Mutagenetix > Incidental Mutation

Incidental Mutation 'R0558:Rsph10b'

45720

Institutional Source

Beutler Lab

Gene Symbol

Rsph10b

Ensembl Gene

ENSMUSG00000075569

Gene Name

radial spoke head 10 homolog B (Chlamydomonas)

Synonyms

4930526H21Rik, Rsph10b2

MMRRC Submission

038750-MU

Accession Numbers

Essential gene?

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

Stock #

R0558 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

143869853-143922537 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 143886156 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Leucine at position 285 (I285L)

Ref Sequence

ENSEMBL: ENSMUSP00000132687 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000166847] [ENSMUST00000169758]

AlphaFold

E9PYQ0

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000031618

Predicted Effect

probably benign
Transcript: ENSMUST00000166847
AA Change: I285L

PolyPhen 2 Score 0.017 (Sensitivity: 0.95; Specificity: 0.80)

SMART Domains

Protein: ENSMUSP00000132687
Gene: ENSMUSG00000075569
AA Change: I285L

Domain	Start	End	E-Value	Type
low complexity region	3	14	N/A	INTRINSIC
low complexity region	39	50	N/A	INTRINSIC
low complexity region	63	75	N/A	INTRINSIC
MORN	107	128	5.9e-7	SMART
MORN	130	151	9.35e-1	SMART
MORN	153	174	1.23e0	SMART
MORN	177	198	1.84e0	SMART
MORN	202	223	3.21e1	SMART
MORN	225	246	1.67e-6	SMART
MORN	249	270	1.85e1	SMART
MORN	282	303	2.71e-6	SMART
MORN	305	326	3.53e-5	SMART
low complexity region	409	420	N/A	INTRINSIC
low complexity region	629	649	N/A	INTRINSIC
coiled coil region	787	841	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000167009

Predicted Effect

probably benign
Transcript: ENSMUST00000169758

SMART Domains

Protein: ENSMUSP00000127770
Gene: ENSMUSG00000075569

Domain	Start	End	E-Value	Type
low complexity region	3	14	N/A	INTRINSIC
low complexity region	39	50	N/A	INTRINSIC
low complexity region	63	75	N/A	INTRINSIC
Blast:MORN	84	105	7e-6	BLAST
MORN	107	128	5.9e-7	SMART
MORN	130	151	9.35e-1	SMART
MORN	153	174	1.23e0	SMART
Pfam:MORN	179	191	2.3e-2	PFAM

Meta Mutation Damage Score

0.1605

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.7%
20x: 93.8%

Validation Efficiency

100% (80/80)

