Incidental Mutation 'R7718:Unc13b'
ID 595019
Institutional Source Beutler Lab
Gene Symbol Unc13b
Ensembl Gene ENSMUSG00000028456
Gene Name unc-13 homolog B
Synonyms Munc13-2, Unc13h2
MMRRC Submission 045775-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.262) question?
Stock # R7718 (G1)
Quality Score 225.009
Status Validated
Chromosome 4
Chromosomal Location 43058953-43264871 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 43173854 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Asparagine at position 1561 (Y1561N)
Ref Sequence ENSEMBL: ENSMUSP00000147100 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000079978] [ENSMUST00000107952] [ENSMUST00000107953] [ENSMUST00000163653] [ENSMUST00000207569]
AlphaFold Q9Z1N9
Predicted Effect probably benign
Transcript: ENSMUST00000079978
SMART Domains Protein: ENSMUSP00000078894
Gene: ENSMUSG00000028456

DomainStartEndE-ValueType
C2 3 94 1.2e-9 SMART
low complexity region 179 193 N/A INTRINSIC
low complexity region 292 303 N/A INTRINSIC
low complexity region 322 333 N/A INTRINSIC
C1 478 527 4.21e-18 SMART
C2 601 708 2.07e-22 SMART
DUF1041 917 1021 2.02e-53 SMART
Pfam:Membr_traf_MHD 1262 1404 4.8e-60 PFAM
C2 1438 1544 7.56e-16 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000107952
SMART Domains Protein: ENSMUSP00000103586
Gene: ENSMUSG00000028456

DomainStartEndE-ValueType
C2 3 94 1.2e-9 SMART
low complexity region 191 205 N/A INTRINSIC
low complexity region 304 315 N/A INTRINSIC
low complexity region 334 345 N/A INTRINSIC
C1 490 539 4.21e-18 SMART
C2 613 720 2.07e-22 SMART
DUF1041 929 1033 2.02e-53 SMART
Pfam:Membr_traf_MHD 1274 1416 4.8e-60 PFAM
C2 1450 1556 7.56e-16 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000107953
SMART Domains Protein: ENSMUSP00000103587
Gene: ENSMUSG00000028456

DomainStartEndE-ValueType
C2 3 94 1.2e-9 SMART
low complexity region 179 193 N/A INTRINSIC
low complexity region 292 303 N/A INTRINSIC
low complexity region 322 333 N/A INTRINSIC
C1 478 527 4.21e-18 SMART
C2 601 708 2.07e-22 SMART
DUF1041 917 1021 2.02e-53 SMART
Pfam:Membr_traf_MHD 1263 1403 2.3e-56 PFAM
C2 1457 1563 7.56e-16 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000163653
SMART Domains Protein: ENSMUSP00000128608
Gene: ENSMUSG00000028456

DomainStartEndE-ValueType
C2 3 94 1.2e-9 SMART
low complexity region 191 205 N/A INTRINSIC
low complexity region 304 315 N/A INTRINSIC
low complexity region 334 345 N/A INTRINSIC
C1 490 539 4.21e-18 SMART
C2 613 720 2.07e-22 SMART
DUF1041 929 1032 4.64e-53 SMART
Pfam:Membr_traf_MHD 1273 1415 4.8e-60 PFAM
C2 1449 1555 7.56e-16 SMART
Predicted Effect unknown
Transcript: ENSMUST00000207569
AA Change: Y1561N
