Incidental Mutation 'R5122:Bltp1'
ID 393327
Institutional Source Beutler Lab
Gene Symbol Bltp1
Ensembl Gene ENSMUSG00000037270
Gene Name bridge-like lipid transfer protein family member 1
Synonyms FSA, 4932438A13Rik, Tweek
MMRRC Submission 042710-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R5122 (G1)
Quality Score 225
Status Not validated
Chromosome 3
Chromosomal Location 36863104-37053033 bp(+) (GRCm38)
Type of Mutation splice site (3 bp from exon)
DNA Base Change (assembly) A to G at 37034757 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000117808 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057272] [ENSMUST00000057272] [ENSMUST00000138950] [ENSMUST00000138950] [ENSMUST00000152564] [ENSMUST00000152564]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000057272
SMART Domains Protein: ENSMUSP00000060199
Gene: ENSMUSG00000037270

DomainStartEndE-ValueType
transmembrane domain 25 47 N/A INTRINSIC
low complexity region 701 716 N/A INTRINSIC
low complexity region 767 779 N/A INTRINSIC
low complexity region 1127 1138 N/A INTRINSIC
low complexity region 1154 1166 N/A INTRINSIC
low complexity region 1226 1240 N/A INTRINSIC
low complexity region 1381 1402 N/A INTRINSIC
low complexity region 1541 1547 N/A INTRINSIC
low complexity region 1593 1607 N/A INTRINSIC
low complexity region 1810 1821 N/A INTRINSIC
low complexity region 1981 1995 N/A INTRINSIC
low complexity region 2182 2191 N/A INTRINSIC
low complexity region 2336 2349 N/A INTRINSIC
low complexity region 2614 2657 N/A INTRINSIC
low complexity region 3468 3480 N/A INTRINSIC
low complexity region 3717 3742 N/A INTRINSIC
low complexity region 3816 3837 N/A INTRINSIC
low complexity region 3919 3929 N/A INTRINSIC
low complexity region 3941 3948 N/A INTRINSIC
low complexity region 4024 4038 N/A INTRINSIC
low complexity region 4041 4049 N/A INTRINSIC
low complexity region 4117 4149 N/A INTRINSIC
low complexity region 4172 4185 N/A INTRINSIC
low complexity region 4359 4380 N/A INTRINSIC
FSA_C 4386 4990 N/A SMART
low complexity region 4993 5004 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000057272
SMART Domains Protein: ENSMUSP00000060199
Gene: ENSMUSG00000037270

DomainStartEndE-ValueType
transmembrane domain 25 47 N/A INTRINSIC
low complexity region 701 716 N/A INTRINSIC
low complexity region 767 779 N/A INTRINSIC
low complexity region 1127 1138 N/A INTRINSIC
low complexity region 1154 1166 N/A INTRINSIC
low complexity region 1226 1240 N/A INTRINSIC
low complexity region 1381 1402 N/A INTRINSIC
low complexity region 1541 1547 N/A INTRINSIC
low complexity region 1593 1607 N/A INTRINSIC
low complexity region 1810 1821 N/A INTRINSIC
low complexity region 1981 1995 N/A INTRINSIC
low complexity region 2182 2191 N/A INTRINSIC
low complexity region 2336 2349 N/A INTRINSIC
low complexity region 2614 2657 N/A INTRINSIC
low complexity region 3468 3480 N/A INTRINSIC
low complexity region 3717 3742 N/A INTRINSIC
low complexity region 3816 3837 N/A INTRINSIC
low complexity region 3919 3929 N/A INTRINSIC
low complexity region 3941 3948 N/A INTRINSIC
low complexity region 4024 4038 N/A INTRINSIC
low complexity region 4041 4049 N/A INTRINSIC
low complexity region 4117 4149 N/A INTRINSIC
low complexity region 4172 4185 N/A INTRINSIC
low complexity region 4359 4380 N/A INTRINSIC
FSA_C 4386 4990 N/A SMART
low complexity region 4993 5004 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000136746
Predicted Effect probably benign
Transcript: ENSMUST00000138152
SMART Domains Protein: ENSMUSP00000117809
Gene: ENSMUSG00000037270

DomainStartEndE-ValueType
low complexity region 81 106 N/A INTRINSIC
