Mutagenetix > Incidental Mutation

Incidental Mutation 'R0725:Cep55'

218388

Institutional Source

Beutler Lab

Gene Symbol

Cep55

Ensembl Gene

ENSMUSG00000024989

Gene Name

centrosomal protein 55

Synonyms

1200008O12Rik, 2700032M20Rik

MMRRC Submission

038907-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.959) question?

Stock #

R0725 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

38043459-38062871 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 38048622 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 93 (S93P)

Ref Sequence

ENSEMBL: ENSMUSP00000127961 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000096096] [ENSMUST00000116506] [ENSMUST00000169673]

AlphaFold

Q8BT07

Predicted Effect

possibly damaging
Transcript: ENSMUST00000096096
AA Change: S93P

PolyPhen 2 Score 0.482 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000093802
Gene: ENSMUSG00000024989
AA Change: S93P

Domain	Start	End	E-Value	Type
low complexity region	11	23	N/A	INTRINSIC
coiled coil region	98	150	N/A	INTRINSIC
Pfam:EABR	171	205	1.2e-22	PFAM
coiled coil region	229	395	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000116506
AA Change: S93P

PolyPhen 2 Score 0.482 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000112205
Gene: ENSMUSG00000024989
AA Change: S93P

Domain	Start	End	E-Value	Type
low complexity region	11	23	N/A	INTRINSIC
coiled coil region	98	150	N/A	INTRINSIC
Pfam:EABR	171	205	1.2e-22	PFAM
coiled coil region	229	371	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000169673
AA Change: S93P

PolyPhen 2 Score 0.482 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000127961
Gene: ENSMUSG00000024989
AA Change: S93P

Domain	Start	End	E-Value	Type
low complexity region	11	23	N/A	INTRINSIC
coiled coil region	98	150	N/A	INTRINSIC
Pfam:EABR	171	204	8.6e-22	PFAM
coiled coil region	229	395	N/A	INTRINSIC

Meta Mutation Damage Score

0.1795

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
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
Cpped1	C	A	16: 11,646,314 (GRCm39)	W170L	probably damaging	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 Cep55

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00420:Cep55	APN	19	38,061,887 (GRCm39)	missense	probably damaging	1.00
IGL02359:Cep55	APN	19	38,058,316 (GRCm39)	missense	probably damaging	1.00
R0079:Cep55	UTSW	19	38,048,769 (GRCm39)	missense	probably benign	0.04
R0308:Cep55	UTSW	19	38,048,659 (GRCm39)	missense	possibly damaging	0.94
R0377:Cep55	UTSW	19	38,060,337 (GRCm39)	nonsense	probably null
R0736:Cep55	UTSW	19	38,061,765 (GRCm39)	missense	probably benign	0.21
R1842:Cep55	UTSW	19	38,046,348 (GRCm39)	missense	probably benign	0.09
R2196:Cep55	UTSW	19	38,057,558 (GRCm39)	missense	probably damaging	1.00
R2227:Cep55	UTSW	19	38,051,082 (GRCm39)	missense	probably benign	0.37
R3832:Cep55	UTSW	19	38,041,560 (GRCm39)	unclassified	probably benign
R4936:Cep55	UTSW	19	38,060,202 (GRCm39)	splice site	probably null
R4938:Cep55	UTSW	19	38,058,364 (GRCm39)	missense	probably damaging	1.00
R5246:Cep55	UTSW	19	38,058,119 (GRCm39)	missense	probably benign	0.39
R5628:Cep55	UTSW	19	38,058,396 (GRCm39)	nonsense	probably null
R5774:Cep55	UTSW	19	38,051,103 (GRCm39)	missense	probably damaging	1.00
R6708:Cep55	UTSW	19	38,048,709 (GRCm39)	missense	probably benign	0.23
R6787:Cep55	UTSW	19	38,046,374 (GRCm39)	missense	probably benign	0.01
R7047:Cep55	UTSW	19	38,048,539 (GRCm39)	missense	possibly damaging	0.65
R7187:Cep55	UTSW	19	38,048,806 (GRCm39)	critical splice donor site	probably null
R7473:Cep55	UTSW	19	38,058,384 (GRCm39)	missense	probably damaging	0.99
R7762:Cep55	UTSW	19	38,057,517 (GRCm39)	splice site	probably null
R7863:Cep55	UTSW	19	38,046,247 (GRCm39)	start gained	probably benign
R9030:Cep55	UTSW	19	38,059,592 (GRCm39)	critical splice donor site	probably null
R9555:Cep55	UTSW	19	38,059,592 (GRCm39)	critical splice donor site	probably null
X0023:Cep55	UTSW	19	38,060,315 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- TGTCTAAGCAGGGGACTGAGCTTC -3'
(R):5'- AGGTGTTGCATCATTTCACAAACCG -3'

Sequencing Primer
(F):5'- GTCCTGATCTCGTAAAATCCAAG -3'
(R):5'- TTATAAGTTGTACCAGACGGGC -3'

Posted On

2014-08-01