Mutagenetix > Incidental Mutation

Incidental Mutation 'R4922:Rnf145'

378705

Institutional Source

Beutler Lab

Gene Symbol

Rnf145

Ensembl Gene

ENSMUSG00000019189

Gene Name

ring finger protein 145

Synonyms

3732413I11Rik

MMRRC Submission

042524-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.206) question?

Stock #

R4922 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

44409791-44456347 bp(+) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to A at 44448063 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000098881 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000019333] [ENSMUST00000101327]

AlphaFold

Q5SWK7

Predicted Effect

probably benign
Transcript: ENSMUST00000019333

SMART Domains

Protein: ENSMUSP00000019333
Gene: ENSMUSG00000019189

Domain	Start	End	E-Value	Type
Pfam:TRC8_N	8	506	2.8e-156	PFAM
RING	537	574	2.12e-8	SMART
low complexity region	590	601	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000101327

SMART Domains

Protein: ENSMUSP00000098881
Gene: ENSMUSG00000019189

Domain	Start	End	E-Value	Type
Pfam:TRC8_N	7	266	1.2e-70	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000129676

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150257

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.5%
20x: 93.0%

Validation Efficiency

97% (76/78)

Allele List at MGI

Other mutations in this stock

Total: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrb2	G	T	4: 129,901,645 (GRCm39)	C423F	probably damaging	Het
Akap11	A	T	14: 78,750,220 (GRCm39)	Y722*	probably null	Het
Albfm1	A	G	5: 90,727,570 (GRCm39)	H396R	possibly damaging	Het
Anxa3	A	T	5: 96,968,288 (GRCm39)	I114F	probably damaging	Het
Arfgef3	T	A	10: 18,467,934 (GRCm39)	R1755S	probably damaging	Het
Atf7ip	A	T	6: 136,537,039 (GRCm39)	T91S	possibly damaging	Het
Bcl2	C	A	1: 106,640,376 (GRCm39)	A79S	probably benign	Het
Bltp1	T	A	3: 37,041,314 (GRCm39)	I2564K	probably damaging	Het
Bmerb1	A	G	16: 13,804,683 (GRCm39)	H10R	possibly damaging	Het
Bmp10	C	T	6: 87,410,557 (GRCm39)	P117S	probably benign	Het
Bmpr2	A	G	1: 59,906,583 (GRCm39)	T559A	probably benign	Het
Cd200r1	A	T	16: 44,610,039 (GRCm39)	Y86F	probably damaging	Het
Cemip	T	A	7: 83,596,308 (GRCm39)		probably benign	Het
Cfap251	T	C	5: 123,394,116 (GRCm39)	V335A	probably benign	Het
Cfap52	A	G	11: 67,822,548 (GRCm39)		probably null	Het
Chml	T	C	1: 175,514,712 (GRCm39)	H60R	possibly damaging	Het
Cic	TCCCCC	TCCCCCCCC	7: 24,991,095 (GRCm39)		probably benign	Het
Clec12a	A	G	6: 129,336,441 (GRCm39)	Y201C	probably damaging	Het
Col15a1	T	C	4: 47,258,719 (GRCm39)	V370A	probably benign	Het
Cpsf3	T	C	12: 21,351,538 (GRCm39)	I353T	probably damaging	Het
Csf2rb	T	A	15: 78,230,667 (GRCm39)	V470E	probably benign	Het
Cyp4a10	C	A	4: 115,378,291 (GRCm39)	Q126K	probably benign	Het
