Mutagenetix > Incidental Mutation

Incidental Mutation 'R0048:Rbm27'

15833

Institutional Source

Beutler Lab

Gene Symbol

Rbm27

Ensembl Gene

ENSMUSG00000024491

Gene Name

RNA binding motif protein 27

Synonyms

Psc1

MMRRC Submission

038342-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0048 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

42408418-42474607 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 42431529 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 112 (D112G)

Ref Sequence

ENSEMBL: ENSMUSP00000089540 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000046972] [ENSMUST00000091920]

AlphaFold

Q5SFM8

Predicted Effect

probably benign
Transcript: ENSMUST00000046972
AA Change: D112G

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000041688
Gene: ENSMUSG00000024491
AA Change: D112G

Domain	Start	End	E-Value	Type
Pfam:PWI	7	77	1.4e-10	PFAM
low complexity region	78	105	N/A	INTRINSIC
low complexity region	123	139	N/A	INTRINSIC
low complexity region	144	158	N/A	INTRINSIC
low complexity region	163	188	N/A	INTRINSIC
low complexity region	213	235	N/A	INTRINSIC
low complexity region	255	268	N/A	INTRINSIC
Pfam:zf-CCCH	274	300	5.2e-7	PFAM
low complexity region	317	358	N/A	INTRINSIC
low complexity region	372	386	N/A	INTRINSIC
low complexity region	448	462	N/A	INTRINSIC
low complexity region	541	555	N/A	INTRINSIC
SCOP:d1l3ka2	598	638	1e-4	SMART
Blast:RRM	601	643	2e-11	BLAST
Blast:RRM_2	744	782	3e-6	BLAST
low complexity region	783	798	N/A	INTRINSIC
low complexity region	853	865	N/A	INTRINSIC
low complexity region	924	938	N/A	INTRINSIC
low complexity region	945	953	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000091920
AA Change: D112G

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000089540
Gene: ENSMUSG00000024491
AA Change: D112G

Domain	Start	End	E-Value	Type
Pfam:PWI	7	77	1.5e-10	PFAM
low complexity region	78	105	N/A	INTRINSIC
low complexity region	123	139	N/A	INTRINSIC
low complexity region	144	158	N/A	INTRINSIC
low complexity region	163	188	N/A	INTRINSIC
low complexity region	213	235	N/A	INTRINSIC
low complexity region	255	268	N/A	INTRINSIC
Pfam:zf-CCCH	274	300	5.5e-7	PFAM
low complexity region	317	358	N/A	INTRINSIC
low complexity region	372	386	N/A	INTRINSIC
low complexity region	486	500	N/A	INTRINSIC
RRM	546	615	7.94e-3	SMART
low complexity region	623	658	N/A	INTRINSIC
Blast:RRM_2	788	826	3e-6	BLAST
low complexity region	827	842	N/A	INTRINSIC
low complexity region	897	909	N/A	INTRINSIC
low complexity region	968	982	N/A	INTRINSIC
low complexity region	989	997	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000175194

Meta Mutation Damage Score

0.0605

Coding Region Coverage

1x: 90.1%
3x: 87.7%
10x: 82.5%
20x: 75.5%

Validation Efficiency

94% (92/98)

