Incidental Mutation 'R1698:Myo9a'
ID 192419
Institutional Source Beutler Lab
Gene Symbol Myo9a
Ensembl Gene ENSMUSG00000039585
Gene Name myosin IXa
Synonyms C130068I12Rik, 4732465J09Rik
MMRRC Submission 039731-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1698 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 59750896-59928866 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 59868181 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 1025 (V1025A)
Ref Sequence ENSEMBL: ENSMUSP00000122852 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000128341] [ENSMUST00000135298] [ENSMUST00000136740]
AlphaFold Q8C170
Predicted Effect probably benign
Transcript: ENSMUST00000128341
AA Change: V1025A

PolyPhen 2 Score 0.044 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000119401
Gene: ENSMUSG00000039585
AA Change: V1025A

DomainStartEndE-ValueType
RA 14 112 5.57e-30 SMART
low complexity region 129 137 N/A INTRINSIC
MYSc 140 1018 N/A SMART
IQ 1019 1041 1.79e1 SMART
IQ 1042 1064 4.11e0 SMART
IQ 1074 1096 1.9e-2 SMART
IQ 1115 1137 1.01e-6 SMART
IQ 1138 1160 8.71e-2 SMART
low complexity region 1161 1173 N/A INTRINSIC
coiled coil region 1265 1285 N/A INTRINSIC
low complexity region 1372 1384 N/A INTRINSIC
coiled coil region 1492 1539 N/A INTRINSIC
Blast:MYSc 1685 1938 6e-89 BLAST
low complexity region 1982 1993 N/A INTRINSIC
C1 2002 2050 2.6e-9 SMART
RhoGAP 2075 2250 3.36e-73 SMART
coiled coil region 2320 2360 N/A INTRINSIC
low complexity region 2419 2438 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000135298
AA Change: V1025A

PolyPhen 2 Score 0.044 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000117432
Gene: ENSMUSG00000039585
AA Change: V1025A

DomainStartEndE-ValueType
RA 14 112 5.57e-30 SMART
low complexity region 129 137 N/A INTRINSIC
MYSc 140 1018 N/A SMART
IQ 1019 1041 1.79e1 SMART
IQ 1042 1064 4.11e0 SMART
IQ 1074 1096 1.9e-2 SMART
IQ 1115 1137 1.01e-6 SMART
IQ 1138 1160 8.71e-2 SMART
low complexity region 1161 1173 N/A INTRINSIC
coiled coil region 1265 1285 N/A INTRINSIC
low complexity region 1372 1384 N/A INTRINSIC
coiled coil region 1492 1539 N/A INTRINSIC
low complexity region 1744 1759 N/A INTRINSIC
low complexity region 2053 2064 N/A INTRINSIC
C1 2073 2121 2.6e-9 SMART
RhoGAP 2146 2321 3.36e-73 SMART
coiled coil region 2391 2431 N/A INTRINSIC
low complexity region 2490 2509 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000136740
AA Change: V1025A

PolyPhen 2 Score 0.054 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000122852
Gene: ENSMUSG00000039585
AA Change: V1025A

DomainStartEndE-ValueType
RA 14 112 5.57e-30 SMART
low complexity region 129 137 N/A INTRINSIC
MYSc 140 1018 N/A SMART
IQ 1019 1041 1.79e1 SMART
IQ 1042 1064 4.11e0 SMART
IQ 1074 1096 1.9e-2 SMART
IQ 1115 1137 1.01e-6 SMART
IQ 1138 1160 8.71e-2 SMART
low complexity region 1161 1173 N/A INTRINSIC
coiled coil region 1265 1285 N/A INTRINSIC
low complexity region 1372 1384 N/A INTRINSIC
coiled coil region 1492 1539 N/A INTRINSIC
