Incidental Mutation 'RF020:Celsr3'
ID 603819
Institutional Source Beutler Lab
Gene Symbol Celsr3
Ensembl Gene ENSMUSG00000023473
Gene Name cadherin, EGF LAG seven-pass G-type receptor 3
Synonyms Fmi1, flamingo
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # RF020 (G1)
Quality Score 225.009
Status Not validated
Chromosome 9
Chromosomal Location 108826320-108852969 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) C to T at 108849057 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Arginine to Cysteine at position 3162 (R3162C)
Ref Sequence ENSEMBL: ENSMUSP00000150759 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000024238] [ENSMUST00000098376] [ENSMUST00000192507] [ENSMUST00000192559] [ENSMUST00000193291] [ENSMUST00000194079] [ENSMUST00000213524]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000024238
AA Change: R3154C

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000024238
Gene: ENSMUSG00000023473
AA Change: R3154C

DomainStartEndE-ValueType
signal peptide 1 31 N/A INTRINSIC
low complexity region 264 293 N/A INTRINSIC
CA 338 422 2.25e-27 SMART
CA 446 534 5.05e-30 SMART
CA 558 640 7.6e-25 SMART
CA 664 745 7.36e-32 SMART
CA 769 847 5.95e-18 SMART
CA 871 950 5.25e-28 SMART
CA 974 1056 2.67e-29 SMART
CA 1080 1158 1.18e-21 SMART
CA 1186 1262 3.2e-1 SMART
low complexity region 1328 1335 N/A INTRINSIC
low complexity region 1350 1360 N/A INTRINSIC
EGF 1369 1424 1.02e-2 SMART
EGF 1429 1464 3.23e0 SMART
EGF 1467 1503 8.78e-2 SMART
LamG 1524 1691 2.27e-35 SMART
EGF 1714 1747 4.22e-4 SMART
LamG 1774 1913 9.02e-21 SMART
EGF 1938 1971 2.43e-4 SMART
EGF 1973 2009 1.3e-4 SMART
EGF_Lam 2066 2111 5.08e-7 SMART
HormR 2114 2176 3.42e-21 SMART
Pfam:GAIN 2188 2441 1.1e-57 PFAM
GPS 2467 2520 7.92e-20 SMART
Pfam:7tm_2 2527 2758 1.5e-56 PFAM
low complexity region 2813 2829 N/A INTRINSIC
low complexity region 2882 2906 N/A INTRINSIC
low complexity region 3058 3072 N/A INTRINSIC
low complexity region 3149 3189 N/A INTRINSIC
low complexity region 3239 3261 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000098376
SMART Domains Protein: ENSMUSP00000095979
Gene: ENSMUSG00000023259

DomainStartEndE-ValueType
Pfam:Sulfate_transp 69 458 4.4e-113 PFAM
low complexity region 471 484 N/A INTRINSIC
PDB:3LLO|A 489 546 2e-16 PDB
low complexity region 554 593 N/A INTRINSIC
low complexity region 638 650 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000192507
SMART Domains Protein: ENSMUSP00000141336
Gene: ENSMUSG00000023259

DomainStartEndE-ValueType
Pfam:Sulfate_tra_GLY 54 137 4.1e-33 PFAM
Pfam:Sulfate_transp 176 454 1.9e-67 PFAM
low complexity region 471 484 N/A INTRINSIC
PDB:3LLO|A 489 546 6e-16 PDB
low complexity region 554 593 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000192559
SMART Domains Protein: ENSMUSP00000141632
