Mutagenetix > Incidental Mutation

Incidental Mutation 'R7275:Dis3'

565534

Institutional Source

Beutler Lab

Gene Symbol

Dis3

Ensembl Gene

ENSMUSG00000033166

Gene Name

DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease

Synonyms

2810028N01Rik

MMRRC Submission

045358-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R7275 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

99314070-99337217 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 99324925 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 502 (V502A)

Ref Sequence

ENSEMBL: ENSMUSP00000041906 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000042471] [ENSMUST00000227022] [ENSMUST00000228643]

AlphaFold

Q9CSH3

Predicted Effect

probably damaging
Transcript: ENSMUST00000042471
AA Change: V502A

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000041906
Gene: ENSMUSG00000033166
AA Change: V502A

Domain	Start	End	E-Value	Type
low complexity region	30	47	N/A	INTRINSIC
PINc	64	182	2.8e-24	SMART
low complexity region	425	436	N/A	INTRINSIC
RNB	467	797	5.56e-141	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000227022

Predicted Effect

probably damaging
Transcript: ENSMUST00000228643
AA Change: V502A

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

Coding Region Coverage

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

Validation Efficiency

98% (64/65)

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930447C04Rik	T	A	12: 72,956,795 (GRCm39)	T132S	possibly damaging	Het
4933412E24Rik	A	G	15: 59,887,738 (GRCm39)	V234A	probably benign	Het
Abtb3	T	A	10: 85,490,346 (GRCm39)	L1004Q	probably damaging	Het
Acsm5	A	G	7: 119,136,511 (GRCm39)	T361A	possibly damaging	Het
Agxt2	G	A	15: 10,358,753 (GRCm39)	R24H	probably benign	Het
Asb16	G	T	11: 102,159,935 (GRCm39)	W96L	probably damaging	Het
Bche	T	A	3: 73,607,969 (GRCm39)	T486S	probably benign	Het
Bpnt2	C	A	4: 4,792,962 (GRCm39)	G48W	probably damaging	Het
Cast	T	C	13: 74,875,453 (GRCm39)	T382A	probably benign	Het
Cdcp1	T	A	9: 123,014,119 (GRCm39)	K218N	possibly damaging	Het
Ceacam18	G	A	7: 43,291,308 (GRCm39)	G250D	probably damaging	Het
Ciao3	T	A	17: 25,994,108 (GRCm39)	V52E	possibly damaging	Het
Ctnnd2	T	C	15: 30,905,855 (GRCm39)	I834T	possibly damaging	Het
Cyp11b2	C	A	15: 74,725,840 (GRCm39)	G136W	probably damaging	Het
Dnai2	T	A	11: 114,648,054 (GRCm39)	M610K	unknown	Het
Drosha	G	A	15: 12,846,169 (GRCm39)	V435I	possibly damaging	Het
Dsc2	T	A	18: 20,184,236 (GRCm39)	R51*	probably null	Het
Ergic2	A	T	6: 148,096,757 (GRCm39)	C170S	probably damaging	Het
Exoc7	A	T	11: 116,195,688 (GRCm39)		probably null	Het
Fbxw25	G	T	9: 109,483,660 (GRCm39)	A184E		Het
