Mutagenetix > Incidental Mutation

Incidental Mutation 'R1770:C4b'

196522

Institutional Source

Beutler Lab

Gene Symbol

C4b

Ensembl Gene

ENSMUSG00000073418

Gene Name

complement component 4B (Chido blood group)

Synonyms

C4, Ss

MMRRC Submission

039801-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1770 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

34728380-34743882 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 34736927 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Isoleucine at position 678 (N678I)

Ref Sequence

ENSEMBL: ENSMUSP00000069418 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000069507]

AlphaFold

P01029

Predicted Effect

possibly damaging
Transcript: ENSMUST00000069507
AA Change: N678I

PolyPhen 2 Score 0.781 (Sensitivity: 0.85; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000069418
Gene: ENSMUSG00000073418
AA Change: N678I

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
Pfam:A2M_N	138	231	2e-19	PFAM
A2M_N_2	470	609	2.87e-26	SMART
ANATO	700	734	3.58e-12	SMART
low complexity region	761	771	N/A	INTRINSIC
A2M	779	867	1.46e-27	SMART
Pfam:Thiol-ester_cl	995	1024	7.7e-13	PFAM
Pfam:A2M_comp	1047	1313	1.3e-82	PFAM
low complexity region	1441	1447	N/A	INTRINSIC
A2M_recep	1475	1564	1.03e-36	SMART
C345C	1608	1720	5.69e-40	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000173057

SMART Domains

Protein: ENSMUSP00000134611
Gene: ENSMUSG00000073418

Domain	Start	End	E-Value	Type
Pfam:A2M	1	62	6.5e-20	PFAM

Meta Mutation Damage Score

0.3140

Coding Region Coverage

1x: 97.4%
3x: 96.8%
10x: 95.1%
20x: 91.8%

Validation Efficiency

92% (69/75)

