Incidental Mutation 'R3975:Kcnma1'
ID 475184
Institutional Source Beutler Lab
Gene Symbol Kcnma1
Ensembl Gene ENSMUSG00000063142
Gene Name potassium large conductance calcium-activated channel, subfamily M, alpha member 1
Synonyms mSlo1, MaxiK, Slo1, 5730414M22Rik, BK channel alpha subunit, BKCa, Slo
MMRRC Submission 040939-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.802) question?
Stock # R3975 (G1)
Quality Score 132
Status Not validated
Chromosome 14
Chromosomal Location 23289431-24014491 bp(-) (GRCm38)
Type of Mutation critical splice donor site (1 bp from exon)
DNA Base Change (assembly) C to T at 24003747 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000152959 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000145596] [ENSMUST00000188210] [ENSMUST00000188285] [ENSMUST00000188991] [ENSMUST00000190044] [ENSMUST00000190339] [ENSMUST00000190339] [ENSMUST00000190985] [ENSMUST00000223655] [ENSMUST00000223727] [ENSMUST00000223749] [ENSMUST00000224232] [ENSMUST00000224812] [ENSMUST00000225315] [ENSMUST00000224468] [ENSMUST00000225556] [ENSMUST00000224077] [ENSMUST00000225431] [ENSMUST00000224285] [ENSMUST00000225794] [ENSMUST00000224787] [ENSMUST00000225471] [ENSMUST00000226051]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000145596
Predicted Effect probably null
Transcript: ENSMUST00000188210
SMART Domains Protein: ENSMUSP00000141069
Gene: ENSMUSG00000063142

DomainStartEndE-ValueType
low complexity region 4 23 N/A INTRINSIC
transmembrane domain 86 108 N/A INTRINSIC
low complexity region 145 156 N/A INTRINSIC
transmembrane domain 179 198 N/A INTRINSIC
Pfam:Ion_trans 216 387 1.3e-18 PFAM
Pfam:Ion_trans_2 305 393 5.2e-16 PFAM
Pfam:TrkA_N 439 538 7.8e-7 PFAM
Pfam:BK_channel_a 536 634 5e-31 PFAM
low complexity region 988 996 N/A INTRINSIC
low complexity region 1044 1055 N/A INTRINSIC
low complexity region 1158 1184 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000188285
SMART Domains Protein: ENSMUSP00000140275
Gene: ENSMUSG00000063142

DomainStartEndE-ValueType
low complexity region 4 23 N/A INTRINSIC
transmembrane domain 86 108 N/A INTRINSIC
low complexity region 145 156 N/A INTRINSIC
transmembrane domain 179 198 N/A INTRINSIC
Pfam:Ion_trans 216 387 1.3e-18 PFAM
Pfam:Ion_trans_2 305 393 5.4e-16 PFAM
Pfam:TrkA_N 439 538 8e-7 PFAM
Pfam:BK_channel_a 536 634 5.2e-31 PFAM
low complexity region 1019 1027 N/A INTRINSIC
low complexity region 1075 1086 N/A INTRINSIC
low complexity region 1189 1215 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000188991
SMART Domains Protein: ENSMUSP00000140751
Gene: ENSMUSG00000063142

DomainStartEndE-ValueType
low complexity region 4 23 N/A INTRINSIC
transmembrane domain 86 108 N/A INTRINSIC
low complexity region 145 156 N/A INTRINSIC
transmembrane domain 179 198 N/A INTRINSIC
Pfam:Ion_trans 216 387 3.3e-18 PFAM
Pfam:Ion_trans_2 305 393 1.1e-15 PFAM
Pfam:TrkA_N 439 538 3.7e-7 PFAM
Pfam:BK_channel_a 536 634 3.4e-31 PFAM
low complexity region 1015 1023 N/A INTRINSIC