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 99% (77/78)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is expressed in the kidney cortical epithelial cells and is upregulated by hyperglycemia. The encoded protein shares a high level of similarity to the rat homolog, and contains 3 C2 domains and a diacylglycerol-binding C1 domain. Hyperglycemia increases the levels of diacylglycerol, which has been shown to induce apoptosis in cells transfected with this gene and thus contribute to the renal cell complications of hyperglycemia. Studies in other species also indicate a role for this protein in the priming step of synaptic vesicle exocytosis. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous mutant mice are grossly phenotypically normal. Mice older than 12 months will exhibit sporadic seizures. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 78 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A430033K04Rik A T 5: 138,646,122 (GRCm39) H669L possibly damaging Het
Abcb1a A T 5: 8,765,788 (GRCm39) N700I probably damaging Het
Abcc6 T C 7: 45,626,816 (GRCm39) K1414E possibly damaging Het
Adcy5 T C 16: 35,100,785 (GRCm39) V779A probably benign Het
Agap2 A G 10: 126,915,734 (GRCm39) S82G possibly damaging Het
Aldh1l1 A G 6: 90,575,305 (GRCm39) N864S probably damaging Het
Ang2 A T 14: 51,433,217 (GRCm39) V55E probably benign Het
Ank2 A G 3: 126,758,662 (GRCm39) M179T possibly damaging Het
Atrnl1 T A 19: 57,728,615 (GRCm39) C1090* probably null Het
Atxn1l A G 8: 110,459,866 (GRCm39) L132P probably damaging Het
Bptf A G 11: 106,972,282 (GRCm39) V862A possibly damaging Het
Capn11 C A 17: 45,954,707 (GRCm39) K143N probably damaging Het
Card6 A G 15: 5,129,269 (GRCm39) V709A possibly damaging Het
Cavin4 C T 4: 48,671,984 (GRCm39) A143V probably benign Het
Cntn5 A G 9: 9,984,133 (GRCm39) I160T probably benign Het
Cyp2c40 T A 19: 39,755,782 (GRCm39) N511Y probably benign Het
Dsc2 A T 18: 20,174,835 (GRCm39) I480N probably damaging Het
Elf2 G T 3: 51,173,385 (GRCm39) probably benign Het
Enoph1 T C 5: 100,210,019 (GRCm39) V133A possibly damaging Het
Ezh2 A T 6: 47,531,125 (GRCm39) D186E probably benign Het
Fcgbpl1 T C 7: 27,846,626 (GRCm39) F1106S probably damaging Het
Gfra1 T C 19: 58,441,889 (GRCm39) D14G possibly damaging Het
Gmip C T 8: 70,270,383 (GRCm39) R698W probably damaging Het
Grk4 A G 5: 34,852,160 (GRCm39) N135D probably benign Het
Hspb6 A G 7: 30,253,772 (GRCm39) D95G probably benign Het
Htatip2 T G 7: 49,420,632 (GRCm39) H159Q possibly damaging Het
Igfn1 T C 1: 135,896,774 (GRCm39) E1264G probably benign Het
Insyn2b T C 11: 34,352,539 (GRCm39) S194P probably benign Het
Katnb1 T A 8: 95,821,836 (GRCm39) V223E possibly damaging Het
Klra6 AGG AG 6: 129,990,315 (GRCm39) probably null Het
Masp2 C T 4: 148,687,204 (GRCm39) R29C probably damaging Het
Mcm3 A T 1: 20,887,498 (GRCm39) C123* probably null Het
Mdn1 T C 4: 32,718,420 (GRCm39) V2225A probably damaging Het
Me1 A G 9: 86,561,953 (GRCm39) L44S probably damaging Het
Mlxip A G 5: 123,583,577 (GRCm39) N380S probably benign Het
Muc21 T C 17: 35,933,728 (GRCm39) T153A unknown Het
Myh14 C T 7: 44,310,464 (GRCm39) V140I probably damaging Het
Myocd A T 11: 65,109,452 (GRCm39) D106E probably damaging Het
Oat T C 7: 132,159,988 (GRCm39) I411V probably benign Het
Or2d2 A T 7: 106,727,925 (GRCm39) V225D probably damaging Het
Or5p59 T C 7: 107,702,855 (GRCm39) V113A probably benign Het
Or8k38 A G 2: 86,488,373 (GRCm39) V143A probably benign Het
Orc2 A T 1: 58,519,476 (GRCm39) H246Q possibly damaging Het
