Mutagenetix > Incidental Mutation

Incidental Mutation 'R8248:Ryr1'

640372

Institutional Source

Beutler Lab

Gene Symbol

Ryr1

Ensembl Gene

ENSMUSG00000030592

Gene Name

ryanodine receptor 1, skeletal muscle

Synonyms

skrr, calcium release channel isoform 1, Ryr

MMRRC Submission

067675-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R8248 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

29003344-29125179 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 29069121 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tryptophan to Arginine at position 2808 (W2808R)

Ref Sequence

ENSEMBL: ENSMUSP00000137123 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000032813] [ENSMUST00000179893]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000032813
AA Change: W2808R

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000032813
Gene: ENSMUSG00000030592
AA Change: W2808R

Domain	Start	End	E-Value	Type
low complexity region	2	11	N/A	INTRINSIC
MIR	99	154	7.52e-4	SMART
MIR	161	206	1.11e-6	SMART
MIR	212	266	1.23e-8	SMART
MIR	272	362	1.05e-25	SMART
Pfam:RYDR_ITPR	441	645	1.2e-73	PFAM
SPRY	660	798	2.79e-27	SMART
Pfam:RyR	851	945	6.5e-33	PFAM
Pfam:RyR	965	1059	1.5e-30	PFAM
SPRY	1086	1209	8.62e-42	SMART
low complexity region	1318	1332	N/A	INTRINSIC
low complexity region	1340	1349	N/A	INTRINSIC
SPRY	1431	1571	3.05e-33	SMART
low complexity region	1787	1798	N/A	INTRINSIC
coiled coil region	1871	1932	N/A	INTRINSIC
low complexity region	1989	1998	N/A	INTRINSIC
low complexity region	2048	2057	N/A	INTRINSIC
low complexity region	2069	2092	N/A	INTRINSIC
Pfam:RYDR_ITPR	2158	2366	7e-66	PFAM
low complexity region	2390	2404	N/A	INTRINSIC
Pfam:RyR	2735	2829	9.7e-34	PFAM
Pfam:RyR	2855	2943	5.7e-32	PFAM
low complexity region	3130	3144	N/A	INTRINSIC
low complexity region	3290	3304	N/A	INTRINSIC
low complexity region	3375	3394	N/A	INTRINSIC
PDB:2BCX\|B	3613	3642	2e-13	PDB
low complexity region	3681	3691	N/A	INTRINSIC
low complexity region	3735	3760	N/A	INTRINSIC
Pfam:RIH_assoc	3872	4004	1.9e-41	PFAM
low complexity region	4010	4023	N/A	INTRINSIC
Pfam:EF-hand_8	4085	4136	9.8e-8	PFAM
transmembrane domain	4283	4305	N/A	INTRINSIC
transmembrane domain	4318	4336	N/A	INTRINSIC
transmembrane domain	4341	4363	N/A	INTRINSIC
Pfam:RR_TM4-6	4377	4666	2e-86	PFAM
Pfam:Ion_trans	4761	4932	3.4e-10	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000179893
AA Change: W2808R

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000137123
Gene: ENSMUSG00000030592
AA Change: W2808R

Domain	Start	End	E-Value	Type
low complexity region	2	11	N/A	INTRINSIC
MIR	99	154	7.52e-4	SMART
MIR	161	206	1.11e-6	SMART
MIR	212	266	1.23e-8	SMART
MIR	272	362	1.05e-25	SMART
Pfam:RYDR_ITPR	443	638	4.5e-63	PFAM
SPRY	660	798	2.79e-27	SMART
Pfam:RyR	852	942	1.3e-37	PFAM
Pfam:RyR	966	1056	1.6e-28	PFAM
SPRY	1086	1209	8.62e-42	SMART
low complexity region	1318	1332	N/A	INTRINSIC
low complexity region	1340	1349	N/A	INTRINSIC
SPRY	1431	1571	3.05e-33	SMART
low complexity region	1787	1798	N/A	INTRINSIC
coiled coil region	1871	1932	N/A	INTRINSIC
low complexity region	1989	1998	N/A	INTRINSIC
low complexity region	2048	2057	N/A	INTRINSIC
low complexity region	2069	2092	N/A	INTRINSIC
Pfam:RYDR_ITPR	2160	2366	2.2e-68	PFAM
low complexity region	2390	2404	N/A	INTRINSIC
Pfam:RyR	2736	2826	7.2e-31	PFAM
Pfam:RyR	2856	2940	5.6e-27	PFAM
low complexity region	3130	3144	N/A	INTRINSIC
low complexity region	3290	3304	N/A	INTRINSIC
low complexity region	3375	3394	N/A	INTRINSIC
PDB:2BCX\|B	3615	3644	2e-13	PDB
low complexity region	3683	3693	N/A	INTRINSIC
low complexity region	3737	3762	N/A	INTRINSIC
Pfam:RIH_assoc	3878	3996	6.2e-35	PFAM
low complexity region	4012	4025	N/A	INTRINSIC
Pfam:EF-hand_8	4087	4137	1.8e-8	PFAM
transmembrane domain	4285	4307	N/A	INTRINSIC
transmembrane domain	4320	4338	N/A	INTRINSIC
transmembrane domain	4343	4365	N/A	INTRINSIC
Pfam:RR_TM4-6	4379	4668	8.4e-76	PFAM
Pfam:Ion_trans	4763	4946	2.8e-15	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

