Incidental Mutation 'R6244:Celsr2'
ID 505433
Institutional Source Beutler Lab
Gene Symbol Celsr2
Ensembl Gene ENSMUSG00000068740
Gene Name cadherin, EGF LAG seven-pass G-type receptor 2
Synonyms mfmi1, EGFL2, flamingo
MMRRC Submission 044435-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6244 (G1)
Quality Score 174.009
Status Validated
Chromosome 3
Chromosomal Location 108390851-108415552 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 108393128 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Histidine to Arginine at position 860 (H860R)
Gene Model predicted gene model for transcript(s): [ENSMUST00000090558] [ENSMUST00000090561] [ENSMUST00000102629]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000090558
AA Change: H2872R

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000088046
Gene: ENSMUSG00000068740
AA Change: H2872R

DomainStartEndE-ValueType
signal peptide 1 31 N/A INTRINSIC
low complexity region 35 53 N/A INTRINSIC
CA 203 287 1.36e-26 SMART
CA 311 397 1.33e-29 SMART
CA 421 503 2.59e-27 SMART
CA 527 608 3.33e-30 SMART
CA 632 710 5.18e-18 SMART
CA 734 813 1.08e-29 SMART
CA 837 919 8.08e-29 SMART
low complexity region 920 932 N/A INTRINSIC
CA 943 1021 4.3e-24 SMART
CA 1049 1125 1.87e-1 SMART
low complexity region 1188 1198 N/A INTRINSIC
EGF 1231 1286 1.81e-3 SMART
EGF_CA 1288 1324 2.24e-8 SMART
EGF 1331 1366 6.65e-2 SMART
LamG 1387 1554 8.4e-30 SMART
EGF 1577 1610 8e-5 SMART
LamG 1636 1770 1.56e-24 SMART
EGF 1796 1829 2.35e-2 SMART
EGF 1831 1867 3.88e-3 SMART
TNFR 1908 1943 1.35e-1 SMART
EGF_Lam 1924 1969 9.54e-12 SMART
HormR 1972 2034 1.57e-20 SMART
Pfam:GAIN 2046 2289 3e-62 PFAM
GPS 2315 2368 1.86e-25 SMART
Pfam:7tm_2 2373 2605 1.1e-48 PFAM
low complexity region 2715 2733 N/A INTRINSIC
low complexity region 2857 2873 N/A INTRINSIC
low complexity region 2874 2881 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000090561
SMART Domains Protein: ENSMUSP00000088049
Gene: ENSMUSG00000068744

DomainStartEndE-ValueType
Pfam:GTSE1_N 7 124 4.8e-24 PFAM
low complexity region 131 143 N/A INTRINSIC
low complexity region 222 231 N/A INTRINSIC
low complexity region 300 316 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000102629
SMART Domains Protein: ENSMUSP00000099689
Gene: ENSMUSG00000068744

DomainStartEndE-ValueType
Pfam:GTSE1_N 8 108 2e-12 PFAM
low complexity region 131 143 N/A INTRINSIC
low complexity region 222 231 N/A INTRINSIC
low complexity region 300 316 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000126349
Predicted Effect noncoding transcript
Transcript: ENSMUST00000126935
Predicted Effect noncoding transcript
Transcript: ENSMUST00000130941
Predicted Effect noncoding transcript
Transcript: ENSMUST00000133216
Predicted Effect probably damaging
Transcript: ENSMUST00000147251
AA Change: H860R

PolyPhen 2 Score 0.964 (Sensitivity: 0.78; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000122329
