Mutagenetix > Incidental Mutation

Incidental Mutation 'R5347:Gm5773'

422660

Institutional Source

Beutler Lab

Gene Symbol

Gm5773

Ensembl Gene

ENSMUSG00000068879

Gene Name

predicted pseudogene 5773

Synonyms

MMRRC Submission

042926-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.860) question?

Stock #

R5347 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

93680307-93681449 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 93681090 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Proline at position 254 (L254P)

Ref Sequence

ENSEMBL: ENSMUSP00000088366 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000090853]

AlphaFold

Q717B2

Predicted Effect

probably damaging
Transcript: ENSMUST00000090853
AA Change: L254P

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000088366
Gene: ENSMUSG00000068879
AA Change: L254P

Domain	Start	End	E-Value	Type
MATH	40	130	2.58e-7	SMART
BTB	188	287	2.82e-24	SMART

Coding Region Coverage

1x: 99.3%
3x: 98.8%
10x: 97.6%
20x: 96.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acvr2a	A	G	2: 48,782,166 (GRCm39)	Y233C	probably damaging	Het
Agl	A	G	3: 116,584,814 (GRCm39)	S169P	probably damaging	Het
Arid1b	C	T	17: 5,341,332 (GRCm39)	Q879*	probably null	Het
Bbs2	A	G	8: 94,819,178 (GRCm39)	S64P	probably damaging	Het
Bend7	G	A	2: 4,768,052 (GRCm39)	R336Q	probably damaging	Het
Cacna2d2	A	G	9: 107,391,313 (GRCm39)	T447A	probably benign	Het
Ccdc168	T	A	1: 44,096,955 (GRCm39)	Y1381F	probably benign	Het
Ccdc169	A	T	3: 55,049,740 (GRCm39)		probably benign	Het
Cdan1	A	G	2: 120,560,546 (GRCm39)	S275P	possibly damaging	Het
Cdh15	A	G	8: 123,588,802 (GRCm39)	N292S	probably null	Het
Cmtm1	CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT	CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT	8: 105,036,102 (GRCm39)		probably benign	Het
Cnnm1	A	G	19: 43,430,301 (GRCm39)	H473R	probably benign	Het
Cplx4	G	A	18: 66,103,157 (GRCm39)		probably benign	Het
Crb1	C	T	1: 139,265,109 (GRCm39)	G103E	probably damaging	Het
Dnaja3	T	A	16: 4,512,346 (GRCm39)	V250E	possibly damaging	Het
Dync2h1	T	G	9: 7,129,727 (GRCm39)	Q1757P	probably damaging	Het
Edem3	A	G	1: 151,683,202 (GRCm39)	Q626R	probably damaging	Het
Eif2b1	T	C	5: 124,716,862 (GRCm39)		probably benign	Het
Esf1	T	A	2: 139,996,801 (GRCm39)	K521*	probably null	Het
Fbxl3	A	C	14: 103,320,730 (GRCm39)	V239G	probably damaging	Het
Fhip2a	A	G	19: 57,367,051 (GRCm39)	D198G	probably benign	Het
Fto	A	G	8: 92,118,107 (GRCm39)		probably benign	Het
Gm5916	A	T	9: 36,032,012 (GRCm39)	W91R	probably benign	Het
Gpam	A	T	19: 55,077,269 (GRCm39)	L174H	probably damaging	Het
Grk1	G	A	8: 13,464,478 (GRCm39)	R450Q	probably damaging	Het
Hc	G	A	2: 34,927,636 (GRCm39)	A326V	probably benign	Het
Hectd4	T	C	5: 121,442,511 (GRCm39)	I1317T	probably benign	Het
Hlcs	A	G	16: 94,068,383 (GRCm39)	V426A	possibly damaging	Het
Ighv1-23	T	C	12: 114,728,376 (GRCm39)		probably benign	Het
Itgax	G	A	7: 127,740,474 (GRCm39)	V754I	probably benign	Het
Krt24	T	A	11: 99,173,556 (GRCm39)	D255V	probably damaging	Het
Lnpk	T	C	2: 74,403,935 (GRCm39)		probably benign	Het
Loxhd1	G	T	18: 77,454,237 (GRCm39)	R478L	probably damaging	Het
Lrrc56	A	G	7: 140,789,537 (GRCm39)	Q518R	probably benign	Het
Mbl1	A	T	14: 40,880,786 (GRCm39)	I225F	probably damaging	Het
Mmp21	T	C	7: 133,277,651 (GRCm39)	S392G	probably benign	Het
Mug2	T	G	6: 122,058,551 (GRCm39)	F1318V	probably damaging	Het
Myo5c	A	G	9: 75,202,487 (GRCm39)	N1447S	probably null	Het
Nbea	A	C	3: 55,948,297 (GRCm39)	V543G	probably damaging	Het
Necap1	A	G	6: 122,857,706 (GRCm39)	I96V	probably benign	Het
Nr3c2	T	A	8: 77,937,377 (GRCm39)	M872K	possibly damaging	Het
Nrf1	C	T	6: 30,118,967 (GRCm39)	T362M	probably benign	Het
Or14j2	T	C	17: 37,885,618 (GRCm39)	E232G	probably damaging	Het
Pcare	A	G	17: 72,056,930 (GRCm39)	S916P	probably benign	Het
Plekhm3	T	C	1: 64,859,149 (GRCm39)	E685G	probably damaging	Het
Robo4	CGG	CG	9: 37,322,786 (GRCm39)		probably null	Het
Sbk3	A	T	7: 4,970,422 (GRCm39)	S316T	probably benign	Het
Serpinb9e	T	C	13: 33,441,767 (GRCm39)	L233P	probably damaging	Het
Set	T	A	2: 29,959,422 (GRCm39)	S132T	possibly damaging	Het
Slc17a4	C	T	13: 24,092,800 (GRCm39)	E11K	possibly damaging	Het
Slc22a6	T	A	19: 8,595,917 (GRCm39)	N86K	possibly damaging	Het
Slco1a6	A	G	6: 142,032,325 (GRCm39)	L600P	probably damaging	Het
Sp8	A	G	12: 118,812,246 (GRCm39)	K34E	possibly damaging	Het
Spen	T	A	4: 141,198,796 (GRCm39)	E3254V	probably benign	Het
Tcf12	G	A	9: 71,792,525 (GRCm39)	P53S	probably damaging	Het
Tcf3	A	G	10: 80,246,045 (GRCm39)	V626A	probably damaging	Het
Trpc4ap	A	G	2: 155,514,908 (GRCm39)		probably null	Het
Ttc3	T	A	16: 94,230,479 (GRCm39)	V892D	probably damaging	Het
Tub	G	T	7: 108,625,978 (GRCm39)	R243L	possibly damaging	Het
Tubgcp5	A	G	7: 55,473,433 (GRCm39)	Y837C	probably damaging	Het
Utp25	A	T	1: 192,810,687 (GRCm39)	D105E	probably benign	Het
Wdhd1	A	T	14: 47,506,181 (GRCm39)	Y244*	probably null	Het
Xdh	T	A	17: 74,232,027 (GRCm39)	T228S	probably benign	Het
Zfp418	A	C	7: 7,185,534 (GRCm39)	Q499P	probably benign	Het
Zfpm1	G	A	8: 123,062,269 (GRCm39)	E443K	possibly damaging	Het
Zfy1	T	C	Y: 725,950 (GRCm39)	H605R	possibly damaging	Het