100% (60/60)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a ryanodine receptor found in skeletal muscle. The encoded protein functions as a calcium release channel in the sarcoplasmic reticulum but also serves to connect the sarcoplasmic reticulum and transverse tubule. Mutations in this gene are associated with malignant hyperthermia susceptibility, central core disease, and minicore myopathy with external ophthalmoplegia. Alternatively spliced transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for a targeted null mutation and a similar ENU-induced mutation are born with a rounded body shape, edema, thin and misshapened ribs, and abnormal muscle fibers. Mutants die perinatally. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A930003A15Rik	T	C	16: 19,883,806 (GRCm38)	D24G	noncoding transcript	Het
Adam32	A	G	8: 24,901,470 (GRCm38)	S343P	possibly damaging	Het
Agbl2	G	A	2: 90,797,564 (GRCm38)	G238R	probably damaging	Het
Ahi1	T	A	10: 20,972,092 (GRCm38)	D466E	probably benign	Het
Ahnak	T	A	19: 9,001,946 (GRCm38)	V198E	probably damaging	Het
Ank2	T	A	3: 126,937,785 (GRCm38)	H658L	possibly damaging	Het
Atp8b5	T	A	4: 43,366,072 (GRCm38)	I781N	probably damaging	Het
Bloc1s6	A	T	2: 122,742,645 (GRCm38)	R47*	probably null	Het
Clk2	G	A	3: 89,173,504 (GRCm38)	V266M	probably damaging	Het
Cul9	A	C	17: 46,530,014 (GRCm38)	Y777D	probably damaging	Het
Dcp1a	A	G	14: 30,522,926 (GRCm38)	T570A	possibly damaging	Het
Dcp1a	C	T	14: 30,479,598 (GRCm38)		probably benign	Het
Dnajb2	T	G	1: 75,243,582 (GRCm38)	D248E		Het
Dpy19l1	T	C	9: 24,502,895 (GRCm38)	H79R	probably benign	Het
Elmo1	T	C	13: 20,600,201 (GRCm38)	S643P	probably damaging	Het
Evi5	A	G	5: 107,818,887 (GRCm38)		probably null	Het
Fam76b	T	C	9: 13,831,102 (GRCm38)	C110R	probably damaging	Het
Galnt7	T	A	8: 57,538,188 (GRCm38)	K429N	probably benign	Het
Gm10142	T	A	10: 77,716,116 (GRCm38)	C104S	probably damaging	Het
Gm7298	A	C	6: 121,787,443 (GRCm38)	H1427P	probably benign	Het
Golga7b	A	T	19: 42,266,871 (GRCm38)	I87F	probably damaging	Het
Gpr165	C	A	X: 96,714,017 (GRCm38)	D7E	probably benign	Het
Gpr25	C	A	1: 136,260,677 (GRCm38)	R66L	probably benign	Het
H2-Q2	A	G	17: 35,344,865 (GRCm38)	N241D	probably benign	Het
Il1a	T	C	2: 129,302,961 (GRCm38)	D179G	probably benign	Het
Itch	T	C	2: 155,206,383 (GRCm38)		probably null	Het
Itsn2	T	C	12: 4,662,052 (GRCm38)	V913A	probably benign	Het
Kdm1b	T	A	13: 47,071,878 (GRCm38)		probably benign	Het
Lama4	T	C	10: 39,061,379 (GRCm38)	I655T	possibly damaging	Het
Lats1	T	A	10: 7,705,903 (GRCm38)	S817R	probably damaging	Het
Lrrc8c	A	T	5: 105,607,867 (GRCm38)	M503L	probably benign	Het
Mast4	T	C	13: 102,738,721 (GRCm38)	T1380A	probably damaging	Het
Mfap1a	G	T	2: 121,506,495 (GRCm38)	T16K	possibly damaging	Het
Mroh2b	C	T	15: 4,931,104 (GRCm38)	T773I	probably benign	Het
Myl10	G	C	5: 136,697,971 (GRCm38)	V70L	probably benign	Het
Nudt7	A	G	8: 114,151,997 (GRCm38)	Y255C	probably benign	Het
Pfas	T	C	11: 69,000,263 (GRCm38)	T310A	probably damaging	Het
Pkhd1l1	T	G	15: 44,543,546 (GRCm38)	I2393R	probably damaging	Het
Pmm1	A	C	15: 81,960,731 (GRCm38)	L24R	possibly damaging	Het
Pram1	T	C	17: 33,641,164 (GRCm38)	V235A	probably benign	Het
Prg4	T	C	1: 150,455,126 (GRCm38)	T599A	unknown	Het
Prpf40b	A	G	15: 99,316,285 (GRCm38)	K812E	unknown	Het
Qars1	G	A	9: 108,509,452 (GRCm38)	A155T	probably benign	Het
Rftn1	G	T	17: 50,047,380 (GRCm38)	A318D	probably damaging	Het
Rgs6	A	G	12: 83,137,704 (GRCm38)		probably benign	Het
Rom1	T	A	19: 8,928,681 (GRCm38)	R165W	probably damaging	Het
Rps6kb2	T	A	19: 4,156,988 (GRCm38)		probably benign	Het
Sh3gl1	A	G	17: 56,019,038 (GRCm38)		probably null	Het
Slc22a30	A	T	19: 8,370,199 (GRCm38)	M279K	probably benign	Het
Snx11	A	G	11: 96,769,933 (GRCm38)	S184P	unknown	Het
Srgap1	A	G	10: 121,804,817 (GRCm38)	C692R	probably damaging	Het
Srgap3	T	C	6: 112,723,143 (GRCm38)	N982S	probably damaging	Het
Stac	T	A	9: 111,593,745 (GRCm38)	D270V	probably benign	Het
Syn3	T	A	10: 86,135,021 (GRCm38)	I246F	probably benign	Het
Tnr	T	C	1: 159,892,093 (GRCm38)	V980A	probably damaging	Het
Usp17le	G	T	7: 104,769,794 (GRCm38)	A47E	possibly damaging	Het
Vmn2r118	T	C	17: 55,610,936 (GRCm38)	N192S	probably benign	Het
Zmym4	C	A	4: 126,905,369 (GRCm38)	V725L	possibly damaging	Het

