Mutagenetix > Incidental Mutation

Incidental Mutation 'R4807:Trpc3'

370734

Institutional Source

Beutler Lab

Gene Symbol

Trpc3

Ensembl Gene

ENSMUSG00000027716

Gene Name

transient receptor potential cation channel, subfamily C, member 3

Synonyms

Trp3, Trcp3, Trrp3

MMRRC Submission

042426-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R4807 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

36674626-36744276 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 36688531 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Glutamine at position 836 (R836Q)

Ref Sequence

ENSEMBL: ENSMUSP00000029271 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000029271]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000029271
AA Change: R836Q

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)

SMART Domains

Protein: ENSMUSP00000029271
Gene: ENSMUSG00000027716
AA Change: R836Q

Domain	Start	End	E-Value	Type
low complexity region	20	45	N/A	INTRINSIC
low complexity region	47	68	N/A	INTRINSIC
ANK	100	129	2.47e2	SMART
ANK	135	163	1.97e1	SMART
ANK	221	250	1.13e1	SMART
Pfam:TRP_2	256	318	3e-28	PFAM
transmembrane domain	414	433	N/A	INTRINSIC
Pfam:Ion_trans	443	744	4.4e-34	PFAM
Pfam:PKD_channel	486	739	1.4e-14	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133542