Gene: ENSMUSG00000023259

DomainStartEndE-ValueType
Pfam:Sulfate_tra_GLY 54 137 7.7e-34 PFAM
Pfam:Sulfate_transp 176 225 1.8e-5 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000193291
SMART Domains Protein: ENSMUSP00000142250
Gene: ENSMUSG00000023259

DomainStartEndE-ValueType
Pfam:Sulfate_tra_GLY 54 137 4.1e-33 PFAM
Pfam:Sulfate_transp 176 454 1.9e-67 PFAM
low complexity region 471 484 N/A INTRINSIC
PDB:3LLO|A 489 546 6e-16 PDB
low complexity region 554 593 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000194079
SMART Domains Protein: ENSMUSP00000141789
Gene: ENSMUSG00000023473

DomainStartEndE-ValueType
Pfam:7tm_2 1 185 6.9e-45 PFAM
low complexity region 240 256 N/A INTRINSIC
low complexity region 309 333 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000213524
AA Change: R3162C

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 99.7%
  • 10x: 99.3%
  • 20x: 98.5%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene belongs to the flamingo subfamily, which is included in the cadherin superfamily. The flamingo cadherins consist of nonclassic-type cadherins that do not interact with catenins. They are plasma membrane proteins containing seven epidermal growth factor-like repeats, nine cadherin domains and two laminin A G-type repeats in their ectodomain. They also have seven transmembrane domains, a characteristic feature of their subfamily. The encoded protein may be involved in the regulation of contact-dependent neurite growth and may play a role in tumor formation. [provided by RefSeq, Jun 2013]
PHENOTYPE: Mice homozygous for a null allele exhibit neonatal lethality, abnormal neurvous system development, and abnormal respiratory system development. [provided by MGI curators]
Allele List at MGI

All alleles(4) : Targeted, knock-out(2) Targeted, other(2)

Other mutations in this stock
Total: 90 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 A G 7: 120,533,657 (GRCm38) K1270E possibly damaging Het
Adgrb2 T C 4: 130,010,084 (GRCm38) S668P probably damaging Het
Ahdc1 T G 4: 133,064,277 (GRCm38) L943R possibly damaging Het
Ank2 T C 3: 126,945,476 (GRCm38) K2253R unknown Het
Arhgap23 T C 11: 97,463,561 (GRCm38) S767P probably damaging Het
Arhgef12 A G 9: 42,989,989 (GRCm38) I839T possibly damaging Het
Begain CGCCGC CGCCGCGGCCGC 12: 109,033,424 (GRCm38) probably benign Het
Btbd19 A T 4: 117,122,275 (GRCm38) C116S probably damaging Het
Cbr1 C T 16: 93,610,179 (GRCm38) A261V probably benign Het
Ccdc137 A G 11: 120,458,196 (GRCm38) R18G probably benign Het
Cdsn AG AGACAGGAAGTAGTAGCTCTCAG 17: 35,554,979 (GRCm38) probably benign Het
Cep350 A T 1: 155,915,478 (GRCm38) V1300E probably benign Het
Cluh G GCCAGAT 11: 74,669,538 (GRCm38) probably benign Het
Cmya5 G T 13: 93,069,291 (GRCm38) Q3357K possibly damaging Het
