Incidental Mutation 'R9133:Cmya5'
ID 693800
Institutional Source Beutler Lab
Gene Symbol Cmya5
Ensembl Gene ENSMUSG00000047419
Gene Name cardiomyopathy associated 5
Synonyms Myospryn, 2310076E21Rik, 2310076E16Rik
MMRRC Submission 068930-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.252) question?
Stock # R9133 (G1)
Quality Score 225.009
Status Validated
Chromosome 13
Chromosomal Location 93040713-93144724 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 93097600 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 327 (S327P)
Ref Sequence ENSEMBL: ENSMUSP00000050408 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000062122]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000062122
AA Change: S327P

PolyPhen 2 Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000050408
Gene: ENSMUSG00000047419
AA Change: S327P

DomainStartEndE-ValueType
low complexity region 20 46 N/A INTRINSIC
low complexity region 129 140 N/A INTRINSIC
internal_repeat_1 448 535 5.09e-18 PROSPERO
internal_repeat_1 543 625 5.09e-18 PROSPERO
low complexity region 626 645 N/A INTRINSIC
low complexity region 679 691 N/A INTRINSIC
low complexity region 734 741 N/A INTRINSIC
low complexity region 1001 1010 N/A INTRINSIC
low complexity region 1166 1183 N/A INTRINSIC
low complexity region 1259 1267 N/A INTRINSIC
low complexity region 1440 1449 N/A INTRINSIC
low complexity region 1876 1889 N/A INTRINSIC
low complexity region 2632 2645 N/A INTRINSIC
low complexity region 3048 3057 N/A INTRINSIC
FN3 3312 3399 7.29e-4 SMART
FN3 3411 3492 1.3e0 SMART
Pfam:SPRY 3551 3668 6.7e-8 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency 100% (65/65)
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acat3 T A 17: 12,940,289 (GRCm38) R4S probably benign Het
Adamdec1 A T 14: 68,577,098 (GRCm38) C143* probably null Het
Adck5 A G 15: 76,576,412 (GRCm38) probably benign Het
Aebp2 A G 6: 140,633,715 (GRCm38) D226G probably damaging Het
Ascc3 A G 10: 50,754,079 (GRCm38) I1755V possibly damaging Het
Aspm C T 1: 139,491,528 (GRCm38) T2977M probably damaging Het
Cacna1a A G 8: 84,549,523 (GRCm38) S582G probably damaging Het
Card14 T C 11: 119,341,009 (GRCm38) F801S probably damaging Het
Casp16-ps T A 17: 23,552,029 (GRCm38) D134V probably damaging Het
Cutc A T 19: 43,767,288 (GRCm38) D229V possibly damaging Het
Cyp21a1 C A 17: 34,804,445 (GRCm38) probably benign Het
Dnah10 A G 5: 124,782,359 (GRCm38) K2130R probably damaging Het
Dsc1 C T 18: 20,101,847 (GRCm38) S250N probably benign Het
Edc4 T C 8: 105,885,146 (GRCm38) probably null Het
Efcab8 G C 2: 153,804,941 (GRCm38) V397L unknown Het
Ehmt1 A T 2: 24,839,623 (GRCm38) I642K possibly damaging Het
Gjd2 T C 2: 114,011,558 (GRCm38) Q146R probably benign Het
Gm26661 A G 14: 7,791,936 (GRCm38) H117R unknown Het
H2-Oa T A 17: 34,094,531 (GRCm38) D185E probably damaging Het