low complexity region 1744 1759 N/A INTRINSIC
low complexity region 2053 2064 N/A INTRINSIC
C1 2073 2121 2.6e-9 SMART
RhoGAP 2146 2321 3.36e-73 SMART
coiled coil region 2409 2449 N/A INTRINSIC
low complexity region 2508 2527 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000147364
Predicted Effect noncoding transcript
Transcript: ENSMUST00000215963
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.6%
  • 20x: 93.6%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional non-muscle myosin-9 (MYH9). Unconventional myosins contain the basic domains of conventional myosins and are further distinguished from class members by their tail domains. They function as actin-based molecular motors. Mutations in this gene have been associated with Bardet-Biedl Syndrome. [provided by RefSeq, Dec 2011]
PHENOTYPE: Homozygous KO leads to obstructive hydrocephaly caused by blockage of the third ventricle and the rostral aqueduct caused by developmental failures of their ependymal cells. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 82 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2m A C 6: 121,645,158 (GRCm38) E340A possibly damaging Het
Abca13 A G 11: 9,314,507 (GRCm38) D2963G probably benign Het
Actn3 T C 19: 4,862,207 (GRCm38) D783G possibly damaging Het
Adamtsl2 A G 2: 27,103,127 (GRCm38) E723G possibly damaging Het
Agrn G T 4: 156,166,558 (GRCm38) Q1931K probably benign Het
Ankrd27 G A 7: 35,614,521 (GRCm38) A426T probably benign Het
Atg9b C A 5: 24,388,188 (GRCm38) G406C probably damaging Het
BC005561 C T 5: 104,520,510 (GRCm38) A966V probably benign Het
C1ra A T 6: 124,522,766 (GRCm38) Q637L probably benign Het
Cdhr2 A T 13: 54,719,581 (GRCm38) M438L probably benign Het
Cep350 T C 1: 155,953,358 (GRCm38) I267V possibly damaging Het
Chrna5 A G 9: 55,004,642 (GRCm38) Y138C probably damaging Het
Chst3 T A 10: 60,185,703 (GRCm38) M441L probably benign Het
Cmya5 G A 13: 93,063,519 (GRCm38) P3434S probably benign Het
Cog2 T A 8: 124,525,683 (GRCm38) L42Q probably damaging Het
Cpq A T 15: 33,250,126 (GRCm38) I210F probably benign Het
Crnn C A 3: 93,148,458 (GRCm38) Q184K probably damaging Het
Csnka2ip A T 16: 64,478,059 (GRCm38) Y647* probably null Het
D5Ertd579e C T 5: 36,604,530 (GRCm38) R1331H probably benign Het
Dennd5a C T 7: 109,917,380 (GRCm38) probably null Het
Dync1h1 A G 12: 110,626,992 (GRCm38) Q1231R possibly damaging Het
Erbin T A 13: 103,833,731 (GRCm38) I1126F possibly damaging Het
Fastkd1 T C 2: 69,702,469 (GRCm38) D518G probably benign Het
Gcc1 A G 6: 28,421,111 (GRCm38) L69P possibly damaging Het
Gkn1 T C 6: 87,347,169 (GRCm38) Y119C probably damaging Het
Gmpr T G 13: 45,517,044 (GRCm38) W81G probably benign Het
Gyg T A 3: 20,138,051 (GRCm38) I236F probably benign Het
Hcrtr2 T C 9: 76,246,453 (GRCm38) Y219C probably damaging Het
Hmcn1 G A 1: 150,565,369 (GRCm38) Q5379* probably null Het
Kank1 T C 19: 25,411,317 (GRCm38) C785R probably benign Het
Lrp1b A T 2: 40,851,806 (GRCm38) C3036* probably null Het
Mdga2 T C 12: 66,689,335 (GRCm38) D373G probably damaging Het