low complexity region 1071 1082 N/A INTRINSIC
low complexity region 1185 1211 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000190044
SMART Domains Protein: ENSMUSP00000140033
Gene: ENSMUSG00000063142

DomainStartEndE-ValueType
low complexity region 4 23 N/A INTRINSIC
transmembrane domain 86 108 N/A INTRINSIC
low complexity region 145 156 N/A INTRINSIC
transmembrane domain 179 198 N/A INTRINSIC
Pfam:Ion_trans 216 387 1.3e-18 PFAM
Pfam:Ion_trans_2 305 393 5.1e-16 PFAM
Pfam:TrkA_N 439 538 7.5e-7 PFAM
Pfam:BK_channel_a 536 634 4.9e-31 PFAM
low complexity region 957 965 N/A INTRINSIC
low complexity region 1013 1024 N/A INTRINSIC
low complexity region 1127 1153 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000190339
SMART Domains Protein: ENSMUSP00000141143
Gene: ENSMUSG00000063142

DomainStartEndE-ValueType
low complexity region 4 23 N/A INTRINSIC
transmembrane domain 86 108 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000190339
SMART Domains Protein: ENSMUSP00000141143
Gene: ENSMUSG00000063142

DomainStartEndE-ValueType
low complexity region 4 23 N/A INTRINSIC
transmembrane domain 86 108 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000190985
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223609
Predicted Effect probably null
Transcript: ENSMUST00000223655
Predicted Effect probably null
Transcript: ENSMUST00000223727
Predicted Effect probably null
Transcript: ENSMUST00000223749
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223837
Predicted Effect probably null
Transcript: ENSMUST00000224025
Predicted Effect probably null
Transcript: ENSMUST00000224232
Predicted Effect probably null
Transcript: ENSMUST00000224812
Predicted Effect probably null
Transcript: ENSMUST00000225315
Predicted Effect probably null
Transcript: ENSMUST00000224468
Predicted Effect probably null
Transcript: ENSMUST00000225556
Predicted Effect probably null
Transcript: ENSMUST00000224077
Predicted Effect probably null
Transcript: ENSMUST00000225431
Predicted Effect probably null
Transcript: ENSMUST00000224285
Predicted Effect probably benign
Transcript: ENSMUST00000225794
Predicted Effect probably null
Transcript: ENSMUST00000224787
Predicted Effect probably null
Transcript: ENSMUST00000225471
Predicted Effect probably benign
Transcript: ENSMUST00000226051
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 93.6%
Validation Efficiency 95% (59/62)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] MaxiK channels are large conductance, voltage and calcium-sensitive potassium channels which are fundamental to the control of smooth muscle tone and neuronal excitability. MaxiK channels can be formed by 2 subunits: the pore-forming alpha subunit, which is the product of this gene, and the modulatory beta subunit. Intracellular calcium regulates the physical association between the alpha and beta subunits. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous inactivation of this gene leads to cerebellar ataxia, Purkinje cell dysfunction, uneven gait patterns, bladder hyperactivity, urinary incontinence, abnormal colonic K+ secretion, and hearing impairment. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam23 T A 1: 63,547,729 (GRCm38) Y416* probably null Het
