Mutagenetix > Incidental Mutation

Incidental Mutation 'R1480:Nol7'

164328

Institutional Source

Beutler Lab

Gene Symbol

Nol7

Ensembl Gene

ENSMUSG00000063200

Gene Name

nucleolar protein 7

Synonyms

RARG-1, 2210008F15Rik, NOP27, 5730556I21Rik

MMRRC Submission

039533-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.909) question?

Stock #

R1480 (G1)

Quality Score

144

Status

Not validated

Chromosome

Chromosomal Location

43551852-43556334 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 43552104 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Valine at position 75 (E75V)

Ref Sequence

ENSEMBL: ENSMUSP00000152581 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000066804] [ENSMUST00000071926] [ENSMUST00000144326] [ENSMUST00000222499] [ENSMUST00000223194] [ENSMUST00000222651]

AlphaFold

Q9D7Z3

Predicted Effect

probably benign
Transcript: ENSMUST00000066804

SMART Domains

Protein: ENSMUSP00000071048
Gene: ENSMUSG00000054021

Domain	Start	End	E-Value	Type
Pfam:SIR2	58	256	5.3e-50	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000071926
AA Change: E75V

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000071818
Gene: ENSMUSG00000063200
AA Change: E75V

Domain	Start	End	E-Value	Type
low complexity region	24	32	N/A	INTRINSIC
low complexity region	44	63	N/A	INTRINSIC
low complexity region	66	85	N/A	INTRINSIC
low complexity region	89	100	N/A	INTRINSIC
low complexity region	150	161	N/A	INTRINSIC
Pfam:NUC129	167	229	1.1e-34	PFAM
low complexity region	236	251	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000144326

SMART Domains

Protein: ENSMUSP00000130636
Gene: ENSMUSG00000038546

Domain	Start	End	E-Value	Type
low complexity region	2	114	N/A	INTRINSIC
SPRY	194	315	1.66e-43	SMART
LisH	347	379	6.82e-5	SMART
CTLH	385	442	9.78e-15	SMART
low complexity region	455	478	N/A	INTRINSIC
CRA	596	698	1.6e-24	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000220601

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000220997

Predicted Effect

probably benign
Transcript: ENSMUST00000221092

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000222305

Predicted Effect

probably damaging
Transcript: ENSMUST00000222499
AA Change: E75V

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

Predicted Effect

probably benign
Transcript: ENSMUST00000223194

Predicted Effect

probably benign
Transcript: ENSMUST00000222651

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000222416

Predicted Effect

probably benign
Transcript: ENSMUST00000222754

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000223188

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.0%
20x: 94.6%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene localizes to the nucleolus, where it maintains nucleolar structure and cell growth rates. The encoded protein also functions as a tumor suppressor and regulator of angiogenesis. The RB tumor suppressor gene recruits transcription factors to this gene and positively regulates its expression. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2015]