low complexity region 180 201 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000138950
SMART Domains Protein: ENSMUSP00000118092
Gene: ENSMUSG00000037270

DomainStartEndE-ValueType
low complexity region 254 279 N/A INTRINSIC
low complexity region 353 374 N/A INTRINSIC
low complexity region 526 540 N/A INTRINSIC
low complexity region 543 551 N/A INTRINSIC
low complexity region 619 651 N/A INTRINSIC
low complexity region 674 687 N/A INTRINSIC
low complexity region 861 882 N/A INTRINSIC
FSA_C 888 1492 N/A SMART
low complexity region 1495 1506 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000138950
SMART Domains Protein: ENSMUSP00000118092
Gene: ENSMUSG00000037270

DomainStartEndE-ValueType
low complexity region 254 279 N/A INTRINSIC
low complexity region 353 374 N/A INTRINSIC
low complexity region 526 540 N/A INTRINSIC
low complexity region 543 551 N/A INTRINSIC
low complexity region 619 651 N/A INTRINSIC
low complexity region 674 687 N/A INTRINSIC
low complexity region 861 882 N/A INTRINSIC
FSA_C 888 1492 N/A SMART
low complexity region 1495 1506 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000141740
SMART Domains Protein: ENSMUSP00000117814
Gene: ENSMUSG00000037270

DomainStartEndE-ValueType
low complexity region 28 40 N/A INTRINSIC
low complexity region 298 323 N/A INTRINSIC
low complexity region 397 418 N/A INTRINSIC
low complexity region 500 510 N/A INTRINSIC
low complexity region 522 529 N/A INTRINSIC
low complexity region 605 619 N/A INTRINSIC
low complexity region 622 630 N/A INTRINSIC
low complexity region 698 730 N/A INTRINSIC
low complexity region 753 766 N/A INTRINSIC
low complexity region 940 961 N/A INTRINSIC
FSA_C 967 1571 N/A SMART
low complexity region 1574 1585 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000146948
SMART Domains Protein: ENSMUSP00000121356
Gene: ENSMUSG00000037270

DomainStartEndE-ValueType
low complexity region 121 133 N/A INTRINSIC
low complexity region 167 177 N/A INTRINSIC
low complexity region 458 483 N/A INTRINSIC
low complexity region 557 578 N/A INTRINSIC
low complexity region 730 744 N/A INTRINSIC
low complexity region 747 755 N/A INTRINSIC
low complexity region 823 855 N/A INTRINSIC
low complexity region 878 891 N/A INTRINSIC
low complexity region 1065 1086 N/A INTRINSIC
FSA_C 1092 1696 N/A SMART
low complexity region 1699 1710 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000146948
SMART Domains Protein: ENSMUSP00000121356
Gene: ENSMUSG00000037270

DomainStartEndE-ValueType
low complexity region 121 133 N/A INTRINSIC
low complexity region 167 177 N/A INTRINSIC
low complexity region 458 483 N/A INTRINSIC
low complexity region 557 578 N/A INTRINSIC
low complexity region 730 744 N/A INTRINSIC
low complexity region 747 755 N/A INTRINSIC
low complexity region 823 855 N/A INTRINSIC
low complexity region 878 891 N/A INTRINSIC
low complexity region 1065 1086 N/A INTRINSIC
FSA_C 1092 1696 N/A SMART
low complexity region 1699 1710 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000148698
Predicted Effect probably null
Transcript: ENSMUST00000152564
SMART Domains Protein: ENSMUSP00000117808
Gene: ENSMUSG00000037270

DomainStartEndE-ValueType
transmembrane domain 25 47 N/A INTRINSIC
low complexity region 701 716 N/A INTRINSIC
low complexity region 767 779 N/A INTRINSIC
low complexity region 1127 1138 N/A INTRINSIC
low complexity region 1154 1166 N/A INTRINSIC
low complexity region 1226 1240 N/A INTRINSIC
low complexity region 1381 1402 N/A INTRINSIC
low complexity region 1541 1547 N/A INTRINSIC
low complexity region 1593 1607 N/A INTRINSIC
low complexity region 1810 1821 N/A INTRINSIC
