Mutagenetix > Incidental Mutation

Incidental Mutation 'R7862:Jmy'

607595

Institutional Source

Beutler Lab

Gene Symbol

Jmy

Ensembl Gene

ENSMUSG00000021690

Gene Name

junction-mediating and regulatory protein

Synonyms

MMRRC Submission

045915-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.159) question?

Stock #

R7862 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

93566609-93636316 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 93635703 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Valine at position 38 (I38V)

Ref Sequence

ENSEMBL: ENSMUSP00000070339 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000065537] [ENSMUST00000220513]

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000065537
AA Change: I38V

PolyPhen 2 Score 0.755 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000070339
Gene: ENSMUSG00000021690
AA Change: I38V

Domain	Start	End	E-Value	Type
Pfam:WHAMM-JMY_N	5	55	6.2e-30	PFAM
low complexity region	77	94	N/A	INTRINSIC
low complexity region	117	128	N/A	INTRINSIC
low complexity region	152	181	N/A	INTRINSIC
low complexity region	202	217	N/A	INTRINSIC
Pfam:JMY	220	574	2.2e-175	PFAM
SCOP:d1jvr__	794	816	4e-3	SMART
WH2	916	933	2.21e-2	SMART
low complexity region	964	975	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000220513
AA Change: I38V

PolyPhen 2 Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)

