Incidental Mutation 'R7182:Map2'
ID 559017
Institutional Source Beutler Lab
Gene Symbol Map2
Ensembl Gene ENSMUSG00000015222
Gene Name microtubule-associated protein 2
Synonyms G1-397-34, MAP-2, Mtap2, repro4
MMRRC Submission 045234-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.751) question?
Stock # R7182 (G1)
Quality Score 225.009
Status Validated
Chromosome 1
Chromosomal Location 66214432-66481742 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 66451812 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 234 (D234G)
Ref Sequence ENSEMBL: ENSMUSP00000109646 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000024639] [ENSMUST00000077355] [ENSMUST00000114012] [ENSMUST00000114013] [ENSMUST00000114015] [ENSMUST00000114017] [ENSMUST00000114018] [ENSMUST00000145419] [ENSMUST00000172886] [ENSMUST00000173778] [ENSMUST00000173800] [ENSMUST00000173855]
AlphaFold P20357
Predicted Effect probably benign
Transcript: ENSMUST00000024639
SMART Domains Protein: ENSMUSP00000024639
Gene: ENSMUSG00000015222

DomainStartEndE-ValueType
low complexity region 120 141 N/A INTRINSIC
low complexity region 182 196 N/A INTRINSIC
low complexity region 206 222 N/A INTRINSIC
low complexity region 229 251 N/A INTRINSIC
Pfam:Tubulin-binding 300 331 2.1e-18 PFAM
Pfam:Tubulin-binding 332 362 9.1e-20 PFAM
Pfam:Tubulin-binding 363 394 1.7e-17 PFAM
low complexity region 422 435 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000077355
SMART Domains Protein: ENSMUSP00000076577
Gene: ENSMUSG00000015222

DomainStartEndE-ValueType
low complexity region 120 141 N/A INTRINSIC
low complexity region 182 196 N/A INTRINSIC
low complexity region 206 222 N/A INTRINSIC
low complexity region 229 251 N/A INTRINSIC
Pfam:Tubulin-binding 300 331 2.1e-18 PFAM
Pfam:Tubulin-binding 332 362 9.1e-20 PFAM
Pfam:Tubulin-binding 363 394 1.7e-17 PFAM
low complexity region 422 435 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000114012
SMART Domains Protein: ENSMUSP00000109645
Gene: ENSMUSG00000015222

DomainStartEndE-ValueType
low complexity region 133 140 N/A INTRINSIC
low complexity region 181 195 N/A INTRINSIC
low complexity region 205 221 N/A INTRINSIC
low complexity region 228 250 N/A INTRINSIC
Pfam:Tubulin-binding 299 330 2.1e-18 PFAM
Pfam:Tubulin-binding 331 361 9.1e-20 PFAM
Pfam:Tubulin-binding 362 393 1.7e-17 PFAM
low complexity region 421 434 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000114013
AA Change: D234G

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000109646
Gene: ENSMUSG00000015222
AA Change: D234G

DomainStartEndE-ValueType
Pfam:RII_binding_1 86 103 1.2e-5 PFAM
low complexity region 120 141 N/A INTRINSIC
Pfam:MAP2_projctn 376 1510 N/A PFAM
low complexity region 1543 1557 N/A INTRINSIC
low complexity region 1567 1583 N/A INTRINSIC
low complexity region 1590 1612 N/A INTRINSIC
Pfam:Tubulin-binding 1662 1692 1.7e-13 PFAM
Pfam:Tubulin-binding 1693 1723 5.8e-18 PFAM
Pfam:Tubulin-binding 1724 1755 5.9e-18 PFAM
low complexity region 1783 1796 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000114015
SMART Domains Protein: ENSMUSP00000109648
Gene: ENSMUSG00000015222

