Mutagenetix > Incidental Mutation

Incidental Mutation 'R2897:Csn1s2a'

260838

Institutional Source

Beutler Lab

Gene Symbol

Csn1s2a

Ensembl Gene

ENSMUSG00000061937

Gene Name

casein alpha s2-like A

Synonyms

Csn1s2a, Csng

MMRRC Submission

040485-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.062) question?

Stock #

R2897 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

87922426-87936656 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 87929680 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Arginine at position 93 (H93R)

Ref Sequence

ENSEMBL: ENSMUSP00000142901 (fasta)

Gene Model

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

AlphaFold

Q02862

Predicted Effect

unknown
Transcript: ENSMUST00000076379
AA Change: H101R

SMART Domains

Protein: ENSMUSP00000075716
Gene: ENSMUSG00000061937
AA Change: H101R

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

unknown
Transcript: ENSMUST00000196585
AA Change: H86R

SMART Domains

Protein: ENSMUSP00000143515
Gene: ENSMUSG00000061937
AA Change: H86R

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

unknown
Transcript: ENSMUST00000196749
AA Change: H100R

SMART Domains

Protein: ENSMUSP00000143715
Gene: ENSMUSG00000061937
AA Change: H100R

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

unknown
Transcript: ENSMUST00000200322
AA Change: H93R

SMART Domains

Protein: ENSMUSP00000142901
Gene: ENSMUSG00000061937
AA Change: H93R

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: ENSMUST00000200210

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000200350

Meta Mutation Damage Score

0.0869

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.5%
20x: 95.8%

Validation Efficiency

99% (72/73)

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2210408I21Rik	T	C	13: 77,471,640 (GRCm39)	V1015A	probably benign	Het
4930480E11Rik	C	T	X: 77,413,868 (GRCm39)	Q198*	probably null	Het
Acap3	G	C	4: 155,989,388 (GRCm39)		probably null	Het
Adamts14	T	C	10: 61,040,689 (GRCm39)	D879G	probably damaging	Het
Akap1	A	T	11: 88,735,605 (GRCm39)	C352*	probably null	Het
Ankk1	T	A	9: 49,333,122 (GRCm39)	T121S	probably benign	Het
Ankrd6	T	C	4: 32,860,438 (GRCm39)	S2G	probably damaging	Het
Anks1	G	T	17: 28,204,337 (GRCm39)		probably null	Het
Apob	G	A	12: 8,060,356 (GRCm39)	G2946D	probably damaging	Het
Atm	A	C	9: 53,419,105 (GRCm39)	C782W	probably damaging	Het
Atp1a4	A	T	1: 172,074,257 (GRCm39)	I332N	probably damaging	Het
Bnc2	T	C	4: 84,211,152 (GRCm39)	I406V	probably damaging	Het
Cdh20	A	T	1: 104,875,199 (GRCm39)	D327V	probably damaging	Het
Cep192	T	A	18: 67,988,341 (GRCm39)		probably null	Het
Chd5	T	C	4: 152,456,572 (GRCm39)	F970L	probably damaging	Het
Coq9	T	C	8: 95,579,752 (GRCm39)	Y236H	probably damaging	Het
Cxcr2	T	C	1: 74,198,130 (GRCm39)	V208A	probably benign	Het
Cyp1b1	G	A	17: 80,021,160 (GRCm39)	T194M	probably benign	Het
Dbt	T	A	3: 116,317,061 (GRCm39)	V79E	probably damaging	Het
Dcx	A	G	X: 142,706,428 (GRCm39)		probably benign	Het
Dnm3	G	A	1: 162,113,643 (GRCm39)		probably benign	Het
Erbin	C	T	13: 104,022,705 (GRCm39)	E45K	probably damaging	Het
Fastkd1	A	G	2: 69,532,960 (GRCm39)	L469P	probably damaging	Het
Gkn3	C	T	6: 87,360,507 (GRCm39)	A163T	probably damaging	Het
Gm10271	A	G	10: 116,808,495 (GRCm39)	L7S	probably damaging	Het
Gm5087	T	C	14: 13,158,805 (GRCm38)		noncoding transcript	Het
Hid1	A	G	11: 115,241,356 (GRCm39)	S645P	probably benign	Het
Hmcn1	C	T	1: 150,678,624 (GRCm39)	C499Y	probably damaging	Het
Ifna1	C	A	4: 88,768,450 (GRCm39)	Q43K	probably benign	Het
Ikbkb	G	T	8: 23,159,693 (GRCm39)	Q432K	possibly damaging	Het
Inpp4a	A	T	1: 37,405,675 (GRCm39)	H148L	probably benign	Het
Itpr2	C	T	6: 146,074,839 (GRCm39)	R2338Q	probably benign	Het
Itpr2	A	T	6: 146,224,667 (GRCm39)	I1441N	probably damaging	Het
Krt78	T	C	15: 101,855,541 (GRCm39)	R757G	probably benign	Het
Lmx1a	T	A	1: 167,658,109 (GRCm39)		probably benign	Het
Lpxn	T	A	19: 12,796,722 (GRCm39)	S81T	probably benign	Het
Lrriq1	T	C	10: 103,063,111 (GRCm39)	N65S	probably damaging	Het
Mis18bp1	T	C	12: 65,180,360 (GRCm39)	D981G	probably benign	Het
Mpp4	T	C	1: 59,183,853 (GRCm39)	I296V	probably benign	Het
Mtrf1l	T	C	10: 5,767,565 (GRCm39)	R184G	probably benign	Het
Muc19	T	C	15: 91,822,550 (GRCm39)		noncoding transcript	Het
Myo6	T	A	9: 80,176,893 (GRCm39)		probably null	Het
Myom1	A	G	17: 71,408,215 (GRCm39)		probably benign	Het
Ndrg4	A	G	8: 96,405,014 (GRCm39)		probably null	Het
Neu2	A	G	1: 87,522,782 (GRCm39)	S72G	probably benign	Het
Nlrc4	T	A	17: 74,755,040 (GRCm39)	M59L	probably benign	Het
Nuak2	A	T	1: 132,252,791 (GRCm39)	H115L	probably damaging	Het
Oog1	T	A	12: 87,655,178 (GRCm39)	I272K	probably damaging	Het
Or10aa1	T	C	1: 173,869,699 (GRCm39)	F61S	probably damaging	Het
Or52a20	A	T	7: 103,366,749 (GRCm39)	Y316F	probably benign	Het
Pcdhb1	A	G	18: 37,399,516 (GRCm39)	Y489C	probably damaging	Het
Pde5a	T	C	3: 122,572,651 (GRCm39)	I344T	probably benign	Het
Pip5kl1	C	A	2: 32,473,359 (GRCm39)	A332D	probably benign	Het
Pja1	T	C	X: 98,510,754 (GRCm39)	E385G	probably benign	Het
Psma6	A	T	12: 55,454,829 (GRCm39)	I53L	probably benign	Het
Ric8b	T	G	10: 84,783,761 (GRCm39)	D206E	probably benign	Het
Sardh	T	C	2: 27,079,559 (GRCm39)	D911G	probably benign	Het
Serpinb8	A	G	1: 107,534,776 (GRCm39)	T32A	unknown	Het
Shroom2	G	T	X: 151,443,035 (GRCm39)	T710K	probably benign	Het
Shroom3	G	T	5: 93,090,945 (GRCm39)	V1151F	probably damaging	Het
Slc38a7	A	G	8: 96,572,424 (GRCm39)		probably benign	Het
Stk36	T	A	1: 74,671,984 (GRCm39)	S895T	probably null	Het
Sycp3	G	A	10: 88,308,544 (GRCm39)	E205K	possibly damaging	Het
Tbc1d16	A	T	11: 119,048,654 (GRCm39)	I333N	probably damaging	Het
Tectb	C	G	19: 55,169,431 (GRCm39)		probably benign	Het
Tmeff1	T	A	4: 48,658,831 (GRCm39)	Y101*	probably null	Het
Tns2	C	T	15: 102,017,369 (GRCm39)	R281C	probably damaging	Het
Ttn	T	A	2: 76,549,500 (GRCm39)	T23399S	probably damaging	Het
Vipas39	A	G	12: 87,289,297 (GRCm39)	V389A	possibly damaging	Het
Vps41	T	C	13: 18,994,598 (GRCm39)		probably benign	Het
Zfp329	A	T	7: 12,544,413 (GRCm39)	H370Q	probably damaging	Het
Zfp37	C	T	4: 62,110,014 (GRCm39)	G350D	probably damaging	Het

