Mutagenetix > Incidental Mutation

Incidental Mutation 'R6466:C2cd2'

516604

Institutional Source

Beutler Lab

Gene Symbol

C2cd2

Ensembl Gene

ENSMUSG00000045975

Gene Name

C2 calcium-dependent domain containing 2

Synonyms

5830404H04Rik, ORF25

MMRRC Submission

044599-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6466 (G1)

Quality Score

219.009

Status

Validated

Chromosome

Chromosomal Location

97656409-97727248 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 97680822 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Arginine at position 331 (C331R)

Ref Sequence

ENSEMBL: ENSMUSP00000127368 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000170757] [ENSMUST00000232165]

AlphaFold

E9Q3C1

Predicted Effect

probably benign
Transcript: ENSMUST00000170757
AA Change: C331R

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000127368
Gene: ENSMUSG00000045975
AA Change: C331R

Domain	Start	End	E-Value	Type
transmembrane domain	12	34	N/A	INTRINSIC
low complexity region	106	122	N/A	INTRINSIC
Pfam:C2	232	359	1.9e-6	PFAM
low complexity region	410	421	N/A	INTRINSIC
low complexity region	491	517	N/A	INTRINSIC
low complexity region	605	616	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000200252

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000231332

Predicted Effect

unknown
Transcript: ENSMUST00000231903
AA Change: C18R

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000232063

Predicted Effect

probably benign
Transcript: ENSMUST00000232165

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000232572

Meta Mutation Damage Score

0.0846

Coding Region Coverage

1x: 99.9%
3x: 99.4%
10x: 97.3%
20x: 91.1%

Validation Efficiency

98% (56/57)

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1190005I06Rik	A	T	8: 121,335,735 (GRCm39)	D69E	probably damaging	Het
AAdacl4fm3	T	A	4: 144,430,437 (GRCm39)	D184V	probably damaging	Het
Adgrv1	G	T	13: 81,723,220 (GRCm39)		probably null	Het
Ahr	A	T	12: 35,554,031 (GRCm39)	V696E	probably benign	Het
Akap13	A	G	7: 75,376,792 (GRCm39)	T2007A	probably benign	Het
Arid1b	T	C	17: 5,377,953 (GRCm39)	F753S	probably damaging	Het
Bpifb3	G	T	2: 153,764,108 (GRCm39)	K105N	probably damaging	Het
Chrm1	T	A	19: 8,655,542 (GRCm39)	Y82*	probably null	Het
Clcn3	A	C	8: 61,382,595 (GRCm39)	V331G	probably damaging	Het
Dchs1	A	T	7: 105,413,748 (GRCm39)	D1022E	probably benign	Het
Dnah2	T	A	11: 69,430,241 (GRCm39)	T106S	probably benign	Het
Fam171a2	T	A	11: 102,330,711 (GRCm39)	D256V	probably damaging	Het
Firrm	G	T	1: 163,781,734 (GRCm39)	R898S	probably benign	Het
Fmn2	T	A	1: 174,437,149 (GRCm39)		probably benign	Het
Fut11	C	T	14: 20,745,377 (GRCm39)	R103W	probably damaging	Het
Gas2l2	A	C	11: 83,320,179 (GRCm39)	S26A	probably damaging	Het
Gramd1a	A	T	7: 30,843,221 (GRCm39)	I29N	probably benign	Het
Grem2	A	G	1: 174,664,450 (GRCm39)	V133A	probably damaging	Het
Hydin	T	A	8: 111,233,600 (GRCm39)	S1813T	possibly damaging	Het
Igkv3-2	T	C	6: 70,676,023 (GRCm39)	F111L	probably benign	Het
Ints8	T	C	4: 11,252,878 (GRCm39)	Q68R	probably damaging	Het
Irx5	A	G	8: 93,086,354 (GRCm39)	I146V	probably damaging	Het
Kcnh3	T	C	15: 99,136,124 (GRCm39)	L707P	probably damaging	Het
Kcnk4	T	A	19: 6,905,665 (GRCm39)	I101F	probably damaging	Het
Klhl9	A	G	4: 88,639,399 (GRCm39)	Y281H	probably benign	Het
Klra9	G	T	6: 130,155,995 (GRCm39)	Y253*	probably null	Het
Lmbr1	C	T	5: 29,583,166 (GRCm39)	A9T	probably benign	Het
Map10	G	T	8: 126,399,123 (GRCm39)	E839*	probably null	Het
Nectin4	C	A	1: 171,214,321 (GRCm39)	A492D	probably damaging	Het
Nfat5	T	A	8: 108,082,140 (GRCm39)		probably null	Het
Or5p5	A	G	7: 107,413,901 (GRCm39)	T37A	probably benign	Het
Plec	A	G	15: 76,062,084 (GRCm39)	Y2608H	probably benign	Het
Pold3	A	G	7: 99,749,839 (GRCm39)	S42P	probably benign	Het
Ppp2r1a	G	T	17: 21,180,893 (GRCm39)	G432*	probably null	Het
Qki	T	C	17: 10,434,394 (GRCm39)	E315G	probably benign	Het
Rfx2	C	T	17: 57,091,397 (GRCm39)	V354I	probably benign	Het
Rp1	T	C	1: 4,418,109 (GRCm39)	Y1001C	probably benign	Het
Sez6l	A	G	5: 112,609,007 (GRCm39)		probably null	Het
Slc39a14	A	G	14: 70,547,335 (GRCm39)	I337T	probably damaging	Het
Slc3a2	G	T	19: 8,686,683 (GRCm39)	L76M	probably damaging	Het
Slco1a5	T	C	6: 142,183,260 (GRCm39)	T555A	probably benign	Het
Sprr2e	A	T	3: 92,260,341 (GRCm39)	K57N	unknown	Het
Syne2	A	G	12: 75,990,675 (GRCm39)	T1886A	probably damaging	Het
Tenm3	A	T	8: 48,689,098 (GRCm39)	I2147N	probably damaging	Het
Thbs1	G	T	2: 117,950,328 (GRCm39)	G654W	probably damaging	Het
Tigd5	A	G	15: 75,782,352 (GRCm39)	Y238C	possibly damaging	Het
Tmem221	A	G	8: 72,010,493 (GRCm39)	F126S	probably damaging	Het
Trp63	C	A	16: 25,582,108 (GRCm39)	P52Q	probably damaging	Het
Ugp2	A	T	11: 21,278,883 (GRCm39)	S434R	probably benign	Het
Vmn2r69	A	C	7: 85,056,378 (GRCm39)	F587V	probably benign	Het
Vps13d	T	A	4: 144,784,065 (GRCm39)	N3872I	possibly damaging	Het
Wdfy2	A	G	14: 63,186,115 (GRCm39)	Y250C	probably damaging	Het
Zbtb16	T	C	9: 48,576,619 (GRCm39)	D487G	possibly damaging	Het