low complexity region 1981 1995 N/A INTRINSIC
low complexity region 2182 2191 N/A INTRINSIC
low complexity region 2336 2349 N/A INTRINSIC
low complexity region 2614 2657 N/A INTRINSIC
low complexity region 3468 3480 N/A INTRINSIC
low complexity region 3717 3742 N/A INTRINSIC
low complexity region 3816 3837 N/A INTRINSIC
low complexity region 3919 3929 N/A INTRINSIC
low complexity region 3941 3948 N/A INTRINSIC
low complexity region 4024 4038 N/A INTRINSIC
low complexity region 4041 4049 N/A INTRINSIC
low complexity region 4117 4149 N/A INTRINSIC
low complexity region 4172 4185 N/A INTRINSIC
low complexity region 4359 4380 N/A INTRINSIC
FSA_C 4386 4990 N/A SMART
low complexity region 4993 5004 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000152564
SMART Domains Protein: ENSMUSP00000117808
Gene: ENSMUSG00000037270

DomainStartEndE-ValueType
transmembrane domain 25 47 N/A INTRINSIC
low complexity region 701 716 N/A INTRINSIC
low complexity region 767 779 N/A INTRINSIC
low complexity region 1127 1138 N/A INTRINSIC
low complexity region 1154 1166 N/A INTRINSIC
low complexity region 1226 1240 N/A INTRINSIC
low complexity region 1381 1402 N/A INTRINSIC
low complexity region 1541 1547 N/A INTRINSIC
low complexity region 1593 1607 N/A INTRINSIC
low complexity region 1810 1821 N/A INTRINSIC
low complexity region 1981 1995 N/A INTRINSIC
low complexity region 2182 2191 N/A INTRINSIC
low complexity region 2336 2349 N/A INTRINSIC
low complexity region 2614 2657 N/A INTRINSIC
low complexity region 3468 3480 N/A INTRINSIC
low complexity region 3717 3742 N/A INTRINSIC
low complexity region 3816 3837 N/A INTRINSIC
low complexity region 3919 3929 N/A INTRINSIC
low complexity region 3941 3948 N/A INTRINSIC
low complexity region 4024 4038 N/A INTRINSIC
low complexity region 4041 4049 N/A INTRINSIC
low complexity region 4117 4149 N/A INTRINSIC
low complexity region 4172 4185 N/A INTRINSIC
low complexity region 4359 4380 N/A INTRINSIC
FSA_C 4386 4990 N/A SMART
low complexity region 4993 5004 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000200245
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.5%
  • 20x: 93.2%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is located on the long arm of chromosome 4 in a region that is associated with susceptibility to celiac disease. The encoded protein is similar to a Chinese hamster protein that is associated with spermatocyte and adipocyte differentiation. The C-terminus of the protein is also similar to a Caenorhabditis elegans protein that plays a role in lipid storage. In mammals, this protein is thought to function in the regulation of epithelial growth and differentiation, and in tumor development. [provided by RefSeq, Oct 2009]
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acan T C 7: 79,100,661 (GRCm38) S1727P probably damaging Het
Actr8 A T 14: 29,982,715 (GRCm38) K57N possibly damaging Het
Bcan G T 3: 87,994,207 (GRCm38) S396Y probably damaging Het
Bmp2k A G 5: 97,087,015 (GRCm38) probably benign Het
Cd274 A G 19: 29,380,565 (GRCm38) H219R possibly damaging Het
Cdc16 A T 8: 13,764,570 (GRCm38) Y118F probably damaging Het
Cdc23 C A 18: 34,651,689 (GRCm38) V7L unknown Het
Chchd3 T C 6: 32,968,305 (GRCm38) R89G probably benign Het
Clstn2 C T 9: 97,461,421 (GRCm38) V658M probably damaging Het
Cpt1b A G 15: 89,424,023 (GRCm38) S160P probably benign Het
Crym T C 7: 120,195,495 (GRCm38) N167S probably benign Het
Dhx16 T A 17: 35,883,310 (GRCm38) Y438N probably damaging Het
Dnah12 A G 14: 26,718,000 (GRCm38) R536G probably benign Het
Dnajc11 A G 4: 151,976,997 (GRCm38) D382G possibly damaging Het
