Mutagenetix > Incidental Mutation

Incidental Mutation 'R0013:Gm4884'

32637

Institutional Source

Beutler Lab

Gene Symbol

Gm4884

Ensembl Gene

ENSMUSG00000048312

Gene Name

predicted gene 4884

Synonyms

MMRRC Submission

038308-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.066) question?

Stock #

R0013 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

40682143-40694726 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 40693716 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 562 (S562P)

Ref Sequence

ENSEMBL: ENSMUSP00000133059 (fasta)

Gene Model

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

AlphaFold

E9PVP9

Predicted Effect

probably damaging
Transcript: ENSMUST00000164422
AA Change: S562P

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

SMART Domains

Protein: ENSMUSP00000133059
Gene: ENSMUSG00000048312
AA Change: S562P

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

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000191289

Meta Mutation Damage Score

0.1017

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.9%
20x: 94.8%

Validation Efficiency

94% (79/84)

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2610028H24Rik	A	G	10: 76,293,346 (GRCm39)	M156V	probably benign	Het
Adnp2	A	T	18: 80,172,960 (GRCm39)	V483D	probably damaging	Het
Aff1	G	T	5: 103,976,350 (GRCm39)	E491*	probably null	Het
Agl	A	T	3: 116,570,257 (GRCm39)	C911*	probably null	Het
Akt2	A	G	7: 27,335,483 (GRCm39)	D284G	probably damaging	Het
Alox15	A	G	11: 70,240,461 (GRCm39)	M240T	possibly damaging	Het
Antxr2	A	G	5: 98,127,844 (GRCm39)	V229A	probably damaging	Het
Arap2	G	A	5: 62,840,827 (GRCm39)	L680F	probably damaging	Het
Btaf1	A	G	19: 36,935,773 (GRCm39)	T188A	probably benign	Het
Btnl6	G	A	17: 34,734,505 (GRCm39)	Q86*	probably null	Het
C2cd3	T	A	7: 100,065,269 (GRCm39)	L685H	probably damaging	Het
Cdh23	T	C	10: 60,248,952 (GRCm39)	T878A	possibly damaging	Het
Clec4b2	T	C	6: 123,179,108 (GRCm39)	Y137H	probably damaging	Het
Dchs1	T	A	7: 105,405,043 (GRCm39)	T2500S	possibly damaging	Het
Def6	A	G	17: 28,436,066 (GRCm39)	Y75C	probably damaging	Het
Dhx33	A	T	11: 70,884,461 (GRCm39)	F448L	probably damaging	Het
Dner	C	T	1: 84,472,614 (GRCm39)		probably benign	Het
Dnmbp	G	A	19: 43,890,670 (GRCm39)	P366S	probably benign	Het
Eif4g3	T	C	4: 137,903,159 (GRCm39)	C1160R	possibly damaging	Het
Elmod1	G	A	9: 53,820,185 (GRCm39)		probably benign	Het
Faah	C	A	4: 115,861,588 (GRCm39)	L305F	probably damaging	Het
Flt1	A	G	5: 147,507,824 (GRCm39)		probably benign	Het
Fyco1	A	T	9: 123,651,471 (GRCm39)	N1196K	probably benign	Het
Galnt18	T	C	7: 111,153,664 (GRCm39)	N320S	probably damaging	Het
Garin3	A	G	11: 46,297,631 (GRCm39)	T312A	unknown	Het
Glp2r	C	A	11: 67,600,538 (GRCm39)	G437V	possibly damaging	Het
Gm9936	A	G	5: 114,995,408 (GRCm39)		probably benign	Het
Gpn2	C	A	4: 133,312,103 (GRCm39)	P112T	probably damaging	Het
Grm4	A	G	17: 27,650,549 (GRCm39)	Y816H	probably benign	Het
Helz2	A	T	2: 180,882,752 (GRCm39)	S14T	probably benign	Het
Htt	T	C	5: 34,977,448 (GRCm39)	L778P	probably benign	Het
Il11ra1	T	C	4: 41,765,060 (GRCm39)	S129P	probably damaging	Het
Ints11	T	C	4: 155,971,625 (GRCm39)	F315S	probably damaging	Het