Mgat2 A T 12: 69,185,719 (GRCm38) I356F probably benign Het
Miga2 A G 2: 30,377,997 (GRCm38) D346G probably damaging Het
Mprip T A 11: 59,760,258 (GRCm38) L1596Q possibly damaging Het
Mroh2b G A 15: 4,914,140 (GRCm38) R386Q probably benign Het
Mst1r T A 9: 107,919,980 (GRCm38) S1349R probably benign Het
Mtmr3 C T 11: 4,492,825 (GRCm38) R403H possibly damaging Het
Mycbpap G A 11: 94,508,143 (GRCm38) Q460* probably null Het
Ncapd2 C T 6: 125,168,590 (GRCm38) E1365K probably null Het
Nkiras2 C A 11: 100,625,163 (GRCm38) D105E probably damaging Het
Nolc1 T G 19: 46,081,431 (GRCm38) probably null Het
Nos1 T C 5: 117,867,232 (GRCm38) F6L probably benign Het
Olfr1112 G T 2: 87,191,737 (GRCm38) V17L probably benign Het
Olfr1278 T A 2: 111,292,560 (GRCm38) C97* probably null Het
Olfr1369-ps1 C T 13: 21,116,565 (GRCm38) T291I probably benign Het
Olfr218 A T 1: 173,203,371 (GRCm38) N5I probably damaging Het
Olfr325 T C 11: 58,581,251 (GRCm38) Y136H probably damaging Het
Olfr910 T A 9: 38,539,256 (GRCm38) Y120* probably null Het
Pfkm A G 15: 98,128,318 (GRCm38) E598G possibly damaging Het
Phf2 A T 13: 48,807,630 (GRCm38) D861E unknown Het
Polr2a A G 11: 69,739,877 (GRCm38) probably null Het
Popdc2 G A 16: 38,369,491 (GRCm38) V167M probably damaging Het
Ptpn22 T C 3: 103,885,798 (GRCm38) S422P probably benign Het
Rasa2 T C 9: 96,568,375 (GRCm38) K490R possibly damaging Het
Rbfox3 T A 11: 118,495,221 (GRCm38) D286V probably damaging Het
Rdh13 A G 7: 4,427,791 (GRCm38) W223R probably damaging Het
Riok3 T C 18: 12,128,929 (GRCm38) S7P probably benign Het
Rnaseh2b A G 14: 62,353,632 (GRCm38) E144G probably benign Het
Rnf20 C T 4: 49,651,498 (GRCm38) Q655* probably null Het
Rpap2 T C 5: 107,603,550 (GRCm38) Y8H probably damaging Het
Slc5a10 T C 11: 61,709,602 (GRCm38) Y181C probably benign Het
Snd1 G T 6: 28,888,253 (GRCm38) G896* probably null Het
Spast C T 17: 74,356,160 (GRCm38) Q158* probably null Het
Tas2r104 G A 6: 131,685,584 (GRCm38) S54F probably damaging Het
Tcaf2 C T 6: 42,628,017 (GRCm38) W611* probably null Het
Timp4 G A 6: 115,250,403 (GRCm38) probably null Het
Tmem45a G A 16: 56,823,570 (GRCm38) S72L probably benign Het
Tnrc18 T C 5: 142,788,703 (GRCm38) T124A possibly damaging Het
Tns2 C T 15: 102,108,934 (GRCm38) R281C probably damaging Het
Ttn T C 2: 76,942,915 (GRCm38) D2381G probably damaging Het
Uevld T C 7: 46,955,624 (GRCm38) T41A possibly damaging Het
Ugcg C T 4: 59,207,798 (GRCm38) P46S probably benign Het
Unc5d T C 8: 28,696,478 (GRCm38) E527G probably damaging Het
Vmn2r125 C T 4: 156,351,038 (GRCm38) T237I probably benign Het
Vmn2r63 A C 7: 42,933,614 (GRCm38) I59S probably benign Het
Vps72 G A 3: 95,118,695 (GRCm38) S106N probably benign Het
Zan A C 5: 137,409,669 (GRCm38) probably benign Het
Zbtb38 T C 9: 96,685,462 (GRCm38) K1190E probably benign Het
Zc3h6 T C 2: 129,017,358 (GRCm38) V1103A probably benign Het
Zfp407 G A 18: 84,562,157 (GRCm38) T277I probably damaging Het
Zfp804b A G 5: 6,769,509 (GRCm38) S1149P probably damaging Het
