Mutagenetix > Incidental Mutation

Incidental Mutation 'R1642:Nolc1'

173649

Institutional Source

Beutler Lab

Gene Symbol

Nolc1

Ensembl Gene

ENSMUSG00000015176

Gene Name

nucleolar and coiled-body phosphoprotein 1

Synonyms

3230402K17Rik, P130, NOPP140

MMRRC Submission

039678-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1642 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

46064302-46073969 bp(+) (GRCm39)

Type of Mutation

critical splice donor site (1 bp from exon)

DNA Base Change (assembly)

G to C at 46067461 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000153545 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000165017] [ENSMUST00000223728] [ENSMUST00000223741] [ENSMUST00000224490] [ENSMUST00000225780]

AlphaFold

E9Q5C9

Predicted Effect

probably null
Transcript: ENSMUST00000165017

SMART Domains

Protein: ENSMUSP00000128331
Gene: ENSMUSG00000015176

Domain	Start	End	E-Value	Type
LisH	10	42	2.3e-2	SMART
low complexity region	76	100	N/A	INTRINSIC
low complexity region	123	187	N/A	INTRINSIC
low complexity region	189	210	N/A	INTRINSIC
low complexity region	224	272	N/A	INTRINSIC
low complexity region	273	285	N/A	INTRINSIC
low complexity region	297	313	N/A	INTRINSIC
low complexity region	315	328	N/A	INTRINSIC
low complexity region	329	342	N/A	INTRINSIC
low complexity region	353	383	N/A	INTRINSIC
low complexity region	429	470	N/A	INTRINSIC
low complexity region	472	486	N/A	INTRINSIC
low complexity region	489	501	N/A	INTRINSIC
low complexity region	509	538	N/A	INTRINSIC
low complexity region	558	579	N/A	INTRINSIC
Pfam:SRP40_C	627	699	1.1e-32	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000223683