Col6a2 T G 10: 76,606,209 (GRCm38) probably null Het
Cyp2j9 T A 4: 96,577,652 (GRCm38) T315S probably damaging Het
Cyp3a13 CATTATT CATT 5: 137,894,263 (GRCm38) probably null Het
Dnah6 T A 6: 73,118,057 (GRCm38) Y2181F probably benign Het
Dnah7b A G 1: 46,373,261 (GRCm38) D4010G possibly damaging Het
E4f1 CCG CCGACG 17: 24,455,195 (GRCm38) probably benign Het
Ep300 A T 15: 81,586,571 (GRCm38) probably benign Het
Fam234a A G 17: 26,218,751 (GRCm38) V90A probably benign Het
Fam71e1 GGA GGAAGGGTGGATCCTGGATACCTGGGTCTGAGGGAAGA 7: 44,500,535 (GRCm38) probably null Het
Gab3 TCT TCTGCT X: 75,000,017 (GRCm38) probably benign Het
Gal3st1 A G 11: 3,998,153 (GRCm38) Y120C possibly damaging Het
Gm5475 GTGGAAGGAAAGGT G 15: 100,427,149 (GRCm38) probably null Het
Gm6665 T TC 18: 31,820,377 (GRCm38) probably null Het
Hdlbp T C 1: 93,440,734 (GRCm38) T8A probably benign Het
Hnrnpa2b1 T A 6: 51,466,694 (GRCm38) K92N probably damaging Het
Hsdl2 GGAGCAGCCACAGCTGCAGGAGAAGCCACAGCTGCAGGAGCAGCCACAGC GGAGCAGCCACAGCTGCAGGAGCAGCCACAGCTGCAGGAGAAGCCACAGCTGCAGGAGCAGCCACAGC 4: 59,610,640 (GRCm38) probably benign Het
Klhl10 C G 11: 100,442,070 (GRCm38) Q14E probably benign Het
Klra2 GAAAGAAATCCA GAAAGAAATCCAAAGAAATCCA 6: 131,221,838 (GRCm38) probably null Het
Kmt2b CC CCTCCTGC 7: 30,586,382 (GRCm38) probably benign Het
Krt2 A G 15: 101,817,968 (GRCm38) I45T unknown Het
Ksr2 T C 5: 117,555,218 (GRCm38) S244P probably benign Het
Lama5 A T 2: 180,196,178 (GRCm38) M915K probably benign Het
Lrp1b A C 2: 41,770,846 (GRCm38) H197Q Het
Lrrc1 T C 9: 77,452,631 (GRCm38) E293G probably damaging Het
Med12l AACA AACAACA 3: 59,275,958 (GRCm38) probably benign Het
Mgam T A 6: 40,685,309 (GRCm38) Y1179N probably damaging Het
Mgat4c A G 10: 102,389,067 (GRCm38) I381V probably benign Het
Mrgprx1 A AGAC 7: 48,021,511 (GRCm38) probably benign Het
Myc A T 15: 61,985,823 (GRCm38) probably benign Het
Nipbl A G 15: 8,358,934 (GRCm38) S401P probably damaging Het
Nlrp9c A T 7: 26,385,224 (GRCm38) I310N probably benign Het
Nwd2 C A 5: 63,805,723 (GRCm38) Y883* probably null Het
Oas1e T A 5: 120,794,318 (GRCm38) T87S possibly damaging Het
Olfr586 A T 7: 103,121,891 (GRCm38) C294S probably benign Het
Olfr653 A G 7: 104,580,290 (GRCm38) M215V probably benign Het
Olfr885 G A 9: 38,061,324 (GRCm38) M1I probably null Het
Olfr964-ps1 GA GATACA 9: 39,686,753 (GRCm38) probably null Het
Pappa T G 4: 65,205,045 (GRCm38) S872R possibly damaging Het
Parp4 T C 14: 56,647,349 (GRCm38) L1295P unknown Het
Pcdh15 A T 10: 74,185,410 (GRCm38) Y152F probably damaging Het
Pdk1 A T 2: 71,883,896 (GRCm38) I217L possibly damaging Het
Phldb1 A C 9: 44,697,946 (GRCm38) C450W probably damaging Het
Pnmal1 C CCATGATGCACCTGCTTCAACATCA 7: 16,961,451 (GRCm38) probably benign Het
