Mutagenetix > Incidental Mutation

Incidental Mutation 'R2010:C1s1'

219468

Institutional Source

Beutler Lab

Gene Symbol

C1s1

Ensembl Gene

ENSMUSG00000038521

Gene Name

complement component 1, s subcomponent 1

Synonyms

C1s

MMRRC Submission

040019-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.091) question?

Stock #

R2010 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

124507304-124519318 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 124514353 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Asparagine at position 168 (Y168N)

Ref Sequence

ENSEMBL: ENSMUSP00000125712 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000159463] [ENSMUST00000160505] [ENSMUST00000162443] [ENSMUST00000162844]

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000159143

Predicted Effect

probably benign
Transcript: ENSMUST00000159463

SMART Domains

Protein: ENSMUSP00000125439
Gene: ENSMUSG00000038521

Domain	Start	End	E-Value	Type
CUB	15	136	1.08e-29	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000160505
AA Change: Y168N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000125531
Gene: ENSMUSG00000038521
AA Change: Y168N

Domain	Start	End	E-Value	Type
CUB	15	136	1.08e-29	SMART
EGF_CA	137	178	1.79e-7	SMART
CUB	181	296	5.89e-31	SMART
CCP	300	360	3.22e-5	SMART
CCP	365	427	5.48e-8	SMART
Tryp_SPc	443	681	1.88e-70	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000160967

Predicted Effect

probably damaging
Transcript: ENSMUST00000162443
AA Change: Y168N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000125712
Gene: ENSMUSG00000038521
AA Change: Y168N

Domain	Start	End	E-Value	Type
CUB	15	136	1.08e-29	SMART
EGF_CA	137	178	1.79e-7	SMART
CUB	181	296	5.89e-31	SMART
CCP	300	360	3.22e-5	SMART
CCP	365	427	5.48e-8	SMART
Tryp_SPc	443	681	1.88e-70	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000162844

