect

probably benign
Transcript: ENSMUST00000103278
AA Change: K68N

PolyPhen 2 Score 0.044 (Sensitivity: 0.94; Specificity: 0.83)

SMART Domains

Protein: ENSMUSP00000100094
Gene: ENSMUSG00000076477
AA Change: K68N

Domain	Start	End	E-Value	Type
Pfam:V-set	1	97	1.6e-14	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000195087
AA Change: K69N

PolyPhen 2 Score 0.044 (Sensitivity: 0.94; Specificity: 0.83)

SMART Domains

Protein: ENSMUSP00000141778
Gene: ENSMUSG00000076477
AA Change: K69N

Domain	Start	End	E-Value	Type
IG_like	19	95	8.7e-7	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

96% (50/52)

Allele List at MGI

Other mutations in this stock

Total: 51 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2210017I01Rik	A	G	3: 92,512,382 (GRCm39)	I59T	unknown	Het
Aspm	C	T	1: 139,406,389 (GRCm39)	Q1759*	probably null	Het
Atn1	A	T	6: 124,724,861 (GRCm39)	I124K	unknown	Het
Catsper2	TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT	TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT	2: 121,228,053 (GRCm39)		probably benign	Het
Ccdc88c	C	T	12: 100,911,198 (GRCm39)	V879M	probably benign	Het
Cd300c	A	G	11: 114,850,609 (GRCm39)	C65R	possibly damaging	Het
Cd69	A	T	6: 129,247,005 (GRCm39)	S112T	possibly damaging	Het
Cdh19	T	C	1: 110,821,137 (GRCm39)	T534A	probably benign	Het
Cdk5rap2	T	A	4: 70,210,145 (GRCm39)	D701V	probably damaging	Het
D130052B06Rik	A	G	11: 33,573,874 (GRCm39)	H157R	possibly damaging	Het
Dpf1	T	A	7: 29,011,052 (GRCm39)	F150L	probably benign	Het
Dsg1c	T	C	18: 20,416,166 (GRCm39)	L689P	probably damaging	Het
Dstyk	G	A	1: 132,381,861 (GRCm39)	M538I	probably benign	Het
E4f1	T	A	17: 24,663,299 (GRCm39)	I669F	probably damaging	Het
Gm7138	T	C	10: 77,612,589 (GRCm39)	T64A	unknown	Het
Gnai2	A	C	9: 107,492,972 (GRCm39)	D310E		Het
Iqca1	A	G	1: 89,998,272 (GRCm39)	V567A	possibly damaging	Het
Iqgap1	A	T	7: 80,409,587 (GRCm39)	N249K	probably benign	Het
Lamc1	A	G	1: 153,110,396 (GRCm39)	V1093A	possibly damaging	Het
Mfap3	A	G	11: 57,420,582 (GRCm39)	K188E	probably damaging	Het
N4bp2	T	A	5: 65,951,888 (GRCm39)	V431D	probably damaging	Het
Notch4	A	G	17: 34,795,445 (GRCm39)	T792A	probably benign	Het
Ntn4	A	G	10: 93,581,603 (GRCm39)	H592R	probably damaging	Het
Ofcc1	A	G	13: 40,362,317 (GRCm39)	C202R	probably benign	Het
Or10j2	T	C	1: 173,098,561 (GRCm39)	I273T	probably benign	Het
Or2a7	A	G	6: 43,151,435 (GRCm39)	K172E	probably benign	Het
Or5p55	T	C	7: 107,567,395 (GRCm39)	S264P	probably benign	Het
Or5p72	A	G	7: 108,022,140 (GRCm39)	M121V	probably damaging	Het
Or8b55	A	G	9: 38,727,009 (GRCm39)	D70G	probably benign	Het
Or8g24	A	T	9: 38,989,906 (GRCm39)	M45K	probably damaging	Het
Parpbp	G	A	10: 87,960,802 (GRCm39)	T228I	probably damaging	Het
Pcdhgb8	G	A	18: 37,896,756 (GRCm39)	V609M	probably damaging	Het
Pla2g4d	T	C	2: 120,100,830 (GRCm39)	N543S	probably damaging	Het
Puf60	A	G	15: 75,944,388 (GRCm39)		probably benign	Het
Rbm6	A	T	9: 107,730,095 (GRCm39)	D184E	probably damaging	Het
Rnase9	A	C	14: 51,276,436 (GRCm39)	S181A	probably benign	Het
Rnpc3	T	A	3: 113,410,480 (GRCm39)	R270S	probably damaging	Het
Rundc1	T	C	11: 101,322,374 (GRCm39)		probably null	Het
Ryr1	T	C	7: 28,751,440 (GRCm39)	S3715G	possibly damaging	Het
Scn3a	A	T	2: 65,299,386 (GRCm39)	D1373E	possibly damaging	Het
Serpina3k	T	G	12: 104,306,861 (GRCm39)	I31S	probably benign	Het
Sipa1l2	A	G	8: 126,196,599 (GRCm39)	F712L	probably damaging	Het
Slc22a29	A	G	19: 8,138,875 (GRCm39)	V529A	probably damaging	Het
Tdrd3	A	G	14: 87,696,239 (GRCm39)	N58S	probably benign	Het
Tmc2	C	T	2: 130,076,724 (GRCm39)	T350I	possibly damaging	Het
Tpst2	T	C	5: 112,455,544 (GRCm39)	C28R	probably benign	Het
Trpm2	A	G	10: 77,771,710 (GRCm39)		probably null	Het
Ttn	A	G	2: 76,679,334 (GRCm39)	V10796A	unknown	Het
Ush2a	A	G	1: 188,643,858 (GRCm39)	T4407A	possibly damaging	Het
Vmn2r95	A	G	17: 18,672,225 (GRCm39)	H726R	probably benign	Het
Zfp777	A	G	6: 48,021,383 (GRCm39)	S80P	probably benign	Het

Other mutations in Trbv21

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0634:Trbv21	UTSW	6	41,179,984 (GRCm39)	unclassified	probably benign
R4302:Trbv21	UTSW	6	41,179,702 (GRCm39)	missense	probably benign	0.04
R4845:Trbv21	UTSW	6	41,179,879 (GRCm39)	missense	probably benign	0.01
R5364:Trbv21	UTSW	6	41,179,764 (GRCm39)	missense	possibly damaging	0.55
R5840:Trbv21	UTSW	6	41,179,792 (GRCm39)	missense	probably damaging	1.00
R6035:Trbv21	UTSW	6	41,179,568 (GRCm39)	splice site	probably benign
R6035:Trbv21	UTSW	6	41,179,568 (GRCm39)	splice site	probably benign
R7485:Trbv21	UTSW	6	41,179,861 (GRCm39)	missense	not run
R8251:Trbv21	UTSW	6	41,179,540 (GRCm39)	start gained	probably benign
R8993:Trbv21	UTSW	6	41,179,924 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- TCCAGAATCCTAGACATCTGGTC -3'
(R):5'- CTGAGAAGGCAGCTGATCAG -3'

Sequencing Primer
(F):5'- ACATCTGGTCAAAGGAAAAGAAC -3'
(R):5'- CACTTTCACATTGTGTTTATGTTAGC -3'

Posted On

2019-06-26