Hjurp A T 1: 88,275,050 (GRCm38) Y71N possibly damaging Het
Hyal6 A G 6: 24,734,586 (GRCm38) R173G possibly damaging Het
Ica1 A T 6: 8,659,921 (GRCm38) V125D probably benign Het
Ift172 T C 5: 31,285,523 (GRCm38) T140A probably benign Het
Ighv9-4 T A 12: 114,300,263 (GRCm38) I17F probably benign Het
Igkv4-92 G T 6: 68,755,264 (GRCm38) T42N probably damaging Het
Kctd16 C A 18: 40,259,016 (GRCm38) P219Q probably damaging Het
Kdm5b A T 1: 134,602,585 (GRCm38) I445F probably benign Het
Ksr2 A G 5: 117,703,254 (GRCm38) T598A probably benign Het
Lrrn1 C T 6: 107,567,607 (GRCm38) T122I probably damaging Het
Mars2 A G 1: 55,237,562 (GRCm38) D108G possibly damaging Het
Ms4a14 A G 19: 11,303,674 (GRCm38) W507R Het
Ncoa3 A G 2: 166,068,461 (GRCm38) T1266A possibly damaging Het
Neb T C 2: 52,193,244 (GRCm38) K5650E possibly damaging Het
Nlrp4f T A 13: 65,185,069 (GRCm38) K92* probably null Het
Nme4 G T 17: 26,095,415 (GRCm38) A13E probably benign Het
Nova1 G T 12: 46,818,741 (GRCm38) A4E unknown Het
Nphs1 G T 7: 30,460,667 (GRCm38) E124* probably null Het
Olfr1162 T C 2: 88,050,438 (GRCm38) Y62C probably damaging Het
Olfr960 T A 9: 39,623,513 (GRCm38) L128* probably null Het
Olfr963 T A 9: 39,669,678 (GRCm38) I207N possibly damaging Het
Pde8a C T 7: 81,332,871 (GRCm38) T746I probably damaging Het
Peg3 GTGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTC GTGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTC 7: 6,709,168 (GRCm38) probably benign Het
Ranbp2 T C 10: 58,477,228 (GRCm38) S1257P probably damaging Het
Ranbp3 T C 17: 56,696,791 (GRCm38) probably null Het
Rasgrf1 A G 9: 89,911,547 (GRCm38) T126A probably benign Het
Rexo5 T G 7: 119,845,444 (GRCm38) L714R probably damaging Het
Rhobtb3 A G 13: 75,872,393 (GRCm38) Y597H probably damaging Het
Riox1 C G 12: 83,951,447 (GRCm38) Y252* probably null Het
Sh2d3c T C 2: 32,744,766 (GRCm38) Y186H possibly damaging Het
Slc16a7 T A 10: 125,230,667 (GRCm38) T368S probably benign Het
Slc25a26 G A 6: 94,534,162 (GRCm38) V107I Het
Slc4a5 A T 6: 83,226,235 (GRCm38) Y39F possibly damaging Het
Smarcad1 A G 6: 65,072,051 (GRCm38) K254E probably damaging Het
Sspo G T 6: 48,457,813 (GRCm38) V1080L possibly damaging Het
Thsd7b A T 1: 129,915,645 (GRCm38) T865S probably benign Het
Top1 C T 2: 160,703,671 (GRCm38) Q320* probably null Het
Trank1 T A 9: 111,391,702 (GRCm38) N2502K possibly damaging Het
Urad T C 5: 147,315,441 (GRCm38) H67R probably damaging Het
Vamp5 A C 6: 72,380,379 (GRCm38) probably null Het
Vmn1r62 A G 7: 5,676,063 (GRCm38) I248V probably benign Het
Wwc2 G T 8: 47,851,972 (GRCm38) Q873K unknown Het
Zcchc2 C A 1: 106,030,805 (GRCm38) S1002Y probably damaging Het
Zdhhc14 G A 17: 5,753,008 (GRCm38) R462H probably benign Het
Zfp788 A G 7: 41,650,060 (GRCm38) N707D Het
Zfp964 A G 8: 69,663,133 (GRCm38) T128A probably benign Het