Gm4846	T	A	1: 166,314,648 (GRCm39)	T332S	probably benign	Het
Greb1l	T	A	18: 10,544,561 (GRCm39)	M1385K	probably benign	Het
Grik1	T	C	16: 87,709,708 (GRCm39)	N871S	probably benign	Het
Il11ra1	T	C	4: 41,765,109 (GRCm39)	L145P	probably damaging	Het
Inpp5e	A	G	2: 26,298,104 (GRCm39)	S166P	probably benign	Het
Kdm4b	T	A	17: 56,703,333 (GRCm39)	L676H	probably damaging	Het
Lrp2	T	A	2: 69,289,875 (GRCm39)	K3655*	probably null	Het
Lrrc74a	A	G	12: 86,787,753 (GRCm39)	N128S	probably damaging	Het
Map3k14	T	C	11: 103,117,848 (GRCm39)	E648G	probably damaging	Het
Mbtps1	A	T	8: 120,269,489 (GRCm39)	D200E	probably benign	Het
Mttp	T	C	3: 137,829,546 (GRCm39)	D114G	probably benign	Het
Mup13	G	A	4: 61,182,752 (GRCm39)	T101M	probably benign	Het
Neb	T	A	2: 52,096,956 (GRCm39)	T4953S	probably benign	Het
Nfasc	A	C	1: 132,562,001 (GRCm39)	L147R	probably damaging	Het
Obox6	T	C	7: 15,567,805 (GRCm39)	E214G	probably benign	Het
Opn3	T	C	1: 175,493,039 (GRCm39)	N175S	probably damaging	Het
Or1j12	A	T	2: 36,342,851 (GRCm39)	M85L	probably benign	Het
Or8g22	T	A	9: 38,958,815 (GRCm39)		probably benign	Het
Or8k22	C	A	2: 86,163,136 (GRCm39)	C188F	possibly damaging	Het
Osbpl3	G	T	6: 50,323,410 (GRCm39)	D224E	probably benign	Het
Osr2	A	G	15: 35,301,032 (GRCm39)	D196G	probably damaging	Het
Pde8b	T	A	13: 95,179,442 (GRCm39)	N405Y	probably damaging	Het
Pirb	A	G	7: 3,719,177 (GRCm39)	S571P	probably benign	Het
Psmc3	T	A	2: 90,886,275 (GRCm39)	I163N	probably damaging	Het
Rapgef4	A	G	2: 72,038,445 (GRCm39)	D532G	probably damaging	Het
Retreg1	A	G	15: 25,971,684 (GRCm39)	D208G	probably benign	Het
Rgsl1	T	G	1: 153,679,876 (GRCm39)		probably null	Het
Ripk4	T	C	16: 97,545,157 (GRCm39)	T497A	probably benign	Het
Slc30a2	T	A	4: 134,076,581 (GRCm39)		probably null	Het
Slc6a19	T	C	13: 73,834,197 (GRCm39)	D335G	probably benign	Het
Slco4c1	G	A	1: 96,799,497 (GRCm39)	T113M	probably benign	Het
Speer1c	T	C	5: 10,295,192 (GRCm39)	N71D		Het
Stxbp6	A	G	12: 44,948,786 (GRCm39)	F108L	probably benign	Het
Sulf1	T	A	1: 12,921,189 (GRCm39)		probably null	Het
Syt16	C	T	12: 74,313,483 (GRCm39)	R470C	probably damaging	Het
Tbc1d19	T	A	5: 54,029,618 (GRCm39)	D326E	probably damaging	Het
Trappc14	T	C	5: 138,261,839 (GRCm39)	S86G	probably benign	Het
Trgv3	A	G	13: 19,427,188 (GRCm39)	T24A	probably benign	Het
Trpm3	T	A	19: 22,956,048 (GRCm39)	M1170K	possibly damaging	Het
Tubgcp6	G	A	15: 88,987,146 (GRCm39)	Q1276*	probably null	Het
Tyrp1	A	G	4: 80,755,821 (GRCm39)	K197E	possibly damaging	Het
Ube3d	T	C	9: 86,322,679 (GRCm39)	D165G	probably damaging	Het
Zfp212	A	G	6: 47,897,678 (GRCm39)	T7A	probably benign	Het
Zhx1	T	C	15: 57,917,758 (GRCm39)	T163A	probably benign	Het
Zp2	A	T	7: 119,734,576 (GRCm39)		probably null	Het

