Mutagenetix > Incidental Mutation

Incidental Mutation 'R7211:Myorg'

561051

Institutional Source

Beutler Lab

Gene Symbol

Myorg

Ensembl Gene

ENSMUSG00000046312

Gene Name

myogenesis regulating glycosidase (putative)

Synonyms

NET37, AI464131

MMRRC Submission

045339-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7211 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

41495604-41503076 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 41498028 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 534 (I534T)

Ref Sequence

ENSEMBL: ENSMUSP00000059038 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000054920] [ENSMUST00000149596]

AlphaFold

Q69ZQ1

Predicted Effect

probably damaging
Transcript: ENSMUST00000054920
AA Change: I534T

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

SMART Domains

Protein: ENSMUSP00000059038
Gene: ENSMUSG00000046312
AA Change: I534T

Domain	Start	End	E-Value	Type
transmembrane domain	56	78	N/A	INTRINSIC
Pfam:Glyco_hydro_31	311	712	9.7e-55	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000149596

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.6%

Validation Efficiency

99% (84/85)

Allele List at MGI

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
a	T	A	2: 154,887,699 (GRCm39)	V53E	probably damaging	Het
A1cf	A	G	19: 31,904,541 (GRCm39)	Y268C	probably benign	Het
Adam34l	T	A	8: 44,078,914 (GRCm39)	S437C	probably damaging	Het
Adamts13	C	T	2: 26,879,310 (GRCm39)	T621I	probably benign	Het
Akr1b7	A	T	6: 34,398,049 (GRCm39)	N293Y	probably benign	Het
Angpt2	T	A	8: 18,791,147 (GRCm39)	T50S	probably benign	Het
Anks1b	C	A	10: 90,346,932 (GRCm39)	A744D	possibly damaging	Het
Aqr	A	G	2: 113,965,204 (GRCm39)	V587A	probably benign	Het
Atm	A	G	9: 53,399,860 (GRCm39)	V1540A	probably benign	Het
Brd10	A	G	19: 29,763,712 (GRCm39)	F121S		Het
C4b	A	G	17: 34,954,508 (GRCm39)	V887A	possibly damaging	Het
Cd200r1	A	G	16: 44,609,120 (GRCm39)	T26A	probably benign	Het
Ciao1	A	G	2: 127,088,928 (GRCm39)		probably null	Het
Clba1	T	A	12: 112,774,632 (GRCm39)		probably null	Het
Clca3a2	A	G	3: 144,519,775 (GRCm39)	C200R	probably benign	Het
Col6a5	T	A	9: 105,805,363 (GRCm39)	Q1181L	unknown	Het
Copb2	T	A	9: 98,456,198 (GRCm39)	I244N	probably damaging	Het
Cpb2	A	G	14: 75,512,430 (GRCm39)	Y281C	probably damaging	Het
Disp3	C	A	4: 148,325,979 (GRCm39)	V1260F	probably damaging	Het
Dnajc2	C	T	5: 21,981,777 (GRCm39)	R123Q	probably damaging	Het
Dpysl2	T	C	14: 67,067,425 (GRCm39)	N162S	probably damaging	Het
Dsp	T	A	13: 38,372,511 (GRCm39)		probably null	Het
Edc4	T	A	8: 106,612,941 (GRCm39)		probably null	Het
Efcab3	C	A	11: 104,601,539 (GRCm39)	A284D	probably benign	Het
Efcab3	G	T	11: 104,615,435 (GRCm39)		probably null	Het
Epm2a	T	C	10: 11,219,419 (GRCm39)	Y69H	probably benign	Het
Frzb	C	A	2: 80,248,669 (GRCm39)	E262*	probably null	Het
Gaa	T	C	11: 119,175,030 (GRCm39)	V877A	possibly damaging	Het
Gpnmb	T	C	6: 49,028,949 (GRCm39)	I489T	possibly damaging	Het
Gpr31b	T	C	17: 13,271,104 (GRCm39)	T22A	probably benign	Het
Gys1	T	A	7: 45,097,684 (GRCm39)	F477Y	possibly damaging	Het
