Mutagenetix > Incidental Mutation

Incidental Mutation 'R8880:Gm4884'

676841

Institutional Source

Beutler Lab

Gene Symbol

Gm4884

Ensembl Gene

ENSMUSG00000048312

Gene Name

predicted gene 4884

Synonyms

MMRRC Submission

068748-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.054) question?

Stock #

R8880 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

40682143-40694726 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 40693911 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Phenylalanine at position 627 (I627F)

Ref Sequence

ENSEMBL: ENSMUSP00000133059 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000164422]

AlphaFold

E9PVP9

Predicted Effect

probably damaging
Transcript: ENSMUST00000164422
AA Change: I627F

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000133059
Gene: ENSMUSG00000048312
AA Change: I627F

Domain	Start	End	E-Value	Type
Pfam:DUF4629	243	387	8e-62	PFAM
low complexity region	509	533	N/A	INTRINSIC
internal_repeat_1	554	584	1.89e-11	PROSPERO
internal_repeat_1	583	613	1.89e-11	PROSPERO

Coding Region Coverage

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

Validation Efficiency

100% (82/82)

Allele List at MGI

Other mutations in this stock

Total: 84 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3425401B19Rik	C	T	14: 32,382,837 (GRCm39)	V1043I	probably benign	Het
5031439G07Rik	T	A	15: 84,839,867 (GRCm39)	I176F	possibly damaging	Het
Adam6b	T	A	12: 113,454,764 (GRCm39)	M527K	probably benign	Het
Atp10b	C	T	11: 43,106,811 (GRCm39)	T615I	probably benign	Het
Atxn2	A	G	5: 121,948,973 (GRCm39)	T1117A	probably benign	Het
AU021092	A	T	16: 5,032,585 (GRCm39)		probably benign	Het
Bcam	C	T	7: 19,492,671 (GRCm39)	V505M	probably damaging	Het
Bco2	A	T	9: 50,461,962 (GRCm39)	L14Q	probably damaging	Het
Caps2	T	G	10: 112,030,824 (GRCm39)		probably benign	Het
Cblb	T	C	16: 51,986,368 (GRCm39)	V537A	probably benign	Het
Ccdc141	A	T	2: 76,845,556 (GRCm39)	N1170K	probably benign	Het
Ccdc154	T	G	17: 25,389,129 (GRCm39)	D442E	probably benign	Het
Col24a1	A	G	3: 145,019,798 (GRCm39)	I60V	probably null	Het
Crb1	A	T	1: 139,164,886 (GRCm39)	N1140K	probably benign	Het
Ddhd1	G	A	14: 45,846,430 (GRCm39)	P621S	probably benign	Het
Ddx46	A	T	13: 55,814,033 (GRCm39)	N663I	probably benign	Het
Dgki	C	T	6: 37,011,652 (GRCm39)		probably benign	Het
Disp2	T	C	2: 118,621,239 (GRCm39)	F657S	probably damaging	Het
Dnajc2	T	C	5: 21,973,670 (GRCm39)	E262G	probably damaging	Het
Dvl2	T	A	11: 69,898,761 (GRCm39)	L408Q	possibly damaging	Het
Egflam	T	C	15: 7,267,249 (GRCm39)	D712G	probably damaging	Het
Entpd7	A	G	19: 43,692,846 (GRCm39)		probably benign	Het
Epb41	A	T	4: 131,695,104 (GRCm39)	W28R		Het
Fabp9	C	T	3: 10,262,231 (GRCm39)		probably benign	Het
Fkbp15	T	A	4: 62,232,602 (GRCm39)	M657L	probably benign	Het
Gfy	A	C	7: 44,827,784 (GRCm39)	L104R	possibly damaging	Het
Gm9195	A	T	14: 72,691,320 (GRCm39)	S1643T	unknown	Het
Gpsm2	C	T	3: 108,610,335 (GRCm39)	A42T	possibly damaging	Het
Gvin2	T	C	7: 105,551,120 (GRCm39)	K644R	probably benign	Het
Gys2	T	C	6: 142,402,113 (GRCm39)	Y242C	probably damaging	Het
Hbs1l	A	G	10: 21,185,868 (GRCm39)	N430S	probably damaging	Het
Idh3b	A	T	2: 130,126,004 (GRCm39)		probably benign	Het