Dync1h1 G A 12: 110,629,680 (GRCm38) G1547D probably damaging Het
Eml3 T A 19: 8,937,696 (GRCm38) probably null Het
Ep400 G A 5: 110,668,170 (GRCm38) P2799S probably damaging Het
Ephb6 T C 6: 41,613,404 (GRCm38) V30A probably benign Het
Fam53b T A 7: 132,779,262 (GRCm38) probably benign Het
Fcrl1 A G 3: 87,385,774 (GRCm38) K246R probably benign Het
Focad G A 4: 88,407,365 (GRCm38) probably null Het
Glipr1l2 T C 10: 112,107,056 (GRCm38) I272T possibly damaging Het
Gm8104 A G 14: 43,109,093 (GRCm38) I101V probably benign Het
Grm5 A G 7: 88,074,820 (GRCm38) I773V probably damaging Het
Hyal1 A T 9: 107,578,069 (GRCm38) T193S probably benign Het
Igkv10-94 C A 6: 68,704,671 (GRCm38) G62* probably null Het
Itsn1 A G 16: 91,893,844 (GRCm38) probably benign Het
Kank4 A G 4: 98,756,567 (GRCm38) S983P probably damaging Het
Krtap16-1 C A 11: 99,985,697 (GRCm38) V294F probably damaging Het
Lama3 T G 18: 12,539,766 (GRCm38) V866G possibly damaging Het
Lrba C T 3: 86,349,154 (GRCm38) R1268* probably null Het
Lrriq1 C T 10: 103,187,453 (GRCm38) V984I probably damaging Het
Macf1 A C 4: 123,452,292 (GRCm38) V4136G probably damaging Het
Mdn1 A T 4: 32,670,593 (GRCm38) E419D probably damaging Het
Nedd4l A G 18: 65,191,447 (GRCm38) Y473C probably damaging Het
Nod2 G T 8: 88,664,120 (GRCm38) D330Y probably damaging Het
Nt5c2 C T 19: 46,889,921 (GRCm38) C458Y probably damaging Het
Numa1 T C 7: 102,013,769 (GRCm38) I681T probably damaging Het
Or10a5 C A 7: 107,036,848 (GRCm38) S231* probably null Het
Papolg C T 11: 23,867,501 (GRCm38) probably null Het
Parn A G 16: 13,654,447 (GRCm38) probably null Het
Pgap2 T C 7: 102,231,391 (GRCm38) F42S probably damaging Het
Phf11d A T 14: 59,353,344 (GRCm38) M188K possibly damaging Het
Pofut2 G C 10: 77,268,565 (GRCm38) R392P probably damaging Het
Prpf18 T C 2: 4,643,709 (GRCm38) D102G probably damaging Het
Rreb1 T A 13: 37,930,768 (GRCm38) I701N probably benign Het
Slc26a5 T C 5: 21,847,196 (GRCm38) K45R probably damaging Het
Slc8a3 A G 12: 81,314,258 (GRCm38) probably null Het
Slf1 T A 13: 77,049,987 (GRCm38) M723L probably benign Het
Spata31e5 A G 1: 28,780,060 (GRCm38) S47P probably benign Het
Sra1 T C 18: 36,667,594 (GRCm38) T187A probably benign Het
Stk17b A C 1: 53,776,558 (GRCm38) N27K probably damaging Het
Tbc1d9 T A 8: 83,236,543 (GRCm38) Y295N probably damaging Het
Tubgcp6 A G 15: 89,116,103 (GRCm38) V353A probably damaging Het
Unc80 A T 1: 66,679,590 (GRCm38) T2991S possibly damaging Het
Urb1 G A 16: 90,752,095 (GRCm38) R2242* probably null Het
Vasp T C 7: 19,264,772 (GRCm38) N20S probably benign Het
Zfp263 A G 16: 3,749,855 (GRCm38) H390R probably damaging Het
Other mutations in Bltp1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00428:Bltp1 APN 3 37,011,727 (GRCm38) missense probably benign 0.00
IGL00434:Bltp1 APN 3 36,987,299 (GRCm38) missense probably damaging 0.98
IGL00640:Bltp1 APN 3 36,908,218 (GRCm38) missense probably damaging 1.00
IGL00693:Bltp1 APN 3 37,052,547 (GRCm38) utr 3 prime probably benign
IGL00721:Bltp1 APN 3 37,030,751 (GRCm38) splice site probably null
IGL00756:Bltp1 APN 3 36,908,218 (GRCm38) missense probably damaging 1.00
IGL00896:Bltp1 APN 3 37,039,462 (GRCm38) missense probably benign
IGL00902:Bltp1 APN 3 37,041,345 (GRCm38) missense probably damaging 1.00
IGL00980:Bltp1 APN 3 37,000,041 (GRCm38) missense probably damaging 1.00
IGL01019:Bltp1 APN 3 37,006,984 (GRCm38) critical splice acceptor site probably null
IGL01025:Bltp1 APN 3 37,046,280 (GRCm38) missense possibly damaging 0.89
IGL01306:Bltp1 APN 3 37,005,013 (GRCm38) splice site probably benign
IGL01370:Bltp1 APN 3 36,947,755 (GRCm38) missense probably benign 0.07