Gene: ENSMUSG00000068740
AA Change: H860R

DomainStartEndE-ValueType
Pfam:GAIN 35 278 5.1e-63 PFAM
GPS 304 357 1.86e-25 SMART
Pfam:7tm_2 362 594 2e-49 PFAM
low complexity region 704 722 N/A INTRINSIC
low complexity region 846 862 N/A INTRINSIC
low complexity region 863 870 N/A INTRINSIC
Meta Mutation Damage Score 0.6329 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.3%
  • 20x: 95.1%
Validation Efficiency 96% (82/85)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the flamingo subfamily, part of the cadherin superfamily. The flamingo subfamily consists of nonclassic-type cadherins; a subpopulation that does not interact with catenins. The flamingo cadherins are located at the plasma membrane and have nine cadherin domains, seven epidermal growth factor-like repeats and two laminin A G-type repeats in their ectodomain. They also have seven transmembrane domains, a characteristic unique to this subfamily. It is postulated that these proteins are receptors involved in contact-mediated communication, with cadherin domains acting as homophilic binding regions and the EGF-like domains involved in cell adhesion and receptor-ligand interactions. The specific function of this particular member has not been determined. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for disruptions in this allele have mild to moderately dilated lateral ventricles in the brain but are otherwise normal. [provided by MGI curators]
Allele List at MGI

All alleles(4) : Targeted, knock-out(1) Targeted, other(3)

Other mutations in this stock
Total: 84 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
6430550D23Rik T C 2: 156,003,230 (GRCm38) H113R possibly damaging Het
Adgrf3 A T 5: 30,197,533 (GRCm38) M499K probably benign Het
Adgrv1 G A 13: 81,106,931 (GRCm38) T211I probably damaging Het
Adss2 C T 1: 177,776,829 (GRCm38) E153K probably benign Het
Ago4 C A 4: 126,511,487 (GRCm38) G431V possibly damaging Het
Araf G T X: 20,860,100 (GRCm38) R601L probably damaging Homo
Atp2b4 T A 1: 133,726,561 (GRCm38) I769F probably damaging Het
Atp9a T C 2: 168,689,352 (GRCm38) probably null Het
Bltp1 T C 3: 36,956,999 (GRCm38) V1782A probably benign Het
Brap C A 5: 121,665,309 (GRCm38) D173E probably benign Het
Brca2 G T 5: 150,566,978 (GRCm38) R3035L probably benign Het
Ccdc8 C A 7: 16,996,251 (GRCm38) P555Q probably benign Het
Ccser2 A G 14: 36,940,718 (GRCm38) S170P probably benign Het
Cenpc1 C A 5: 86,046,385 (GRCm38) R174M probably damaging Het
Cfap57 T G 4: 118,579,410 (GRCm38) I930L probably damaging Het
Cx3cr1 C T 9: 120,051,694 (GRCm38) R214H probably damaging Het
Cyp4f14 T A 17: 32,906,317 (GRCm38) H429L probably benign Het
D5Ertd579e A G 5: 36,615,276 (GRCm38) F592L probably damaging Het
Ddb1 A G 19: 10,625,923 (GRCm38) E865G probably damaging Het
Ddx50 A T 10: 62,621,566 (GRCm38) probably null Het
Dpp6 A G 5: 27,049,628 (GRCm38) T14A probably damaging Het