Itga11	A	T	9: 62,683,895 (GRCm39)	N1059Y	possibly damaging	Het
Jak3	A	G	8: 72,136,971 (GRCm39)	S716G	probably damaging	Het
Kcns1	G	T	2: 164,010,563 (GRCm39)	D65E	probably benign	Het
Kdm5d	A	T	Y: 941,715 (GRCm39)	K1305N	probably benign	Het
Kif26a	G	T	12: 112,144,314 (GRCm39)	V1523L	probably benign	Het
Mboat7	A	G	7: 3,686,821 (GRCm39)	S340P	probably damaging	Het
Mctp2	T	C	7: 71,879,156 (GRCm39)	I234V	probably benign	Het
Mex3c	G	A	18: 73,723,622 (GRCm39)	A572T	probably benign	Het
Mpp3	C	A	11: 101,896,251 (GRCm39)	R424L	probably benign	Het
Mroh4	T	A	15: 74,480,086 (GRCm39)		probably benign	Het
Myo9a	A	T	9: 59,767,489 (GRCm39)		probably benign	Het
Myog	T	A	1: 134,217,973 (GRCm39)	H60Q	probably damaging	Het
Nlrp9a	T	A	7: 26,270,650 (GRCm39)		probably null	Het
Notch1	A	G	2: 26,363,830 (GRCm39)	V868A	possibly damaging	Het
Or10g9b	A	T	9: 39,917,651 (GRCm39)	I198N	probably damaging	Het
Or1j20	A	G	2: 36,760,172 (GRCm39)	N198S	probably damaging	Het
Or1p1	T	A	11: 74,179,877 (GRCm39)	I135N	possibly damaging	Het
Or5d18	T	C	2: 87,864,610 (GRCm39)	Y291C	possibly damaging	Het
Pink1	T	C	4: 138,044,712 (GRCm39)	T342A	probably benign	Het
Plb1	T	A	5: 32,506,959 (GRCm39)		probably benign	Het
Plec	T	C	15: 76,062,446 (GRCm39)	D2524G	probably damaging	Het
Plekhg4	G	T	8: 106,102,028 (GRCm39)	E6*	probably null	Het
Polq	T	C	16: 36,882,201 (GRCm39)	F1455S	possibly damaging	Het
Ppm1e	A	G	11: 87,139,884 (GRCm39)		probably benign	Het
Prkaca	G	A	8: 84,714,932 (GRCm39)	M119I	possibly damaging	Het
Prss46	G	T	9: 110,679,123 (GRCm39)	S108I	probably damaging	Het
Ptma	C	T	1: 86,457,498 (GRCm39)		probably benign	Het
Rab11fip4	C	T	11: 79,580,479 (GRCm39)	T437M	probably benign	Het
Rngtt	T	A	4: 33,379,409 (GRCm39)	M437K	probably benign	Het
Rrn3	T	A	16: 13,630,977 (GRCm39)	D604E	possibly damaging	Het
Scn4a	A	G	11: 106,239,231 (GRCm39)		probably benign	Het
Sis	A	G	3: 72,817,809 (GRCm39)	L1468P	possibly damaging	Het
Slit3	A	G	11: 35,598,745 (GRCm39)	M1450V	probably benign	Het
Smg5	T	C	3: 88,256,540 (GRCm39)	S269P	probably benign	Het
Sntg1	T	C	1: 8,533,686 (GRCm39)	T323A	probably damaging	Het
Son	C	T	16: 91,448,550 (GRCm39)	T37I	probably damaging	Het
Stk17b	T	C	1: 53,803,291 (GRCm39)	I41M	probably benign	Het
Tgm5	T	A	2: 120,907,363 (GRCm39)	Y120F	probably damaging	Het
Tppp	A	G	13: 74,169,479 (GRCm39)	K73R	possibly damaging	Het
Ttn	C	A	2: 76,569,502 (GRCm39)	K27130N	probably damaging	Het
Ttn	C	T	2: 76,738,096 (GRCm39)	V4148I	probably benign	Het
Tut4	T	A	4: 108,388,152 (GRCm39)		probably benign	Het
Uba7	A	T	9: 107,855,448 (GRCm39)	Y375F	probably damaging	Het
Ugcg	T	C	4: 59,213,931 (GRCm39)	L171P	possibly damaging	Het
Vsig2	T	C	9: 37,453,872 (GRCm39)		probably benign	Het
Zfp839	T	A	12: 110,834,820 (GRCm39)	S692T	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
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
R8880:Gm4884	UTSW	7	40,693,911 (GRCm39)	missense	probably damaging	1.00
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'- ATCTCCATCCCAGTATGAGCTGCC -3'
(R):5'- GAGACAACTGGTCCCAGAATGTCG -3'

Sequencing Primer
(F):5'- AAGGTCAAGTTAGTTCCTCTGC -3'
(R):5'- CTGAAGTCATGCAGCAGATATTG -3'

Posted On

2013-05-09