Prl2c5 G A 13: 13,185,912 (GRCm38) G55S probably benign Het
Psme2b A T 11: 48,945,570 (GRCm38) H183Q probably damaging Het
Ptms CCTCCTC CCTCCTCCTC 6: 124,914,449 (GRCm38) probably benign Het
Rln3 T C 8: 84,043,302 (GRCm38) T73A probably benign Het
Rprd1a T A 18: 24,530,005 (GRCm38) Q21L probably damaging Het
Sept3 A T 15: 82,284,461 (GRCm38) D155V probably damaging Het
Sh3rf3 T A 10: 58,813,768 (GRCm38) V65E probably damaging Het
Shank3 A G 15: 89,500,390 (GRCm38) N155S probably benign Het
Shox2 G T 3: 66,973,813 (GRCm38) P278Q probably damaging Het
Slc1a1 T C 19: 28,879,155 (GRCm38) probably null Het
Slc39a10 A T 1: 46,810,015 (GRCm38) F814I probably damaging Het
Slc5a1 T C 5: 33,133,429 (GRCm38) I119T probably damaging Het
Slc6a13 T C 6: 121,324,351 (GRCm38) probably null Het
Spta1 A G 1: 174,213,444 (GRCm38) D1270G probably benign Het
Spta1 T A 1: 174,217,903 (GRCm38) F1542L probably damaging Het
Tacc3 T A 5: 33,661,224 (GRCm38) M1K probably null Het
Tax1bp1 T C 6: 52,721,354 (GRCm38) V17A probably damaging Het
Thegl CAGCGATCCTCCCCAGTCCCGCAAGGC CAGCGATCCTCCCCAGTCCCGCAAGGCGAGCGATCCTCCCCAGTCCCGCAAGGC 5: 77,016,400 (GRCm38) probably benign Het
Tmem156 T A 5: 65,091,547 (GRCm38) E3D probably benign Het
Tmem209 T A 6: 30,487,418 (GRCm38) M530L probably benign Het
Trpc2 A G 7: 102,096,226 (GRCm38) D883G unknown Het
Tsen34 GGAGCCAAAAT G 7: 3,695,796 (GRCm38) probably null Het
Uhrf2 T C 19: 30,086,391 (GRCm38) Y585H probably damaging Het
Vmn1r26 T A 6: 58,008,720 (GRCm38) K161N probably benign Het
Vmn1r29 A G 6: 58,307,543 (GRCm38) S83G probably benign Het
Vps13b G T 15: 35,925,406 (GRCm38) W3829L probably null Het
Vwce G A 19: 10,653,085 (GRCm38) G503R probably damaging Het
Zc3h11a T C 1: 133,626,997 (GRCm38) E415G possibly damaging Het
Zc3h14 T A 12: 98,780,282 (GRCm38) probably null Het
Zfp119b A T 17: 55,939,499 (GRCm38) M229K probably benign Het
Zfp384 GGCCCAGGC GGCCCAGGCCCACGCCCAGGC 6: 125,036,488 (GRCm38) probably benign Het
Zfp384 CCAAGCTCAAGC CCAAGC 6: 125,036,455 (GRCm38) probably benign Het
Zyx T A 6: 42,357,396 (GRCm38) L518Q probably damaging Het
Other mutations in Celsr3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00233:Celsr3 APN 9 108,848,925 (GRCm38) missense probably damaging 1.00
IGL00536:Celsr3 APN 9 108,829,192 (GRCm38) missense probably benign 0.33
IGL00552:Celsr3 APN 9 108,841,263 (GRCm38) missense possibly damaging 0.88
IGL00801:Celsr3 APN 9 108,842,576 (GRCm38) missense probably benign
IGL01420:Celsr3 APN 9 108,841,190 (GRCm38) critical splice acceptor site probably null
IGL01541:Celsr3 APN 9 108,831,708 (GRCm38) missense probably damaging 1.00
IGL01619:Celsr3 APN 9 108,834,557 (GRCm38) missense probably damaging 1.00
IGL01619:Celsr3 APN 9 108,837,404 (GRCm38) missense probably benign 0.00
