Mutagenetix > Incidental Mutation

Incidental Mutation 'R0399:C4b'

38085

Institutional Source

Beutler Lab

Gene Symbol

C4b

Ensembl Gene

ENSMUSG00000073418

Gene Name

complement component 4B (Chido blood group)

Synonyms

C4, Ss

MMRRC Submission

038604-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0399 (G1)

Quality Score

220

Status

Validated

Chromosome

Chromosomal Location

34728380-34743882 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 34728869 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Histidine at position 1657 (Q1657H)

Ref Sequence

ENSEMBL: ENSMUSP00000069418 (fasta)

Gene Model

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

AlphaFold

P01029

Predicted Effect

probably damaging
Transcript: ENSMUST00000069507
AA Change: Q1657H

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000069418
Gene: ENSMUSG00000073418
AA Change: Q1657H

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

noncoding transcript
Transcript: ENSMUST00000173669

Meta Mutation Damage Score

0.1797

Coding Region Coverage

1x: 99.2%
3x: 98.4%
10x: 96.5%
20x: 93.4%

Validation Efficiency

99% (71/72)

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: 70 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310035C23Rik	A	G	1: 105,750,959 (GRCm38)		probably benign	Het
6030452D12Rik	T	C	8: 106,504,542 (GRCm38)	M120T	unknown	Het
Actr1a	A	T	19: 46,385,011 (GRCm38)		probably null	Het
AI314180	T	C	4: 58,827,047 (GRCm38)	T1029A	possibly damaging	Het
Anapc5	A	T	5: 122,791,753 (GRCm38)	V555D	probably damaging	Het
Aox1	A	G	1: 58,068,849 (GRCm38)		probably null	Het
Arhgap30	A	G	1: 171,404,816 (GRCm38)	E343G	probably damaging	Het
Asap2	C	T	12: 21,217,997 (GRCm38)	T291I	possibly damaging	Het
Atp5a1	T	A	18: 77,781,836 (GRCm38)	Y439*	probably null	Het
Auts2	A	T	5: 131,440,524 (GRCm38)	S428T	probably benign	Het
B3gnt7	T	A	1: 86,305,711 (GRCm38)	C109*	probably null	Het
Cadm2	A	T	16: 66,747,339 (GRCm38)	L268*	probably null	Het
Cep290	G	A	10: 100,554,400 (GRCm38)		probably benign	Het
Cep68	T	G	11: 20,230,571 (GRCm38)	I687L	probably benign	Het
Chd6	T	A	2: 161,052,688 (GRCm38)	D84V	probably damaging	Het
Clpx	A	G	9: 65,322,769 (GRCm38)	T514A	probably benign	Het
Cox18	A	T	5: 90,215,028 (GRCm38)	C324S	probably benign	Het
Cryzl2	T	C	1: 157,462,016 (GRCm38)	Y75H	probably damaging	Het
Cxcr6	C	T	9: 123,810,951 (GRCm38)	A339V	possibly damaging	Het
Dock1	T	C	7: 135,163,442 (GRCm38)	L1721P	probably benign	Het
Dstyk	T	C	1: 132,453,080 (GRCm38)		probably benign	Het
Ehf	A	G	2: 103,266,870 (GRCm38)	Y246H	probably damaging	Het
Epas1	T	C	17: 86,805,193 (GRCm38)	V73A	probably benign	Het
Filip1	A	G	9: 79,818,310 (GRCm38)	I1009T	possibly damaging	Het
Glis3	A	T	19: 28,298,768 (GRCm38)		probably benign	Het
Gm17333	A	T	16: 77,852,790 (GRCm38)		noncoding transcript	Het
Gpc1	G	A	1: 92,857,309 (GRCm38)	R358H	possibly damaging	Het
Gpr155	A	T	2: 73,370,002 (GRCm38)	I387N	possibly damaging	Het