DomainStartEndE-ValueType
low complexity region 120 141 N/A INTRINSIC
low complexity region 182 196 N/A INTRINSIC
low complexity region 206 222 N/A INTRINSIC
low complexity region 229 251 N/A INTRINSIC
Pfam:Tubulin-binding 300 331 2.1e-18 PFAM
Pfam:Tubulin-binding 332 362 9.1e-20 PFAM
Pfam:Tubulin-binding 363 394 1.7e-17 PFAM
low complexity region 422 435 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000114017
SMART Domains Protein: ENSMUSP00000109650
Gene: ENSMUSG00000015222

DomainStartEndE-ValueType
low complexity region 120 141 N/A INTRINSIC
low complexity region 182 196 N/A INTRINSIC
low complexity region 206 222 N/A INTRINSIC
low complexity region 229 251 N/A INTRINSIC
Pfam:Tubulin-binding 300 331 2.3e-18 PFAM
Pfam:Tubulin-binding 332 362 2.3e-19 PFAM
Pfam:Tubulin-binding 363 393 9.9e-20 PFAM
Pfam:Tubulin-binding 394 425 1.9e-17 PFAM
low complexity region 453 466 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000114018
SMART Domains Protein: ENSMUSP00000109651
Gene: ENSMUSG00000015222

DomainStartEndE-ValueType
low complexity region 120 141 N/A INTRINSIC
low complexity region 182 196 N/A INTRINSIC
low complexity region 206 222 N/A INTRINSIC
low complexity region 229 251 N/A INTRINSIC
Pfam:Tubulin-binding 300 331 2.3e-18 PFAM
Pfam:Tubulin-binding 332 362 2.3e-19 PFAM
Pfam:Tubulin-binding 363 393 9.9e-20 PFAM
Pfam:Tubulin-binding 394 425 1.9e-17 PFAM
low complexity region 453 466 N/A INTRINSIC
Predicted Effect
SMART Domains Protein: ENSMUSP00000117996
Gene: ENSMUSG00000015222
AA Change: D169G

DomainStartEndE-ValueType
Pfam:RII_binding_1 23 40 3.2e-6 PFAM
low complexity region 70 77 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000145419
AA Change: D76G

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000134538
Gene: ENSMUSG00000015222
AA Change: D76G

DomainStartEndE-ValueType
Pfam:MAP2_projctn 218 608 1.7e-250 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000172886
SMART Domains Protein: ENSMUSP00000133446
Gene: ENSMUSG00000015222

DomainStartEndE-ValueType
Pfam:MAP2_projctn 1 107 3.9e-54 PFAM
low complexity region 112 126 N/A INTRINSIC
low complexity region 136 152 N/A INTRINSIC
low complexity region 159 181 N/A INTRINSIC
Pfam:Tubulin-binding 230 261 1.4e-18 PFAM
Pfam:Tubulin-binding 262 292 1.4e-19 PFAM
Pfam:Tubulin-binding 293 323 6e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000173778
SMART Domains Protein: ENSMUSP00000134651
Gene: ENSMUSG00000015222

DomainStartEndE-ValueType
Pfam:MAP2_projctn 1 124 4.8e-84 PFAM
low complexity region 157 171 N/A INTRINSIC
low complexity region 181 197 N/A INTRINSIC
low complexity region 204 226 N/A INTRINSIC
Pfam:Tubulin-binding 275 306 1.6e-18 PFAM
Pfam:Tubulin-binding 307 337 1.6e-19 PFAM
Pfam:Tubulin-binding 338 368 7e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000173800
SMART Domains Protein: ENSMUSP00000134518
Gene: ENSMUSG00000015222

DomainStartEndE-ValueType
Pfam:MAP2_projctn 1 23 2.2e-11 PFAM
low complexity region 55 69 N/A INTRINSIC
low complexity region 79 95 N/A INTRINSIC
low complexity region 102 124 N/A INTRINSIC
Pfam:Tubulin-binding 173 204 8.7e-19 PFAM
Pfam:Tubulin-binding 205 235 3.8e-20 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000173855
AA Change: D316G

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000134471
Gene: ENSMUSG00000015222
AA Change: D316G