Coding Region Coverage

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

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2410004B18Rik	A	C	3: 145,649,624 (GRCm39)	*181S	probably null	Het
Abcc10	G	T	17: 46,626,458 (GRCm39)	S661*	probably null	Het
Abtb2	C	T	2: 103,532,626 (GRCm39)	R475W	probably damaging	Het
Cep97	T	C	16: 55,726,084 (GRCm39)	D673G	probably benign	Het
Chaf1b	T	C	16: 93,684,983 (GRCm39)	M144T	possibly damaging	Het
Chd8	T	C	14: 52,451,734 (GRCm39)	D1372G	probably damaging	Het
Chmp6	G	A	11: 119,807,836 (GRCm39)		probably null	Het
Cst12	T	C	2: 148,631,495 (GRCm39)	V72A	probably damaging	Het
D1Pas1	G	A	1: 186,700,349 (GRCm39)	G93R	probably damaging	Het
Dhx34	C	A	7: 15,944,448 (GRCm39)	V589F	probably damaging	Het
Dlg5	G	A	14: 24,295,280 (GRCm39)	P80L	probably damaging	Het
Dmrta1	C	A	4: 89,576,561 (GRCm39)	H6N	probably benign	Het
Dop1b	T	C	16: 93,546,851 (GRCm39)	L285P	probably damaging	Het
Dpy19l1	T	C	9: 24,386,730 (GRCm39)	Y188C	probably damaging	Het
Ehbp1l1	C	T	19: 5,770,851 (GRCm39)	R230Q	probably benign	Het
Ep300	T	G	15: 81,534,954 (GRCm39)	V2337G	probably damaging	Het
Fh1	A	T	1: 175,442,400 (GRCm39)	V150E	probably damaging	Het
Fkbp11	G	A	15: 98,624,389 (GRCm39)	R122*	probably null	Het
Fkbp5	C	T	17: 28,631,013 (GRCm39)	E251K	probably damaging	Het
Fmnl1	A	G	11: 103,071,756 (GRCm39)	K88E	probably damaging	Het
Frrs1	T	C	3: 116,685,529 (GRCm39)	V300A	possibly damaging	Het
Glud1	T	G	14: 34,047,479 (GRCm39)	L198V	possibly damaging	Het
Gsdmc	A	T	15: 63,649,845 (GRCm39)	W349R	possibly damaging	Het
Hacd1	T	C	2: 14,050,013 (GRCm39)	H64R	probably damaging	Het
Haus2	T	A	2: 120,443,570 (GRCm39)	D75E	probably benign	Het
Hmcn1	A	T	1: 150,682,172 (GRCm39)	F459L	probably damaging	Het
Ighe	A	T	12: 113,235,428 (GRCm39)	V272E		Het
Iqgap1	C	T	7: 80,393,636 (GRCm39)	R647H	probably benign	Het
Kcnh1	G	T	1: 191,873,167 (GRCm39)		probably benign	Het
Kctd20	C	T	17: 29,181,849 (GRCm39)	A167V	probably damaging	Het
Klhl38	A	T	15: 58,178,395 (GRCm39)	V525E	probably damaging	Het
Krit1	A	G	5: 3,862,788 (GRCm39)	D259G	probably damaging	Het
Med1	A	T	11: 98,052,036 (GRCm39)	C443S	probably benign	Het
Mllt6	T	C	11: 97,556,631 (GRCm39)	V107A	probably benign	Het
Myl7	A	G	11: 5,847,157 (GRCm39)	M132T	probably benign	Het
Myo10	T	C	15: 25,666,522 (GRCm39)	V11A	probably damaging	Het
Nipbl	T	C	15: 8,355,236 (GRCm39)	I1642V	probably benign	Het
Or4a47	T	C	2: 89,665,468 (GRCm39)	T274A	probably benign	Het
Or6c214	T	C	10: 129,591,224 (GRCm39)	T32A	probably benign	Het
Or7g25	C	A	9: 19,160,736 (GRCm39)		probably benign	Het
Or8b3b	C	T	9: 38,584,624 (GRCm39)	V39M	probably benign	Het
Pcdhb2	C	T	18: 37,429,113 (GRCm39)	A362V	probably benign	Het
Pnp2	A	T	14: 51,201,016 (GRCm39)	D167V	possibly damaging	Het
Rasa1	G	A	13: 85,403,530 (GRCm39)	T282I	probably damaging	Het
Rp1l1	A	G	14: 64,265,476 (GRCm39)	D354G	probably damaging	Het
Rpap1	C	T	2: 119,605,893 (GRCm39)		probably null	Het
Rsf1	CGGCGGCGG	CGGCGGCGGGGGCGGCGG	7: 97,229,130 (GRCm39)		probably benign	Het
Shank3	A	G	15: 89,389,648 (GRCm39)	D415G	possibly damaging	Het
Slc12a1	A	G	2: 125,003,014 (GRCm39)	I182V	probably damaging	Het
Slc6a13	A	G	6: 121,312,589 (GRCm39)	Y441C	probably damaging	Het
Sltm	G	T	9: 70,479,446 (GRCm39)	E193*	probably null	Het
Spag9	T	C	11: 94,002,892 (GRCm39)	I1134T	possibly damaging	Het
Spta1	G	A	1: 174,025,351 (GRCm39)		probably null	Het
Stk3	A	G	15: 35,115,732 (GRCm39)	V29A	possibly damaging	Het
Tgfbr1	A	T	4: 47,403,489 (GRCm39)	I365F	probably damaging	Het
Thpo	C	T	16: 20,547,540 (GRCm39)	V24I	probably benign	Het
Tle1	A	C	4: 72,117,552 (GRCm39)	L36R	probably damaging	Het
Togaram2	T	C	17: 71,996,168 (GRCm39)	V57A	probably benign	Het
Ttll9	C	T	2: 152,848,895 (GRCm39)	A459V	probably benign	Het
Ush1c	T	C	7: 45,870,848 (GRCm39)	I330V	probably damaging	Het
Usp34	T	C	11: 23,414,718 (GRCm39)	M2906T		Het
Vmn2r28	A	T	7: 5,493,613 (GRCm39)	M111K	probably benign	Het
Vmn2r97	T	C	17: 19,167,416 (GRCm39)	C557R	probably damaging	Het
Zfp873	T	A	10: 81,896,109 (GRCm39)	I280K	probably benign	Het