IGL01631:Celsr3 APN 9 108,837,404 (GRCm38) missense probably benign 0.00
IGL01777:Celsr3 APN 9 108,835,942 (GRCm38) missense probably benign 0.08
IGL01938:Celsr3 APN 9 108,828,415 (GRCm38) missense probably benign 0.34
IGL02135:Celsr3 APN 9 108,827,556 (GRCm38) missense probably benign 0.11
IGL02231:Celsr3 APN 9 108,842,510 (GRCm38) missense probably damaging 1.00
IGL02234:Celsr3 APN 9 108,829,960 (GRCm38) missense probably benign
IGL02392:Celsr3 APN 9 108,834,721 (GRCm38) splice site probably benign
IGL02416:Celsr3 APN 9 108,832,119 (GRCm38) missense probably damaging 1.00
IGL02421:Celsr3 APN 9 108,840,463 (GRCm38) missense probably damaging 1.00
IGL02455:Celsr3 APN 9 108,842,893 (GRCm38) missense probably benign 0.15
IGL02798:Celsr3 APN 9 108,843,575 (GRCm38) missense probably damaging 1.00
IGL02939:Celsr3 APN 9 108,849,453 (GRCm38) missense probably damaging 1.00
IGL02947:Celsr3 APN 9 108,845,935 (GRCm38) missense probably benign 0.12
IGL02986:Celsr3 APN 9 108,841,255 (GRCm38) splice site probably null
IGL03089:Celsr3 APN 9 108,826,607 (GRCm38) missense probably benign 0.04
IGL03162:Celsr3 APN 9 108,842,558 (GRCm38) missense probably damaging 1.00
IGL03267:Celsr3 APN 9 108,836,525 (GRCm38) splice site probably benign
Diminishment UTSW 9 108,842,708 (GRCm38) intron probably benign
little_d UTSW 9 108,827,692 (GRCm38) missense probably damaging 0.98
nogal UTSW 9 108,835,838 (GRCm38) missense probably benign
F6893:Celsr3 UTSW 9 108,835,067 (GRCm38) missense probably benign 0.00
PIT4243001:Celsr3 UTSW 9 108,832,308 (GRCm38) missense probably benign 0.13
PIT4810001:Celsr3 UTSW 9 108,845,733 (GRCm38) missense probably damaging 1.00
R0110:Celsr3 UTSW 9 108,827,005 (GRCm38) missense possibly damaging 0.62
R0243:Celsr3 UTSW 9 108,843,724 (GRCm38) splice site probably benign
R0382:Celsr3 UTSW 9 108,829,218 (GRCm38) missense probably damaging 1.00
R0482:Celsr3 UTSW 9 108,829,073 (GRCm38) nonsense probably null
R0510:Celsr3 UTSW 9 108,827,005 (GRCm38) missense possibly damaging 0.62
R0630:Celsr3 UTSW 9 108,827,692 (GRCm38) missense probably damaging 0.98
R0656:Celsr3 UTSW 9 108,834,655 (GRCm38) missense possibly damaging 0.89
R0764:Celsr3 UTSW 9 108,827,818 (GRCm38) missense probably damaging 1.00
R0883:Celsr3 UTSW 9 108,842,633 (GRCm38) missense probably damaging 1.00
R0924:Celsr3 UTSW 9 108,846,025 (GRCm38) missense possibly damaging 0.78
R1015:Celsr3 UTSW 9 108,833,176 (GRCm38) missense probably benign 0.17
R1321:Celsr3 UTSW 9 108,835,870 (GRCm38) missense probably damaging 1.00
R1423:Celsr3 UTSW 9 108,826,905 (GRCm38) missense probably benign 0.00
R1497:Celsr3 UTSW 9 108,848,865 (GRCm38) missense probably benign 0.14
R1520:Celsr3 UTSW 9 108,848,658 (GRCm38) missense probably damaging 1.00
R1534:Celsr3 UTSW 9 108,848,884 (GRCm38) missense probably damaging 0.99
