Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03033:Vmn1r68'

408545

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Vmn1r68

Ensembl Gene

ENSMUSG00000047031

Gene Name

vomeronasal 1 receptor 68

Synonyms

Gm6898

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.055) question?

Stock #

IGL03033

Quality Score

Status

Chromosome

Chromosomal Location

10261137-10262096 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 10262074 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Valine at position 8 (E8V)

Ref Sequence

ENSEMBL: ENSMUSP00000050927 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000058362]

AlphaFold

E9Q0V3

Predicted Effect

probably damaging
Transcript: ENSMUST00000058362
AA Change: E8V

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000050927
Gene: ENSMUSG00000047031
AA Change: E8V

Domain	Start	End	E-Value	Type
Pfam:V1R	49	306	2e-33	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aoc1l2	A	T	6: 48,909,452 (GRCm39)	T566S	probably benign	Het
Ap3b1	A	G	13: 94,585,003 (GRCm39)	T405A	probably benign	Het
Bicd2	G	T	13: 49,533,396 (GRCm39)	V587L	probably benign	Het
Bsn	A	T	9: 107,993,192 (GRCm39)	D853E	probably damaging	Het
Cacna1i	C	A	15: 80,246,440 (GRCm39)	N611K	probably damaging	Het
Capn11	A	G	17: 45,953,473 (GRCm39)	L227P	probably damaging	Het
Copb2	A	G	9: 98,452,426 (GRCm39)	N70S	probably benign	Het
Ddb1	T	C	19: 10,603,290 (GRCm39)	V866A	possibly damaging	Het
Dst	A	G	1: 34,208,826 (GRCm39)		probably benign	Het
Ero1b	A	G	13: 12,596,551 (GRCm39)	Y117C	probably damaging	Het
Esyt1	T	G	10: 128,352,252 (GRCm39)	R758S	probably benign	Het
Gm20441	A	G	10: 75,607,326 (GRCm39)	F55S	probably damaging	Het
Gm20547	A	T	17: 35,078,492 (GRCm39)	M362K	probably damaging	Het
Gucy1b2	A	G	14: 62,653,393 (GRCm39)	V334A	probably benign	Het
Hnrnph3	A	T	10: 62,853,958 (GRCm39)	F53L	probably benign	Het
Kcnk18	C	T	19: 59,223,616 (GRCm39)	P254S	probably benign	Het
Lrfn5	T	A	12: 61,886,833 (GRCm39)	L207Q	probably damaging	Het
Lrp3	T	C	7: 34,902,052 (GRCm39)	M589V	possibly damaging	Het
Nlrp1b	A	G	11: 71,052,665 (GRCm39)	V918A	probably benign	Het
Nsg2	A	G	11: 31,951,836 (GRCm39)	T29A	probably damaging	Het
Or51b4	T	A	7: 103,530,724 (GRCm39)	H242L	probably damaging	Het
Pank4	C	T	4: 155,059,172 (GRCm39)	T435I	probably damaging	Het
Prom1	C	T	5: 44,163,502 (GRCm39)		probably null	Het
Prr14	G	T	7: 127,071,135 (GRCm39)	L3F	probably damaging	Het
Rfx7	A	T	9: 72,440,271 (GRCm39)		probably benign	Het
Rhbdl3	A	G	11: 80,237,653 (GRCm39)	N295S	probably damaging	Het
Ripk3	A	G	14: 56,024,622 (GRCm39)		probably benign	Het
Ror1	A	T	4: 100,269,092 (GRCm39)	N310I	possibly damaging	Het
Rpl23a	T	C	11: 78,072,408 (GRCm39)	Y74C	possibly damaging	Het
Rtp3	A	T	9: 110,815,162 (GRCm39)		probably benign	Het
Sbno1	A	T	5: 124,514,213 (GRCm39)	N1326K	probably damaging	Het
Sepsecs	T	C	5: 52,818,018 (GRCm39)	N253S	probably damaging	Het
Setd2	A	C	9: 110,380,343 (GRCm39)	E1386A	possibly damaging	Het
Sf3b3	T	C	8: 111,537,596 (GRCm39)	I1211V	possibly damaging	Het
Sh3tc2	G	A	18: 62,107,549 (GRCm39)	V187M	possibly damaging	Het
Slc30a6	G	T	17: 74,716,373 (GRCm39)	E136*	probably null	Het
Sptan1	T	A	2: 29,881,045 (GRCm39)	V438E	probably damaging	Het
Stab2	A	G	10: 86,832,667 (GRCm39)		probably null	Het
Sult2a1	T	A	7: 13,566,635 (GRCm39)		probably benign	Het
Tmem198	A	G	1: 75,459,612 (GRCm39)	D189G	possibly damaging	Het
Tnfrsf8	C	A	4: 145,019,219 (GRCm39)	L205F	possibly damaging	Het
Wnk3	G	A	X: 150,059,924 (GRCm39)	D742N	probably damaging	Het
Xpc	A	T	6: 91,468,297 (GRCm39)		probably null	Het
Zfp113	A	T	5: 138,149,458 (GRCm39)		probably benign	Het
Zfp120	A	T	2: 149,961,794 (GRCm39)	D51E	probably benign	Het
Zfp473	C	T	7: 44,382,522 (GRCm39)	V603M	probably benign	Het