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.5%
20x: 92.6%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 78 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1810062G17Rik	G	A	3: 36,535,955 (GRCm39)	G74S	unknown	Het
Aimp1	A	T	3: 132,373,253 (GRCm39)	L229Q	probably benign	Het
Arhgef6	T	C	X: 56,344,865 (GRCm39)	T52A	possibly damaging	Het
Aste1	C	A	9: 105,280,701 (GRCm39)	H25Q	probably damaging	Het
Atp13a1	G	A	8: 70,244,010 (GRCm39)	G36R	possibly damaging	Het
Bahcc1	T	C	11: 120,163,604 (GRCm39)	V634A	probably damaging	Het
Bltp1	T	G	3: 36,982,700 (GRCm39)	N788K	probably benign	Het
Camsap2	T	C	1: 136,202,606 (GRCm39)	S612G	probably damaging	Het
Cdh23	C	A	10: 60,150,006 (GRCm39)	R2611L	probably damaging	Het
Cfap20dc	A	T	14: 8,511,021 (GRCm38)	F464L	probably damaging	Het
Cilp2	A	G	8: 70,334,344 (GRCm39)	Y885H	probably damaging	Het
Dhrs3	C	T	4: 144,653,758 (GRCm39)	T227I	possibly damaging	Het
Dnah2	A	T	11: 69,349,184 (GRCm39)		probably null	Het
Dnah3	T	G	7: 119,694,400 (GRCm39)	M1L	probably benign	Het
Ehbp1l1	A	G	19: 5,769,311 (GRCm39)	I664T	probably benign	Het
Eif4e	C	T	3: 138,261,219 (GRCm39)	T171I	probably benign	Het
Elfn1	C	T	5: 139,959,071 (GRCm39)	R692W	probably damaging	Het
Eps8l3	T	A	3: 107,786,688 (GRCm39)	M1K	probably null	Het
Evi5	C	A	5: 107,961,411 (GRCm39)		probably null	Het
Fancd2	A	T	6: 113,570,252 (GRCm39)	D1401V	probably damaging	Het
Fat2	G	A	11: 55,144,653 (GRCm39)	R4074C	probably damaging	Het
Fkbp4	A	T	6: 128,412,765 (GRCm39)	V55E	probably benign	Het
Fnip1	A	G	11: 54,373,329 (GRCm39)	D180G	probably damaging	Het
Galc	A	G	12: 98,220,489 (GRCm39)	F126S	possibly damaging	Het
Gdf7	C	T	12: 8,351,729 (GRCm39)	V69M	unknown	Het
Glis2	A	G	16: 4,426,575 (GRCm39)	E22G	probably damaging	Het
H2bc3	G	A	13: 23,931,111 (GRCm39)	V112M	possibly damaging	Het
Hps4	T	A	5: 112,517,342 (GRCm39)	V243E	probably damaging	Het
Ighe	T	A	12: 113,235,108 (GRCm39)	I351F	unknown	Het
Irak4	A	T	15: 94,449,687 (GRCm39)	R55S	probably damaging	Het
Itpr2	G	A	6: 146,129,022 (GRCm39)		probably null	Het
Katnip	A	G	7: 125,472,128 (GRCm39)	I1544M	possibly damaging	Het
Kirrel3	T	C	9: 34,850,494 (GRCm39)	Y41H	probably damaging	Het
Krr1	A	G	10: 111,811,474 (GRCm39)	E56G	possibly damaging	Het
Lgi1	G	A	19: 38,289,683 (GRCm39)	V250I	probably damaging	Het
Lipf	A	G	19: 33,950,946 (GRCm39)	N306D	probably benign	Het
Lman2l	C	T	1: 36,484,262 (GRCm39)	W18*	probably null	Het
Lztfl1	T	A	9: 123,531,251 (GRCm39)	N239I	possibly damaging	Het
Mief1	T	C	15: 80,132,126 (GRCm39)	S66P	possibly damaging	Het
Mmp8	C	A	9: 7,567,535 (GRCm39)	S465*	probably null	Het
Muc2	A	T	7: 141,287,444 (GRCm39)	T208S	probably damaging	Het
Myh8	A	T	11: 67,187,990 (GRCm39)	K921*	probably null	Het
Myh9	T	C	15: 77,656,147 (GRCm39)	E1121G	probably benign	Het
Nbn	T	C	4: 15,969,393 (GRCm39)	S213P	probably damaging	Het
Nol10	A	G	12: 17,466,102 (GRCm39)	E499G	probably benign	Het
Nxn	T	C	11: 76,289,627 (GRCm39)	E87G	probably damaging	Het
Or14c40	A	G	7: 86,313,811 (GRCm39)	T314A	probably benign	Het
Or51f2	T	A	7: 102,526,892 (GRCm39)	C188*	probably null	Het
Or8g23	T	C	9: 38,971,395 (GRCm39)	H189R	probably benign	Het
Pds5b	CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT	CATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTAT	5: 150,698,819 (GRCm39)		probably benign	Het
Pigk	A	G	3: 152,472,151 (GRCm39)	I354M	probably damaging	Het
Pigl	T	A	11: 62,349,508 (GRCm39)	C75S	probably damaging	Het
Pm20d1	T	A	1: 131,739,852 (GRCm39)	I400N	probably benign	Het
Prkg2	T	A	5: 99,172,664 (GRCm39)	H17L	probably benign	Het
Psmd1	T	A	1: 86,003,719 (GRCm39)	L168Q	probably damaging	Het
Rab3gap2	A	T	1: 185,010,478 (GRCm39)	H1136L	possibly damaging	Het
Rb1	T	C	14: 73,532,433 (GRCm39)	T134A	probably benign	Het
Rims1	T	C	1: 22,367,220 (GRCm39)	E1024G	probably damaging	Het
Rrp12	A	G	19: 41,861,376 (GRCm39)	V977A	probably benign	Het
Rusc2	C	T	4: 43,415,212 (GRCm39)	P173S	probably benign	Het
Selenov	A	T	7: 27,987,447 (GRCm39)	D310E	probably damaging	Het
Serpina3f	T	A	12: 104,183,582 (GRCm39)	L148Q	probably damaging	Het
Slc10a1	C	T	12: 81,007,221 (GRCm39)	V187I	probably benign	Het
Spsb2	A	G	6: 124,787,339 (GRCm39)	K258E	probably damaging	Het
Tas2r105	A	C	6: 131,664,365 (GRCm39)	V21G	probably benign	Het
Tmem229b-ps	T	A	10: 53,351,295 (GRCm39)		noncoding transcript	Het
Tnrc6a	C	G	7: 122,770,269 (GRCm39)	H686Q	probably benign	Het
Trpc2	T	A	7: 101,743,780 (GRCm39)	F715L	probably benign	Het
Ube2t	T	A	1: 134,897,036 (GRCm39)	I56N	probably benign	Het
Ubr4	T	C	4: 139,207,963 (GRCm39)	Y4915H	possibly damaging	Het
Usp32	T	A	11: 84,930,830 (GRCm39)	E533D	probably damaging	Het
Vipr2	T	G	12: 116,086,430 (GRCm39)		probably null	Het
Vmn1r15	A	G	6: 57,235,269 (GRCm39)	T46A	probably benign	Het
Vmn1r203	T	G	13: 22,708,617 (GRCm39)	S133A	possibly damaging	Het
Vmn1r215	T	G	13: 23,260,378 (GRCm39)	N139K	probably damaging	Het
Vmn1r232	C	T	17: 21,133,601 (GRCm39)	R333H	probably benign	Het
Wdr20rt	C	A	12: 65,273,988 (GRCm39)	H311N	possibly damaging	Het
Zranb1	T	C	7: 132,568,425 (GRCm39)		probably null	Het