R1569:Celsr3 UTSW 9 108,829,068 (GRCm38) missense probably damaging 1.00
R1657:Celsr3 UTSW 9 108,842,952 (GRCm38) nonsense probably null
R1753:Celsr3 UTSW 9 108,831,857 (GRCm38) missense probably damaging 0.99
R1764:Celsr3 UTSW 9 108,828,958 (GRCm38) missense probably damaging 1.00
R1801:Celsr3 UTSW 9 108,834,626 (GRCm38) missense possibly damaging 0.88
R1838:Celsr3 UTSW 9 108,829,906 (GRCm38) missense probably benign
R1839:Celsr3 UTSW 9 108,829,906 (GRCm38) missense probably benign
R1874:Celsr3 UTSW 9 108,835,838 (GRCm38) missense probably benign
R1875:Celsr3 UTSW 9 108,835,838 (GRCm38) missense probably benign
R1953:Celsr3 UTSW 9 108,843,182 (GRCm38) missense probably benign 0.19
R1960:Celsr3 UTSW 9 108,845,817 (GRCm38) missense probably benign
R2113:Celsr3 UTSW 9 108,838,470 (GRCm38) missense probably damaging 1.00
R2290:Celsr3 UTSW 9 108,843,224 (GRCm38) missense probably damaging 1.00
R2369:Celsr3 UTSW 9 108,842,552 (GRCm38) missense probably benign
R2373:Celsr3 UTSW 9 108,842,552 (GRCm38) missense probably benign
R2374:Celsr3 UTSW 9 108,842,552 (GRCm38) missense probably benign
R2375:Celsr3 UTSW 9 108,842,552 (GRCm38) missense probably benign
R2844:Celsr3 UTSW 9 108,829,308 (GRCm38) missense probably damaging 1.00
R2968:Celsr3 UTSW 9 108,832,191 (GRCm38) missense probably damaging 1.00
R3103:Celsr3 UTSW 9 108,837,139 (GRCm38) missense probably benign 0.31
R3159:Celsr3 UTSW 9 108,827,710 (GRCm38) missense possibly damaging 0.94
R3791:Celsr3 UTSW 9 108,842,552 (GRCm38) missense probably benign
R4194:Celsr3 UTSW 9 108,843,302 (GRCm38) critical splice donor site probably null
R4329:Celsr3 UTSW 9 108,846,049 (GRCm38) missense probably benign 0.00
R4365:Celsr3 UTSW 9 108,829,847 (GRCm38) missense possibly damaging 0.47
R4419:Celsr3 UTSW 9 108,843,244 (GRCm38) missense possibly damaging 0.84
R4484:Celsr3 UTSW 9 108,846,063 (GRCm38) critical splice donor site probably null
R4582:Celsr3 UTSW 9 108,845,723 (GRCm38) missense probably damaging 1.00
R4681:Celsr3 UTSW 9 108,827,754 (GRCm38) missense possibly damaging 0.58
R4729:Celsr3 UTSW 9 108,847,652 (GRCm38) missense probably benign 0.05
R4881:Celsr3 UTSW 9 108,843,941 (GRCm38) missense probably damaging 1.00
R4893:Celsr3 UTSW 9 108,849,421 (GRCm38) missense probably damaging 1.00
R5183:Celsr3 UTSW 9 108,837,560 (GRCm38) missense probably damaging 0.99
R5207:Celsr3 UTSW 9 108,832,759 (GRCm38) missense probably benign 0.01
R5290:Celsr3 UTSW 9 108,843,158 (GRCm38) missense probably benign 0.01
R5327:Celsr3 UTSW 9 108,842,708 (GRCm38) intron probably benign
R5345:Celsr3 UTSW 9 108,832,124 (GRCm38) missense probably damaging 1.00
R5358:Celsr3 UTSW 9 108,832,025 (GRCm38) missense possibly damaging 0.96
R5396:Celsr3 UTSW 9 108,828,582 (GRCm38) missense probably damaging 1.00