IGL01377:Bltp1 APN 3 36,973,452 (GRCm38) critical splice donor site probably null
IGL01401:Bltp1 APN 3 36,942,292 (GRCm38) missense probably benign
IGL01419:Bltp1 APN 3 37,048,121 (GRCm38) missense probably damaging 1.00
IGL01432:Bltp1 APN 3 37,003,759 (GRCm38) missense possibly damaging 0.87
IGL01433:Bltp1 APN 3 36,887,770 (GRCm38) missense probably damaging 1.00
IGL01452:Bltp1 APN 3 36,996,308 (GRCm38) unclassified probably benign
IGL01520:Bltp1 APN 3 36,973,260 (GRCm38) nonsense probably null
IGL01524:Bltp1 APN 3 36,942,382 (GRCm38) missense possibly damaging 0.90
IGL01628:Bltp1 APN 3 37,008,485 (GRCm38) missense probably damaging 1.00
IGL01638:Bltp1 APN 3 36,974,311 (GRCm38) missense probably damaging 1.00
IGL01650:Bltp1 APN 3 36,992,673 (GRCm38) splice site probably benign
IGL01717:Bltp1 APN 3 37,034,736 (GRCm38) missense probably benign
IGL01767:Bltp1 APN 3 37,041,363 (GRCm38) missense probably benign 0.29
IGL01813:Bltp1 APN 3 36,928,520 (GRCm38) missense possibly damaging 0.90
IGL01998:Bltp1 APN 3 36,957,016 (GRCm38) missense possibly damaging 0.49
IGL02172:Bltp1 APN 3 37,004,873 (GRCm38) missense probably damaging 0.99
IGL02197:Bltp1 APN 3 36,906,735 (GRCm38) missense probably damaging 1.00
IGL02248:Bltp1 APN 3 36,969,290 (GRCm38) critical splice donor site probably null
IGL02273:Bltp1 APN 3 36,921,437 (GRCm38) splice site probably benign
IGL02403:Bltp1 APN 3 37,030,664 (GRCm38) missense probably benign
IGL02492:Bltp1 APN 3 37,048,113 (GRCm38) missense probably benign 0.04
IGL02517:Bltp1 APN 3 36,958,868 (GRCm38) missense probably damaging 1.00
IGL02519:Bltp1 APN 3 36,895,315 (GRCm38) missense probably damaging 1.00
IGL02586:Bltp1 APN 3 37,044,608 (GRCm38) nonsense probably null
IGL02620:Bltp1 APN 3 37,035,945 (GRCm38) missense possibly damaging 0.95
IGL02621:Bltp1 APN 3 37,041,484 (GRCm38) splice site probably benign
IGL02670:Bltp1 APN 3 36,967,305 (GRCm38) nonsense probably null
IGL02806:Bltp1 APN 3 36,946,494 (GRCm38) missense possibly damaging 0.95
IGL02985:Bltp1 APN 3 36,958,757 (GRCm38) missense probably damaging 0.99
IGL03004:Bltp1 APN 3 36,965,677 (GRCm38) splice site probably benign
IGL03037:Bltp1 APN 3 36,969,207 (GRCm38) missense probably benign 0.23
IGL03037:Bltp1 APN 3 36,969,208 (GRCm38) missense probably damaging 1.00
IGL03062:Bltp1 APN 3 37,038,517 (GRCm38) splice site probably benign
IGL03137:Bltp1 APN 3 37,034,602 (GRCm38) missense probably damaging 0.98
IGL03150:Bltp1 APN 3 36,948,066 (GRCm38) missense probably damaging 1.00
IGL03204:Bltp1 APN 3 37,050,934 (GRCm38) splice site probably benign
IGL03207:Bltp1 APN 3 36,949,996 (GRCm38) missense possibly damaging 0.73
IGL03256:Bltp1 APN 3 36,906,683 (GRCm38) splice site probably benign
IGL03264:Bltp1 APN 3 37,002,635 (GRCm38) missense probably damaging 1.00
IGL03265:Bltp1 APN 3 37,047,991 (GRCm38) missense probably benign 0.00
IGL03303:Bltp1 APN 3 36,870,077 (GRCm38) missense possibly damaging 0.90
admonished UTSW 3 36,948,304 (GRCm38) missense probably damaging 1.00
alerted UTSW 3 37,033,265 (GRCm38) missense possibly damaging 0.85
informed UTSW 3 36,965,849 (GRCm38) missense probably damaging 1.00
resolved UTSW 3 36,921,221 (GRCm38) missense possibly damaging 0.60
tipped UTSW 3 36,988,085 (GRCm38) missense possibly damaging 0.81
warned UTSW 3 36,965,621 (GRCm38) missense probably damaging 1.00
FR4340:Bltp1 UTSW 3 37,050,752 (GRCm38) critical splice acceptor site probably benign
FR4737:Bltp1 UTSW 3 37,050,754 (GRCm38) critical splice acceptor site probably benign
PIT4515001:Bltp1 UTSW 3 36,974,236 (GRCm38) missense probably damaging 1.00
R0035:Bltp1 UTSW 3 36,987,598 (GRCm38) nonsense probably null