Pank4 A G 4: 155,059,100 (GRCm39) E411G probably damaging Het
Patl2 A T 2: 121,957,255 (GRCm39) probably null Het
Pcdhb15 A G 18: 37,608,216 (GRCm39) N483D probably damaging Het
Pcdhb20 A G 18: 37,638,704 (GRCm39) D410G probably damaging Het
Pdcl2 A G 5: 76,465,846 (GRCm39) C125R probably damaging Het
Peli3 C G 19: 4,984,584 (GRCm39) probably null Het
Pkd1 A G 17: 24,805,474 (GRCm39) D3313G probably benign Het
Plec A C 15: 76,061,639 (GRCm39) M2766R probably damaging Het
Ppargc1a C T 5: 51,655,504 (GRCm39) V99M probably damaging Het
Prr35 T A 17: 26,165,998 (GRCm39) R430* probably null Het
Psg19 G A 7: 18,526,368 (GRCm39) A374V probably benign Het
Psmd7 A T 8: 108,313,261 (GRCm39) F54L possibly damaging Het
Ptbp2 C T 3: 119,514,637 (GRCm39) G397R probably null Het
Ranbp3 A G 17: 57,003,718 (GRCm39) D39G probably damaging Het
Rcor3 T C 1: 191,786,021 (GRCm39) T406A probably benign Het
Rhbdl2 T A 4: 123,718,712 (GRCm39) I222K probably damaging Het
Ripk2 T C 4: 16,151,968 (GRCm39) N197S possibly damaging Het
Rpia A T 6: 70,743,602 (GRCm39) M283K probably damaging Het
Rps6kc1 T C 1: 190,604,022 (GRCm39) D200G probably benign Het
Sipa1l1 A T 12: 82,389,271 (GRCm39) K499M probably damaging Het
Slc5a4b A G 10: 75,906,407 (GRCm39) L404P probably damaging Het
Son AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG 16: 91,457,222 (GRCm39) probably benign Het
Spmip4 G A 6: 50,566,078 (GRCm39) probably null Het
St7 A C 6: 17,854,998 (GRCm39) T312P probably damaging Het
Strbp T C 2: 37,515,294 (GRCm39) E244G probably damaging Het
Tbc1d8 T G 1: 39,416,061 (GRCm39) T871P probably benign Het
Tcp1 T A 17: 13,141,049 (GRCm39) I286N probably damaging Het
Tead3 C A 17: 28,552,491 (GRCm39) V327F probably damaging Het
Tmem132c A T 5: 127,640,504 (GRCm39) T892S probably benign Het
Trmt2a T C 16: 18,068,487 (GRCm39) S65P probably benign Het
Ubp1 A G 9: 113,802,597 (GRCm39) N479S possibly damaging Het
Ubtfl1 A T 9: 18,320,527 (GRCm39) L18F possibly damaging Het
Uevld T G 7: 46,587,804 (GRCm39) M299L probably benign Het
Ylpm1 A G 12: 85,075,896 (GRCm39) K874E probably damaging Het
Zbtb37 G A 1: 160,859,802 (GRCm39) R168W possibly damaging Het
Other mutations in Unc13b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00392:Unc13b APN 4 43,240,285 (GRCm39) missense probably damaging 1.00
IGL00832:Unc13b APN 4 43,258,921 (GRCm39) missense probably damaging 1.00
IGL01111:Unc13b APN 4 43,096,927 (GRCm39) missense possibly damaging 0.76
IGL01115:Unc13b APN 4 43,258,492 (GRCm39) missense probably damaging 1.00
IGL01137:Unc13b APN 4 43,091,291 (GRCm39) missense probably damaging 1.00
IGL01637:Unc13b APN 4 43,241,066 (GRCm39) missense probably damaging 1.00
IGL01789:Unc13b APN 4 43,239,462 (GRCm39) missense probably damaging 1.00
IGL01792:Unc13b APN 4 43,250,218 (GRCm39) missense probably damaging 0.99
IGL01877:Unc13b APN 4 43,249,583 (GRCm39) critical splice donor site probably null
IGL01924:Unc13b APN 4 43,239,385 (GRCm39) nonsense probably null
IGL02087:Unc13b APN 4 43,091,270 (GRCm39) missense probably null 1.00