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.9%
20x: 94.2%

Validation Efficiency

98% (86/88)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a membrane protein that can form a non-selective channel permeable to calcium and other cations. The encoded protein appears to be induced to form channels by a receptor tyrosine kinase-activated phosphatidylinositol second messenger system and also by depletion of intracellular calcium stores. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]
PHENOTYPE: Homozygous knockout mice or mice heterozygoous for a point mutation in exon 7 display an abnormal gait. Abnormal nervous system electrophysiology is also described. An A1903G point mutation in exon 7 results in homozygous lethality. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 84 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca16	C	T	7: 120,139,832 (GRCm39)	A1499V	probably damaging	Het
Agap3	T	A	5: 24,682,114 (GRCm39)	D386E	probably damaging	Het
Ahdc1	C	A	4: 132,791,624 (GRCm39)	T955K	possibly damaging	Het
Ankrd9	A	G	12: 110,943,669 (GRCm39)	Y122H	probably benign	Het
Apc2	G	T	10: 80,150,196 (GRCm39)	R1721L	probably benign	Het
Arfgef3	A	G	10: 18,522,385 (GRCm39)	V547A	probably benign	Het
Arhgap42	T	C	9: 9,046,629 (GRCm39)	N203D	possibly damaging	Het
Arl6ip1	AAAATAAATAAATAAATAAATAAATA	AAAATAAATAAATAAATAAATAAATAAATA	7: 117,721,122 (GRCm39)		probably benign	Het
Arsi	G	A	18: 61,049,723 (GRCm39)	G202E	probably benign	Het
Aspm	T	A	1: 139,405,657 (GRCm39)	F1515I	probably damaging	Het
Baz1a	T	C	12: 54,945,267 (GRCm39)	T1363A	probably benign	Het
Cacng3	C	T	7: 122,353,732 (GRCm39)	A72V	probably benign	Het
Casp8ap2	T	C	4: 32,644,505 (GRCm39)	C1193R	possibly damaging	Het
Ccr3	A	G	9: 123,829,334 (GRCm39)	Y223C	probably damaging	Het
Clcn3	C	A	8: 61,387,564 (GRCm39)	L201F	probably damaging	Het
Cltc	A	C	11: 86,591,902 (GRCm39)		probably benign	Het
Cyp19a1	G	T	9: 54,083,930 (GRCm39)	T86K	possibly damaging	Het
Ddx24	A	T	12: 103,385,720 (GRCm39)	F248L	probably damaging	Het
Ddx60	G	A	8: 62,432,372 (GRCm39)	V885I	probably damaging	Het
Dync2h1	T	C	9: 7,139,422 (GRCm39)	I1404M	probably benign	Het
Emilin2	A	T	17: 71,580,443 (GRCm39)	V761E	probably damaging	Het
Endou	C	T	15: 97,629,113 (GRCm39)	C13Y	probably benign	Het
Ep400	C	A	5: 110,843,444 (GRCm39)		probably null	Het
Fbxo33	C	A	12: 59,265,998 (GRCm39)	D90Y	probably damaging	Het
Fryl	A	G	5: 73,198,705 (GRCm39)	F2641L	probably benign	Het
Gbp2b	A	G	3: 142,304,006 (GRCm39)	I34V	probably benign	Het
Ghdc	T	C	11: 100,661,051 (GRCm39)	H38R	probably damaging	Het
Gm10722	T	C	9: 3,000,937 (GRCm39)	C6R	probably benign	Het
Gpr63	A	C	4: 25,007,446 (GRCm39)	M57L	probably benign	Het
Gprc5c	A	G	11: 114,755,324 (GRCm39)	S3G	probably damaging	Het
Grk4	A	T	5: 34,909,552 (GRCm39)	M539L	probably benign	Het
Gulo	C	T	14: 66,227,833 (GRCm39)	M366I	probably benign	Het
Heatr5a	T	C	12: 51,924,303 (GRCm39)	H1970R	probably damaging	Het
Hmbox1	T	C	14: 65,062,998 (GRCm39)		probably benign	Het
