Mutagenetix > Incidental Mutation

Incidental Mutation 'R9544:Cep97'

720029

Institutional Source

Beutler Lab

Gene Symbol

Cep97

Ensembl Gene

ENSMUSG00000022604

Gene Name

centrosomal protein 97

Synonyms

Lrriq2, 4932439K18Rik, E130116N02Rik, 2810403B08Rik

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R9544 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

55720251-55755218 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 55735303 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Lysine at position 570 (N570K)

Ref Sequence

ENSEMBL: ENSMUSP00000023270 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000023270] [ENSMUST00000117468] [ENSMUST00000118500]

AlphaFold

Q9CZ62

Predicted Effect

possibly damaging
Transcript: ENSMUST00000023270
AA Change: N570K

PolyPhen 2 Score 0.858 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000023270
Gene: ENSMUSG00000022604
AA Change: N570K

Domain	Start	End	E-Value	Type
Pfam:LRR_9	98	259	1.8e-12	PFAM
IQ	549	571	2e-1	SMART
coiled coil region	576	609	N/A	INTRINSIC
low complexity region	661	673	N/A	INTRINSIC
low complexity region	715	728	N/A	INTRINSIC
low complexity region	775	789	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000117468
AA Change: N498K

PolyPhen 2 Score 0.858 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000112687
Gene: ENSMUSG00000022604
AA Change: N498K

Domain	Start	End	E-Value	Type
Pfam:LRR_9	7	187	4.1e-12	PFAM
Pfam:LRR_8	30	86	1e-7	PFAM
Pfam:LRR_4	52	94	3.6e-8	PFAM
Pfam:LRR_1	53	73	1.3e-2	PFAM
IQ	477	499	2e-1	SMART
coiled coil region	504	537	N/A	INTRINSIC
low complexity region	589	601	N/A	INTRINSIC
low complexity region	643	656	N/A	INTRINSIC
low complexity region	703	717	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000118500
AA Change: N498K

PolyPhen 2 Score 0.858 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000112663
Gene: ENSMUSG00000022604
AA Change: N498K

