Mutagenetix > Incidental Mutations

Incidental Mutation 'IGL03057:C4b'

409308

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

C4b

Ensembl Gene

ENSMUSG00000073418

Gene Name

complement component 4B (Chido blood group)

Synonyms

C4, Ss

Accession Numbers

Is this an essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL03057

Quality Score

Status

Chromosome

Chromosomal Location

34728380-34743882 bp(-) (GRCm38)

Type of Mutation

unclassified

DNA Base Change (assembly)

C to A at 34737764 bp

Zygosity

Heterozygous

Amino Acid Change

Gene Model

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

Predicted Effect

probably benign
Transcript: ENSMUST00000069507

SMART Domains

Protein: ENSMUSP00000069418
Gene: ENSMUSG00000073418

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

Coding Region Coverage

Validation Efficiency

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: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abi3bp	C	T	16: 56,668,391	A1295V	possibly damaging	Het
Adgre4	T	C	17: 55,799,602		probably benign	Het
Atp8b2	A	T	3: 89,944,186	Y901N	probably damaging	Het
Bud31	A	G	5: 145,146,568	T74A	probably benign	Het
Ccdc92	G	A	5: 124,835,689	Q259*	probably null	Het
Chfr	C	A	5: 110,143,609	Q98K	probably benign	Het
Ciita	T	A	16: 10,520,959		probably benign	Het
Cnbd2	A	T	2: 156,367,672	I512F	possibly damaging	Het
Cpa2	A	G	6: 30,557,727	Y346C	probably damaging	Het
Cpxm1	A	G	2: 130,393,189	L570P	probably damaging	Het
Cylc1	G	A	X: 111,122,601	G217D	unknown	Het
Dennd2a	T	C	6: 39,508,248	I366V	probably damaging	Het
Dis3	A	T	14: 99,089,990	M359K	possibly damaging	Het
Dock10	T	C	1: 80,567,371	N848S	probably damaging	Het
Dyrk3	C	T	1: 131,129,078	V453I	probably benign	Het
Ercc5	A	G	1: 44,167,001	E358G	probably damaging	Het
Fam167b	C	A	4: 129,578,167	C70F	possibly damaging	Het
Fam71a	A	T	1: 191,162,944	S501T	probably benign	Het
Flt1	G	T	5: 147,681,924	Y200*	probably null	Het
Ggh	T	C	4: 20,065,770	V288A	probably benign	Het
Glb1l2	T	C	9: 26,806,290		probably benign	Het
Gm28042	A	G	2: 120,032,156	Y302C	probably damaging	Het
Gsta2	A	G	9: 78,333,910		probably benign	Het
Idh3b	T	A	2: 130,284,401	N6I	probably benign	Het
Irs4	A	G	X: 141,722,528	S891P	unknown	Het
Kcmf1	G	T	6: 72,843,027	R330S	probably benign	Het
Kif26a	G	T	12: 112,175,774	E821*	probably null	Het
L3mbtl1	A	G	2: 162,967,383	E670G	probably damaging	Het
Met	A	T	6: 17,558,766	D1131V	probably damaging	Het
Neo1	T	C	9: 58,878,059	E1428G	probably damaging	Het
Odf2	A	G	2: 29,923,645		probably benign	Het
Ogfod1	T	A	8: 94,056,138	L294H	possibly damaging	Het
Olfr933	G	T	9: 38,976,218	V181F	probably benign	Het
Pcdhb20	A	T	18: 37,504,798	I126L	possibly damaging	Het
Pcdhb9	A	T	18: 37,401,277	Q108L	probably benign	Het
Prdm10	G	T	9: 31,349,185	R645L	probably damaging	Het
Psmb11	T	A	14: 54,625,779	C151*	probably null	Het
Reep1	T	A	6: 71,807,781		probably benign	Het
Reg3a	G	A	6: 78,381,956	A46T	possibly damaging	Het
Rnf213	T	A	11: 119,441,087	I2374N	probably damaging	Het
Slc17a7	T	C	7: 45,170,939	Y273H	probably damaging	Het
Smg6	T	A	11: 74,935,434	Y238*	probably null	Het
Sorcs1	T	A	19: 50,259,756	K411*	probably null	Het
Spta1	G	T	1: 174,181,058	A243S	probably benign	Het
Tas2r135	A	T	6: 42,401,127		probably benign	Het
Tbx18	T	C	9: 87,730,829	R6G	probably damaging	Het
Timp3	A	G	10: 86,300,951	D33G	possibly damaging	Het
Ttf1	A	G	2: 29,071,345	K582E	probably damaging	Het
Ubr5	C	A	15: 38,040,906		probably benign	Het
Ugt2b1	A	G	5: 86,926,341	V53A	possibly damaging	Het
Ush2a	G	T	1: 188,797,838	G3275W	probably damaging	Het
Usp19	G	A	9: 108,499,130	V1023M	probably benign	Het
Usp26	T	C	X: 51,757,258	I47V	possibly damaging	Het
Vapa	A	G	17: 65,594,907	V76A	probably damaging	Het
Vmn1r202	G	A	13: 22,501,470	T259I	probably benign	Het
Vps13a	T	C	19: 16,668,694	N1993S	probably damaging	Het
Wdr59	G	A	8: 111,476,118	R598C	probably damaging	Het
Wisp1	T	C	15: 66,891,640		probably benign	Het