Zkscan16 T C 4: 58,957,722 (GRCm38) L668S possibly damaging Het
Other mutations in Cmya5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00489:Cmya5 APN 13 93,093,120 (GRCm38) missense probably benign 0.13
IGL00516:Cmya5 APN 13 93,098,167 (GRCm38) missense possibly damaging 0.73
IGL00654:Cmya5 APN 13 93,094,161 (GRCm38) missense probably benign 0.00
IGL00948:Cmya5 APN 13 93,091,036 (GRCm38) missense probably benign
IGL00966:Cmya5 APN 13 93,097,906 (GRCm38) missense probably benign 0.33
IGL00988:Cmya5 APN 13 93,097,933 (GRCm38) missense possibly damaging 0.96
IGL01106:Cmya5 APN 13 93,084,612 (GRCm38) missense probably damaging 1.00
IGL01331:Cmya5 APN 13 93,096,946 (GRCm38) missense possibly damaging 0.53
IGL01392:Cmya5 APN 13 93,089,206 (GRCm38) missense probably damaging 0.99
IGL01508:Cmya5 APN 13 93,094,027 (GRCm38) missense probably benign
IGL01679:Cmya5 APN 13 93,065,320 (GRCm38) missense probably damaging 1.00
IGL01749:Cmya5 APN 13 93,089,299 (GRCm38) missense probably benign 0.00
IGL01861:Cmya5 APN 13 93,089,748 (GRCm38) missense probably damaging 1.00
IGL02021:Cmya5 APN 13 93,094,549 (GRCm38) missense probably benign 0.00
IGL02034:Cmya5 APN 13 93,084,535 (GRCm38) splice site probably benign
IGL02103:Cmya5 APN 13 93,092,127 (GRCm38) missense probably benign 0.05
IGL02174:Cmya5 APN 13 93,048,907 (GRCm38) missense possibly damaging 0.76
IGL02176:Cmya5 APN 13 93,090,150 (GRCm38) missense probably damaging 1.00
IGL02210:Cmya5 APN 13 93,092,734 (GRCm38) missense probably benign 0.14
IGL02229:Cmya5 APN 13 93,092,686 (GRCm38) missense possibly damaging 0.54
IGL02306:Cmya5 APN 13 93,098,019 (GRCm38) missense probably damaging 1.00
IGL02311:Cmya5 APN 13 93,090,655 (GRCm38) missense probably benign 0.40
IGL02409:Cmya5 APN 13 93,090,198 (GRCm38) missense probably damaging 0.96
IGL02561:Cmya5 APN 13 93,091,858 (GRCm38) missense probably benign 0.00
IGL02676:Cmya5 APN 13 93,092,853 (GRCm38) missense probably damaging 1.00
IGL02683:Cmya5 APN 13 93,090,997 (GRCm38) nonsense probably null
IGL02685:Cmya5 APN 13 93,090,997 (GRCm38) nonsense probably null
IGL02686:Cmya5 APN 13 93,090,997 (GRCm38) nonsense probably null
IGL02724:Cmya5 APN 13 93,096,655 (GRCm38) missense probably benign
IGL02727:Cmya5 APN 13 93,098,245 (GRCm38) missense possibly damaging 0.73
IGL02965:Cmya5 APN 13 93,092,557 (GRCm38) missense probably benign 0.41
IGL03079:Cmya5 APN 13 93,097,701 (GRCm38) missense possibly damaging 0.85
IGL03144:Cmya5 APN 13 93,090,868 (GRCm38) missense probably damaging 1.00
IGL03253:Cmya5 APN 13 93,091,270 (GRCm38) nonsense probably null
IGL03336:Cmya5 APN 13 93,093,505 (GRCm38) missense possibly damaging 0.84
IGL03138:Cmya5 UTSW 13 93,065,342 (GRCm38) missense probably damaging 1.00
P0023:Cmya5 UTSW 13 93,089,346 (GRCm38) missense probably benign 0.22
P4748:Cmya5 UTSW 13 93,074,475 (GRCm38) splice site probably benign