Other mutations in Ryr1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00321:Ryr1	APN	7	29,102,810 (GRCm38)	missense	probably damaging	1.00
IGL00335:Ryr1	APN	7	29,124,960 (GRCm38)	splice site	probably null
IGL00427:Ryr1	APN	7	29,104,737 (GRCm38)	splice site	probably benign
IGL00559:Ryr1	APN	7	29,012,242 (GRCm38)	splice site	probably benign
IGL00803:Ryr1	APN	7	29,069,645 (GRCm38)	missense	possibly damaging	0.95
IGL00886:Ryr1	APN	7	29,024,229 (GRCm38)	missense	probably damaging	1.00
IGL00948:Ryr1	APN	7	29,020,195 (GRCm38)	missense	possibly damaging	0.78
IGL01017:Ryr1	APN	7	29,082,543 (GRCm38)	missense	probably damaging	0.99
IGL01116:Ryr1	APN	7	29,100,202 (GRCm38)	splice site	probably benign
IGL01385:Ryr1	APN	7	29,056,985 (GRCm38)	missense	probably damaging	1.00
IGL01482:Ryr1	APN	7	29,052,337 (GRCm38)	missense	probably damaging	1.00
IGL01529:Ryr1	APN	7	29,075,227 (GRCm38)	missense	probably damaging	1.00
IGL01543:Ryr1	APN	7	29,091,076 (GRCm38)	missense	probably damaging	1.00
IGL01653:Ryr1	APN	7	29,078,597 (GRCm38)	missense	probably damaging	0.99
IGL01701:Ryr1	APN	7	29,059,810 (GRCm38)	missense	probably damaging	0.98
IGL02051:Ryr1	APN	7	29,071,658 (GRCm38)	missense	probably benign	0.16
IGL02152:Ryr1	APN	7	29,052,015 (GRCm38)	missense	possibly damaging	0.95
IGL02271:Ryr1	APN	7	29,094,047 (GRCm38)	missense	probably benign	0.07
IGL02321:Ryr1	APN	7	29,078,696 (GRCm38)	missense	probably damaging	1.00
IGL02448:Ryr1	APN	7	29,105,066 (GRCm38)	splice site	probably benign
IGL02472:Ryr1	APN	7	29,040,844 (GRCm38)	missense	probably damaging	1.00
IGL02544:Ryr1	APN	7	29,115,599 (GRCm38)	missense	probably benign	0.24
IGL02666:Ryr1	APN	7	29,019,763 (GRCm38)	missense	unknown
IGL02672:Ryr1	APN	7	29,004,519 (GRCm38)	unclassified	probably benign
IGL02677:Ryr1	APN	7	29,110,608 (GRCm38)	missense	probably benign	0.18
IGL02686:Ryr1	APN	7	29,069,550 (GRCm38)	splice site	probably benign
IGL02751:Ryr1	APN	7	29,078,774 (GRCm38)	missense	probably damaging	1.00
IGL02899:Ryr1	APN	7	29,048,795 (GRCm38)	missense	possibly damaging	0.53
IGL02926:Ryr1	APN	7	29,061,540 (GRCm38)	missense	probably damaging	1.00
IGL02950:Ryr1	APN	7	29,097,459 (GRCm38)	missense	probably damaging	1.00
IGL02960:Ryr1	APN	7	29,060,053 (GRCm38)	missense	probably damaging	1.00
IGL02968:Ryr1	APN	7	29,043,893 (GRCm38)	missense	probably damaging	1.00
IGL03070:Ryr1	APN	7	29,070,659 (GRCm38)	missense	probably damaging	1.00
IGL03091:Ryr1	APN	7	29,083,486 (GRCm38)	missense	possibly damaging	0.85
IGL03100:Ryr1	APN	7	29,104,593 (GRCm38)	missense	probably damaging	1.00
IGL03107:Ryr1	APN	7	29,075,199 (GRCm38)	missense	probably damaging	1.00
IGL03117:Ryr1	APN	7	29,102,964 (GRCm38)	missense	probably damaging	1.00
IGL03118:Ryr1	APN	7	29,015,786 (GRCm38)	missense	unknown
IGL03146:Ryr1	APN	7	29,094,032 (GRCm38)	missense	probably benign	0.09
