Mutagenetix > Incidental Mutation

Incidental Mutation 'R0334:Rnf139'

26171

Institutional Source

Beutler Lab

Gene Symbol

Rnf139

Ensembl Gene

ENSMUSG00000037075

Gene Name

ring finger protein 139

Synonyms

4930555P18Rik

MMRRC Submission

038543-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.221) question?

Stock #

R0334 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

58760975-58774239 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 58771322 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 449 (Y449C)

Ref Sequence

ENSEMBL: ENSMUSP00000046467 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000036904] [ENSMUST00000110155] [ENSMUST00000226707] [ENSMUST00000227540] [ENSMUST00000228538] [ENSMUST00000228787]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000036904
AA Change: Y449C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000046467
Gene: ENSMUSG00000037075
AA Change: Y449C

Domain	Start	End	E-Value	Type
Pfam:TRC8_N	19	516	5.1e-187	PFAM
RING	547	585	1.2e-7	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000110155

SMART Domains

Protein: ENSMUSP00000105783
Gene: ENSMUSG00000050891

Domain	Start	End	E-Value	Type
Pfam:TatD_DNase	7	263	2.4e-51	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000226707

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000226908

Predicted Effect

probably benign
Transcript: ENSMUST00000227540

Predicted Effect

probably benign
Transcript: ENSMUST00000228538

Predicted Effect

probably benign
Transcript: ENSMUST00000228787

Meta Mutation Damage Score

0.2528

Coding Region Coverage

1x: 99.1%
3x: 98.3%
10x: 96.4%
20x: 93.6%

Validation Efficiency

99% (68/69)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a multi-membrane spanning protein containing a RING-H2 finger. This protein is located in the endoplasmic reticulum, and has been shown to possess ubiquitin ligase activity. This gene was found to be interrupted by a t(3:8) translocation in a family with hereditary renal and non-medulary thyroid cancer. Studies of the Drosophila counterpart suggested that this protein may interact with tumor suppressor protein VHL, as well as with COPS5/JAB1, a protein responsible for the degradation of tumor suppressor CDKN1B/P27KIP. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased diet-induced liver apoptosis, inflammation and fibrosis. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aggf1	T	C	13: 95,508,105 (GRCm39)	N87S	probably benign	Het
Ap2b1	T	C	11: 83,258,700 (GRCm39)		probably benign	Het
Arfgef3	A	G	10: 18,468,029 (GRCm39)	Y1724H	probably damaging	Het
Arhgef10l	G	A	4: 140,311,237 (GRCm39)	Q243*	probably null	Het
Atp8a2	A	T	14: 59,928,961 (GRCm39)	F1031Y	probably damaging	Het
Bmp8b	A	G	4: 123,008,553 (GRCm39)		probably null	Het
Brinp2	G	T	1: 158,123,155 (GRCm39)	T37K	probably benign	Het
Bsph1	T	A	7: 13,184,864 (GRCm39)	L9*	probably null	Het
C6	T	G	15: 4,784,849 (GRCm39)	N238K	probably benign	Het
Cbs	T	C	17: 31,838,130 (GRCm39)	D373G	probably damaging	Het
Clec4a3	T	C	6: 122,946,329 (GRCm39)	F191S	possibly damaging	Het
Cpz	A	G	5: 35,661,025 (GRCm39)	V530A	probably damaging	Het
Ctsc	G	T	7: 87,927,550 (GRCm39)	S47I	possibly damaging	Het
Cyp7b1	T	G	3: 18,157,960 (GRCm39)	Y53S	probably damaging	Het
