Mutagenetix > Incidental Mutations

Incidental Mutation 'R0105:C1qtnf4'

33240

Institutional Source

Beutler Lab

Gene Symbol

C1qtnf4

Ensembl Gene

ENSMUSG00000040794

Gene Name

C1q and tumor necrosis factor related protein 4

Synonyms

0710001E10Rik, CTRP4, 9430004J15Rik

MMRRC Submission

038391-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.078) question?

Stock #

R0105 (G1)

Quality Score

131

Status

Validated (trace)

Chromosome

Chromosomal Location

90885860-90890525 bp(+) (GRCm38)

Type of Mutation

makesense

DNA Base Change (assembly)

T to A at 90890363 bp

Zygosity

Heterozygous

Amino Acid Change

Stop codon to Arginine at position 327 (*327R)

Ref Sequence

ENSEMBL: ENSMUSP00000107091 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000005647] [ENSMUST00000111466]

Predicted Effect

probably benign
Transcript: ENSMUST00000005647

SMART Domains

Protein: ENSMUSP00000005647
Gene: ENSMUSG00000005510

Domain	Start	End	E-Value	Type
Pfam:Complex1_30kDa	85	207	1.9e-43	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000111466
AA Change: *327R

SMART Domains

Protein: ENSMUSP00000107091
Gene: ENSMUSG00000040794
AA Change: *327R

Domain	Start	End	E-Value	Type
signal peptide	1	16	N/A	INTRINSIC
C1Q	22	158	1.51e-28	SMART
C1Q	166	312	2.47e-24	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000123426

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000139400

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000140248

Meta Mutation Damage Score

0.8588

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.0%
20x: 94.9%

Validation Efficiency

100% (70/70)