IGL03165:Ryr1	APN	7	29,105,040 (GRCm38)	missense	probably benign	0.22
IGL03220:Ryr1	APN	7	29,059,855 (GRCm38)	missense	probably damaging	1.00
R0017:Ryr1	UTSW	7	29,047,542 (GRCm38)	missense	probably damaging	1.00
R0066:Ryr1	UTSW	7	29,005,567 (GRCm38)	unclassified	probably benign
R0066:Ryr1	UTSW	7	29,005,567 (GRCm38)	unclassified	probably benign
R0069:Ryr1	UTSW	7	29,110,505 (GRCm38)	splice site	probably benign
R0148:Ryr1	UTSW	7	29,052,035 (GRCm38)	missense	probably damaging	0.99
R0266:Ryr1	UTSW	7	29,040,679 (GRCm38)	missense	probably damaging	1.00
R0346:Ryr1	UTSW	7	29,067,588 (GRCm38)	splice site	probably benign
R0387:Ryr1	UTSW	7	29,083,367 (GRCm38)	splice site	probably benign
R0454:Ryr1	UTSW	7	29,036,075 (GRCm38)	missense	probably damaging	0.99
R0494:Ryr1	UTSW	7	29,003,793 (GRCm38)	splice site	probably benign
R0533:Ryr1	UTSW	7	29,078,780 (GRCm38)	missense	probably damaging	1.00
R0585:Ryr1	UTSW	7	29,036,076 (GRCm38)	missense	probably damaging	1.00
R0591:Ryr1	UTSW	7	29,104,795 (GRCm38)	missense	possibly damaging	0.68
R0624:Ryr1	UTSW	7	29,074,609 (GRCm38)	missense	probably damaging	1.00
R0662:Ryr1	UTSW	7	29,100,189 (GRCm38)	missense	probably damaging	1.00
R0849:Ryr1	UTSW	7	29,040,679 (GRCm38)	missense	probably damaging	1.00
R0961:Ryr1	UTSW	7	29,009,697 (GRCm38)	missense	unknown
R1052:Ryr1	UTSW	7	29,096,258 (GRCm38)	missense	probably damaging	0.96
R1218:Ryr1	UTSW	7	29,086,109 (GRCm38)	missense	possibly damaging	0.79
R1340:Ryr1	UTSW	7	29,116,012 (GRCm38)	missense	probably damaging	0.99
R1513:Ryr1	UTSW	7	29,070,621 (GRCm38)	missense	probably damaging	1.00
R1543:Ryr1	UTSW	7	29,083,537 (GRCm38)	missense	possibly damaging	0.67
R1566:Ryr1	UTSW	7	29,092,175 (GRCm38)	missense	possibly damaging	0.95
R1572:Ryr1	UTSW	7	29,062,191 (GRCm38)	missense	probably damaging	1.00
R1623:Ryr1	UTSW	7	29,095,490 (GRCm38)	missense	probably damaging	1.00
R1632:Ryr1	UTSW	7	29,094,261 (GRCm38)	missense	probably benign	0.03
R1661:Ryr1	UTSW	7	29,101,738 (GRCm38)	missense	probably damaging	0.98
R1665:Ryr1	UTSW	7	29,036,078 (GRCm38)	missense	probably damaging	1.00
R1678:Ryr1	UTSW	7	29,116,154 (GRCm38)	missense	probably damaging	0.99
R1705:Ryr1	UTSW	7	29,078,564 (GRCm38)	missense	probably damaging	1.00
R1712:Ryr1	UTSW	7	29,047,503 (GRCm38)	missense	probably benign	0.25
R1720:Ryr1	UTSW	7	29,101,870 (GRCm38)	missense	probably damaging	0.99
R1799:Ryr1	UTSW	7	29,067,621 (GRCm38)	missense	probably damaging	1.00
R1847:Ryr1	UTSW	7	29,079,811 (GRCm38)	missense	probably benign	0.43
R1860:Ryr1	UTSW	7	29,009,552 (GRCm38)	missense	unknown
R1861:Ryr1	UTSW	7	29,009,552 (GRCm38)	missense	unknown
R1921:Ryr1	UTSW	7	29,054,944 (GRCm38)	missense	probably damaging	1.00
R1983:Ryr1	UTSW	7	29,059,472 (GRCm38)	missense	possibly damaging	0.74
R2043:Ryr1	UTSW	7	29,059,631 (GRCm38)	missense	probably damaging	0.99