Dach1	C	T	14: 98,406,184 (GRCm39)	G188R	probably damaging	Het
Defb4	T	C	8: 19,251,220 (GRCm39)	I29T	probably benign	Het
Disc1	A	T	8: 125,987,836 (GRCm39)		probably null	Het
Dnah2	A	G	11: 69,327,662 (GRCm39)	M3429T	probably damaging	Het
Dnah7a	A	T	1: 53,472,213 (GRCm39)	I3518N	possibly damaging	Het
Dnah8	A	T	17: 31,090,325 (GRCm39)	H4609L	probably damaging	Het
Evi5	C	A	5: 107,968,401 (GRCm39)	C182F	probably damaging	Het
Fam149b	G	A	14: 20,413,492 (GRCm39)	R237H	probably damaging	Het
Fut8	T	A	12: 77,440,536 (GRCm39)	D174E	possibly damaging	Het
Ghr	T	C	15: 3,370,580 (GRCm39)		probably benign	Het
Gm10801	G	C	2: 98,494,352 (GRCm39)	R143T	possibly damaging	Het
Gpr176	T	C	2: 118,110,189 (GRCm39)	S357G	probably benign	Het
Grwd1	A	T	7: 45,476,601 (GRCm39)		probably null	Het
H2-T24	A	G	17: 36,325,772 (GRCm39)	V273A	possibly damaging	Het
Hdac4	A	C	1: 91,883,760 (GRCm39)		probably benign	Het
Herc3	A	G	6: 58,895,802 (GRCm39)	T1017A	probably damaging	Het
Hsd11b1	T	C	1: 192,924,476 (GRCm39)		probably benign	Het
Igsf23	T	C	7: 19,675,678 (GRCm39)	S143G	probably benign	Het
Kbtbd12	T	A	6: 88,594,888 (GRCm39)	Y314F	probably damaging	Het
Kcnmb2	A	G	3: 32,252,508 (GRCm39)		probably null	Het
Kdm5b	A	G	1: 134,532,260 (GRCm39)	I479M	probably damaging	Het
Kidins220	A	G	12: 25,058,068 (GRCm39)	T600A	probably damaging	Het
Mrgprb2	A	C	7: 48,202,077 (GRCm39)	I216S	probably damaging	Het
Muc21	A	G	17: 35,933,614 (GRCm39)		probably benign	Het
Myo1g	A	G	11: 6,461,084 (GRCm39)		probably benign	Het
Nrxn3	T	C	12: 89,780,412 (GRCm39)		probably null	Het
Or2ag2	A	G	7: 106,485,622 (GRCm39)	V134A	probably benign	Het
Or8b54	A	T	9: 38,686,535 (GRCm39)		probably null	Het
Or8g26	A	G	9: 39,095,980 (GRCm39)	I169V	probably benign	Het
Pdia5	A	T	16: 35,284,760 (GRCm39)	S66T	possibly damaging	Het
Plec	T	C	15: 76,062,206 (GRCm39)	E2604G	probably damaging	Het
Plekha6	G	T	1: 133,209,918 (GRCm39)	A654S	probably benign	Het
Pnpla2	G	A	7: 141,039,433 (GRCm39)		probably null	Het
Pramel19	T	C	4: 101,798,781 (GRCm39)	F251L	probably benign	Het
Prb1c	T	A	6: 132,341,021 (GRCm39)	Q17L	unknown	Het
Prkdc	A	G	16: 15,554,663 (GRCm39)	D2128G	probably benign	Het
Rabggta	A	T	14: 55,958,268 (GRCm39)	L131Q	probably damaging	Het
Rbks	A	T	5: 31,781,863 (GRCm39)	Y312*	probably null	Het
Sanbr	A	G	11: 23,567,129 (GRCm39)		probably benign	Het
Sbno1	A	G	5: 124,524,931 (GRCm39)	V1058A	possibly damaging	Het
Sema3a	A	T	5: 13,607,268 (GRCm39)	N321I	probably damaging	Het
Slit3	T	A	11: 35,469,928 (GRCm39)	V310E	probably damaging	Het
Slitrk5	T	C	14: 111,918,256 (GRCm39)	S627P	probably benign	Het
Stat2	T	A	10: 128,113,736 (GRCm39)	F172I	probably damaging	Het
Tchh	C	A	3: 93,352,923 (GRCm39)	R788S	unknown	Het
Tnks	T	A	8: 35,320,413 (GRCm39)	K753*	probably null	Het
Trank1	T	A	9: 111,194,421 (GRCm39)	V815D	probably benign	Het
Trank1	T	A	9: 111,222,008 (GRCm39)	I2915N	probably damaging	Het
Trpc6	T	C	9: 8,610,344 (GRCm39)	S271P	probably damaging	Het
Trpm5	T	C	7: 142,640,613 (GRCm39)	Q213R	probably benign	Het
Ulk3	C	T	9: 57,501,510 (GRCm39)		probably benign	Het
Usp31	T	C	7: 121,258,185 (GRCm39)	D694G	probably damaging	Het
Wnt3a	A	G	11: 59,147,144 (GRCm39)	S181P	probably damaging	Het
Yipf3	T	C	17: 46,559,238 (GRCm39)	F22S	possibly damaging	Het
Zbtb40	A	T	4: 136,713,867 (GRCm39)	H1094Q	probably damaging	Het

