Mutagenetix > Incidental Mutation

Incidental Mutation 'R4965:Csn1s2a'

383889

Institutional Source

Beutler Lab

Gene Symbol

Csn1s2a

Ensembl Gene

ENSMUSG00000061937

Gene Name

casein alpha s2-like A

Synonyms

Csn1s2a, Csng

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.064) question?

Stock #

R4965 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

87774567-87788797 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 87781838 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Arginine at position 99 (S99R)

Ref Sequence

ENSEMBL: ENSMUSP00000142901 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000076379] [ENSMUST00000196585] [ENSMUST00000196749] [ENSMUST00000200322]

AlphaFold

Q02862

Predicted Effect

possibly damaging
Transcript: ENSMUST00000076379
AA Change: S107R

PolyPhen 2 Score 0.827 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000075716
Gene: ENSMUSG00000061937
AA Change: S107R

Domain	Start	End	E-Value	Type
low complexity region	23	31	N/A	INTRINSIC
coiled coil region	58	86	N/A	INTRINSIC
low complexity region	102	115	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000196585
AA Change: S92R

PolyPhen 2 Score 0.827 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000143515
Gene: ENSMUSG00000061937
AA Change: S92R

Domain	Start	End	E-Value	Type
low complexity region	23	31	N/A	INTRINSIC
low complexity region	51	80	N/A	INTRINSIC
low complexity region	87	100	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000196749
AA Change: S106R

PolyPhen 2 Score 0.827 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000143715
Gene: ENSMUSG00000061937
AA Change: S106R

Domain	Start	End	E-Value	Type
low complexity region	23	31	N/A	INTRINSIC
coiled coil region	57	85	N/A	INTRINSIC
low complexity region	101	114	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000197019

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000197544

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000199200

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000200200

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000200210

Predicted Effect

possibly damaging
Transcript: ENSMUST00000200322
AA Change: S99R

PolyPhen 2 Score 0.827 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000142901
Gene: ENSMUSG00000061937
AA Change: S99R

Domain	Start	End	E-Value	Type
low complexity region	23	31	N/A	INTRINSIC
low complexity region	51	57	N/A	INTRINSIC
low complexity region	72	87	N/A	INTRINSIC
low complexity region	94	107	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000200350