R5414:Celsr3 UTSW 9 108,840,042 (GRCm38) missense possibly damaging 0.88
R5452:Celsr3 UTSW 9 108,844,034 (GRCm38) missense possibly damaging 0.68
R5467:Celsr3 UTSW 9 108,828,637 (GRCm38) missense probably damaging 1.00
R5479:Celsr3 UTSW 9 108,844,544 (GRCm38) critical splice donor site probably null
R5629:Celsr3 UTSW 9 108,849,067 (GRCm38) missense probably benign 0.41
R5637:Celsr3 UTSW 9 108,837,133 (GRCm38) missense probably damaging 1.00
R5652:Celsr3 UTSW 9 108,838,472 (GRCm38) missense probably benign 0.03
R5739:Celsr3 UTSW 9 108,827,158 (GRCm38) missense probably benign
R5785:Celsr3 UTSW 9 108,827,797 (GRCm38) missense probably damaging 1.00
R5877:Celsr3 UTSW 9 108,845,727 (GRCm38) missense probably damaging 0.98
R5961:Celsr3 UTSW 9 108,831,794 (GRCm38) missense probably damaging 1.00
R6046:Celsr3 UTSW 9 108,837,151 (GRCm38) missense probably benign 0.01
R6176:Celsr3 UTSW 9 108,828,355 (GRCm38) missense probably damaging 1.00
R6291:Celsr3 UTSW 9 108,828,842 (GRCm38) missense probably damaging 1.00
R6468:Celsr3 UTSW 9 108,835,790 (GRCm38) missense probably benign 0.08
R6481:Celsr3 UTSW 9 108,837,084 (GRCm38) missense possibly damaging 0.92
R6547:Celsr3 UTSW 9 108,829,128 (GRCm38) missense probably damaging 1.00
R6763:Celsr3 UTSW 9 108,827,350 (GRCm38) missense probably damaging 1.00
R6870:Celsr3 UTSW 9 108,829,191 (GRCm38) missense probably benign 0.02
R6977:Celsr3 UTSW 9 108,827,715 (GRCm38) missense probably benign
R7061:Celsr3 UTSW 9 108,847,594 (GRCm38) nonsense probably null
R7122:Celsr3 UTSW 9 108,828,567 (GRCm38) missense possibly damaging 0.90
R7156:Celsr3 UTSW 9 108,838,004 (GRCm38) missense possibly damaging 0.95
R7166:Celsr3 UTSW 9 108,842,951 (GRCm38) missense probably damaging 1.00
R7176:Celsr3 UTSW 9 108,845,762 (GRCm38) missense probably benign
R7213:Celsr3 UTSW 9 108,849,040 (GRCm38) missense probably damaging 0.98
R7314:Celsr3 UTSW 9 108,829,144 (GRCm38) missense probably damaging 1.00
R7478:Celsr3 UTSW 9 108,843,578 (GRCm38) missense probably benign 0.37
R7508:Celsr3 UTSW 9 108,836,622 (GRCm38) missense probably benign
R7554:Celsr3 UTSW 9 108,841,209 (GRCm38) missense probably benign
R7615:Celsr3 UTSW 9 108,837,652 (GRCm38) missense possibly damaging 0.75
R7653:Celsr3 UTSW 9 108,835,070 (GRCm38) nonsense probably null
R7747:Celsr3 UTSW 9 108,829,978 (GRCm38) missense possibly damaging 0.61
R7881:Celsr3 UTSW 9 108,828,072 (GRCm38) missense probably benign 0.28
R7935:Celsr3 UTSW 9 108,829,641 (GRCm38) missense probably benign 0.01
R7995:Celsr3 UTSW 9 108,845,083 (GRCm38) missense probably damaging 0.99
R8006:Celsr3 UTSW 9 108,829,107 (GRCm38) missense probably damaging 1.00
R8077:Celsr3 UTSW 9 108,828,331 (GRCm38) missense probably benign 0.15
R8284:Celsr3 UTSW 9 108,846,413 (GRCm38) missense probably damaging 0.99