R2089:Ryr1	UTSW	7	29,086,049 (GRCm38)	missense	probably damaging	1.00
R2091:Ryr1	UTSW	7	29,086,049 (GRCm38)	missense	probably damaging	1.00
R2091:Ryr1	UTSW	7	29,086,049 (GRCm38)	missense	probably damaging	1.00
R2105:Ryr1	UTSW	7	29,090,150 (GRCm38)	missense	probably damaging	0.99
R2175:Ryr1	UTSW	7	29,068,442 (GRCm38)	missense	probably damaging	1.00
R2259:Ryr1	UTSW	7	29,019,741 (GRCm38)	missense	unknown
R2291:Ryr1	UTSW	7	29,098,777 (GRCm38)	missense	probably damaging	1.00
R2351:Ryr1	UTSW	7	29,075,293 (GRCm38)	missense	probably benign	0.18
R2512:Ryr1	UTSW	7	29,103,542 (GRCm38)	missense	possibly damaging	0.64
R2571:Ryr1	UTSW	7	29,036,126 (GRCm38)	missense	possibly damaging	0.94
R2571:Ryr1	UTSW	7	29,009,562 (GRCm38)	missense	unknown
R2885:Ryr1	UTSW	7	29,074,798 (GRCm38)	missense	probably damaging	0.99
R2886:Ryr1	UTSW	7	29,074,798 (GRCm38)	missense	probably damaging	0.99
R2889:Ryr1	UTSW	7	29,078,741 (GRCm38)	missense	possibly damaging	0.76
R3051:Ryr1	UTSW	7	29,053,090 (GRCm38)	missense	probably damaging	1.00
R3052:Ryr1	UTSW	7	29,053,090 (GRCm38)	missense	probably damaging	1.00
R3053:Ryr1	UTSW	7	29,053,090 (GRCm38)	missense	probably damaging	1.00
R3082:Ryr1	UTSW	7	29,045,646 (GRCm38)	missense	probably damaging	1.00
R3103:Ryr1	UTSW	7	29,074,948 (GRCm38)	missense	probably damaging	1.00
R3237:Ryr1	UTSW	7	29,069,650 (GRCm38)	critical splice acceptor site	probably null
R3551:Ryr1	UTSW	7	29,056,997 (GRCm38)	missense	probably damaging	1.00
R3552:Ryr1	UTSW	7	29,056,997 (GRCm38)	missense	probably damaging	1.00
R3807:Ryr1	UTSW	7	29,020,152 (GRCm38)	missense	probably damaging	1.00
R3815:Ryr1	UTSW	7	29,072,902 (GRCm38)	missense	probably damaging	0.98
R4010:Ryr1	UTSW	7	29,095,124 (GRCm38)	missense	probably benign	0.41
R4041:Ryr1	UTSW	7	29,085,931 (GRCm38)	missense	possibly damaging	0.77
R4226:Ryr1	UTSW	7	29,062,151 (GRCm38)	nonsense	probably null
R4257:Ryr1	UTSW	7	29,082,450 (GRCm38)	missense	possibly damaging	0.93
R4328:Ryr1	UTSW	7	29,083,059 (GRCm38)	missense	probably damaging	1.00
R4394:Ryr1	UTSW	7	29,094,242 (GRCm38)	missense	possibly damaging	0.69
R4485:Ryr1	UTSW	7	29,090,156 (GRCm38)	missense	probably damaging	0.97
R4550:Ryr1	UTSW	7	29,098,735 (GRCm38)	missense	probably benign	0.05
R4554:Ryr1	UTSW	7	29,105,008 (GRCm38)	missense	probably benign	0.03
R4562:Ryr1	UTSW	7	29,074,580 (GRCm38)	intron	probably benign
R4642:Ryr1	UTSW	7	29,086,038 (GRCm38)	missense	possibly damaging	0.91
R4669:Ryr1	UTSW	7	29,059,831 (GRCm38)	missense	probably null	0.99
R4707:Ryr1	UTSW	7	29,045,662 (GRCm38)	missense	probably damaging	1.00
R4766:Ryr1	UTSW	7	29,085,833 (GRCm38)	missense	probably damaging	0.96
R4768:Ryr1	UTSW	7	29,004,821 (GRCm38)	unclassified	probably benign
R4770:Ryr1	UTSW	7	29,109,282 (GRCm38)	missense	probably damaging	0.99
R4780:Ryr1	UTSW	7	29,095,097 (GRCm38)	missense	possibly damaging	0.85