Gria1	A	G	11: 57,186,027 (GRCm38)	D83G	probably damaging	Het
Grid2	A	G	6: 64,666,052 (GRCm38)	I933V	probably benign	Het
Hhatl	C	T	9: 121,788,762 (GRCm38)	A254T	probably benign	Het
Hook2	A	G	8: 84,993,567 (GRCm38)		probably benign	Het
Ift140	T	A	17: 25,050,340 (GRCm38)	S656R	possibly damaging	Het
Il11ra1	A	T	4: 41,766,185 (GRCm38)	T241S	probably benign	Het
Kank1	A	G	19: 25,411,242 (GRCm38)	I760V	probably benign	Het
Kansl1	T	C	11: 104,424,132 (GRCm38)	E360G	possibly damaging	Het
Klf9	A	T	19: 23,142,082 (GRCm38)	S110C	probably damaging	Het
Klhl31	A	G	9: 77,650,653 (GRCm38)	N217S	probably benign	Het
Lct	T	C	1: 128,300,525 (GRCm38)	Y1077C	probably damaging	Het
Lrrc49	A	T	9: 60,610,246 (GRCm38)		probably benign	Het
Lrrn1	T	A	6: 107,569,120 (GRCm38)	H626Q	probably benign	Het
Mmp28	A	T	11: 83,451,732 (GRCm38)	L40Q	probably damaging	Het
Mroh1	C	T	15: 76,452,099 (GRCm38)	A1530V	probably benign	Het
Myo1e	A	G	9: 70,301,793 (GRCm38)		probably benign	Het
Naa25	A	T	5: 121,435,490 (GRCm38)	M761L	probably benign	Het
Ncln	G	A	10: 81,488,297 (GRCm38)	A465V	probably damaging	Het
Nktr	A	G	9: 121,731,484 (GRCm38)	N98S	probably damaging	Het
Olfr1012	T	C	2: 85,759,904 (GRCm38)	I157M	possibly damaging	Het
Olfr215	C	A	6: 116,582,781 (GRCm38)	S55I	probably benign	Het
Olfr651	T	A	7: 104,553,369 (GRCm38)	V150E	probably benign	Het
Olfr76	G	C	19: 12,120,370 (GRCm38)	A114G	possibly damaging	Het
Olfr878	G	T	9: 37,919,553 (GRCm38)	A304S	possibly damaging	Het
Pacsin2	T	C	15: 83,386,782 (GRCm38)	Y222C	probably damaging	Het
Pcdhb15	C	T	18: 37,474,168 (GRCm38)	T151M	possibly damaging	Het
Plcz1	C	A	6: 140,023,230 (GRCm38)	V161L	possibly damaging	Het
Ppp6c	G	A	2: 39,200,124 (GRCm38)		probably benign	Het
Rhbdf2	T	A	11: 116,603,992 (GRCm38)	Y286F	probably benign	Het
Rtn3	A	T	19: 7,457,876 (GRCm38)	D231E	probably damaging	Het
Slc35c2	A	C	2: 165,280,895 (GRCm38)	Y156*	probably null	Het
Spata46	A	G	1: 170,311,537 (GRCm38)	D35G	probably damaging	Het
Tmed3	A	G	9: 89,702,873 (GRCm38)	F110L	possibly damaging	Het
Tmem104	T	G	11: 115,201,308 (GRCm38)		probably benign	Het
Tpbg	T	A	9: 85,844,938 (GRCm38)	V320E	possibly damaging	Het
Trib2	T	C	12: 15,793,663 (GRCm38)	D190G	probably damaging	Het
Tspan2	A	G	3: 102,759,385 (GRCm38)	T26A	probably damaging	Het
Usp17lb	A	C	7: 104,841,151 (GRCm38)	Y190D	possibly damaging	Het
Utp18	C	T	11: 93,880,147 (GRCm38)		probably benign	Het
Utp20	A	T	10: 88,820,979 (GRCm38)	D121E	probably damaging	Het
Vmn1r80	T	A	7: 12,193,317 (GRCm38)	M118K	possibly damaging	Het
Vmn1r84	T	C	7: 12,361,867 (GRCm38)	S300G	probably benign	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
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
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'- CCCCAAAAGGAAGGTCACAGGTATG -3'
(R):5'- CGTCTCTTTGAGTCCAAGATCACCC -3'

Sequencing Primer
(F):5'- GTCACAGGTATGAGGAGAGC -3'
(R):5'- CAAGTCCTGCATTTCAGTAGGAAG -3'

Posted On

2013-05-23