Allele List at MGI

Other mutations in this stock

Total: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrb3	A	G	1: 25,140,563 (GRCm39)	I299T	probably benign	Het
Ankrd12	A	G	17: 66,291,798 (GRCm39)	S1212P	probably damaging	Het
Ankrd50	A	G	3: 38,537,198 (GRCm39)	S52P	probably benign	Het
Aox1	A	G	1: 58,112,371 (GRCm39)	E715G	probably damaging	Het
Arid1b	T	C	17: 5,364,309 (GRCm39)		probably null	Het
Brca1	A	G	11: 101,415,803 (GRCm39)	V777A	possibly damaging	Het
Btaf1	G	T	19: 36,980,924 (GRCm39)	A1582S	probably benign	Het
Cblif	G	A	19: 11,727,120 (GRCm39)	V110M	possibly damaging	Het
Ccdc184	G	A	15: 98,066,341 (GRCm39)	A49T	probably damaging	Het
Cd109	A	C	9: 78,587,303 (GRCm39)	Y657S	possibly damaging	Het
Cfap53	A	T	18: 74,432,244 (GRCm39)	Y44F	probably benign	Het
Cped1	T	A	6: 22,119,601 (GRCm39)	N353K	probably benign	Het
Dcaf10	T	G	4: 45,374,262 (GRCm39)	Y562*	probably null	Het
Eno4	T	C	19: 58,952,970 (GRCm39)	M328T	possibly damaging	Het
Etv3l	T	C	3: 87,462,275 (GRCm39)		noncoding transcript	Het
Eya2	T	A	2: 165,557,931 (GRCm39)	Y176N	probably damaging	Het
Fat2	G	T	11: 55,200,865 (GRCm39)	H736Q	probably benign	Het
Fgfr2	A	T	7: 129,782,218 (GRCm39)		probably benign	Het
Grhl1	A	T	12: 24,662,150 (GRCm39)		probably benign	Het
H60b	T	A	10: 22,163,130 (GRCm39)	M235K	probably benign	Het
Hal	T	A	10: 93,334,853 (GRCm39)	Y395N	probably damaging	Het
Hmcn2	T	C	2: 31,318,249 (GRCm39)	S3865P	possibly damaging	Het
Inpp5j	A	G	11: 3,451,417 (GRCm39)	V463A	probably damaging	Het
Iqgap3	A	T	3: 88,023,256 (GRCm39)	T516S	probably benign	Het
Itpr2	T	C	6: 146,133,789 (GRCm39)		probably null	Het
Jmjd4	C	A	11: 59,344,778 (GRCm39)	H244N	probably benign	Het
Klkb1	G	A	8: 45,742,233 (GRCm39)		probably benign	Het
Loxhd1	A	T	18: 77,496,474 (GRCm39)	Y1578F	probably damaging	Het
Lrp2	A	T	2: 69,295,971 (GRCm39)	D3379E	probably damaging	Het
Lrrfip1	C	T	1: 91,021,369 (GRCm39)		probably benign	Het
Mblac1	A	G	5: 138,192,727 (GRCm39)	Y23C	probably damaging	Het
Mfsd12	G	A	10: 81,198,648 (GRCm39)	V380I	possibly damaging	Het
Mroh9	G	A	1: 162,890,056 (GRCm39)	T227M	probably damaging	Het
Mtor	C	T	4: 148,623,338 (GRCm39)	Q2063*	probably null	Het
Ncstn	A	G	1: 171,897,528 (GRCm39)		probably benign	Het
Nek9	T	C	12: 85,348,673 (GRCm39)	T954A	probably benign	Het
Nlrc5	A	T	8: 95,201,284 (GRCm39)	Y126F	possibly damaging	Het
Nr1d1	A	G	11: 98,661,304 (GRCm39)	S321P	probably benign	Het
Or13c3	C	A	4: 52,856,196 (GRCm39)	A106S	probably damaging	Het
Pkn2	T	C	3: 142,516,588 (GRCm39)	I513V	probably damaging	Het
Pls1	T	C	9: 95,669,116 (GRCm39)	E35G	probably damaging	Het
Polr3a	A	G	14: 24,519,323 (GRCm39)		probably benign	Het
Ptgfr	A	G	3: 151,540,728 (GRCm39)	V260A	possibly damaging	Het
Rabgap1l	A	G	1: 160,454,939 (GRCm39)		probably benign	Het
Raph1	T	C	1: 60,539,764 (GRCm39)	K423E	probably benign	Het
Rbm46	A	T	3: 82,771,537 (GRCm39)	S359R	probably damaging	Het
Rhobtb3	A	T	13: 76,050,364 (GRCm39)	*100R	probably null	Het
Ryr2	T	C	13: 11,610,670 (GRCm39)	E4052G	probably damaging	Het
Sart3	G	T	5: 113,893,458 (GRCm39)	D346E	possibly damaging	Het
Sgsm1	A	G	5: 113,416,616 (GRCm39)	F629S	probably damaging	Het
Siglec1	T	C	2: 130,915,317 (GRCm39)	T1425A	possibly damaging	Het
Slc12a2	A	T	18: 58,048,594 (GRCm39)		probably benign	Het
Slc38a10	G	T	11: 120,001,138 (GRCm39)	P561T	probably benign	Het
Slc45a4	A	G	15: 73,477,285 (GRCm39)		probably benign	Het
Snx25	A	T	8: 46,558,146 (GRCm39)		probably benign	Het
Son	T	A	16: 91,455,865 (GRCm39)	H1537Q	possibly damaging	Het
Synpo2l	A	T	14: 20,716,340 (GRCm39)		probably benign	Het
Tarbp1	A	G	8: 127,174,269 (GRCm39)	Y846H	probably damaging	Het
Tgfb1	T	A	7: 25,393,779 (GRCm39)		probably benign	Het
Tigd2	C	A	6: 59,188,369 (GRCm39)	T412K	possibly damaging	Het
Umodl1	A	T	17: 31,187,451 (GRCm39)	N172Y	probably damaging	Het
Urah	C	T	7: 140,416,665 (GRCm39)	T46I	probably damaging	Het
Usp8	C	T	2: 126,579,809 (GRCm39)	P353L	probably damaging	Het
Vamp2	A	G	11: 68,980,585 (GRCm39)	D51G	possibly damaging	Het
Vps13a	A	T	19: 16,653,504 (GRCm39)	V1959E	probably damaging	Het
Wdr76	C	T	2: 121,365,900 (GRCm39)		probably benign	Het
Zbtb38	C	T	9: 96,569,729 (GRCm39)	V452M	probably damaging	Het
Zbtb41	A	G	1: 139,369,572 (GRCm39)	K650E	probably damaging	Het
Zfp532	A	G	18: 65,777,404 (GRCm39)	Y887C	probably damaging	Het

