Mutagenetix > Incidental Mutation

Incidental Mutation 'R3980:Nuggc'

311285

Institutional Source

Beutler Lab

Gene Symbol

Nuggc

Ensembl Gene

ENSMUSG00000061356

Gene Name

nuclear GTPase, germinal center associated

Synonyms

SLIP-GC, Gm600, LOC239151

MMRRC Submission

040843-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.088) question?

Stock #

R3980 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

65835995-65885980 bp(+) (GRCm39)

Type of Mutation

critical splice donor site (2 bp from exon)

DNA Base Change (assembly)

T to C at 65856542 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000118402 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000079469] [ENSMUST00000150897]

AlphaFold

D3YWJ0

Predicted Effect

probably null
Transcript: ENSMUST00000079469

SMART Domains

Protein: ENSMUSP00000078434
Gene: ENSMUSG00000061356

Domain	Start	End	E-Value	Type
Pfam:Dynamin_N	119	372	2.2e-15	PFAM
low complexity region	406	421	N/A	INTRINSIC
Blast:AAA	434	739	4e-14	BLAST
coiled coil region	758	792	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000150897

SMART Domains

Protein: ENSMUSP00000118402
Gene: ENSMUSG00000061356

Domain	Start	End	E-Value	Type
Pfam:Dynamin_N	103	356	6.1e-16	PFAM
low complexity region	390	405	N/A	INTRINSIC
Blast:AAA	418	723	4e-14	BLAST
coiled coil region	742	776	N/A	INTRINSIC