Coding Region Coverage

1x: 99.0%
3x: 98.2%
10x: 95.7%
20x: 90.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 117 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110002E22Rik	A	G	3: 138,069,672	T1541A	probably benign	Het
2810474O19Rik	G	T	6: 149,328,398	G981*	probably null	Het
4931423N10Rik	C	A	2: 23,245,115	T312K	probably benign	Het
9530002B09Rik	T	C	4: 122,700,492	M59T	probably benign	Het
Adam18	C	T	8: 24,641,811	C428Y	probably damaging	Het
Adcy5	A	G	16: 35,278,502	E700G	possibly damaging	Het
Adprh	G	T	16: 38,445,780	Y333*	probably null	Het
Agfg2	C	A	5: 137,667,177		probably null	Het
Akip1	A	T	7: 109,711,754	E167V	probably damaging	Het
Akr1c21	A	T	13: 4,580,305	Q199L	probably damaging	Het
Aldh9a1	C	A	1: 167,365,789	A455E	probably damaging	Het
Amph	G	A	13: 19,137,699	S520N	probably benign	Het
Ankrd52	A	G	10: 128,390,507	D1006G	probably benign	Het
Ap5z1	A	C	5: 142,467,676	Q133P	probably damaging	Het
Babam1	C	T	8: 71,404,388	A331V	possibly damaging	Het
Btc	T	C	5: 91,362,301		probably null	Het
Cacna2d3	A	G	14: 28,982,332	F831L	probably benign	Het
Cadm3	G	A	1: 173,337,097	P372L	probably damaging	Het
Capn5	A	T	7: 98,126,417	M439K	probably damaging	Het
Carf	T	C	1: 60,150,637	S639P	probably damaging	Het
Casp12	C	T	9: 5,352,250	R81C	probably benign	Het
Ces2e	G	T	8: 104,933,698	R555M	probably benign	Het
Cfap54	T	A	10: 93,066,799	I164F	probably benign	Het
Cltc	C	T	11: 86,707,501	V1012I	probably damaging	Het
Cmya5	G	A	13: 93,095,787	T931I	possibly damaging	Het
Cntn6	A	G	6: 104,774,474	I364V	probably damaging	Het
Cntnap1	A	T	11: 101,177,425	I59F	possibly damaging	Het
Cop1	T	C	1: 159,239,597	M80T	probably damaging	Het
Cplx2	A	G	13: 54,379,647	S115G	possibly damaging	Het
Crtac1	A	G	19: 42,318,740	Y195H	probably damaging	Het
Csn1s2b	T	A	5: 87,813,961	D41E	possibly damaging	Het
Cul9	C	T	17: 46,538,525	D565N	probably damaging	Het
Cux1	A	T	5: 136,311,556	N625K	possibly damaging	Het
Cyp2c37	A	T	19: 40,011,762	M443L	possibly damaging	Het
Cyp2s1	G	A	7: 25,809,285	T244I	possibly damaging	Het
Dgkh	C	T	14: 78,624,421	V135M	probably damaging	Het
Dtl	T	C	1: 191,546,565	E395G	possibly damaging	Het
Dyrk1a	G	T	16: 94,691,995	G658*	probably null	Het
Erlin2	T	C	8: 27,029,595	F117S	probably damaging	Het
Fkbp8	A	G	8: 70,531,523		probably null	Het
Fras1	T	C	5: 96,726,580	F2288S	possibly damaging	Het
Frmd3	A	G	4: 74,153,600	T240A	probably damaging	Het
H2-D1	A	G	17: 35,263,905	Y137C	probably damaging	Het
Helz2	A	G	2: 181,240,916	V28A	possibly damaging	Het
Hydin	A	G	8: 110,398,095	I579V	probably benign	Het
Il6	A	T	5: 30,013,493	Y29F	possibly damaging	Het
Ildr2	A	G	1: 166,307,840	D368G	probably damaging	Het
Junb	T	A	8: 84,978,159	I91F	probably damaging	Het
Kat2a	C	A	11: 100,712,203		probably benign	Het
Kat2a	A	T	11: 100,712,204		probably benign	Het
Kcnh5	T	A	12: 74,965,151	T665S	probably benign	Het
Kdm1b	A	T	13: 47,074,367	D608V	probably damaging	Het
Krcc1	A	G	6: 71,284,637	K218E	probably damaging	Het
Krt8	C	T	15: 101,996,951	V488M	probably benign	Het
Lzts1	C	T	8: 69,138,762	A245T	probably benign	Het
Mcm6	T	A	1: 128,359,486	Q27L	probably damaging	Het
Mfsd4b3	G	T	10: 39,947,690	Y191*	probably null	Het
Mgme1	C	T	2: 144,276,404	Q199*	probably null	Het
Mgme1	T	C	2: 144,279,620	L332P	probably benign	Het
Morc3	G	T	16: 93,860,587	E25*	probably null	Het
Mroh7	G	A	4: 106,690,987	A1098V	possibly damaging	Het
Mtrf1	G	A	14: 79,406,587	R174H	probably benign	Het
Mybpc3	G	A	2: 91,119,247	G45D	possibly damaging	Het
Mycbpap	A	T	11: 94,504,938	N733K	probably damaging	Het
N4bp1	T	C	8: 86,851,686	I684V	possibly damaging	Het
Nav2	A	T	7: 49,552,877	R1470*	probably null	Het
Ndufa9	A	T	6: 126,822,063	S364T	probably benign	Het
Nipal4	C	A	11: 46,162,010	A43S	possibly damaging	Het
Nlrp1a	T	A	11: 71,092,315	Y1275F	possibly damaging	Het
Nova1	A	T	12: 46,720,835	L8*	probably null	Het
Odam	G	T	5: 87,890,108	G181*	probably null	Het
Olfr1111	T	A	2: 87,150,659	M1L	possibly damaging	Het
Olfr1297	T	C	2: 111,621,534	D180G	probably damaging	Het
Olfr15	T	C	16: 3,839,570	L199P	probably damaging	Het
Olfr186	A	T	16: 59,027,333	D191E	probably damaging	Het
Olfr283	T	C	15: 98,379,149		probably benign	Het
Olfr33	A	T	7: 102,713,495	I306N	probably damaging	Het
Olfr723	C	T	14: 49,928,897	V216I	probably benign	Het
Optn	T	A	2: 5,021,379	Q576L	probably benign	Het
Patl2	G	T	2: 122,128,848	S45*	probably null	Het
Pde2a	G	A	7: 101,502,933	G349E	probably benign	Het
Pdlim2	T	A	14: 70,168,015		probably benign	Het
Per1	T	C	11: 69,104,401	V653A	probably benign	Het
Phlda2	A	G	7: 143,502,268	S75P	probably damaging	Het
Poldip3	A	T	15: 83,137,505	M167K	possibly damaging	Het
Prpf38a	T	C	4: 108,579,081	I12V	probably benign	Het
Prrc1	G	A	18: 57,374,550	V259I	possibly damaging	Het
Ptges3l	A	T	11: 101,424,622	M1K	probably null	Het
Rdh5	A	G	10: 128,913,784	Y296H	probably damaging	Het
Rnf2	T	A	1: 151,473,217	K51*	probably null	Het
Rpusd3	C	A	6: 113,416,848	R215L	probably benign	Het
Rsph4a	A	T	10: 33,909,240	E382D	probably damaging	Het
S1pr2	G	A	9: 20,968,449	Q28*	probably null	Het
Sesn1	A	T	10: 41,895,009	I179F	probably damaging	Het
Setd3	T	A	12: 108,113,371	E291V	probably benign	Het
Shc1	G	T	3: 89,426,996	R323L	probably damaging	Het
Slc22a5	T	C	11: 53,891,526	D5G	possibly damaging	Het
Slc6a19	T	C	13: 73,700,558	K26E	probably benign	Het
Slc9a3	A	G	13: 74,164,293	N670D	possibly damaging	Het
Spata19	A	T	9: 27,400,465	I127L	probably benign	Het
Speg	G	T	1: 75,427,703	V2751L	probably damaging	Het
Sptbn2	A	G	19: 4,729,309	D298G	probably benign	Het
Srm	T	C	4: 148,594,183	V289A	possibly damaging	Het
Stip1	C	T	19: 7,035,570	A49T	probably benign	Het
Tas2r118	C	A	6: 23,969,628	V145F	probably benign	Het
Tbc1d12	A	T	19: 38,865,725	K284*	probably null	Het
Tfcp2	T	C	15: 100,525,650	H125R	probably damaging	Het
Tfdp1	T	C	8: 13,373,073	V206A	probably damaging	Het
Tgtp2	A	G	11: 49,059,410	W112R	probably damaging	Het
Tmem71	T	G	15: 66,538,861	M221L	probably benign	Het
Tpcn1	T	C	5: 120,547,487	N436S	possibly damaging	Het
Usp4	C	T	9: 108,362,620	L183F	probably damaging	Het
Vmn2r55	A	T	7: 12,670,551	N308K	possibly damaging	Het
Zfp106	T	A	2: 120,533,919	D669V	probably damaging	Het
Zfp108	A	T	7: 24,260,148	I55L	probably benign	Het
Zfp512b	A	T	2: 181,586,338	S8R	probably damaging	Het
Zfp827	T	C	8: 79,061,281	S359P	probably benign	Het