Echs1 C A 7: 140,113,069 (GRCm38) Q51H possibly damaging Het
Ecm2 A T 13: 49,530,307 (GRCm38) D587V probably damaging Het
Ect2l A T 10: 18,140,397 (GRCm38) Y666N possibly damaging Het
Epha2 G A 4: 141,316,912 (GRCm38) G342S probably benign Het
Fbxo33 C A 12: 59,206,079 (GRCm38) K211N probably benign Het
Fchsd2 A G 7: 101,259,776 (GRCm38) probably null Het
Fen1 A G 19: 10,200,687 (GRCm38) V131A probably damaging Het
Fetub C T 16: 22,932,331 (GRCm38) R143C probably damaging Het
Flnb A G 14: 7,892,092 (GRCm38) E587G probably damaging Het
Foxd3 A G 4: 99,657,240 (GRCm38) T206A possibly damaging Het
Fut1 A G 7: 45,619,306 (GRCm38) E228G possibly damaging Het
Galnt13 T C 2: 54,933,548 (GRCm38) F379L probably damaging Het
Gcnt2 A C 13: 40,861,241 (GRCm38) E296A probably damaging Het
Gm7145 T A 1: 117,986,140 (GRCm38) C251S probably damaging Het
Gpam G A 19: 55,070,985 (GRCm38) P810L probably damaging Het
Il1rl2 T A 1: 40,327,566 (GRCm38) L87M possibly damaging Het
Itgae A G 11: 73,145,601 (GRCm38) S1122G probably damaging Het
Kcnh7 T A 2: 63,182,226 (GRCm38) D46V probably damaging Het
Kcnn3 T G 3: 89,645,523 (GRCm38) Y511* probably null Het
Kdm3b T A 18: 34,793,005 (GRCm38) I66N probably damaging Het
Klk1b27 A T 7: 44,054,550 (GRCm38) H39L probably benign Het
Kmo C T 1: 175,659,695 (GRCm38) T404I possibly damaging Het
Krt222 C T 11: 99,235,058 (GRCm38) probably null Het
Magi3 G C 3: 104,015,697 (GRCm38) H1235D probably benign Het
Mapk8ip1 C A 2: 92,389,244 (GRCm38) G81C probably damaging Het
Med15 G A 16: 17,652,745 (GRCm38) Q583* probably null Het
Mroh2a T C 1: 88,256,754 (GRCm38) V1453A probably benign Het
Myh13 A G 11: 67,362,501 (GRCm38) M1488V probably benign Het
Naip2 A T 13: 100,152,137 (GRCm38) F1193L probably damaging Het
Nop58 T A 1: 59,702,855 (GRCm38) M181K probably damaging Het
Npepps A T 11: 97,213,790 (GRCm38) V796D probably damaging Het
Nr1d1 A G 11: 98,770,537 (GRCm38) F301S probably damaging Het
Nynrin G A 14: 55,868,028 (GRCm38) V832I probably damaging Het
Or13a28 C A 7: 140,638,433 (GRCm38) S244Y probably damaging Het
Or1j14 T A 2: 36,528,341 (GRCm38) C310S probably benign Het
Or2ak7 A T 11: 58,684,004 (GRCm38) T44S possibly damaging Het
Or4e1 T A 14: 52,463,895 (GRCm38) Y38F probably damaging Het
Or8k1 T A 2: 86,217,222 (GRCm38) T163S possibly damaging Het
Phrf1 T A 7: 141,237,673 (GRCm38) C132S probably damaging Het
Plekhn1 T C 4: 156,230,558 (GRCm38) probably null Het
Polr2a G A 11: 69,744,226 (GRCm38) T569M probably damaging Het
Prr29 A G 11: 106,376,632 (GRCm38) probably null Het
Rsf1 CG CGACGGCGGAG 7: 97,579,908 (GRCm38) probably benign Homo
Sc5d T C 9: 42,255,421 (GRCm38) E274G probably benign Het
Serpina1d A T 12: 103,764,828 (GRCm38) probably null Het
Serpinb11 T A 1: 107,372,242 (GRCm38) I106N probably damaging Het
Setd2 G A 9: 110,548,665 (GRCm38) R516K probably damaging Het
Sirt2 G T 7: 28,787,797 (GRCm38) C291F probably damaging Het