R4927:Ryr1	UTSW	7	29,019,983 (GRCm38)	missense	unknown
R4933:Ryr1	UTSW	7	29,104,298 (GRCm38)	missense	probably damaging	1.00
R4934:Ryr1	UTSW	7	29,068,095 (GRCm38)	missense	probably damaging	1.00
R4942:Ryr1	UTSW	7	29,069,573 (GRCm38)	missense	probably damaging	0.98
R4960:Ryr1	UTSW	7	29,078,783 (GRCm38)	missense	possibly damaging	0.82
R5007:Ryr1	UTSW	7	29,069,115 (GRCm38)	missense	probably damaging	1.00
R5011:Ryr1	UTSW	7	29,102,809 (GRCm38)	splice site	probably null
R5013:Ryr1	UTSW	7	29,102,809 (GRCm38)	splice site	probably null
R5137:Ryr1	UTSW	7	29,101,858 (GRCm38)	missense	possibly damaging	0.94
R5167:Ryr1	UTSW	7	29,067,693 (GRCm38)	missense	probably damaging	1.00
R5239:Ryr1	UTSW	7	29,036,128 (GRCm38)	missense	probably damaging	1.00
R5291:Ryr1	UTSW	7	29,115,598 (GRCm38)	missense	probably benign	0.03
R5303:Ryr1	UTSW	7	29,068,482 (GRCm38)	missense	probably damaging	1.00
R5386:Ryr1	UTSW	7	29,117,416 (GRCm38)	missense	probably damaging	0.98
R5431:Ryr1	UTSW	7	29,109,812 (GRCm38)	missense	probably benign	0.39
R5460:Ryr1	UTSW	7	29,071,961 (GRCm38)	missense	probably damaging	1.00
R5463:Ryr1	UTSW	7	29,024,023 (GRCm38)	missense	possibly damaging	0.79
R5503:Ryr1	UTSW	7	29,069,028 (GRCm38)	missense	possibly damaging	0.87
R5541:Ryr1	UTSW	7	29,086,185 (GRCm38)	missense	probably damaging	1.00
R5573:Ryr1	UTSW	7	29,015,723 (GRCm38)	missense	unknown
R5575:Ryr1	UTSW	7	29,078,693 (GRCm38)	missense	possibly damaging	0.77
R5610:Ryr1	UTSW	7	29,111,974 (GRCm38)	missense	probably benign	0.05
R5658:Ryr1	UTSW	7	29,091,089 (GRCm38)	splice site	probably null
R5918:Ryr1	UTSW	7	29,009,152 (GRCm38)	missense	probably benign	0.39
R5926:Ryr1	UTSW	7	29,104,360 (GRCm38)	missense	probably damaging	1.00
R5938:Ryr1	UTSW	7	29,046,865 (GRCm38)	missense	probably damaging	1.00
R5939:Ryr1	UTSW	7	29,116,127 (GRCm38)	missense	probably damaging	0.97
R5947:Ryr1	UTSW	7	29,071,924 (GRCm38)	missense	probably null	0.98
R5991:Ryr1	UTSW	7	29,104,610 (GRCm38)	missense	probably damaging	0.99
R5992:Ryr1	UTSW	7	29,067,637 (GRCm38)	missense	probably damaging	1.00
R5996:Ryr1	UTSW	7	29,024,241 (GRCm38)	missense	probably benign	0.38
R6075:Ryr1	UTSW	7	29,087,438 (GRCm38)	missense	probably damaging	1.00
R6091:Ryr1	UTSW	7	29,071,973 (GRCm38)	missense	probably benign	0.01
R6126:Ryr1	UTSW	7	29,076,239 (GRCm38)	missense	probably null	1.00
R6147:Ryr1	UTSW	7	29,085,914 (GRCm38)	missense	possibly damaging	0.88
R6235:Ryr1	UTSW	7	29,116,181 (GRCm38)	missense	probably benign	0.07
R6279:Ryr1	UTSW	7	29,087,428 (GRCm38)	missense	possibly damaging	0.93
R6381:Ryr1	UTSW	7	29,075,257 (GRCm38)	missense	possibly damaging	0.87
R6441:Ryr1	UTSW	7	29,059,695 (GRCm38)	missense	possibly damaging	0.95
R6443:Ryr1	UTSW	7	29,077,078 (GRCm38)	missense	probably damaging	0.97
R6459:Ryr1	UTSW	7	29,015,654 (GRCm38)	missense	probably benign	0.39
