Mutagenetix > Incidental Mutation

Incidental Mutation 'R3731:Nol10'

271001

Institutional Source

Beutler Lab

Gene Symbol

Nol10

Ensembl Gene

ENSMUSG00000061458

Gene Name

nucleolar protein 10

Synonyms

LOC217431

Accession Numbers

Essential gene?

Probably essential (E-score: 0.969) question?

Stock #

R3731 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

17398459-17480096 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 17474674 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Isoleucine at position 622 (K622I)

Ref Sequence

ENSEMBL: ENSMUSP00000035930 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000046011]

AlphaFold

Q5RJG1

Predicted Effect

probably benign
Transcript: ENSMUST00000046011
AA Change: K622I

PolyPhen 2 Score 0.418 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000035930
Gene: ENSMUSG00000061458
AA Change: K622I

Domain	Start	End	E-Value	Type
WD40	42	81	1.1e1	SMART
Blast:WD40	84	123	1e-8	BLAST
WD40	165	204	3.3e1	SMART
WD40	223	257	4.42e1	SMART
WD40	260	299	1.19e1	SMART
WD40	302	340	1.97e2	SMART
low complexity region	451	476	N/A	INTRINSIC
Pfam:NUC153	482	509	1.4e-15	PFAM
low complexity region	515	536	N/A	INTRINSIC
low complexity region	542	553	N/A	INTRINSIC
coiled coil region	557	588	N/A	INTRINSIC
low complexity region	650	660	N/A	INTRINSIC

Meta Mutation Damage Score

0.0727

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.5%
20x: 95.8%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 49 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A630010A05Rik	T	A	16: 14,427,485 (GRCm39)		probably null	Het
Abcc5	A	T	16: 20,217,684 (GRCm39)	Y5*	probably null	Het
Acbd6	T	A	1: 155,434,471 (GRCm39)	S30T	probably benign	Het
Adar	T	C	3: 89,653,962 (GRCm39)	I325T	probably damaging	Het
Akap13	T	C	7: 75,261,125 (GRCm39)	S92P	probably benign	Het
Atp1a4	A	T	1: 172,061,528 (GRCm39)	V771E	probably damaging	Het
Cfh	A	G	1: 140,047,708 (GRCm39)	S492P	possibly damaging	Het
Crlf1	A	G	8: 70,952,092 (GRCm39)	T95A	probably benign	Het
Dennd2d	T	G	3: 106,407,271 (GRCm39)	F441V	probably damaging	Het
Dhx33	T	C	11: 70,879,978 (GRCm39)	D344G	probably benign	Het
Disp3	A	G	4: 148,337,284 (GRCm39)	S844P	probably benign	Het
Dock2	T	C	11: 34,599,722 (GRCm39)	K286E	probably damaging	Het
Fam228a	T	C	12: 4,768,671 (GRCm39)	E203G	probably benign	Het
Fbxo38	GTGCTGCTGCTGCTGCTGCTGC	GTGCTGCTGCTGCTGCTGC	18: 62,648,399 (GRCm39)		probably benign	Het
Frmpd4	G	A	X: 166,269,803 (GRCm39)	T493M	probably damaging	Het
Galnt13	A	G	2: 54,823,519 (GRCm39)	N365S	possibly damaging	Het
Hrob	A	G	11: 102,148,732 (GRCm39)	E381G	possibly damaging	Het
Ighv1-19	C	A	12: 114,672,497 (GRCm39)	C40F	probably damaging	Het
Ints4	A	G	7: 97,155,308 (GRCm39)	Q320R	probably benign	Het
Kctd5	T	C	17: 24,278,212 (GRCm39)	D146G	probably benign	Het
Loxl3	T	C	6: 83,027,652 (GRCm39)		probably null	Het
Lrp2	G	A	2: 69,294,923 (GRCm39)	P3465L	probably damaging	Het
Lrp2	A	T	2: 69,365,251 (GRCm39)		probably null	Het
Manba	G	A	3: 135,260,611 (GRCm39)	V599I	probably benign	Het
Mbd6	A	G	10: 127,121,637 (GRCm39)		probably benign	Het
Mrc2	G	A	11: 105,239,257 (GRCm39)		probably null	Het
Nepn	A	T	10: 52,280,110 (GRCm39)	N401Y	probably damaging	Het
Npas3	T	C	12: 53,401,175 (GRCm39)	I40T	probably benign	Het
Or1e29	T	C	11: 73,667,565 (GRCm39)	E196G	probably benign	Het
Or1j19	A	T	2: 36,676,578 (GRCm39)	I14F	possibly damaging	Het
Or2d4	T	A	7: 106,543,684 (GRCm39)	N175Y	probably damaging	Het
Or4n4b	T	A	14: 50,535,962 (GRCm39)	D268V	probably damaging	Het
Or5p73	T	C	7: 108,064,633 (GRCm39)	I34T	possibly damaging	Het
Or8g33	T	A	9: 39,338,365 (GRCm39)	M1L	probably benign	Het
Phtf1	A	G	3: 103,893,095 (GRCm39)	M120V	probably benign	Het
Plxna2	A	G	1: 194,471,193 (GRCm39)	Y988C	probably benign	Het
Rgs12	G	A	5: 35,189,595 (GRCm39)	E658K	probably damaging	Het
Ripor3	C	G	2: 167,834,739 (GRCm39)	E251Q	probably damaging	Het
Sec24b	T	C	3: 129,827,482 (GRCm39)	K203R	possibly damaging	Het
Serpina1d	T	A	12: 103,734,164 (GRCm39)	N47Y	possibly damaging	Het
Setx	GTGGCT	GT	2: 29,044,073 (GRCm39)	1814	probably null	Het
Sirpb1c	T	C	3: 15,887,287 (GRCm39)	K184R	probably damaging	Het
Slc16a10	G	C	10: 39,932,620 (GRCm39)	H314D	possibly damaging	Het
Upp2	T	C	2: 58,645,379 (GRCm39)	S41P	probably benign	Het
Vmn1r10	A	G	6: 57,090,719 (GRCm39)	T104A	probably damaging	Het
Wdhd1	A	C	14: 47,485,349 (GRCm39)	S838R	possibly damaging	Het
Zer1	A	G	2: 30,000,923 (GRCm39)	V166A	probably benign	Het
Zfp217	T	C	2: 169,956,308 (GRCm39)	N897D	probably benign	Het
Zfp960	T	A	17: 17,308,633 (GRCm39)	L449H	probably damaging	Het