Stac3 T C 10: 127,508,175 (GRCm38) V314A probably damaging Het
Stat6 C T 10: 127,657,712 (GRCm38) probably null Het
Strn3 A G 12: 51,610,107 (GRCm38) V712A probably damaging Het
Tmc5 G T 7: 118,634,214 (GRCm38) G84C possibly damaging Het
Tnik C A 3: 28,650,179 (GRCm38) L996I probably damaging Het
Trim30d G T 7: 104,487,610 (GRCm38) T129K probably damaging Het
Triml1 G T 8: 43,138,756 (GRCm38) Y188* probably null Het
Trpc7 A G 13: 56,773,892 (GRCm38) Y760H probably damaging Het
Uaca G A 9: 60,870,044 (GRCm38) R571Q probably damaging Het
Ubash3a A T 17: 31,239,272 (GRCm38) Q575L possibly damaging Het
Usp49 T A 17: 47,672,902 (GRCm38) C61* probably null Het
Vmn2r18 A T 5: 151,584,651 (GRCm38) V336E probably damaging Het
Vwa8 T C 14: 79,086,662 (GRCm38) V1135A probably benign Het
Zcchc4 T C 5: 52,783,161 (GRCm38) V24A probably benign Het
Zfp354c A G 11: 50,814,971 (GRCm38) Y426H probably benign Het
Other mutations in Celsr2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00898:Celsr2 APN 3 108,413,879 (GRCm38) missense possibly damaging 0.49
IGL01020:Celsr2 APN 3 108,403,270 (GRCm38) missense probably damaging 0.99
IGL01420:Celsr2 APN 3 108,393,763 (GRCm38) missense probably benign 0.13
IGL01448:Celsr2 APN 3 108,393,239 (GRCm38) missense probably damaging 0.99
IGL01559:Celsr2 APN 3 108,406,867 (GRCm38) missense possibly damaging 0.75
IGL01674:Celsr2 APN 3 108,414,843 (GRCm38) missense probably damaging 1.00
IGL01863:Celsr2 APN 3 108,394,022 (GRCm38) missense probably benign 0.00
IGL02309:Celsr2 APN 3 108,396,011 (GRCm38) missense probably damaging 1.00
IGL02325:Celsr2 APN 3 108,412,871 (GRCm38) missense probably damaging 1.00
IGL02409:Celsr2 APN 3 108,413,955 (GRCm38) missense probably damaging 1.00
IGL02514:Celsr2 APN 3 108,397,510 (GRCm38) missense probably benign 0.01
IGL02812:Celsr2 APN 3 108,414,113 (GRCm38) missense probably benign 0.25
IGL02894:Celsr2 APN 3 108,395,210 (GRCm38) missense probably damaging 1.00
IGL03281:Celsr2 APN 3 108,412,940 (GRCm38) missense probably damaging 1.00
barrow UTSW 3 108,394,965 (GRCm38) missense possibly damaging 0.92
goldeneye UTSW 3 108,394,919 (GRCm38) missense probably damaging 1.00
1mM(1):Celsr2 UTSW 3 108,400,838 (GRCm38) missense probably benign 0.01
ANU74:Celsr2 UTSW 3 108,412,499 (GRCm38) missense probably damaging 1.00
IGL02799:Celsr2 UTSW 3 108,414,062 (GRCm38) missense probably damaging 1.00
R0011:Celsr2 UTSW 3 108,413,402 (GRCm38) missense probably benign 0.19
R0031:Celsr2 UTSW 3 108,413,063 (GRCm38) missense probably damaging 1.00
R0049:Celsr2 UTSW 3 108,397,254 (GRCm38) missense probably benign 0.12
R0049:Celsr2 UTSW 3 108,397,254 (GRCm38) missense probably benign 0.12
R0090:Celsr2 UTSW 3 108,393,327 (GRCm38) splice site probably benign
R0140:Celsr2 UTSW 3 108,397,933 (GRCm38) missense probably benign 0.00
R0524:Celsr2 UTSW 3 108,401,587 (GRCm38) missense probably damaging 1.00