Other mutations in Vmn1r68

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01892:Vmn1r68	APN	7	10,261,334 (GRCm39)	missense	possibly damaging	0.76
IGL02051:Vmn1r68	APN	7	10,261,948 (GRCm39)	missense	probably benign	0.00
IGL02112:Vmn1r68	APN	7	10,261,787 (GRCm39)	missense	probably damaging	0.96
IGL02619:Vmn1r68	APN	7	10,261,603 (GRCm39)	missense	probably benign	0.14
IGL03184:Vmn1r68	APN	7	10,261,799 (GRCm39)	missense	probably benign	0.16
PIT4354001:Vmn1r68	UTSW	7	10,261,958 (GRCm39)	missense	probably benign
R0141:Vmn1r68	UTSW	7	10,261,252 (GRCm39)	missense	possibly damaging	0.69
R0359:Vmn1r68	UTSW	7	10,261,201 (GRCm39)	missense	probably damaging	1.00
R0634:Vmn1r68	UTSW	7	10,261,162 (GRCm39)	missense	probably benign	0.00
R1731:Vmn1r68	UTSW	7	10,261,802 (GRCm39)	missense	probably damaging	1.00
R2021:Vmn1r68	UTSW	7	10,261,918 (GRCm39)	missense	probably damaging	1.00
R2022:Vmn1r68	UTSW	7	10,261,918 (GRCm39)	missense	probably damaging	1.00
R2243:Vmn1r68	UTSW	7	10,262,089 (GRCm39)	missense	probably damaging	0.98
R2262:Vmn1r68	UTSW	7	10,261,372 (GRCm39)	missense	probably damaging	1.00
R3877:Vmn1r68	UTSW	7	10,261,408 (GRCm39)	missense	probably damaging	1.00
R4470:Vmn1r68	UTSW	7	10,261,275 (GRCm39)	missense	probably benign	0.23
R4843:Vmn1r68	UTSW	7	10,261,904 (GRCm39)	missense	probably benign	0.00
R5198:Vmn1r68	UTSW	7	10,261,723 (GRCm39)	missense	probably benign	0.00
R5835:Vmn1r68	UTSW	7	10,261,747 (GRCm39)	missense	possibly damaging	0.68
R5906:Vmn1r68	UTSW	7	10,261,550 (GRCm39)	missense	probably benign	0.02
R6015:Vmn1r68	UTSW	7	10,261,616 (GRCm39)	missense	probably benign	0.31
R7073:Vmn1r68	UTSW	7	10,261,778 (GRCm39)	missense	probably benign	0.00
R7614:Vmn1r68	UTSW	7	10,261,553 (GRCm39)	missense	probably benign	0.05
R7699:Vmn1r68	UTSW	7	10,261,559 (GRCm39)	missense	probably benign	0.15
R7700:Vmn1r68	UTSW	7	10,261,559 (GRCm39)	missense	probably benign	0.15
R7912:Vmn1r68	UTSW	7	10,261,237 (GRCm39)	missense	probably benign	0.01
R8166:Vmn1r68	UTSW	7	10,261,888 (GRCm39)	missense	probably benign	0.10
R8426:Vmn1r68	UTSW	7	10,261,382 (GRCm39)	missense	probably benign	0.02
R9466:Vmn1r68	UTSW	7	10,261,417 (GRCm39)	missense	probably damaging	1.00
R9466:Vmn1r68	UTSW	7	10,261,317 (GRCm39)	nonsense	probably null

Posted On

2016-08-02