Dennd1b	T	C	1: 139,013,652 (GRCm39)	S249P	probably damaging	Het
Dnase2a	A	G	8: 85,635,625 (GRCm39)		probably null	Het
Dpp10	T	C	1: 123,305,882 (GRCm39)	N490S	probably benign	Het
Drgx	A	T	14: 32,330,363 (GRCm39)	N160I	probably damaging	Het
Enc1	C	T	13: 97,382,243 (GRCm39)	A251V	probably benign	Het
Fancd2	T	C	6: 113,562,434 (GRCm39)	V1258A	probably benign	Het
Fancm	G	A	12: 65,153,666 (GRCm39)		probably null	Het
Fbxo16	C	T	14: 65,536,657 (GRCm39)	T177I	probably benign	Het
Gm1965	T	C	6: 89,123,525 (GRCm39)		noncoding transcript	Het
Hal	A	T	10: 93,339,401 (GRCm39)	M497L	probably damaging	Het
Hectd4	T	C	5: 121,497,378 (GRCm39)	L3936S	possibly damaging	Het
Hs3st4	G	T	7: 123,996,410 (GRCm39)	G359W	probably damaging	Het
Il6st	C	T	13: 112,639,399 (GRCm39)	P608L	probably damaging	Het
Kctd18	A	C	1: 58,004,707 (GRCm39)		probably benign	Het
Kntc1	T	A	5: 123,940,309 (GRCm39)	S1636T	probably damaging	Het
Lrrn1	A	T	6: 107,545,311 (GRCm39)	S370C	probably damaging	Het
Mtcl1	A	C	17: 66,655,474 (GRCm39)	C968G	probably benign	Het
Mylip	G	A	13: 45,562,238 (GRCm39)	A347T	probably damaging	Het
Naip2	T	C	13: 100,291,468 (GRCm39)	S1157G	probably benign	Het
Ncoa4-ps	A	G	12: 119,226,252 (GRCm39)		noncoding transcript	Het
Neu4	T	A	1: 93,950,200 (GRCm39)	V53E	probably damaging	Het
Nxpe3	T	C	16: 55,680,687 (GRCm39)	I302V	probably benign	Het
Or11i1	A	T	3: 106,729,576 (GRCm39)	C100S	probably damaging	Het
Or4c15b	A	T	2: 89,112,811 (GRCm39)	L243Q	possibly damaging	Het
Otos	T	C	1: 92,572,090 (GRCm39)	T79A	probably damaging	Het
Pde4a	T	C	9: 21,122,009 (GRCm39)	I578T	probably damaging	Het
Pramel17	T	A	4: 101,692,729 (GRCm39)	M424L	probably benign	Het
Prex2	C	T	1: 11,240,164 (GRCm39)	P927S	probably damaging	Het
Prune2	A	T	19: 17,100,116 (GRCm39)	K1873N	probably benign	Het
Ptk7	C	A	17: 46,887,417 (GRCm39)		probably null	Het
Reln	T	A	5: 22,200,585 (GRCm39)		probably null	Het
Rgl2	A	G	17: 34,151,749 (GRCm39)		probably benign	Het
Ryr2	T	C	13: 11,724,849 (GRCm39)	E2488G	probably damaging	Het
Sgo2b	A	T	8: 64,379,664 (GRCm39)	M1056K	possibly damaging	Het
Snapc4	A	G	2: 26,259,245 (GRCm39)	V635A	probably benign	Het
Snx19	T	A	9: 30,348,763 (GRCm39)	Y101N	probably benign	Het
Sorl1	C	A	9: 41,925,746 (GRCm39)		probably null	Het
Sp110	C	G	1: 85,516,839 (GRCm39)	E219D	probably damaging	Het
Speer4a2	A	T	5: 26,289,791 (GRCm39)	I212N	probably damaging	Het
Tmem30b	G	A	12: 73,592,488 (GRCm39)	P209L	probably damaging	Het
Trbv12-2	G	T	6: 41,096,081 (GRCm39)	C52F	probably damaging	Het
Tsc2	T	A	17: 24,819,343 (GRCm39)	D1304V	probably benign	Het
Ugt2b36	T	C	5: 87,214,183 (GRCm39)	Y487C	probably damaging	Het
Vmn1r10	T	A	6: 57,090,811 (GRCm39)	N134K	probably damaging	Het
Wdr27	C	A	17: 15,141,016 (GRCm39)		probably null	Het
Wdr75	T	C	1: 45,855,638 (GRCm39)	F430L	probably damaging	Het
Zfp629	A	G	7: 127,211,299 (GRCm39)	I170T	probably damaging	Het