R0607:Celsr2 UTSW 3 108,403,895 (GRCm38) critical splice donor site probably null
R0662:Celsr2 UTSW 3 108,398,520 (GRCm38) missense probably damaging 0.99
R0690:Celsr2 UTSW 3 108,414,977 (GRCm38) missense probably damaging 1.00
R0691:Celsr2 UTSW 3 108,412,623 (GRCm38) missense probably damaging 1.00
R0710:Celsr2 UTSW 3 108,412,712 (GRCm38) missense probably benign 0.42
R0730:Celsr2 UTSW 3 108,398,606 (GRCm38) missense probably damaging 1.00
R0815:Celsr2 UTSW 3 108,401,301 (GRCm38) missense possibly damaging 0.56
R0848:Celsr2 UTSW 3 108,414,338 (GRCm38) missense probably benign
R0989:Celsr2 UTSW 3 108,403,272 (GRCm38) missense probably benign 0.00
R1185:Celsr2 UTSW 3 108,399,709 (GRCm38) missense possibly damaging 0.95
R1185:Celsr2 UTSW 3 108,399,709 (GRCm38) missense possibly damaging 0.95
R1185:Celsr2 UTSW 3 108,399,709 (GRCm38) missense possibly damaging 0.95
R1469:Celsr2 UTSW 3 108,414,108 (GRCm38) missense probably damaging 1.00
R1469:Celsr2 UTSW 3 108,414,108 (GRCm38) missense probably damaging 1.00
R1474:Celsr2 UTSW 3 108,393,739 (GRCm38) missense possibly damaging 0.91
R1608:Celsr2 UTSW 3 108,402,483 (GRCm38) missense probably damaging 1.00
R1653:Celsr2 UTSW 3 108,413,520 (GRCm38) missense possibly damaging 0.52
R1659:Celsr2 UTSW 3 108,414,095 (GRCm38) missense probably benign
R1689:Celsr2 UTSW 3 108,407,304 (GRCm38) missense possibly damaging 0.63
R1848:Celsr2 UTSW 3 108,401,310 (GRCm38) missense probably benign 0.35
R1859:Celsr2 UTSW 3 108,396,630 (GRCm38) missense probably damaging 1.00
R1918:Celsr2 UTSW 3 108,398,650 (GRCm38) missense probably benign 0.05
R1974:Celsr2 UTSW 3 108,414,214 (GRCm38) missense probably damaging 1.00
R2042:Celsr2 UTSW 3 108,402,495 (GRCm38) missense probably damaging 0.98
R2167:Celsr2 UTSW 3 108,413,193 (GRCm38) missense probably damaging 0.96
R2333:Celsr2 UTSW 3 108,398,605 (GRCm38) missense probably benign 0.16
R2434:Celsr2 UTSW 3 108,404,479 (GRCm38) missense probably damaging 1.00
R2504:Celsr2 UTSW 3 108,413,591 (GRCm38) missense probably benign 0.11
R3420:Celsr2 UTSW 3 108,414,416 (GRCm38) missense probably benign 0.03
R3712:Celsr2 UTSW 3 108,400,839 (GRCm38) missense probably benign
R3723:Celsr2 UTSW 3 108,397,415 (GRCm38) splice site probably benign
R3809:Celsr2 UTSW 3 108,403,239 (GRCm38) missense possibly damaging 0.67
R4018:Celsr2 UTSW 3 108,394,965 (GRCm38) missense possibly damaging 0.92
R4126:Celsr2 UTSW 3 108,402,097 (GRCm38) missense possibly damaging 0.71
R4177:Celsr2 UTSW 3 108,413,978 (GRCm38) missense probably damaging 0.96
R4232:Celsr2 UTSW 3 108,413,772 (GRCm38) missense probably benign 0.02
R4293:Celsr2 UTSW 3 108,393,677 (GRCm38) missense probably benign 0.01
R4458:Celsr2 UTSW 3 108,394,997 (GRCm38) missense probably damaging 0.98
R4621:Celsr2 UTSW 3 108,395,216 (GRCm38) missense possibly damaging 0.86
R4645:Celsr2 UTSW 3 108,395,969 (GRCm38) missense probably damaging 1.00
R4700:Celsr2 UTSW 3 108,397,231 (GRCm38) missense probably benign 0.24
