Mutagenetix > Incidental Mutation

Incidental Mutation 'R0725:Cpped1'

63662

Institutional Source

Beutler Lab

Gene Symbol

Cpped1

Ensembl Gene

ENSMUSG00000065979

Gene Name

calcineurin-like phosphoesterase domain containing 1

Synonyms

C530044N13Rik

MMRRC Submission

038907-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.060) question?

Stock #

R0725 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

11621585-11727309 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 11646314 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tryptophan to Leucine at position 170 (W170L)

Ref Sequence

ENSEMBL: ENSMUSP00000119989 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000096272] [ENSMUST00000121750] [ENSMUST00000127972]

AlphaFold

Q8BFS6

Predicted Effect

possibly damaging
Transcript: ENSMUST00000096272
AA Change: W146L

PolyPhen 2 Score 0.911 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000093992
Gene: ENSMUSG00000065979
AA Change: W146L

Domain	Start	End	E-Value	Type
Pfam:Metallophos	33	250	4.6e-14	PFAM
Pfam:Metallophos_2	63	285	6e-10	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000121750
AA Change: W132L

PolyPhen 2 Score 0.781 (Sensitivity: 0.85; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000112587
Gene: ENSMUSG00000065979
AA Change: W132L

Domain	Start	End	E-Value	Type
Pfam:Metallophos	25	236	1e-14	PFAM
Pfam:Metallophos_2	45	271	6.8e-12	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000127972
AA Change: W170L

PolyPhen 2 Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000119989
Gene: ENSMUSG00000065979
AA Change: W170L

Domain	Start	End	E-Value	Type
Pfam:Metallophos	57	239	2e-10	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000145169

Meta Mutation Damage Score

0.5700

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.1%
20x: 93.7%

Validation Efficiency

100% (70/70)

Allele List at MGI

Other mutations in this stock

Total: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Asph	C	T	4: 9,542,275 (GRCm39)	D305N	probably damaging	Het
Atp13a3	T	C	16: 30,170,205 (GRCm39)	K327R	probably damaging	Het
Cacna1s	T	C	1: 136,026,264 (GRCm39)		probably benign	Het
Ccnk	T	C	12: 108,161,834 (GRCm39)		probably benign	Het
Cep55	T	C	19: 38,048,622 (GRCm39)	S93P	possibly damaging	Het
Cfap300	A	T	9: 8,027,144 (GRCm39)	D131E	probably damaging	Het
Cfh	A	G	1: 140,085,081 (GRCm39)		probably benign	Het
Clptm1l	A	G	13: 73,754,462 (GRCm39)	T129A	probably benign	Het
Cntnap5a	A	G	1: 116,220,206 (GRCm39)	E672G	probably benign	Het
Crygb	T	C	1: 65,121,100 (GRCm39)	I76V	probably benign	Het
Cyp3a25	A	G	5: 145,931,746 (GRCm39)	S121P	probably damaging	Het
Cyp4b1	T	C	4: 115,484,024 (GRCm39)	D395G	probably damaging	Het
Dll4	T	C	2: 119,163,170 (GRCm39)	V597A	probably damaging	Het
Dock7	T	C	4: 98,833,528 (GRCm39)	D1891G	probably damaging	Het
Dsel	T	C	1: 111,787,682 (GRCm39)	D951G	possibly damaging	Het
Dync2h1	C	A	9: 7,015,497 (GRCm39)	V3603F	possibly damaging	Het
Fam167b	C	A	4: 129,472,078 (GRCm39)	A31S	probably damaging	Het
Fgfrl1	T	A	5: 108,852,539 (GRCm39)	I25N	probably damaging	Het
Gzf1	C	T	2: 148,526,569 (GRCm39)	R347*	probably null	Het
Heatr5b	T	A	17: 79,103,825 (GRCm39)	I1117F	probably benign	Het
Kntc1	T	C	5: 123,907,767 (GRCm39)	V456A	possibly damaging	Het
Macc1	C	A	12: 119,411,251 (GRCm39)	S673*	probably null	Het
Mpp4	T	C	1: 59,160,581 (GRCm39)	E574G	probably damaging	Het
Muc20	C	T	16: 32,613,858 (GRCm39)	M506I	probably benign	Het
Ncbp1	A	G	4: 46,152,056 (GRCm39)	T218A	probably benign	Het
Nfxl1	A	T	5: 72,716,473 (GRCm39)	V46E	probably benign	Het
Nfyc	G	T	4: 120,625,931 (GRCm39)		probably benign	Het
Niban1	A	G	1: 151,581,766 (GRCm39)	E454G	probably benign	Het
Or51f5	T	A	7: 102,423,739 (GRCm39)	S3T	probably benign	Het
Or8g55	A	T	9: 39,784,643 (GRCm39)	Q24L	probably damaging	Het
Osbpl8	T	C	10: 111,122,101 (GRCm39)	F681S	possibly damaging	Het
Pcm1	G	C	8: 41,740,848 (GRCm39)	E1031D	probably damaging	Het
Pdcd11	A	G	19: 47,115,730 (GRCm39)	E1486G	probably benign	Het
Pex12	G	T	11: 83,188,860 (GRCm39)	A45E	probably damaging	Het
Pheta1	T	A	5: 121,991,314 (GRCm39)	H225Q	probably benign	Het
Pigm	A	G	1: 172,204,384 (GRCm39)	D40G	probably damaging	Het
Pkp1	G	T	1: 135,808,478 (GRCm39)	N496K	probably benign	Het
Psmc4	T	C	7: 27,748,287 (GRCm39)	I54V	probably benign	Het
Rbm33	T	C	5: 28,599,481 (GRCm39)	V951A	unknown	Het
Selenbp2	G	T	3: 94,604,809 (GRCm39)		probably benign	Het
Slc3a1	G	A	17: 85,368,263 (GRCm39)	W510*	probably null	Het
Stx12	A	C	4: 132,584,701 (GRCm39)		probably benign	Het
Tas2r125	G	T	6: 132,887,085 (GRCm39)	D158Y	probably benign	Het
Tchp	C	A	5: 114,857,682 (GRCm39)	Q392K	probably benign	Het
Tmed11	T	A	5: 108,926,855 (GRCm39)	D139V	probably damaging	Het
Ttn	C	T	2: 76,578,654 (GRCm39)	V24080M	probably damaging	Het
Ush2a	G	A	1: 188,683,722 (GRCm39)	G4967D	probably damaging	Het
Vezf1	T	C	11: 87,964,156 (GRCm39)	S103P	probably benign	Het
Xpnpep3	T	C	15: 81,315,043 (GRCm39)	S248P	probably damaging	Het
Yipf2	G	C	9: 21,503,519 (GRCm39)		probably null	Het
Zfp110	A	T	7: 12,570,290 (GRCm39)	Q39L	possibly damaging	Het
Zfp287	A	T	11: 62,605,039 (GRCm39)	C623S	probably damaging	Het

