Mutagenetix > Incidental Mutation

Incidental Mutation 'R6283:Rnf150'

508056

Institutional Source

Beutler Lab

Gene Symbol

Rnf150

Ensembl Gene

ENSMUSG00000047747

Gene Name

ring finger protein 150

Synonyms

Greul5, A630007N06Rik, C030044C12Rik

MMRRC Submission

044453-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.496) question?

Stock #

R6283 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

83589985-83817897 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 83717183 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 230 (Y230C)

Ref Sequence

ENSEMBL: ENSMUSP00000077610 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078525]

AlphaFold

Q5DTZ6

Predicted Effect

probably damaging
Transcript: ENSMUST00000078525
AA Change: Y230C

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

SMART Domains

Protein: ENSMUSP00000077610
Gene: ENSMUSG00000047747
AA Change: Y230C

Domain	Start	End	E-Value	Type
signal peptide	1	34	N/A	INTRINSIC
low complexity region	54	64	N/A	INTRINSIC
Pfam:PA	84	180	2.1e-12	PFAM
transmembrane domain	207	229	N/A	INTRINSIC
RING	277	317	1.29e-7	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000211020

Meta Mutation Damage Score

0.7493

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.0%
20x: 94.1%

Validation Efficiency

100% (59/59)

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acsf3	C	A	8: 123,512,694 (GRCm39)	R372S	probably damaging	Het
Adamts20	A	G	15: 94,249,602 (GRCm39)	S472P	probably benign	Het
Bhlhe40	T	C	6: 108,641,992 (GRCm39)	L312P	probably damaging	Het
Ccdc180	A	G	4: 45,902,486 (GRCm39)	E305G	possibly damaging	Het
Ccdc83	T	A	7: 89,885,615 (GRCm39)	R257*	probably null	Het
Cd209e	G	A	8: 3,899,212 (GRCm39)	Q167*	probably null	Het
Cd300e	G	A	11: 114,945,380 (GRCm39)	T138I	probably benign	Het
Ces2c	A	T	8: 105,576,331 (GRCm39)	M115L	probably benign	Het
Cfap61	T	A	2: 145,971,022 (GRCm39)		probably null	Het
Chd1l	G	A	3: 97,494,483 (GRCm39)	A399V	probably damaging	Het
Cic	C	T	7: 24,985,459 (GRCm39)	S301L	probably damaging	Het
Cks2	A	G	13: 51,799,495 (GRCm39)	H16R	probably benign	Het
Copa	A	T	1: 171,946,415 (GRCm39)	H953L	possibly damaging	Het
Ctdsp2	T	C	10: 126,831,749 (GRCm39)	V145A	possibly damaging	Het
Cyp2j13	A	G	4: 95,945,074 (GRCm39)	V377A	possibly damaging	Het
Dhx57	A	G	17: 80,582,234 (GRCm39)	V404A	probably benign	Het
Dock2	T	C	11: 34,598,152 (GRCm39)	S340G	probably damaging	Het
Ggps1	A	G	13: 14,232,379 (GRCm39)		probably null	Het
Gm10549	C	A	18: 33,597,358 (GRCm39)		probably benign	Het
Gm11444	T	C	11: 85,737,617 (GRCm39)		probably null	Het
Grina	A	G	15: 76,132,751 (GRCm39)	T173A	possibly damaging	Het
Hcrtr1	G	A	4: 130,029,133 (GRCm39)	T223I	probably benign	Het
Igsf10	T	A	3: 59,226,870 (GRCm39)	T2268S	probably damaging	Het
Inhca	G	A	9: 103,159,834 (GRCm39)	R14*	probably null	Het
Ino80d	C	T	1: 63,101,285 (GRCm39)	R447Q	probably damaging	Het
Inpp4b	C	T	8: 82,497,462 (GRCm39)	T94M	probably damaging	Het
Itga2	A	G	13: 115,005,786 (GRCm39)	Y465H	probably damaging	Het
Knl1	A	G	2: 118,900,767 (GRCm39)	T823A	probably damaging	Het
Krtap4-16	A	G	11: 99,741,861 (GRCm39)	S180P	unknown	Het
Ldc1	A	G	4: 130,115,534 (GRCm39)	S5P	probably benign	Het
Lpar6	A	T	14: 73,476,297 (GRCm39)	D86V	probably damaging	Het
Muc5ac	C	A	7: 141,370,601 (GRCm39)	C2500*	probably null	Het
Mzf1	T	C	7: 12,787,296 (GRCm39)		probably benign	Het
Or4f58	A	C	2: 111,851,605 (GRCm39)	M198R	possibly damaging	Het
Or5d46	T	A	2: 88,170,002 (GRCm39)	I31N	probably benign	Het
Or5m3	G	T	2: 85,838,443 (GRCm39)	V108L	possibly damaging	Het
Or7a36	T	C	10: 78,820,113 (GRCm39)	V163A	probably benign	Het
Otogl	T	G	10: 107,626,361 (GRCm39)	E1501A	probably damaging	Het
Pcdh10	T	A	3: 45,335,989 (GRCm39)	S768T	possibly damaging	Het
Pcnx2	G	T	8: 126,604,325 (GRCm39)	Q644K	probably damaging	Het
Pdzd9	T	A	7: 120,259,449 (GRCm39)	I180F	possibly damaging	Het
Pinx1	A	C	14: 64,115,621 (GRCm39)	N152T	probably benign	Het
Prr14l	T	C	5: 32,987,608 (GRCm39)	E629G	probably benign	Het
Qpctl	T	A	7: 18,882,345 (GRCm39)	I104F	probably benign	Het
Rabep1	C	T	11: 70,808,505 (GRCm39)	A444V	probably damaging	Het
Slc25a27	A	C	17: 43,968,621 (GRCm39)	V152G	probably damaging	Het
Swt1	A	G	1: 151,260,084 (GRCm39)	S772P	possibly damaging	Het
Tenm4	A	G	7: 96,523,701 (GRCm39)	T1711A	probably benign	Het
Tfap2d	G	C	1: 19,174,702 (GRCm39)	G52R	probably benign	Het
Tmem265	T	G	7: 127,164,044 (GRCm39)	V86G	possibly damaging	Het
Trpm8	C	T	1: 88,276,054 (GRCm39)	H551Y	probably benign	Het
Ttc6	T	G	12: 57,749,048 (GRCm39)	Y1327D	possibly damaging	Het
Uevld	G	T	7: 46,587,729 (GRCm39)	Q324K	possibly damaging	Het
Vmn2r111	T	C	17: 22,778,032 (GRCm39)	N549S	possibly damaging	Het
Vmn2r73	C	T	7: 85,521,049 (GRCm39)	M306I	probably benign	Het
Vmn2r93	T	A	17: 18,524,366 (GRCm39)	M120K	probably benign	Het
Zfp804b	T	A	5: 6,819,908 (GRCm39)	I1016F	probably benign	Het
Zfp90	T	C	8: 107,152,026 (GRCm39)	C580R	probably damaging	Het