IGL02197:Unc13b APN 4 43,165,828 (GRCm39) missense probably damaging 0.99
IGL02504:Unc13b APN 4 43,263,031 (GRCm39) missense probably damaging 1.00
IGL02659:Unc13b APN 4 43,235,332 (GRCm39) missense probably damaging 1.00
IGL03031:Unc13b APN 4 43,235,368 (GRCm39) missense probably damaging 1.00
IGL03036:Unc13b APN 4 43,235,249 (GRCm39) missense probably damaging 1.00
IGL03209:Unc13b APN 4 43,239,351 (GRCm39) missense probably damaging 0.99
IGL03352:Unc13b APN 4 43,237,110 (GRCm39) missense possibly damaging 0.90
BB006:Unc13b UTSW 4 43,174,399 (GRCm39) missense unknown
BB016:Unc13b UTSW 4 43,174,399 (GRCm39) missense unknown
G1Funyon:Unc13b UTSW 4 43,263,568 (GRCm39) missense probably benign
P0028:Unc13b UTSW 4 43,256,225 (GRCm39) missense probably damaging 1.00
PIT4585001:Unc13b UTSW 4 43,091,298 (GRCm39) missense probably benign 0.03
R0019:Unc13b UTSW 4 43,096,990 (GRCm39) missense possibly damaging 0.58
R0019:Unc13b UTSW 4 43,096,990 (GRCm39) missense possibly damaging 0.58
R0335:Unc13b UTSW 4 43,236,983 (GRCm39) missense possibly damaging 0.95
R0504:Unc13b UTSW 4 43,263,559 (GRCm39) missense probably damaging 0.99
R0631:Unc13b UTSW 4 43,182,849 (GRCm39) missense possibly damaging 0.47
R0748:Unc13b UTSW 4 43,241,164 (GRCm39) splice site probably benign
R1275:Unc13b UTSW 4 43,235,366 (GRCm39) missense probably damaging 1.00
R1293:Unc13b UTSW 4 43,235,190 (GRCm39) missense probably damaging 1.00
R1434:Unc13b UTSW 4 43,239,385 (GRCm39) nonsense probably null
R1552:Unc13b UTSW 4 43,237,144 (GRCm39) missense probably damaging 0.99
R1591:Unc13b UTSW 4 43,244,747 (GRCm39) missense probably damaging 1.00
R1628:Unc13b UTSW 4 43,263,371 (GRCm39) missense probably damaging 1.00
R1740:Unc13b UTSW 4 43,240,285 (GRCm39) missense probably damaging 1.00
R1839:Unc13b UTSW 4 43,258,308 (GRCm39) splice site probably benign
R2045:Unc13b UTSW 4 43,091,266 (GRCm39) missense probably damaging 1.00
R2191:Unc13b UTSW 4 43,245,566 (GRCm39) nonsense probably null
R2259:Unc13b UTSW 4 43,182,780 (GRCm39) missense possibly damaging 0.87
R2307:Unc13b UTSW 4 43,239,854 (GRCm39) missense probably damaging 0.98
R2317:Unc13b UTSW 4 43,245,514 (GRCm39) missense probably damaging 1.00
R2402:Unc13b UTSW 4 43,095,843 (GRCm39) missense probably benign
R2847:Unc13b UTSW 4 43,180,404 (GRCm39) missense probably benign 0.04
R3414:Unc13b UTSW 4 43,234,658 (GRCm39) splice site probably benign
R3436:Unc13b UTSW 4 43,097,028 (GRCm39) splice site probably benign
R3955:Unc13b UTSW 4 43,256,834 (GRCm39) missense probably damaging 1.00
R3957:Unc13b UTSW 4 43,256,834 (GRCm39) missense probably damaging 1.00
R4015:Unc13b UTSW 4 43,237,801 (GRCm39) missense probably damaging 1.00
R4650:Unc13b UTSW 4 43,261,035 (GRCm39) missense probably damaging 0.97
R4836:Unc13b UTSW 4 43,237,137 (GRCm39) missense probably damaging 1.00
R5041:Unc13b UTSW 4 43,237,836 (GRCm39) missense probably benign 0.41
R5413:Unc13b UTSW 4 43,257,936 (GRCm39) critical splice donor site probably null
R5994:Unc13b UTSW 4 43,172,596 (GRCm39) intron probably benign
R6015:Unc13b UTSW 4 43,177,995 (GRCm39) nonsense probably null