Other mutations in Csn1s2a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00985:Csn1s2a	APN	5	87,932,439 (GRCm39)	missense	possibly damaging	0.83
IGL01829:Csn1s2a	APN	5	87,934,569 (GRCm39)	missense	unknown
R0137:Csn1s2a	UTSW	5	87,926,826 (GRCm39)	missense	possibly damaging	0.46
R1503:Csn1s2a	UTSW	5	87,923,658 (GRCm39)	missense	possibly damaging	0.66
R1799:Csn1s2a	UTSW	5	87,926,052 (GRCm39)	missense	probably damaging	0.97
R1870:Csn1s2a	UTSW	5	87,926,058 (GRCm39)	missense	probably benign	0.27
R2400:Csn1s2a	UTSW	5	87,928,014 (GRCm39)	critical splice donor site	probably null
R4034:Csn1s2a	UTSW	5	87,929,746 (GRCm39)	missense	probably benign	0.27
R4360:Csn1s2a	UTSW	5	87,929,700 (GRCm39)	missense	possibly damaging	0.46
R4377:Csn1s2a	UTSW	5	87,923,680 (GRCm39)	missense	probably benign
R4834:Csn1s2a	UTSW	5	87,929,637 (GRCm39)	missense	probably benign	0.27
R4965:Csn1s2a	UTSW	5	87,929,697 (GRCm39)	missense	possibly damaging	0.83
R6807:Csn1s2a	UTSW	5	87,929,731 (GRCm39)	missense	probably benign
R7115:Csn1s2a	UTSW	5	87,929,664 (GRCm39)	missense	probably benign	0.00
R7353:Csn1s2a	UTSW	5	87,933,161 (GRCm39)	missense	possibly damaging	0.66
R7420:Csn1s2a	UTSW	5	87,927,865 (GRCm39)	missense	possibly damaging	0.83
R8932:Csn1s2a	UTSW	5	87,933,164 (GRCm39)	missense	probably benign	0.05
R9074:Csn1s2a	UTSW	5	87,934,458 (GRCm39)	missense	probably benign

Predicted Primers

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

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

Posted On

2015-01-23