Other mutations in Rbm27

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01064:Rbm27	APN	18	42,452,879 (GRCm39)	missense	possibly damaging	0.82
IGL01630:Rbm27	APN	18	42,434,905 (GRCm39)	missense	probably damaging	1.00
IGL02045:Rbm27	APN	18	42,452,978 (GRCm39)	missense	possibly damaging	0.52
IGL03031:Rbm27	APN	18	42,466,464 (GRCm39)	critical splice donor site	probably null
IGL03085:Rbm27	APN	18	42,460,589 (GRCm39)	splice site	probably benign
IGL03249:Rbm27	APN	18	42,434,812 (GRCm39)	missense	probably damaging	0.99
IGL03372:Rbm27	APN	18	42,438,781 (GRCm39)	missense	probably damaging	0.99
messenger	UTSW	18	42,466,468 (GRCm39)	splice site	probably null
R0048:Rbm27	UTSW	18	42,431,529 (GRCm39)	missense	probably benign	0.02
R0111:Rbm27	UTSW	18	42,438,737 (GRCm39)	splice site	probably benign
R0122:Rbm27	UTSW	18	42,447,033 (GRCm39)	intron	probably benign
R0707:Rbm27	UTSW	18	42,459,091 (GRCm39)	critical splice donor site	probably null
R1253:Rbm27	UTSW	18	42,434,839 (GRCm39)	missense	probably damaging	0.99
R1268:Rbm27	UTSW	18	42,466,367 (GRCm39)	missense	probably damaging	1.00
R1317:Rbm27	UTSW	18	42,457,116 (GRCm39)	splice site	probably benign
R1403:Rbm27	UTSW	18	42,450,746 (GRCm39)	missense	probably damaging	0.97
R1403:Rbm27	UTSW	18	42,450,746 (GRCm39)	missense	probably damaging	0.97
R2187:Rbm27	UTSW	18	42,459,022 (GRCm39)	missense	probably damaging	1.00
R2358:Rbm27	UTSW	18	42,425,177 (GRCm39)	splice site	probably benign
R3123:Rbm27	UTSW	18	42,460,230 (GRCm39)	missense	probably damaging	1.00
R3711:Rbm27	UTSW	18	42,425,177 (GRCm39)	splice site	probably benign
R3712:Rbm27	UTSW	18	42,425,177 (GRCm39)	splice site	probably benign
R4616:Rbm27	UTSW	18	42,434,840 (GRCm39)	missense	probably damaging	0.96
R4839:Rbm27	UTSW	18	42,460,510 (GRCm39)	missense	probably damaging	1.00
R5151:Rbm27	UTSW	18	42,471,509 (GRCm39)	missense	probably damaging	1.00
R5308:Rbm27	UTSW	18	42,460,275 (GRCm39)	missense	probably damaging	1.00
R5696:Rbm27	UTSW	18	42,450,731 (GRCm39)	missense	probably damaging	1.00
R5868:Rbm27	UTSW	18	42,433,450 (GRCm39)	missense	possibly damaging	0.86
R6058:Rbm27	UTSW	18	42,460,570 (GRCm39)	missense	probably damaging	1.00
R6477:Rbm27	UTSW	18	42,466,383 (GRCm39)	missense	probably damaging	1.00
R6499:Rbm27	UTSW	18	42,470,076 (GRCm39)	missense	probably damaging	1.00
R6658:Rbm27	UTSW	18	42,457,178 (GRCm39)	missense	probably damaging	1.00
R6700:Rbm27	UTSW	18	42,459,004 (GRCm39)	missense	probably damaging	1.00
R6784:Rbm27	UTSW	18	42,434,929 (GRCm39)	missense	probably benign	0.00
R6812:Rbm27	UTSW	18	42,466,468 (GRCm39)	splice site	probably null
R7162:Rbm27	UTSW	18	42,447,092 (GRCm39)	missense	unknown
R7606:Rbm27	UTSW	18	42,460,578 (GRCm39)	missense	probably damaging	1.00
R7904:Rbm27	UTSW	18	42,465,921 (GRCm39)	missense	probably damaging	1.00
R7969:Rbm27	UTSW	18	42,408,545 (GRCm39)	start gained	probably benign
R8177:Rbm27	UTSW	18	42,457,175 (GRCm39)	missense	probably damaging	1.00
R9052:Rbm27	UTSW	18	42,465,893 (GRCm39)	missense	probably damaging	1.00
R9091:Rbm27	UTSW	18	42,438,829 (GRCm39)	missense	probably benign	0.06
R9206:Rbm27	UTSW	18	42,447,163 (GRCm39)	nonsense	probably null
R9269:Rbm27	UTSW	18	42,460,572 (GRCm39)	missense	probably benign	0.02
R9270:Rbm27	UTSW	18	42,438,829 (GRCm39)	missense	probably benign	0.06
R9680:Rbm27	UTSW	18	42,455,186 (GRCm39)	missense	probably damaging	0.98
X0065:Rbm27	UTSW	18	42,432,385 (GRCm39)	missense	possibly damaging	0.70
Z1176:Rbm27	UTSW	18	42,466,299 (GRCm39)	frame shift	probably null
Z1177:Rbm27	UTSW	18	42,471,517 (GRCm39)	nonsense	probably null

Posted On

2013-01-08