Other mutations in C2cd2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00482:C2cd2	APN	16	97,671,420 (GRCm39)	missense	probably damaging	1.00
IGL01633:C2cd2	APN	16	97,676,323 (GRCm39)	splice site	probably benign
IGL01731:C2cd2	APN	16	97,671,372 (GRCm39)	missense	probably damaging	1.00
IGL02071:C2cd2	APN	16	97,671,432 (GRCm39)	missense	probably damaging	1.00
IGL02086:C2cd2	APN	16	97,691,208 (GRCm39)	splice site	probably benign
IGL02502:C2cd2	APN	16	97,677,590 (GRCm39)	missense	possibly damaging	0.85
IGL02933:C2cd2	APN	16	97,693,401 (GRCm39)	missense	probably benign	0.22
IGL03005:C2cd2	APN	16	97,660,632 (GRCm39)	missense	probably damaging	0.99
IGL03493:C2cd2	APN	16	97,682,861 (GRCm39)	missense	probably damaging	0.97
H8562:C2cd2	UTSW	16	97,680,840 (GRCm39)	missense	possibly damaging	0.91
H8786:C2cd2	UTSW	16	97,680,840 (GRCm39)	missense	possibly damaging	0.91
R0480:C2cd2	UTSW	16	97,678,348 (GRCm39)	missense	probably benign	0.45
R0483:C2cd2	UTSW	16	97,660,788 (GRCm39)	splice site	probably benign
R0541:C2cd2	UTSW	16	97,723,496 (GRCm39)	missense	possibly damaging	0.66
R1294:C2cd2	UTSW	16	97,723,469 (GRCm39)	missense	probably damaging	1.00
R1986:C2cd2	UTSW	16	97,671,471 (GRCm39)	missense	probably damaging	1.00
R2518:C2cd2	UTSW	16	97,723,286 (GRCm39)	missense	probably benign	0.01
R5468:C2cd2	UTSW	16	97,669,791 (GRCm39)	splice site	probably null
R5507:C2cd2	UTSW	16	97,682,820 (GRCm39)	missense	probably benign	0.01
R5979:C2cd2	UTSW	16	97,676,418 (GRCm39)	missense	probably benign	0.01
R7264:C2cd2	UTSW	16	97,677,419 (GRCm39)	critical splice donor site	probably null
R7372:C2cd2	UTSW	16	97,676,580 (GRCm39)	missense
R8003:C2cd2	UTSW	16	97,687,286 (GRCm39)	critical splice donor site	probably null
R8181:C2cd2	UTSW	16	97,693,502 (GRCm39)	missense	probably benign	0.21
R8340:C2cd2	UTSW	16	97,670,013 (GRCm39)	missense	probably benign	0.00
R8506:C2cd2	UTSW	16	97,676,621 (GRCm39)	missense
R9072:C2cd2	UTSW	16	97,676,403 (GRCm39)	missense	probably damaging	1.00
R9145:C2cd2	UTSW	16	97,677,486 (GRCm39)	missense	probably damaging	1.00
R9175:C2cd2	UTSW	16	97,678,421 (GRCm39)	missense	probably benign	0.00
R9369:C2cd2	UTSW	16	97,723,333 (GRCm39)	missense	possibly damaging	0.58
R9659:C2cd2	UTSW	16	97,723,473 (GRCm39)	missense	possibly damaging	0.87
R9668:C2cd2	UTSW	16	97,671,418 (GRCm39)	missense	probably damaging	1.00
R9788:C2cd2	UTSW	16	97,723,473 (GRCm39)	missense	possibly damaging	0.87

Predicted Primers

PCR Primer
(F):5'- CCCCAAAGGAATGACACTGTTG -3'
(R):5'- AACCCTTGGTTGAATTGGTGGC -3'

Sequencing Primer
(F):5'- AGGAATGACACTGTTGATTCTTAAC -3'
(R):5'- GACTGACAACCATGTGTCTTTAG -3'

Posted On

2018-05-21