Mutagenetix > Incidental Mutation

Incidental Mutation 'R9417:Isg20'

712106

Institutional Source

Beutler Lab

Gene Symbol

Isg20

Ensembl Gene

ENSMUSG00000039236

Gene Name

interferon-stimulated protein

Synonyms

DnaQl, HEM45, 20kDa, 2010107M23Rik, 1600023I01Rik

MMRRC Submission

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R9417 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

78563172-78570144 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 78569605 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Proline to Leucine at position 192 (P192L)

Ref Sequence

ENSEMBL: ENSMUSP00000112621 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000038142] [ENSMUST00000118867] [ENSMUST00000120331] [ENSMUST00000121645] [ENSMUST00000205981]

AlphaFold

Q9JL16

Predicted Effect

probably benign
Transcript: ENSMUST00000038142

SMART Domains

Protein: ENSMUSP00000040080
Gene: ENSMUSG00000039236

Domain	Start	End	E-Value	Type
EXOIII	6	171	6.23e-47	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000118867

SMART Domains

Protein: ENSMUSP00000112480
Gene: ENSMUSG00000039236

Domain	Start	End	E-Value	Type
EXOIII	6	171	6.23e-47	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000120331

SMART Domains

Protein: ENSMUSP00000113255
Gene: ENSMUSG00000039236

Domain	Start	End	E-Value	Type
EXOIII	6	171	6.23e-47	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000121645
AA Change: P192L

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000112621
Gene: ENSMUSG00000039236
AA Change: P192L

Domain	Start	End	E-Value	Type
EXOIII	6	176	8.25e-29	SMART
low complexity region	182	201	N/A	INTRINSIC
low complexity region	208	224	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000205981

Coding Region Coverage

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

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930553M12Rik	A	G	4: 88,786,202 (GRCm39)	Y139H	unknown	Het
Akr1b10	T	C	6: 34,371,027 (GRCm39)	V259A	probably benign	Het
Aldh5a1	A	T	13: 25,095,673 (GRCm39)	N481K	probably damaging	Het
Ankrd26	A	T	6: 118,504,725 (GRCm39)	M728K	possibly damaging	Het
Asic1	A	G	15: 99,590,405 (GRCm39)	M52V	probably benign	Het
Bean1	CT	C	8: 104,908,664 (GRCm39)		probably null	Het
Cacna2d2	C	A	9: 107,392,689 (GRCm39)	Y544*	probably null	Het
Cdcp3	A	G	7: 130,852,218 (GRCm39)	D818G	possibly damaging	Het
Chd4	A	G	6: 125,097,688 (GRCm39)	N1403S	probably damaging	Het
Cldn4	G	T	5: 134,975,174 (GRCm39)	N142K	probably benign	Het
Cracd	GCGCGAGGCCGAGAGGCAGGAGGAGGAAGCAAGACAACGCGAGGCCGAGAGGCAGG	GCGCGAGGCCGAGAGGCAGG	5: 77,004,801 (GRCm39)		probably benign	Het
Dll1	T	C	17: 15,593,710 (GRCm39)	Y219C	probably damaging	Het
Dnah2	T	A	11: 69,326,990 (GRCm39)	I3539F	probably damaging	Het
Egfr	T	A	11: 16,825,067 (GRCm39)	L469*	probably null	Het
Elmo1	A	G	13: 20,756,573 (GRCm39)	N554D	possibly damaging	Het
Fam234a	A	C	17: 26,435,225 (GRCm39)	F306L	probably benign	Het
Fbl	G	A	7: 27,874,052 (GRCm39)	G45D	unknown	Het
Fbxw10	C	A	11: 62,753,522 (GRCm39)	C505*	probably null	Het
Ftcd	G	A	10: 76,417,153 (GRCm39)	G221S	probably damaging	Het
Gad1	A	G	2: 70,417,716 (GRCm39)	D305G	possibly damaging	Het
Gdpd4	A	G	7: 97,607,074 (GRCm39)	D16G	probably benign	Het
Gsdmc3	T	A	15: 63,738,663 (GRCm39)	D133V	possibly damaging	Het
Hpdl	T	C	4: 116,677,817 (GRCm39)	T215A	possibly damaging	Het
Ift56	T	C	6: 38,386,386 (GRCm39)	F369S	probably damaging	Het
Igsf10	A	T	3: 59,236,526 (GRCm39)	N1218K	possibly damaging	Het
Itga7	C	T	10: 128,793,543 (GRCm39)	T126M	unknown	Het
Krr1	A	G	10: 111,813,026 (GRCm39)	I134V	probably benign	Het
Krt71	T	A	15: 101,646,731 (GRCm39)	T326S	probably benign	Het
Lamb1	T	A	12: 31,337,983 (GRCm39)	V480E	probably damaging	Het
Mmp19	T	A	10: 128,630,523 (GRCm39)	L102Q	possibly damaging	Het
Mtor	T	A	4: 148,622,776 (GRCm39)	L1952*	probably null	Het
Myo15a	T	A	11: 60,378,243 (GRCm39)	V215E		Het
Nfs1	T	A	2: 155,965,851 (GRCm39)	K77*	probably null	Het
Or52s1	A	T	7: 102,861,156 (GRCm39)	I30F	possibly damaging	Het
Or9a4	T	A	6: 40,549,096 (GRCm39)	Y259N		Het
Pcdhga4	T	C	18: 37,820,560 (GRCm39)	F703S	probably damaging	Het
Pdzd7	A	G	19: 45,034,022 (GRCm39)	S21P	probably damaging	Het
Pitrm1	A	T	13: 6,617,394 (GRCm39)	I583F	possibly damaging	Het
Ppox	A	G	1: 171,107,855 (GRCm39)	L77P	unknown	Het
Ppp1r37	G	T	7: 19,269,658 (GRCm39)	R114S	probably damaging	Het
Ppp4r3b	T	C	11: 29,144,598 (GRCm39)	V316A	probably benign	Het
Ptprd	A	G	4: 75,865,335 (GRCm39)	I1214T	probably damaging	Het
Rasal3	A	G	17: 32,615,441 (GRCm39)	F466L	probably benign	Het
Ric8b	A	T	10: 84,761,447 (GRCm39)	D41V	probably benign	Het
Rin2	T	C	2: 145,686,713 (GRCm39)	S81P	probably benign	Het
Sft2d1	T	A	17: 8,542,139 (GRCm39)	C128S	probably damaging	Het
Skint1	T	C	4: 111,878,509 (GRCm39)	V147A	probably benign	Het
Slc9c1	T	C	16: 45,413,848 (GRCm39)	V992A	probably benign	Het
Sst	A	G	16: 23,708,487 (GRCm39)	S115P	probably damaging	Het
Sv2b	G	T	7: 74,769,772 (GRCm39)	S590Y	probably damaging	Het
Syne1	C	T	10: 5,082,021 (GRCm39)	V868I	probably benign	Het
Tex35	T	C	1: 156,934,789 (GRCm39)	I42V	possibly damaging	Het
Tlr2	T	C	3: 83,744,892 (GRCm39)	N397S	probably damaging	Het
Tmem202	A	G	9: 59,431,999 (GRCm39)		probably null	Het
Usp20	A	G	2: 30,873,030 (GRCm39)		probably null	Het
Usp32	C	T	11: 84,885,369 (GRCm39)	R1226Q	probably damaging	Het
Usp47	C	T	7: 111,688,801 (GRCm39)	A736V	possibly damaging	Het
Vmn2r-ps117	T	A	17: 19,044,037 (GRCm39)	L371*	probably null	Het
Wwp1	T	A	4: 19,662,215 (GRCm39)	N127Y	possibly damaging	Het
Yae1d1	A	T	13: 18,167,770 (GRCm39)	V41D	probably damaging	Het
Zbtb8b	T	C	4: 129,326,517 (GRCm39)	D216G	probably benign	Het
Zfp462	T	C	4: 55,016,988 (GRCm39)	S903P	probably benign	Het
Zranb1	G	A	7: 132,585,466 (GRCm39)	G638D	probably damaging	Het