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 97.2%
20x: 94.8%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased somatic mutation frequency immunoglobulin and non-immunoglobulin loci in B cells. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrb1	G	A	15: 74,454,792 (GRCm39)	G268R	probably damaging	Het
Amacr	T	A	15: 10,989,015 (GRCm39)	Y240*	probably null	Het
Ankhd1	A	T	18: 36,780,666 (GRCm39)	H1906L	probably damaging	Het
Arhgef25	C	A	10: 127,023,089 (GRCm39)	C106F	probably damaging	Het
Bean1	A	T	8: 104,937,730 (GRCm39)	Q103L	possibly damaging	Het
Ccr9	A	T	9: 123,608,441 (GRCm39)	N41I	probably benign	Het
Ceacam16	A	G	7: 19,592,558 (GRCm39)	F117L	probably benign	Het
Col4a1	T	C	8: 11,289,155 (GRCm39)		probably benign	Het
Csk	A	G	9: 57,538,063 (GRCm39)	Y48H	probably damaging	Het
Csmd1	T	A	8: 15,956,056 (GRCm39)	K3384*	probably null	Het
Ctnnd2	T	A	15: 30,669,589 (GRCm39)	H399Q	probably benign	Het
Cutal	T	C	2: 34,772,325 (GRCm39)	Y30H	possibly damaging	Het
Cybb	T	C	X: 9,310,827 (GRCm39)	Y425C	probably damaging	Het
Dab2	A	G	15: 6,464,644 (GRCm39)		probably null	Het
Defb30	C	A	14: 63,273,421 (GRCm39)	C64F	probably damaging	Het
Eif2a	T	C	3: 58,446,960 (GRCm39)	I45T	probably benign	Het
Esyt1	T	A	10: 128,347,393 (GRCm39)	D1044V	probably damaging	Het
Gabpb2	A	T	3: 95,096,081 (GRCm39)	V382E	probably damaging	Het
Glb1	T	A	9: 114,246,132 (GRCm39)	I61K	probably damaging	Het
Insyn2b	G	A	11: 34,352,678 (GRCm39)	C240Y	probably benign	Het
Kcnt1	T	C	2: 25,783,226 (GRCm39)	V263A	possibly damaging	Het
Kdm5b	A	G	1: 134,547,408 (GRCm39)	D1019G	probably benign	Het
Klhl2	A	T	8: 65,196,109 (GRCm39)	L545M	probably damaging	Het
Klhl2	C	A	8: 65,196,115 (GRCm39)	G543C	probably damaging	Het
Krt31	G	T	11: 99,939,030 (GRCm39)	Q264K	probably damaging	Het
Lmnb1	A	G	18: 56,864,091 (GRCm39)	D232G	probably damaging	Het
Loxhd1	T	C	18: 77,501,855 (GRCm39)	F859L	probably damaging	Het
Map7	C	A	10: 20,143,099 (GRCm39)	T416K	unknown	Het
Med18	T	A	4: 132,190,251 (GRCm39)	I45F	probably benign	Het
Mn1	A	T	5: 111,569,636 (GRCm39)	H1202L	possibly damaging	Het
Mpp7	T	C	18: 7,444,062 (GRCm39)	D120G	probably benign	Het
Nlrp1b	A	T	11: 71,072,437 (GRCm39)	F469I	possibly damaging	Het
Nos3	T	A	5: 24,582,929 (GRCm39)	D685E	probably damaging	Het
Nrap	G	A	19: 56,369,984 (GRCm39)	A206V	probably benign	Het
Oasl1	C	T	5: 115,070,957 (GRCm39)	T274I	probably damaging	Het
Or10ak12	T	A	4: 118,666,500 (GRCm39)	Y187F	probably benign	Het
Or51a25	T	C	7: 102,372,959 (GRCm39)	N246S	probably damaging	Het
Parp3	T	C	9: 106,351,267 (GRCm39)	D278G	probably damaging	Het
Phc3	T	A	3: 30,991,080 (GRCm39)	Q346L	probably damaging	Het
Pigo	A	G	4: 43,019,231 (GRCm39)	L1029P	probably damaging	Het
Plcb3	A	G	19: 6,943,803 (GRCm39)	I66T	probably damaging	Het
Plch2	T	C	4: 155,069,255 (GRCm39)	S1019G	probably benign	Het
Plekhg6	C	A	6: 125,350,146 (GRCm39)	C264F	probably damaging	Het
Plxna2	C	T	1: 194,431,625 (GRCm39)	S538F	probably damaging	Het
Pou4f2	G	T	8: 79,162,067 (GRCm39)	H179N	possibly damaging	Het
Prpf39	T	C	12: 65,108,231 (GRCm39)		probably benign	Het
Rapgef1	G	A	2: 29,609,662 (GRCm39)	V700I	probably benign	Het
Rdh14	A	G	12: 10,444,703 (GRCm39)	I185V	probably benign	Het
Rnf111	A	T	9: 70,349,607 (GRCm39)	H785Q	probably damaging	Het
Rttn	C	T	18: 89,035,399 (GRCm39)	R758W	probably benign	Het
Sik3	G	A	9: 46,113,361 (GRCm39)	V601M	probably damaging	Het
Slc22a14	T	C	9: 119,007,552 (GRCm39)	T286A	probably benign	Het
Slc36a3	G	A	11: 55,026,209 (GRCm39)	T203I	probably benign	Het
Spata31	A	T	13: 65,070,468 (GRCm39)	Q872L	probably benign	Het
Spata31d1c	A	G	13: 65,182,974 (GRCm39)	D172G	possibly damaging	Het
Sphkap	A	T	1: 83,245,215 (GRCm39)		probably null	Het
Stat6	T	C	10: 127,491,248 (GRCm39)	V463A	probably damaging	Het
Stx7	T	C	10: 24,060,947 (GRCm39)	S225P	probably damaging	Het
Sult2a7	A	T	7: 14,207,334 (GRCm39)		probably benign	Het
Tada2a	A	T	11: 83,993,946 (GRCm39)	F179L	probably benign	Het
Tas2r103	A	G	6: 133,013,280 (GRCm39)	L262P	probably benign	Het
Tfap2d	A	G	1: 19,236,187 (GRCm39)	I382V	possibly damaging	Het
Tshr	C	A	12: 91,504,517 (GRCm39)	A485D	probably damaging	Het
Vmn1r32	T	A	6: 66,530,698 (GRCm39)	Y26F	probably damaging	Het
Vmn1r5	A	G	6: 56,962,636 (GRCm39)	T104A	probably damaging	Het
Wbp1l	T	A	19: 46,642,396 (GRCm39)		probably null	Het

