Mutagenetix > Incidental Mutation

Incidental Mutation 'R1598:Ubr7'

175971

Institutional Source

Beutler Lab

Gene Symbol

Ubr7

Ensembl Gene

ENSMUSG00000041712

Gene Name

ubiquitin protein ligase E3 component n-recognin 7 (putative)

Synonyms

5730410I19Rik

MMRRC Submission

039635-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.406) question?

Stock #

R1598 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

102724234-102743960 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 102736153 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Isoleucine at position 358 (M358I)

Ref Sequence

ENSEMBL: ENSMUSP00000041247 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000046404]

AlphaFold

Q8BU04

Predicted Effect

probably damaging
Transcript: ENSMUST00000046404
AA Change: M358I

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000041247
Gene: ENSMUSG00000041712
AA Change: M358I

Domain	Start	End	E-Value	Type
low complexity region	13	33	N/A	INTRINSIC
Pfam:zf-UBR	45	113	2.4e-15	PFAM
PHD	134	186	1.78e-1	SMART
low complexity region	261	267	N/A	INTRINSIC

Coding Region Coverage

1x: 99.0%
3x: 98.2%
10x: 95.7%
20x: 90.9%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a UBR box-containing protein that belongs to the E3 ubiquitin ligase family. The protein also contains a plant homeodomain (PHD) in the C-terminus. In mammals, the encoded protein recognizes N-degrons, the destabilizing N-terminal residues of short-lived proteins, which results in ubiquitinylation, and proteolysis via the proteasome. [provided by RefSeq, Jul 2016]

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5730455P16Rik	G	A	11: 80,254,838 (GRCm39)	Q328*	probably null	Het
Aadacl4fm4	T	A	4: 144,396,994 (GRCm39)	K246I	possibly damaging	Het
Adamts1	G	A	16: 85,595,399 (GRCm39)	Q260*	probably null	Het
Add2	A	T	6: 86,075,628 (GRCm39)	Y259F	probably benign	Het
Bora	T	C	14: 99,305,840 (GRCm39)	V403A	probably benign	Het
Ccnl1	G	A	3: 65,854,191 (GRCm39)	R477W	probably damaging	Het
Cdc25a	CG	CGG	9: 109,708,961 (GRCm39)		probably null	Het
Cdr2l	T	C	11: 115,284,203 (GRCm39)	S180P	probably damaging	Het
Cep290	T	A	10: 100,385,191 (GRCm39)	L1889Q	probably damaging	Het
Ces4a	T	C	8: 105,869,453 (GRCm39)	V208A	probably damaging	Het
Col2a1	T	C	15: 97,877,131 (GRCm39)	D1049G	probably damaging	Het
Coro1a	A	T	7: 126,300,864 (GRCm39)	N154K	possibly damaging	Het
Cubn	T	A	2: 13,474,600 (GRCm39)	R401S	probably benign	Het
Cul7	A	T	17: 46,974,017 (GRCm39)	Q1434L	probably benign	Het
Dab1	C	T	4: 104,588,948 (GRCm39)	A524V	probably benign	Het
Dars1	G	T	1: 128,301,709 (GRCm39)	D308E	probably benign	Het
Dna2	T	A	10: 62,797,436 (GRCm39)	F604I	probably damaging	Het
Dnah1	T	G	14: 31,023,219 (GRCm39)	I1033L	probably benign	Het
Erlin1	T	C	19: 44,036,112 (GRCm39)	E206G	probably damaging	Het
Esrp2	T	A	8: 106,859,905 (GRCm39)	E345D	probably damaging	Het
Foxa1	T	C	12: 57,589,473 (GRCm39)	D249G	possibly damaging	Het
Ghsr	C	A	3: 27,426,426 (GRCm39)	L161M	probably benign	Het
Gm57858	C	T	3: 36,073,146 (GRCm39)	A379T	probably damaging	Het
Gpr155	C	A	2: 73,200,434 (GRCm39)	V358F	probably damaging	Het
H2-Eb2	A	T	17: 34,553,348 (GRCm39)	N178I	probably damaging	Het
Hydin	T	A	8: 111,137,306 (GRCm39)	I703N	possibly damaging	Het
Kctd15	A	G	7: 34,341,417 (GRCm39)	V170A	probably damaging	Het
Klhl31	A	T	9: 77,558,298 (GRCm39)	Y338F	possibly damaging	Het
Krt5	C	T	15: 101,620,876 (GRCm39)	A124T	probably benign	Het
Krt72	T	A	15: 101,688,688 (GRCm39)	I331F	probably benign	Het
Lrp1b	T	A	2: 41,401,490 (GRCm39)	D388V	probably damaging	Het
Ly9	A	G	1: 171,424,075 (GRCm39)	V382A	probably benign	Het
Mon2	T	C	10: 122,852,301 (GRCm39)	Y1024C	probably damaging	Het
Myh14	A	G	7: 44,287,818 (GRCm39)	F572L	probably damaging	Het
Myh3	A	T	11: 66,983,997 (GRCm39)	D987V	probably damaging	Het
Ndn	C	T	7: 61,998,256 (GRCm39)	P34L	probably benign	Het
Nphp4	A	G	4: 152,646,547 (GRCm39)	T1360A	probably benign	Het
Oog4	A	G	4: 143,164,571 (GRCm39)	L320P	probably damaging	Het
Or4k49	G	T	2: 111,495,099 (GRCm39)	S176I	probably damaging	Het
Or5m9	C	T	2: 85,877,657 (GRCm39)	T277I	probably damaging	Het
Or5w8	T	A	2: 87,688,095 (GRCm39)	I192K	probably benign	Het
Pcnx2	T	C	8: 126,498,825 (GRCm39)	N1558S	probably benign	Het
Pde10a	A	G	17: 9,147,976 (GRCm39)	E147G	probably damaging	Het
Pgbd5	T	A	8: 125,101,026 (GRCm39)	H410L	probably benign	Het
Plce1	A	C	19: 38,709,440 (GRCm39)	D1098A	probably damaging	Het
Psg25	G	A	7: 18,265,928 (GRCm39)	Q16*	probably null	Het
Psmd9	T	A	5: 123,379,980 (GRCm39)	V133E	probably damaging	Het
Rabgap1	C	T	2: 37,451,911 (GRCm39)	S937F	probably damaging	Het
Rbck1	A	G	2: 152,165,090 (GRCm39)		probably null	Het
Rprd2	C	G	3: 95,726,051 (GRCm39)		probably benign	Het
Rrs1	A	G	1: 9,616,137 (GRCm39)	N130S	probably benign	Het
Scmh1	A	T	4: 120,372,327 (GRCm39)	I377F	possibly damaging	Het
Skor1	G	T	9: 63,053,286 (GRCm39)	R228S	probably damaging	Het
Slc2a4	A	G	11: 69,835,844 (GRCm39)	V335A	probably benign	Het
Slc4a9	G	A	18: 36,661,424 (GRCm39)	W62*	probably null	Het
Styxl2	G	A	1: 165,937,828 (GRCm39)	T77I	probably benign	Het
Taar9	G	T	10: 23,985,305 (GRCm39)	A43D	possibly damaging	Het
Tns4	T	C	11: 98,961,243 (GRCm39)	Y645C	probably damaging	Het
Tpcn2	G	T	7: 144,830,957 (GRCm39)	Y129*	probably null	Het
Trpm3	T	C	19: 22,710,388 (GRCm39)	S278P	possibly damaging	Het
Ttc3	T	C	16: 94,223,156 (GRCm39)	W615R	probably damaging	Het
Ttll5	T	C	12: 85,910,372 (GRCm39)	V207A	probably damaging	Het
Urb1	C	A	16: 90,574,328 (GRCm39)	V918F	possibly damaging	Het
Vmn2r51	G	A	7: 9,839,432 (GRCm39)	T52I	probably benign	Het
Vmn2r95	A	T	17: 18,672,575 (GRCm39)	I771F	probably benign	Het
Wfdc16	T	C	2: 164,477,350 (GRCm39)	S107G	probably benign	Het
Zmym2	A	G	14: 57,140,226 (GRCm39)	T22A	possibly damaging	Het
Zmym2	G	A	14: 57,151,524 (GRCm39)	G470R	probably damaging	Het