Other mutations in C1s1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02225:C1s1	APN	6	124,518,293 (GRCm39)	missense	probably benign	0.02
IGL02590:C1s1	APN	6	124,508,235 (GRCm39)	missense	possibly damaging	0.89
IGL02968:C1s1	APN	6	124,517,310 (GRCm39)	missense	probably damaging	0.99
IGL03301:C1s1	APN	6	124,518,283 (GRCm39)	splice site	probably benign
BB008:C1s1	UTSW	6	124,510,359 (GRCm39)	missense	probably damaging	1.00
BB018:C1s1	UTSW	6	124,510,359 (GRCm39)	missense	probably damaging	1.00
R0105:C1s1	UTSW	6	124,518,277 (GRCm39)	splice site	probably benign
R0396:C1s1	UTSW	6	124,510,313 (GRCm39)	missense	probably benign	0.03
R0759:C1s1	UTSW	6	124,508,396 (GRCm39)	missense	probably damaging	1.00
R1145:C1s1	UTSW	6	124,517,759 (GRCm39)	missense	probably damaging	1.00
R1145:C1s1	UTSW	6	124,517,759 (GRCm39)	missense	probably damaging	1.00
R1396:C1s1	UTSW	6	124,508,010 (GRCm39)	missense	probably damaging	1.00
R1466:C1s1	UTSW	6	124,508,090 (GRCm39)	missense	probably damaging	1.00
R1466:C1s1	UTSW	6	124,508,090 (GRCm39)	missense	probably damaging	1.00
R1627:C1s1	UTSW	6	124,514,439 (GRCm39)	missense	probably damaging	1.00
R1855:C1s1	UTSW	6	124,511,315 (GRCm39)	critical splice donor site	probably null
R2349:C1s1	UTSW	6	124,518,432 (GRCm39)	start gained	probably benign
R4544:C1s1	UTSW	6	124,508,499 (GRCm39)	missense	probably benign	0.31
R4661:C1s1	UTSW	6	124,513,449 (GRCm39)	missense	probably benign	0.22
R5383:C1s1	UTSW	6	124,511,360 (GRCm39)	missense	probably damaging	1.00
R5687:C1s1	UTSW	6	124,517,909 (GRCm39)	missense	probably benign	0.01
R5846:C1s1	UTSW	6	124,517,912 (GRCm39)	missense	possibly damaging	0.93
R6289:C1s1	UTSW	6	124,508,135 (GRCm39)	missense	probably damaging	0.99
R6410:C1s1	UTSW	6	124,508,117 (GRCm39)	missense	probably damaging	1.00
R6983:C1s1	UTSW	6	124,517,855 (GRCm39)	missense	possibly damaging	0.93
R7931:C1s1	UTSW	6	124,510,359 (GRCm39)	missense	probably damaging	1.00
R8141:C1s1	UTSW	6	124,508,321 (GRCm39)	missense	probably damaging	1.00
R8341:C1s1	UTSW	6	124,508,115 (GRCm39)	missense	probably damaging	1.00
R8399:C1s1	UTSW	6	124,512,252 (GRCm39)	missense	probably benign	0.00
R8926:C1s1	UTSW	6	124,513,322 (GRCm39)	missense	possibly damaging	0.95
R8926:C1s1	UTSW	6	124,510,325 (GRCm39)	missense	probably damaging	1.00
R9008:C1s1	UTSW	6	124,509,499 (GRCm39)	critical splice donor site	probably null
R9147:C1s1	UTSW	6	124,517,758 (GRCm39)	missense	probably damaging	1.00
R9148:C1s1	UTSW	6	124,517,758 (GRCm39)	missense	probably damaging	1.00
R9153:C1s1	UTSW	6	124,517,906 (GRCm39)	missense	possibly damaging	0.78
R9177:C1s1	UTSW	6	124,508,362 (GRCm39)	missense	probably damaging	0.98
RF029:C1s1	UTSW	6	124,518,310 (GRCm39)	start codon destroyed	probably null

Predicted Primers

PCR Primer
(F):5'- TCCTGAGGATCCTATTCAGTTTG -3'
(R):5'- TGGAGAGTATTTAAGCAACAAACC -3'

Sequencing Primer
(F):5'- CAGTTTGTGAACAGCTAACAGC -3'
(R):5'- GTATTTAAGCAACAAACCTTTTCTGG -3'

Posted On

2014-08-25