R0123:Cmya5 UTSW 13 93,095,904 (GRCm38) missense possibly damaging 0.84
R0206:Cmya5 UTSW 13 93,095,557 (GRCm38) missense probably damaging 0.98
R0206:Cmya5 UTSW 13 93,095,557 (GRCm38) missense probably damaging 0.98
R0242:Cmya5 UTSW 13 93,095,600 (GRCm38) missense probably benign
R0242:Cmya5 UTSW 13 93,095,600 (GRCm38) missense probably benign
R0331:Cmya5 UTSW 13 93,144,403 (GRCm38) missense possibly damaging 0.53
R0363:Cmya5 UTSW 13 93,094,869 (GRCm38) missense possibly damaging 0.77
R0382:Cmya5 UTSW 13 93,092,748 (GRCm38) missense probably benign 0.06
R0416:Cmya5 UTSW 13 93,089,856 (GRCm38) missense probably benign 0.05
R0446:Cmya5 UTSW 13 93,093,656 (GRCm38) missense probably benign
R0457:Cmya5 UTSW 13 93,095,587 (GRCm38) missense possibly damaging 0.84
R0673:Cmya5 UTSW 13 93,089,997 (GRCm38) missense probably damaging 1.00
R0674:Cmya5 UTSW 13 93,092,791 (GRCm38) missense probably damaging 1.00
R0692:Cmya5 UTSW 13 93,093,849 (GRCm38) nonsense probably null
R0698:Cmya5 UTSW 13 93,095,557 (GRCm38) missense probably damaging 0.98
R1227:Cmya5 UTSW 13 93,094,446 (GRCm38) missense probably damaging 0.99
R1272:Cmya5 UTSW 13 93,095,112 (GRCm38) missense possibly damaging 0.79
R1335:Cmya5 UTSW 13 93,041,535 (GRCm38) missense possibly damaging 0.65
R1353:Cmya5 UTSW 13 93,041,525 (GRCm38) missense probably damaging 1.00
R1354:Cmya5 UTSW 13 93,092,058 (GRCm38) missense possibly damaging 0.46
R1458:Cmya5 UTSW 13 93,065,327 (GRCm38) missense probably benign 0.44
R1572:Cmya5 UTSW 13 93,094,269 (GRCm38) missense possibly damaging 0.61
R1698:Cmya5 UTSW 13 93,063,519 (GRCm38) missense probably benign 0.27
R1735:Cmya5 UTSW 13 93,089,789 (GRCm38) missense probably benign 0.11
R1743:Cmya5 UTSW 13 93,097,317 (GRCm38) missense probably benign 0.33
R1750:Cmya5 UTSW 13 93,095,663 (GRCm38) missense probably benign
R1827:Cmya5 UTSW 13 93,074,448 (GRCm38) missense possibly damaging 0.80
R2068:Cmya5 UTSW 13 93,090,524 (GRCm38) missense possibly damaging 0.93
R2088:Cmya5 UTSW 13 93,092,812 (GRCm38) missense probably damaging 1.00
R2132:Cmya5 UTSW 13 93,069,383 (GRCm38) missense probably damaging 1.00
R2216:Cmya5 UTSW 13 93,093,495 (GRCm38) missense probably damaging 1.00
R2363:Cmya5 UTSW 13 93,093,702 (GRCm38) missense probably benign 0.15
R2497:Cmya5 UTSW 13 93,098,005 (GRCm38) missense possibly damaging 0.53
R2509:Cmya5 UTSW 13 93,093,558 (GRCm38) missense probably benign 0.41
R2917:Cmya5 UTSW 13 93,091,064 (GRCm38) nonsense probably null
R2944:Cmya5 UTSW 13 93,092,842 (GRCm38) nonsense probably null
R3039:Cmya5 UTSW 13 93,092,250 (GRCm38) missense probably benign 0.12
R3078:Cmya5 UTSW 13 93,048,927 (GRCm38) missense probably damaging 0.99
R3708:Cmya5 UTSW 13 93,095,366 (GRCm38) nonsense probably null
R3717:Cmya5 UTSW 13 93,092,487 (GRCm38) missense probably benign 0.12