Allele List at MGI

Other mutations in this stock

Total: 78 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca2	C	T	2: 25,323,409 (GRCm39)	R126C	possibly damaging	Het
Abcb9	C	A	5: 124,216,889 (GRCm39)	A443S	probably benign	Het
Adcy3	A	G	12: 4,262,171 (GRCm39)	M1074V	probably damaging	Het
Adnp	A	G	2: 168,025,454 (GRCm39)	Y614H	probably damaging	Het
Agbl4	G	A	4: 111,423,914 (GRCm39)	M313I	possibly damaging	Het
AI987944	T	C	7: 41,024,343 (GRCm39)	D212G	probably benign	Het
Anxa2	TCCC	TCC	9: 69,397,036 (GRCm39)		probably null	Het
Aplp1	A	G	7: 30,135,448 (GRCm39)	S537P	probably benign	Het
Arap2	T	A	5: 62,826,472 (GRCm39)	R1031*	probably null	Het
Arid1a	A	G	4: 133,407,700 (GRCm39)	M2269T	unknown	Het
Ash1l	C	A	3: 88,892,359 (GRCm39)	P1413T	probably damaging	Het
Auh	G	A	13: 52,989,532 (GRCm39)	P308L	probably benign	Het
B3gnt5	A	T	16: 19,588,617 (GRCm39)	I279L	probably damaging	Het
Camkk2	T	C	5: 122,872,341 (GRCm39)		probably null	Het
Ccdc158	T	C	5: 92,796,903 (GRCm39)	K478E	probably damaging	Het
Ces1f	T	C	8: 94,000,782 (GRCm39)	I121V	probably benign	Het
Chad	A	T	11: 94,455,963 (GRCm39)		probably benign	Het
Col6a1	T	C	10: 76,545,752 (GRCm39)	I907V	unknown	Het
Cpe	T	A	8: 65,047,969 (GRCm39)	T432S	probably benign	Het
Csmd3	T	C	15: 47,595,325 (GRCm39)	T1941A	possibly damaging	Het
Dennd3	G	A	15: 73,404,695 (GRCm39)	V257I	probably benign	Het
Dnajc21	T	C	15: 10,460,037 (GRCm39)		probably null	Het
Dqx1	A	G	6: 83,036,433 (GRCm39)	R146G	possibly damaging	Het
Etf1	T	C	18: 35,042,276 (GRCm39)	E261G	probably damaging	Het
Fermt2	C	T	14: 45,699,244 (GRCm39)	V617I	possibly damaging	Het
Gabarap	T	C	11: 69,882,551 (GRCm39)	Y5H	probably damaging	Het
Gdap1	A	G	1: 17,215,781 (GRCm39)	Y29C	probably damaging	Het
Gimap5	A	G	6: 48,729,964 (GRCm39)	E178G	probably damaging	Het
Gpatch1	C	T	7: 35,002,763 (GRCm39)	G249E	probably damaging	Het
Gse1	T	G	8: 121,299,133 (GRCm39)		probably benign	Het
Kifc3	T	C	8: 95,836,515 (GRCm39)	D82G	probably damaging	Het
Kit	G	A	5: 75,797,977 (GRCm39)	D422N	probably benign	Het
Klhl28	A	T	12: 65,003,995 (GRCm39)	F173I	probably damaging	Het
Klk1b22	A	G	7: 43,766,278 (GRCm39)	D253G	possibly damaging	Het
Lias	T	A	5: 65,549,634 (GRCm39)	H39Q	probably benign	Het
Lrp1b	T	A	2: 40,793,401 (GRCm39)	D2504V	probably damaging	Het
Mgat5	A	T	1: 127,387,716 (GRCm39)	R557S	probably damaging	Het
Mrpl54	T	C	10: 81,101,489 (GRCm39)	T91A	probably benign	Het
Myh3	T	A	11: 66,984,371 (GRCm39)	D1069E	possibly damaging	Het
Nek1	T	A	8: 61,577,360 (GRCm39)		probably null	Het
Nfyc	A	C	4: 120,625,921 (GRCm39)		probably null	Het
Nomo1	T	A	7: 45,710,337 (GRCm39)	V606E	probably damaging	Het
Npat	TGGTAAAA	T	9: 53,474,366 (GRCm39)		probably null	Het
Nt5c1b	A	G	12: 10,424,886 (GRCm39)	E142G	probably damaging	Het
Ogdh	A	T	11: 6,297,827 (GRCm39)		probably null	Het
Or1o4	A	G	17: 37,590,636 (GRCm39)	V225A	probably benign	Het
Parg	A	T	14: 31,931,585 (GRCm39)	K402*	probably null	Het
Patj	G	A	4: 98,357,819 (GRCm39)	G695E	probably damaging	Het
Pde3a	G	A	6: 141,433,300 (GRCm39)	S777N	probably benign	Het
Phactr2	G	A	10: 13,129,536 (GRCm39)	P174L	possibly damaging	Het
Phtf1	C	T	3: 103,894,750 (GRCm39)	R113*	probably null	Het
Pik3r4	G	T	9: 105,564,443 (GRCm39)	V1346L	probably benign	Het
Prkcb	T	C	7: 122,193,865 (GRCm39)	W525R	probably damaging	Het
Prl8a1	C	T	13: 27,758,055 (GRCm39)	R218H	possibly damaging	Het
Pum3	T	C	19: 27,376,310 (GRCm39)	E536G	probably benign	Het
Rb1	T	C	14: 73,500,042 (GRCm39)	N535S	probably benign	Het
Rbm7	G	T	9: 48,401,016 (GRCm39)	D237E	probably benign	Het
Ripor1	T	C	8: 106,342,180 (GRCm39)	V122A	probably damaging	Het
Sdhc	C	T	1: 170,973,370 (GRCm39)	R11H	probably benign	Het
Sema3c	A	G	5: 17,887,029 (GRCm39)	N360S	possibly damaging	Het
Serpinb5	T	A	1: 106,809,437 (GRCm39)	M281K	probably benign	Het
Serpinc1	A	G	1: 160,822,889 (GRCm39)	E210G	probably benign	Het
Shoc2	T	C	19: 53,976,202 (GRCm39)	S31P	probably benign	Het
Sult2a3	T	A	7: 13,856,836 (GRCm39)	N28I	possibly damaging	Het
Svil	C	T	18: 5,057,345 (GRCm39)	P598S	probably damaging	Het
Tacc3	G	A	5: 33,821,941 (GRCm39)	V234I	probably benign	Het
Tacr1	A	T	6: 82,469,511 (GRCm39)	M132L	possibly damaging	Het
Tas2r104	C	A	6: 131,662,257 (GRCm39)	V151F	probably benign	Het
Tbc1d10b	C	T	7: 126,802,950 (GRCm39)	S326N	probably benign	Het
Trim12c	C	T	7: 103,997,451 (GRCm39)	C35Y	probably damaging	Het
Trrap	T	C	5: 144,755,123 (GRCm39)	I2067T	probably benign	Het
Upk1a	T	C	7: 30,306,311 (GRCm39)	I152V	probably benign	Het
Vmn2r39	T	G	7: 9,017,955 (GRCm39)	T794P	probably damaging	Het
Wnk2	G	A	13: 49,210,708 (GRCm39)	P1704S	probably damaging	Het
Zfp609	T	C	9: 65,610,593 (GRCm39)	E790G	possibly damaging	Het
Zmym1	G	T	4: 126,942,405 (GRCm39)	T563K	probably damaging	Het
Zranb1	T	A	7: 132,551,745 (GRCm39)	F132Y	probably benign	Het
Zranb3	C	T	1: 128,019,599 (GRCm39)	A48T	probably damaging	Het

