Mutagenetix > Incidental Mutation

Incidental Mutation 'R2213:Rbm25'

239539

Institutional Source

Beutler Lab

Gene Symbol

Rbm25

Ensembl Gene

ENSMUSG00000010608

Gene Name

RNA binding motif protein 25

Synonyms

2610015J01Rik, A130095G20Rik, 2600011C06Rik

MMRRC Submission

040215-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R2213 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

83678990-83729901 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 83722856 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Leucine at position 760 (I760L)

Ref Sequence

ENSEMBL: ENSMUSP00000048470 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000048155] [ENSMUST00000181983] [ENSMUST00000182450]

AlphaFold

B2RY56

Predicted Effect

probably benign
Transcript: ENSMUST00000048155
AA Change: I760L

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)

SMART Domains

Protein: ENSMUSP00000048470
Gene: ENSMUSG00000010608
AA Change: I760L

Domain	Start	End	E-Value	Type
low complexity region	10	44	N/A	INTRINSIC
RRM	88	160	2.52e-11	SMART
low complexity region	234	241	N/A	INTRINSIC
coiled coil region	270	351	N/A	INTRINSIC
coiled coil region	382	549	N/A	INTRINSIC
low complexity region	556	606	N/A	INTRINSIC
low complexity region	616	625	N/A	INTRINSIC
PWI	758	831	2.79e-38	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000181983

SMART Domains

Protein: ENSMUSP00000138572
Gene: ENSMUSG00000010608

Domain	Start	End	E-Value	Type
low complexity region	10	44	N/A	INTRINSIC
RRM	88	160	2.52e-11	SMART
internal_repeat_1	187	203	3e-5	PROSPERO
low complexity region	234	241	N/A	INTRINSIC
internal_repeat_1	258	274	3e-5	PROSPERO
coiled coil region	382	549	N/A	INTRINSIC
low complexity region	556	571	N/A	INTRINSIC
low complexity region	575	584	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000182450

SMART Domains

Protein: ENSMUSP00000138416
Gene: ENSMUSG00000010608

Domain	Start	End	E-Value	Type
low complexity region	10	44	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000182840

