Mutagenetix > Incidental Mutation

Incidental Mutation 'R0373:U2surp'

65624

Institutional Source

Beutler Lab

Gene Symbol

U2surp

Ensembl Gene

ENSMUSG00000032407

Gene Name

U2 snRNP-associated SURP domain containing

Synonyms

2610101N10Rik

MMRRC Submission

038579-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.956) question?

Stock #

R0373 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

95456898-95511996 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 95484443 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Isoleucine at position 470 (V470I)

Ref Sequence

ENSEMBL: ENSMUSP00000151121 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078374] [ENSMUST00000079659] [ENSMUST00000191213] [ENSMUST00000217176]

AlphaFold

Q6NV83

Predicted Effect

probably benign
Transcript: ENSMUST00000078374
AA Change: V427I

PolyPhen 2 Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)

SMART Domains

Protein: ENSMUSP00000077482
Gene: ENSMUSG00000032407
AA Change: V427I

Domain	Start	End	E-Value	Type
low complexity region	18	27	N/A	INTRINSIC
low complexity region	54	75	N/A	INTRINSIC
coiled coil region	148	186	N/A	INTRINSIC
RRM	231	307	1.85e-18	SMART
low complexity region	313	323	N/A	INTRINSIC
SWAP	384	438	1.07e-20	SMART
RPR	493	632	1.42e-41	SMART
internal_repeat_1	648	665	6.09e-7	PROSPERO
internal_repeat_1	678	698	6.09e-7	PROSPERO
coiled coil region	742	769	N/A	INTRINSIC
cwf21	792	843	6.31e-17	SMART
low complexity region	881	933	N/A	INTRINSIC
low complexity region	939	985	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000079659
AA Change: V471I

PolyPhen 2 Score 0.052 (Sensitivity: 0.94; Specificity: 0.83)

SMART Domains

Protein: ENSMUSP00000078602
Gene: ENSMUSG00000032407
AA Change: V471I

Domain	Start	End	E-Value	Type
low complexity region	18	27	N/A	INTRINSIC
low complexity region	98	119	N/A	INTRINSIC
coiled coil region	192	230	N/A	INTRINSIC
RRM	275	351	1.85e-18	SMART
low complexity region	357	367	N/A	INTRINSIC
SWAP	428	482	1.07e-20	SMART
RPR	537	676	1.42e-41	SMART
internal_repeat_1	692	709	1.14e-6	PROSPERO
internal_repeat_1	722	742	1.14e-6	PROSPERO
coiled coil region	786	813	N/A	INTRINSIC
cwf21	836	887	6.31e-17	SMART
low complexity region	925	977	N/A	INTRINSIC
low complexity region	983	1029	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000186139

Predicted Effect

probably benign
Transcript: ENSMUST00000191213

SMART Domains

Protein: ENSMUSP00000140614
Gene: ENSMUSG00000032407

Domain	Start	End	E-Value	Type
low complexity region	18	27	N/A	INTRINSIC
low complexity region	98	119	N/A	INTRINSIC
coiled coil region	192	230	N/A	INTRINSIC
RRM	275	351	7.8e-21	SMART
low complexity region	357	367	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000217176
AA Change: V470I

PolyPhen 2 Score 0.076 (Sensitivity: 0.93; Specificity: 0.85)

