Mutagenetix > Incidental Mutation

Incidental Mutation 'R8821:Atp2c2'

686588

Institutional Source

Beutler Lab

Gene Symbol

Atp2c2

Ensembl Gene

ENSMUSG00000034112

Gene Name

ATPase, Ca++ transporting, type 2C, member 2

Synonyms

1810010G06Rik

MMRRC Submission

068654-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R8821 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

120426748-120484456 bp(+) (GRCm39)

Type of Mutation

splice site (100 bp from exon)

DNA Base Change (assembly)

A to G at 120476033 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000092794 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000095171]

AlphaFold

A7L9Z8

Predicted Effect

probably null
Transcript: ENSMUST00000095171

SMART Domains

Protein: ENSMUSP00000092794
Gene: ENSMUSG00000034112

Domain	Start	End	E-Value	Type
Cation_ATPase_N	54	128	1.27e-12	SMART
Pfam:E1-E2_ATPase	133	366	1.7e-62	PFAM
Pfam:Hydrolase	371	684	5.3e-18	PFAM
Pfam:HAD	374	681	7.4e-11	PFAM
Pfam:Cation_ATPase	437	521	1.1e-17	PFAM
Pfam:Cation_ATPase_C	754	927	1.1e-47	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

100% (74/74)

Allele List at MGI

Other mutations in this stock

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A230072I06Rik	A	T	8: 12,329,688 (GRCm39)	I48L	unknown	Het
Abca8a	A	T	11: 109,949,362 (GRCm39)	I927K	probably damaging	Het
Abcc3	A	C	11: 94,241,787 (GRCm39)	C1415G	probably damaging	Het
Abcf3	C	T	16: 20,369,214 (GRCm39)	R205C	probably damaging	Het
Aldh3a1	A	G	11: 61,107,142 (GRCm39)	Y282C	probably damaging	Het
Alyref	CCCGCGCGGCGGCCTGCACTGCGCCGCCGCGGCCGCCCTGGGAGCCGGCCCTGCCGCG	CCCGCG	11: 120,489,023 (GRCm39)		probably null	Het
Arfgef3	A	G	10: 18,528,491 (GRCm39)	S299P	possibly damaging	Het
Asic2	A	T	11: 81,858,726 (GRCm39)	N95K	probably damaging	Het
Btbd18	A	G	2: 84,497,601 (GRCm39)	D413G	probably damaging	Het
C8b	A	G	4: 104,647,874 (GRCm39)	Y355C	probably damaging	Het
Carm1	A	G	9: 21,491,663 (GRCm39)	E244G	probably damaging	Het
Castor2	T	A	5: 134,164,092 (GRCm39)	V96E	possibly damaging	Het
Catsperg1	A	T	7: 28,904,361 (GRCm39)		probably benign	Het
Cish	T	A	9: 107,177,671 (GRCm39)	F116I	probably damaging	Het
Ckmt1	G	A	2: 121,191,302 (GRCm39)		probably benign	Het
Clasrp	C	T	7: 19,320,362 (GRCm39)	R432H	unknown	Het
Clstn1	G	A	4: 149,730,780 (GRCm39)	R837Q	probably benign	Het
Col27a1	A	G	4: 63,143,148 (GRCm39)	T279A	probably benign	Het
Cox10	A	G	11: 63,855,306 (GRCm39)	F325S	probably damaging	Het
Cpne5	T	C	17: 29,430,668 (GRCm39)	I81V	probably benign	Het
Ctps1	A	T	4: 120,424,507 (GRCm39)	S36T	possibly damaging	Het
Dchs2	T	C	3: 83,192,670 (GRCm39)	L1705P	probably benign	Het
Dcstamp	A	G	15: 39,618,185 (GRCm39)	H198R	probably benign	Het
Dhx58	T	A	11: 100,594,806 (GRCm39)	K30M	probably damaging	Het
Dnah1	C	T	14: 31,018,455 (GRCm39)	A1392T	probably benign	Het
Dnah14	C	A	1: 181,619,569 (GRCm39)	Y3964*	probably null	Het
Dnah8	T	C	17: 31,013,712 (GRCm39)	S3818P	probably damaging	Het
Dnmt3b	T	A	2: 153,518,734 (GRCm39)	N632K	probably benign	Het