Akr1b10 G T 6: 34,392,496 (GRCm38) probably null Het
Arap2 G T 5: 62,748,894 (GRCm38) P261T possibly damaging Het
Bckdha C A 7: 25,631,433 (GRCm38) D53Y probably damaging Het
Bfsp2 A G 9: 103,480,072 (GRCm38) V52A probably benign Het
Bola3 T C 6: 83,351,267 (GRCm38) L45P probably benign Het
Cacna2d4 A G 6: 119,278,173 (GRCm38) probably null Het
Ccn6 C G 10: 39,155,098 (GRCm38) C143S probably damaging Het
Ceacam16 C A 7: 19,853,612 (GRCm38) Q410H probably damaging Het
Cenpe A G 3: 135,235,225 (GRCm38) probably null Het
Cenpe T C 3: 135,238,472 (GRCm38) probably null Het
Clca1 A T 3: 145,032,639 (GRCm38) V36D probably damaging Het
Copa T A 1: 172,121,245 (GRCm38) S1155T probably benign Het
Crb2 C A 2: 37,793,668 (GRCm38) P1061T possibly damaging Het
Crot T C 5: 8,977,541 (GRCm38) T264A probably benign Het
Cyp51 C T 5: 4,091,877 (GRCm38) G346S probably damaging Het
Dnah6 A G 6: 73,121,992 (GRCm38) S2027P possibly damaging Het
Fbh1 T C 2: 11,767,210 (GRCm38) H220R possibly damaging Het
Gdf2 T A 14: 33,944,834 (GRCm38) V171D probably damaging Het
Golgb1 T G 16: 36,918,571 (GRCm38) V2424G probably damaging Het
Gpbp1l1 T C 4: 116,570,985 (GRCm38) probably null Het
Gpx6 C A 13: 21,317,658 (GRCm38) S150Y probably damaging Het
Greb1l A G 18: 10,522,247 (GRCm38) N672S possibly damaging Het
Lrba T C 3: 86,351,255 (GRCm38) F1350L probably damaging Het
Nat8f4 A G 6: 85,901,070 (GRCm38) V157A possibly damaging Het
Niban1 T C 1: 151,649,335 (GRCm38) Y164H probably damaging Het
Nt5dc2 T C 14: 31,138,875 (GRCm38) S439P probably damaging Het
Or2ag12 T C 7: 106,677,785 (GRCm38) R234G probably damaging Het
Or2n1 A G 17: 38,175,495 (GRCm38) N137S probably benign Het
Or5t18 G A 2: 86,806,460 (GRCm38) P180S possibly damaging Het
Or8k40 T A 2: 86,754,543 (GRCm38) H65L probably damaging Het
Orm3 A T 4: 63,356,158 (GRCm38) probably null Het
Otof A G 5: 30,370,712 (GRCm38) L1929P probably damaging Het
Pex5l C A 3: 33,015,015 (GRCm38) C111F probably damaging Het
Plcl1 T A 1: 55,698,215 (GRCm38) M905K probably benign Het
Prdm6 T C 18: 53,540,206 (GRCm38) I186T possibly damaging Het
Rara T G 11: 98,970,569 (GRCm38) I236S probably damaging Het
Reln A T 5: 21,995,366 (GRCm38) S1379T possibly damaging Het
Rnps1-ps A T 6: 7,983,149 (GRCm38) noncoding transcript Het
Rp1l1 T A 14: 64,030,309 (GRCm38) Y1115N probably damaging Het
Rpe65 A T 3: 159,604,585 (GRCm38) N135I probably damaging Het
Rps6 A G 4: 86,856,813 (GRCm38) V18A probably benign Het
Scrn3 T C 2: 73,335,777 (GRCm38) S385P possibly damaging Het
Sis T C 3: 72,943,635 (GRCm38) T577A probably damaging Het
Slx1b G A 7: 126,691,807 (GRCm38) L239F probably damaging Het
Smad4 G T 18: 73,677,736 (GRCm38) T59K possibly damaging Het
Smad6 A G 9: 64,020,930 (GRCm38) V32A probably benign Het
Smc6 T A 12: 11,274,074 (GRCm38) F73L probably damaging Het