Other mutations in Nuggc

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01359:Nuggc	APN	14	65,860,656 (GRCm39)	missense	probably damaging	1.00
IGL01403:Nuggc	APN	14	65,860,635 (GRCm39)	missense	probably benign	0.01
IGL01413:Nuggc	APN	14	65,876,030 (GRCm39)	missense	probably benign	0.23
IGL02588:Nuggc	APN	14	65,855,226 (GRCm39)	splice site	probably benign
R0102:Nuggc	UTSW	14	65,851,000 (GRCm39)	missense	probably null	1.00
R0102:Nuggc	UTSW	14	65,851,000 (GRCm39)	missense	probably null	1.00
R0395:Nuggc	UTSW	14	65,850,921 (GRCm39)	nonsense	probably null
R0827:Nuggc	UTSW	14	65,846,340 (GRCm39)	missense	probably damaging	1.00
R1496:Nuggc	UTSW	14	65,861,582 (GRCm39)	missense	probably damaging	0.96
R1861:Nuggc	UTSW	14	65,879,450 (GRCm39)	splice site	probably benign
R1986:Nuggc	UTSW	14	65,879,370 (GRCm39)	missense	probably damaging	0.98
R1995:Nuggc	UTSW	14	65,848,623 (GRCm39)	missense	probably benign	0.02
R2283:Nuggc	UTSW	14	65,876,061 (GRCm39)	missense	possibly damaging	0.89
R2317:Nuggc	UTSW	14	65,861,591 (GRCm39)	missense	possibly damaging	0.81
R3799:Nuggc	UTSW	14	65,857,087 (GRCm39)	missense	probably benign	0.00
R4303:Nuggc	UTSW	14	65,848,621 (GRCm39)	missense	possibly damaging	0.77
R4431:Nuggc	UTSW	14	65,848,659 (GRCm39)	missense	probably benign	0.19
R4734:Nuggc	UTSW	14	65,860,679 (GRCm39)	missense	probably damaging	1.00
R5095:Nuggc	UTSW	14	65,872,539 (GRCm39)	nonsense	probably null
R5108:Nuggc	UTSW	14	65,876,129 (GRCm39)	missense	probably damaging	0.99
R5360:Nuggc	UTSW	14	65,876,075 (GRCm39)	missense	probably damaging	1.00
R5547:Nuggc	UTSW	14	65,879,330 (GRCm39)	missense	possibly damaging	0.87
R5636:Nuggc	UTSW	14	65,885,637 (GRCm39)	nonsense	probably null
R6494:Nuggc	UTSW	14	65,885,671 (GRCm39)	missense	probably damaging	1.00
R6922:Nuggc	UTSW	14	65,855,092 (GRCm39)	missense	probably damaging	1.00
R6971:Nuggc	UTSW	14	65,846,305 (GRCm39)	missense	probably benign	0.04
R7124:Nuggc	UTSW	14	65,846,251 (GRCm39)	missense	probably damaging	1.00
R7273:Nuggc	UTSW	14	65,857,057 (GRCm39)	missense	probably damaging	0.99
R7282:Nuggc	UTSW	14	65,855,072 (GRCm39)	missense	probably damaging	1.00
R7578:Nuggc	UTSW	14	65,885,623 (GRCm39)	missense	probably damaging	1.00
R7670:Nuggc	UTSW	14	65,850,975 (GRCm39)	missense	probably damaging	1.00
R7780:Nuggc	UTSW	14	65,882,490 (GRCm39)	missense	probably damaging	1.00
R7871:Nuggc	UTSW	14	65,860,700 (GRCm39)	missense	probably benign	0.01
R8250:Nuggc	UTSW	14	65,879,318 (GRCm39)	missense	probably benign	0.10
R8329:Nuggc	UTSW	14	65,878,731 (GRCm39)	missense	probably benign	0.01
R8334:Nuggc	UTSW	14	65,882,478 (GRCm39)	missense	probably benign	0.04
R8463:Nuggc	UTSW	14	65,851,011 (GRCm39)	missense	probably damaging	1.00
R8503:Nuggc	UTSW	14	65,878,797 (GRCm39)	critical splice donor site	probably null
R8737:Nuggc	UTSW	14	65,882,535 (GRCm39)	missense	probably benign	0.00
R8861:Nuggc	UTSW	14	65,847,484 (GRCm39)	critical splice donor site	probably null
R8914:Nuggc	UTSW	14	65,879,354 (GRCm39)	missense	probably benign
R9573:Nuggc	UTSW	14	65,848,603 (GRCm39)	missense	probably benign	0.37
R9666:Nuggc	UTSW	14	65,857,045 (GRCm39)	missense	possibly damaging	0.86
R9792:Nuggc	UTSW	14	65,847,345 (GRCm39)	missense	probably damaging	1.00
R9793:Nuggc	UTSW	14	65,847,345 (GRCm39)	missense	probably damaging	1.00
R9795:Nuggc	UTSW	14	65,847,345 (GRCm39)	missense	probably damaging	1.00
RF019:Nuggc	UTSW	14	65,885,713 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGGCTTCCGATCCAAGACAC -3'
(R):5'- GATTATGTACCACCAGACACAAAGG -3'

Sequencing Primer
(F):5'- TTCCGATCCAAGACACTAGAAGAGG -3'
(R):5'- CAGATGACCTGAATTTGGTTCCCAG -3'

Posted On

2015-04-29