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2410089E03Rik	T	A	15: 8,187,392	V698D	probably benign	Het
5530400C23Rik	G	A	6: 133,294,314	R107K	probably benign	Het
A530053G22Rik	T	C	6: 60,402,152		noncoding transcript	Het
Adcy9	A	G	16: 4,288,388	V954A	probably damaging	Het
Aldh8a1	T	A	10: 21,395,539	M388K	probably damaging	Het
Ankhd1	A	G	18: 36,646,766	I1720M	probably damaging	Het
Atp6v0a4	T	C	6: 38,053,129		probably benign	Het
C1s1	T	C	6: 124,541,318		probably benign	Het
Cdsn	A	C	17: 35,556,138	R521S	possibly damaging	Het
Cgnl1	T	C	9: 71,656,102	M848V	probably benign	Het
Cog3	A	G	14: 75,722,140	S591P	probably damaging	Het
Col6a3	A	G	1: 90,798,161	V1375A	possibly damaging	Het
Cr1l	A	G	1: 195,112,412		probably benign	Het
Crmp1	T	A	5: 37,284,135	D520E	probably damaging	Het
Ctdspl2	T	A	2: 121,977,320		probably benign	Het
Dnah6	C	T	6: 73,155,279	A1147T	probably damaging	Het
Dsg2	T	C	18: 20,602,054	S1030P	probably benign	Het
Elavl3	C	A	9: 22,036,833	V12F	possibly damaging	Het
Fam20b	T	C	1: 156,690,570	E218G	probably damaging	Het
Fam227a	T	C	15: 79,620,832	D466G	possibly damaging	Het
Fto	G	A	8: 91,522,802	E421K	probably damaging	Het
Gab2	T	C	7: 97,299,072	Y290H	probably damaging	Het
Gm973	A	G	1: 59,582,474	Q591R	probably null	Het
Gsdmc2	T	C	15: 63,828,177	T249A	probably benign	Het
Il15ra	T	A	2: 11,730,648		probably null	Het
Il1rl1	CTTGTTGTTGTTGTTGTTG	CTTGTTGTTGTTGTTGTTGTTG	1: 40,442,574		probably benign	Het
Il6ra	A	G	3: 89,876,818	I382T	probably damaging	Het
Isy1	G	A	6: 87,819,185	R257W	probably damaging	Het
Krt76	T	C	15: 101,884,912	T564A	unknown	Het
Lhpp	T	C	7: 132,630,525	S57P	probably damaging	Het
Lrrk1	G	T	7: 66,292,341	D716E	probably damaging	Het
Mcm3ap	T	A	10: 76,499,534	D1263E	probably damaging	Het
Mogat1	A	G	1: 78,523,670	T124A	probably benign	Het
Mroh7	T	C	4: 106,711,270	T48A	possibly damaging	Het
Nccrp1	T	C	7: 28,547,038	D33G	probably benign	Het
Neurog1	G	T	13: 56,251,237	D232E	probably benign	Het
Olfr1202	T	A	2: 88,817,909	V246D	probably damaging	Het
Olfr1243	T	C	2: 89,528,363	T16A	probably benign	Het
Otog	C	A	7: 46,288,366	T1833K	possibly damaging	Het
Perm1	C	A	4: 156,218,225	H409N	probably benign	Het
Pik3r5	A	T	11: 68,490,511	E174D	probably damaging	Het
Pkhd1	G	A	1: 20,523,732	Q1386*	probably null	Het
Pla2r1	T	C	2: 60,514,981	R344G	possibly damaging	Het
Plekha5	G	A	6: 140,591,747	R646K	possibly damaging	Het
Plekhg4	G	A	8: 105,382,012	V1202M	possibly damaging	Het
Ppil4	A	G	10: 7,798,446	Y118C	probably damaging	Het
Prrc2b	G	T	2: 32,213,311	E934*	probably null	Het
Psmb9	A	G	17: 34,187,275	F12S	probably benign	Het
Ptdss2	T	C	7: 141,152,880	W183R	probably damaging	Het
Ptpn4	C	T	1: 119,687,605		probably null	Het
Reln	G	A	5: 22,048,815	R600W	probably damaging	Het
Scml4	T	A	10: 42,930,599	V161E	probably damaging	Het
Sdcbp2	A	T	2: 151,589,558	T284S	probably benign	Het
Slc22a29	T	C	19: 8,160,627		probably benign	Het
Slc35e1	T	C	8: 72,492,571		probably benign	Het
Spen	T	C	4: 141,469,810		probably benign	Het
Sumf2	T	A	5: 129,849,894		probably benign	Het
Tbx10	A	G	19: 3,993,121		probably benign	Het
Tex10	C	A	4: 48,468,957	V73F	probably damaging	Het
Tgm5	C	A	2: 121,077,012	G77W	probably damaging	Het
Tnfrsf21	T	A	17: 43,040,191		probably null	Het
Treml2	C	T	17: 48,302,828	T96I	probably damaging	Het
Trim65	T	C	11: 116,126,066	*523W	probably null	Het
Zcchc17	T	A	4: 130,349,306	D28V	probably benign	Het
Zhx2	T	C	15: 57,822,695	F487L	probably damaging	Het
Zkscan6	T	A	11: 65,821,985	L248Q	probably damaging	Het

Other mutations in C1qtnf4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0078:C1qtnf4	UTSW	2	90889549	missense	probably damaging	1.00
R1970:C1qtnf4	UTSW	2	90889659	missense	probably damaging	0.99
R4647:C1qtnf4	UTSW	2	90889652	missense	probably damaging	1.00
R5748:C1qtnf4	UTSW	2	90889533	missense	probably damaging	1.00
R6995:C1qtnf4	UTSW	2	90889953	missense	probably benign
R7274:C1qtnf4	UTSW	2	90889541	missense	probably damaging	1.00
X0063:C1qtnf4	UTSW	2	90890312	missense	probably damaging	1.00
Z1177:C1qtnf4	UTSW	2	90889505	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ACGCTGTCGGTGAAGCTGATGAAG -3'
(R):5'- TCATGACACAGGGCAGGACCATAAG -3'

Sequencing Primer
(F):5'- TGCAGGCCATGATTTACGAC -3'
(R):5'- GCAGGACCATAAGGCTGAC -3'

Posted On

2013-05-09