R6090:Unc13b UTSW 4 43,239,306 (GRCm39) missense probably damaging 1.00
R6242:Unc13b UTSW 4 43,165,800 (GRCm39) missense possibly damaging 0.92
R6246:Unc13b UTSW 4 43,216,246 (GRCm39) missense probably benign 0.18
R6427:Unc13b UTSW 4 43,176,966 (GRCm39) unclassified probably benign
R6660:Unc13b UTSW 4 43,177,412 (GRCm39) unclassified probably benign
R6670:Unc13b UTSW 4 43,255,562 (GRCm39) missense probably damaging 0.99
R6753:Unc13b UTSW 4 43,239,331 (GRCm39) missense probably damaging 1.00
R6858:Unc13b UTSW 4 43,165,828 (GRCm39) missense possibly damaging 0.85
R6886:Unc13b UTSW 4 43,170,156 (GRCm39) intron probably benign
R6969:Unc13b UTSW 4 43,263,538 (GRCm39) missense possibly damaging 0.94
R6994:Unc13b UTSW 4 43,173,203 (GRCm39) intron probably benign
R6994:Unc13b UTSW 4 43,171,403 (GRCm39) intron probably benign
R7080:Unc13b UTSW 4 43,171,926 (GRCm39) missense unknown
R7117:Unc13b UTSW 4 43,216,544 (GRCm39) missense probably benign 0.33
R7132:Unc13b UTSW 4 43,215,757 (GRCm39) missense probably benign 0.17
R7181:Unc13b UTSW 4 43,258,893 (GRCm39) missense probably damaging 0.99
R7192:Unc13b UTSW 4 43,258,519 (GRCm39) missense probably damaging 1.00
R7246:Unc13b UTSW 4 43,172,910 (GRCm39) missense unknown
R7342:Unc13b UTSW 4 43,258,703 (GRCm39) missense probably damaging 0.99
R7345:Unc13b UTSW 4 43,173,966 (GRCm39) missense unknown
R7355:Unc13b UTSW 4 43,237,754 (GRCm39) missense probably damaging 1.00
R7391:Unc13b UTSW 4 43,216,459 (GRCm39) missense probably benign 0.03
R7419:Unc13b UTSW 4 43,174,023 (GRCm39) missense unknown
R7424:Unc13b UTSW 4 43,172,235 (GRCm39) missense unknown
R7517:Unc13b UTSW 4 43,215,765 (GRCm39) missense probably benign
R7532:Unc13b UTSW 4 43,249,565 (GRCm39) missense probably benign 0.44
R7564:Unc13b UTSW 4 43,091,258 (GRCm39) missense probably damaging 1.00
R7598:Unc13b UTSW 4 43,263,569 (GRCm39) missense probably benign 0.20
R7604:Unc13b UTSW 4 43,256,776 (GRCm39) missense possibly damaging 0.95
R7604:Unc13b UTSW 4 43,170,102 (GRCm39) missense unknown
R7643:Unc13b UTSW 4 43,216,333 (GRCm39) missense probably benign
R7735:Unc13b UTSW 4 43,165,791 (GRCm39) missense probably damaging 1.00
R7756:Unc13b UTSW 4 43,177,312 (GRCm39) small deletion probably benign
R7757:Unc13b UTSW 4 43,177,341 (GRCm39) small insertion probably benign
R7757:Unc13b UTSW 4 43,177,330 (GRCm39) small insertion probably benign
R7757:Unc13b UTSW 4 43,177,312 (GRCm39) small deletion probably benign
R7758:Unc13b UTSW 4 43,177,344 (GRCm39) small insertion probably benign
R7758:Unc13b UTSW 4 43,177,312 (GRCm39) small insertion probably benign
R7781:Unc13b UTSW 4 43,259,546 (GRCm39) missense possibly damaging 0.87
R7793:Unc13b UTSW 4 43,172,737 (GRCm39) missense unknown
R7858:Unc13b UTSW 4 43,176,285 (GRCm39) missense unknown
R7867:Unc13b UTSW 4 43,232,573 (GRCm39) nonsense probably null
R7897:Unc13b UTSW 4 43,171,860 (GRCm39) missense unknown
R7904:Unc13b UTSW 4 43,217,075 (GRCm39) missense probably benign
R7929:Unc13b UTSW 4 43,174,399 (GRCm39) missense unknown
R7984:Unc13b UTSW 4 43,173,973 (GRCm39) missense unknown