R6514:Ryr1	UTSW	7	29,046,841 (GRCm38)	missense	probably damaging	1.00
R6563:Ryr1	UTSW	7	29,095,492 (GRCm38)	missense	possibly damaging	0.92
R6660:Ryr1	UTSW	7	29,038,345 (GRCm38)	critical splice donor site	probably null
R6746:Ryr1	UTSW	7	29,117,404 (GRCm38)	missense	possibly damaging	0.56
R6785:Ryr1	UTSW	7	29,064,874 (GRCm38)	missense	probably benign	0.12
R6800:Ryr1	UTSW	7	29,024,316 (GRCm38)	missense	possibly damaging	0.95
R6939:Ryr1	UTSW	7	29,052,326 (GRCm38)	missense	possibly damaging	0.91
R6980:Ryr1	UTSW	7	29,109,387 (GRCm38)	missense	probably benign	0.03
R6995:Ryr1	UTSW	7	29,094,182 (GRCm38)	missense	probably damaging	0.97
R7065:Ryr1	UTSW	7	29,103,643 (GRCm38)	missense	probably damaging	1.00
R7123:Ryr1	UTSW	7	29,046,854 (GRCm38)	missense	probably benign	0.37
R7238:Ryr1	UTSW	7	29,095,382 (GRCm38)	missense	probably benign	0.24
R7240:Ryr1	UTSW	7	29,052,015 (GRCm38)	missense	possibly damaging	0.95
R7300:Ryr1	UTSW	7	29,059,511 (GRCm38)	missense	probably damaging	1.00
R7365:Ryr1	UTSW	7	29,085,755 (GRCm38)	missense	probably benign	0.05
R7403:Ryr1	UTSW	7	29,013,867 (GRCm38)	missense	probably benign	0.34
R7422:Ryr1	UTSW	7	29,085,870 (GRCm38)	missense	probably benign	0.00
R7493:Ryr1	UTSW	7	29,095,205 (GRCm38)	missense	probably benign	0.44
R7570:Ryr1	UTSW	7	29,078,585 (GRCm38)	missense	probably damaging	0.98
R7593:Ryr1	UTSW	7	29,036,103 (GRCm38)	missense	probably damaging	1.00
R7769:Ryr1	UTSW	7	29,098,785 (GRCm38)	missense	probably damaging	1.00
R7781:Ryr1	UTSW	7	29,067,630 (GRCm38)	missense	probably damaging	1.00
R7790:Ryr1	UTSW	7	29,104,832 (GRCm38)	missense	probably benign	0.39
R7799:Ryr1	UTSW	7	29,003,560 (GRCm38)	splice site	probably null
R7916:Ryr1	UTSW	7	29,090,939 (GRCm38)	nonsense	probably null
R7922:Ryr1	UTSW	7	29,097,224 (GRCm38)	missense	probably benign	0.09
R7988:Ryr1	UTSW	7	29,096,171 (GRCm38)	missense	probably benign	0.29
R7997:Ryr1	UTSW	7	29,003,543 (GRCm38)	missense	unknown
R8052:Ryr1	UTSW	7	29,083,385 (GRCm38)	missense	probably benign	0.05
R8096:Ryr1	UTSW	7	29,009,201 (GRCm38)	missense	unknown
R8116:Ryr1	UTSW	7	29,110,883 (GRCm38)	missense	probably benign	0.03
R8202:Ryr1	UTSW	7	29,091,032 (GRCm38)	missense	probably benign	0.18
R8207:Ryr1	UTSW	7	29,090,225 (GRCm38)	missense	probably damaging	1.00
R8257:Ryr1	UTSW	7	29,064,639 (GRCm38)	missense	possibly damaging	0.82
R8354:Ryr1	UTSW	7	29,015,717 (GRCm38)	missense	unknown
R8454:Ryr1	UTSW	7	29,015,717 (GRCm38)	missense	unknown
R8487:Ryr1	UTSW	7	29,040,867 (GRCm38)	missense	probably damaging	0.97
R8529:Ryr1	UTSW	7	29,070,084 (GRCm38)	missense	possibly damaging	0.86
R8545:Ryr1	UTSW	7	29,004,814 (GRCm38)	unclassified	probably benign
R8678:Ryr1	UTSW	7	29,077,064 (GRCm38)	missense	probably damaging	0.99
R8717:Ryr1	UTSW	7	29,052,328 (GRCm38)	missense	probably benign	0.03
R8724:Ryr1	UTSW	7	29,117,377 (GRCm38)	missense	probably benign	0.04
