Mutagenetix > Incidental Mutation

Incidental Mutation 'R7570:Ryr1'

585708

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

045631-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R7570 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

29003344-29125179 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 29078585 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Leucine at position 2169 (Q2169L)

Ref Sequence

ENSEMBL: ENSMUSP00000149042 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000032813] [ENSMUST00000179893] [ENSMUST00000214374]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000032813
AA Change: Q2162L

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000032813
Gene: ENSMUSG00000030592
AA Change: Q2162L

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 benign
Transcript: ENSMUST00000179893
AA Change: Q2162L

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

SMART Domains

Protein: ENSMUSP00000137123
Gene: ENSMUSG00000030592
AA Change: Q2162L

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

Predicted Effect

probably damaging
Transcript: ENSMUST00000214374
AA Change: Q2169L

PolyPhen 2 Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)

Coding Region Coverage

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

Validation Efficiency

98% (104/106)

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: 106 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930590J08Rik	C	T	6: 91,934,610 (GRCm38)	T613I	probably benign	Het
Ajuba	T	C	14: 54,576,402 (GRCm38)	E288G	probably damaging	Het
Ankrd12	C	T	17: 65,985,360 (GRCm38)	R1026K	probably benign	Het
Apol7b	T	C	15: 77,423,474 (GRCm38)	T274A	probably benign	Het
Arid4a	A	T	12: 71,063,142 (GRCm38)	R86*	probably null	Het
Asnsd1	C	T	1: 53,348,258 (GRCm38)	G70D	probably damaging	Het
Atg4c	T	A	4: 99,228,560 (GRCm38)	V313D	possibly damaging	Het
Atp13a5	A	C	16: 29,266,963 (GRCm38)	C885G	probably damaging	Het
Bpifb9a	A	T	2: 154,262,263 (GRCm38)	I209F	possibly damaging	Het
Bsn	T	C	9: 108,113,543 (GRCm38)	D1670G	probably damaging	Het
Cct8	T	A	16: 87,491,322 (GRCm38)	I121F	probably benign	Het
Cd209a	T	G	8: 3,744,151 (GRCm38)	D217A	probably damaging	Het
Cdk19	C	T	10: 40,477,958 (GRCm38)	S456L	possibly damaging	Het
Chd9	C	T	8: 90,994,580 (GRCm38)	H999Y	unknown	Het
Col5a1	G	A	2: 27,951,383 (GRCm38)	V339M	unknown	Het
Cr2	G	A	1: 195,169,340 (GRCm38)	R115*	probably null	Het
Cyb561	A	T	11: 105,937,644 (GRCm38)	F62I	probably damaging	Het
Cyp2c38	A	T	19: 39,404,743 (GRCm38)	N293K	possibly damaging	Het
Cyp2c69	A	T	19: 39,859,898 (GRCm38)	D293E	probably damaging	Het
Dcbld2	T	A	16: 58,424,569 (GRCm38)	C69S	possibly damaging	Het
Dcdc2a	T	C	13: 25,119,373 (GRCm38)	S296P	probably benign	Het