Igdcc3	C	T	9: 65,088,550 (GRCm39)	A384V	probably benign	Het
Ighv3-4	C	T	12: 114,217,535 (GRCm39)	D19N	possibly damaging	Het
Igkv19-93	G	T	6: 68,713,494 (GRCm39)	A45E	probably damaging	Het
Il10ra	G	A	9: 45,175,631 (GRCm39)	T230M	probably damaging	Het
Kalrn	A	G	16: 34,038,305 (GRCm39)	V1009A	probably damaging	Het
Kcnma1	G	T	14: 23,417,718 (GRCm39)	A837D	probably damaging	Het
Kif7	T	A	7: 79,348,650 (GRCm39)	R1231S	probably benign	Het
Klhdc1	A	G	12: 69,298,817 (GRCm39)	D134G	possibly damaging	Het
Klk14	T	C	7: 43,343,459 (GRCm39)	V97A	probably damaging	Het
Lamb3	G	A	1: 193,003,363 (GRCm39)	V101M	possibly damaging	Het
Lrrc7	C	T	3: 157,867,381 (GRCm39)	E787K	probably damaging	Het
Mep1a	A	G	17: 43,808,808 (GRCm39)	I94T	possibly damaging	Het
Mtrex	T	A	13: 113,051,034 (GRCm39)	K180N	probably benign	Het
Ncr1	C	T	7: 4,341,336 (GRCm39)	S109L	probably benign	Het
Nell2	A	T	15: 95,129,329 (GRCm39)	M678K	probably damaging	Het
Or12j5	C	A	7: 140,084,172 (GRCm39)	A67S	probably benign	Het
Or14c42-ps1	G	A	7: 86,211,549 (GRCm39)	C203Y	unknown	Het
Or2m13	A	T	16: 19,226,396 (GRCm39)	Y123*	probably null	Het
Or8g19	T	A	9: 39,055,899 (GRCm39)	F168I	probably damaging	Het
Pnpla1	A	C	17: 29,098,438 (GRCm39)	Y248S	probably damaging	Het
Pramel27	T	C	4: 143,573,140 (GRCm39)		probably null	Het
Prdm10	T	C	9: 31,264,742 (GRCm39)	F726L	probably damaging	Het
Prdm16	T	C	4: 154,613,370 (GRCm39)	N19S	probably damaging	Het
Prss44	A	G	9: 110,643,263 (GRCm39)	R53G	probably benign	Het
Rasgrp1	C	T	2: 117,115,425 (GRCm39)	R721Q	probably benign	Het
Rassf1	A	T	9: 107,434,740 (GRCm39)	N149I	probably damaging	Het
Rbp3	A	C	14: 33,678,796 (GRCm39)	T915P	probably benign	Het
Reg3g	A	T	6: 78,444,788 (GRCm39)	D63E	probably benign	Het
Relch	T	C	1: 105,592,220 (GRCm39)	Y130H	probably damaging	Het
Rgs3	C	A	4: 62,543,373 (GRCm39)	T236K	probably damaging	Het
Rin2	T	C	2: 145,690,772 (GRCm39)	F147L	probably damaging	Het
Slc17a1	T	C	13: 24,062,732 (GRCm39)	I266T	probably benign	Het
Slc34a3	A	T	2: 25,119,267 (GRCm39)	N534K	probably benign	Het
Smc2	A	T	4: 52,462,856 (GRCm39)	E615D	probably benign	Het
Snx16	A	C	3: 10,484,193 (GRCm39)	D343E	probably benign	Het
St18	T	A	1: 6,865,619 (GRCm39)	Y32*	probably null	Het
Svep1	C	T	4: 58,064,204 (GRCm39)	V3260I	possibly damaging	Het
Synm	C	T	7: 67,386,456 (GRCm39)	R402H	possibly damaging	Het
Tacc2	A	T	7: 130,318,564 (GRCm39)	E67V	possibly damaging	Het
Tarbp1	G	T	8: 127,198,044 (GRCm39)	N302K	probably damaging	Het
Tenm2	A	G	11: 35,942,788 (GRCm39)	S1294P	probably damaging	Het
Ttk	T	C	9: 83,751,304 (GRCm39)	S794P	probably damaging	Het
Ulk1	G	A	5: 110,934,288 (GRCm39)	A999V	probably damaging	Het
Upf2	A	G	2: 6,030,983 (GRCm39)	I808V	unknown	Het
Ush2a	A	G	1: 188,460,733 (GRCm39)	T2665A	probably benign	Het
Usp8	A	G	2: 126,590,229 (GRCm39)	K672E	probably damaging	Het
Vmn2r105	T	A	17: 20,429,229 (GRCm39)	I616F	probably damaging	Het
Vps33a	T	C	5: 123,707,506 (GRCm39)	M154V	probably damaging	Het
Wdfy4	A	C	14: 32,795,492 (GRCm39)	Y2083*	probably null	Het
Zc3hav1	A	G	6: 38,288,212 (GRCm39)	F875L	probably benign	Het
Zfp979	T	C	4: 147,697,836 (GRCm39)	N291S	probably benign	Het
Zp2	T	A	7: 119,742,835 (GRCm39)	Y99F	possibly damaging	Het