Other mutations in Cpped1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02221:Cpped1	APN	16	11,646,392 (GRCm39)	missense	probably damaging	1.00
IGL02448:Cpped1	APN	16	11,623,253 (GRCm39)	missense	probably benign	0.30
IGL03048:Cpped1	UTSW	16	11,646,339 (GRCm39)	missense	probably benign	0.23
R2084:Cpped1	UTSW	16	11,646,365 (GRCm39)	missense	probably damaging	1.00
R2276:Cpped1	UTSW	16	11,712,745 (GRCm39)	critical splice donor site	probably null
R3702:Cpped1	UTSW	16	11,646,304 (GRCm39)	missense	probably damaging	1.00
R4321:Cpped1	UTSW	16	11,705,610 (GRCm39)	missense	probably benign	0.35
R4407:Cpped1	UTSW	16	11,623,285 (GRCm39)	missense	probably damaging	0.96
R4421:Cpped1	UTSW	16	11,623,221 (GRCm39)	makesense	probably null
R4672:Cpped1	UTSW	16	11,623,238 (GRCm39)	nonsense	probably null
R4704:Cpped1	UTSW	16	11,703,493 (GRCm39)	intron	probably benign
R4928:Cpped1	UTSW	16	11,646,143 (GRCm39)	missense	probably damaging	1.00
R5647:Cpped1	UTSW	16	11,646,010 (GRCm39)	unclassified	probably benign
R7260:Cpped1	UTSW	16	11,646,327 (GRCm39)	missense	possibly damaging	0.90
R7610:Cpped1	UTSW	16	11,712,742 (GRCm39)	splice site	probably null
R8008:Cpped1	UTSW	16	11,646,260 (GRCm39)	missense	probably damaging	1.00
R8324:Cpped1	UTSW	16	11,623,340 (GRCm39)	missense	probably benign	0.00
R8356:Cpped1	UTSW	16	11,712,793 (GRCm39)	nonsense	probably null
R9100:Cpped1	UTSW	16	11,646,419 (GRCm39)	missense
X0017:Cpped1	UTSW	16	11,646,156 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GGCACTGTTTCTGCTCTGCAATG -3'
(R):5'- GCCCTTGTTCAAAACCAGGTCCAC -3'

Sequencing Primer
(F):5'- CTGCTCTGCAATGTTCAGC -3'
(R):5'- CAGTGAACTCATCAGGTTGC -3'

Posted On

2013-07-30