Domain	Start	End	E-Value	Type
Pfam:LRR_9	7	187	4.1e-12	PFAM
Pfam:LRR_8	30	86	1e-7	PFAM
Pfam:LRR_4	52	94	3.6e-8	PFAM
Pfam:LRR_1	53	73	1.3e-2	PFAM
IQ	477	499	2e-1	SMART
coiled coil region	504	537	N/A	INTRINSIC
low complexity region	589	601	N/A	INTRINSIC
low complexity region	643	656	N/A	INTRINSIC
low complexity region	703	717	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.1%
20x: 96.7%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5530400C23Rik	A	G	6: 133,271,202 (GRCm39)	E82G	possibly damaging	Het
Adra2a	C	G	19: 54,035,454 (GRCm39)	P270R	probably benign	Het
Alox12b	A	T	11: 69,054,812 (GRCm39)	I272F	possibly damaging	Het
Als2	C	A	1: 59,250,468 (GRCm39)	E425D	probably benign	Het
Arhgap21	C	A	2: 20,858,938 (GRCm39)	C1252F	possibly damaging	Het
Arhgap31	T	G	16: 38,423,976 (GRCm39)	T697P	probably damaging	Het
Aspm	C	A	1: 139,385,523 (GRCm39)	T389K	probably benign	Het
B4galnt3	T	A	6: 120,209,905 (GRCm39)	I73F	probably damaging	Het
Btn2a2	A	G	13: 23,672,008 (GRCm39)	V27A	probably benign	Het
Cfh	T	C	1: 140,036,266 (GRCm39)	I751V	probably benign	Het
Chd3	A	G	11: 69,241,046 (GRCm39)	C1516R	probably damaging	Het
Cul3	A	G	1: 80,258,576 (GRCm39)	F487L	probably damaging	Het
Dock1	T	C	7: 134,348,186 (GRCm39)	S266P	possibly damaging	Het
Dock6	A	T	9: 21,732,830 (GRCm39)	Y1118*	probably null	Het
Dolpp1	T	A	2: 30,282,515 (GRCm39)	Y23N	probably damaging	Het
Egf	T	C	3: 129,511,617 (GRCm39)	M517V	probably benign	Het
Endou	C	A	15: 97,609,969 (GRCm39)	K442N	probably damaging	Het
Fam210b	C	T	2: 172,194,633 (GRCm39)	R162W	probably damaging	Het
Fbxw27	ATGT	AT	9: 109,602,322 (GRCm39)		probably null	Het
Flt3	T	A	5: 147,291,442 (GRCm39)	Q641L	possibly damaging	Het
Ighv3-3	T	A	12: 114,160,270 (GRCm39)	I47F	probably damaging	Het
Il4	C	T	11: 53,504,837 (GRCm39)	R76H	probably damaging	Het
Inpp5f	A	C	7: 128,278,515 (GRCm39)	D435A	possibly damaging	Het
Kcnq2	T	G	2: 180,729,407 (GRCm39)	D532A	probably damaging	Het
Krtap11-1	A	C	16: 89,368,062 (GRCm39)		probably benign	Het
Lamp3	T	A	16: 19,494,832 (GRCm39)		probably null	Het
Lcn3	A	T	2: 25,656,151 (GRCm39)	I69L	probably benign	Het
Lrrc43	A	T	5: 123,641,307 (GRCm39)	H497L	probably damaging	Het
Luc7l2	T	G	6: 38,580,315 (GRCm39)	S305A	unknown	Het
Malrd1	C	T	2: 15,640,809 (GRCm39)	T513I	unknown	Het
Mllt3	T	A	4: 87,759,418 (GRCm39)	D210V	probably damaging	Het
Mmp14	A	G	14: 54,673,251 (GRCm39)	H53R	possibly damaging	Het
Ndst4	A	C	3: 125,476,808 (GRCm39)	H11P	probably damaging	Het
Nln	G	A	13: 104,198,356 (GRCm39)	T152M	probably benign	Het
Oas1c	A	G	5: 120,946,202 (GRCm39)	F99L	probably benign	Het
Or10s1	T	C	9: 39,986,353 (GRCm39)	L254P	probably damaging	Het
Or1e35	T	C	11: 73,797,637 (GRCm39)	K227R	probably benign	Het
Or1j11	G	T	2: 36,311,784 (GRCm39)	A125S	probably damaging	Het
Or5w15	G	A	2: 87,568,644 (GRCm39)	T8I	probably benign	Het
Or7g25	T	A	9: 19,160,561 (GRCm39)	I45F	probably damaging	Het
Pappa2	C	A	1: 158,784,817 (GRCm39)	Q64H	probably damaging	Het
Pcdhb15	T	C	18: 37,608,948 (GRCm39)	F727L	probably benign	Het
Pcsk1	A	T	13: 75,259,039 (GRCm39)	N271I	probably damaging	Het
Pkhd1l1	G	A	15: 44,410,239 (GRCm39)	G2582D	probably damaging	Het
Psma4	A	T	9: 54,862,245 (GRCm39)	Q123L	probably damaging	Het
Selenbp2	A	T	3: 94,605,368 (GRCm39)	I127F	possibly damaging	Het
Shank1	G	A	7: 43,962,342 (GRCm39)	S71N	unknown	Het
Slc29a3	G	T	10: 60,551,960 (GRCm39)	C361*	probably null	Het
Slx4	C	A	16: 3,797,917 (GRCm39)	R1489L	probably damaging	Het
Sorl1	A	C	9: 41,993,105 (GRCm39)	Y306*	probably null	Het
Tbc1d16	G	T	11: 119,101,335 (GRCm39)	H58Q	probably damaging	Het
Tfdp2	A	G	9: 96,169,663 (GRCm39)	T5A	probably damaging	Het
Thbs1	G	T	2: 117,953,932 (GRCm39)	G1061V	probably damaging	Het
Timm29	G	A	9: 21,504,662 (GRCm39)	R110H	probably damaging	Het
Tmf1	C	T	6: 97,147,293 (GRCm39)	E558K	possibly damaging	Het
Trappc11	T	C	8: 47,972,713 (GRCm39)	T287A	possibly damaging	Het
Unc119b	G	A	5: 115,272,827 (GRCm39)	T48M	probably benign	Het
Vmn1r123	T	C	7: 20,896,987 (GRCm39)	I293T	probably benign	Het
Vmn2r67	G	A	7: 84,786,317 (GRCm39)	H563Y	possibly damaging	Het
Vps8	G	T	16: 21,336,893 (GRCm39)	V763L	probably benign	Het
Wdr3	A	T	3: 100,050,752 (GRCm39)	Y722*	probably null	Het
Xrn1	A	G	9: 95,920,756 (GRCm39)	T1339A	probably benign	Het
Zfp827	T	A	8: 79,905,604 (GRCm39)	H860Q	probably damaging	Het