Meta Mutation Damage Score

0.0844

Coding Region Coverage

1x: 99.1%
3x: 98.1%
10x: 95.8%
20x: 91.5%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 93 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930579F01Rik	A	T	3: 138,173,582	L235Q	probably damaging	Het
Adam6b	T	A	12: 113,490,655	V364D	probably benign	Het
Akap13	T	C	7: 75,609,929	L767P	probably benign	Het
Akap13	T	A	7: 75,730,500	S2193T	probably damaging	Het
Anapc11	T	C	11: 120,605,377	V69A	probably benign	Het
Ankmy1	C	T	1: 92,896,190	R118Q	probably damaging	Het
Ankrd27	T	C	7: 35,638,053	S931P	probably benign	Het
Atp6v1c2	G	A	12: 17,288,168	R280C	probably damaging	Het
Bbs10	T	A	10: 111,300,052	I342N	probably damaging	Het
Calhm2	T	C	19: 47,132,950	D260G	possibly damaging	Het
Camk2a	A	G	18: 60,958,238	E264G	probably damaging	Het
Ccdc146	T	A	5: 21,319,545	M270L	probably benign	Het
Cdc16	A	G	8: 13,779,264	T517A	probably benign	Het
Ces1g	T	C	8: 93,331,193	H160R	probably benign	Het
Chst4	T	C	8: 110,030,394	N196S	probably damaging	Het
Ciz1	A	T	2: 32,367,467	N175Y	probably damaging	Het
Cyb5r4	G	A	9: 87,027,040	V57I	probably damaging	Het
Cyth3	A	G	5: 143,684,426		probably benign	Het
Def6	A	G	17: 28,220,180	E255G	probably damaging	Het
Dhtkd1	T	G	2: 5,911,870	Q665P	probably damaging	Het
Dsg3	A	C	18: 20,539,747	D825A	probably damaging	Het
Eif3m	T	C	2: 105,005,000	T242A	probably benign	Het
Emilin3	A	G	2: 160,909,817	F101L	probably benign	Het
Epha7	A	G	4: 28,935,700		probably null	Het
Fam205a1	T	C	4: 42,851,161	I332V	probably benign	Het
Fbxo45	A	T	16: 32,238,405	Y224N	probably damaging	Het
Fhod3	A	T	18: 25,090,104	M836L	possibly damaging	Het
Fut4	C	A	9: 14,751,210	V263F	probably damaging	Het
Ggt1	C	T	10: 75,579,270	T206M	probably benign	Het
Gls	T	C	1: 52,188,699	R79G	probably damaging	Het
Gm436	A	T	4: 144,686,220	M50K	possibly damaging	Het
Grhl1	T	C	12: 24,581,515	S156P	probably benign	Het
Ipo8	C	T	6: 148,775,042	S983N	probably benign	Het
Kcna7	C	T	7: 45,409,444	A385V	probably damaging	Het
Kpnb1	A	T	11: 97,185,090	L40Q	probably damaging	Het
Matn1	A	T	4: 130,950,106	S209C	probably damaging	Het
Mcc	A	G	18: 44,475,222	I501T	probably benign	Het
Mdp1	A	T	14: 55,659,375	F104L	probably damaging	Het
Mib2	A	T	4: 155,656,288	N626K	probably damaging	Het
Mrgprh	T	C	17: 12,876,956	S28P	possibly damaging	Het
Mup-ps23	T	A	4: 61,856,149		noncoding transcript	Het
Myh15	A	G	16: 49,182,959	T1794A	possibly damaging	Het
Myo18a	C	G	11: 77,821,042	P680A	probably benign	Het
Myom2	G	T	8: 15,098,419	D532Y	possibly damaging	Het
Ndufaf5	A	G	2: 140,170,881	N57S	probably benign	Het