R0047:Bltp1 UTSW 3 36,908,192 (GRCm38) missense possibly damaging 0.83
R0047:Bltp1 UTSW 3 36,908,192 (GRCm38) missense possibly damaging 0.83
R0068:Bltp1 UTSW 3 36,952,221 (GRCm38) missense probably benign 0.28
R0068:Bltp1 UTSW 3 36,952,221 (GRCm38) missense probably benign 0.28
R0092:Bltp1 UTSW 3 37,028,159 (GRCm38) missense probably benign 0.41
R0233:Bltp1 UTSW 3 36,948,563 (GRCm38) nonsense probably null
R0233:Bltp1 UTSW 3 36,948,563 (GRCm38) nonsense probably null
R0256:Bltp1 UTSW 3 36,917,773 (GRCm38) missense probably benign 0.01
R0277:Bltp1 UTSW 3 36,943,182 (GRCm38) nonsense probably null
R0321:Bltp1 UTSW 3 36,906,788 (GRCm38) splice site probably null
R0323:Bltp1 UTSW 3 36,943,182 (GRCm38) nonsense probably null
R0335:Bltp1 UTSW 3 36,969,152 (GRCm38) missense probably damaging 1.00
R0375:Bltp1 UTSW 3 37,046,252 (GRCm38) missense probably damaging 0.99
R0437:Bltp1 UTSW 3 36,989,804 (GRCm38) missense possibly damaging 0.81
R0445:Bltp1 UTSW 3 37,000,065 (GRCm38) missense probably damaging 0.99
R0496:Bltp1 UTSW 3 36,987,635 (GRCm38) missense probably damaging 1.00
R0531:Bltp1 UTSW 3 37,036,825 (GRCm38) missense probably damaging 1.00
R0543:Bltp1 UTSW 3 36,996,458 (GRCm38) missense probably benign 0.22
R0545:Bltp1 UTSW 3 36,987,690 (GRCm38) splice site probably benign
R0674:Bltp1 UTSW 3 37,044,626 (GRCm38) missense possibly damaging 0.86
R0745:Bltp1 UTSW 3 36,928,463 (GRCm38) missense probably damaging 1.00
R0755:Bltp1 UTSW 3 36,946,364 (GRCm38) missense probably damaging 1.00
R0785:Bltp1 UTSW 3 36,959,334 (GRCm38) splice site probably benign
R1056:Bltp1 UTSW 3 37,044,680 (GRCm38) missense probably benign 0.44
R1056:Bltp1 UTSW 3 36,983,453 (GRCm38) missense possibly damaging 0.69
R1080:Bltp1 UTSW 3 36,988,255 (GRCm38) missense probably damaging 1.00
R1103:Bltp1 UTSW 3 36,996,523 (GRCm38) missense probably benign
R1119:Bltp1 UTSW 3 36,987,045 (GRCm38) missense probably damaging 1.00
R1170:Bltp1 UTSW 3 37,044,631 (GRCm38) missense probably damaging 0.98
R1183:Bltp1 UTSW 3 36,895,303 (GRCm38) missense possibly damaging 0.51
R1186:Bltp1 UTSW 3 36,996,312 (GRCm38) unclassified probably benign
R1201:Bltp1 UTSW 3 36,948,375 (GRCm38) missense probably benign
R1219:Bltp1 UTSW 3 36,946,470 (GRCm38) nonsense probably null
R1270:Bltp1 UTSW 3 36,952,184 (GRCm38) missense probably damaging 1.00
R1273:Bltp1 UTSW 3 36,987,210 (GRCm38) missense probably damaging 1.00
R1338:Bltp1 UTSW 3 37,052,535 (GRCm38) missense unknown
R1364:Bltp1 UTSW 3 36,987,030 (GRCm38) missense probably damaging 1.00
R1437:Bltp1 UTSW 3 36,942,429 (GRCm38) missense possibly damaging 0.65
R1447:Bltp1 UTSW 3 36,965,586 (GRCm38) missense probably damaging 0.98
R1467:Bltp1 UTSW 3 37,035,945 (GRCm38) missense probably damaging 0.99
R1467:Bltp1 UTSW 3 37,035,945 (GRCm38) missense probably damaging 0.99
R1470:Bltp1 UTSW 3 36,998,331 (GRCm38) missense probably benign 0.31
R1470:Bltp1 UTSW 3 36,998,331 (GRCm38) missense probably benign 0.31
R1481:Bltp1 UTSW 3 37,008,434 (GRCm38) missense probably damaging 0.99
R1528:Bltp1 UTSW 3 37,052,535 (GRCm38) missense unknown
R1533:Bltp1 UTSW 3 37,041,375 (GRCm38) missense probably damaging 1.00
R1546:Bltp1 UTSW 3 36,870,056 (GRCm38) missense possibly damaging 0.64
R1606:Bltp1 UTSW 3 36,942,399 (GRCm38) missense probably damaging 1.00
R1638:Bltp1 UTSW 3 37,035,812 (GRCm38) nonsense probably null
R1772:Bltp1 UTSW 3 36,959,432 (GRCm38) missense probably damaging 1.00
R1896:Bltp1 UTSW 3 36,908,231 (GRCm38) nonsense probably null
R1919:Bltp1 UTSW 3 37,006,983 (GRCm38) critical splice acceptor site probably null
R1983:Bltp1 UTSW 3 36,887,865 (GRCm38) missense probably null 1.00