Other mutations in Nol7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01821:Nol7	APN	13	43,552,216 (GRCm39)	missense	probably benign	0.02
IGL03011:Nol7	APN	13	43,554,769 (GRCm39)	unclassified	probably benign
R0743:Nol7	UTSW	13	43,554,091 (GRCm39)	missense	probably benign	0.19
R0884:Nol7	UTSW	13	43,554,091 (GRCm39)	missense	probably benign	0.19
R4379:Nol7	UTSW	13	43,555,051 (GRCm39)	missense	probably damaging	1.00
R5435:Nol7	UTSW	13	43,554,848 (GRCm39)	missense	possibly damaging	0.54
R7185:Nol7	UTSW	13	43,560,307 (GRCm39)	critical splice acceptor site	probably null
R7487:Nol7	UTSW	13	43,552,076 (GRCm39)	missense	probably damaging	1.00
R8052:Nol7	UTSW	13	43,554,990 (GRCm39)	missense	probably damaging	1.00
R8986:Nol7	UTSW	13	43,554,985 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGCATCTCACAAGCAACGATGGTC -3'
(R):5'- TTTAGCAAGGGAACTCTAGCCCCG -3'

Sequencing Primer
(F):5'- aaaaaaaaaaaaaaaaaaaaGGCGGC -3'
(R):5'- GCCGAGTTTACATAAGCGAC -3'

Posted On

2014-03-28