DomainStartEndE-ValueType
low complexity region 120 141 N/A INTRINSIC
low complexity region 142 163 N/A INTRINSIC
Pfam:MAP2_projctn 458 565 1.1e-52 PFAM
Meta Mutation Damage Score 0.0799 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.8%
Validation Efficiency 96% (70/73)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that belongs to the microtubule-associated protein family. The proteins of this family are thought to be involved in microtubule assembly, which is an essential step in neurogenesis. The products of similar genes in rat and mouse are neuron-specific cytoskeletal proteins that are enriched in dentrites, implicating a role in determining and stabilizing dentritic shape during neuron development. A number of alternatively spliced variants encoding distinct isoforms have been described. [provided by RefSeq, Jan 2010]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit altered contextual memory. Mice homozygous for another knock-out allele display decreased body weight, altered microtubule density and organization in Purkinje cell dendrites, and reduced dendritic length inhippocampal neurons. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930562C15Rik T C 16: 4,667,578 (GRCm39) V323A unknown Het
AC117241.1 A G 17: 7,620,087 (GRCm39) V158A unknown Het
Acadm A G 3: 153,647,518 (GRCm39) probably null Het
Adcy10 T G 1: 165,371,039 (GRCm39) probably null Het
Aldh6a1 C T 12: 84,488,605 (GRCm39) A94T probably benign Het
Ano2 T A 6: 125,767,256 (GRCm39) L229Q probably damaging Het
Cacna1h C T 17: 25,596,629 (GRCm39) R1828H probably damaging Het
Ccdc33 A T 9: 57,941,456 (GRCm39) probably null Het
Cep112 A C 11: 108,573,670 (GRCm39) D6A probably benign Het
Chd9 T C 8: 91,733,250 (GRCm39) F1373S unknown Het
Cog5 T C 12: 31,735,707 (GRCm39) L158P probably damaging Het
Col6a3 G A 1: 90,731,400 (GRCm39) Q1618* probably null Het
Dlg5 A G 14: 24,294,924 (GRCm39) V3A Het
Dnah7a T A 1: 53,659,620 (GRCm39) probably null Het
Dpp10 A T 1: 123,268,880 (GRCm39) H716Q probably benign Het
Epor A G 9: 21,874,625 (GRCm39) F35L probably benign Het
Ergic1 A T 17: 26,873,856 (GRCm39) Y92F Het
Fam98a G A 17: 75,846,013 (GRCm39) Q273* probably null Het
Fhdc1 G A 3: 84,356,157 (GRCm39) T429I probably damaging Het
Fmnl2 T A 2: 52,997,453 (GRCm39) L468Q unknown Het
Fmnl3 C T 15: 99,219,663 (GRCm39) R695Q probably damaging Het
Gabrg2 T C 11: 41,811,333 (GRCm39) M271V probably damaging Het
Garin4 C T 1: 190,895,548 (GRCm39) R365H probably damaging Het
Gk5 G T 9: 96,001,579 (GRCm39) V26L possibly damaging Het
Gm14412 A C 2: 177,007,408 (GRCm39) N162K probably benign Het
Gm3604 T C 13: 62,519,689 (GRCm39) D22G probably damaging Het
Gm5565 G T 5: 146,094,865 (GRCm39) H294N probably benign Het
Hsf2 T A 10: 57,381,272 (GRCm39) D287E possibly damaging Het
Ift70b A T 2: 75,768,293 (GRCm39) Y153* probably null Het