MGI Phenotype

PHENOTYPE: Homozygous C4 deficient mice have compromised immune responses. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9330182L06Rik	A	T	5: 9,418,021 (GRCm38)	T230S	probably benign	Het
Abcd4	T	C	12: 84,615,100 (GRCm38)	T84A	probably benign	Het
Adgra1	T	A	7: 139,874,031 (GRCm38)	Y161*	probably null	Het
Aldoart1	G	T	4: 72,851,936 (GRCm38)	H212N	probably benign	Het
Aldob	A	G	4: 49,536,861 (GRCm38)	Y343H	probably damaging	Het
Ankrd17	A	T	5: 90,243,376 (GRCm38)	V2036E	possibly damaging	Het
Ass1	A	G	2: 31,486,516 (GRCm38)	T131A	probably benign	Het
Baz1a	C	T	12: 54,898,508 (GRCm38)	R1354H	probably damaging	Het
C2cd2l	A	G	9: 44,316,811 (GRCm38)	V71A	probably benign	Het
Carmil1	A	G	13: 24,173,674 (GRCm38)	L64P	probably damaging	Het
Cdh18	T	C	15: 23,474,401 (GRCm38)	S786P	probably benign	Het
Cep135	A	G	5: 76,603,195 (GRCm38)	E296G	possibly damaging	Het
Chml	G	A	1: 175,687,878 (GRCm38)	T159I	probably benign	Het
Cntn3	C	T	6: 102,269,205 (GRCm38)	E328K	possibly damaging	Het
Cstf1	A	G	2: 172,373,063 (GRCm38)	I35V	possibly damaging	Het
Cyp2c65	A	G	19: 39,082,198 (GRCm38)	K275R	probably benign	Het
Dab1	C	T	4: 104,731,751 (GRCm38)	A524V	probably benign	Het
Dbx2	T	C	15: 95,624,734 (GRCm38)	E364G	probably benign	Het
Dcaf13	A	T	15: 39,130,238 (GRCm38)	N242I	probably damaging	Het
Dcc	A	G	18: 71,446,399 (GRCm38)	V701A	probably benign	Het
Fastkd5	A	T	2: 130,614,280 (GRCm38)	Y797N	probably damaging	Het
Fat4	T	A	3: 39,010,268 (GRCm38)	I4791K	probably damaging	Het
Gm3852	T	C	1: 46,011,888 (GRCm38)	I45V	possibly damaging	Het
Gng4	A	G	13: 13,825,266 (GRCm38)	D40G	probably damaging	Het
Gns	A	G	10: 121,378,047 (GRCm38)	D209G	probably benign	Het
Kif6	C	A	17: 49,903,649 (GRCm38)	Q791K	possibly damaging	Het
Klhl35	G	A	7: 99,473,875 (GRCm38)	V569M	possibly damaging	Het
Krt2	A	G	15: 101,811,154 (GRCm38)	S694P	unknown	Het
Lrrc8c	A	G	5: 105,606,737 (GRCm38)	Y126C	probably damaging	Het
Mad2l1bp	A	G	17: 46,152,912 (GRCm38)	V62A	probably benign	Het
Map1b	T	C	13: 99,430,493 (GRCm38)	R1907G	unknown	Het
Mertk	A	G	2: 128,750,174 (GRCm38)	I273V	probably benign	Het
Mfsd4b1	A	G	10: 40,003,227 (GRCm38)	Y225H	probably damaging	Het
Mrc2	T	C	11: 105,338,793 (GRCm38)	V684A	probably damaging	Het
Msh6	G	A	17: 87,980,223 (GRCm38)	W97*	probably null	Het
Mtmr10	A	G	7: 64,336,721 (GRCm38)	I516V	possibly damaging	Het
Myo7a	A	T	7: 98,112,606 (GRCm38)		probably benign	Het
Ndufs5	T	C	4: 123,712,868 (GRCm38)	Y92C	probably benign	Het
Nlrp1b	C	T	11: 71,160,153 (GRCm38)	V1035I	probably benign	Het
Ntrk2	A	G	13: 58,861,318 (GRCm38)	R308G	possibly damaging	Het
Olfr1148	A	G	2: 87,833,299 (GRCm38)	I87V	probably benign	Het
Pcdhb16	G	T	18: 37,479,180 (GRCm38)	G398W	probably damaging	Het
Plpbp	T	A	8: 27,053,298 (GRCm38)	S237T	probably damaging	Het
Pnpla6	T	A	8: 3,534,634 (GRCm38)	F769I	possibly damaging	Het
Polk	A	G	13: 96,495,442 (GRCm38)	V261A	probably damaging	Het
Prss52	C	T	14: 64,113,633 (GRCm38)	A289V	probably damaging	Het
Puf60	T	C	15: 76,070,874 (GRCm38)	K407E	probably benign	Het
Pzp	T	C	6: 128,485,617 (GRCm38)	D1455G	probably damaging	Het
Ranbp17	T	C	11: 33,217,301 (GRCm38)	N1054S	probably benign	Het
Sdk2	A	G	11: 113,793,741 (GRCm38)	S1965P	probably benign	Het
Spryd7	T	C	14: 61,540,205 (GRCm38)	Y142C	probably damaging	Het
Srrt	A	T	5: 137,299,860 (GRCm38)		probably benign	Het
Stk10	A	G	11: 32,622,464 (GRCm38)	E935G	possibly damaging	Het
Tas2r115	G	A	6: 132,737,971 (GRCm38)	R6C	probably damaging	Het
Tdrd7	T	A	4: 45,987,681 (GRCm38)		probably benign	Het
Trim29	A	T	9: 43,332,376 (GRCm38)	Q564L	probably damaging	Het
Trim5	T	C	7: 104,276,661 (GRCm38)	D231G	probably damaging	Het
Trpv2	A	G	11: 62,596,961 (GRCm38)	K676E	probably benign	Het
Ttn	T	C	2: 76,753,515 (GRCm38)	R22383G	probably damaging	Het
Ugt1a2	A	G	1: 88,201,438 (GRCm38)	I268V	probably benign	Het
Ugt8a	T	C	3: 125,874,203 (GRCm38)	N330D	probably benign	Het
Utrn	G	A	10: 12,475,296 (GRCm38)	H2822Y	probably damaging	Het
Vmn1r176	G	A	7: 23,835,521 (GRCm38)	A69V	probably benign	Het
Vmn2r106	T	C	17: 20,268,298 (GRCm38)	Y613C	probably damaging	Het
Wdfy1	A	T	1: 79,709,140 (GRCm38)	W296R	probably damaging	Het
Zfp11	G	A	5: 129,657,758 (GRCm38)	T213I	possibly damaging	Het
Zfp142	A	T	1: 74,579,631 (GRCm38)	F193I	probably damaging	Het
Zfp764	G	A	7: 127,405,567 (GRCm38)	Q131*	probably null	Het