Nectin3	C	T	16: 46,458,187	V282M	probably damaging	Het
Nup188	G	T	2: 30,330,988	D997Y	probably damaging	Het
Olfm3	T	C	3: 115,122,805	V462A	probably damaging	Het
Olfr1044	A	C	2: 86,171,706	F37C	probably damaging	Het
Olfr1225	A	T	2: 89,170,413	F266L	probably benign	Het
Olfr305	A	T	7: 86,363,805	C177*	probably null	Het
Opcml	A	G	9: 28,813,398	H164R	possibly damaging	Het
Pacrg	A	G	17: 10,403,418	I209T	probably damaging	Het
Pcf11	T	C	7: 92,661,215	M522V	probably benign	Het
Pck1	T	A	2: 173,153,390	M1K	probably null	Het
Pcm1	G	T	8: 41,276,111	E707*	probably null	Het
Pcsk5	G	A	19: 17,654,849	R318W	probably damaging	Het
Phf11d	A	T	14: 59,353,344	M188K	possibly damaging	Het
Ppip5k2	A	T	1: 97,740,537	C615*	probably null	Het
Prkdc	T	A	16: 15,791,927	S3132T	probably damaging	Het
Prl2c5	A	T	13: 13,183,024		probably benign	Het
Prpsap2	A	G	11: 61,741,000	I177T	possibly damaging	Het
Rad50	A	G	11: 53,650,519	S1297P	probably damaging	Het
Rasip1	T	A	7: 45,635,244	N678K	possibly damaging	Het
Rubcn	A	G	16: 32,835,980	S544P	probably damaging	Het
Rwdd2a	A	T	9: 86,574,400	T210S	possibly damaging	Het
Scd2	A	G	19: 44,303,040	D306G	probably damaging	Het
Sema3b	T	C	9: 107,602,918	N207S	probably benign	Het
Sf3b2	C	T	19: 5,274,824	D845N	probably damaging	Het
Sipa1l2	C	A	8: 125,464,410	C947F	probably damaging	Het
Slc12a1	A	T	2: 125,226,031	T1013S	probably damaging	Het
Slc18a2	A	T	19: 59,287,367	I461L	probably benign	Het
Slc1a6	C	A	10: 78,801,922	Y427*	probably null	Het
Slc30a4	A	T	2: 122,689,399	I231K	probably damaging	Het
Sos1	G	T	17: 80,453,763	A168D	probably damaging	Het
Sptb	T	C	12: 76,621,371	S651G	probably benign	Het
Stk36	T	C	1: 74,633,620	L1007P	probably damaging	Het
Tek	A	T	4: 94,804,341	N229Y	probably damaging	Het
Tep1	A	G	14: 50,836,768	F1887L	possibly damaging	Het
Tet1	A	T	10: 62,878,209	C602*	probably null	Het
Tnfrsf19	A	G	14: 60,972,036	S262P	possibly damaging	Het
Trim5	T	C	7: 104,265,684	I393V	probably benign	Het
Trpm6	A	G	19: 18,853,587	E1272G	probably benign	Het
Ttc21b	A	T	2: 66,188,326	Y1246N	probably damaging	Het
Ttll3	T	A	6: 113,398,777	L151H	probably damaging	Het
Ubr1	A	T	2: 120,946,657	Y276N	probably benign	Het
Uggt1	A	G	1: 36,179,670	S59P	probably benign	Het
Unc45a	T	C	7: 80,326,344	T796A	probably damaging	Het
Unc5b	C	A	10: 60,778,940	V193F	possibly damaging	Het
Upp1	G	T	11: 9,129,590	M50I	probably benign	Het
Vps18	C	T	2: 119,293,905	R438C	probably damaging	Het
Zfp715	T	C	7: 43,299,336	Y400C	possibly damaging	Het
Zfp955b	T	C	17: 33,302,522	Y322H	probably benign	Het