Ighg2b	T	C	12: 113,267,965 (GRCm39)		probably benign	Het
Il1b	A	T	2: 129,212,226 (GRCm39)	C9S	probably benign	Het
Itpkb	A	T	1: 180,162,440 (GRCm39)		probably benign	Het
Kcnn1	T	A	8: 71,300,822 (GRCm39)	H473L	probably damaging	Het
Kidins220	C	T	12: 25,107,284 (GRCm39)	S1579L	probably damaging	Het
Kif1b	A	T	4: 149,332,378 (GRCm39)		probably benign	Het
Lyg2	A	T	1: 37,950,148 (GRCm39)	M60K	possibly damaging	Het
Mak16	G	T	8: 31,656,161 (GRCm39)	H107Q	probably benign	Het
Mapkap1	G	A	2: 34,487,434 (GRCm39)		probably null	Het
Mastl	A	G	2: 23,022,855 (GRCm39)	S623P	probably benign	Het
Mccc1	T	C	3: 36,039,195 (GRCm39)	Y46C	probably damaging	Het
Mdn1	T	G	4: 32,685,651 (GRCm39)		probably null	Het
Med25	T	A	7: 44,534,043 (GRCm39)	T31S	probably benign	Het
Mprip	G	A	11: 59,648,846 (GRCm39)	G850D	probably benign	Het
Mrpl10	T	C	11: 96,932,449 (GRCm39)	I8T	probably benign	Het
Msr1	T	C	8: 40,095,668 (GRCm39)		probably benign	Het
Myo3b	T	A	2: 69,936,056 (GRCm39)	I99N	probably damaging	Het
Neurod6	A	T	6: 55,655,640 (GRCm39)	N332K	probably damaging	Het
Npc1l1	T	C	11: 6,168,723 (GRCm39)	Y886C	probably damaging	Het
Nsmaf	T	C	4: 6,398,542 (GRCm39)		probably null	Het
Ntn4	C	T	10: 93,480,362 (GRCm39)	R29C	probably damaging	Het
Or5d47	T	A	2: 87,804,095 (GRCm39)	I305L	probably benign	Het
Plppr2	A	G	9: 21,855,810 (GRCm39)	N261S	probably damaging	Het
Prkar2a	T	A	9: 108,617,584 (GRCm39)		probably benign	Het
Pxk	G	A	14: 8,144,133 (GRCm38)	V294M	probably damaging	Het
Rars1	A	G	11: 35,699,973 (GRCm39)	F608L	possibly damaging	Het
Rasa3	A	G	8: 13,664,633 (GRCm39)	F60L	probably damaging	Het
Rbm47	C	T	5: 66,176,647 (GRCm39)	A490T	possibly damaging	Het
Sardh	T	C	2: 27,079,539 (GRCm39)	I918V	probably benign	Het
Saxo5	A	G	8: 3,529,004 (GRCm39)	K193R	possibly damaging	Het
Sdhc	T	C	1: 170,963,626 (GRCm39)	Y80C	probably damaging	Het
Selp	T	A	1: 163,971,505 (GRCm39)	M653K	probably damaging	Het
Slc6a17	T	C	3: 107,407,803 (GRCm39)	D56G	possibly damaging	Het
Slco1b2	T	C	6: 141,615,195 (GRCm39)	S367P	probably damaging	Het
Spry4	TTGAGGTCC	T	18: 38,723,328 (GRCm39)		probably null	Het
Strip2	T	A	6: 29,925,092 (GRCm39)	Y143*	probably null	Het
Sycp2	T	C	2: 178,035,754 (GRCm39)		probably benign	Het
Tex30	C	A	1: 44,126,118 (GRCm39)	V204L	possibly damaging	Het
Tln2	G	T	9: 67,239,015 (GRCm39)	T1087K	probably benign	Het
Tmeff2	A	C	1: 51,018,546 (GRCm39)	N176T	probably benign	Het
Togaram2	C	G	17: 72,004,918 (GRCm39)	T324R	probably damaging	Het
Trpm7	A	C	2: 126,673,149 (GRCm39)	L535V	probably benign	Het
Vmn1r213	G	A	13: 23,195,775 (GRCm39)	W119*	probably null	Het
Vps29	T	G	5: 122,500,951 (GRCm39)	V176G	probably damaging	Het
Vsig10l	A	G	7: 43,113,173 (GRCm39)	T144A	possibly damaging	Het
Wdr11	T	C	7: 129,229,746 (GRCm39)	Y844H	probably benign	Het
Zbp1	A	T	2: 173,053,999 (GRCm39)	M174K	probably damaging	Het
Zfp341	G	A	2: 154,487,786 (GRCm39)		probably benign	Het
Zfp638	G	A	6: 83,920,040 (GRCm39)	R546H	probably damaging	Het
Zfp820	A	T	17: 22,042,853 (GRCm39)	M1K	probably null	Het

