Mutagenetix > Incidental Mutation

Incidental Mutation 'R5095:Rnf149'

395797

Institutional Source

Beutler Lab

Gene Symbol

Rnf149

Ensembl Gene

ENSMUSG00000048234

Gene Name

ring finger protein 149

Synonyms

1600023E10Rik, Greul4

MMRRC Submission

042684-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.166) question?

Stock #

R5095 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

39551296-39577405 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 39555656 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glutamic Acid at position 321 (D321E)

Ref Sequence

ENSEMBL: ENSMUSP00000050388 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000062525] [ENSMUST00000195136]

AlphaFold

Q3U2C5

Predicted Effect

probably benign
Transcript: ENSMUST00000062525
AA Change: D321E

PolyPhen 2 Score 0.191 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000050388
Gene: ENSMUSG00000048234
AA Change: D321E

Domain	Start	End	E-Value	Type
low complexity region	2	24	N/A	INTRINSIC
Pfam:PA	72	169	3.9e-13	PFAM
transmembrane domain	196	218	N/A	INTRINSIC
RING	265	305	2.09e-7	SMART
low complexity region	347	362	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000146314

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000153381

Predicted Effect

unknown
Transcript: ENSMUST00000195136
AA Change: I132K

SMART Domains

Protein: ENSMUSP00000141667
Gene: ENSMUSG00000048234
AA Change: I132K

Domain	Start	End	E-Value	Type
transmembrane domain	39	61	N/A	INTRINSIC
SCOP:d1ldjb_	74	127	3e-3	SMART
Blast:RING	108	127	9e-7	BLAST

Meta Mutation Damage Score

0.1281

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.4%
20x: 95.5%

Validation Efficiency

98% (59/60)

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700021A07Rik	G	C	10: 21,425,593		noncoding transcript	Het
4932415D10Rik	G	T	10: 82,283,667	A4503E	probably damaging	Het
Adgrv1	C	T	13: 81,095,487	V6265I	probably benign	Het
Agbl1	G	A	7: 76,720,133	G660D	probably damaging	Het
Arap2	A	G	5: 62,654,049	Y1140H	probably damaging	Het
Atp6v1c1	T	C	15: 38,679,413		probably null	Het
C1rb	A	T	6: 124,580,313	R470W	possibly damaging	Het
Caskin2	T	C	11: 115,800,738	T1074A	probably benign	Het
Cdh19	T	A	1: 110,954,661	T34S	probably benign	Het
Csnk1a1	T	A	18: 61,575,476	Y175N	probably damaging	Het
F2	CAGAAAG	CAG	2: 91,634,957		probably benign	Het
Flt4	T	A	11: 49,627,159	V342D	possibly damaging	Het
Frmd5	A	T	2: 121,548,921	C394S	possibly damaging	Het
Gm5414	T	G	15: 101,624,038	N550T	probably benign	Het
Hcn3	C	A	3: 89,149,923	R456L	probably damaging	Het
Htt	T	C	5: 34,824,395	V893A	possibly damaging	Het
Ift46	A	G	9: 44,786,849	D203G	probably damaging	Het
Itga10	G	T	3: 96,648,164	V145L	probably benign	Het
Kcnh6	A	G	11: 106,017,254	D232G	possibly damaging	Het
Mbtd1	T	C	11: 93,929,671	S431P	probably damaging	Het
Mmp27	T	A	9: 7,572,158	W120R	probably damaging	Het
Mmp27	A	T	9: 7,579,000	D418V	probably damaging	Het
Myo5a	A	G	9: 75,152,020	D510G	probably damaging	Het
Myo5a	A	T	9: 75,184,389	K1179*	probably null	Het
Neto1	T	C	18: 86,398,281	S38P	probably benign	Het
Nos3	A	G	5: 24,368,918		probably benign	Het
Nuggc	C	T	14: 65,635,090	R512*	probably null	Het
Oas1e	T	A	5: 120,794,264	K105*	probably null	Het
Olfr135	A	C	17: 38,208,317	E24A	possibly damaging	Het
Olfr512	T	C	7: 108,713,812	F141S	probably damaging	Het
Omd	T	A	13: 49,589,698	S75T	possibly damaging	Het
Pbrm1	A	G	14: 31,032,530	N190S	probably benign	Het
Picalm	T	C	7: 90,170,633	F85L	probably damaging	Het
Polg	A	G	7: 79,460,300	V360A	possibly damaging	Het
Prex1	T	C	2: 166,581,921	D1017G	probably damaging	Het
Prss56	G	C	1: 87,188,111	R569P	probably damaging	Het
Rab6b	G	A	9: 103,140,384	G25R	probably damaging	Het
Rdh10	A	G	1: 16,131,385	T332A	probably benign	Het
Rheb	A	T	5: 24,807,641	M115K	probably benign	Het
Rps28	C	T	17: 33,823,203		probably null	Het
Slc6a20b	A	G	9: 123,595,054	V616A	probably benign	Het
Smarcc2	A	G	10: 128,469,300	K300R	probably damaging	Het
Sparcl1	C	T	5: 104,085,763	M573I	probably damaging	Het
Srp68	C	T	11: 116,248,747	V459M	probably damaging	Het
Stxbp4	C	T	11: 90,548,975	V346I	probably benign	Het
Syne2	A	G	12: 75,952,826	D2331G	probably damaging	Het
Ttn	A	T	2: 76,734,192	Y28534N	probably damaging	Het
Usp44	A	T	10: 93,846,845	I386F	possibly damaging	Het
Vmn2r15	T	C	5: 109,288,451		probably null	Het
Vmn2r72	T	A	7: 85,737,853	L834F	probably damaging	Het
Vps13b	T	A	15: 35,923,202	I3741K	probably damaging	Het
Zdbf2	A	G	1: 63,309,073	T2204A	possibly damaging	Het
Zfp607b	T	A	7: 27,693,636		probably benign	Het

Other mutations in Rnf149

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02586:Rnf149	APN	1	39565215	missense	probably benign	0.19
R1316:Rnf149	UTSW	1	39565320	makesense	probably null
R2917:Rnf149	UTSW	1	39552483	missense	probably benign	0.00
R4690:Rnf149	UTSW	1	39577214	intron	probably benign
R6084:Rnf149	UTSW	1	39577174	missense	probably benign	0.01
R6338:Rnf149	UTSW	1	39560742	missense	probably null	1.00
R7773:Rnf149	UTSW	1	39565218	missense	possibly damaging	0.78
R8090:Rnf149	UTSW	1	39577223	missense	unknown

Predicted Primers

PCR Primer
(F):5'- AGTAATGCTGTGTCCTCCCCTG -3'
(R):5'- AAAGGGCGAGATACAACTTCC -3'

Sequencing Primer
(F):5'- CCTGCATCTTCTTTAAGACAGGGG -3'
(R):5'- CGAGATACAACTTCCATCAAGTAGGG -3'

Posted On

2016-06-21