Sorbs2 T C 8: 45,772,710 (GRCm38) probably null Het
Svbp T A 4: 119,195,893 (GRCm38) F32I probably benign Het
Tap1 C A 17: 34,189,567 (GRCm38) probably benign Het
Tesk1 C T 4: 43,445,786 (GRCm38) P280S possibly damaging Het
Thrb A G 14: 18,033,456 (GRCm38) I406M probably damaging Het
Tsc22d1 T C 14: 76,418,609 (GRCm38) S761P probably damaging Het
Ttn T C 2: 76,876,653 (GRCm38) probably benign Het
Umodl1 C A 17: 30,984,789 (GRCm38) Y525* probably null Het
Vmn2r70 C T 7: 85,559,332 (GRCm38) V646I probably benign Het
Wipf1 C T 2: 73,437,169 (GRCm38) G295D probably benign Het
Zim1 A T 7: 6,677,130 (GRCm38) H511Q probably damaging Het
Other mutations in Kcnma1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01318:Kcnma1 APN 14 23,314,322 (GRCm38) splice site probably benign
IGL01520:Kcnma1 APN 14 23,501,143 (GRCm38) missense possibly damaging 0.94
IGL01977:Kcnma1 APN 14 23,530,299 (GRCm38) splice site probably benign
IGL02140:Kcnma1 APN 14 23,309,045 (GRCm38) missense probably damaging 1.00
IGL02165:Kcnma1 APN 14 23,336,967 (GRCm38) missense possibly damaging 0.93
IGL02186:Kcnma1 APN 14 23,526,813 (GRCm38) missense probably benign 0.28
IGL02268:Kcnma1 APN 14 23,543,076 (GRCm38) missense probably damaging 1.00
IGL02353:Kcnma1 APN 14 23,591,613 (GRCm38) missense probably damaging 1.00
IGL02360:Kcnma1 APN 14 23,591,613 (GRCm38) missense probably damaging 1.00
IGL02491:Kcnma1 APN 14 23,311,689 (GRCm38) missense probably damaging 1.00
IGL02552:Kcnma1 APN 14 23,386,259 (GRCm38) critical splice donor site probably null
IGL02625:Kcnma1 APN 14 23,363,832 (GRCm38) missense probably damaging 1.00
IGL02677:Kcnma1 APN 14 23,463,156 (GRCm38) missense probably damaging 1.00
IGL02706:Kcnma1 APN 14 23,309,154 (GRCm38) missense probably damaging 1.00
G1citation:Kcnma1 UTSW 14 24,003,744 (GRCm38) splice site probably null
PIT4495001:Kcnma1 UTSW 14 23,425,597 (GRCm38) missense probably benign 0.00
PIT4514001:Kcnma1 UTSW 14 23,309,035 (GRCm38) splice site probably null
PIT4576001:Kcnma1 UTSW 14 23,309,035 (GRCm38) splice site probably null
R0071:Kcnma1 UTSW 14 23,526,767 (GRCm38) missense probably damaging 1.00
R0071:Kcnma1 UTSW 14 23,526,767 (GRCm38) missense probably damaging 1.00
R0115:Kcnma1 UTSW 14 23,314,175 (GRCm38) missense probably damaging 1.00
R0172:Kcnma1 UTSW 14 23,803,166 (GRCm38) missense probably damaging 1.00
R0178:Kcnma1 UTSW 14 23,526,767 (GRCm38) missense probably damaging 1.00
R0183:Kcnma1 UTSW 14 23,508,052 (GRCm38) missense probably damaging 1.00
R0240:Kcnma1 UTSW 14 23,494,579 (GRCm38) missense probably damaging 1.00
R0240:Kcnma1 UTSW 14 23,494,579 (GRCm38) missense probably damaging 1.00
R0328:Kcnma1 UTSW 14 23,373,197 (GRCm38) missense probably damaging 1.00
R0501:Kcnma1 UTSW 14 23,311,716 (GRCm38) missense possibly damaging 0.80
R0631:Kcnma1 UTSW 14 23,509,784 (GRCm38) splice site probably benign
R0668:Kcnma1 UTSW 14 23,367,495 (GRCm38) missense probably damaging 1.00
R0811:Kcnma1 UTSW 14 23,300,018 (GRCm38) missense probably damaging 0.96