Impdh2 G A 9: 108,440,407 (GRCm39) R231H possibly damaging Het
Irak3 T C 10: 120,002,416 (GRCm39) H234R probably damaging Het
Lrba GTTCCCTTC GTTC 3: 86,648,765 (GRCm39) probably null Het
Lrch3 T A 16: 32,814,149 (GRCm39) D551E probably benign Het
Manba A T 3: 135,273,274 (GRCm39) N736I probably benign Het
Mdk C A 2: 91,761,197 (GRCm39) K121N unknown Het
Mfn1 T A 3: 32,618,369 (GRCm39) L526Q probably damaging Het
Mfsd2b A G 12: 4,916,157 (GRCm39) probably null Het
Mnat1 G T 12: 73,277,452 (GRCm39) E233* probably null Het
Mtmr4 T C 11: 87,495,431 (GRCm39) probably null Het
Mtrf1 A G 14: 79,660,904 (GRCm39) E432G possibly damaging Het
Muc5b C T 7: 141,396,382 (GRCm39) R165C unknown Het
Naip6 T A 13: 100,452,657 (GRCm39) I135F probably benign Het
Nod2 A G 8: 89,390,460 (GRCm39) T256A probably benign Het
Notch4 T A 17: 34,802,473 (GRCm39) V1298E probably damaging Het
Nudc G T 4: 133,261,776 (GRCm39) D169E possibly damaging Het
Obscn A T 11: 58,925,927 (GRCm39) I5602N probably damaging Het
Or5b114-ps1 G A 19: 13,353,208 (GRCm39) G294E unknown Het
Osbpl10 G A 9: 114,896,319 (GRCm39) D18N probably damaging Het
Pigk G A 3: 152,428,188 (GRCm39) V72I possibly damaging Het
Prl8a6 C T 13: 27,621,153 (GRCm39) E26K probably damaging Het
Prpf8 A G 11: 75,381,553 (GRCm39) Y318C possibly damaging Het
Rab13 A G 3: 90,132,070 (GRCm39) D159G possibly damaging Het
Rgl2 T C 17: 34,153,964 (GRCm39) F457L possibly damaging Het
Ryr2 T C 13: 11,774,643 (GRCm39) H1171R probably benign Het
Scn4a T A 11: 106,221,134 (GRCm39) I842F probably benign Het
Scnm1 A T 3: 95,041,165 (GRCm39) N14K possibly damaging Het
Serinc1 A T 10: 57,400,457 (GRCm39) I137N probably benign Het
Slc30a3 T C 5: 31,244,169 (GRCm39) Q371R probably benign Het
Slc30a3 A C 5: 31,247,014 (GRCm39) M103R probably damaging Het
Slco1a1 A T 6: 141,857,565 (GRCm39) C589S probably damaging Het
Slco1b2 A G 6: 141,602,656 (GRCm39) Y203C probably damaging Het
Spty2d1 A T 7: 46,648,271 (GRCm39) D219E probably benign Het
Svep1 A T 4: 58,043,991 (GRCm39) S3552T probably benign Het
Tmem62 A G 2: 120,835,224 (GRCm39) I516M probably benign Het
Trim61 A T 8: 65,466,266 (GRCm39) S332T probably damaging Het
Trmt10b A C 4: 45,308,520 (GRCm39) T227P probably benign Het
Trpc3 T C 3: 36,709,258 (GRCm39) Q406R probably benign Het
Ush2a A T 1: 188,485,740 (GRCm39) Y2950F probably benign Het
Usp32 C T 11: 84,930,996 (GRCm39) G478D probably benign Het
Wdfy3 A G 5: 102,091,758 (GRCm39) L527P possibly damaging Het
Wdr73 A G 7: 80,543,426 (GRCm39) V163A possibly damaging Het
Other mutations in Map2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01518:Map2 APN 1 66,464,490 (GRCm39) missense probably damaging 1.00
IGL02135:Map2 APN 1 66,419,920 (GRCm39) nonsense probably null
IGL02526:Map2 APN 1 66,419,876 (GRCm39) missense possibly damaging 0.94
Annas UTSW 1 66,472,756 (GRCm39) critical splice donor site probably null