Other mutations in C4b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00402:C4b	APN	17	34734428	missense	probably damaging	1.00
IGL00433:C4b	APN	17	34742041	missense	possibly damaging	0.75
IGL00471:C4b	APN	17	34734429	missense	probably damaging	1.00
IGL00515:C4b	APN	17	34728891	missense	probably damaging	1.00
IGL01599:C4b	APN	17	34743019	splice site	probably benign
IGL01761:C4b	APN	17	34739938	missense	possibly damaging	0.56
IGL02004:C4b	APN	17	34739010	unclassified	probably benign
IGL02215:C4b	APN	17	34734491	missense	probably damaging	1.00
IGL02517:C4b	APN	17	34734408	missense	probably benign	0.01
IGL02926:C4b	APN	17	34730712	missense	possibly damaging	0.95
IGL03031:C4b	APN	17	34731130	missense	possibly damaging	0.47
IGL03165:C4b	APN	17	34739955	missense	probably benign	0.13
IGL03380:C4b	APN	17	34740286	missense	probably benign	0.01
Aspiration	UTSW	17	34734442	missense	probably benign	0.00
Inspiration	UTSW	17	34732166	splice site	probably null
Peroration	UTSW	17	34729399	critical splice donor site	probably null
perspiration	UTSW	17	34729831	missense	probably damaging	1.00
FR4548:C4b	UTSW	17	34740997	missense	probably benign	0.00
PIT4142001:C4b	UTSW	17	34733701	missense	probably benign	0.01
R0064:C4b	UTSW	17	34738856	missense	probably damaging	1.00
R0113:C4b	UTSW	17	34741240	missense	probably damaging	0.98
R0143:C4b	UTSW	17	34734219	unclassified	probably benign
R0254:C4b	UTSW	17	34734776	missense	probably benign	0.00
R0320:C4b	UTSW	17	34733161	missense	probably benign	0.01
R0391:C4b	UTSW	17	34735614	splice site	probably benign
R0399:C4b	UTSW	17	34728869	missense	probably damaging	1.00
R0467:C4b	UTSW	17	34736127	missense	probably benign	0.01
R0549:C4b	UTSW	17	34735415	missense	probably damaging	1.00
R0561:C4b	UTSW	17	34734417	missense	probably damaging	0.99
R0662:C4b	UTSW	17	34730888	missense	probably damaging	1.00
R0941:C4b	UTSW	17	34740055	missense	probably benign
R1161:C4b	UTSW	17	34729593	missense	probably damaging	1.00
R1169:C4b	UTSW	17	34742972	missense	probably benign	0.14
R1186:C4b	UTSW	17	34736309	missense	possibly damaging	0.47
R1310:C4b	UTSW	17	34729593	missense	probably damaging	1.00
R1398:C4b	UTSW	17	34730719	unclassified	probably benign
R1472:C4b	UTSW	17	34743769	nonsense	probably null
R1496:C4b	UTSW	17	34740021	missense	probably benign	0.30
R1544:C4b	UTSW	17	34738967	missense	probably benign	0.13
R1588:C4b	UTSW	17	34741025	missense	probably benign
R1645:C4b	UTSW	17	34740597	missense	probably damaging	1.00
R1664:C4b	UTSW	17	34732978	missense	probably damaging	1.00
R1678:C4b	UTSW	17	34743650	missense	probably benign	0.05
R1710:C4b	UTSW	17	34743664	splice site	probably benign
R1713:C4b	UTSW	17	34729271	splice site	probably benign
R1770:C4b	UTSW	17	34736927	missense	possibly damaging	0.78
R1859:C4b	UTSW	17	34735553	missense	probably benign
R1924:C4b	UTSW	17	34729657	missense	probably damaging	1.00
R2057:C4b	UTSW	17	34728620	missense	probably damaging	1.00
R2060:C4b	UTSW	17	34736101	missense	probably damaging	1.00
R2184:C4b	UTSW	17	34737702	missense	probably benign	0.27
R2306:C4b	UTSW	17	34728518	missense	probably benign	0.00
R2363:C4b	UTSW	17	34736058	splice site	probably benign
R2365:C4b	UTSW	17	34736058	splice site	probably benign