Predicted Effect

probably null
Transcript: ENSMUST00000223728

Predicted Effect

probably null
Transcript: ENSMUST00000223741

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000224034

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000224434

Predicted Effect

probably benign
Transcript: ENSMUST00000224490

Predicted Effect

probably null
Transcript: ENSMUST00000225780

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000225758

Coding Region Coverage

1x: 99.0%
3x: 98.1%
10x: 95.4%
20x: 89.7%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310057J18Rik	A	G	10: 28,862,233 (GRCm39)	V19A	probably benign	Het
6820408C15Rik	T	C	2: 152,282,774 (GRCm39)	Y210H	probably damaging	Het
Aars1	T	A	8: 111,769,882 (GRCm39)	I327N	possibly damaging	Het
Abca6	T	A	11: 110,109,107 (GRCm39)	N688Y	possibly damaging	Het
Ablim3	T	C	18: 61,947,382 (GRCm39)	K457R	probably benign	Het
Acsm2	A	T	7: 119,162,860 (GRCm39)	N45Y	probably damaging	Het
Agxt2	T	C	15: 10,373,917 (GRCm39)	S108P	probably damaging	Het
Akr1cl	A	T	1: 65,060,588 (GRCm39)	M174K	probably benign	Het
Armh4	T	C	14: 50,005,867 (GRCm39)		probably null	Het
Bfsp1	G	A	2: 143,683,683 (GRCm39)	R214W	probably damaging	Het
Cby3	A	G	11: 50,250,343 (GRCm39)	D183G	probably damaging	Het
Clip2	T	C	5: 134,532,107 (GRCm39)	D566G	possibly damaging	Het
Colgalt1	A	G	8: 72,073,401 (GRCm39)	I341V	probably benign	Het
Cyp2c38	T	A	19: 39,390,153 (GRCm39)	D349V	probably damaging	Het
Cyp3a16	T	A	5: 145,406,399 (GRCm39)	I18F	unknown	Het
Degs2	C	T	12: 108,658,451 (GRCm39)	C176Y	probably benign	Het
Dhx16	A	T	17: 36,201,957 (GRCm39)	T995S	probably damaging	Het
Dicer1	A	T	12: 104,679,415 (GRCm39)	C521S	probably damaging	Het
Dop1b	T	C	16: 93,559,203 (GRCm39)	S532P	probably benign	Het
Dpysl4	T	G	7: 138,670,254 (GRCm39)	M124R	probably damaging	Het
Eml6	A	G	11: 29,727,001 (GRCm39)		probably null	Het
Erbb4	A	T	1: 68,370,393 (GRCm39)	V395D	probably damaging	Het
Esf1	T	C	2: 140,000,406 (GRCm39)	D460G	possibly damaging	Het
F830045P16Rik	G	A	2: 129,305,634 (GRCm39)	H247Y	probably benign	Het
Fsbp	T	A	4: 11,583,965 (GRCm39)	S221R	probably benign	Het
Fstl5	T	A	3: 76,317,929 (GRCm39)	N198K	possibly damaging	Het
Gemin5	G	T	11: 58,029,906 (GRCm39)	H855Q	probably damaging	Het
Gjd3	T	C	11: 98,873,535 (GRCm39)	E103G	probably benign	Het
I0C0044D17Rik	A	G	4: 98,708,471 (GRCm39)		probably benign	Het
Iqca1l	C	A	5: 24,757,686 (GRCm39)	R177L	probably damaging	Het
Itgb4	A	T	11: 115,898,183 (GRCm39)	R1646W	probably damaging	Het
Klri2	A	T	6: 129,715,837 (GRCm39)	C121S	probably benign	Het
Lamc3	A	G	2: 31,806,008 (GRCm39)	Y703C	probably damaging	Het
Lrrc10	A	G	10: 116,881,788 (GRCm39)	N154S	probably damaging	Het
Lrriq1	A	G	10: 103,050,317 (GRCm39)	F812L	probably benign	Het
Naip2	C	T	13: 100,298,489 (GRCm39)	A516T	possibly damaging	Het
Nav1	T	C	1: 135,380,010 (GRCm39)	Y1564C	probably damaging	Het
Ndufc1	T	C	3: 51,315,664 (GRCm39)	T25A	probably benign	Het
Neurl4	A	G	11: 69,794,485 (GRCm39)	M23V	probably benign	Het
Nnt	A	G	13: 119,541,086 (GRCm39)		probably null	Het
Nrg1	A	T	8: 32,314,536 (GRCm39)	M289K	probably benign	Het
Oas3	G	T	5: 120,915,639 (GRCm39)	H17Q	possibly damaging	Het
Or10h1	A	G	17: 33,418,430 (GRCm39)	Y132C	probably damaging	Het
Or2z2	A	G	11: 58,346,664 (GRCm39)	I37T	probably benign	Het
Or5m5	A	G	2: 85,814,201 (GRCm39)	K6E	probably benign	Het
Or8g36	C	T	9: 39,422,650 (GRCm39)	R122H	possibly damaging	Het
Parp9	T	C	16: 35,788,067 (GRCm39)	Y612H	probably benign	Het
Pcdh1	A	T	18: 38,332,283 (GRCm39)	M240K	possibly damaging	Het
Pcdhb9	A	G	18: 37,533,987 (GRCm39)		probably benign	Het
Plpp2	A	G	10: 79,366,518 (GRCm39)	V42A	probably damaging	Het
Ppic	C	T	18: 53,540,134 (GRCm39)	V172M	probably damaging	Het
Ppp1r9b	A	G	11: 94,892,150 (GRCm39)		silent	Het
Prop1	A	G	11: 50,844,152 (GRCm39)	V27A	possibly damaging	Het
Psmc5	A	G	11: 106,153,242 (GRCm39)	T295A	probably benign	Het
Rpa1	A	G	11: 75,203,517 (GRCm39)		probably null	Het
Rrp12	A	G	19: 41,860,176 (GRCm39)	F1016L	probably damaging	Het
Scn2a	A	T	2: 65,514,041 (GRCm39)	I242F	probably damaging	Het
Slco1a6	T	A	6: 142,032,160 (GRCm39)	H655L	probably benign	Het
Sp140	G	A	1: 85,538,545 (GRCm39)		probably null	Het
Syne1	A	G	10: 5,298,694 (GRCm39)	I1071T	possibly damaging	Het
Tbc1d9b	A	G	11: 50,040,659 (GRCm39)	D392G	probably damaging	Het
Tcaim	G	A	9: 122,647,838 (GRCm39)		probably null	Het
Tgm3	T	A	2: 129,889,702 (GRCm39)	V632E	probably damaging	Het
Triobp	C	A	15: 78,886,348 (GRCm39)	R1830S	probably damaging	Het
Ttn	A	T	2: 76,641,587 (GRCm39)	L5176Q	possibly damaging	Het
Vps8	A	G	16: 21,400,329 (GRCm39)	T1266A	probably benign	Het
Znfx1	T	C	2: 166,880,930 (GRCm39)	I285V	possibly damaging	Het