R4732:Celsr2 UTSW 3 108,398,952 (GRCm38) missense probably damaging 0.99
R4733:Celsr2 UTSW 3 108,398,952 (GRCm38) missense probably damaging 0.99
R4901:Celsr2 UTSW 3 108,406,987 (GRCm38) missense possibly damaging 0.81
R4932:Celsr2 UTSW 3 108,402,758 (GRCm38) missense probably damaging 1.00
R4989:Celsr2 UTSW 3 108,412,629 (GRCm38) missense possibly damaging 0.62
R5052:Celsr2 UTSW 3 108,412,358 (GRCm38) missense probably damaging 1.00
R5093:Celsr2 UTSW 3 108,413,373 (GRCm38) missense possibly damaging 0.66
R5114:Celsr2 UTSW 3 108,393,996 (GRCm38) missense probably benign 0.05
R5120:Celsr2 UTSW 3 108,393,120 (GRCm38) missense probably benign 0.02
R5135:Celsr2 UTSW 3 108,398,659 (GRCm38) missense probably damaging 1.00
R5247:Celsr2 UTSW 3 108,397,630 (GRCm38) missense probably benign 0.34
R5381:Celsr2 UTSW 3 108,402,757 (GRCm38) missense probably damaging 1.00
R5412:Celsr2 UTSW 3 108,399,995 (GRCm38) missense probably damaging 1.00
R5445:Celsr2 UTSW 3 108,392,658 (GRCm38) missense probably benign 0.01
R5528:Celsr2 UTSW 3 108,413,294 (GRCm38) missense probably damaging 1.00
R5598:Celsr2 UTSW 3 108,402,803 (GRCm38) missense possibly damaging 0.82
R5652:Celsr2 UTSW 3 108,396,735 (GRCm38) missense probably null 0.49
R5697:Celsr2 UTSW 3 108,403,921 (GRCm38) nonsense probably null
R5718:Celsr2 UTSW 3 108,393,358 (GRCm38) missense probably benign
R5869:Celsr2 UTSW 3 108,413,909 (GRCm38) missense probably damaging 1.00
R5876:Celsr2 UTSW 3 108,413,943 (GRCm38) missense probably damaging 0.96
R6021:Celsr2 UTSW 3 108,401,245 (GRCm38) missense probably benign
R6054:Celsr2 UTSW 3 108,406,963 (GRCm38) missense possibly damaging 0.95
R6313:Celsr2 UTSW 3 108,401,214 (GRCm38) missense probably damaging 0.99
R6322:Celsr2 UTSW 3 108,412,574 (GRCm38) missense probably damaging 1.00
R6555:Celsr2 UTSW 3 108,394,919 (GRCm38) missense probably damaging 1.00
R6682:Celsr2 UTSW 3 108,400,501 (GRCm38) critical splice donor site probably null
R7062:Celsr2 UTSW 3 108,402,510 (GRCm38) missense possibly damaging 0.95
R7110:Celsr2 UTSW 3 108,397,865 (GRCm38) missense probably damaging 1.00
R7139:Celsr2 UTSW 3 108,415,359 (GRCm38) missense unknown
R7326:Celsr2 UTSW 3 108,394,995 (GRCm38) missense possibly damaging 0.85
R7425:Celsr2 UTSW 3 108,402,457 (GRCm38) missense probably damaging 1.00
R7452:Celsr2 UTSW 3 108,413,090 (GRCm38) missense possibly damaging 0.95
R7461:Celsr2 UTSW 3 108,395,640 (GRCm38) missense probably damaging 1.00
R7502:Celsr2 UTSW 3 108,398,902 (GRCm38) missense probably benign 0.00
R7613:Celsr2 UTSW 3 108,395,640 (GRCm38) missense probably damaging 1.00
R7644:Celsr2 UTSW 3 108,413,490 (GRCm38) missense probably damaging 0.99
R7666:Celsr2 UTSW 3 108,398,588 (GRCm38) missense probably benign
R7687:Celsr2 UTSW 3 108,397,769 (GRCm38) missense probably benign 0.27
R7695:Celsr2 UTSW 3 108,402,753 (GRCm38) missense probably damaging 1.00