R0812:Kcnma1 UTSW 14 23,300,018 (GRCm38) missense probably damaging 0.96
R1080:Kcnma1 UTSW 14 23,494,607 (GRCm38) missense probably damaging 1.00
R1419:Kcnma1 UTSW 14 23,367,642 (GRCm38) missense probably damaging 0.99
R1446:Kcnma1 UTSW 14 23,311,724 (GRCm38) missense probably damaging 1.00
R1454:Kcnma1 UTSW 14 23,463,200 (GRCm38) missense probably damaging 1.00
R1651:Kcnma1 UTSW 14 23,314,194 (GRCm38) missense probably damaging 1.00
R1826:Kcnma1 UTSW 14 23,330,929 (GRCm38) missense probably damaging 1.00
R1827:Kcnma1 UTSW 14 23,330,929 (GRCm38) missense probably damaging 1.00
R1828:Kcnma1 UTSW 14 23,330,929 (GRCm38) missense probably damaging 1.00
R1864:Kcnma1 UTSW 14 23,803,162 (GRCm38) missense probably damaging 1.00
R2002:Kcnma1 UTSW 14 23,337,029 (GRCm38) missense probably damaging 0.99
R2140:Kcnma1 UTSW 14 23,314,220 (GRCm38) missense probably damaging 1.00
R2278:Kcnma1 UTSW 14 23,543,083 (GRCm38) nonsense probably null
R2866:Kcnma1 UTSW 14 23,373,207 (GRCm38) missense probably benign 0.16
R2867:Kcnma1 UTSW 14 23,373,207 (GRCm38) missense probably benign 0.16
R2867:Kcnma1 UTSW 14 23,373,207 (GRCm38) missense probably benign 0.16
R2900:Kcnma1 UTSW 14 23,803,160 (GRCm38) missense probably damaging 1.00
R3820:Kcnma1 UTSW 14 23,299,938 (GRCm38) missense possibly damaging 0.66
R3821:Kcnma1 UTSW 14 23,367,611 (GRCm38) missense probably damaging 1.00
R3901:Kcnma1 UTSW 14 23,505,255 (GRCm38) missense probably damaging 0.98
R3976:Kcnma1 UTSW 14 24,003,747 (GRCm38) critical splice donor site probably null
R4352:Kcnma1 UTSW 14 23,311,652 (GRCm38) missense probably damaging 1.00
R4517:Kcnma1 UTSW 14 23,337,029 (GRCm38) missense probably damaging 1.00
R4598:Kcnma1 UTSW 14 23,803,160 (GRCm38) missense probably damaging 1.00
R4604:Kcnma1 UTSW 14 23,309,038 (GRCm38) critical splice donor site probably null
R4743:Kcnma1 UTSW 14 23,803,202 (GRCm38) missense probably damaging 1.00
R4754:Kcnma1 UTSW 14 23,363,836 (GRCm38) missense probably damaging 0.96
R4908:Kcnma1 UTSW 14 23,309,152 (GRCm38) missense probably damaging 0.99
R4960:Kcnma1 UTSW 14 24,004,118 (GRCm38) intron probably benign
R5175:Kcnma1 UTSW 14 23,336,038 (GRCm38) critical splice donor site probably null
R5218:Kcnma1 UTSW 14 23,463,185 (GRCm38) missense probably damaging 0.96
R5435:Kcnma1 UTSW 14 23,528,404 (GRCm38) nonsense probably null
R5705:Kcnma1 UTSW 14 24,003,771 (GRCm38) missense possibly damaging 0.73
R5746:Kcnma1 UTSW 14 23,494,567 (GRCm38) missense probably damaging 1.00
R5780:Kcnma1 UTSW 14 23,386,351 (GRCm38) nonsense probably null
R5793:Kcnma1 UTSW 14 23,309,035 (GRCm38) splice site probably null
R6039:Kcnma1 UTSW 14 23,309,037 (GRCm38) missense probably benign 0.42
R6039:Kcnma1 UTSW 14 23,309,037 (GRCm38) missense probably benign 0.42
R6133:Kcnma1 UTSW 14 24,003,868 (GRCm38) missense probably damaging 0.98
R6271:Kcnma1 UTSW 14 23,509,889 (GRCm38) missense probably damaging 1.00
R6490:Kcnma1 UTSW 14 23,336,097 (GRCm38) missense possibly damaging 0.46
