Mutagenetix > Incidental Mutation

Incidental Mutation 'R5410:Cenps'

426492

Institutional Source

Beutler Lab

Gene Symbol

Cenps

Ensembl Gene

ENSMUSG00000073705

Gene Name

centromere protein S

Synonyms

2610040C18Rik, Apitd1, 2810407L01Rik

MMRRC Submission

042979-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.261) question?

Stock #

R5410 (G1)

Quality Score

145

Status

Not validated

Chromosome

Chromosomal Location

149212806-149222057 bp(-) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

C to A at 149214658 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000101321 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000030813] [ENSMUST00000030815] [ENSMUST00000105695] [ENSMUST00000105696] [ENSMUST00000150150] [ENSMUST00000176124] [ENSMUST00000177408]

AlphaFold

Q9D084

Predicted Effect

silent
Transcript: ENSMUST00000030813

SMART Domains

Protein: ENSMUSP00000030813
Gene: ENSMUSG00000073705

Domain	Start	End	E-Value	Type
Pfam:CENP-S	16	91	1.4e-36	PFAM
Pfam:CENP-T_C	18	116	2.3e-12	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000030815

SMART Domains

Protein: ENSMUSP00000030815
Gene: ENSMUSG00000028971

Domain	Start	End	E-Value	Type
signal peptide	1	27	N/A	INTRINSIC
low complexity region	65	78	N/A	INTRINSIC
Pfam:Somatostatin	91	108	9.3e-14	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000105695

SMART Domains

Protein: ENSMUSP00000101320
Gene: ENSMUSG00000073705

Domain	Start	End	E-Value	Type
Pfam:CENP-S	16	75	3.4e-23	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000105696

SMART Domains

Protein: ENSMUSP00000101321
Gene: ENSMUSG00000073705

Domain	Start	End	E-Value	Type
Pfam:CENP-S	16	76	2e-23	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000132672

Predicted Effect

silent
Transcript: ENSMUST00000150150

SMART Domains

Protein: ENSMUSP00000121878
Gene: ENSMUSG00000073705

Domain	Start	End	E-Value	Type
Pfam:CENP-S	1	26	7.3e-14	PFAM
low complexity region	43	51	N/A	INTRINSIC

Predicted Effect

silent
Transcript: ENSMUST00000176124

SMART Domains

Protein: ENSMUSP00000134756
Gene: ENSMUSG00000073705

Domain	Start	End	E-Value	Type
Pfam:CENP-S	1	26	1.4e-13	PFAM
low complexity region	43	62	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000177408
AA Change: R69L

