Mutagenetix > Incidental Mutation

Incidental Mutation 'R2861:C4b'

252763

Institutional Source

Beutler Lab

Gene Symbol

C4b

Ensembl Gene

ENSMUSG00000073418

Gene Name

complement component 4B (Chido blood group)

Synonyms

C4, Ss

MMRRC Submission

040451-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2861 (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 34734758 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Cysteine at position 959 (S959C)

Ref Sequence

ENSEMBL: ENSMUSP00000069418 (fasta)

Gene Model

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

AlphaFold

P01029

Predicted Effect

probably damaging
Transcript: ENSMUST00000069507
AA Change: S959C

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000069418
Gene: ENSMUSG00000073418
AA Change: S959C

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

0.6467

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.7%
20x: 96.1%

Validation Efficiency

100% (54/54)

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: 74 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4932438A13Rik	G	A	3: 36,965,849 (GRCm38)	S2079N	probably damaging	Het
Abca13	A	G	11: 9,309,057 (GRCm38)	S2928G	probably damaging	Het
Abcc9	C	T	6: 142,626,010 (GRCm38)	V1131M	probably benign	Het
Abcd1	T	A	X: 73,737,458 (GRCm38)	L713H	probably damaging	Het
Actg1	T	C	11: 120,346,801 (GRCm38)	I52V	probably benign	Het
Ang	G	T	14: 51,101,818 (GRCm38)	D139Y	probably damaging	Het
Ano1	C	T	7: 144,590,012 (GRCm38)	G1011E	probably damaging	Het
Apoe	T	C	7: 19,697,554 (GRCm38)	Y46C	probably damaging	Het
Ash1l	T	C	3: 89,054,478 (GRCm38)	W2386R	probably damaging	Het
Asph	T	C	4: 9,598,277 (GRCm38)	D250G	probably damaging	Het
Atr	A	G	9: 95,874,243 (GRCm38)	N836S	probably benign	Het
Btg3	A	G	16: 78,364,980 (GRCm38)	V114A	probably damaging	Het
C2	T	C	17: 34,863,878 (GRCm38)	T471A	possibly damaging	Het
Cap1	A	T	4: 122,864,725 (GRCm38)	S221T	probably benign	Het
Capn2	A	T	1: 182,472,920 (GRCm38)		probably benign	Het
Cd38	A	G	5: 43,901,433 (GRCm38)	S130G	probably damaging	Het
Cd8b1	A	G	6: 71,334,101 (GRCm38)	R202G	probably damaging	Het
Col22a1	A	G	15: 71,815,943 (GRCm38)		probably null	Het
Cps1	A	T	1: 67,166,375 (GRCm38)	E519V	probably benign	Het
Cyp2c38	G	A	19: 39,460,694 (GRCm38)	R72W	probably benign	Het
Cyp3a16	A	T	5: 145,455,499 (GRCm38)	Y215*	probably null	Het
F5	A	T	1: 164,184,964 (GRCm38)	K482N	probably damaging	Het
Fam212a	T	C	9: 107,984,404 (GRCm38)	T238A	probably benign	Het
Fam45a	T	C	19: 60,814,794 (GRCm38)	S80P	probably benign	Het
Gab1	T	C	8: 80,784,753 (GRCm38)	M488V	probably benign	Het
Gabpb1	A	G	2: 126,653,574 (GRCm38)	I86T	probably damaging	Het
Gbx2	C	T	1: 89,929,131 (GRCm38)	R179Q	probably damaging	Het
Gm11938	C	A	11: 99,603,146 (GRCm38)	R41L	probably damaging	Het
Gpn1	A	G	5: 31,497,320 (GRCm38)	D72G	probably damaging	Het
Greb1	A	G	12: 16,711,745 (GRCm38)	S545P	probably benign	Het
Hsd3b7	T	G	7: 127,802,270 (GRCm38)	L189R	probably damaging	Het