Other mutations in Nolc1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02679:Nolc1	APN	19	46,071,468 (GRCm39)	unclassified	probably benign
FR4976:Nolc1	UTSW	19	46,069,814 (GRCm39)	small insertion	probably benign
FR4976:Nolc1	UTSW	19	46,069,795 (GRCm39)	small insertion	probably benign
R0106:Nolc1	UTSW	19	46,068,528 (GRCm39)	splice site	probably benign
R0121:Nolc1	UTSW	19	46,069,817 (GRCm39)	unclassified	probably benign
R0140:Nolc1	UTSW	19	46,069,817 (GRCm39)	unclassified	probably benign
R0501:Nolc1	UTSW	19	46,067,359 (GRCm39)	missense	probably damaging	1.00
R0513:Nolc1	UTSW	19	46,072,598 (GRCm39)	missense	probably damaging	1.00
R0676:Nolc1	UTSW	19	46,068,528 (GRCm39)	splice site	probably benign
R1553:Nolc1	UTSW	19	46,069,814 (GRCm39)	small insertion	probably benign
R1698:Nolc1	UTSW	19	46,069,870 (GRCm39)	splice site	probably null
R2067:Nolc1	UTSW	19	46,072,046 (GRCm39)	missense	probably damaging	1.00
R2113:Nolc1	UTSW	19	46,069,800 (GRCm39)	small insertion	probably benign
R2113:Nolc1	UTSW	19	46,069,798 (GRCm39)	small insertion	probably benign
R2300:Nolc1	UTSW	19	46,069,807 (GRCm39)	small insertion	probably benign
R2300:Nolc1	UTSW	19	46,069,798 (GRCm39)	small insertion	probably benign
R2895:Nolc1	UTSW	19	46,069,791 (GRCm39)	small insertion	probably benign
R2999:Nolc1	UTSW	19	46,071,594 (GRCm39)	small deletion	probably benign
R3737:Nolc1	UTSW	19	46,069,816 (GRCm39)	small insertion	probably benign
R3737:Nolc1	UTSW	19	46,069,792 (GRCm39)	small insertion	probably benign
R3737:Nolc1	UTSW	19	46,069,809 (GRCm39)	small insertion	probably benign
R3747:Nolc1	UTSW	19	46,069,795 (GRCm39)	small insertion	probably benign
R3806:Nolc1	UTSW	19	46,069,791 (GRCm39)	small insertion	probably benign
R3807:Nolc1	UTSW	19	46,069,791 (GRCm39)	small insertion	probably benign
R3807:Nolc1	UTSW	19	46,069,798 (GRCm39)	small insertion	probably benign
R3807:Nolc1	UTSW	19	46,069,810 (GRCm39)	small insertion	probably benign
R4035:Nolc1	UTSW	19	46,069,797 (GRCm39)	small insertion	probably benign
R4619:Nolc1	UTSW	19	46,071,959 (GRCm39)	missense	probably damaging	1.00
R4856:Nolc1	UTSW	19	46,071,594 (GRCm39)	small deletion	probably benign
R4999:Nolc1	UTSW	19	46,067,359 (GRCm39)	missense	probably damaging	1.00
R5103:Nolc1	UTSW	19	46,070,103 (GRCm39)	nonsense	probably null
R5559:Nolc1	UTSW	19	46,071,594 (GRCm39)	small deletion	probably benign
R5837:Nolc1	UTSW	19	46,071,622 (GRCm39)	unclassified	probably benign
R6457:Nolc1	UTSW	19	46,071,509 (GRCm39)	unclassified	probably benign
R7467:Nolc1	UTSW	19	46,070,773 (GRCm39)	missense	unknown
R7497:Nolc1	UTSW	19	46,071,257 (GRCm39)	missense	probably benign	0.23
R8011:Nolc1	UTSW	19	46,070,023 (GRCm39)	missense	unknown
R8806:Nolc1	UTSW	19	46,071,471 (GRCm39)	missense	unknown
RF027:Nolc1	UTSW	19	46,069,802 (GRCm39)	small insertion	probably benign
RF031:Nolc1	UTSW	19	46,069,810 (GRCm39)	small insertion	probably benign
RF034:Nolc1	UTSW	19	46,069,810 (GRCm39)	small insertion	probably benign
RF040:Nolc1	UTSW	19	46,069,802 (GRCm39)	small insertion	probably benign
RF044:Nolc1	UTSW	19	46,069,810 (GRCm39)	small insertion	probably benign
X0050:Nolc1	UTSW	19	46,069,791 (GRCm39)	small deletion	probably benign
Y5377:Nolc1	UTSW	19	46,069,808 (GRCm39)	small insertion	probably benign
Y5379:Nolc1	UTSW	19	46,069,798 (GRCm39)	small insertion	probably benign
Z1088:Nolc1	UTSW	19	46,071,537 (GRCm39)	unclassified	probably benign

Predicted Primers

PCR Primer
(F):5'- TGCATCAGCAGGTCCACCAAAG -3'
(R):5'- CAGAATTCATGCAATGCGGAGCAG -3'

Sequencing Primer
(F):5'- AGCCCCAAAGGTGAAGTTAC -3'
(R):5'- ACAAACCTGGACAGGCTTTTTC -3'

Posted On

2014-04-24