Other mutations in Myo9a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00427:Myo9a APN 9 59,843,059 (GRCm38) splice site probably benign
IGL00510:Myo9a APN 9 59,832,181 (GRCm38) splice site probably benign
IGL00710:Myo9a APN 9 59,875,311 (GRCm38) missense probably damaging 1.00
IGL00963:Myo9a APN 9 59,900,372 (GRCm38) missense probably damaging 0.98
IGL01087:Myo9a APN 9 59,790,078 (GRCm38) missense possibly damaging 0.93
IGL01145:Myo9a APN 9 59,855,375 (GRCm38) missense probably benign 0.18
IGL01403:Myo9a APN 9 59,871,563 (GRCm38) missense probably damaging 0.98
IGL01528:Myo9a APN 9 59,779,674 (GRCm38) missense probably damaging 1.00
IGL01608:Myo9a APN 9 59,870,836 (GRCm38) nonsense probably null
IGL01701:Myo9a APN 9 59,884,594 (GRCm38) critical splice donor site probably null
IGL01918:Myo9a APN 9 59,779,702 (GRCm38) missense probably damaging 1.00
IGL02026:Myo9a APN 9 59,905,962 (GRCm38) missense probably damaging 0.99
IGL02139:Myo9a APN 9 59,779,992 (GRCm38) missense probably benign 0.07
IGL02176:Myo9a APN 9 59,870,553 (GRCm38) missense probably benign 0.45
IGL02272:Myo9a APN 9 59,884,600 (GRCm38) splice site probably benign
IGL02283:Myo9a APN 9 59,871,673 (GRCm38) missense probably benign 0.00
IGL02499:Myo9a APN 9 59,815,386 (GRCm38) splice site probably benign
IGL02652:Myo9a APN 9 59,863,928 (GRCm38) missense probably damaging 1.00
IGL02666:Myo9a APN 9 59,924,904 (GRCm38) missense probably benign 0.02
IGL02878:Myo9a APN 9 59,908,300 (GRCm38) critical splice donor site probably null
IGL02982:Myo9a APN 9 59,908,208 (GRCm38) nonsense probably null
IGL03072:Myo9a APN 9 59,809,442 (GRCm38) missense possibly damaging 0.83
IGL03090:Myo9a APN 9 59,894,135 (GRCm38) splice site probably benign
IGL03111:Myo9a APN 9 59,827,243 (GRCm38) missense probably benign 0.19
IGL03389:Myo9a APN 9 59,869,607 (GRCm38) missense probably damaging 1.00
essentials UTSW 9 59,894,866 (GRCm38) missense probably benign 0.09
necessities UTSW 9 59,815,334 (GRCm38) missense probably damaging 1.00
PIT4402001:Myo9a UTSW 9 59,870,436 (GRCm38) missense possibly damaging 0.83
R0013:Myo9a UTSW 9 59,860,206 (GRCm38) splice site probably benign
R0013:Myo9a UTSW 9 59,860,206 (GRCm38) splice site probably benign
R0018:Myo9a UTSW 9 59,871,724 (GRCm38) missense probably benign 0.00
R0018:Myo9a UTSW 9 59,871,724 (GRCm38) missense probably benign 0.00
R0329:Myo9a UTSW 9 59,923,677 (GRCm38) missense probably damaging 1.00
R0423:Myo9a UTSW 9 59,895,336 (GRCm38) missense probably damaging 1.00
R0521:Myo9a UTSW 9 59,894,352 (GRCm38) missense probably damaging 1.00
R0607:Myo9a UTSW 9 59,921,793 (GRCm38) missense probably benign 0.02
R0652:Myo9a UTSW 9 59,871,926 (GRCm38) missense probably benign
R0653:Myo9a UTSW 9 59,924,991 (GRCm38) missense probably damaging 1.00
R0723:Myo9a UTSW 9 59,871,100 (GRCm38) missense probably benign 0.01
R0784:Myo9a UTSW 9 59,896,545 (GRCm38) splice site probably benign
R0842:Myo9a UTSW 9 59,871,067 (GRCm38) missense probably benign 0.02
R1055:Myo9a UTSW 9 59,855,370 (GRCm38) missense probably benign 0.01