R3768:Cmya5 UTSW 13 93,096,693 (GRCm38) missense possibly damaging 0.73
R3769:Cmya5 UTSW 13 93,096,693 (GRCm38) missense possibly damaging 0.73
R3840:Cmya5 UTSW 13 93,094,632 (GRCm38) missense probably damaging 0.96
R3841:Cmya5 UTSW 13 93,094,632 (GRCm38) missense probably damaging 0.96
R3882:Cmya5 UTSW 13 93,091,219 (GRCm38) missense probably benign 0.07
R3888:Cmya5 UTSW 13 93,093,656 (GRCm38) missense probably benign
R3897:Cmya5 UTSW 13 93,096,681 (GRCm38) missense possibly damaging 0.72
R3952:Cmya5 UTSW 13 93,089,199 (GRCm38) missense possibly damaging 0.89
R4366:Cmya5 UTSW 13 93,091,956 (GRCm38) missense probably benign 0.36
R4471:Cmya5 UTSW 13 93,092,325 (GRCm38) missense probably benign 0.01
R4493:Cmya5 UTSW 13 93,094,065 (GRCm38) missense probably benign
R4495:Cmya5 UTSW 13 93,094,065 (GRCm38) missense probably benign
R4544:Cmya5 UTSW 13 93,091,918 (GRCm38) nonsense probably null
R4545:Cmya5 UTSW 13 93,091,918 (GRCm38) nonsense probably null
R4624:Cmya5 UTSW 13 93,063,551 (GRCm38) missense probably damaging 1.00
R4648:Cmya5 UTSW 13 93,093,828 (GRCm38) missense possibly damaging 0.84
R4824:Cmya5 UTSW 13 93,093,574 (GRCm38) missense probably benign 0.04
R4965:Cmya5 UTSW 13 93,095,787 (GRCm38) missense possibly damaging 0.84
R4967:Cmya5 UTSW 13 93,090,585 (GRCm38) missense probably damaging 1.00
R5101:Cmya5 UTSW 13 93,091,603 (GRCm38) missense possibly damaging 0.61
R5133:Cmya5 UTSW 13 93,093,372 (GRCm38) missense possibly damaging 0.79
R5139:Cmya5 UTSW 13 93,096,061 (GRCm38) missense probably benign 0.00
R5220:Cmya5 UTSW 13 93,092,296 (GRCm38) missense probably damaging 0.99
R5332:Cmya5 UTSW 13 93,096,195 (GRCm38) missense probably damaging 0.96
R5337:Cmya5 UTSW 13 93,083,273 (GRCm38) missense probably benign 0.28
R5356:Cmya5 UTSW 13 93,063,485 (GRCm38) missense probably damaging 1.00
R5401:Cmya5 UTSW 13 93,091,968 (GRCm38) missense probably damaging 1.00
R5438:Cmya5 UTSW 13 93,095,199 (GRCm38) missense possibly damaging 0.89
R5604:Cmya5 UTSW 13 93,092,763 (GRCm38) missense probably benign 0.15
R5628:Cmya5 UTSW 13 93,089,710 (GRCm38) missense probably damaging 1.00
R5666:Cmya5 UTSW 13 93,045,949 (GRCm38) missense possibly damaging 0.75
R5687:Cmya5 UTSW 13 93,098,176 (GRCm38) missense possibly damaging 0.53
R5695:Cmya5 UTSW 13 93,045,866 (GRCm38) critical splice donor site probably null
R5806:Cmya5 UTSW 13 93,093,937 (GRCm38) missense possibly damaging 0.84
R5820:Cmya5 UTSW 13 93,092,780 (GRCm38) missense probably benign 0.04
R5872:Cmya5 UTSW 13 93,097,435 (GRCm38) missense probably benign 0.01
R5875:Cmya5 UTSW 13 93,095,184 (GRCm38) missense probably benign 0.13
R5896:Cmya5 UTSW 13 93,045,865 (GRCm38) critical splice donor site probably null
R5910:Cmya5 UTSW 13 93,092,643 (GRCm38) missense probably damaging 0.98
R5969:Cmya5 UTSW 13 93,089,544 (GRCm38) missense possibly damaging 0.78