R1987:Bltp1 UTSW 3 36,953,985 (GRCm38) critical splice donor site probably null
R1992:Bltp1 UTSW 3 37,000,032 (GRCm38) missense probably benign 0.32
R1999:Bltp1 UTSW 3 36,908,211 (GRCm38) missense probably damaging 1.00
R2004:Bltp1 UTSW 3 36,895,378 (GRCm38) missense possibly damaging 0.77
R2010:Bltp1 UTSW 3 36,928,551 (GRCm38) missense probably benign 0.09
R2027:Bltp1 UTSW 3 37,047,961 (GRCm38) splice site probably benign
R2039:Bltp1 UTSW 3 37,003,878 (GRCm38) missense possibly damaging 0.66
R2054:Bltp1 UTSW 3 36,947,853 (GRCm38) missense probably benign 0.01
R2089:Bltp1 UTSW 3 36,988,256 (GRCm38) missense probably damaging 1.00
R2091:Bltp1 UTSW 3 36,988,256 (GRCm38) missense probably damaging 1.00
R2091:Bltp1 UTSW 3 36,988,256 (GRCm38) missense probably damaging 1.00
R2091:Bltp1 UTSW 3 36,953,970 (GRCm38) missense probably damaging 1.00
R2220:Bltp1 UTSW 3 36,875,530 (GRCm38) critical splice donor site probably null
R2374:Bltp1 UTSW 3 36,885,396 (GRCm38) missense probably benign 0.00
R2437:Bltp1 UTSW 3 36,958,685 (GRCm38) splice site probably null
R2860:Bltp1 UTSW 3 36,965,849 (GRCm38) missense probably damaging 1.00
R2861:Bltp1 UTSW 3 36,965,849 (GRCm38) missense probably damaging 1.00
R2909:Bltp1 UTSW 3 36,947,953 (GRCm38) missense probably damaging 1.00
R2925:Bltp1 UTSW 3 37,007,122 (GRCm38) missense probably damaging 0.99
R2940:Bltp1 UTSW 3 36,958,805 (GRCm38) missense probably damaging 1.00
R3015:Bltp1 UTSW 3 36,875,462 (GRCm38) missense probably damaging 1.00
R3086:Bltp1 UTSW 3 37,011,703 (GRCm38) missense possibly damaging 0.56
R3159:Bltp1 UTSW 3 36,959,415 (GRCm38) missense probably benign 0.17
R3440:Bltp1 UTSW 3 37,041,912 (GRCm38) nonsense probably null
R3703:Bltp1 UTSW 3 36,987,581 (GRCm38) missense probably damaging 1.00
R3705:Bltp1 UTSW 3 36,987,581 (GRCm38) missense probably damaging 1.00
R3795:Bltp1 UTSW 3 37,030,565 (GRCm38) missense probably benign 0.30
R3820:Bltp1 UTSW 3 37,040,434 (GRCm38) missense probably damaging 1.00
R3862:Bltp1 UTSW 3 36,885,398 (GRCm38) missense possibly damaging 0.73
R3944:Bltp1 UTSW 3 37,030,061 (GRCm38) missense possibly damaging 0.90
R4020:Bltp1 UTSW 3 37,012,575 (GRCm38) intron probably benign
R4091:Bltp1 UTSW 3 37,030,589 (GRCm38) missense probably benign 0.00
R4159:Bltp1 UTSW 3 36,931,083 (GRCm38) missense probably benign 0.00
R4231:Bltp1 UTSW 3 36,920,236 (GRCm38) missense probably benign 0.10
R4368:Bltp1 UTSW 3 36,988,147 (GRCm38) nonsense probably null
R4413:Bltp1 UTSW 3 36,958,681 (GRCm38) splice site probably null
R4475:Bltp1 UTSW 3 37,040,395 (GRCm38) missense probably damaging 1.00
R4488:Bltp1 UTSW 3 37,003,933 (GRCm38) missense probably null 0.93
R4489:Bltp1 UTSW 3 37,003,933 (GRCm38) missense probably null 0.93
R4516:Bltp1 UTSW 3 36,895,311 (GRCm38) missense possibly damaging 0.90
R4580:Bltp1 UTSW 3 37,030,025 (GRCm38) missense probably benign 0.02
R4672:Bltp1 UTSW 3 36,889,990 (GRCm38) makesense probably null
R4705:Bltp1 UTSW 3 37,041,889 (GRCm38) missense probably benign 0.03
R4735:Bltp1 UTSW 3 37,004,967 (GRCm38) missense possibly damaging 0.84
R4741:Bltp1 UTSW 3 36,942,375 (GRCm38) missense probably damaging 0.99
R4754:Bltp1 UTSW 3 37,022,466 (GRCm38) nonsense probably null
R4778:Bltp1 UTSW 3 36,937,065 (GRCm38) missense possibly damaging 0.90
R4833:Bltp1 UTSW 3 36,964,968 (GRCm38) missense probably damaging 0.96
R4896:Bltp1 UTSW 3 36,965,937 (GRCm38) missense probably damaging 1.00
R4910:Bltp1 UTSW 3 36,998,199 (GRCm38) missense probably damaging 1.00
R4922:Bltp1 UTSW 3 36,987,165 (GRCm38) missense probably damaging 1.00
R4941:Bltp1 UTSW 3 36,919,901 (GRCm38) missense probably benign 0.41
