Mutagenetix > Incidental Mutation

Incidental Mutation 'R6502:Rnf145'

519807

Institutional Source

Beutler Lab

Gene Symbol

Rnf145

Ensembl Gene

ENSMUSG00000019189

Gene Name

ring finger protein 145

Synonyms

3732413I11Rik

MMRRC Submission

044634-MU

Accession Numbers

Essential gene?

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

Stock #

R6502 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

44409791-44456347 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 44415932 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Serine at position 49 (F49S)

Ref Sequence

ENSEMBL: ENSMUSP00000019333 (fasta)

Gene Model

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

AlphaFold

Q5SWK7

Predicted Effect

probably damaging
Transcript: ENSMUST00000019333
AA Change: F49S

PolyPhen 2 Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000019333
Gene: ENSMUSG00000019189
AA Change: F49S

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 damaging
Transcript: ENSMUST00000101327
AA Change: F49S

PolyPhen 2 Score 0.969 (Sensitivity: 0.77; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000098881
Gene: ENSMUSG00000019189
AA Change: F49S

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

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000124959

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000127907

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.2%
20x: 94.7%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 78 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700013D24Rik	A	T	6: 124,333,908 (GRCm39)	I24K	probably benign	Het
Adamts9	A	T	6: 92,849,316 (GRCm39)	C467S	probably damaging	Het
Adcy7	G	A	8: 89,052,107 (GRCm39)	R925Q	probably damaging	Het
Akap6	G	A	12: 53,186,998 (GRCm39)	G1471S	probably damaging	Het
Ap2b1	T	C	11: 83,233,505 (GRCm39)	V506A	probably damaging	Het
Apob	A	G	12: 8,051,814 (GRCm39)	I1113M	probably damaging	Het
Arsg	A	T	11: 109,408,162 (GRCm39)	N105Y	probably damaging	Het
Blm	T	A	7: 80,131,223 (GRCm39)	Y872F	probably damaging	Het
Btaf1	A	T	19: 36,961,017 (GRCm39)	N797Y	probably benign	Het
Camsap1	T	C	2: 25,846,320 (GRCm39)	E201G	probably damaging	Het
Ccdc122	T	A	14: 77,279,509 (GRCm39)		probably null	Homo
Ccdc141	A	G	2: 77,000,745 (GRCm39)	V29A	probably damaging	Het
Cd244a	T	A	1: 171,405,447 (GRCm39)	D277E	probably benign	Het
Cfap157	T	C	2: 32,670,690 (GRCm39)	Y186C	probably damaging	Het
Ciita	C	T	16: 10,329,774 (GRCm39)	A686V	probably damaging	Het
Clptm1l	T	C	13: 73,765,884 (GRCm39)		probably null	Het
Col16a1	C	T	4: 129,949,787 (GRCm39)	P50L	probably damaging	Het
Crisp3	A	T	17: 40,546,804 (GRCm39)	V38D	probably damaging	Het
Cyfip2	T	C	11: 46,112,173 (GRCm39)	E1010G	probably damaging	Het
Dvl3	G	A	16: 20,346,133 (GRCm39)	E488K	probably damaging	Het
Eed	C	A	7: 89,626,237 (GRCm39)	E45D	probably benign	Het
Eln	A	G	5: 134,754,628 (GRCm39)		probably benign	Het
Fah	T	A	7: 84,244,043 (GRCm39)	I239F	probably damaging	Het
Fbxw5	T	A	2: 25,392,448 (GRCm39)	Y77N	possibly damaging	Het
Garnl3	T	C	2: 32,896,833 (GRCm39)	E602G	possibly damaging	Het
Gkn3	A	T	6: 87,365,786 (GRCm39)	M11K	probably benign	Het
Glt1d1	A	G	5: 127,784,045 (GRCm39)	Y333C	probably damaging	Het
Gm10762	A	T	2: 128,809,090 (GRCm39)	Y86*	probably null	Het
Gm14496	A	G	2: 181,642,386 (GRCm39)	M686V	probably benign	Het
Gse1	T	A	8: 121,280,428 (GRCm39)		probably null	Het
