Mutagenetix > Incidental Mutation

Incidental Mutation 'R9234:Ubxn7'

701009

Institutional Source

Beutler Lab

Gene Symbol

Ubxn7

Ensembl Gene

ENSMUSG00000053774

Gene Name

UBX domain protein 7

Synonyms

Ubxd7

MMRRC Submission

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R9234 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

32151075-32212565 bp(+) (GRCm39)

Type of Mutation

critical splice donor site (2 bp from exon)

DNA Base Change (assembly)

T to C at 32178895 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000110804 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000115151] [ENSMUST00000232137]

AlphaFold

Q6P5G6

Predicted Effect

probably null
Transcript: ENSMUST00000115151

SMART Domains

Protein: ENSMUSP00000110804
Gene: ENSMUSG00000053774

Domain	Start	End	E-Value	Type
low complexity region	2	12	N/A	INTRINSIC
Pfam:UBA_4	15	56	4.3e-15	PFAM
UAS	137	260	3.05e-50	SMART
low complexity region	312	328	N/A	INTRINSIC
UBX	405	487	1.16e-15	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000232137

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
6430550D23Rik	A	G	2: 155,845,798 (GRCm39)	Y20H	probably benign	Het
Arid5b	A	G	10: 67,964,628 (GRCm39)	F348L	possibly damaging	Het
Bms1	C	A	6: 118,375,044 (GRCm39)	A777S	probably damaging	Het
C2cd3	A	G	7: 100,049,012 (GRCm39)	Y61C		Het
Caprin2	A	T	6: 148,744,337 (GRCm39)	Y1029*	probably null	Het
Casp1	A	T	9: 5,303,128 (GRCm39)	D194V	probably benign	Het
Crkl	A	G	16: 17,286,822 (GRCm39)	E126G	probably damaging	Het
Crp	A	T	1: 172,526,413 (GRCm39)	D166V	probably damaging	Het
Dnah10	A	C	5: 124,818,989 (GRCm39)	D425A	possibly damaging	Het
Dnah11	A	T	12: 117,951,095 (GRCm39)	L3071Q	probably damaging	Het
Dnah9	T	A	11: 65,924,751 (GRCm39)	I2168F	possibly damaging	Het
Elp3	T	A	14: 65,788,920 (GRCm39)	I388F	probably damaging	Het
Espn	C	A	4: 152,217,380 (GRCm39)		probably null	Het
Fbrsl1	G	T	5: 110,511,250 (GRCm39)	F504L	probably benign	Het
Fzd9	A	C	5: 135,279,540 (GRCm39)	M115R	probably damaging	Het
Git2	A	T	5: 114,899,682 (GRCm39)	Y224N	possibly damaging	Het
Gm9195	A	T	14: 72,695,786 (GRCm39)	Y1415*	probably null	Het
Gnpat	T	A	8: 125,610,179 (GRCm39)	L454Q	probably damaging	Het
Grm5	C	T	7: 87,723,440 (GRCm39)	P577S	probably damaging	Het
Hfm1	T	C	5: 107,041,334 (GRCm39)	N683S	probably benign	Het
Hps4	G	A	5: 112,525,905 (GRCm39)	S642N	possibly damaging	Het
Leng8	C	A	7: 4,145,247 (GRCm39)	P216T	probably damaging	Het
Letm2	C	A	8: 26,084,102 (GRCm39)	R43L	probably benign	Het
Lims2	A	T	18: 32,090,943 (GRCm39)	Y309F	probably benign	Het
Llgl1	T	C	11: 60,600,956 (GRCm39)		probably null	Het
Ltn1	A	T	16: 87,194,089 (GRCm39)	D1417E	probably damaging	Het
Map4k4	T	A	1: 40,029,261 (GRCm39)	N345K	unknown	Het
Mapre2	T	C	18: 23,937,236 (GRCm39)	I26T	probably benign	Het
Nfe2	A	G	15: 103,159,636 (GRCm39)		probably benign	Het
Nlgn3	T	C	X: 100,352,390 (GRCm39)	V179A	probably damaging	Het
Ntrk1	A	G	3: 87,695,622 (GRCm39)		probably null	Het
Or51b6b	T	A	7: 103,309,950 (GRCm39)	Y169F	possibly damaging	Het
Or52e18	A	G	7: 104,609,651 (GRCm39)	F96S	probably damaging	Het
Or5h19	T	C	16: 58,856,789 (GRCm39)	N104D	probably benign	Het
Otud7b	G	T	3: 96,047,771 (GRCm39)	Q43H	probably damaging	Het
Pcdhb5	T	C	18: 37,453,695 (GRCm39)	V25A	probably benign	Het
Pcolce2	A	G	9: 95,560,439 (GRCm39)	T163A	probably benign	Het
Pdgfra	T	A	5: 75,324,262 (GRCm39)	V39E	possibly damaging	Het
Pdgfrb	T	A	18: 61,194,300 (GRCm39)	W26R	probably null	Het
Pigp	T	A	16: 94,165,522 (GRCm39)	*206Y	probably null	Het
Pip5kl1	G	T	2: 32,468,211 (GRCm39)	G126C	probably benign	Het
Plekhg2	G	T	7: 28,064,215 (GRCm39)	T442K	probably benign	Het
Prmt5	A	T	14: 54,748,674 (GRCm39)	S375T	possibly damaging	Het
Rnf213	T	A	11: 119,340,943 (GRCm39)	M3529K		Het
Ror2	C	A	13: 53,265,374 (GRCm39)	D573Y	probably damaging	Het
Shank1	A	G	7: 43,962,579 (GRCm39)	T98A	unknown	Het
Shcbp1	A	T	8: 4,798,800 (GRCm39)	I373K	possibly damaging	Het
Slc25a42	A	G	8: 70,642,736 (GRCm39)	S64P	probably damaging	Het
Smco3	T	A	6: 136,808,410 (GRCm39)	I155F	probably damaging	Het
Snx4	C	A	16: 33,087,161 (GRCm39)	S102*	probably null	Het
Snx4	T	A	16: 33,108,069 (GRCm39)	S288T	probably benign	Het
Socs4	A	G	14: 47,527,716 (GRCm39)	N217S	probably benign	Het
Tatdn2	G	A	6: 113,679,683 (GRCm39)		probably null	Het
Tmprss2	A	G	16: 97,379,821 (GRCm39)	Y160H	probably damaging	Het
Trim37	T	C	11: 87,036,393 (GRCm39)	I158T	possibly damaging	Het
Trip11	C	T	12: 101,811,990 (GRCm39)		probably null	Het
Ubr3	G	A	2: 69,727,990 (GRCm39)	A118T	probably benign	Het
Unc5cl	C	T	17: 48,770,658 (GRCm39)	H369Y	probably damaging	Het
Unc5d	A	T	8: 29,250,877 (GRCm39)	N263K	probably damaging	Het
Vmn2r59	A	G	7: 41,661,907 (GRCm39)	I636T	possibly damaging	Het
Vps13d	G	T	4: 144,875,792 (GRCm39)	Q1578K		Het
Wnk2	T	C	13: 49,224,274 (GRCm39)	D1171G	probably damaging	Het
Zfpm2	A	G	15: 40,966,470 (GRCm39)	Y985C	probably damaging	Het
Zpbp2	A	T	11: 98,443,398 (GRCm39)	N77I	probably damaging	Het