Other mutations in Gm4884

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00429:Gm4884	APN	7	40,693,809 (GRCm39)	missense	probably benign	0.22
IGL00980:Gm4884	APN	7	40,693,150 (GRCm39)	missense	probably damaging	1.00
IGL02230:Gm4884	APN	7	40,692,829 (GRCm39)	missense	probably damaging	1.00
IGL03271:Gm4884	APN	7	40,692,699 (GRCm39)	missense	probably benign	0.33
IGL03274:Gm4884	APN	7	40,693,969 (GRCm39)	missense	probably damaging	1.00
R0013:Gm4884	UTSW	7	40,693,716 (GRCm39)	missense	probably damaging	1.00
R0139:Gm4884	UTSW	7	40,692,387 (GRCm39)	missense	probably benign	0.00
R0179:Gm4884	UTSW	7	40,693,252 (GRCm39)	missense	probably benign	0.26
R0960:Gm4884	UTSW	7	40,692,232 (GRCm39)	missense	possibly damaging	0.55
R1167:Gm4884	UTSW	7	40,693,336 (GRCm39)	missense	possibly damaging	0.92
R1311:Gm4884	UTSW	7	40,692,539 (GRCm39)	missense	possibly damaging	0.73
R1466:Gm4884	UTSW	7	40,692,552 (GRCm39)	missense	probably damaging	0.96
R1466:Gm4884	UTSW	7	40,692,552 (GRCm39)	missense	probably damaging	0.96
R1581:Gm4884	UTSW	7	40,693,255 (GRCm39)	missense	probably benign	0.09
R1622:Gm4884	UTSW	7	40,692,265 (GRCm39)	missense	probably damaging	0.99
R1891:Gm4884	UTSW	7	40,692,539 (GRCm39)	missense	possibly damaging	0.73
R1952:Gm4884	UTSW	7	40,693,671 (GRCm39)	missense	probably benign	0.02
R2198:Gm4884	UTSW	7	40,690,229 (GRCm39)	missense	probably benign
R2209:Gm4884	UTSW	7	40,692,745 (GRCm39)	missense	possibly damaging	0.47
R2210:Gm4884	UTSW	7	40,692,970 (GRCm39)	missense	possibly damaging	0.72
R2219:Gm4884	UTSW	7	40,692,910 (GRCm39)	missense	possibly damaging	0.75
R3688:Gm4884	UTSW	7	40,692,910 (GRCm39)	missense	possibly damaging	0.75
R4437:Gm4884	UTSW	7	40,692,514 (GRCm39)	missense	probably damaging	0.97
R4472:Gm4884	UTSW	7	40,692,687 (GRCm39)	missense	probably benign	0.35
R5137:Gm4884	UTSW	7	40,692,318 (GRCm39)	missense	probably damaging	0.99
R5700:Gm4884	UTSW	7	40,692,643 (GRCm39)	missense	probably benign	0.22
R5875:Gm4884	UTSW	7	40,692,360 (GRCm39)	missense	possibly damaging	0.75
R6479:Gm4884	UTSW	7	40,690,211 (GRCm39)	missense	probably damaging	0.99
R6659:Gm4884	UTSW	7	40,694,046 (GRCm39)	missense	probably damaging	1.00
R7180:Gm4884	UTSW	7	40,693,633 (GRCm39)	missense	possibly damaging	0.89
R7844:Gm4884	UTSW	7	40,690,122 (GRCm39)	missense	probably benign	0.11
R8153:Gm4884	UTSW	7	40,692,582 (GRCm39)	missense	probably benign	0.17
R8436:Gm4884	UTSW	7	40,692,810 (GRCm39)	missense	probably damaging	0.97
R8885:Gm4884	UTSW	7	40,694,108 (GRCm39)	nonsense	probably null
R9406:Gm4884	UTSW	7	40,692,565 (GRCm39)	missense	probably damaging	1.00
R9621:Gm4884	UTSW	7	40,693,111 (GRCm39)	missense	possibly damaging	0.76
R9728:Gm4884	UTSW	7	40,692,689 (GRCm39)	missense	probably benign	0.00
RF013:Gm4884	UTSW	7	40,690,233 (GRCm39)	missense	probably damaging	1.00
Z1088:Gm4884	UTSW	7	40,692,300 (GRCm39)	missense	possibly damaging	0.71
Z1177:Gm4884	UTSW	7	40,682,161 (GRCm39)	start gained	probably benign

Predicted Primers

PCR Primer
(F):5'- AGAGCTTGTTTCTGCTGCC -3'
(R):5'- GCAATGATCTGGCAAGCTGTTAC -3'

Sequencing Primer
(F):5'- TTTCTGCTGCCAGGAACAAG -3'
(R):5'- GGCAAGCTGTTACATTGCATAGC -3'

Posted On

2021-07-15