Mutagenetix > Incidental Mutations

Incidental Mutation 'R8399:Ighv1-11'

647784

Institutional Source

Beutler Lab

Gene Symbol

Ighv1-11

Ensembl Gene

ENSMUSG00000102888

Gene Name

immunoglobulin heavy variable V1-11

Synonyms

MMRRC Submission

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.243) question?

Stock #

R8399 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

114612243-114612675 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 114612427 bp

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 56 (V56A)

Ref Sequence

ENSEMBL: ENSMUSP00000141570 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000103500] [ENSMUST00000109711] [ENSMUST00000191801] [ENSMUST00000195469]

Predicted Effect

probably benign
Transcript: ENSMUST00000103500

SMART Domains

Protein: ENSMUSP00000100281
Gene: ENSMUSG00000095416

Domain	Start	End	E-Value	Type
IGv	17	98	5.55e-29	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000109711

SMART Domains

Protein: ENSMUSP00000105333
Gene: ENSMUSG00000095416

Domain	Start	End	E-Value	Type
IG_like	1	60	4.1e-5	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000191801
AA Change: V56A

PolyPhen 2 Score 0.803 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000141570
Gene: ENSMUSG00000102888
AA Change: V56A

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
IGv	36	117	1.8e-28	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000195469

SMART Domains

Protein: ENSMUSP00000142024
Gene: ENSMUSG00000095416

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
IGv	36	117	2.2e-31	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.2%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 51 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrv1	A	T	13: 81,489,170	V3384D	possibly damaging	Het
Apba3	C	A	10: 81,268,998	T35N	probably benign	Het
Bcl6	T	C	16: 23,972,948	M219V	probably benign	Het
Bco2	T	A	9: 50,541,118	T217S	probably benign	Het
C1s1	C	T	6: 124,535,293	V277I	probably benign	Het
Ccdc162	T	A	10: 41,539,521	R2149W	probably damaging	Het
Cers6	T	C	2: 68,861,771	F46L	probably benign	Het
Chpf	T	C	1: 75,476,220	I359V	probably benign	Het
Chrnb4	A	C	9: 55,043,823	L52R	probably benign	Het
Cox6a1	T	C	5: 115,345,899	T95A	probably damaging	Het
Def8	T	A	8: 123,455,499	Y197*	probably null	Het
Dmbt1	C	G	7: 131,082,587	D778E	unknown	Het
Dnaaf3	C	T	7: 4,523,937		probably null	Het
Dnm1l	T	A	16: 16,321,672	H484L	probably damaging	Het
Eml1	G	A	12: 108,538,131	S783N	possibly damaging	Het
Frmd4a	T	C	2: 4,572,433	S367P	probably damaging	Het
Hck	A	C	2: 153,138,317	K355N	probably damaging	Het
Hexim2	G	T	11: 103,138,503	R127L	probably damaging	Het
Hivep2	T	C	10: 14,132,434	L1592P	possibly damaging	Het
Htr1d	G	A	4: 136,443,375	G305E	probably damaging	Het
Ifi207	G	A	1: 173,730,278	S298L	unknown	Het
Ighv7-1	G	A	12: 113,896,912	T12I	unknown	Het
Kctd14	T	C	7: 97,457,604	L22P	probably damaging	Het
Klra17	T	C	6: 129,874,937		probably benign	Het
Kndc1	C	T	7: 139,913,518	R467W	probably damaging	Het
Maf	T	A	8: 115,706,512	I118F	unknown	Het
Mppe1	T	C	18: 67,225,875	T341A	probably benign	Het
Mtmr2	T	A	9: 13,792,067	V186E	probably benign	Het
Nedd9	G	T	13: 41,318,474	Y176*	probably null	Het
Olfr1145	A	C	2: 87,810,224	M135L	probably damaging	Het
Olfr1238	T	C	2: 89,406,684	T132A	probably benign	Het
Omd	A	G	13: 49,589,869	I132V	possibly damaging	Het
Pcnx4	T	A	12: 72,574,211	M935K	probably benign	Het
Pecr	G	A	1: 72,267,465	T219I	probably benign	Het
Pkd1l3	C	T	8: 109,623,888	P455L	possibly damaging	Het
Plcg2	T	C	8: 117,596,362	Y719H	probably damaging	Het
Plk4	C	T	3: 40,808,830	R479*	probably null	Het
Pms1	T	A	1: 53,267,932		probably null	Het
Raph1	C	T	1: 60,489,318	S928N	unknown	Het
Rtp4	G	T	16: 23,520,414		probably benign	Het
Skor1	C	T	9: 63,145,158	V510I	possibly damaging	Het
Smg1	T	C	7: 118,190,571	T699A	unknown	Het
Tcp11l1	T	C	2: 104,685,375	D381G	probably benign	Het
Tnik	T	A	3: 28,494,010	M56K	unknown	Het
Trappc9	G	A	15: 73,052,282	R204C	probably damaging	Het
Trmt10b	A	T	4: 45,305,870	M184L	possibly damaging	Het
Vmn1r224	T	A	17: 20,419,749	I196N	probably damaging	Het
Vmn1r49	A	T	6: 90,072,707	C104*	probably null	Het
Vmn2r35	A	C	7: 7,816,898	S124R	probably benign	Het
Wdr62	T	C	7: 30,258,061	E547G	probably damaging	Het
Zfp68	A	T	5: 138,607,820	D80E	probably benign	Het

Other mutations in Ighv1-11

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL03253:Ighv1-11	APN	12	114615848	unclassified	probably benign
R5492:Ighv1-11	UTSW	12	114612464	missense	probably damaging	0.99
R5778:Ighv1-11	UTSW	12	114612431	missense	probably damaging	1.00
R6169:Ighv1-11	UTSW	12	114612298	missense	probably damaging	0.97
R8262:Ighv1-11	UTSW	12	114612457	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CACACTCAGGATGTGGTTGTAG -3'
(R):5'- AGTTCCAGACCTGAGGATGG -3'

Sequencing Primer
(F):5'- TTCCACAGTAATAGACAGCAGGGTC -3'
(R):5'- GGCCACACACTCAGGTGATAATG -3'

Posted On

2020-09-02