Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03350:Rbm11'

419670

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Rbm11

Ensembl Gene

ENSMUSG00000032940

Gene Name

RNA binding motif protein 11

Synonyms

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.073) question?

Stock #

IGL03350

Quality Score

Status

Chromosome

Chromosomal Location

75592844-75602829 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 75600808 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Proline to Serine at position 209 (P209S)

Ref Sequence

ENSEMBL: ENSMUSP00000109891 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000046378] [ENSMUST00000114249] [ENSMUST00000114253]

AlphaFold

Q80YT9

Predicted Effect

probably benign
Transcript: ENSMUST00000046378
AA Change: P209S

PolyPhen 2 Score 0.312 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000038956
Gene: ENSMUSG00000032940
AA Change: P209S

Domain	Start	End	E-Value	Type
RRM	11	83	3.25e-23	SMART
low complexity region	210	217	N/A	INTRINSIC
low complexity region	228	237	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000114249
AA Change: P209S

PolyPhen 2 Score 0.312 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000109887
Gene: ENSMUSG00000032940
AA Change: P209S

Domain	Start	End	E-Value	Type
RRM	11	83	3.25e-23	SMART
low complexity region	210	217	N/A	INTRINSIC
low complexity region	228	237	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000114253
AA Change: P209S

PolyPhen 2 Score 0.312 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000109891
Gene: ENSMUSG00000032940
AA Change: P209S

Domain	Start	End	E-Value	Type
RRM	11	83	3.25e-23	SMART
low complexity region	210	217	N/A	INTRINSIC
low complexity region	228	237	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 45 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4922502D21Rik	C	A	6: 129,331,023	V28L	probably benign	Het
Adam26a	A	T	8: 43,569,552	Y300*	probably null	Het
Adgre1	T	A	17: 57,401,908	V33E	probably benign	Het
AI987944	A	G	7: 41,393,237		probably benign	Het
Atp4a	T	C	7: 30,720,867	L813P	probably damaging	Het
Blmh	A	G	11: 76,971,948	N396D	probably damaging	Het
Brat1	T	C	5: 140,705,995	L9P	probably damaging	Het
Ccdc171	T	C	4: 83,681,378	I810T	possibly damaging	Het
Cyp2a22	T	C	7: 26,934,854	T292A	possibly damaging	Het
Ecm2	C	T	13: 49,520,944	T280I	probably benign	Het
Fa2h	C	T	8: 111,349,296	V232I	probably benign	Het
Fbxw24	T	C	9: 109,607,013	D317G	probably damaging	Het
Flt4	C	A	11: 49,634,793	S722*	probably null	Het
Fryl	T	C	5: 73,133,306	Q85R	probably damaging	Het
Gm3239	A	G	14: 4,667,115	R188G	possibly damaging	Het
Hspa13	A	T	16: 75,757,829	S456R	probably damaging	Het
Htr1b	T	C	9: 81,632,122	Y144C	probably damaging	Het
Hydin	A	G	8: 110,312,224	H198R	possibly damaging	Het
Krt78	A	T	15: 101,946,517	M953K	probably benign	Het
Lgr5	G	T	10: 115,471,988	T255K	probably damaging	Het
Lrp2	T	A	2: 69,438,453	D4162V	probably damaging	Het
Map3k2	A	G	18: 32,212,148	D342G	probably damaging	Het
Miip	A	G	4: 147,862,522	V258A	probably benign	Het
Muc6	T	C	7: 141,652,059	H52R	probably damaging	Het
Nfs1	T	C	2: 156,127,740	E329G	probably benign	Het
Npsr1	T	C	9: 24,098,309	V37A	probably benign	Het
Olfr1107	A	C	2: 87,071,560	D191E	probably damaging	Het
Olfr23	A	T	11: 73,940,838	L197F	probably damaging	Het
Olfr356	T	C	2: 36,937,583	Y155H	probably damaging	Het
Pex16	T	A	2: 92,377,497	M98K	probably damaging	Het
Pla2r1	C	T	2: 60,455,173	C699Y	probably damaging	Het
Plcd4	A	T	1: 74,549,301	D103V	probably damaging	Het
Pnpla1	A	G	17: 28,876,992	D129G	probably damaging	Het
Rad23a	T	C	8: 84,837,479	E265G	possibly damaging	Het
Ribc2	T	A	15: 85,135,502	W162R	probably damaging	Het
Rnf4	A	G	5: 34,346,860	E32G	possibly damaging	Het
Rpe65	A	T	3: 159,614,517	S269C	possibly damaging	Het
Slc7a14	T	A	3: 31,237,409	Y240F	probably benign	Het
Sorbs2	C	T	8: 45,805,807	P1047L	probably damaging	Het
Ttn	T	C	2: 76,749,822	I23576V	probably damaging	Het
Usp24	T	G	4: 106,371,079	Y780*	probably null	Het
Wee2	T	C	6: 40,449,731	S145P	probably damaging	Het
Zcchc7	A	G	4: 44,931,188	T126A	probably benign	Het
Zpld1	A	G	16: 55,241,329		probably benign	Het
Zufsp	G	A	10: 33,928,111	R456C	probably benign	Het

Other mutations in Rbm11

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01732:Rbm11	APN	16	75600622	missense	probably benign	0.01
IGL02245:Rbm11	APN	16	75593008	missense	possibly damaging	0.74
R0060:Rbm11	UTSW	16	75598779	missense	probably damaging	0.98
R0815:Rbm11	UTSW	16	75596637	missense	probably damaging	1.00
R1351:Rbm11	UTSW	16	75596643	missense	possibly damaging	0.91
R1562:Rbm11	UTSW	16	75596535	missense	probably damaging	1.00
R1793:Rbm11	UTSW	16	75600797	missense	probably damaging	1.00
R1891:Rbm11	UTSW	16	75600787	missense	possibly damaging	0.87
R1965:Rbm11	UTSW	16	75598768	splice site	probably null
R3757:Rbm11	UTSW	16	75596581	missense	probably damaging	1.00
R3928:Rbm11	UTSW	16	75593044	critical splice donor site	probably null
R4513:Rbm11	UTSW	16	75596587	missense	probably damaging	1.00
R5314:Rbm11	UTSW	16	75596586	missense	probably damaging	1.00
R5418:Rbm11	UTSW	16	75596535	missense	probably damaging	1.00
R5530:Rbm11	UTSW	16	75592973	missense	possibly damaging	0.66
R5891:Rbm11	UTSW	16	75598837	missense	possibly damaging	0.55
R6293:Rbm11	UTSW	16	75596767	splice site	probably null
R7853:Rbm11	UTSW	16	75593035	missense	probably damaging	1.00
R8167:Rbm11	UTSW	16	75598785	missense	probably benign	0.01
R8356:Rbm11	UTSW	16	75600806	missense	probably benign
R9571:Rbm11	UTSW	16	75600655	missense	possibly damaging	0.73

Posted On

2016-08-02