Other mutations in Cep97

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00978:Cep97	APN	16	55,745,323 (GRCm39)	splice site	probably benign
IGL01142:Cep97	APN	16	55,742,561 (GRCm39)	missense	probably damaging	1.00
IGL01383:Cep97	APN	16	55,731,970 (GRCm39)	missense	probably damaging	1.00
IGL01529:Cep97	APN	16	55,750,981 (GRCm39)	splice site	probably benign
IGL01693:Cep97	APN	16	55,750,957 (GRCm39)	missense	probably damaging	1.00
IGL01759:Cep97	APN	16	55,750,936 (GRCm39)	missense	probably damaging	1.00
IGL02085:Cep97	APN	16	55,735,868 (GRCm39)	missense	probably damaging	1.00
IGL02135:Cep97	APN	16	55,743,330 (GRCm39)	missense	probably damaging	1.00
IGL02582:Cep97	APN	16	55,742,539 (GRCm39)	missense	probably damaging	1.00
IGL02631:Cep97	APN	16	55,742,541 (GRCm39)	nonsense	probably null
IGL02899:Cep97	APN	16	55,738,903 (GRCm39)	missense	probably damaging	0.98
IGL03086:Cep97	APN	16	55,735,659 (GRCm39)	missense	probably benign
R0067:Cep97	UTSW	16	55,735,924 (GRCm39)	missense	possibly damaging	0.96
R0067:Cep97	UTSW	16	55,735,924 (GRCm39)	missense	possibly damaging	0.96
R0309:Cep97	UTSW	16	55,745,421 (GRCm39)	missense	probably damaging	0.96
R0504:Cep97	UTSW	16	55,726,142 (GRCm39)	missense	probably benign	0.00
R0507:Cep97	UTSW	16	55,726,245 (GRCm39)	splice site	probably benign
R0508:Cep97	UTSW	16	55,750,969 (GRCm39)	missense	probably benign	0.02
R0658:Cep97	UTSW	16	55,735,265 (GRCm39)	missense	probably benign	0.09
R1588:Cep97	UTSW	16	55,748,184 (GRCm39)	missense	probably damaging	1.00
R1619:Cep97	UTSW	16	55,748,159 (GRCm39)	missense	probably damaging	1.00
R1710:Cep97	UTSW	16	55,735,385 (GRCm39)	missense	probably damaging	0.99
R1872:Cep97	UTSW	16	55,748,229 (GRCm39)	missense	probably damaging	1.00
R1878:Cep97	UTSW	16	55,725,589 (GRCm39)	missense	probably damaging	1.00
R1896:Cep97	UTSW	16	55,748,107 (GRCm39)	missense	probably damaging	1.00
R5401:Cep97	UTSW	16	55,745,315 (GRCm39)	missense	probably benign	0.03
R5520:Cep97	UTSW	16	55,735,659 (GRCm39)	missense	probably benign
R5627:Cep97	UTSW	16	55,745,330 (GRCm39)	critical splice donor site	probably null
R5632:Cep97	UTSW	16	55,735,946 (GRCm39)	missense	probably benign	0.02
R5903:Cep97	UTSW	16	55,739,889 (GRCm39)	missense	probably damaging	1.00
R5914:Cep97	UTSW	16	55,725,820 (GRCm39)	missense	probably benign	0.02
R6185:Cep97	UTSW	16	55,735,455 (GRCm39)	missense	probably benign
R6381:Cep97	UTSW	16	55,742,534 (GRCm39)	missense	probably damaging	1.00
R7041:Cep97	UTSW	16	55,726,117 (GRCm39)	missense	probably benign
R7056:Cep97	UTSW	16	55,725,935 (GRCm39)	missense	probably damaging	1.00
R7371:Cep97	UTSW	16	55,725,683 (GRCm39)	missense	probably benign	0.00
R7862:Cep97	UTSW	16	55,726,084 (GRCm39)	missense	probably benign	0.26
R7951:Cep97	UTSW	16	55,725,820 (GRCm39)	missense	probably benign	0.02
R8042:Cep97	UTSW	16	55,731,965 (GRCm39)	missense	probably benign
R8337:Cep97	UTSW	16	55,735,394 (GRCm39)	nonsense	probably null
R8782:Cep97	UTSW	16	55,726,084 (GRCm39)	missense	probably benign	0.26
R8876:Cep97	UTSW	16	55,742,467 (GRCm39)	missense	possibly damaging	0.55
R9028:Cep97	UTSW	16	55,739,915 (GRCm39)	nonsense	probably null
R9514:Cep97	UTSW	16	55,726,093 (GRCm39)	missense	probably benign	0.01
Z1176:Cep97	UTSW	16	55,748,098 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCAGTGCATCACAGGAGATGAG -3'
(R):5'- ACATCTCTCCCTGAGTCAGCTG -3'

Sequencing Primer
(F):5'- ATGAGGTATAGCAGTGGCCTG -3'
(R):5'- ACACAGTGCGTCTCGTAC -3'

Posted On

2022-07-18