R8002:Celsr2 UTSW 3 108,403,969 (GRCm38) missense probably damaging 1.00
R8052:Celsr2 UTSW 3 108,412,655 (GRCm38) missense probably damaging 1.00
R8283:Celsr2 UTSW 3 108,396,455 (GRCm38) missense probably damaging 1.00
R8356:Celsr2 UTSW 3 108,413,531 (GRCm38) missense possibly damaging 0.90
R8381:Celsr2 UTSW 3 108,395,636 (GRCm38) missense probably damaging 1.00
R8427:Celsr2 UTSW 3 108,392,633 (GRCm38) makesense probably null
R8435:Celsr2 UTSW 3 108,414,399 (GRCm38) missense probably benign
R8438:Celsr2 UTSW 3 108,393,823 (GRCm38) missense probably damaging 1.00
R8458:Celsr2 UTSW 3 108,398,902 (GRCm38) missense probably benign 0.00
R8460:Celsr2 UTSW 3 108,396,777 (GRCm38) missense possibly damaging 0.84
R8462:Celsr2 UTSW 3 108,412,851 (GRCm38) nonsense probably null
R8479:Celsr2 UTSW 3 108,398,902 (GRCm38) missense probably benign 0.00
R8480:Celsr2 UTSW 3 108,398,902 (GRCm38) missense probably benign 0.00
R8512:Celsr2 UTSW 3 108,413,838 (GRCm38) missense probably damaging 1.00
R8694:Celsr2 UTSW 3 108,406,860 (GRCm38) missense probably damaging 1.00
R8772:Celsr2 UTSW 3 108,397,073 (GRCm38) missense possibly damaging 0.84
R8843:Celsr2 UTSW 3 108,396,127 (GRCm38) splice site probably benign
R8888:Celsr2 UTSW 3 108,413,564 (GRCm38) missense possibly damaging 0.95
R8895:Celsr2 UTSW 3 108,413,564 (GRCm38) missense possibly damaging 0.95
R8917:Celsr2 UTSW 3 108,396,566 (GRCm38) missense probably benign 0.00
R9119:Celsr2 UTSW 3 108,401,972 (GRCm38) missense possibly damaging 0.90
R9169:Celsr2 UTSW 3 108,402,546 (GRCm38) missense probably benign 0.04
R9209:Celsr2 UTSW 3 108,414,033 (GRCm38) missense probably benign 0.02
R9342:Celsr2 UTSW 3 108,413,126 (GRCm38) missense probably damaging 1.00
R9416:Celsr2 UTSW 3 108,414,768 (GRCm38) missense probably damaging 0.96
R9493:Celsr2 UTSW 3 108,393,758 (GRCm38) missense probably damaging 1.00
R9564:Celsr2 UTSW 3 108,414,518 (GRCm38) missense probably damaging 1.00
R9598:Celsr2 UTSW 3 108,415,262 (GRCm38) missense possibly damaging 0.72
R9629:Celsr2 UTSW 3 108,401,599 (GRCm38) missense probably damaging 1.00
R9691:Celsr2 UTSW 3 108,394,235 (GRCm38) missense probably damaging 1.00
X0020:Celsr2 UTSW 3 108,396,110 (GRCm38) missense probably damaging 1.00
X0050:Celsr2 UTSW 3 108,401,272 (GRCm38) missense probably benign 0.09
Z1088:Celsr2 UTSW 3 108,414,117 (GRCm38) missense probably damaging 1.00
Z1176:Celsr2 UTSW 3 108,412,341 (GRCm38) missense probably benign 0.07
Z1176:Celsr2 UTSW 3 108,393,131 (GRCm38) missense probably benign 0.10
Z1177:Celsr2 UTSW 3 108,413,571 (GRCm38) missense probably benign 0.32
Z1177:Celsr2 UTSW 3 108,412,220 (GRCm38) missense probably damaging 1.00
Z1191:Celsr2 UTSW 3 108,414,549 (GRCm38) missense possibly damaging 0.68
Predicted Primers PCR Primer
(F):5'- CTTGGGTTAGCAAGGACCTC -3'
(R):5'- ACAAAGGTGAGTGGAGTCTCTC -3'

Sequencing Primer
(F):5'- TTAGCAAGGACCTCAGGCAG -3'
(R):5'- GGAGTCTCTCCCATCAGCTC -3'
Posted On 2018-02-28