Other mutations in C4b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00402:C4b	APN	17	34,734,428 (GRCm38)	missense	probably damaging	1.00
IGL00433:C4b	APN	17	34,742,041 (GRCm38)	missense	possibly damaging	0.75
IGL00471:C4b	APN	17	34,734,429 (GRCm38)	missense	probably damaging	1.00
IGL00515:C4b	APN	17	34,728,891 (GRCm38)	missense	probably damaging	1.00
IGL01599:C4b	APN	17	34,743,019 (GRCm38)	splice site	probably benign
IGL01761:C4b	APN	17	34,739,938 (GRCm38)	missense	possibly damaging	0.56
IGL02004:C4b	APN	17	34,739,010 (GRCm38)	unclassified	probably benign
IGL02215:C4b	APN	17	34,734,491 (GRCm38)	missense	probably damaging	1.00
IGL02517:C4b	APN	17	34,734,408 (GRCm38)	missense	probably benign	0.01
IGL02926:C4b	APN	17	34,730,712 (GRCm38)	missense	possibly damaging	0.95
IGL03031:C4b	APN	17	34,731,130 (GRCm38)	missense	possibly damaging	0.47
IGL03057:C4b	APN	17	34,737,764 (GRCm38)	unclassified	probably benign
IGL03165:C4b	APN	17	34,739,955 (GRCm38)	missense	probably benign	0.13
IGL03380:C4b	APN	17	34,740,286 (GRCm38)	missense	probably benign	0.01
Aspiration	UTSW	17	34,734,442 (GRCm38)	missense	probably benign	0.00
Inspiration	UTSW	17	34,732,166 (GRCm38)	splice site	probably null
Peroration	UTSW	17	34,729,399 (GRCm38)	critical splice donor site	probably null
perspiration	UTSW	17	34,729,831 (GRCm38)	missense	probably damaging	1.00
FR4548:C4b	UTSW	17	34,740,997 (GRCm38)	missense	probably benign	0.00
PIT4142001:C4b	UTSW	17	34,733,701 (GRCm38)	missense	probably benign	0.01
R0064:C4b	UTSW	17	34,738,856 (GRCm38)	missense	probably damaging	1.00
R0113:C4b	UTSW	17	34,741,240 (GRCm38)	missense	probably damaging	0.98
R0143:C4b	UTSW	17	34,734,219 (GRCm38)	unclassified	probably benign
R0254:C4b	UTSW	17	34,734,776 (GRCm38)	missense	probably benign	0.00
R0320:C4b	UTSW	17	34,733,161 (GRCm38)	missense	probably benign	0.01
R0391:C4b	UTSW	17	34,735,614 (GRCm38)	splice site	probably benign
R0399:C4b	UTSW	17	34,728,869 (GRCm38)	missense	probably damaging	1.00
R0467:C4b	UTSW	17	34,736,127 (GRCm38)	missense	probably benign	0.01
R0549:C4b	UTSW	17	34,735,415 (GRCm38)	missense	probably damaging	1.00
R0561:C4b	UTSW	17	34,734,417 (GRCm38)	missense	probably damaging	0.99
R0662:C4b	UTSW	17	34,730,888 (GRCm38)	missense	probably damaging	1.00
R0941:C4b	UTSW	17	34,740,055 (GRCm38)	missense	probably benign
R1161:C4b	UTSW	17	34,729,593 (GRCm38)	missense	probably damaging	1.00
R1169:C4b	UTSW	17	34,742,972 (GRCm38)	missense	probably benign	0.14
R1186:C4b	UTSW	17	34,736,309 (GRCm38)	missense	possibly damaging	0.47
R1310:C4b	UTSW	17	34,729,593 (GRCm38)	missense	probably damaging	1.00
R1398:C4b	UTSW	17	34,730,719 (GRCm38)	unclassified	probably benign
R1472:C4b	UTSW	17	34,743,769 (GRCm38)	nonsense	probably null
R1496:C4b	UTSW	17	34,740,021 (GRCm38)	missense	probably benign	0.30
R1544:C4b	UTSW	17	34,738,967 (GRCm38)	missense	probably benign	0.13