Iglc1	T	C	16: 19,061,910 (GRCm38)		probably benign	Het
Il18r1	T	C	1: 40,498,557 (GRCm38)	V494A	possibly damaging	Het
Itsn2	C	A	12: 4,700,315 (GRCm38)		probably benign	Het
Kcnn1	T	C	8: 70,846,535 (GRCm38)	K487R	probably benign	Het
Kdf1	G	A	4: 133,528,541 (GRCm38)	E190K	probably damaging	Het
Klhdc10	G	A	6: 30,402,140 (GRCm38)	R48H	unknown	Het
Lama3	G	T	18: 12,453,750 (GRCm38)	L723F	probably damaging	Het
Lama5	T	C	2: 180,187,247 (GRCm38)	T2034A	probably benign	Het
Maged1	G	A	X: 94,538,924 (GRCm38)	P366S	probably damaging	Het
Med14	A	G	X: 12,719,697 (GRCm38)	I521T	probably benign	Het
Mia2	A	G	12: 59,154,410 (GRCm38)	K841E	probably damaging	Het
Mrgbp	G	A	2: 180,583,410 (GRCm38)	R53Q	possibly damaging	Het
Mum1l1	G	A	X: 139,236,680 (GRCm38)	G656S	possibly damaging	Het
Nmnat2	G	A	1: 153,112,425 (GRCm38)	V267I	probably benign	Het
Olfr1305	G	T	2: 111,873,473 (GRCm38)	C127*	probably null	Het
Olfr231	A	G	1: 174,117,732 (GRCm38)	Y95H	probably damaging	Het
Olfr490	A	G	7: 108,286,962 (GRCm38)	S55P	probably damaging	Het
Olfr715b	T	A	7: 107,106,468 (GRCm38)	H131L	probably benign	Het
Opn4	A	G	14: 34,593,828 (GRCm38)		probably null	Het
Ovgp1	T	C	3: 105,986,567 (GRCm38)		probably benign	Het
Parp16	G	T	9: 65,233,804 (GRCm38)	D219Y	probably damaging	Het
Pitpnm2	G	C	5: 124,121,437 (GRCm38)	H1224Q	probably damaging	Het
Pkd1	C	T	17: 24,565,446 (GRCm38)	T322I	probably benign	Het
Pkhd1l1	A	C	15: 44,540,871 (GRCm38)	T2299P	probably damaging	Het
Plin4	T	C	17: 56,106,668 (GRCm38)	D319G	probably damaging	Het
Ppp6r3	A	C	19: 3,521,782 (GRCm38)	S122R	possibly damaging	Het
Rims1	A	T	1: 22,432,976 (GRCm38)	F653I	probably benign	Het
Rnf113a1	A	G	X: 37,192,083 (GRCm38)	E231G	probably damaging	Het
Rnf41	T	C	10: 128,438,154 (GRCm38)	L225P	possibly damaging	Het
Ryr2	T	C	13: 11,593,093 (GRCm38)	E876G	probably damaging	Het
Slc25a10	G	A	11: 120,495,177 (GRCm38)	V115M	probably damaging	Het
Snx13	T	A	12: 35,138,117 (GRCm38)	I798N	probably benign	Het
Sri	A	T	5: 8,067,540 (GRCm38)	Q178L	probably benign	Het
Tex14	T	G	11: 87,474,417 (GRCm38)	D62E	probably damaging	Het
Tshz1	G	T	18: 84,014,980 (GRCm38)	H434Q	probably damaging	Het
Vegfd	A	G	X: 164,385,883 (GRCm38)	E57G	probably damaging	Het
Vmn2r112	T	A	17: 22,603,115 (GRCm38)	V258E	probably damaging	Het
Vmn2r59	A	G	7: 42,047,003 (GRCm38)	I105T	possibly damaging	Het
Vmn2r6	G	T	3: 64,547,339 (GRCm38)	T513N	probably benign	Het
Vmn2r72	A	T	7: 85,750,836 (GRCm38)	I335N	probably damaging	Het
Wiz	G	T	17: 32,361,706 (GRCm38)	T257K	probably damaging	Het
Xirp1	A	G	9: 120,018,378 (GRCm38)	S41P	probably benign	Het
Xirp1	T	C	9: 120,019,815 (GRCm38)	M1V	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
R1770:C4b	UTSW	17	34,736,927 (GRCm38)	missense	possibly damaging	0.78
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
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'- GTTCCGAGGCTAAAGGACAG -3'
(R):5'- GGAAGTTCACATGCCAAGACC -3'

Sequencing Primer
(F):5'- TTCCGAGGCTAAAGGACAGAGAAG -3'
(R):5'- TTCACATGCCAAGACCCTGGG -3'

Posted On

2014-12-04