Other mutations in Rnf145

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00087:Rnf145	APN	11	44,446,039 (GRCm39)	missense	possibly damaging	0.90
IGL02972:Rnf145	APN	11	44,454,865 (GRCm39)	missense	probably benign	0.26
IGL03168:Rnf145	APN	11	44,445,985 (GRCm39)	missense	probably damaging	1.00
IGL03185:Rnf145	APN	11	44,422,157 (GRCm39)	missense	probably damaging	1.00
IGL02980:Rnf145	UTSW	11	44,452,484 (GRCm39)	missense	probably benign
R0112:Rnf145	UTSW	11	44,454,978 (GRCm39)	missense	probably benign
R0346:Rnf145	UTSW	11	44,445,991 (GRCm39)	missense	probably damaging	1.00
R0415:Rnf145	UTSW	11	44,415,965 (GRCm39)	missense	probably damaging	0.99
R0452:Rnf145	UTSW	11	44,452,587 (GRCm39)	missense	probably damaging	1.00
R0487:Rnf145	UTSW	11	44,446,056 (GRCm39)	missense	probably benign	0.21
R0598:Rnf145	UTSW	11	44,439,770 (GRCm39)	missense	probably damaging	1.00
R0631:Rnf145	UTSW	11	44,450,851 (GRCm39)	missense	probably damaging	0.99
R0837:Rnf145	UTSW	11	44,415,815 (GRCm39)	missense	probably benign	0.00
R1611:Rnf145	UTSW	11	44,442,625 (GRCm39)	missense	probably damaging	1.00
R1971:Rnf145	UTSW	11	44,439,642 (GRCm39)	missense	probably damaging	1.00
R1991:Rnf145	UTSW	11	44,452,293 (GRCm39)	missense	possibly damaging	0.90
R2157:Rnf145	UTSW	11	44,445,997 (GRCm39)	missense	probably damaging	1.00
R2340:Rnf145	UTSW	11	44,422,205 (GRCm39)	missense	probably benign	0.04
R3855:Rnf145	UTSW	11	44,422,120 (GRCm39)	missense	possibly damaging	0.46
R4483:Rnf145	UTSW	11	44,455,104 (GRCm39)	missense	probably benign	0.10
R4564:Rnf145	UTSW	11	44,439,635 (GRCm39)	missense	probably benign	0.25
R5633:Rnf145	UTSW	11	44,450,915 (GRCm39)	missense	probably damaging	1.00
R5672:Rnf145	UTSW	11	44,422,120 (GRCm39)	missense	possibly damaging	0.46
R5673:Rnf145	UTSW	11	44,422,120 (GRCm39)	missense	possibly damaging	0.46
R5701:Rnf145	UTSW	11	44,422,120 (GRCm39)	missense	possibly damaging	0.46
R5915:Rnf145	UTSW	11	44,433,549 (GRCm39)	critical splice donor site	probably null
R6128:Rnf145	UTSW	11	44,446,018 (GRCm39)	missense	probably damaging	1.00
R6502:Rnf145	UTSW	11	44,415,932 (GRCm39)	missense	probably damaging	0.98
R6717:Rnf145	UTSW	11	44,452,317 (GRCm39)	missense	probably benign	0.00
R6963:Rnf145	UTSW	11	44,455,104 (GRCm39)	missense	probably benign	0.10
R7035:Rnf145	UTSW	11	44,452,583 (GRCm39)	missense	probably damaging	1.00
R7154:Rnf145	UTSW	11	44,415,822 (GRCm39)	missense	probably damaging	1.00
R7351:Rnf145	UTSW	11	44,439,623 (GRCm39)	missense	possibly damaging	0.91
R7639:Rnf145	UTSW	11	44,422,184 (GRCm39)	missense	probably damaging	1.00
R8074:Rnf145	UTSW	11	44,448,263 (GRCm39)	missense	probably damaging	0.98
R8536:Rnf145	UTSW	11	44,450,942 (GRCm39)	missense	probably damaging	1.00
R8861:Rnf145	UTSW	11	44,445,984 (GRCm39)	missense	probably damaging	1.00
R9123:Rnf145	UTSW	11	44,450,819 (GRCm39)	missense	probably damaging	1.00
R9125:Rnf145	UTSW	11	44,450,819 (GRCm39)	missense	probably damaging	1.00
R9172:Rnf145	UTSW	11	44,448,262 (GRCm39)	missense	possibly damaging	0.95
R9520:Rnf145	UTSW	11	44,452,336 (GRCm39)	missense	possibly damaging	0.91
R9711:Rnf145	UTSW	11	44,415,830 (GRCm39)	nonsense	probably null
R9801:Rnf145	UTSW	11	44,448,112 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- TGCCTGTAAATCGGTGTGCC -3'
(R):5'- CCGTGGGAAGAGAGTCCATTAAC -3'

Sequencing Primer
(F):5'- TGTGCCGCCACACTGAAG -3'
(R):5'- TGCCAAAACAATGGGATCTGC -3'

Posted On

2016-04-15