Other mutations in Gm5773

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02954:Gm5773	APN	3	93,680,358 (GRCm39)	missense	probably benign	0.15
IGL03411:Gm5773	APN	3	93,681,264 (GRCm39)	missense	probably damaging	1.00
BB005:Gm5773	UTSW	3	93,680,997 (GRCm39)	missense	probably damaging	0.96
BB015:Gm5773	UTSW	3	93,680,997 (GRCm39)	missense	probably damaging	0.96
R0239:Gm5773	UTSW	3	93,681,339 (GRCm39)	missense	probably benign	0.01
R0239:Gm5773	UTSW	3	93,681,339 (GRCm39)	missense	probably benign	0.01
R1087:Gm5773	UTSW	3	93,681,065 (GRCm39)	missense	probably damaging	1.00
R1884:Gm5773	UTSW	3	93,681,348 (GRCm39)	missense	probably benign	0.00
R2122:Gm5773	UTSW	3	93,680,624 (GRCm39)	missense	possibly damaging	0.78
R2182:Gm5773	UTSW	3	93,680,820 (GRCm39)	missense	probably benign	0.00
R4615:Gm5773	UTSW	3	93,681,339 (GRCm39)	missense	probably benign	0.01
R4650:Gm5773	UTSW	3	93,680,712 (GRCm39)	missense	probably benign	0.04
R5127:Gm5773	UTSW	3	93,680,735 (GRCm39)	missense	probably benign
R5141:Gm5773	UTSW	3	93,681,034 (GRCm39)	missense	probably benign	0.04
R6883:Gm5773	UTSW	3	93,681,162 (GRCm39)	missense	probably benign	0.31
R6962:Gm5773	UTSW	3	93,681,234 (GRCm39)	missense	possibly damaging	0.90
R7444:Gm5773	UTSW	3	93,680,850 (GRCm39)	missense	probably damaging	1.00
R7549:Gm5773	UTSW	3	93,680,323 (GRCm39)	start gained	probably benign
R7743:Gm5773	UTSW	3	93,680,565 (GRCm39)	missense	probably damaging	0.97
R7916:Gm5773	UTSW	3	93,680,586 (GRCm39)	missense	possibly damaging	0.52
R7928:Gm5773	UTSW	3	93,680,997 (GRCm39)	missense	probably damaging	0.96
R7992:Gm5773	UTSW	3	93,680,373 (GRCm39)	missense	possibly damaging	0.66
R8024:Gm5773	UTSW	3	93,680,475 (GRCm39)	missense	probably benign	0.06
R8500:Gm5773	UTSW	3	93,680,835 (GRCm39)	missense	probably benign	0.00
R8805:Gm5773	UTSW	3	93,681,042 (GRCm39)	missense	probably damaging	1.00
R9135:Gm5773	UTSW	3	93,681,179 (GRCm39)	missense	possibly damaging	0.94
R9281:Gm5773	UTSW	3	93,680,891 (GRCm39)	missense	probably benign	0.12
R9554:Gm5773	UTSW	3	93,680,340 (GRCm39)	missense	probably benign	0.00
R9566:Gm5773	UTSW	3	93,680,742 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TAGCTGGCCATGAAATCAGG -3'
(R):5'- CCGGAGCTTTTAGAGACCTC -3'

Sequencing Primer
(F):5'- CATGAAATCAGGGCTCACAAAG -3'
(R):5'- GCTTTTAGAGACCTCAGAAGCATG -3'

Posted On

2016-08-04