R1056:Myo9a UTSW 9 59,832,201 (GRCm38) missense possibly damaging 0.64
R1195:Myo9a UTSW 9 59,895,200 (GRCm38) missense probably damaging 1.00
R1195:Myo9a UTSW 9 59,895,200 (GRCm38) missense probably damaging 1.00
R1195:Myo9a UTSW 9 59,895,200 (GRCm38) missense probably damaging 1.00
R1615:Myo9a UTSW 9 59,788,456 (GRCm38) missense possibly damaging 0.68
R1715:Myo9a UTSW 9 59,832,300 (GRCm38) missense probably damaging 0.99
R1981:Myo9a UTSW 9 59,894,146 (GRCm38) missense probably benign
R2228:Myo9a UTSW 9 59,894,180 (GRCm38) missense probably benign 0.06
R2272:Myo9a UTSW 9 59,815,301 (GRCm38) missense probably damaging 1.00
R2327:Myo9a UTSW 9 59,779,765 (GRCm38) missense probably benign 0.11
R2990:Myo9a UTSW 9 59,924,889 (GRCm38) missense possibly damaging 0.95
R3161:Myo9a UTSW 9 59,832,315 (GRCm38) splice site probably benign
R3721:Myo9a UTSW 9 59,868,180 (GRCm38) missense probably benign
R3928:Myo9a UTSW 9 59,895,283 (GRCm38) missense probably damaging 1.00
R4197:Myo9a UTSW 9 59,894,866 (GRCm38) missense probably benign 0.09
R4212:Myo9a UTSW 9 59,906,066 (GRCm38) nonsense probably null
R4610:Myo9a UTSW 9 59,871,882 (GRCm38) missense probably benign
R4616:Myo9a UTSW 9 59,821,649 (GRCm38) missense probably damaging 1.00
R4621:Myo9a UTSW 9 59,871,072 (GRCm38) missense probably benign 0.00
R4623:Myo9a UTSW 9 59,871,072 (GRCm38) missense probably benign 0.00
R4632:Myo9a UTSW 9 59,869,664 (GRCm38) missense probably benign 0.00
R4657:Myo9a UTSW 9 59,875,416 (GRCm38) critical splice donor site probably null
R4892:Myo9a UTSW 9 59,824,242 (GRCm38) missense probably damaging 0.98
R4897:Myo9a UTSW 9 59,896,517 (GRCm38) missense probably benign 0.07
R4966:Myo9a UTSW 9 59,871,734 (GRCm38) missense probably benign 0.00
R4993:Myo9a UTSW 9 59,861,472 (GRCm38) nonsense probably null
R5160:Myo9a UTSW 9 59,871,802 (GRCm38) missense probably benign 0.24
R5233:Myo9a UTSW 9 59,910,617 (GRCm38) missense probably damaging 1.00
R5271:Myo9a UTSW 9 59,907,382 (GRCm38) missense probably damaging 1.00
R5308:Myo9a UTSW 9 59,863,961 (GRCm38) missense probably damaging 1.00
R5367:Myo9a UTSW 9 59,900,449 (GRCm38) missense probably damaging 0.96
R5432:Myo9a UTSW 9 59,865,670 (GRCm38) missense possibly damaging 0.94
R5459:Myo9a UTSW 9 59,884,520 (GRCm38) missense probably damaging 0.98
R5511:Myo9a UTSW 9 59,780,212 (GRCm38) missense probably damaging 1.00
R5568:Myo9a UTSW 9 59,874,628 (GRCm38) missense probably benign
R5573:Myo9a UTSW 9 59,871,001 (GRCm38) missense probably benign
R5589:Myo9a UTSW 9 59,895,244 (GRCm38) nonsense probably null
R5607:Myo9a UTSW 9 59,863,944 (GRCm38) missense probably damaging 1.00
R5633:Myo9a UTSW 9 59,868,184 (GRCm38) missense possibly damaging 0.60
R5885:Myo9a UTSW 9 59,871,220 (GRCm38) missense probably benign
R6024:Myo9a UTSW 9 59,855,388 (GRCm38) missense possibly damaging 0.68
R6086:Myo9a UTSW 9 59,790,057 (GRCm38) nonsense probably null
R6146:Myo9a UTSW 9 59,871,229 (GRCm38) missense probably benign 0.01
R6194:Myo9a UTSW 9 59,869,750 (GRCm38) missense probably benign 0.00