R6704:Kcnma1 UTSW 14 24,002,814 (GRCm38) nonsense probably null
R6822:Kcnma1 UTSW 14 24,003,744 (GRCm38) splice site probably null
R6855:Kcnma1 UTSW 14 23,367,611 (GRCm38) missense probably damaging 1.00
R6920:Kcnma1 UTSW 14 23,526,534 (GRCm38) critical splice donor site probably null
R7017:Kcnma1 UTSW 14 23,494,643 (GRCm38) missense possibly damaging 0.79
R7081:Kcnma1 UTSW 14 23,300,018 (GRCm38) missense probably damaging 0.96
R7113:Kcnma1 UTSW 14 23,463,156 (GRCm38) missense probably damaging 1.00
R7131:Kcnma1 UTSW 14 23,367,494 (GRCm38) missense probably damaging 1.00
R7172:Kcnma1 UTSW 14 23,526,623 (GRCm38) missense probably damaging 1.00
R7207:Kcnma1 UTSW 14 23,309,015 (GRCm38) makesense probably null
R7308:Kcnma1 UTSW 14 23,330,935 (GRCm38) missense probably damaging 0.99
R7371:Kcnma1 UTSW 14 23,494,570 (GRCm38) missense possibly damaging 0.94
R7404:Kcnma1 UTSW 14 24,002,834 (GRCm38) missense unknown
R7560:Kcnma1 UTSW 14 23,530,242 (GRCm38) missense probably benign 0.15
R7693:Kcnma1 UTSW 14 23,367,612 (GRCm38) missense probably damaging 1.00
R7763:Kcnma1 UTSW 14 23,300,006 (GRCm38) missense possibly damaging 0.66
R7809:Kcnma1 UTSW 14 23,373,256 (GRCm38) missense probably benign 0.16
R7832:Kcnma1 UTSW 14 23,390,923 (GRCm38) missense probably benign
R7884:Kcnma1 UTSW 14 23,336,989 (GRCm38) missense probably benign 0.01
R8013:Kcnma1 UTSW 14 23,373,143 (GRCm38) missense probably benign 0.31
R8014:Kcnma1 UTSW 14 23,373,143 (GRCm38) missense probably benign 0.31
R8066:Kcnma1 UTSW 14 23,311,676 (GRCm38) missense probably benign 0.00
R8097:Kcnma1 UTSW 14 23,330,964 (GRCm38) missense probably damaging 1.00
R8154:Kcnma1 UTSW 14 23,311,754 (GRCm38) missense possibly damaging 0.62
R8507:Kcnma1 UTSW 14 23,591,638 (GRCm38) missense probably benign 0.00
R8672:Kcnma1 UTSW 14 23,501,162 (GRCm38) missense probably damaging 1.00
R8677:Kcnma1 UTSW 14 23,386,350 (GRCm38) missense probably benign 0.36
R8725:Kcnma1 UTSW 14 23,386,264 (GRCm38) missense probably benign 0.00
R8727:Kcnma1 UTSW 14 23,386,264 (GRCm38) missense probably benign 0.00
R8827:Kcnma1 UTSW 14 23,367,480 (GRCm38) missense probably damaging 1.00
R8880:Kcnma1 UTSW 14 23,367,650 (GRCm38) missense probably damaging 1.00
R8997:Kcnma1 UTSW 14 23,462,969 (GRCm38) intron probably benign
R9056:Kcnma1 UTSW 14 23,650,146 (GRCm38) missense possibly damaging 0.80
R9346:Kcnma1 UTSW 14 23,650,165 (GRCm38) missense possibly damaging 0.94
R9403:Kcnma1 UTSW 14 23,543,077 (GRCm38) missense probably benign 0.05
R9438:Kcnma1 UTSW 14 23,367,585 (GRCm38) missense probably benign 0.00
R9482:Kcnma1 UTSW 14 23,390,965 (GRCm38) missense probably benign
R9511:Kcnma1 UTSW 14 23,311,725 (GRCm38) missense possibly damaging 0.90
R9649:Kcnma1 UTSW 14 23,451,598 (GRCm38) critical splice donor site probably null
R9663:Kcnma1 UTSW 14 24,003,829 (GRCm38) missense probably benign 0.15
R9673:Kcnma1 UTSW 14 23,508,055 (GRCm38) missense probably benign 0.01
RF001:Kcnma1 UTSW 14 23,311,697 (GRCm38) missense probably damaging 1.00
Predicted Primers
Posted On 2017-04-14