calliope UTSW 1 66,464,457 (GRCm39) missense probably damaging 1.00
carthage UTSW 1 66,453,807 (GRCm39) missense probably damaging 1.00
costas UTSW 1 66,451,812 (GRCm39) missense possibly damaging 0.94
Jacobin UTSW 1 66,438,578 (GRCm39) missense probably damaging 1.00
Nectar UTSW 1 66,454,522 (GRCm39) nonsense probably null
ruby_throat UTSW 1 66,454,043 (GRCm39) missense possibly damaging 0.67
Rufous UTSW 1 66,419,927 (GRCm39) missense probably damaging 1.00
Speckled UTSW 1 66,451,886 (GRCm39) nonsense probably null
Sunbird UTSW 1 66,454,646 (GRCm39) missense probably benign 0.01
swift UTSW 1 66,455,523 (GRCm39) missense probably damaging 1.00
E0370:Map2 UTSW 1 66,455,883 (GRCm39) unclassified probably benign
PIT4362001:Map2 UTSW 1 66,451,677 (GRCm39) missense probably benign 0.05
R0067:Map2 UTSW 1 66,452,322 (GRCm39) missense probably benign 0.04
R0238:Map2 UTSW 1 66,455,265 (GRCm39) missense probably damaging 1.00
R0238:Map2 UTSW 1 66,455,265 (GRCm39) missense probably damaging 1.00
R0239:Map2 UTSW 1 66,455,265 (GRCm39) missense probably damaging 1.00
R0239:Map2 UTSW 1 66,455,265 (GRCm39) missense probably damaging 1.00
R0268:Map2 UTSW 1 66,419,881 (GRCm39) nonsense probably null
R0302:Map2 UTSW 1 66,453,987 (GRCm39) missense probably benign 0.15
R0305:Map2 UTSW 1 66,452,253 (GRCm39) missense probably benign 0.00
R0409:Map2 UTSW 1 66,472,739 (GRCm39) missense probably damaging 1.00
R0561:Map2 UTSW 1 66,464,656 (GRCm39) missense probably damaging 1.00
R0674:Map2 UTSW 1 66,452,361 (GRCm39) missense probably damaging 1.00
R0738:Map2 UTSW 1 66,464,348 (GRCm39) splice site probably benign
R0893:Map2 UTSW 1 66,419,927 (GRCm39) missense probably damaging 1.00
R1305:Map2 UTSW 1 66,464,554 (GRCm39) missense probably damaging 1.00
R1534:Map2 UTSW 1 66,452,339 (GRCm39) missense probably benign 0.33
R1632:Map2 UTSW 1 66,454,245 (GRCm39) missense possibly damaging 0.60
R1682:Map2 UTSW 1 66,454,781 (GRCm39) splice site probably null
R1774:Map2 UTSW 1 66,453,233 (GRCm39) missense probably damaging 1.00
R2014:Map2 UTSW 1 66,455,295 (GRCm39) missense possibly damaging 0.55
R2017:Map2 UTSW 1 66,451,958 (GRCm39) missense probably damaging 1.00
R2050:Map2 UTSW 1 66,453,473 (GRCm39) missense probably damaging 0.98
R2093:Map2 UTSW 1 66,438,599 (GRCm39) missense probably damaging 1.00
R2214:Map2 UTSW 1 66,459,345 (GRCm39) missense probably damaging 0.99
R2284:Map2 UTSW 1 66,453,227 (GRCm39) missense probably damaging 1.00
R3011:Map2 UTSW 1 66,453,771 (GRCm39) missense probably damaging 1.00
R3105:Map2 UTSW 1 66,472,756 (GRCm39) critical splice donor site probably null
R3708:Map2 UTSW 1 66,455,714 (GRCm39) unclassified probably benign
R3709:Map2 UTSW 1 66,455,015 (GRCm39) nonsense probably null
R3729:Map2 UTSW 1 66,451,605 (GRCm39) missense possibly damaging 0.80
R3760:Map2 UTSW 1 66,478,077 (GRCm39) missense probably damaging 1.00