Allele List at MGI

Other mutations in this stock

Total: 78 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc2	G	A	19: 43,789,163 (GRCm39)	G273R	probably benign	Het
Adamts10	T	C	17: 33,769,583 (GRCm39)	V935A	probably benign	Het
Anapc15-ps	T	C	10: 95,508,983 (GRCm39)	D90G	probably damaging	Het
Atic	T	A	1: 71,602,947 (GRCm39)	V107E	probably benign	Het
Atp4b	T	C	8: 13,443,523 (GRCm39)	T52A	possibly damaging	Het
Cacna1h	C	T	17: 25,600,524 (GRCm39)	A1606T	probably damaging	Het
Cacng6	T	A	7: 3,483,324 (GRCm39)	Y217*	probably null	Het
Cc2d2a	T	G	5: 43,881,729 (GRCm39)		probably benign	Het
Cd226	T	A	18: 89,225,338 (GRCm39)	H78Q	probably benign	Het
Cers3	A	G	7: 66,433,166 (GRCm39)	D161G	probably damaging	Het
Ces1f	T	C	8: 94,002,017 (GRCm39)	H37R	probably benign	Het
Cfhr4	A	G	1: 139,667,230 (GRCm39)	V376A	probably damaging	Het
Chek1	T	A	9: 36,623,411 (GRCm39)	N421I	possibly damaging	Het
Cibar1	T	C	4: 12,164,095 (GRCm39)	D248G	probably damaging	Het
Cma2	T	C	14: 56,210,249 (GRCm39)	Y45H	probably damaging	Het
Cmas	C	A	6: 142,720,970 (GRCm39)	Y401*	probably null	Het
Cyp2j8	A	T	4: 96,332,871 (GRCm39)	S492T	probably benign	Het
Dnah12	T	C	14: 26,430,465 (GRCm39)	S358P	probably benign	Het
Dnajc13	T	C	9: 104,079,151 (GRCm39)		probably null	Het
Ep400	A	C	5: 110,832,933 (GRCm39)		probably benign	Het
Fam209	T	A	2: 172,314,758 (GRCm39)	N82K	probably benign	Het
G3bp2	A	T	5: 92,221,056 (GRCm39)	Y20N	probably damaging	Het
Gli2	T	C	1: 118,765,379 (GRCm39)	D924G	probably benign	Het
Gm10787	T	C	10: 76,857,850 (GRCm39)		noncoding transcript	Het
Gm11568	A	G	11: 99,748,872 (GRCm39)	R26G	unknown	Het
Hivep3	T	G	4: 119,953,763 (GRCm39)	L693R	probably damaging	Het
Hook1	A	G	4: 95,881,449 (GRCm39)		probably benign	Het
Ibtk	A	C	9: 85,619,591 (GRCm39)	D116E	probably damaging	Het
Insrr	C	T	3: 87,718,288 (GRCm39)	T927I	possibly damaging	Het
Irx1	T	G	13: 72,107,747 (GRCm39)	S312R	probably benign	Het
Itga11	T	C	9: 62,659,570 (GRCm39)	Y441H	probably benign	Het
Itsn1	A	G	16: 91,696,511 (GRCm39)	D38G	possibly damaging	Het
Kat6b	G	T	14: 21,719,489 (GRCm39)	E1280D	probably benign	Het
Kcnk10	T	A	12: 98,402,560 (GRCm39)	Y293F	possibly damaging	Het
Krt74	T	A	15: 101,669,398 (GRCm39)		noncoding transcript	Het
Lars1	T	G	18: 42,347,902 (GRCm39)	I974L	probably benign	Het
Limch1	A	G	5: 67,126,498 (GRCm39)	D42G	probably damaging	Het
Mau2	G	C	8: 70,495,082 (GRCm39)	T85R	probably damaging	Het
Mkrn3	A	G	7: 62,068,612 (GRCm39)	I393T	probably benign	Het
Mpl	A	C	4: 118,301,217 (GRCm39)	S541R	probably damaging	Het
Nfrkb	T	C	9: 31,321,564 (GRCm39)	S754P	possibly damaging	Het
Or4c125	A	G	2: 89,170,580 (GRCm39)	L22P	probably benign	Het
Or5bw2	T	C	7: 6,573,652 (GRCm39)	Y221H	possibly damaging	Het
Or5d41	A	G	2: 88,054,818 (GRCm39)	V186A	possibly damaging	Het
Or8g18	T	A	9: 39,149,496 (GRCm39)	T75S	probably damaging	Het
P2rx7	A	T	5: 122,811,861 (GRCm39)	I391F	possibly damaging	Het
Pbrm1	T	A	14: 30,807,016 (GRCm39)		probably null	Het
Pcdh8	T	C	14: 80,007,516 (GRCm39)	D349G	probably damaging	Het
Pias1	A	G	9: 62,789,291 (GRCm39)	S639P	possibly damaging	Het
Pkhd1l1	A	T	15: 44,347,820 (GRCm39)	I232F	probably damaging	Het
Plxnc1	C	T	10: 94,673,797 (GRCm39)	R995Q	probably damaging	Het
Pnliprp2	T	A	19: 58,762,519 (GRCm39)	S375T	probably benign	Het
Prkar1b	C	T	5: 139,005,847 (GRCm39)	V313M	probably benign	Het
Prr35	T	C	17: 26,166,523 (GRCm39)	N338S	probably benign	Het
Ptpn13	T	C	5: 103,677,583 (GRCm39)	S734P	probably damaging	Het
Rdh1	T	C	10: 127,595,810 (GRCm39)	W2R	possibly damaging	Het
Rubcnl	T	C	14: 75,284,987 (GRCm39)	F502S	probably damaging	Het
Ryr2	T	A	13: 11,653,329 (GRCm39)	I3693F	probably damaging	Het
Ryr2	T	C	13: 11,814,747 (GRCm39)	Y675C	probably damaging	Het
Scaper	T	C	9: 55,593,207 (GRCm39)	T477A	probably benign	Het
Scn2a	G	T	2: 65,542,269 (GRCm39)	V791L	probably benign	Het
Sdk1	A	T	5: 142,117,820 (GRCm39)	T1573S	probably damaging	Het
Sema3c	A	T	5: 17,919,413 (GRCm39)	H483L	probably benign	Het
Sema6c	T	C	3: 95,076,002 (GRCm39)	S219P	probably damaging	Het
Slc10a5	T	G	3: 10,400,177 (GRCm39)	E161A	probably damaging	Het
Slc22a23	C	T	13: 34,528,366 (GRCm39)	G139S	possibly damaging	Het
Slc34a3	C	T	2: 25,123,077 (GRCm39)		probably benign	Het
Slc38a9	A	T	13: 112,865,730 (GRCm39)		probably null	Het
Taok1	A	C	11: 77,450,670 (GRCm39)	S367R	possibly damaging	Het
Tlr6	G	A	5: 65,112,203 (GRCm39)	Q235*	probably null	Het
Top2a	A	G	11: 98,887,665 (GRCm39)	V1281A	probably benign	Het
Tpgs1	T	C	10: 79,511,616 (GRCm39)	Y253H	probably damaging	Het
Tubgcp3	T	C	8: 12,703,462 (GRCm39)	T288A	probably benign	Het
Ubr4	A	G	4: 139,154,213 (GRCm39)	E2140G	probably benign	Het
Uso1	A	G	5: 92,321,878 (GRCm39)	Q257R	probably benign	Het
Zfp106	A	G	2: 120,362,677 (GRCm39)	V48A	probably damaging	Het
Zfp174	T	A	16: 3,666,118 (GRCm39)	S128T	possibly damaging	Het
Zscan26	T	A	13: 21,629,225 (GRCm39)	D426V	probably benign	Het