Herc4	C	A	10: 63,153,197 (GRCm39)	T1035K	probably benign	Het
Hmcn2	T	A	2: 31,272,490 (GRCm39)	N1323K	probably damaging	Het
Hnrnpd	T	A	5: 100,114,025 (GRCm39)	E3D	probably damaging	Het
Htr7	T	A	19: 35,947,010 (GRCm39)	I335F	probably damaging	Het
Ift70b	T	A	2: 75,767,448 (GRCm39)	N435I	possibly damaging	Het
Itgae	A	T	11: 73,036,418 (GRCm39)	I1119F	probably benign	Het
Lcn11	T	C	2: 25,669,103 (GRCm39)	F137S	probably benign	Het
Lrp3	T	G	7: 34,903,413 (GRCm39)	D311A	possibly damaging	Het
Lrrc1	G	T	9: 77,349,473 (GRCm39)	D364E	probably damaging	Het
Lrrc37a	T	A	11: 103,383,005 (GRCm39)	E2456V	unknown	Het
Lrriq1	T	C	10: 103,063,045 (GRCm39)	Y87C	probably damaging	Het
Mcc	A	T	18: 44,601,457 (GRCm39)	L449*	probably null	Het
Mcc	A	T	18: 44,601,458 (GRCm39)	L624M	probably damaging	Het
Mcm9	T	C	10: 53,488,935 (GRCm39)	T496A	probably damaging	Het
Myef2	T	A	2: 124,958,602 (GRCm39)	D109V	probably damaging	Het
Myom3	C	T	4: 135,489,824 (GRCm39)		probably benign	Het
Nanos1	G	T	19: 60,744,977 (GRCm39)	G92W	possibly damaging	Het
Ncor1	T	A	11: 62,272,240 (GRCm39)	K84*	probably null	Het
Neb	T	A	2: 52,181,094 (GRCm39)	D1171V	probably benign	Het
Notch3	A	G	17: 32,377,191 (GRCm39)	W267R	probably damaging	Het
Or5d39	A	T	2: 87,980,360 (GRCm39)	M1K	probably null	Het
Or8d1	A	C	9: 38,766,933 (GRCm39)	T192P	probably damaging	Het
Per2	A	G	1: 91,355,485 (GRCm39)	S758P	probably benign	Het
Pi4k2a	A	G	19: 42,079,371 (GRCm39)	Q144R	probably benign	Het
Pirb	A	T	7: 3,720,392 (GRCm39)	V327E	probably benign	Het
Pla2g4a	C	T	1: 149,748,367 (GRCm39)	W272*	probably null	Het
Plekha4	T	A	7: 45,180,000 (GRCm39)	M1K	probably null	Het
Ppt2	A	G	17: 34,844,894 (GRCm39)	C117R	probably damaging	Het
Prph	A	T	15: 98,954,267 (GRCm39)	I222F	probably damaging	Het
Rbm43	T	C	2: 51,815,588 (GRCm39)	D211G	probably damaging	Het
Rims2	A	G	15: 39,398,251 (GRCm39)	D1072G	probably benign	Het
Rnf123	G	T	9: 107,945,531 (GRCm39)	Q380K	possibly damaging	Het
Sall4	A	G	2: 168,597,628 (GRCm39)	I404T	probably damaging	Het
Slc25a39	G	A	11: 102,295,286 (GRCm39)	P228L	probably damaging	Het
Tbc1d14	T	C	5: 36,677,825 (GRCm39)	T377A	possibly damaging	Het
Tbc1d17	A	G	7: 44,491,049 (GRCm39)	I555T	probably benign	Het
Tmem131l	A	T	3: 83,829,715 (GRCm39)	S980T	probably damaging	Het
Tmem14a	G	T	1: 21,299,662 (GRCm39)	L97F	possibly damaging	Het
Tmem98	T	C	11: 80,703,461 (GRCm39)	V26A	probably benign	Het
Tmppe	G	T	9: 114,234,720 (GRCm39)	G340W	probably damaging	Het
Tsc1	T	C	2: 28,555,613 (GRCm39)	S237P	probably damaging	Het
Ubr4	C	T	4: 139,171,982 (GRCm39)	R2992W	probably damaging	Het
Ugt2a2	A	G	5: 87,608,318 (GRCm39)	V673A	possibly damaging	Het
Vmn2r19	T	C	6: 123,293,067 (GRCm39)	Y370H	possibly damaging	Het
Vmn2r20	A	G	6: 123,373,342 (GRCm39)	F500S	possibly damaging	Het
Zc3h7b	A	G	15: 81,653,252 (GRCm39)	Y47C	probably benign	Het
Zdhhc13	A	G	7: 48,465,308 (GRCm39)	E406G	possibly damaging	Het
Zfp418	T	C	7: 7,185,599 (GRCm39)	S521P	possibly 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
R4922:Rnf145	UTSW	11	44,448,063 (GRCm39)	unclassified	probably benign
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
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'- GGTCTGCTCCGAGGAAACAATC -3'
(R):5'- ACATGGATGTAGTGGCAACTAATC -3'

Sequencing Primer
(F):5'- TCCAAAAGCAACCATGGCTG -3'
(R):5'- TGGCAACTAATCAAAAGATGCTG -3'

Posted On

2018-06-06