Other mutations in Csn1s2a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00985:Csn1s2a	APN	5	87784580	missense	possibly damaging	0.83
IGL01829:Csn1s2a	APN	5	87786710	missense	unknown
R0137:Csn1s2a	UTSW	5	87778967	missense	possibly damaging	0.46
R1503:Csn1s2a	UTSW	5	87775799	missense	possibly damaging	0.66
R1799:Csn1s2a	UTSW	5	87778193	missense	probably damaging	0.97
R1870:Csn1s2a	UTSW	5	87778199	missense	probably benign	0.27
R2400:Csn1s2a	UTSW	5	87780155	critical splice donor site	probably null
R2897:Csn1s2a	UTSW	5	87781821	missense	unknown
R4034:Csn1s2a	UTSW	5	87781887	missense	probably benign	0.27
R4360:Csn1s2a	UTSW	5	87781841	missense	possibly damaging	0.46
R4377:Csn1s2a	UTSW	5	87775821	missense	probably benign
R4834:Csn1s2a	UTSW	5	87781778	missense	probably benign	0.27
R6807:Csn1s2a	UTSW	5	87781872	missense	probably benign
R7115:Csn1s2a	UTSW	5	87781805	missense	probably benign	0.00
R7353:Csn1s2a	UTSW	5	87785302	missense	possibly damaging	0.66
R7420:Csn1s2a	UTSW	5	87780006	missense	possibly damaging	0.83
R8932:Csn1s2a	UTSW	5	87785305	missense	probably benign	0.05
R9074:Csn1s2a	UTSW	5	87786599	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- TGCTTTGTCAAACTGGCATAG -3'
(R):5'- AATCACACATGAATGGTTTTGCGTG -3'

Sequencing Primer
(F):5'- GACCTATGAAGAATAGTCACTAC -3'
(R):5'- CACATGAATGGTTTTGCGTGATTTAC -3'

Posted On

2016-04-27