Hoxc11	A	C	15: 102,863,487 (GRCm39)	E176A	possibly damaging	Het
Kcnk13	T	A	12: 100,028,076 (GRCm39)	F384I	probably damaging	Het
Ky	A	G	9: 102,386,349 (GRCm39)	E59G	probably benign	Het
Lama4	T	A	10: 38,881,491 (GRCm39)	D93E	probably damaging	Het
Lrrc23	A	T	6: 124,755,152 (GRCm39)	N128K	probably benign	Het
Lrrc71	G	T	3: 87,650,633 (GRCm39)	Q210K	possibly damaging	Het
Map1a	G	A	2: 121,135,124 (GRCm39)	R1980H	probably benign	Het
Med15	T	C	16: 17,515,977 (GRCm39)	D15G	unknown	Het
Mfng	A	T	15: 78,657,268 (GRCm39)	S69T	probably benign	Het
Muc16	T	G	9: 18,409,866 (GRCm39)	S181R	probably damaging	Het
Mug1	A	T	6: 121,857,498 (GRCm39)	Q1074L	possibly damaging	Het
Nbea	T	A	3: 55,912,322 (GRCm39)	N1155I	probably benign	Het
Nbeal1	T	G	1: 60,240,110 (GRCm39)	L159V	probably damaging	Het
Nudt1	C	A	5: 140,323,402 (GRCm39)	P118Q	possibly damaging	Het
Or2q1	A	T	6: 42,794,950 (GRCm39)	T182S	probably benign	Het
Or8g37	A	C	9: 39,731,154 (GRCm39)	Q73P	possibly damaging	Het
Pcdhga6	T	A	18: 37,842,173 (GRCm39)	V631D	probably benign	Het
Pcna	A	C	2: 132,091,792 (GRCm39)	V203G	probably damaging	Het
Pgf	G	T	12: 85,222,549 (GRCm39)	N33K	probably benign	Het
Pgm2	T	C	5: 64,263,193 (GRCm39)	L280P	probably damaging	Het
Plcg1	G	A	2: 160,573,794 (GRCm39)	A20T	probably benign	Het
Pou2af2	G	T	9: 51,201,733 (GRCm39)	Q108K	probably damaging	Het
Prdx5	G	T	19: 6,884,958 (GRCm39)	D126E	probably damaging	Het
Prkag2	T	C	5: 25,200,296 (GRCm39)	T20A	probably benign	Het
Prr14l	T	A	5: 32,987,431 (GRCm39)	Q688L	probably damaging	Het
Pxdn	T	G	12: 30,034,903 (GRCm39)	D253E	possibly damaging	Het
Rbm18	A	T	2: 36,012,905 (GRCm39)	C53*	probably null	Het
Rprm	A	T	2: 53,975,270 (GRCm39)	L16Q	probably benign	Het
Saysd1	A	G	14: 20,127,576 (GRCm39)	F116S	probably damaging	Het
Scg3	A	G	9: 75,589,366 (GRCm39)	S96P	probably benign	Het
Scgb1b3	C	T	7: 31,075,078 (GRCm39)	L16F	unknown	Het
Sh3tc2	A	G	18: 62,122,474 (GRCm39)	T412A	probably benign	Het
Skint6	T	C	4: 113,095,566 (GRCm39)	N31S	probably benign	Het
Slc22a2	T	C	17: 12,805,770 (GRCm39)		probably null	Het
Slc8a2	C	T	7: 15,874,538 (GRCm39)	T262I	possibly damaging	Het
Smarcc1	A	T	9: 109,979,082 (GRCm39)	K188N	probably damaging	Het
Taf6	T	C	5: 138,177,088 (GRCm39)	T660A	possibly damaging	Het
Tbx2	C	T	11: 85,725,540 (GRCm39)	R164C	probably damaging	Het
Tec	T	C	5: 72,939,355 (GRCm39)	D220G	probably null	Het
Tfec	A	T	6: 16,867,464 (GRCm39)	W59R	probably damaging	Het
Tmtc2	G	T	10: 105,409,587 (GRCm39)	S8R	probably benign	Het
Tmtc3	A	T	10: 100,283,467 (GRCm39)	M696K	probably benign	Het
Trpc3	A	T	3: 36,694,882 (GRCm39)	S691T	possibly damaging	Het
Ttf2	A	T	3: 100,866,623 (GRCm39)	M503K	probably benign	Het
Ttll7	A	G	3: 146,619,031 (GRCm39)	H312R	probably damaging	Het
Ttn	T	C	2: 76,598,032 (GRCm39)	Y19627C	probably damaging	Het
Ugt2b35	T	C	5: 87,149,177 (GRCm39)	S143P	probably benign	Het
Usp53	A	G	3: 122,751,299 (GRCm39)	S253P	probably damaging	Het
Utp18	A	G	11: 93,776,206 (GRCm39)	V93A	probably benign	Het
Utrn	T	C	10: 12,277,079 (GRCm39)	N3413D	possibly damaging	Het
Zhx1	T	C	15: 57,916,647 (GRCm39)	D533G	possibly damaging	Het