R8069:Unc13b UTSW 4 43,177,597 (GRCm39) missense unknown
R8101:Unc13b UTSW 4 43,239,918 (GRCm39) missense probably benign 0.08
R8246:Unc13b UTSW 4 43,175,954 (GRCm39) missense unknown
R8289:Unc13b UTSW 4 43,172,524 (GRCm39) nonsense probably null
R8301:Unc13b UTSW 4 43,263,568 (GRCm39) missense probably benign
R8397:Unc13b UTSW 4 43,217,290 (GRCm39) missense probably benign 0.12
R8421:Unc13b UTSW 4 43,178,304 (GRCm39) missense unknown
R8738:Unc13b UTSW 4 43,177,564 (GRCm39) missense unknown
R8746:Unc13b UTSW 4 43,176,120 (GRCm39) missense unknown
R8766:Unc13b UTSW 4 43,174,722 (GRCm39) missense unknown
R8825:Unc13b UTSW 4 43,237,683 (GRCm39) splice site probably benign
R8834:Unc13b UTSW 4 43,175,954 (GRCm39) missense unknown
R8862:Unc13b UTSW 4 43,235,207 (GRCm39) missense probably damaging 1.00
R8864:Unc13b UTSW 4 43,174,724 (GRCm39) missense unknown
R8889:Unc13b UTSW 4 43,176,484 (GRCm39) missense unknown
R8892:Unc13b UTSW 4 43,176,484 (GRCm39) missense unknown
R8904:Unc13b UTSW 4 43,178,531 (GRCm39) intron probably benign
R9089:Unc13b UTSW 4 43,095,847 (GRCm39) missense probably damaging 1.00
R9144:Unc13b UTSW 4 43,173,649 (GRCm39) missense unknown
R9149:Unc13b UTSW 4 43,176,186 (GRCm39) missense unknown
R9173:Unc13b UTSW 4 43,177,421 (GRCm39) missense unknown
R9200:Unc13b UTSW 4 43,257,352 (GRCm39) missense possibly damaging 0.50
R9232:Unc13b UTSW 4 43,240,321 (GRCm39) missense probably benign 0.03
R9269:Unc13b UTSW 4 43,171,955 (GRCm39) missense unknown
R9320:Unc13b UTSW 4 43,171,044 (GRCm39) missense unknown
R9335:Unc13b UTSW 4 43,255,551 (GRCm39) missense probably damaging 0.99
R9335:Unc13b UTSW 4 43,216,123 (GRCm39) missense possibly damaging 0.86
R9352:Unc13b UTSW 4 43,177,313 (GRCm39) nonsense probably null
R9352:Unc13b UTSW 4 43,177,312 (GRCm39) small insertion probably benign
R9378:Unc13b UTSW 4 43,173,282 (GRCm39) missense unknown
R9382:Unc13b UTSW 4 43,172,512 (GRCm39) missense unknown
R9569:Unc13b UTSW 4 43,177,312 (GRCm39) small deletion probably benign
R9622:Unc13b UTSW 4 43,172,513 (GRCm39) missense
R9687:Unc13b UTSW 4 43,174,920 (GRCm39) missense unknown
R9704:Unc13b UTSW 4 43,237,102 (GRCm39) missense probably benign 0.31
R9721:Unc13b UTSW 4 43,101,869 (GRCm39) missense probably benign
R9753:Unc13b UTSW 4 43,182,842 (GRCm39) nonsense probably null
RF016:Unc13b UTSW 4 43,177,350 (GRCm39) small insertion probably benign
RF016:Unc13b UTSW 4 43,177,347 (GRCm39) small insertion probably benign
RF041:Unc13b UTSW 4 43,177,338 (GRCm39) small insertion probably benign
RF056:Unc13b UTSW 4 43,177,359 (GRCm39) small insertion probably benign
Z1176:Unc13b UTSW 4 43,177,764 (GRCm39) missense unknown
Z1176:Unc13b UTSW 4 43,177,191 (GRCm39) missense unknown
Z1176:Unc13b UTSW 4 43,171,419 (GRCm39) missense unknown
Z1176:Unc13b UTSW 4 43,261,043 (GRCm39) missense probably benign 0.11
Z1177:Unc13b UTSW 4 43,173,669 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- CCGACTCATGTGGAAATTCTGG -3'
(R):5'- GGCAGAAATAGTGTTGTCATCTAAC -3'

Sequencing Primer
(F):5'- CGACTCATGTGGAAATTCTGGTTATC -3'
(R):5'- CATCTAACATAATGCTTGGGAGAGC -3'
Posted On 2019-11-12