Other mutations in U2surp

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00583:U2surp	APN	9	95461524	utr 3 prime	probably benign
IGL01122:U2surp	APN	9	95490234	missense	probably benign	0.02
IGL01985:U2surp	APN	9	95490226	missense	probably damaging	1.00
IGL01992:U2surp	APN	9	95464419	missense	possibly damaging	0.46
IGL01992:U2surp	APN	9	95482181	missense	probably damaging	0.99
IGL02300:U2surp	APN	9	95488770	missense	probably damaging	1.00
IGL02491:U2surp	APN	9	95490220	missense	probably damaging	0.98
IGL02503:U2surp	APN	9	95502569	missense	probably benign	0.03
IGL02615:U2surp	APN	9	95493231	missense	probably benign	0.00
IGL02628:U2surp	APN	9	95472090	missense	possibly damaging	0.89
IGL02682:U2surp	APN	9	95481651	critical splice donor site	probably null
IGL02721:U2surp	APN	9	95474435	missense	probably benign	0.10
IGL03200:U2surp	APN	9	95491391	nonsense	probably null
coup	UTSW	9	95477512	missense	probably damaging	1.00
R0095:U2surp	UTSW	9	95500684	splice site	probably null
R0376:U2surp	UTSW	9	95484443	missense	probably benign	0.08
R0377:U2surp	UTSW	9	95484443	missense	probably benign	0.08
R0416:U2surp	UTSW	9	95485607	missense	probably damaging	1.00
R0682:U2surp	UTSW	9	95484443	missense	probably benign	0.08
R0948:U2surp	UTSW	9	95461497	utr 3 prime	probably benign
R1420:U2surp	UTSW	9	95462803	missense	probably benign	0.33
R1474:U2surp	UTSW	9	95493198	missense	possibly damaging	0.49
R1555:U2surp	UTSW	9	95466577	missense	probably damaging	1.00
R1597:U2surp	UTSW	9	95481740	splice site	probably benign
R1638:U2surp	UTSW	9	95484227	missense	possibly damaging	0.95
R1693:U2surp	UTSW	9	95511860	start codon destroyed	probably null	0.53
R1851:U2surp	UTSW	9	95482097	nonsense	probably null
R2271:U2surp	UTSW	9	95491420	missense	possibly damaging	0.80
R2679:U2surp	UTSW	9	95476232	missense	possibly damaging	0.82
R2851:U2surp	UTSW	9	95500682	splice site	probably null
R3769:U2surp	UTSW	9	95493697	splice site	probably benign
R4596:U2surp	UTSW	9	95485628	missense	probably damaging	1.00
R4672:U2surp	UTSW	9	95493145	missense	possibly damaging	0.83
R4763:U2surp	UTSW	9	95511791	intron	probably benign
R4995:U2surp	UTSW	9	95462794	utr 3 prime	probably benign
R5805:U2surp	UTSW	9	95479304	missense	possibly damaging	0.51
R6006:U2surp	UTSW	9	95479307	missense	probably damaging	0.96
R6249:U2surp	UTSW	9	95500816	missense	probably benign	0.07
R6260:U2surp	UTSW	9	95476157	missense	probably damaging	0.99
R6378:U2surp	UTSW	9	95491421	missense	probably benign	0.41
R6487:U2surp	UTSW	9	95477512	missense	probably damaging	1.00
R6585:U2surp	UTSW	9	95472071	missense	probably damaging	1.00
R6721:U2surp	UTSW	9	95491104	missense	probably damaging	0.99
R6760:U2surp	UTSW	9	95493711	missense	probably benign	0.27
R7065:U2surp	UTSW	9	95485659	missense	probably benign	0.01
R7167:U2surp	UTSW	9	95481673	missense	probably damaging	0.98
R7219:U2surp	UTSW	9	95490162	nonsense	probably null
R7232:U2surp	UTSW	9	95493717	missense	probably benign	0.03
R7460:U2surp	UTSW	9	95462824	missense	unknown
R7547:U2surp	UTSW	9	95479349	missense	possibly damaging	0.94
R7609:U2surp	UTSW	9	95485679	splice site	probably null
R7761:U2surp	UTSW	9	95488761	missense	probably damaging	1.00
R8520:U2surp	UTSW	9	95502554	missense	possibly damaging	0.88
R9059:U2surp	UTSW	9	95481663	missense	probably damaging	1.00
R9065:U2surp	UTSW	9	95477510	missense	probably benign
R9124:U2surp	UTSW	9	95464415	nonsense	probably null
R9266:U2surp	UTSW	9	95484415	missense	probably damaging	1.00
R9488:U2surp	UTSW	9	95474482	missense
X0018:U2surp	UTSW	9	95475288	missense	probably benign	0.14
X0018:U2surp	UTSW	9	95485597	missense	probably damaging	0.98

Predicted Primers

Posted On

2013-08-08