Other mutations in Jmy

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00798:Jmy	APN	13	93,577,910 (GRCm39)	missense	probably benign	0.00
IGL00949:Jmy	APN	13	93,590,510 (GRCm39)	missense	probably damaging	1.00
IGL01111:Jmy	APN	13	93,577,529 (GRCm39)	missense	probably damaging	1.00
IGL01734:Jmy	APN	13	93,596,159 (GRCm39)	missense	probably damaging	1.00
IGL01926:Jmy	APN	13	93,596,294 (GRCm39)	missense	probably damaging	1.00
IGL01985:Jmy	APN	13	93,596,144 (GRCm39)	missense	possibly damaging	0.58
IGL02183:Jmy	APN	13	93,635,750 (GRCm39)	missense	possibly damaging	0.78
IGL02517:Jmy	APN	13	93,589,316 (GRCm39)	missense	probably benign	0.01
IGL02524:Jmy	APN	13	93,609,268 (GRCm39)	missense	probably damaging	1.00
IGL02697:Jmy	APN	13	93,596,209 (GRCm39)	nonsense	probably null
IGL03024:Jmy	APN	13	93,635,707 (GRCm39)	missense	probably damaging	1.00
R0242:Jmy	UTSW	13	93,578,126 (GRCm39)	missense	probably benign	0.07
R0242:Jmy	UTSW	13	93,578,126 (GRCm39)	missense	probably benign	0.07
R0623:Jmy	UTSW	13	93,589,325 (GRCm39)	missense	probably benign	0.37
R0623:Jmy	UTSW	13	93,589,325 (GRCm39)	missense	probably benign	0.37
R0722:Jmy	UTSW	13	93,589,325 (GRCm39)	missense	probably benign	0.37
R1533:Jmy	UTSW	13	93,577,819 (GRCm39)	missense	probably benign
R1667:Jmy	UTSW	13	93,634,878 (GRCm39)	missense	probably damaging	1.00
R1737:Jmy	UTSW	13	93,635,303 (GRCm39)	missense	probably damaging	0.99
R1815:Jmy	UTSW	13	93,590,585 (GRCm39)	missense	probably damaging	1.00
R2057:Jmy	UTSW	13	93,596,211 (GRCm39)	missense	probably damaging	1.00
R3522:Jmy	UTSW	13	93,590,558 (GRCm39)	missense	probably damaging	1.00
R3765:Jmy	UTSW	13	93,601,219 (GRCm39)	missense	possibly damaging	0.78
R4231:Jmy	UTSW	13	93,635,433 (GRCm39)	missense	probably benign
R4279:Jmy	UTSW	13	93,635,781 (GRCm39)	missense	probably damaging	1.00
R4279:Jmy	UTSW	13	93,635,390 (GRCm39)	missense	probably damaging	1.00
R4330:Jmy	UTSW	13	93,635,390 (GRCm39)	missense	probably damaging	1.00
R4330:Jmy	UTSW	13	93,635,781 (GRCm39)	missense	probably damaging	1.00
R4845:Jmy	UTSW	13	93,576,246 (GRCm39)	missense	possibly damaging	0.80
R5047:Jmy	UTSW	13	93,578,080 (GRCm39)	missense	possibly damaging	0.65
R5403:Jmy	UTSW	13	93,577,904 (GRCm39)	missense	probably benign	0.08
R5941:Jmy	UTSW	13	93,635,333 (GRCm39)	missense	probably benign
R5953:Jmy	UTSW	13	93,635,624 (GRCm39)	missense	possibly damaging	0.62
R6022:Jmy	UTSW	13	93,590,086 (GRCm39)	splice site	probably null
R6150:Jmy	UTSW	13	93,577,641 (GRCm39)	missense	probably benign	0.10
R6520:Jmy	UTSW	13	93,590,547 (GRCm39)	missense	probably benign	0.10
R7073:Jmy	UTSW	13	93,577,841 (GRCm39)	missense	probably benign	0.01
R7074:Jmy	UTSW	13	93,590,439 (GRCm39)	missense	probably benign	0.15
R7325:Jmy	UTSW	13	93,609,251 (GRCm39)	missense	probably damaging	0.99
R7575:Jmy	UTSW	13	93,601,103 (GRCm39)	nonsense	probably null
R7641:Jmy	UTSW	13	93,579,107 (GRCm39)	missense	probably damaging	1.00
R7674:Jmy	UTSW	13	93,579,107 (GRCm39)	missense	probably damaging	1.00
R8278:Jmy	UTSW	13	93,601,224 (GRCm39)	missense	probably damaging	1.00
R8416:Jmy	UTSW	13	93,634,949 (GRCm39)	missense	probably damaging	1.00
R8987:Jmy	UTSW	13	93,589,397 (GRCm39)	missense	probably damaging	1.00
R9063:Jmy	UTSW	13	93,635,580 (GRCm39)	missense	probably benign	0.22
R9196:Jmy	UTSW	13	93,601,209 (GRCm39)	missense	probably damaging	1.00
R9255:Jmy	UTSW	13	93,589,894 (GRCm39)	critical splice donor site	probably null
R9402:Jmy	UTSW	13	93,635,678 (GRCm39)	missense	probably damaging	0.99
Z1088:Jmy	UTSW	13	93,577,589 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CCATTTCCAGGACCTCGATC -3'
(R):5'- GACCATGTGAACTACCTGCTC -3'

Sequencing Primer
(F):5'- ATCTCGGGATTCGGCGCTTC -3'
(R):5'- TCTTCTGAGAGCCGCACCAC -3'

Posted On

2019-12-20