Other mutations in Myorg

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01287:Myorg	APN	4	41,498,923 (GRCm39)	missense	possibly damaging	0.68
IGL01352:Myorg	APN	4	41,499,469 (GRCm39)	nonsense	probably null
IGL01384:Myorg	APN	4	41,498,151 (GRCm39)	missense	probably damaging	0.99
IGL02150:Myorg	APN	4	41,499,183 (GRCm39)	missense	possibly damaging	0.48
IGL02557:Myorg	APN	4	41,497,900 (GRCm39)	missense	possibly damaging	0.51
R0238:Myorg	UTSW	4	41,498,912 (GRCm39)	missense	probably benign	0.11
R0238:Myorg	UTSW	4	41,498,912 (GRCm39)	missense	probably benign	0.11
R0413:Myorg	UTSW	4	41,498,585 (GRCm39)	missense	probably benign	0.00
R0455:Myorg	UTSW	4	41,499,538 (GRCm39)	nonsense	probably null
R0511:Myorg	UTSW	4	41,498,538 (GRCm39)	missense	probably damaging	0.96
R0560:Myorg	UTSW	4	41,498,167 (GRCm39)	missense	probably damaging	0.99
R0785:Myorg	UTSW	4	41,497,539 (GRCm39)	missense	probably benign	0.02
R0940:Myorg	UTSW	4	41,497,996 (GRCm39)	missense	probably damaging	1.00
R1677:Myorg	UTSW	4	41,497,947 (GRCm39)	missense	probably benign	0.00
R1762:Myorg	UTSW	4	41,498,553 (GRCm39)	missense	possibly damaging	0.91
R1984:Myorg	UTSW	4	41,497,501 (GRCm39)	missense	possibly damaging	0.95
R2192:Myorg	UTSW	4	41,497,704 (GRCm39)	missense	probably damaging	0.99
R2496:Myorg	UTSW	4	41,499,165 (GRCm39)	missense	probably benign	0.28
R4212:Myorg	UTSW	4	41,498,307 (GRCm39)	missense	probably benign	0.01
R4321:Myorg	UTSW	4	41,498,767 (GRCm39)	missense	probably benign	0.00
R4672:Myorg	UTSW	4	41,499,061 (GRCm39)	missense	probably benign	0.00
R4890:Myorg	UTSW	4	41,498,877 (GRCm39)	missense	probably benign	0.00
R4954:Myorg	UTSW	4	41,498,241 (GRCm39)	missense	possibly damaging	0.89
R5177:Myorg	UTSW	4	41,498,407 (GRCm39)	nonsense	probably null
R5967:Myorg	UTSW	4	41,497,830 (GRCm39)	missense	probably benign	0.00
R6005:Myorg	UTSW	4	41,498,895 (GRCm39)	missense	probably benign	0.31
R6128:Myorg	UTSW	4	41,498,445 (GRCm39)	missense	probably damaging	1.00
R6162:Myorg	UTSW	4	41,497,899 (GRCm39)	missense	possibly damaging	0.51
R7202:Myorg	UTSW	4	41,498,268 (GRCm39)	missense	probably damaging	0.99
R7311:Myorg	UTSW	4	41,498,577 (GRCm39)	missense	probably damaging	1.00
R7524:Myorg	UTSW	4	41,498,779 (GRCm39)	missense	probably benign	0.03
R7680:Myorg	UTSW	4	41,497,978 (GRCm39)	missense	probably damaging	1.00
R8177:Myorg	UTSW	4	41,497,568 (GRCm39)	nonsense	probably null
R8809:Myorg	UTSW	4	41,498,812 (GRCm39)	missense	probably benign
R8981:Myorg	UTSW	4	41,498,209 (GRCm39)	missense	possibly damaging	0.56
R9257:Myorg	UTSW	4	41,499,030 (GRCm39)	missense	probably benign
X0024:Myorg	UTSW	4	41,498,107 (GRCm39)	missense	possibly damaging	0.92
Z1088:Myorg	UTSW	4	41,497,557 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- TTGTGTGCGATGGCTACCAC -3'
(R):5'- AGGGACTTCAGCACCTACAG -3'

Sequencing Primer
(F):5'- GTGCGATGGCTACCACTTCTG -3'
(R):5'- TCAGCACCTACAGGCCTCTG -3'

Posted On

2019-06-26