Other mutations in Ubxn7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00821:Ubxn7	APN	16	32,188,216 (GRCm39)	missense	probably damaging	0.97
IGL02149:Ubxn7	APN	16	32,194,088 (GRCm39)	missense	probably damaging	1.00
IGL02183:Ubxn7	APN	16	32,188,201 (GRCm39)	missense	probably damaging	1.00
IGL02690:Ubxn7	APN	16	32,200,423 (GRCm39)	missense	probably benign	0.01
IGL03133:Ubxn7	APN	16	32,200,599 (GRCm39)	missense	probably damaging	1.00
R0268:Ubxn7	UTSW	16	32,178,864 (GRCm39)	missense	probably benign	0.05
R0583:Ubxn7	UTSW	16	32,194,732 (GRCm39)	missense	probably damaging	1.00
R0635:Ubxn7	UTSW	16	32,186,235 (GRCm39)	intron	probably benign
R0787:Ubxn7	UTSW	16	32,200,581 (GRCm39)	splice site	probably benign
R1658:Ubxn7	UTSW	16	32,200,054 (GRCm39)	splice site	probably null
R1916:Ubxn7	UTSW	16	32,200,577 (GRCm39)	splice site	probably benign
R2070:Ubxn7	UTSW	16	32,191,287 (GRCm39)	missense	possibly damaging	0.47
R2071:Ubxn7	UTSW	16	32,191,287 (GRCm39)	missense	possibly damaging	0.47
R3031:Ubxn7	UTSW	16	32,194,125 (GRCm39)	missense	probably benign	0.34
R3871:Ubxn7	UTSW	16	32,200,248 (GRCm39)	missense	possibly damaging	0.94
R4994:Ubxn7	UTSW	16	32,200,322 (GRCm39)	missense	probably damaging	1.00
R5629:Ubxn7	UTSW	16	32,151,117 (GRCm39)	missense	unknown
R6334:Ubxn7	UTSW	16	32,191,007 (GRCm39)	splice site	probably null
R6599:Ubxn7	UTSW	16	32,203,743 (GRCm39)	missense	probably damaging	1.00
R8230:Ubxn7	UTSW	16	32,194,094 (GRCm39)	missense	probably benign	0.08
R8714:Ubxn7	UTSW	16	32,186,229 (GRCm39)	critical splice donor site	probably benign
R9633:Ubxn7	UTSW	16	32,200,248 (GRCm39)	missense	probably benign	0.08
R9778:Ubxn7	UTSW	16	32,200,471 (GRCm39)	missense	probably benign	0.20

Predicted Primers

PCR Primer
(F):5'- TCAGGTAATCTCTGTGGAAATCAC -3'
(R):5'- GTTTCCATAAAAGGCAGCAATTCC -3'

Sequencing Primer
(F):5'- CTGGAACTCACTTTGTAGACCAGG -3'
(R):5'- TGAGTTCCAGGCCAGCTAGAAC -3'

Posted On

2022-03-25