Other mutations in Rnf139

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00595:Rnf139	APN	15	58,770,391 (GRCm39)	missense	possibly damaging	0.75
IGL01288:Rnf139	APN	15	58,771,028 (GRCm39)	missense	probably damaging	1.00
IGL01290:Rnf139	APN	15	58,770,175 (GRCm39)	missense	probably benign
IGL02078:Rnf139	APN	15	58,771,880 (GRCm39)	missense	possibly damaging	0.94
IGL02302:Rnf139	APN	15	58,770,606 (GRCm39)	missense	probably damaging	0.99
IGL03029:Rnf139	APN	15	58,770,967 (GRCm39)	missense	probably damaging	1.00
IGL03355:Rnf139	APN	15	58,771,881 (GRCm39)	missense	probably benign	0.05
R0099:Rnf139	UTSW	15	58,771,264 (GRCm39)	missense	probably damaging	1.00
R0158:Rnf139	UTSW	15	58,770,727 (GRCm39)	missense	probably benign
R0331:Rnf139	UTSW	15	58,771,755 (GRCm39)	missense	probably benign	0.01
R0606:Rnf139	UTSW	15	58,771,676 (GRCm39)	missense	probably damaging	1.00
R0680:Rnf139	UTSW	15	58,771,501 (GRCm39)	missense	probably damaging	1.00
R1338:Rnf139	UTSW	15	58,771,064 (GRCm39)	missense	probably damaging	0.97
R1524:Rnf139	UTSW	15	58,761,266 (GRCm39)	missense	probably damaging	0.99
R1528:Rnf139	UTSW	15	58,771,064 (GRCm39)	missense	probably damaging	0.97
R1577:Rnf139	UTSW	15	58,771,367 (GRCm39)	missense	probably damaging	1.00
R1870:Rnf139	UTSW	15	58,771,202 (GRCm39)	missense	probably benign	0.00
R1889:Rnf139	UTSW	15	58,771,346 (GRCm39)	missense	probably damaging	1.00
R4647:Rnf139	UTSW	15	58,771,836 (GRCm39)	missense	probably benign	0.11
R4992:Rnf139	UTSW	15	58,770,325 (GRCm39)	nonsense	probably null
R5088:Rnf139	UTSW	15	58,771,790 (GRCm39)	missense	possibly damaging	0.74
R5246:Rnf139	UTSW	15	58,771,552 (GRCm39)	missense	probably damaging	1.00
R5982:Rnf139	UTSW	15	58,770,687 (GRCm39)	missense	possibly damaging	0.76
R5984:Rnf139	UTSW	15	58,770,595 (GRCm39)	missense	probably benign	0.41
R8920:Rnf139	UTSW	15	58,771,529 (GRCm39)	missense	possibly damaging	0.93
R9120:Rnf139	UTSW	15	58,771,685 (GRCm39)	missense	probably damaging	1.00
R9507:Rnf139	UTSW	15	58,770,664 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- CTGGTTTAAGTGGGCTAAGACCTGAAG -3'
(R):5'- GGTTACACGGTGTTATACGAGCAGATG -3'

Sequencing Primer
(F):5'- ACCTGAAGAGAGACTTATTCGC -3'
(R):5'- TACGAGCAGATGTTGTGAACTC -3'

Posted On

2013-04-16