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000183181

Coding Region Coverage

1x: 99.1%
3x: 98.6%
10x: 97.3%
20x: 95.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Akr1c12	T	C	13: 4,326,247 (GRCm39)	D78G	probably damaging	Het
Anxa1	C	T	19: 20,360,239 (GRCm39)	R124H	probably damaging	Het
Arhgef4	G	A	1: 34,846,230 (GRCm39)		probably null	Het
C87436	G	A	6: 86,422,455 (GRCm39)	V10I	probably benign	Het
Ces1a	G	T	8: 93,751,853 (GRCm39)	P427Q	probably damaging	Het
Cpm	T	C	10: 117,495,744 (GRCm39)	Y78H	probably damaging	Het
Csmd3	G	A	15: 47,683,843 (GRCm39)	T1663I	possibly damaging	Het
Cul7	T	C	17: 46,962,398 (GRCm39)	F10L	probably damaging	Het
Cyp2j5	T	C	4: 96,547,852 (GRCm39)	N130S	probably benign	Het
Dclk1	G	A	3: 55,387,854 (GRCm39)	C100Y	probably damaging	Het
Ddb1	T	C	19: 10,585,691 (GRCm39)	L135P	probably damaging	Het
Dixdc1	A	G	9: 50,613,245 (GRCm39)	S211P	probably benign	Het
Dnah12	G	T	14: 26,460,485 (GRCm39)	K970N	probably benign	Het
Eps15	A	G	4: 109,218,417 (GRCm39)	K391E	probably damaging	Het
Fabp9	A	G	3: 10,259,860 (GRCm39)	V51A	probably damaging	Het
Flg	T	C	3: 93,200,335 (GRCm39)		probably benign	Het
Flnb	AAGGAG	AAG	14: 7,881,652 (GRCm38)		probably benign	Het
Fscb	A	T	12: 64,520,890 (GRCm39)	I192N	possibly damaging	Het
Galntl5	A	G	5: 25,422,527 (GRCm39)	I333V	probably benign	Het
Gcnt3	A	T	9: 69,941,989 (GRCm39)	V193E	probably benign	Het
Gle1	T	C	2: 29,839,313 (GRCm39)	F535S	probably damaging	Het
Gpr87	A	T	3: 59,086,465 (GRCm39)	S347T	probably damaging	Het
Gstm2	C	T	3: 107,893,409 (GRCm39)	R18H	probably damaging	Het
H1f7	T	A	15: 98,154,219 (GRCm39)	Q310L	unknown	Het
Haus6	C	T	4: 86,500,229 (GRCm39)	E927K	possibly damaging	Het
Hunk	A	G	16: 90,229,505 (GRCm39)	N122S	probably damaging	Het
Itih4	T	A	14: 30,612,670 (GRCm39)	V232E	probably damaging	Het
Jag1	G	T	2: 136,931,812 (GRCm39)	D586E	probably benign	Het
Klk1b1	T	C	7: 43,619,905 (GRCm39)	S155P	probably damaging	Het
Lama1	G	T	17: 68,084,029 (GRCm39)	G1424*	probably null	Het
Lrp1	T	A	10: 127,376,571 (GRCm39)	N4279I	probably damaging	Het
Lrrc43	G	A	5: 123,641,640 (GRCm39)	V525I	possibly damaging	Het
Lrrc4c	G	A	2: 97,460,816 (GRCm39)	V481M	probably benign	Het
Mecr	T	A	4: 131,581,126 (GRCm39)		probably null	Het
Megf10	T	A	18: 57,421,081 (GRCm39)	Y906*	probably null	Het
Mpdz	A	G	4: 81,228,409 (GRCm39)	F1319L	probably damaging	Het
Mtf2	A	G	5: 108,248,780 (GRCm39)	E364G	possibly damaging	Het
Nelfe	T	A	17: 35,072,859 (GRCm39)	D160E	probably benign	Het
Nin	A	G	12: 70,092,128 (GRCm39)	L727P	probably damaging	Het
Npat	A	G	9: 53,463,681 (GRCm39)	T155A	probably benign	Het
Nup58	T	C	14: 60,476,945 (GRCm39)	D242G	probably benign	Het
Or4a78	A	T	2: 89,497,891 (GRCm39)	L113Q	probably damaging	Het
Pnlip	T	C	19: 58,662,202 (GRCm39)	V116A	probably benign	Het
Prl7a2	T	A	13: 27,849,051 (GRCm39)	L79F	probably benign	Het
Rbms3	A	T	9: 116,788,534 (GRCm39)		probably null	Het
Rif1	GCCACCA	GCCA	2: 52,000,336 (GRCm39)		probably benign	Het
Rps10	C	A	17: 27,849,473 (GRCm39)		probably benign	Het
Slc35e4	T	C	11: 3,863,159 (GRCm39)	E10G	possibly damaging	Het
Smad2	A	T	18: 76,437,697 (GRCm39)	T434S	probably damaging	Het
Sox30	C	T	11: 45,875,679 (GRCm39)	S477F	probably damaging	Het
Speer4a3	G	T	5: 26,158,175 (GRCm39)	T59K	probably benign	Het
Stat4	A	T	1: 52,053,014 (GRCm39)	D65V	probably damaging	Het
Strip2	A	G	6: 29,931,147 (GRCm39)	D366G	probably damaging	Het
Syngap1	C	A	17: 27,172,043 (GRCm39)	R84S	probably damaging	Het
Synpo2l	A	G	14: 20,710,734 (GRCm39)	Y629H	probably damaging	Het
Taf4	A	T	2: 179,577,683 (GRCm39)		probably null	Het
Ttc21a	A	G	9: 119,769,527 (GRCm39)	H68R	probably benign	Het
Txndc8	T	A	4: 57,984,199 (GRCm39)	Q144L	probably benign	Het
Tyr	T	G	7: 87,142,086 (GRCm39)	Q158P	probably damaging	Het
Uchl3	T	A	14: 101,904,106 (GRCm39)		probably null	Het
Vwa5b1	T	C	4: 138,332,123 (GRCm39)	K298R	probably benign	Het
Wrn	T	C	8: 33,747,043 (GRCm39)	N891S	probably benign	Het
Ylpm1	A	G	12: 85,116,492 (GRCm39)	S2125G	probably benign	Het