Other mutations in Rnf150

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02183:Rnf150	APN	8	83,730,234 (GRCm39)	missense	probably damaging	0.96
R0512:Rnf150	UTSW	8	83,590,807 (GRCm39)	missense	probably benign	0.01
R1848:Rnf150	UTSW	8	83,590,639 (GRCm39)	start codon destroyed	possibly damaging	0.67
R2078:Rnf150	UTSW	8	83,730,234 (GRCm39)	missense	probably damaging	0.96
R2192:Rnf150	UTSW	8	83,591,020 (GRCm39)	missense	probably damaging	0.98
R3918:Rnf150	UTSW	8	83,591,090 (GRCm39)	missense	probably benign	0.25
R4365:Rnf150	UTSW	8	83,590,744 (GRCm39)	missense	probably benign	0.05
R4781:Rnf150	UTSW	8	83,590,781 (GRCm39)	missense	probably damaging	1.00
R4810:Rnf150	UTSW	8	83,716,991 (GRCm39)	missense	possibly damaging	0.66
R4859:Rnf150	UTSW	8	83,590,712 (GRCm39)	missense	probably damaging	1.00
R5677:Rnf150	UTSW	8	83,730,228 (GRCm39)	nonsense	probably null
R6022:Rnf150	UTSW	8	83,769,358 (GRCm39)	missense	probably benign	0.00
R6241:Rnf150	UTSW	8	83,591,093 (GRCm39)	missense	possibly damaging	0.82
R6306:Rnf150	UTSW	8	83,810,131 (GRCm39)	missense	possibly damaging	0.90
R7014:Rnf150	UTSW	8	83,769,292 (GRCm39)	missense	probably benign
R7023:Rnf150	UTSW	8	83,590,706 (GRCm39)	missense	probably damaging	0.97
R7394:Rnf150	UTSW	8	83,717,100 (GRCm39)	nonsense	probably null
R7710:Rnf150	UTSW	8	83,590,781 (GRCm39)	missense	probably damaging	1.00
R7771:Rnf150	UTSW	8	83,590,832 (GRCm39)	missense	probably benign	0.00
R8073:Rnf150	UTSW	8	83,590,546 (GRCm39)	start gained	probably benign
R8856:Rnf150	UTSW	8	83,762,715 (GRCm39)	missense	probably damaging	1.00
R8980:Rnf150	UTSW	8	83,717,087 (GRCm39)	missense	probably benign	0.19
R9139:Rnf150	UTSW	8	83,590,588 (GRCm39)	start gained	probably benign
R9289:Rnf150	UTSW	8	83,716,982 (GRCm39)	missense	probably benign
R9410:Rnf150	UTSW	8	83,762,722 (GRCm39)	missense	possibly damaging	0.91
R9594:Rnf150	UTSW	8	83,717,144 (GRCm39)	missense	probably damaging	1.00
R9603:Rnf150	UTSW	8	83,717,208 (GRCm39)	missense	possibly damaging	0.64
R9763:Rnf150	UTSW	8	83,732,968 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- ATGATTCCTGAGCCCAAAGG -3'
(R):5'- GTGGGGATAACTCATCAACACC -3'

Sequencing Primer
(F):5'- GGAAGGAGATAGTGAGCCTGCTG -3'
(R):5'- TGCCTAAGCACAACAGAAGTTAG -3'

Posted On

2018-03-15