Other mutations in Rsph10b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00419:Rsph10b	APN	5	143,873,905 (GRCm39)	makesense	probably null
K7894:Rsph10b	UTSW	5	143,881,338 (GRCm39)	missense	probably damaging	1.00
R0136:Rsph10b	UTSW	5	143,896,639 (GRCm39)	missense	probably benign	0.05
R0149:Rsph10b	UTSW	5	143,875,727 (GRCm39)	unclassified	probably benign
R0326:Rsph10b	UTSW	5	143,903,946 (GRCm39)	missense	probably damaging	1.00
R1185:Rsph10b	UTSW	5	143,903,280 (GRCm39)	splice site	probably benign
R1185:Rsph10b	UTSW	5	143,903,280 (GRCm39)	splice site	probably benign
R1712:Rsph10b	UTSW	5	143,873,967 (GRCm39)	missense	probably damaging	0.96
R1832:Rsph10b	UTSW	5	143,903,997 (GRCm39)	missense	possibly damaging	0.79
R1909:Rsph10b	UTSW	5	143,922,309 (GRCm39)	missense	probably benign	0.09
R2044:Rsph10b	UTSW	5	143,904,068 (GRCm39)	splice site	probably null
R2155:Rsph10b	UTSW	5	143,898,074 (GRCm39)	missense	probably benign	0.05
R2842:Rsph10b	UTSW	5	143,916,710 (GRCm39)	missense	possibly damaging	0.81
R3805:Rsph10b	UTSW	5	143,895,206 (GRCm39)	critical splice donor site	probably null
R4031:Rsph10b	UTSW	5	143,922,486 (GRCm39)	splice site	probably null
R4792:Rsph10b	UTSW	5	143,874,135 (GRCm39)	missense	probably damaging	1.00
R4866:Rsph10b	UTSW	5	143,885,347 (GRCm39)	missense	probably benign	0.28
R6090:Rsph10b	UTSW	5	143,913,946 (GRCm39)	missense	probably benign	0.00
R6252:Rsph10b	UTSW	5	143,873,939 (GRCm39)	missense	possibly damaging	0.70
R6255:Rsph10b	UTSW	5	143,896,564 (GRCm39)	missense	probably damaging	1.00
R6518:Rsph10b	UTSW	5	143,900,691 (GRCm39)	missense	probably damaging	1.00
R7085:Rsph10b	UTSW	5	143,886,102 (GRCm39)	missense	possibly damaging	0.82
R7206:Rsph10b	UTSW	5	143,898,010 (GRCm39)	missense	possibly damaging	0.86
R7337:Rsph10b	UTSW	5	143,898,033 (GRCm39)	missense	probably benign	0.11
R7353:Rsph10b	UTSW	5	143,904,038 (GRCm39)	missense	possibly damaging	0.73
R7567:Rsph10b	UTSW	5	143,886,244 (GRCm39)	missense	possibly damaging	0.78
R8022:Rsph10b	UTSW	5	143,904,050 (GRCm39)	missense	probably benign	0.00
R8109:Rsph10b	UTSW	5	143,922,348 (GRCm39)	missense	probably benign	0.00
R8275:Rsph10b	UTSW	5	143,903,323 (GRCm39)	missense	possibly damaging	0.50
R8679:Rsph10b	UTSW	5	143,887,112 (GRCm39)	missense	possibly damaging	0.80
R8947:Rsph10b	UTSW	5	143,913,952 (GRCm39)	missense	probably benign	0.01
R9020:Rsph10b	UTSW	5	143,922,283 (GRCm39)	missense	probably benign	0.05
R9189:Rsph10b	UTSW	5	143,896,504 (GRCm39)	missense	probably benign	0.05
R9319:Rsph10b	UTSW	5	143,903,337 (GRCm39)	missense	probably benign	0.00
Z1177:Rsph10b	UTSW	5	143,913,952 (GRCm39)	missense	probably benign	0.01

Predicted Primers

PCR Primer
(F):5'- CTACAATCCCTAAAGGGCTCACTGC -3'
(R):5'- TGGCATAGACATGCTGAAGTCACTG -3'

Sequencing Primer
(F):5'- CTAAAGGGCTCACTGCCAGAG -3'
(R):5'- TATGAACGATCAGGCTACACTG -3'

Posted On

2013-06-11