Other mutations in Rbm25

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01614:Rbm25	APN	12	83,706,341 (GRCm39)	missense	probably damaging	1.00
IGL02095:Rbm25	APN	12	83,718,748 (GRCm39)	missense	probably damaging	1.00
IGL02227:Rbm25	APN	12	83,719,527 (GRCm39)	missense	probably damaging	1.00
IGL02454:Rbm25	APN	12	83,707,096 (GRCm39)	missense	probably benign	0.02
IGL02704:Rbm25	APN	12	83,689,500 (GRCm39)	missense	probably damaging	1.00
IGL02726:Rbm25	APN	12	83,719,626 (GRCm39)	missense	probably damaging	1.00
IGL03384:Rbm25	APN	12	83,706,297 (GRCm39)	missense	probably benign	0.28
Complexities	UTSW	12	83,724,630 (GRCm39)	missense	probably damaging	1.00
R0380:Rbm25	UTSW	12	83,707,130 (GRCm39)	missense	probably benign	0.02
R0829:Rbm25	UTSW	12	83,707,150 (GRCm39)	splice site	probably benign
R1330:Rbm25	UTSW	12	83,724,666 (GRCm39)	missense	probably damaging	1.00
R1346:Rbm25	UTSW	12	83,691,167 (GRCm39)	splice site	probably benign
R1518:Rbm25	UTSW	12	83,715,219 (GRCm39)	missense	possibly damaging	0.91
R1566:Rbm25	UTSW	12	83,721,828 (GRCm39)	missense	probably damaging	0.98
R1660:Rbm25	UTSW	12	83,714,924 (GRCm39)	unclassified	probably benign
R1809:Rbm25	UTSW	12	83,719,501 (GRCm39)	splice site	probably benign
R2336:Rbm25	UTSW	12	83,698,192 (GRCm39)	missense	probably damaging	1.00
R2943:Rbm25	UTSW	12	83,707,415 (GRCm39)	missense	probably damaging	1.00
R3971:Rbm25	UTSW	12	83,721,982 (GRCm39)	missense	probably benign	0.03
R4349:Rbm25	UTSW	12	83,721,947 (GRCm39)	missense	probably damaging	0.99
R4740:Rbm25	UTSW	12	83,691,181 (GRCm39)	missense	possibly damaging	0.61
R4987:Rbm25	UTSW	12	83,724,630 (GRCm39)	missense	probably damaging	1.00
R5205:Rbm25	UTSW	12	83,719,643 (GRCm39)	missense	probably benign	0.03
R5579:Rbm25	UTSW	12	83,715,281 (GRCm39)	missense	probably benign	0.41
R5603:Rbm25	UTSW	12	83,710,990 (GRCm39)	nonsense	probably null
R5909:Rbm25	UTSW	12	83,728,362 (GRCm39)	missense	probably damaging	0.97
R5930:Rbm25	UTSW	12	83,724,640 (GRCm39)	missense	possibly damaging	0.46
R5982:Rbm25	UTSW	12	83,718,725 (GRCm39)	missense	probably damaging	0.99
R6233:Rbm25	UTSW	12	83,706,200 (GRCm39)	missense	probably benign	0.24
R6275:Rbm25	UTSW	12	83,691,206 (GRCm39)	missense	probably damaging	0.98
R6282:Rbm25	UTSW	12	83,722,863 (GRCm39)	missense	probably damaging	0.98
R7156:Rbm25	UTSW	12	83,710,965 (GRCm39)	missense	unknown
R7188:Rbm25	UTSW	12	83,710,772 (GRCm39)	missense	unknown
R7217:Rbm25	UTSW	12	83,710,991 (GRCm39)	missense	unknown
R7403:Rbm25	UTSW	12	83,722,908 (GRCm39)	missense	probably damaging	1.00
R7508:Rbm25	UTSW	12	83,719,651 (GRCm39)	missense	probably damaging	0.99
R7703:Rbm25	UTSW	12	83,721,864 (GRCm39)	missense	possibly damaging	0.69
R8004:Rbm25	UTSW	12	83,721,166 (GRCm39)	missense	possibly damaging	0.61
R8154:Rbm25	UTSW	12	83,691,205 (GRCm39)	missense	unknown
R8444:Rbm25	UTSW	12	83,711,025 (GRCm39)	missense	unknown
Z1176:Rbm25	UTSW	12	83,719,658 (GRCm39)	missense	possibly damaging	0.92

Predicted Primers

PCR Primer
(F):5'- TTCCCTGCACCGTACAACTTAATAG -3'
(R):5'- GCTGACTTCAAATATCAGGTCAC -3'

Sequencing Primer
(F):5'- CCATGGAAATTCAAATGGCTGTTTGG -3'
(R):5'- TTGTGTAGATGCAGGCA -3'

Posted On

2014-10-15