Mutagenetix > Incidental Mutations

Incidental Mutation 'R6941:Nufip2'

540561

Institutional Source

Beutler Lab

Gene Symbol

Nufip2

Ensembl Gene

ENSMUSG00000037857

Gene Name

nuclear fragile X mental retardation protein interacting protein 2

Synonyms

9530056D24Rik, 1110001M19Rik

MMRRC Submission

Accession Numbers

Is this an essential gene?

Probably essential (E-score: 0.962) question?

Stock #

R6941 (G1)

Quality Score

108.467

Status

Not validated

Chromosome

Chromosomal Location

77686155-77741921 bp(+) (GRCm38)

Type of Mutation

small deletion (1 aa in frame mutation)

DNA Base Change (assembly)

CCAGCAGCAGCAGCAGCAGCAG to CCAGCAGCAGCAGCAGCAG at 77686296 bp

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000137922 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000100802] [ENSMUST00000181023]

Predicted Effect

probably benign
Transcript: ENSMUST00000100802

SMART Domains

Protein: ENSMUSP00000098365
Gene: ENSMUSG00000037857

Domain	Start	End	E-Value	Type
low complexity region	7	61	N/A	INTRINSIC
Pfam:NUFIP2	90	685	2.4e-292	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000126942

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000155238

Predicted Effect

probably benign
Transcript: ENSMUST00000181023

SMART Domains

Protein: ENSMUSP00000137922
Gene: ENSMUSG00000037857

Domain	Start	End	E-Value	Type
low complexity region	7	61	N/A	INTRINSIC
Pfam:NUFIP2	89	681	7e-293	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.1%
20x: 97.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca16	A	T	7: 120,541,147	I1557F	probably damaging	Het
Acad10	A	T	5: 121,649,357	D176E	probably damaging	Het
Acta2	A	T	19: 34,252,522	V11E	probably damaging	Het
Ampd2	T	C	3: 108,079,293	H225R	probably damaging	Het
Arfgef3	A	G	10: 18,625,455	Y1016H	possibly damaging	Het
Atg7	C	T	6: 114,673,678	T83M	possibly damaging	Het
AU018091	A	G	7: 3,159,427		probably null	Het
Birc2	A	G	9: 7,819,468	V481A	probably benign	Het
C130060K24Rik	G	A	6: 65,447,401	M126I	probably damaging	Het
Cabp1	A	T	5: 115,172,901	D295E	probably damaging	Het
Cd180	A	T	13: 102,706,191	T582S	probably benign	Het
Cnksr3	A	G	10: 7,126,758	S145P	probably damaging	Het
Ddx27	A	G	2: 167,015,377	D15G	possibly damaging	Het
Dsc1	T	C	18: 20,097,189	Y353C	probably benign	Het
Dsg1c	C	T	18: 20,267,923	T161I	probably damaging	Het
Epm2a	A	G	10: 11,391,085		probably null	Het
Fat2	T	C	11: 55,262,088	H3766R	probably benign	Het
Fjx1	A	G	2: 102,450,558	V344A	probably benign	Het
Frmd3	A	G	4: 74,098,126	I93V	probably benign	Het
Gbe1	TAGTAAGAGT	TAGT	16: 70,433,556		probably benign	Het
Gdf15	A	G	8: 70,630,144	L104P	possibly damaging	Het
Glra3	G	A	8: 55,940,926	R24Q	probably benign	Het
Gm4070	G	A	7: 105,901,980	Q622*	probably null	Het
Ighv1-9	A	T	12: 114,583,828	M31K	probably benign	Het
Ipmk	G	A	10: 71,348,090	G47S	probably null	Het
Itsn2	T	C	12: 4,629,641	I150T	probably benign	Het
Kcnq5	T	C	1: 21,405,844	Y545C	probably damaging	Het
Klk1b8	C	A	7: 43,952,789	H48Q	possibly damaging	Het
Lrit1	G	C	14: 37,060,095	V242L	probably damaging	Het
Lrrc34	T	C	3: 30,624,820	Y376C	probably benign	Het
Mast4	A	T	13: 102,804,714	D278E	probably damaging	Het
Mtmr3	T	C	11: 4,487,505	Y982C	possibly damaging	Het
Ndst4	T	G	3: 125,609,511	H422Q	possibly damaging	Het
Nek7	T	C	1: 138,502,638	E206G	probably damaging	Het
Olfr1451	T	A	19: 12,999,497	N170K	possibly damaging	Het
Pglyrp2	T	C	17: 32,416,074	Y438C	probably damaging	Het
Pigr	G	T	1: 130,847,327	W497L	probably damaging	Het
Pkd2l2	G	T	18: 34,416,883	V194L	probably benign	Het
Ppp1r16b	A	T	2: 158,696,148	K5M	probably damaging	Het
Psat1	A	T	19: 15,920,943	S35R	probably damaging	Het
Rab11fip1	G	A	8: 27,156,275	Q258*	probably null	Het
Rad51d	A	G	11: 82,889,797	L53P	probably damaging	Het
Rell2	G	A	18: 37,958,288	A169T	probably benign	Het
Rnf19b	T	C	4: 129,082,779	I545T	probably benign	Het
Slc12a1	G	T	2: 125,214,079	E843D	possibly damaging	Het
Slc1a4	A	G	11: 20,304,346	S507P	probably damaging	Het
Slc6a1	G	A	6: 114,313,512	W316*	probably null	Het
Spesp1	A	G	9: 62,272,870	L252P	probably damaging	Het
Sphkap	G	A	1: 83,408,090		probably benign	Het
Srcap	A	G	7: 127,542,597	T1850A	probably damaging	Het
Supv3l1	T	C	10: 62,430,586	T604A	possibly damaging	Het
Tacr1	A	G	6: 82,403,865	T86A	possibly damaging	Het
Tenm3	T	C	8: 48,674,416	R76G	probably damaging	Het
Tmprss6	C	A	15: 78,446,777	A419S	probably damaging	Het
Usp54	T	G	14: 20,562,109	I880L	probably benign	Het
Wwp2	T	A	8: 107,548,502	V377D	probably damaging	Het
Zfp735	A	T	11: 73,690,333	E65D	probably benign	Het
Zfy2	T	C	Y: 2,121,491	E134G	probably benign	Het