R8291:Celsr3 UTSW 9 108,837,970 (GRCm38) missense probably damaging 1.00
R8322:Celsr3 UTSW 9 108,848,794 (GRCm38) missense probably damaging 1.00
R8334:Celsr3 UTSW 9 108,841,272 (GRCm38) frame shift probably null
R8337:Celsr3 UTSW 9 108,841,272 (GRCm38) frame shift probably null
R8338:Celsr3 UTSW 9 108,827,340 (GRCm38) nonsense probably null
R8353:Celsr3 UTSW 9 108,826,535 (GRCm38) missense probably benign 0.00
R8407:Celsr3 UTSW 9 108,829,057 (GRCm38) missense probably damaging 1.00
R8408:Celsr3 UTSW 9 108,831,789 (GRCm38) missense probably damaging 1.00
R8459:Celsr3 UTSW 9 108,829,630 (GRCm38) missense probably damaging 1.00
R8510:Celsr3 UTSW 9 108,838,120 (GRCm38) missense possibly damaging 0.93
R8713:Celsr3 UTSW 9 108,829,863 (GRCm38) missense probably benign
R8728:Celsr3 UTSW 9 108,846,741 (GRCm38) missense probably benign 0.24
R8829:Celsr3 UTSW 9 108,840,383 (GRCm38) missense probably benign
R8877:Celsr3 UTSW 9 108,829,678 (GRCm38) missense probably damaging 1.00
R8905:Celsr3 UTSW 9 108,841,302 (GRCm38) missense probably damaging 1.00
R9008:Celsr3 UTSW 9 108,828,952 (GRCm38) missense possibly damaging 0.94
R9072:Celsr3 UTSW 9 108,827,094 (GRCm38) missense probably benign
R9157:Celsr3 UTSW 9 108,829,986 (GRCm38) missense probably damaging 1.00
R9183:Celsr3 UTSW 9 108,829,396 (GRCm38) missense probably damaging 1.00
R9275:Celsr3 UTSW 9 108,838,490 (GRCm38) missense probably benign 0.27
R9361:Celsr3 UTSW 9 108,849,322 (GRCm38) missense probably damaging 1.00
R9382:Celsr3 UTSW 9 108,829,762 (GRCm38) missense possibly damaging 0.60
R9407:Celsr3 UTSW 9 108,846,397 (GRCm38) missense probably damaging 1.00
R9432:Celsr3 UTSW 9 108,848,833 (GRCm38) missense probably benign 0.00
R9607:Celsr3 UTSW 9 108,840,502 (GRCm38) critical splice donor site probably null
R9626:Celsr3 UTSW 9 108,849,322 (GRCm38) missense probably damaging 1.00
R9628:Celsr3 UTSW 9 108,826,360 (GRCm38) nonsense probably null
R9630:Celsr3 UTSW 9 108,827,097 (GRCm38) missense probably benign
R9645:Celsr3 UTSW 9 108,827,492 (GRCm38) nonsense probably null
R9683:Celsr3 UTSW 9 108,827,323 (GRCm38) missense probably damaging 1.00
R9794:Celsr3 UTSW 9 108,851,303 (GRCm38) missense probably benign 0.00
R9798:Celsr3 UTSW 9 108,828,595 (GRCm38) missense probably damaging 1.00
X0018:Celsr3 UTSW 9 108,840,412 (GRCm38) missense probably benign 0.01
X0018:Celsr3 UTSW 9 108,827,778 (GRCm38) missense possibly damaging 0.65
X0026:Celsr3 UTSW 9 108,828,930 (GRCm38) missense probably damaging 0.99
Z1177:Celsr3 UTSW 9 108,826,477 (GRCm38) missense probably benign 0.34
Predicted Primers PCR Primer
(F):5'- AGAAGAGGTCCCAGTTCCTG -3'
(R):5'- AATGTCCAGTTGCTCTGTGGAG -3'

Sequencing Primer
(F):5'- GGTCCCAGTTCCTGCACCTG -3'
(R):5'- TCCTCCCTGGCTCTGAGAAG -3'
Posted On 2019-12-04