Other mutations in Ubr7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02152:Ubr7	APN	12	102,734,535 (GRCm39)	nonsense	probably null
IGL02493:Ubr7	APN	12	102,734,479 (GRCm39)	missense	probably benign	0.00
IGL02750:Ubr7	APN	12	102,737,537 (GRCm39)	missense	possibly damaging	0.68
IGL03229:Ubr7	APN	12	102,735,414 (GRCm39)	missense	probably damaging	1.00
dwindled	UTSW	12	102,727,723 (GRCm39)	missense	probably damaging	1.00
Hair	UTSW	12	102,724,342 (GRCm39)	missense	probably damaging	0.98
Inch	UTSW	12	102,732,099 (GRCm39)	nonsense	probably null
R0519:Ubr7	UTSW	12	102,734,465 (GRCm39)	missense	probably benign	0.00
R0894:Ubr7	UTSW	12	102,735,450 (GRCm39)	missense	probably damaging	1.00
R1453:Ubr7	UTSW	12	102,735,437 (GRCm39)	missense	probably benign	0.00
R2201:Ubr7	UTSW	12	102,727,764 (GRCm39)	critical splice donor site	probably null
R4731:Ubr7	UTSW	12	102,735,485 (GRCm39)	missense	probably benign	0.03
R4834:Ubr7	UTSW	12	102,727,761 (GRCm39)	missense	probably damaging	1.00
R5222:Ubr7	UTSW	12	102,741,964 (GRCm39)	missense	probably benign	0.09
R5662:Ubr7	UTSW	12	102,734,526 (GRCm39)	missense	probably benign	0.00
R5845:Ubr7	UTSW	12	102,732,571 (GRCm39)	missense	probably damaging	0.99
R5867:Ubr7	UTSW	12	102,727,753 (GRCm39)	missense	probably damaging	1.00
R6257:Ubr7	UTSW	12	102,732,099 (GRCm39)	nonsense	probably null
R6543:Ubr7	UTSW	12	102,734,494 (GRCm39)	missense	probably benign	0.01
R6601:Ubr7	UTSW	12	102,727,723 (GRCm39)	missense	probably damaging	1.00
R6849:Ubr7	UTSW	12	102,724,342 (GRCm39)	missense	probably damaging	0.98
R7330:Ubr7	UTSW	12	102,741,971 (GRCm39)	missense	probably damaging	0.99
R7576:Ubr7	UTSW	12	102,735,398 (GRCm39)	missense	probably damaging	1.00
R8256:Ubr7	UTSW	12	102,736,170 (GRCm39)	missense	probably damaging	1.00
R8334:Ubr7	UTSW	12	102,724,397 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTCACAGAGTAGACACTGCGAGACTTA -3'
(R):5'- AGTTCATGCTGAGGGCTTCTTTCTTT -3'

Sequencing Primer
(F):5'- agacacacaagaagagagcac -3'
(R):5'- aaacttacaaaaatcctcctgcc -3'

Posted On

2014-04-24