Other mutations in Nol10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00916:Nol10	APN	12	17,411,130 (GRCm39)	splice site	probably benign
R1769:Nol10	UTSW	12	17,466,709 (GRCm39)	splice site	probably benign
R1884:Nol10	UTSW	12	17,418,390 (GRCm39)	critical splice donor site	probably null
R1930:Nol10	UTSW	12	17,398,555 (GRCm39)	start codon destroyed	probably null	0.99
R1931:Nol10	UTSW	12	17,398,555 (GRCm39)	start codon destroyed	probably null	0.99
R2010:Nol10	UTSW	12	17,466,102 (GRCm39)	missense	probably benign	0.00
R2037:Nol10	UTSW	12	17,411,152 (GRCm39)	missense	probably benign	0.01
R2168:Nol10	UTSW	12	17,423,585 (GRCm39)	missense	probably damaging	1.00
R3729:Nol10	UTSW	12	17,474,674 (GRCm39)	missense	probably benign	0.42
R4368:Nol10	UTSW	12	17,429,293 (GRCm39)	missense	probably damaging	1.00
R4618:Nol10	UTSW	12	17,398,562 (GRCm39)	missense	probably damaging	0.98
R4736:Nol10	UTSW	12	17,405,288 (GRCm39)	missense	probably damaging	1.00
R5342:Nol10	UTSW	12	17,419,621 (GRCm39)	splice site	probably null
R5451:Nol10	UTSW	12	17,409,103 (GRCm39)	nonsense	probably null
R5536:Nol10	UTSW	12	17,466,138 (GRCm39)	nonsense	probably null
R5586:Nol10	UTSW	12	17,466,829 (GRCm39)	missense	possibly damaging	0.73
R6045:Nol10	UTSW	12	17,398,479 (GRCm39)	start gained	probably benign
R6833:Nol10	UTSW	12	17,402,728 (GRCm39)	missense	probably benign	0.03
R7039:Nol10	UTSW	12	17,479,185 (GRCm39)	missense	possibly damaging	0.94
R7189:Nol10	UTSW	12	17,423,562 (GRCm39)	critical splice acceptor site	probably null
R7251:Nol10	UTSW	12	17,452,108 (GRCm39)	missense	probably damaging	1.00
R7399:Nol10	UTSW	12	17,452,174 (GRCm39)	missense	probably damaging	1.00
R7600:Nol10	UTSW	12	17,419,481 (GRCm39)	missense	probably damaging	0.99
R7650:Nol10	UTSW	12	17,412,683 (GRCm39)	critical splice donor site	probably null
R7729:Nol10	UTSW	12	17,474,676 (GRCm39)	missense	possibly damaging	0.62
R7772:Nol10	UTSW	12	17,398,586 (GRCm39)	missense	probably damaging	1.00
R7869:Nol10	UTSW	12	17,408,239 (GRCm39)	missense	probably null	0.93
R7972:Nol10	UTSW	12	17,402,648 (GRCm39)	missense	probably benign	0.15
R8686:Nol10	UTSW	12	17,419,772 (GRCm39)	intron	probably benign
R8926:Nol10	UTSW	12	17,466,871 (GRCm39)	missense	probably benign	0.00
R8936:Nol10	UTSW	12	17,466,863 (GRCm39)	missense	probably benign	0.08
R8966:Nol10	UTSW	12	17,419,507 (GRCm39)	missense	possibly damaging	0.64
R8994:Nol10	UTSW	12	17,402,717 (GRCm39)	missense	probably damaging	1.00
R9002:Nol10	UTSW	12	17,408,134 (GRCm39)	missense	probably damaging	1.00
R9096:Nol10	UTSW	12	17,466,199 (GRCm39)	missense	probably benign
R9196:Nol10	UTSW	12	17,455,316 (GRCm39)	missense	probably benign	0.04
R9548:Nol10	UTSW	12	17,466,144 (GRCm39)	missense	possibly damaging	0.49
Z1177:Nol10	UTSW	12	17,409,089 (GRCm39)	critical splice acceptor site	probably null

Predicted Primers

PCR Primer
(F):5'- ATGACAGTTTGAGGGCAGCTG -3'
(R):5'- CTCTGGCTATAGGAAACACTGG -3'

Sequencing Primer
(F):5'- GACTCTGGGCTCTGCTAGACAAG -3'
(R):5'- CTGGAGTAGGGAACACAGCTTTCTC -3'

Posted On

2015-03-18