R3788:Map2 UTSW 1 66,456,022 (GRCm39) missense probably damaging 0.99
R3789:Map2 UTSW 1 66,456,022 (GRCm39) missense probably damaging 0.99
R4003:Map2 UTSW 1 66,454,899 (GRCm39) missense probably damaging 1.00
R4120:Map2 UTSW 1 66,455,063 (GRCm39) missense probably damaging 1.00
R4172:Map2 UTSW 1 66,452,759 (GRCm39) missense possibly damaging 0.89
R4198:Map2 UTSW 1 66,464,457 (GRCm39) missense probably damaging 1.00
R4200:Map2 UTSW 1 66,464,457 (GRCm39) missense probably damaging 1.00
R4205:Map2 UTSW 1 66,464,449 (GRCm39) missense probably damaging 1.00
R4613:Map2 UTSW 1 66,464,628 (GRCm39) missense probably damaging 1.00
R4700:Map2 UTSW 1 66,449,796 (GRCm39) missense probably damaging 0.96
R4974:Map2 UTSW 1 66,452,664 (GRCm39) missense probably benign 0.15
R5007:Map2 UTSW 1 66,452,448 (GRCm39) missense possibly damaging 0.86
R5039:Map2 UTSW 1 66,477,955 (GRCm39) missense probably damaging 1.00
R5237:Map2 UTSW 1 66,478,169 (GRCm39) unclassified probably benign
R5313:Map2 UTSW 1 66,464,538 (GRCm39) missense probably damaging 1.00
R5455:Map2 UTSW 1 66,438,550 (GRCm39) missense probably damaging 1.00
R5490:Map2 UTSW 1 66,452,292 (GRCm39) missense probably damaging 1.00
R5517:Map2 UTSW 1 66,454,415 (GRCm39) missense probably benign 0.00
R5532:Map2 UTSW 1 66,453,779 (GRCm39) missense probably damaging 1.00
R5583:Map2 UTSW 1 66,455,196 (GRCm39) missense probably damaging 1.00
R5764:Map2 UTSW 1 66,454,034 (GRCm39) missense probably damaging 0.99
R5996:Map2 UTSW 1 66,454,043 (GRCm39) missense possibly damaging 0.67
R6058:Map2 UTSW 1 66,454,573 (GRCm39) missense probably benign 0.05
R6199:Map2 UTSW 1 66,464,637 (GRCm39) missense probably damaging 1.00
R6208:Map2 UTSW 1 66,470,749 (GRCm39) missense probably damaging 1.00
R6276:Map2 UTSW 1 66,438,578 (GRCm39) missense probably damaging 1.00
R6378:Map2 UTSW 1 66,454,488 (GRCm39) missense probably damaging 1.00
R6424:Map2 UTSW 1 66,453,946 (GRCm39) missense possibly damaging 0.67
R6743:Map2 UTSW 1 66,454,766 (GRCm39) missense probably benign 0.04
R6837:Map2 UTSW 1 66,453,731 (GRCm39) missense probably damaging 1.00
R6901:Map2 UTSW 1 66,460,932 (GRCm39) missense possibly damaging 0.94
R6984:Map2 UTSW 1 66,454,395 (GRCm39) missense possibly damaging 0.90
R6989:Map2 UTSW 1 66,454,065 (GRCm39) missense probably benign 0.00
R7001:Map2 UTSW 1 66,454,646 (GRCm39) missense probably benign 0.01
R7055:Map2 UTSW 1 66,455,983 (GRCm39) missense probably damaging 1.00
R7094:Map2 UTSW 1 66,451,886 (GRCm39) nonsense probably null
R7106:Map2 UTSW 1 66,449,903 (GRCm39) missense possibly damaging 0.92
R7235:Map2 UTSW 1 66,453,807 (GRCm39) missense probably damaging 1.00
R7424:Map2 UTSW 1 66,453,983 (GRCm39) missense possibly damaging 0.69
R7473:Map2 UTSW 1 66,454,617 (GRCm39) missense probably damaging 1.00
R7642:Map2 UTSW 1 66,452,466 (GRCm39) missense probably benign 0.01