Other mutations in Trpc3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00913:Trpc3	APN	3	36,694,788 (GRCm39)	missense	possibly damaging	0.95
IGL01701:Trpc3	APN	3	36,725,743 (GRCm39)	missense	possibly damaging	0.92
IGL02254:Trpc3	APN	3	36,705,669 (GRCm39)	missense	probably null	0.98
IGL02723:Trpc3	APN	3	36,704,377 (GRCm39)	missense	probably benign	0.02
IGL02816:Trpc3	APN	3	36,705,851 (GRCm39)	missense	probably damaging	1.00
IGL02867:Trpc3	APN	3	36,694,850 (GRCm39)	missense	probably benign	0.10
IGL02929:Trpc3	APN	3	36,692,623 (GRCm39)	nonsense	probably null
IGL03076:Trpc3	APN	3	36,694,804 (GRCm39)	missense	probably damaging	1.00
R0032:Trpc3	UTSW	3	36,698,405 (GRCm39)	missense	probably damaging	1.00
R0032:Trpc3	UTSW	3	36,698,405 (GRCm39)	missense	probably damaging	1.00
R0115:Trpc3	UTSW	3	36,678,566 (GRCm39)	missense	probably benign	0.05
R0481:Trpc3	UTSW	3	36,678,566 (GRCm39)	missense	probably benign	0.05
R0645:Trpc3	UTSW	3	36,725,654 (GRCm39)	missense	probably benign	0.00
R0694:Trpc3	UTSW	3	36,725,704 (GRCm39)	missense	possibly damaging	0.48
R1190:Trpc3	UTSW	3	36,725,497 (GRCm39)	missense	probably benign	0.00
R1635:Trpc3	UTSW	3	36,694,776 (GRCm39)	missense	probably damaging	1.00
R1828:Trpc3	UTSW	3	36,692,695 (GRCm39)	missense	possibly damaging	0.95
R2204:Trpc3	UTSW	3	36,704,298 (GRCm39)	missense	possibly damaging	0.79
R2937:Trpc3	UTSW	3	36,688,532 (GRCm39)	nonsense	probably null
R3732:Trpc3	UTSW	3	36,692,708 (GRCm39)	missense	probably benign
R3732:Trpc3	UTSW	3	36,692,708 (GRCm39)	missense	probably benign
R3733:Trpc3	UTSW	3	36,692,708 (GRCm39)	missense	probably benign
R4063:Trpc3	UTSW	3	36,725,172 (GRCm39)	missense	probably damaging	1.00
R4270:Trpc3	UTSW	3	36,717,074 (GRCm39)	nonsense	probably null
R4996:Trpc3	UTSW	3	36,716,967 (GRCm39)	missense	probably benign	0.00
R5098:Trpc3	UTSW	3	36,717,047 (GRCm39)	missense	probably benign	0.07
R5139:Trpc3	UTSW	3	36,725,706 (GRCm39)	missense	possibly damaging	0.46
R5251:Trpc3	UTSW	3	36,725,103 (GRCm39)	missense	probably damaging	1.00
R5337:Trpc3	UTSW	3	36,692,519 (GRCm39)	intron	probably benign
R5891:Trpc3	UTSW	3	36,725,171 (GRCm39)	missense	probably damaging	1.00
R6512:Trpc3	UTSW	3	36,716,907 (GRCm39)	missense	possibly damaging	0.59
R6618:Trpc3	UTSW	3	36,694,844 (GRCm39)	missense	possibly damaging	0.82
R6750:Trpc3	UTSW	3	36,678,542 (GRCm39)	missense	probably damaging	1.00
R6950:Trpc3	UTSW	3	36,692,739 (GRCm39)	missense	probably damaging	1.00
R6986:Trpc3	UTSW	3	36,709,165 (GRCm39)	critical splice donor site	probably null
R7031:Trpc3	UTSW	3	36,675,459 (GRCm39)	missense	probably benign
R7100:Trpc3	UTSW	3	36,704,216 (GRCm39)	missense	probably benign	0.00
R7182:Trpc3	UTSW	3	36,709,258 (GRCm39)	missense	probably benign	0.02
R7211:Trpc3	UTSW	3	36,694,882 (GRCm39)	missense	possibly damaging	0.81
R7214:Trpc3	UTSW	3	36,704,286 (GRCm39)	missense	possibly damaging	0.94
R7284:Trpc3	UTSW	3	36,678,562 (GRCm39)	missense	probably damaging	0.98
R7468:Trpc3	UTSW	3	36,678,565 (GRCm39)	missense	probably damaging	0.99
R7652:Trpc3	UTSW	3	36,692,677 (GRCm39)	missense	probably benign	0.06
R7815:Trpc3	UTSW	3	36,709,294 (GRCm39)	missense	probably benign	0.28
R7833:Trpc3	UTSW	3	36,694,821 (GRCm39)	missense	probably damaging	0.96
R7977:Trpc3	UTSW	3	36,698,318 (GRCm39)	missense	probably benign	0.13
R7987:Trpc3	UTSW	3	36,698,318 (GRCm39)	missense	probably benign	0.13
R8778:Trpc3	UTSW	3	36,725,070 (GRCm39)	missense	probably damaging	0.99
R8959:Trpc3	UTSW	3	36,709,258 (GRCm39)	missense	probably benign	0.02
R9072:Trpc3	UTSW	3	36,694,831 (GRCm39)	missense	probably benign	0.01
R9175:Trpc3	UTSW	3	36,709,279 (GRCm39)	missense	probably benign	0.15
R9401:Trpc3	UTSW	3	36,675,503 (GRCm39)	nonsense	probably null
R9429:Trpc3	UTSW	3	36,705,777 (GRCm39)	missense	probably benign	0.01
R9563:Trpc3	UTSW	3	36,705,683 (GRCm39)	missense	probably benign	0.03
R9571:Trpc3	UTSW	3	36,694,909 (GRCm39)	missense	probably damaging	1.00
R9711:Trpc3	UTSW	3	36,692,713 (GRCm39)	missense	possibly damaging	0.81
Z1177:Trpc3	UTSW	3	36,675,428 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- CCCTGGGGTCAAACTCAATC -3'
(R):5'- AGTGTGGATTCCAGAAACGC -3'

Sequencing Primer
(F):5'- CCTGGGGTCAAACTCAATCTTAAG -3'
(R):5'- GTGGATTCCAGAAACGCCATCC -3'

Posted On

2016-02-04