Dmxl1	T	A	18: 49,893,957 (GRCm38)	I2044K	possibly damaging	Het
Dnah5	A	G	15: 28,346,952 (GRCm38)	D2527G	probably damaging	Het
Dnah6	T	C	6: 73,149,430 (GRCm38)	T1305A	probably benign	Het
Dnajc9	A	G	14: 20,388,644 (GRCm38)	V47A	probably benign	Het
Dnmt3b	A	G	2: 153,676,699 (GRCm38)	Y594C	probably damaging	Het
Dph7	A	G	2: 24,965,630 (GRCm38)	D147G	probably damaging	Het
Drap1	T	C	19: 5,423,352 (GRCm38)	H164R	possibly damaging	Het
Dsg3	T	A	18: 20,527,780 (GRCm38)	V392E	possibly damaging	Het
Dxo	A	G	17: 34,837,640 (GRCm38)	D81G	probably benign	Het
E230025N22Rik	G	T	18: 36,695,592 (GRCm38)	T11K	probably benign	Het
Esyt1	A	G	10: 128,518,932 (GRCm38)	V533A	possibly damaging	Het
Etv3	T	A	3: 87,536,031 (GRCm38)	C307*	probably null	Het
Fam114a1	T	A	5: 65,030,059 (GRCm38)		probably null	Het
Fam3c	T	A	6: 22,326,405 (GRCm38)		probably benign	Het
Fbn1	G	T	2: 125,397,852 (GRCm38)	T305K	probably benign	Het
Ggt1	A	T	10: 75,585,594 (GRCm38)	I484F	probably damaging	Het
Gpatch1	T	C	7: 35,293,812 (GRCm38)	D536G	probably damaging	Het
Gpx4	T	C	10: 80,055,041 (GRCm38)	I189T	probably damaging	Het
Gsr	T	A	8: 33,669,165 (GRCm38)	C85S	probably damaging	Het
Gsta5	A	T	9: 78,304,469 (GRCm38)	D171V	possibly damaging	Het
Havcr1	T	A	11: 46,770,542 (GRCm38)		probably null	Het
Heatr4	T	C	12: 83,979,644 (GRCm38)	T280A	probably benign	Het
Hmcn2	A	T	2: 31,423,911 (GRCm38)	E3532D	probably benign	Het
Hnrnpc	T	C	14: 52,075,099 (GRCm38)	N308S	possibly damaging	Het
Ighv8-9	A	G	12: 115,468,738 (GRCm38)	V13A	probably benign	Het
Itgb2l	A	T	16: 96,426,239 (GRCm38)	F535I	probably benign	Het
Kdm5a	T	G	6: 120,427,842 (GRCm38)	D1348E	probably damaging	Het
Kndc1	CT	C	7: 139,923,775 (GRCm38)		probably null	Het
Ky	A	G	9: 102,542,329 (GRCm38)	I512V	probably benign	Het
Lamc1	A	T	1: 153,243,275 (GRCm38)	F866Y	possibly damaging	Het
Lbx1	C	A	19: 45,235,248 (GRCm38)		probably benign	Het
Magel2	A	G	7: 62,378,910 (GRCm38)	T521A	possibly damaging	Het
Mgam	A	T	6: 40,746,433 (GRCm38)	I491L	probably benign	Het
Mitd1	T	C	1: 37,890,192 (GRCm38)	E40G	probably damaging	Het
Mpzl3	A	G	9: 45,070,687 (GRCm38)	T218A	probably benign	Het
Mrpl42	A	G	10: 95,480,965 (GRCm38)	S77P	probably benign	Het
Mup5	C	T	4: 61,834,674 (GRCm38)	W37*	probably null	Het
Myh14	T	C	7: 44,632,426 (GRCm38)	I803V	probably benign	Het
Ncor2	T	A	5: 125,030,089 (GRCm38)	T744S		Het
Ndufv3	A	G	17: 31,527,622 (GRCm38)	D162G	probably damaging	Het
Nostrin	A	G	2: 69,175,806 (GRCm38)	E278G	probably damaging	Het
Nrxn1	T	G	17: 90,162,379 (GRCm38)	E1288A	probably benign	Het
Or4c11c	A	G	2: 88,831,128 (GRCm38)	N4D	possibly damaging	Het
Or51b6b	C	A	7: 103,660,881 (GRCm38)	R123L	probably damaging	Het
Or52h1	T	A	7: 104,179,748 (GRCm38)	Y220F	probably damaging	Het