Other mutations in Isg20

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00589:Isg20	APN	7	78,566,332 (GRCm39)	missense	probably damaging	1.00
IGL01399:Isg20	APN	7	78,569,836 (GRCm39)	missense	possibly damaging	0.92
IGL01680:Isg20	APN	7	78,566,333 (GRCm39)	missense	probably damaging	1.00
IGL01769:Isg20	APN	7	78,564,129 (GRCm39)	missense	probably damaging	1.00
R0233:Isg20	UTSW	7	78,566,334 (GRCm39)	missense	probably damaging	1.00
R0233:Isg20	UTSW	7	78,566,334 (GRCm39)	missense	probably damaging	1.00
R0233:Isg20	UTSW	7	78,564,243 (GRCm39)	missense	probably damaging	0.99
R0233:Isg20	UTSW	7	78,564,243 (GRCm39)	missense	probably damaging	0.99
R0400:Isg20	UTSW	7	78,566,473 (GRCm39)	missense	possibly damaging	0.89
R1562:Isg20	UTSW	7	78,569,891 (GRCm39)	missense	probably benign	0.17
R1610:Isg20	UTSW	7	78,564,257 (GRCm39)	missense	possibly damaging	0.48
R1894:Isg20	UTSW	7	78,569,647 (GRCm39)	missense	probably benign	0.01
R2033:Isg20	UTSW	7	78,566,281 (GRCm39)	missense	probably damaging	0.98
R2992:Isg20	UTSW	7	78,569,632 (GRCm39)	missense	probably benign	0.10
R3159:Isg20	UTSW	7	78,564,201 (GRCm39)	missense	possibly damaging	0.62
R4678:Isg20	UTSW	7	78,564,076 (GRCm39)	unclassified	probably benign
R5787:Isg20	UTSW	7	78,569,558 (GRCm39)	missense	probably benign	0.04
R7834:Isg20	UTSW	7	78,569,867 (GRCm39)	missense	probably damaging	0.99
R8554:Isg20	UTSW	7	78,566,425 (GRCm39)	missense	probably benign	0.14
R9046:Isg20	UTSW	7	78,569,823 (GRCm39)	nonsense	probably null
R9052:Isg20	UTSW	7	78,566,390 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGTTCCACTGTGTGCTCTGC -3'
(R):5'- TTGTTCTGCAGACACAGGG -3'

Sequencing Primer
(F):5'- AAAGAGCTTCTGTTTTAGCGCC -3'
(R):5'- TTCTGCAGACACAGGGAGAGC -3'

Posted On

2022-05-16