R6064:Cmya5 UTSW 13 93,089,649 (GRCm38) missense probably damaging 1.00
R6081:Cmya5 UTSW 13 93,144,513 (GRCm38) unclassified probably benign
R6102:Cmya5 UTSW 13 93,094,231 (GRCm38) missense probably benign
R6117:Cmya5 UTSW 13 93,095,166 (GRCm38) missense probably damaging 0.98
R6188:Cmya5 UTSW 13 93,097,276 (GRCm38) missense possibly damaging 0.73
R6188:Cmya5 UTSW 13 93,093,444 (GRCm38) missense possibly damaging 0.61
R6219:Cmya5 UTSW 13 93,094,443 (GRCm38) missense probably damaging 1.00
R6229:Cmya5 UTSW 13 93,093,306 (GRCm38) missense probably benign 0.41
R6346:Cmya5 UTSW 13 93,092,190 (GRCm38) missense probably damaging 1.00
R6431:Cmya5 UTSW 13 93,074,464 (GRCm38) missense possibly damaging 0.60
R6436:Cmya5 UTSW 13 93,089,215 (GRCm38) missense probably damaging 0.98
R6598:Cmya5 UTSW 13 93,089,808 (GRCm38) missense probably benign 0.05
R6649:Cmya5 UTSW 13 93,098,025 (GRCm38) missense possibly damaging 0.91
R6652:Cmya5 UTSW 13 93,093,039 (GRCm38) missense probably damaging 0.99
R6652:Cmya5 UTSW 13 93,092,895 (GRCm38) missense probably benign 0.04
R6669:Cmya5 UTSW 13 93,093,259 (GRCm38) missense probably benign 0.03
R6881:Cmya5 UTSW 13 93,090,292 (GRCm38) missense probably damaging 1.00
R6909:Cmya5 UTSW 13 93,091,252 (GRCm38) missense probably benign 0.04
R6933:Cmya5 UTSW 13 93,095,136 (GRCm38) missense probably benign 0.03
R7021:Cmya5 UTSW 13 93,093,555 (GRCm38) missense possibly damaging 0.62
R7022:Cmya5 UTSW 13 93,069,278 (GRCm38) critical splice donor site probably null
R7068:Cmya5 UTSW 13 93,092,697 (GRCm38) missense possibly damaging 0.59
R7087:Cmya5 UTSW 13 93,090,975 (GRCm38) missense probably benign 0.00
R7088:Cmya5 UTSW 13 93,091,864 (GRCm38) missense possibly damaging 0.95
R7126:Cmya5 UTSW 13 93,089,940 (GRCm38) missense probably benign 0.41
R7177:Cmya5 UTSW 13 93,095,328 (GRCm38) missense probably benign 0.00
R7188:Cmya5 UTSW 13 93,046,038 (GRCm38) missense probably damaging 1.00
R7217:Cmya5 UTSW 13 93,090,430 (GRCm38) missense probably damaging 1.00
R7278:Cmya5 UTSW 13 93,095,700 (GRCm38) missense probably damaging 0.96
R7293:Cmya5 UTSW 13 93,092,797 (GRCm38) missense possibly damaging 0.90
R7332:Cmya5 UTSW 13 93,092,553 (GRCm38) missense possibly damaging 0.60
R7375:Cmya5 UTSW 13 93,091,661 (GRCm38) missense probably damaging 0.97
R7386:Cmya5 UTSW 13 93,069,323 (GRCm38) missense probably damaging 1.00
R7489:Cmya5 UTSW 13 93,091,838 (GRCm38) missense possibly damaging 0.87
R7529:Cmya5 UTSW 13 93,097,434 (GRCm38) missense probably benign 0.02
R7552:Cmya5 UTSW 13 93,069,312 (GRCm38) missense probably benign 0.41
R7624:Cmya5 UTSW 13 93,090,357 (GRCm38) missense possibly damaging 0.79
R7637:Cmya5 UTSW 13 93,083,212 (GRCm38) missense possibly damaging 0.87
R7673:Cmya5 UTSW 13 93,094,121 (GRCm38) missense probably benign 0.13
R7753:Cmya5 UTSW 13 93,098,172 (GRCm38) missense probably benign 0.18