Other mutations in Dis3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00492:Dis3	APN	14	99,320,110 (GRCm39)	missense	probably damaging	1.00
IGL00821:Dis3	APN	14	99,328,922 (GRCm39)	missense	probably benign	0.00
IGL00975:Dis3	APN	14	99,316,670 (GRCm39)	missense	probably damaging	1.00
IGL01536:Dis3	APN	14	99,316,859 (GRCm39)	missense	probably damaging	1.00
IGL01538:Dis3	APN	14	99,335,181 (GRCm39)	missense	probably benign	0.00
IGL02143:Dis3	APN	14	99,328,754 (GRCm39)	splice site	probably benign
IGL02270:Dis3	APN	14	99,315,790 (GRCm39)	missense	probably benign	0.01
IGL02354:Dis3	APN	14	99,317,148 (GRCm39)	nonsense	probably null
IGL02361:Dis3	APN	14	99,317,148 (GRCm39)	nonsense	probably null
IGL02650:Dis3	APN	14	99,336,221 (GRCm39)	missense	probably benign	0.00
IGL03053:Dis3	APN	14	99,336,170 (GRCm39)	missense	probably benign	0.00
IGL03057:Dis3	APN	14	99,327,426 (GRCm39)	missense	possibly damaging	0.95
IGL03389:Dis3	APN	14	99,332,783 (GRCm39)	splice site	probably benign
R0415:Dis3	UTSW	14	99,324,892 (GRCm39)	missense	probably damaging	1.00
R0504:Dis3	UTSW	14	99,318,826 (GRCm39)	splice site	probably benign
R1535:Dis3	UTSW	14	99,316,862 (GRCm39)	missense	probably damaging	1.00
R1756:Dis3	UTSW	14	99,323,539 (GRCm39)	missense	probably damaging	1.00
R1767:Dis3	UTSW	14	99,321,578 (GRCm39)	missense	probably damaging	1.00
R1883:Dis3	UTSW	14	99,328,905 (GRCm39)	missense	probably benign	0.21
R1938:Dis3	UTSW	14	99,335,026 (GRCm39)	missense	probably benign	0.09
R2056:Dis3	UTSW	14	99,336,251 (GRCm39)	missense	possibly damaging	0.90
R2133:Dis3	UTSW	14	99,317,313 (GRCm39)	missense	probably benign	0.18
R2448:Dis3	UTSW	14	99,324,848 (GRCm39)	missense	probably damaging	0.99
R3407:Dis3	UTSW	14	99,336,212 (GRCm39)	missense	probably benign	0.15
R4052:Dis3	UTSW	14	99,332,752 (GRCm39)	missense	probably benign	0.00
R4207:Dis3	UTSW	14	99,332,752 (GRCm39)	missense	probably benign	0.00
R4208:Dis3	UTSW	14	99,332,752 (GRCm39)	missense	probably benign	0.00
R4465:Dis3	UTSW	14	99,321,550 (GRCm39)	missense	possibly damaging	0.88
R4612:Dis3	UTSW	14	99,328,871 (GRCm39)	missense	probably benign	0.07
R4859:Dis3	UTSW	14	99,325,226 (GRCm39)	missense	probably damaging	1.00
R4932:Dis3	UTSW	14	99,326,340 (GRCm39)	missense	probably damaging	1.00
R5273:Dis3	UTSW	14	99,336,242 (GRCm39)	missense	probably benign	0.32
R5335:Dis3	UTSW	14	99,335,089 (GRCm39)	missense	possibly damaging	0.72
R5409:Dis3	UTSW	14	99,323,368 (GRCm39)	missense	possibly damaging	0.95
R5802:Dis3	UTSW	14	99,337,100 (GRCm39)	missense	probably damaging	1.00
R6156:Dis3	UTSW	14	99,336,215 (GRCm39)	missense	probably benign	0.10
R6309:Dis3	UTSW	14	99,323,358 (GRCm39)	missense	probably benign	0.00
R7511:Dis3	UTSW	14	99,337,042 (GRCm39)	missense	possibly damaging	0.94
R7535:Dis3	UTSW	14	99,327,415 (GRCm39)	missense	probably benign	0.15
R7794:Dis3	UTSW	14	99,336,233 (GRCm39)	missense	probably benign	0.04
R8013:Dis3	UTSW	14	99,314,835 (GRCm39)	missense	possibly damaging	0.50
R8014:Dis3	UTSW	14	99,314,835 (GRCm39)	missense	possibly damaging	0.50
R8077:Dis3	UTSW	14	99,327,471 (GRCm39)	missense	probably benign	0.03
R8957:Dis3	UTSW	14	99,337,027 (GRCm39)	missense	probably damaging	1.00
R9072:Dis3	UTSW	14	99,332,647 (GRCm39)	missense	probably benign	0.44
R9073:Dis3	UTSW	14	99,332,647 (GRCm39)	missense	probably benign	0.44
R9345:Dis3	UTSW	14	99,318,814 (GRCm39)	missense	probably damaging	1.00
R9542:Dis3	UTSW	14	99,316,975 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTGAGGCAATCAAGACCCCG -3'
(R):5'- TACACTCTTAGCTAATGTGGTTCAG -3'

Sequencing Primer
(F):5'- TCAAGACCCCGTGCCCATC -3'
(R):5'- CATTGCATTTTGATCCGGGACAGAC -3'

Posted On

2019-06-26