R1588:C4b	UTSW	17	34,741,025 (GRCm38)	missense	probably benign
R1645:C4b	UTSW	17	34,740,597 (GRCm38)	missense	probably damaging	1.00
R1664:C4b	UTSW	17	34,732,978 (GRCm38)	missense	probably damaging	1.00
R1678:C4b	UTSW	17	34,743,650 (GRCm38)	missense	probably benign	0.05
R1710:C4b	UTSW	17	34,743,664 (GRCm38)	splice site	probably benign
R1713:C4b	UTSW	17	34,729,271 (GRCm38)	splice site	probably benign
R1859:C4b	UTSW	17	34,735,553 (GRCm38)	missense	probably benign
R1924:C4b	UTSW	17	34,729,657 (GRCm38)	missense	probably damaging	1.00
R2057:C4b	UTSW	17	34,728,620 (GRCm38)	missense	probably damaging	1.00
R2060:C4b	UTSW	17	34,736,101 (GRCm38)	missense	probably damaging	1.00
R2184:C4b	UTSW	17	34,737,702 (GRCm38)	missense	probably benign	0.27
R2306:C4b	UTSW	17	34,728,518 (GRCm38)	missense	probably benign	0.00
R2363:C4b	UTSW	17	34,736,058 (GRCm38)	splice site	probably benign
R2365:C4b	UTSW	17	34,736,058 (GRCm38)	splice site	probably benign
R2379:C4b	UTSW	17	34,735,743 (GRCm38)	missense	possibly damaging	0.81
R2860:C4b	UTSW	17	34,734,758 (GRCm38)	missense	probably damaging	0.99
R2861:C4b	UTSW	17	34,734,758 (GRCm38)	missense	probably damaging	0.99
R3551:C4b	UTSW	17	34,741,872 (GRCm38)	missense	possibly damaging	0.75
R3765:C4b	UTSW	17	34,729,840 (GRCm38)	missense	probably damaging	0.98
R4157:C4b	UTSW	17	34,742,855 (GRCm38)	missense	probably damaging	1.00
R4299:C4b	UTSW	17	34,731,144 (GRCm38)	missense	possibly damaging	0.52
R4365:C4b	UTSW	17	34,734,743 (GRCm38)	missense	possibly damaging	0.65
R4411:C4b	UTSW	17	34,728,864 (GRCm38)	missense	probably damaging	1.00
R4613:C4b	UTSW	17	34,734,551 (GRCm38)	missense	probably benign	0.12
R4784:C4b	UTSW	17	34,733,406 (GRCm38)	missense	probably benign	0.00
R4790:C4b	UTSW	17	34,734,143 (GRCm38)	missense	probably benign	0.01
R4831:C4b	UTSW	17	34,736,890 (GRCm38)	splice site	probably null
R4879:C4b	UTSW	17	34,743,647 (GRCm38)	missense	probably damaging	0.99
R5036:C4b	UTSW	17	34,740,445 (GRCm38)	critical splice acceptor site	probably null
R5361:C4b	UTSW	17	34,741,238 (GRCm38)	missense	probably benign	0.15
R5384:C4b	UTSW	17	34,737,661 (GRCm38)	missense	possibly damaging	0.89
R5518:C4b	UTSW	17	34,734,442 (GRCm38)	missense	probably benign	0.00
R5590:C4b	UTSW	17	34,740,335 (GRCm38)	missense	probably damaging	0.98
R5643:C4b	UTSW	17	34,742,417 (GRCm38)	missense	probably benign	0.01
R5644:C4b	UTSW	17	34,742,417 (GRCm38)	missense	probably benign	0.01
R5833:C4b	UTSW	17	34,730,673 (GRCm38)	missense	probably damaging	1.00
R5931:C4b	UTSW	17	34,729,193 (GRCm38)	missense	probably damaging	0.99
R6178:C4b	UTSW	17	34,733,406 (GRCm38)	missense	probably benign	0.00
R6209:C4b	UTSW	17	34,741,087 (GRCm38)	missense	possibly damaging	0.93
R6225:C4b	UTSW	17	34,738,874 (GRCm38)	missense	possibly damaging	0.64
R6518:C4b	UTSW	17	34,734,205 (GRCm38)	missense	probably damaging	0.98
R6613:C4b	UTSW	17	34,733,565 (GRCm38)	missense	probably damaging	0.99