R2379:C4b	UTSW	17	34735743	missense	possibly damaging	0.81
R2860:C4b	UTSW	17	34734758	missense	probably damaging	0.99
R2861:C4b	UTSW	17	34734758	missense	probably damaging	0.99
R3551:C4b	UTSW	17	34741872	missense	possibly damaging	0.75
R3765:C4b	UTSW	17	34729840	missense	probably damaging	0.98
R4157:C4b	UTSW	17	34742855	missense	probably damaging	1.00
R4299:C4b	UTSW	17	34731144	missense	possibly damaging	0.52
R4365:C4b	UTSW	17	34734743	missense	possibly damaging	0.65
R4411:C4b	UTSW	17	34728864	missense	probably damaging	1.00
R4613:C4b	UTSW	17	34734551	missense	probably benign	0.12
R4784:C4b	UTSW	17	34733406	missense	probably benign	0.00
R4790:C4b	UTSW	17	34734143	missense	probably benign	0.01
R4831:C4b	UTSW	17	34736890	splice site	probably null
R4879:C4b	UTSW	17	34743647	missense	probably damaging	0.99
R5036:C4b	UTSW	17	34740445	critical splice acceptor site	probably null
R5361:C4b	UTSW	17	34741238	missense	probably benign	0.15
R5384:C4b	UTSW	17	34737661	missense	possibly damaging	0.89
R5518:C4b	UTSW	17	34734442	missense	probably benign	0.00
R5590:C4b	UTSW	17	34740335	missense	probably damaging	0.98
R5643:C4b	UTSW	17	34742417	missense	probably benign	0.01
R5644:C4b	UTSW	17	34742417	missense	probably benign	0.01
R5833:C4b	UTSW	17	34730673	missense	probably damaging	1.00
R5931:C4b	UTSW	17	34729193	missense	probably damaging	0.99
R6178:C4b	UTSW	17	34733406	missense	probably benign	0.00
R6209:C4b	UTSW	17	34741087	missense	possibly damaging	0.93
R6225:C4b	UTSW	17	34738874	missense	possibly damaging	0.64
R6518:C4b	UTSW	17	34734205	missense	probably damaging	0.98
R6613:C4b	UTSW	17	34733565	missense	probably damaging	0.99
R6781:C4b	UTSW	17	34742954	missense	probably damaging	0.99
R6807:C4b	UTSW	17	34730956	missense	probably benign	0.17
R6858:C4b	UTSW	17	34729831	missense	probably damaging	1.00
R6962:C4b	UTSW	17	34732166	splice site	probably null
R7068:C4b	UTSW	17	34733477	missense	probably damaging	1.00
R7081:C4b	UTSW	17	34735443	missense	probably benign	0.27
R7105:C4b	UTSW	17	34730911	missense	possibly damaging	0.52
R7211:C4b	UTSW	17	34735534	missense	possibly damaging	0.92
R7296:C4b	UTSW	17	34743659	missense	probably damaging	1.00
R7314:C4b	UTSW	17	34740356	missense	probably benign
R7330:C4b	UTSW	17	34730472	missense	probably damaging	1.00
R7397:C4b	UTSW	17	34742390	missense	possibly damaging	0.80
R7437:C4b	UTSW	17	34734733	missense	probably benign	0.10
R7490:C4b	UTSW	17	34731080	nonsense	probably null
R7597:C4b	UTSW	17	34739675	missense	probably benign
R7633:C4b	UTSW	17	34729399	critical splice donor site	probably null
R7900:C4b	UTSW	17	34739777	missense	probably benign	0.03
R7910:C4b	UTSW	17	34740352	missense	probably benign	0.00
R7923:C4b	UTSW	17	34742380	missense	probably damaging	1.00
R7960:C4b	UTSW	17	34741278	splice site	probably null
R8420:C4b	UTSW	17	34734539	missense	probably damaging	0.97
R8467:C4b	UTSW	17	34732813	missense	possibly damaging	0.51
R8558:C4b	UTSW	17	34736567	missense	probably damaging	1.00
R8725:C4b	UTSW	17	34734485	missense	probably damaging	1.00
R8727:C4b	UTSW	17	34734485	missense	probably damaging	1.00
Z1176:C4b	UTSW	17	34731147	missense	probably damaging	0.97

Posted On

2016-08-02