R8755:Ryr1	UTSW	7	29,092,268 (GRCm38)	missense	probably benign	0.19
R8772:Ryr1	UTSW	7	29,116,132 (GRCm38)	missense	probably benign	0.05
R8790:Ryr1	UTSW	7	29,076,872 (GRCm38)	missense	probably damaging	1.00
R8793:Ryr1	UTSW	7	29,064,859 (GRCm38)	missense	probably damaging	1.00
R8836:Ryr1	UTSW	7	29,074,666 (GRCm38)	missense	probably damaging	1.00
R8858:Ryr1	UTSW	7	29,109,213 (GRCm38)	missense	probably benign	0.00
R8910:Ryr1	UTSW	7	29,071,915 (GRCm38)	missense	probably damaging	1.00
R8920:Ryr1	UTSW	7	29,090,215 (GRCm38)	missense	possibly damaging	0.89
R8938:Ryr1	UTSW	7	29,101,933 (GRCm38)	missense	probably damaging	1.00
R9035:Ryr1	UTSW	7	29,090,997 (GRCm38)	missense	probably damaging	0.97
R9115:Ryr1	UTSW	7	29,104,564 (GRCm38)	nonsense	probably null
R9123:Ryr1	UTSW	7	29,071,804 (GRCm38)	missense	probably damaging	1.00
R9154:Ryr1	UTSW	7	29,069,858 (GRCm38)	missense	probably benign	0.08
R9189:Ryr1	UTSW	7	29,077,046 (GRCm38)	missense	probably damaging	1.00
R9200:Ryr1	UTSW	7	29,095,099 (GRCm38)	missense	probably benign	0.00
R9214:Ryr1	UTSW	7	29,085,762 (GRCm38)	missense	possibly damaging	0.52
R9216:Ryr1	UTSW	7	29,101,852 (GRCm38)	missense	probably damaging	0.97
R9240:Ryr1	UTSW	7	29,043,888 (GRCm38)	missense	probably damaging	1.00
R9261:Ryr1	UTSW	7	29,052,388 (GRCm38)	missense	possibly damaging	0.91
R9276:Ryr1	UTSW	7	29,102,829 (GRCm38)	missense	probably damaging	0.99
R9280:Ryr1	UTSW	7	29,102,964 (GRCm38)	missense	probably damaging	1.00
R9316:Ryr1	UTSW	7	29,017,962 (GRCm38)	missense	unknown
R9333:Ryr1	UTSW	7	29,074,789 (GRCm38)	critical splice donor site	probably null
R9459:Ryr1	UTSW	7	29,068,643 (GRCm38)	missense	probably damaging	1.00
R9468:Ryr1	UTSW	7	29,073,085 (GRCm38)	missense	probably damaging	1.00
R9486:Ryr1	UTSW	7	29,078,540 (GRCm38)	missense	probably benign	0.15
R9524:Ryr1	UTSW	7	29,024,175 (GRCm38)	missense	probably damaging	1.00
R9620:Ryr1	UTSW	7	29,015,713 (GRCm38)	missense	unknown
R9664:Ryr1	UTSW	7	29,059,667 (GRCm38)	missense	probably damaging	1.00
R9776:Ryr1	UTSW	7	29,075,239 (GRCm38)	missense	probably damaging	1.00
X0021:Ryr1	UTSW	7	29,061,531 (GRCm38)	missense	probably damaging	1.00
Z1176:Ryr1	UTSW	7	29,103,498 (GRCm38)	missense	probably damaging	1.00
Z1176:Ryr1	UTSW	7	29,086,035 (GRCm38)	missense	probably benign	0.10
Z1176:Ryr1	UTSW	7	29,020,214 (GRCm38)	missense	probably damaging	1.00
Z1177:Ryr1	UTSW	7	29,101,922 (GRCm38)	missense	probably damaging	1.00
Z1177:Ryr1	UTSW	7	29,048,792 (GRCm38)	nonsense	probably null
Z1177:Ryr1	UTSW	7	29,017,985 (GRCm38)	missense	unknown
Z1186:Ryr1	UTSW	7	29,082,477 (GRCm38)	missense	possibly damaging	0.61

Predicted Primers

PCR Primer
(F):5'- GTCAGTCCTCATTGCAACCC -3'
(R):5'- AGGTTAGAGTCCTGGATTCCAATC -3'

Sequencing Primer
(F):5'- ACAGTCCCTCGATCACCTGG -3'
(R):5'- GATTCCAATCCTGACTGACCC -3'

Posted On

2020-07-28