R6781:C4b	UTSW	17	34,742,954 (GRCm38)	missense	probably damaging	0.99
R6807:C4b	UTSW	17	34,730,956 (GRCm38)	missense	probably benign	0.17
R6858:C4b	UTSW	17	34,729,831 (GRCm38)	missense	probably damaging	1.00
R6962:C4b	UTSW	17	34,732,166 (GRCm38)	splice site	probably null
R7068:C4b	UTSW	17	34,733,477 (GRCm38)	missense	probably damaging	1.00
R7081:C4b	UTSW	17	34,735,443 (GRCm38)	missense	probably benign	0.27
R7105:C4b	UTSW	17	34,730,911 (GRCm38)	missense	possibly damaging	0.52
R7211:C4b	UTSW	17	34,735,534 (GRCm38)	missense	possibly damaging	0.92
R7296:C4b	UTSW	17	34,743,659 (GRCm38)	missense	probably damaging	1.00
R7314:C4b	UTSW	17	34,740,356 (GRCm38)	missense	probably benign
R7330:C4b	UTSW	17	34,730,472 (GRCm38)	missense	probably damaging	1.00
R7397:C4b	UTSW	17	34,742,390 (GRCm38)	missense	possibly damaging	0.80
R7437:C4b	UTSW	17	34,734,733 (GRCm38)	missense	probably benign	0.10
R7490:C4b	UTSW	17	34,731,080 (GRCm38)	nonsense	probably null
R7597:C4b	UTSW	17	34,739,675 (GRCm38)	missense	probably benign
R7633:C4b	UTSW	17	34,729,399 (GRCm38)	critical splice donor site	probably null
R7900:C4b	UTSW	17	34,739,777 (GRCm38)	missense	probably benign	0.03
R7910:C4b	UTSW	17	34,740,352 (GRCm38)	missense	probably benign	0.00
R7923:C4b	UTSW	17	34,742,380 (GRCm38)	missense	probably damaging	1.00
R7960:C4b	UTSW	17	34,741,278 (GRCm38)	splice site	probably null
R8420:C4b	UTSW	17	34,734,539 (GRCm38)	missense	probably damaging	0.97
R8467:C4b	UTSW	17	34,732,813 (GRCm38)	missense	possibly damaging	0.51
R8558:C4b	UTSW	17	34,736,567 (GRCm38)	missense	probably damaging	1.00
R8725:C4b	UTSW	17	34,734,485 (GRCm38)	missense	probably damaging	1.00
R8727:C4b	UTSW	17	34,734,485 (GRCm38)	missense	probably damaging	1.00
R8853:C4b	UTSW	17	34,729,905 (GRCm38)	missense	possibly damaging	0.91
R8934:C4b	UTSW	17	34,732,984 (GRCm38)	missense	possibly damaging	0.78
R8944:C4b	UTSW	17	34,742,939 (GRCm38)	missense	probably benign	0.00
R8960:C4b	UTSW	17	34,733,918 (GRCm38)	missense	probably damaging	1.00
R8982:C4b	UTSW	17	34,734,364 (GRCm38)	critical splice donor site	probably null
R9104:C4b	UTSW	17	34,729,259 (GRCm38)	missense	probably benign	0.39
R9114:C4b	UTSW	17	34,729,430 (GRCm38)	missense	probably damaging	0.99
R9348:C4b	UTSW	17	34,733,185 (GRCm38)	missense	probably benign	0.01
R9428:C4b	UTSW	17	34,730,911 (GRCm38)	missense	possibly damaging	0.52
R9533:C4b	UTSW	17	34,737,724 (GRCm38)	nonsense	probably null
R9591:C4b	UTSW	17	34,738,955 (GRCm38)	missense	probably benign	0.00
R9678:C4b	UTSW	17	34,741,789 (GRCm38)	critical splice donor site	probably null
Z1176:C4b	UTSW	17	34,731,147 (GRCm38)	missense	probably damaging	0.97

Predicted Primers

PCR Primer
(F):5'- ATGGACTGCACCAGCCAGC -3'
(R):5'- ATCGACTAACTCAAACCAGAGAGGGTAA -3'

Sequencing Primer
(F):5'- AGCCAGCCTCCACCCTC -3'
(R):5'- ctcctttttctgtgataactcctg -3'

Posted On

2014-05-23