R7757:Cmya5 UTSW 13 93,098,272 (GRCm38) missense possibly damaging 0.53
R7806:Cmya5 UTSW 13 93,094,262 (GRCm38) missense probably benign 0.00
R7825:Cmya5 UTSW 13 93,097,628 (GRCm38) missense possibly damaging 0.53
R7878:Cmya5 UTSW 13 93,089,757 (GRCm38) missense probably damaging 0.98
R7892:Cmya5 UTSW 13 93,096,357 (GRCm38) missense probably damaging 0.96
R7952:Cmya5 UTSW 13 93,097,004 (GRCm38) small deletion probably benign
R8127:Cmya5 UTSW 13 93,094,614 (GRCm38) missense probably damaging 0.99
R8256:Cmya5 UTSW 13 93,093,478 (GRCm38) missense possibly damaging 0.62
R8339:Cmya5 UTSW 13 93,091,634 (GRCm38) nonsense probably null
R8446:Cmya5 UTSW 13 93,093,828 (GRCm38) missense possibly damaging 0.84
R8553:Cmya5 UTSW 13 93,093,796 (GRCm38) missense probably benign 0.00
R8686:Cmya5 UTSW 13 93,095,380 (GRCm38) missense possibly damaging 0.91
R8748:Cmya5 UTSW 13 93,089,721 (GRCm38) missense probably damaging 1.00
R8783:Cmya5 UTSW 13 93,089,380 (GRCm38) missense possibly damaging 0.58
R8803:Cmya5 UTSW 13 93,041,483 (GRCm38) missense probably damaging 1.00
R8810:Cmya5 UTSW 13 93,063,540 (GRCm38) missense possibly damaging 0.47
R8937:Cmya5 UTSW 13 93,096,332 (GRCm38) missense probably benign 0.01
R8985:Cmya5 UTSW 13 93,097,156 (GRCm38) missense possibly damaging 0.73
R9017:Cmya5 UTSW 13 93,092,064 (GRCm38) missense probably benign 0.03
R9087:Cmya5 UTSW 13 93,097,203 (GRCm38) missense possibly damaging 0.72
R9156:Cmya5 UTSW 13 93,097,370 (GRCm38) missense unknown
R9209:Cmya5 UTSW 13 93,090,358 (GRCm38) missense probably benign 0.45
R9222:Cmya5 UTSW 13 93,094,071 (GRCm38) missense probably benign 0.00
R9229:Cmya5 UTSW 13 93,095,668 (GRCm38) missense possibly damaging 0.92
R9382:Cmya5 UTSW 13 93,093,376 (GRCm38) missense probably benign
R9385:Cmya5 UTSW 13 93,094,372 (GRCm38) missense probably damaging 0.99
R9418:Cmya5 UTSW 13 93,089,701 (GRCm38) missense probably benign 0.22
R9452:Cmya5 UTSW 13 93,095,886 (GRCm38) missense probably benign
R9492:Cmya5 UTSW 13 93,041,314 (GRCm38) makesense probably null
R9600:Cmya5 UTSW 13 93,090,096 (GRCm38) missense probably damaging 1.00
R9712:Cmya5 UTSW 13 93,065,373 (GRCm38) critical splice acceptor site probably null
R9742:Cmya5 UTSW 13 93,095,427 (GRCm38) missense possibly damaging 0.89
RF020:Cmya5 UTSW 13 93,069,291 (GRCm38) missense possibly damaging 0.56
X0028:Cmya5 UTSW 13 93,096,687 (GRCm38) missense possibly damaging 0.53
Z1088:Cmya5 UTSW 13 93,063,579 (GRCm38) missense probably benign
Z1176:Cmya5 UTSW 13 93,096,790 (GRCm38) missense unknown
Z1176:Cmya5 UTSW 13 93,063,579 (GRCm38) missense probably benign
Z1177:Cmya5 UTSW 13 93,063,579 (GRCm38) missense probably benign
Predicted Primers PCR Primer
(F):5'- ACCATGGTTGCTGGAATGC -3'
(R):5'- GGGACGTTGCCAAAAGGTTATG -3'

Sequencing Primer
(F):5'- AATGCTTGGTGGCTCCATTC -3'
(R):5'- GATTCATCTATTAGTCTAGAGCCGG -3'
Posted On 2022-01-20