Other mutations in Nufip2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01361:Nufip2	APN	11	77692370	missense	possibly damaging	0.93
R0646:Nufip2	UTSW	11	77686453	missense	probably benign	0.33
R0667:Nufip2	UTSW	11	77692013	missense	possibly damaging	0.94
R1544:Nufip2	UTSW	11	77691907	missense	possibly damaging	0.57
R1546:Nufip2	UTSW	11	77691606	missense	probably damaging	0.99
R1629:Nufip2	UTSW	11	77693008	missense	probably benign	0.03
R1719:Nufip2	UTSW	11	77693090	missense	probably damaging	1.00
R1864:Nufip2	UTSW	11	77692298	missense	probably damaging	1.00
R3855:Nufip2	UTSW	11	77692889	missense	probably damaging	0.97
R4489:Nufip2	UTSW	11	77686229	start codon destroyed	probably null
R4584:Nufip2	UTSW	11	77741728	missense	unknown
R4585:Nufip2	UTSW	11	77741728	missense	unknown
R4586:Nufip2	UTSW	11	77741728	missense	unknown
R4779:Nufip2	UTSW	11	77686328	missense	unknown
R5111:Nufip2	UTSW	11	77691843	missense	probably benign	0.01
R5354:Nufip2	UTSW	11	77686277	missense	unknown
R6051:Nufip2	UTSW	11	77691916	missense	probably damaging	1.00
R6324:Nufip2	UTSW	11	77691661	missense	probably benign
R6505:Nufip2	UTSW	11	77691613	missense	probably benign	0.36
R7237:Nufip2	UTSW	11	77692770	missense	probably benign	0.00
R8351:Nufip2	UTSW	11	77692355	missense	probably damaging	0.98
R8355:Nufip2	UTSW	11	77692433	missense	probably damaging	1.00
R8451:Nufip2	UTSW	11	77692355	missense	probably damaging	0.98
R8455:Nufip2	UTSW	11	77692433	missense	probably damaging	1.00
R8547:Nufip2	UTSW	11	77692565	missense	probably damaging	1.00
Z1176:Nufip2	UTSW	11	77741791	makesense	probably null

Predicted Primers

PCR Primer
(F):5'- AATGCTGACGTTGAAGGCCC -3'
(R):5'- TTCTGCTCATGTTTCAGCGG -3'

Sequencing Primer
(F):5'- TCGCTTAACCAGTGCGCTG -3'
(R):5'- CTCATGTTTCAGCGGCTTGG -3'

Posted On

2018-11-06