R7660:Map2 UTSW 1 66,453,536 (GRCm39) missense probably damaging 1.00
R7673:Map2 UTSW 1 66,452,933 (GRCm39) missense probably benign 0.03
R7768:Map2 UTSW 1 66,453,642 (GRCm39) missense possibly damaging 0.94
R7796:Map2 UTSW 1 66,455,654 (GRCm39) splice site probably null
R7834:Map2 UTSW 1 66,455,647 (GRCm39) missense probably damaging 1.00
R7842:Map2 UTSW 1 66,455,570 (GRCm39) missense probably benign
R7955:Map2 UTSW 1 66,452,875 (GRCm39) missense probably damaging 1.00
R8056:Map2 UTSW 1 66,454,779 (GRCm39) missense probably damaging 0.99
R8118:Map2 UTSW 1 66,464,550 (GRCm39) missense probably damaging 1.00
R8135:Map2 UTSW 1 66,452,828 (GRCm39) missense probably damaging 1.00
R8152:Map2 UTSW 1 66,453,902 (GRCm39) missense probably benign 0.00
R8223:Map2 UTSW 1 66,464,649 (GRCm39) missense probably damaging 1.00
R8329:Map2 UTSW 1 66,454,272 (GRCm39) missense probably benign 0.01
R8344:Map2 UTSW 1 66,460,872 (GRCm39) missense probably damaging 1.00
R8475:Map2 UTSW 1 66,453,164 (GRCm39) missense probably damaging 1.00
R8548:Map2 UTSW 1 66,452,499 (GRCm39) missense probably damaging 1.00
R8680:Map2 UTSW 1 66,460,872 (GRCm39) missense probably damaging 1.00
R8713:Map2 UTSW 1 66,453,781 (GRCm39) missense probably damaging 1.00
R8745:Map2 UTSW 1 66,452,556 (GRCm39) missense probably benign 0.00
R8786:Map2 UTSW 1 66,472,755 (GRCm39) critical splice donor site probably benign
R8790:Map2 UTSW 1 66,477,997 (GRCm39) missense probably damaging 1.00
R8874:Map2 UTSW 1 66,455,523 (GRCm39) missense probably damaging 1.00
R8887:Map2 UTSW 1 66,454,758 (GRCm39) missense possibly damaging 0.48
R8948:Map2 UTSW 1 66,419,684 (GRCm39) missense probably damaging 1.00
R8950:Map2 UTSW 1 66,419,684 (GRCm39) missense probably damaging 1.00
R8998:Map2 UTSW 1 66,452,473 (GRCm39) missense possibly damaging 0.91
R8999:Map2 UTSW 1 66,452,473 (GRCm39) missense possibly damaging 0.91
R9072:Map2 UTSW 1 66,453,312 (GRCm39) missense probably damaging 1.00
R9088:Map2 UTSW 1 66,453,773 (GRCm39) missense probably damaging 1.00
R9089:Map2 UTSW 1 66,452,098 (GRCm39) missense probably benign 0.09
R9106:Map2 UTSW 1 66,454,522 (GRCm39) nonsense probably null
R9112:Map2 UTSW 1 66,472,723 (GRCm39) nonsense probably null
R9120:Map2 UTSW 1 66,453,218 (GRCm39) missense probably damaging 1.00
R9161:Map2 UTSW 1 66,477,503 (GRCm39) missense possibly damaging 0.65
R9464:Map2 UTSW 1 66,454,497 (GRCm39) missense probably damaging 1.00
R9589:Map2 UTSW 1 66,449,753 (GRCm39) missense probably benign
V8831:Map2 UTSW 1 66,455,004 (GRCm39) missense probably damaging 1.00
Z1177:Map2 UTSW 1 66,477,520 (GRCm39) missense probably damaging 0.96
Z1177:Map2 UTSW 1 66,419,839 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- TCGCTGAGCCTTTAGACAAG -3'
(R):5'- AGAGTCAAACTGCTTCCCTTCC -3'

Sequencing Primer
(F):5'- GGGAGAAATGGAGTTTAAGATGCC -3'
(R):5'- ATCTTGGGATATCCTCTAGCACATC -3'
Posted On 2019-06-26