Drc7	G	A	8: 95,788,845 (GRCm39)	R301Q	probably damaging	Het
Dsg1a	T	C	18: 20,453,365 (GRCm39)	V21A	probably damaging	Het
Dtd1	T	C	2: 144,459,261 (GRCm39)	L95P	probably benign	Het
Efhb	A	T	17: 53,707,772 (GRCm39)		probably benign	Het
Fam186b	T	A	15: 99,178,733 (GRCm39)	M198L	possibly damaging	Het
Fam193a	A	G	5: 34,616,374 (GRCm39)	T850A	probably benign	Het
Fan1	G	A	7: 64,004,249 (GRCm39)	P739L	probably damaging	Het
Flii	A	T	11: 60,616,074 (GRCm39)	N28K	probably benign	Het
Fmo3	T	C	1: 162,796,407 (GRCm39)	Y55C	probably damaging	Het
Gfi1	G	A	5: 107,868,138 (GRCm39)	R377C	probably damaging	Het
Gm9195	C	T	14: 72,717,536 (GRCm39)	E266K	possibly damaging	Het
Hdac1-ps	T	A	17: 78,799,969 (GRCm39)	L320Q	probably damaging	Het
Helz	A	T	11: 107,525,919 (GRCm39)	M825L	probably damaging	Het
Hsd3b9	A	T	3: 98,354,047 (GRCm39)	W151R	probably benign	Het
Ift80	G	A	3: 68,869,583 (GRCm39)	A236V	probably damaging	Het
Il1rn	A	T	2: 24,239,505 (GRCm39)	T134S	possibly damaging	Het
Imp4	T	C	1: 34,483,445 (GRCm39)	M257T	probably benign	Het
Impdh2	T	C	9: 108,441,957 (GRCm39)	L377S	probably damaging	Het
Kcnrg	T	C	14: 61,844,981 (GRCm39)	V7A	possibly damaging	Het
Kdm1b	C	A	13: 47,217,617 (GRCm39)	L359I	possibly damaging	Het
Lima1	T	A	15: 99,704,306 (GRCm39)	T288S	probably benign	Het
Lrrc37	A	T	11: 103,510,470 (GRCm39)	D499E	unknown	Het
Lrrc4c	A	T	2: 97,460,040 (GRCm39)	D222V	possibly damaging	Het
Mybpc3	T	A	2: 90,948,524 (GRCm39)	V4E	probably null	Het
Ncor1	A	T	11: 62,260,234 (GRCm39)	D505E	probably benign	Het
Nell1	A	G	7: 50,476,097 (GRCm39)	S579G	probably damaging	Het
Npc1	T	A	18: 12,333,877 (GRCm39)	M735L	probably benign	Het
Or1j13	G	A	2: 36,369,794 (GRCm39)	T116I	possibly damaging	Het
Or2at4	A	G	7: 99,384,893 (GRCm39)	H181R	possibly damaging	Het
Or4a73	A	G	2: 89,420,880 (GRCm39)	I193T	probably damaging	Het
Pcdhb12	A	G	18: 37,570,386 (GRCm39)	M511V	probably benign	Het
Peli2	G	A	14: 48,490,130 (GRCm39)	E201K	possibly damaging	Het
Phf3	T	A	1: 30,860,347 (GRCm39)	K828*	probably null	Het
Pih1d1	A	G	7: 44,806,196 (GRCm39)	D44G	possibly damaging	Het
Prag1	A	T	8: 36,613,891 (GRCm39)	T1148S	probably benign	Het
Ptpn18	A	T	1: 34,511,271 (GRCm39)	R338W	probably null	Het
Slc7a6os	A	T	8: 106,937,189 (GRCm39)	D90E	probably benign	Het
Sp7	T	A	15: 102,267,227 (GRCm39)	H211L	possibly damaging	Het
Ssh3	A	G	19: 4,319,053 (GRCm39)	V19A	possibly damaging	Het
Tcp11l2	A	G	10: 84,449,522 (GRCm39)	I496V	probably damaging	Het
Tenm3	C	T	8: 48,729,417 (GRCm39)	A1530T		Het
Tmem232	A	G	17: 65,743,367 (GRCm39)	L308P	probably damaging	Het
Tulp4	A	G	17: 6,189,409 (GRCm39)	N77S	probably damaging	Het
Unc13d	AATGCCTCCCATGCC	AATGCCTCCCATGCCTCCCATGCC	11: 115,958,998 (GRCm39)		probably benign	Het
Usp48	A	T	4: 137,341,080 (GRCm39)	D360V	probably damaging	Het
Vmn2r84	G	A	10: 130,226,968 (GRCm39)	A290V	probably benign	Het
Zfp1007	A	T	5: 109,824,174 (GRCm39)	S425R	probably benign	Het
Zfp512b	T	C	2: 181,228,525 (GRCm39)	N738S	probably benign	Het