SMART Domains

Protein: ENSMUSP00000135536
Gene: ENSMUSG00000073705
AA Change: R69L

Domain	Start	End	E-Value	Type
Pfam:CENP-S	16	64	1.2e-12	PFAM

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.5%
20x: 92.8%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam24	A	G	8: 41,134,103 (GRCm39)	M524V	probably benign	Het
Adamts20	T	A	15: 94,179,838 (GRCm39)	N1788I	possibly damaging	Het
Arfgef3	T	G	10: 18,486,985 (GRCm39)	I1350L	probably damaging	Het
Arhgap17	A	G	7: 122,896,716 (GRCm39)		probably null	Het
Ascl5	A	T	1: 135,978,926 (GRCm39)	I129F	probably damaging	Het
AU040320	A	T	4: 126,717,509 (GRCm39)	H362L	possibly damaging	Het
Bpifb9a	A	T	2: 154,112,155 (GRCm39)	N564Y	probably benign	Het
Cdon	G	T	9: 35,381,331 (GRCm39)	D574Y	probably damaging	Het
Ces1e	T	A	8: 93,937,070 (GRCm39)	I334F	possibly damaging	Het
Clip2	G	A	5: 134,551,645 (GRCm39)	T159M	possibly damaging	Het
Cntn3	T	A	6: 102,255,314 (GRCm39)	T195S	probably benign	Het
Csmd2	C	A	4: 128,442,612 (GRCm39)	H3221Q	probably benign	Het
Cyp2c68	T	C	19: 39,687,728 (GRCm39)	D423G	possibly damaging	Het
Dennd3	C	T	15: 73,419,297 (GRCm39)	T696M	probably benign	Het
Ep300	T	C	15: 81,533,055 (GRCm39)	M1704T	unknown	Het
Exoc2	A	G	13: 31,048,839 (GRCm39)	F738S	probably damaging	Het
Fis1	A	G	5: 136,994,420 (GRCm39)	E36G	probably damaging	Het
Galnt1	A	G	18: 24,400,604 (GRCm39)	I237V	probably benign	Het
Gspt1	A	T	16: 11,048,374 (GRCm39)	I416N	probably benign	Het
Hjurp	GT	GTT	1: 88,194,246 (GRCm39)		probably null	Het
Hykk	G	A	9: 54,853,350 (GRCm39)	C224Y	probably damaging	Het
Ifi211	T	C	1: 173,733,829 (GRCm39)	T111A	probably benign	Het
Il17rd	T	C	14: 26,817,868 (GRCm39)	Y186H	probably damaging	Het
Klhl29	G	T	12: 5,141,366 (GRCm39)	N539K	probably benign	Het
Lmbr1l	T	C	15: 98,807,143 (GRCm39)	T213A	probably damaging	Het
Madd	C	T	2: 90,984,859 (GRCm39)	R1318Q	probably damaging	Het
Mecom	C	A	3: 30,051,870 (GRCm39)	A182S	probably benign	Het
Or13c25	C	A	4: 52,910,991 (GRCm39)	A268S	probably benign	Het
Or1e1	C	T	11: 73,244,632 (GRCm39)	P18S	probably benign	Het
Or4f56	C	T	2: 111,703,637 (GRCm39)	A188T	probably damaging	Het
Or52z1	A	T	7: 103,436,581 (GRCm39)	V301E	probably damaging	Het
Otud4	T	A	8: 80,399,626 (GRCm39)	M780K	probably benign	Het
Pdia5	A	G	16: 35,273,906 (GRCm39)	V130A	probably damaging	Het
Phldb2	T	A	16: 45,645,975 (GRCm39)	H202L	possibly damaging	Het
Ppig	G	A	2: 69,566,241 (GRCm39)	G136E	probably null	Het
Prr14l	C	A	5: 32,985,121 (GRCm39)	R1458L	probably damaging	Het
Ptpn3	T	C	4: 57,205,019 (GRCm39)	Y714C	probably damaging	Het
Ptprr	T	C	10: 116,024,235 (GRCm39)	V182A	possibly damaging	Het
Rai14	A	G	15: 10,575,024 (GRCm39)	Y645H	probably damaging	Het
Rasgrp3	T	C	17: 75,804,042 (GRCm39)	I115T	probably benign	Het
Rc3h1	G	T	1: 160,792,533 (GRCm39)	R990L	possibly damaging	Het
Rdh5	T	A	10: 128,754,160 (GRCm39)	Q21L	probably benign	Het
Rfx8	A	G	1: 39,749,316 (GRCm39)		probably null	Het
Scap	A	G	9: 110,203,250 (GRCm39)		probably null	Het
Shank1	T	A	7: 44,001,246 (GRCm39)	S988R	unknown	Het
Slc16a14	T	A	1: 84,885,145 (GRCm39)	I465F	probably damaging	Het
Slc41a2	A	G	10: 83,117,232 (GRCm39)		probably null	Het
Tab2	T	C	10: 7,795,585 (GRCm39)	H225R	possibly damaging	Het
Tbx19	T	A	1: 164,987,941 (GRCm39)	N64I	probably damaging	Het
Tmprss11f	A	T	5: 86,677,965 (GRCm39)	I268K	probably damaging	Het
Tox2	A	G	2: 163,162,293 (GRCm39)	M388V	probably benign	Het
Trbv17	T	C	6: 41,140,472 (GRCm39)	L109P	probably damaging	Het
Trim72	A	G	7: 127,609,095 (GRCm39)	H299R	probably damaging	Het
Ulbp3	G	A	10: 3,076,473 (GRCm39)		noncoding transcript	Het
Vmn1r63	C	T	7: 5,806,189 (GRCm39)	V148I	possibly damaging	Het
Zfp938	A	C	10: 82,061,092 (GRCm39)	H509Q	possibly damaging	Het
Zfyve16	A	G	13: 92,657,739 (GRCm39)	V724A	probably benign	Het
Zscan10	T	C	17: 23,829,395 (GRCm39)	F569L	probably damaging	Het

Other mutations in Cenps

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02212:Cenps	APN	4	149,213,303 (GRCm39)	missense	probably damaging	1.00
R5408:Cenps	UTSW	4	149,214,658 (GRCm39)	intron	probably benign
R5457:Cenps	UTSW	4	149,216,094 (GRCm39)	critical splice donor site	probably null
R5939:Cenps	UTSW	4	149,214,658 (GRCm39)	intron	probably benign
R5951:Cenps	UTSW	4	149,214,658 (GRCm39)	intron	probably benign
R5952:Cenps	UTSW	4	149,214,658 (GRCm39)	intron	probably benign
R5953:Cenps	UTSW	4	149,214,658 (GRCm39)	intron	probably benign
R5954:Cenps	UTSW	4	149,214,658 (GRCm39)	intron	probably benign
R5957:Cenps	UTSW	4	149,214,658 (GRCm39)	intron	probably benign
R7601:Cenps	UTSW	4	149,216,772 (GRCm39)	missense	possibly damaging	0.82

Predicted Primers

Posted On

2016-09-01