R6213:Myo9a UTSW 9 59,827,258 (GRCm38) missense probably damaging 1.00
R6368:Myo9a UTSW 9 59,924,948 (GRCm38) missense probably benign 0.01
R6550:Myo9a UTSW 9 59,868,199 (GRCm38) missense probably damaging 1.00
R6612:Myo9a UTSW 9 59,827,196 (GRCm38) missense probably damaging 1.00
R6665:Myo9a UTSW 9 59,871,872 (GRCm38) missense probably benign 0.09
R6951:Myo9a UTSW 9 59,894,768 (GRCm38) missense probably damaging 1.00
R7026:Myo9a UTSW 9 59,815,334 (GRCm38) missense probably damaging 1.00
R7107:Myo9a UTSW 9 59,870,815 (GRCm38) missense probably benign 0.44
R7310:Myo9a UTSW 9 59,871,153 (GRCm38) missense probably benign 0.08
R7473:Myo9a UTSW 9 59,895,244 (GRCm38) missense probably benign 0.31
R7723:Myo9a UTSW 9 59,779,858 (GRCm38) missense probably damaging 1.00
R7823:Myo9a UTSW 9 59,811,950 (GRCm38) missense probably damaging 1.00
R7824:Myo9a UTSW 9 59,860,109 (GRCm38) missense probably damaging 1.00
R7965:Myo9a UTSW 9 59,788,438 (GRCm38) missense probably damaging 1.00
R8031:Myo9a UTSW 9 59,780,091 (GRCm38) missense probably benign 0.33
R8055:Myo9a UTSW 9 59,907,460 (GRCm38) missense probably damaging 1.00
R8071:Myo9a UTSW 9 59,874,648 (GRCm38) missense probably benign
R8250:Myo9a UTSW 9 59,860,109 (GRCm38) missense probably damaging 1.00
R8260:Myo9a UTSW 9 59,910,678 (GRCm38) missense probably benign 0.08
R8355:Myo9a UTSW 9 59,909,847 (GRCm38) missense probably damaging 1.00
R8432:Myo9a UTSW 9 59,780,265 (GRCm38) missense probably damaging 1.00
R8470:Myo9a UTSW 9 59,832,290 (GRCm38) missense probably damaging 1.00
R8528:Myo9a UTSW 9 59,860,140 (GRCm38) missense probably damaging 1.00
R8681:Myo9a UTSW 9 59,868,111 (GRCm38) missense probably benign 0.16
R8690:Myo9a UTSW 9 59,875,374 (GRCm38) missense probably benign
R8793:Myo9a UTSW 9 59,884,567 (GRCm38) missense probably benign 0.03
R8812:Myo9a UTSW 9 59,779,747 (GRCm38) missense probably benign 0.14
R9016:Myo9a UTSW 9 59,868,144 (GRCm38) nonsense probably null
R9026:Myo9a UTSW 9 59,809,474 (GRCm38) missense probably damaging 0.96
R9036:Myo9a UTSW 9 59,780,301 (GRCm38) nonsense probably null
R9130:Myo9a UTSW 9 59,832,231 (GRCm38) missense probably damaging 0.98
R9131:Myo9a UTSW 9 59,861,489 (GRCm38) missense probably damaging 1.00
R9213:Myo9a UTSW 9 59,865,639 (GRCm38) missense probably benign 0.04
R9498:Myo9a UTSW 9 59,827,183 (GRCm38) missense probably damaging 1.00
R9575:Myo9a UTSW 9 59,905,907 (GRCm38) missense probably damaging 1.00
R9651:Myo9a UTSW 9 59,871,481 (GRCm38) missense probably damaging 0.96
R9672:Myo9a UTSW 9 59,780,049 (GRCm38) missense probably benign 0.16
RF018:Myo9a UTSW 9 59,869,586 (GRCm38) missense probably benign 0.00
RF019:Myo9a UTSW 9 59,921,772 (GRCm38) missense probably benign 0.00
Z1176:Myo9a UTSW 9 59,895,259 (GRCm38) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GGTGCTTTGTTTGCATTTCTGCCATTAC -3'
(R):5'- GTCAGACTACTTATCCAAGGACACCTCA -3'

Sequencing Primer
(F):5'- CATGTGTTCTCTGAAAGCTTACCAC -3'
(R):5'- aggagaaaagggtggtaggg -3'
Posted On 2014-05-14