Other mutations in Atp2c2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00966:Atp2c2	APN	8	120,472,329 (GRCm39)	missense	probably benign
IGL01624:Atp2c2	APN	8	120,484,189 (GRCm39)	missense	probably benign	0.00
IGL02133:Atp2c2	APN	8	120,481,074 (GRCm39)	missense	probably benign	0.00
IGL02221:Atp2c2	APN	8	120,471,073 (GRCm39)	missense	probably damaging	1.00
IGL02606:Atp2c2	APN	8	120,457,013 (GRCm39)	missense	probably benign
IGL02657:Atp2c2	APN	8	120,479,771 (GRCm39)	missense	probably damaging	1.00
IGL02839:Atp2c2	APN	8	120,475,859 (GRCm39)	missense	possibly damaging	0.85
IGL03122:Atp2c2	APN	8	120,469,414 (GRCm39)	missense	possibly damaging	0.77
R0031:Atp2c2	UTSW	8	120,475,801 (GRCm39)	missense	probably benign	0.15
R0372:Atp2c2	UTSW	8	120,484,180 (GRCm39)	missense	probably benign
R0502:Atp2c2	UTSW	8	120,461,316 (GRCm39)	missense	probably null	0.99
R0503:Atp2c2	UTSW	8	120,461,316 (GRCm39)	missense	probably null	0.99
R0584:Atp2c2	UTSW	8	120,465,157 (GRCm39)	missense	probably benign	0.01
R1225:Atp2c2	UTSW	8	120,461,984 (GRCm39)	missense	probably damaging	1.00
R1580:Atp2c2	UTSW	8	120,479,726 (GRCm39)	missense	probably benign	0.00
R1620:Atp2c2	UTSW	8	120,475,865 (GRCm39)	missense	probably benign
R1638:Atp2c2	UTSW	8	120,482,742 (GRCm39)	missense	possibly damaging	0.82
R1745:Atp2c2	UTSW	8	120,451,833 (GRCm39)	missense	probably benign	0.02
R1746:Atp2c2	UTSW	8	120,461,182 (GRCm39)	unclassified	probably benign
R1907:Atp2c2	UTSW	8	120,476,615 (GRCm39)	splice site	probably benign
R2104:Atp2c2	UTSW	8	120,476,584 (GRCm39)	missense	probably benign
R2151:Atp2c2	UTSW	8	120,482,841 (GRCm39)	missense	probably benign
R2152:Atp2c2	UTSW	8	120,482,841 (GRCm39)	missense	probably benign
R2154:Atp2c2	UTSW	8	120,482,841 (GRCm39)	missense	probably benign
R2207:Atp2c2	UTSW	8	120,475,048 (GRCm39)	missense	probably damaging	1.00
R3874:Atp2c2	UTSW	8	120,462,035 (GRCm39)	missense	possibly damaging	0.74
R3912:Atp2c2	UTSW	8	120,448,015 (GRCm39)	missense	probably damaging	1.00
R4093:Atp2c2	UTSW	8	120,476,610 (GRCm39)	critical splice donor site	probably null
R4782:Atp2c2	UTSW	8	120,475,891 (GRCm39)	missense	probably damaging	0.97
R4801:Atp2c2	UTSW	8	120,474,426 (GRCm39)	missense	probably damaging	1.00
R4973:Atp2c2	UTSW	8	120,481,002 (GRCm39)	missense	probably benign	0.00
R5485:Atp2c2	UTSW	8	120,479,801 (GRCm39)	critical splice donor site	probably null
R5978:Atp2c2	UTSW	8	120,476,614 (GRCm39)	splice site	probably null
R6377:Atp2c2	UTSW	8	120,453,093 (GRCm39)	missense	probably benign	0.10
R6613:Atp2c2	UTSW	8	120,482,760 (GRCm39)	missense	probably damaging	0.99
R6765:Atp2c2	UTSW	8	120,479,756 (GRCm39)	missense	probably damaging	1.00
R6836:Atp2c2	UTSW	8	120,461,154 (GRCm39)	missense	probably damaging	1.00
R6963:Atp2c2	UTSW	8	120,457,006 (GRCm39)	nonsense	probably null
R7220:Atp2c2	UTSW	8	120,472,300 (GRCm39)	missense	probably benign	0.00
R7238:Atp2c2	UTSW	8	120,469,160 (GRCm39)	missense	possibly damaging	0.73
R7373:Atp2c2	UTSW	8	120,456,991 (GRCm39)	missense	probably benign	0.02
R7438:Atp2c2	UTSW	8	120,474,936 (GRCm39)	missense	probably damaging	1.00
R7573:Atp2c2	UTSW	8	120,478,008 (GRCm39)	missense	probably damaging	1.00
R7677:Atp2c2	UTSW	8	120,474,915 (GRCm39)	missense	probably benign	0.00
R7737:Atp2c2	UTSW	8	120,469,134 (GRCm39)	missense	probably damaging	1.00
R7912:Atp2c2	UTSW	8	120,456,917 (GRCm39)	missense	possibly damaging	0.81
R8831:Atp2c2	UTSW	8	120,476,033 (GRCm39)	splice site	probably null
R9200:Atp2c2	UTSW	8	120,474,999 (GRCm39)	nonsense	probably null
R9211:Atp2c2	UTSW	8	120,446,032 (GRCm39)	missense	probably benign
R9246:Atp2c2	UTSW	8	120,456,989 (GRCm39)	missense	probably damaging	1.00
R9285:Atp2c2	UTSW	8	120,465,141 (GRCm39)	missense	probably benign	0.00
RF004:Atp2c2	UTSW	8	120,479,561 (GRCm39)	missense	probably damaging	1.00
RF012:Atp2c2	UTSW	8	120,472,253 (GRCm39)	missense	possibly damaging	0.91
Z1177:Atp2c2	UTSW	8	120,461,124 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- TGACATTCCTGGGTCTCGTG -3'
(R):5'- GGACAGAATCAACATGACTGC -3'

Sequencing Primer
(F):5'- TCTCGTGGGCATCATCGAC -3'
(R):5'- TGACTGCCCCAAACCATAATGATG -3'

Posted On

2021-11-17