Or8g55	A	T	9: 39,873,455 (GRCm38)	Y60F	possibly damaging	Het
Patj	T	A	4: 98,424,500 (GRCm38)		probably null	Het
Pcm1	T	G	8: 41,267,344 (GRCm38)	I314R	possibly damaging	Het
Pcsk6	A	G	7: 66,033,898 (GRCm38)	T754A	probably benign	Het
Pde2a	A	T	7: 101,502,834 (GRCm38)	N326I	probably benign	Het
Plekhg4	T	C	8: 105,378,684 (GRCm38)	S594P	possibly damaging	Het
Plekhm3	T	C	1: 64,937,906 (GRCm38)	D135G	probably damaging	Het
Plin4	A	T	17: 56,106,776 (GRCm38)	M283K	probably benign	Het
Ppfia3	T	C	7: 45,340,748 (GRCm38)		probably null	Het
Prdm9	T	C	17: 15,555,652 (GRCm38)	N179S	probably benign	Het
Prrt3	T	C	6: 113,494,488 (GRCm38)	S908G	probably damaging	Het
Psg22	C	A	7: 18,722,735 (GRCm38)	S181Y	possibly damaging	Het
Rcor3	C	A	1: 192,137,876 (GRCm38)	G8V	probably damaging	Het
Rp1l1	T	A	14: 64,031,574 (GRCm38)	C1536*	probably null	Het
Rpp25l	T	C	4: 41,712,529 (GRCm38)	H82R	probably damaging	Het
Rps3a1	T	A	3: 86,139,089 (GRCm38)	M172L	probably benign	Het
Rtbdn	T	C	8: 84,952,927 (GRCm38)	L110P	probably damaging	Het
Scn4a	A	T	11: 106,320,473 (GRCm38)	C1573S	possibly damaging	Het
Sec16b	A	T	1: 157,531,395 (GRCm38)		probably null	Het
Serpina1a	A	T	12: 103,853,837 (GRCm38)	D383E	possibly damaging	Het
Sh3gl3	T	C	7: 82,285,077 (GRCm38)	M262T	probably benign	Het
Sos2	G	A	12: 69,590,880 (GRCm38)	T1052M	probably damaging	Het
Spag16	G	A	1: 69,996,841 (GRCm38)	V343I	probably benign	Het
Spocd1	T	G	4: 129,930,164 (GRCm38)	D251E		Het
Stc2	G	T	11: 31,367,798 (GRCm38)	N74K	probably damaging	Het
Tasor2	A	G	13: 3,573,621 (GRCm38)	Y2110H	probably damaging	Het
Thbs3	C	T	3: 89,219,052 (GRCm38)	Q227*	probably null	Het
Tmem92	A	C	11: 94,778,990 (GRCm38)	I105R	probably benign	Het
Tmod1	T	A	4: 46,083,632 (GRCm38)	N20K	probably benign	Het
Tns1	T	C	1: 73,953,479 (GRCm38)	D53G	probably damaging	Het
Tspan33	T	A	6: 29,717,338 (GRCm38)	L246Q	probably damaging	Het
Ttc16	A	G	2: 32,768,968 (GRCm38)	L392P	probably damaging	Het
Uggt1	T	A	1: 36,185,838 (GRCm38)	T572S	probably benign	Het
Usp17la	A	T	7: 104,860,397 (GRCm38)	T70S	probably damaging	Het
Usp31	C	T	7: 121,674,963 (GRCm38)	R370H	probably damaging	Het
Wdr83	C	T	8: 85,079,834 (GRCm38)	V112M	probably damaging	Het
Zbtb25	T	A	12: 76,369,592 (GRCm38)		probably benign	Het
Zfp110	T	A	7: 12,849,340 (GRCm38)	N638K	possibly damaging	Het
Zfp747l1	T	A	7: 127,385,283 (GRCm38)	S216C	probably benign	Het
Zfp820	T	C	17: 21,819,013 (GRCm38)	T445A	probably benign	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
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
R8248:Ryr1	UTSW	7	29,069,121 (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'- AAGGGACATCATGGCGGTAC -3'
(R):5'- AGAGATGCAACCCAGTGTCC -3'

Sequencing Primer
(F):5'- ATCATGGCGGTACAGCGTG -3'
(R):5'- TTCCCCAGAGTCCTTGCAGG -3'

Posted On

2019-10-17