R4941:Bltp1 UTSW 3 36,917,702 (GRCm38) missense probably damaging 1.00
R4980:Bltp1 UTSW 3 36,943,312 (GRCm38) missense probably damaging 1.00
R5030:Bltp1 UTSW 3 36,943,399 (GRCm38) intron probably benign
R5049:Bltp1 UTSW 3 37,041,390 (GRCm38) missense probably damaging 1.00
R5049:Bltp1 UTSW 3 37,040,506 (GRCm38) intron probably benign
R5089:Bltp1 UTSW 3 36,987,502 (GRCm38) missense probably benign 0.02
R5092:Bltp1 UTSW 3 37,000,085 (GRCm38) missense probably benign 0.14
R5210:Bltp1 UTSW 3 37,033,265 (GRCm38) missense possibly damaging 0.85
R5246:Bltp1 UTSW 3 37,048,050 (GRCm38) missense probably damaging 1.00
R5289:Bltp1 UTSW 3 37,000,109 (GRCm38) missense probably damaging 0.97
R5348:Bltp1 UTSW 3 37,048,146 (GRCm38) missense probably damaging 1.00
R5394:Bltp1 UTSW 3 36,917,668 (GRCm38) missense probably damaging 1.00
R5434:Bltp1 UTSW 3 36,875,516 (GRCm38) missense probably damaging 1.00
R5667:Bltp1 UTSW 3 36,917,677 (GRCm38) missense probably benign 0.00
R5686:Bltp1 UTSW 3 36,917,660 (GRCm38) missense probably benign 0.00
R5701:Bltp1 UTSW 3 36,921,360 (GRCm38) missense probably benign 0.10
R5778:Bltp1 UTSW 3 36,958,714 (GRCm38) missense probably damaging 1.00
R5787:Bltp1 UTSW 3 36,992,733 (GRCm38) splice site probably null
R5800:Bltp1 UTSW 3 37,052,443 (GRCm38) missense probably damaging 1.00
R5819:Bltp1 UTSW 3 37,048,600 (GRCm38) missense probably benign 0.12
R5820:Bltp1 UTSW 3 37,039,526 (GRCm38) missense probably benign 0.00
R5952:Bltp1 UTSW 3 36,965,621 (GRCm38) missense probably damaging 1.00
R5975:Bltp1 UTSW 3 36,969,221 (GRCm38) missense possibly damaging 0.64
R5996:Bltp1 UTSW 3 36,931,116 (GRCm38) missense probably benign 0.07
R6192:Bltp1 UTSW 3 36,988,169 (GRCm38) missense probably benign 0.00
R6225:Bltp1 UTSW 3 36,948,304 (GRCm38) missense probably damaging 1.00
R6234:Bltp1 UTSW 3 36,983,471 (GRCm38) missense probably benign 0.00
R6244:Bltp1 UTSW 3 36,956,999 (GRCm38) missense probably benign
R6263:Bltp1 UTSW 3 36,931,111 (GRCm38) missense probably benign 0.06
R6351:Bltp1 UTSW 3 36,908,228 (GRCm38) missense probably damaging 1.00
R6380:Bltp1 UTSW 3 37,033,307 (GRCm38) missense probably benign 0.19
R6468:Bltp1 UTSW 3 37,008,443 (GRCm38) missense probably damaging 1.00
R6759:Bltp1 UTSW 3 36,988,085 (GRCm38) missense possibly damaging 0.81
R6792:Bltp1 UTSW 3 37,011,566 (GRCm38) critical splice acceptor site probably null
R6809:Bltp1 UTSW 3 36,874,282 (GRCm38) missense probably damaging 0.98
R6841:Bltp1 UTSW 3 37,021,481 (GRCm38) missense probably damaging 1.00
R6959:Bltp1 UTSW 3 36,967,189 (GRCm38) missense probably damaging 1.00
R7102:Bltp1 UTSW 3 36,940,798 (GRCm38) missense probably damaging 0.99
R7188:Bltp1 UTSW 3 36,950,013 (GRCm38) missense probably benign 0.06
R7212:Bltp1 UTSW 3 37,048,009 (GRCm38) missense
R7425:Bltp1 UTSW 3 36,983,394 (GRCm38) missense probably benign 0.02
R7425:Bltp1 UTSW 3 36,948,341 (GRCm38) missense probably benign
R7451:Bltp1 UTSW 3 37,022,807 (GRCm38) splice site probably null
R7604:Bltp1 UTSW 3 36,949,843 (GRCm38) splice site probably null
R7622:Bltp1 UTSW 3 36,948,413 (GRCm38) nonsense probably null
R7671:Bltp1 UTSW 3 36,943,231 (GRCm38) missense probably damaging 0.99
R7699:Bltp1 UTSW 3 37,026,154 (GRCm38) missense probably benign 0.00
R7699:Bltp1 UTSW 3 36,974,172 (GRCm38) missense possibly damaging 0.67
R7700:Bltp1 UTSW 3 36,974,172 (GRCm38) missense possibly damaging 0.67
R7700:Bltp1 UTSW 3 37,026,154 (GRCm38) missense probably benign 0.00
R7748:Bltp1 UTSW 3 36,959,335 (GRCm38) critical splice acceptor site probably null
R7767:Bltp1 UTSW 3 36,920,287 (GRCm38) critical splice donor site probably null
R7787:Bltp1 UTSW 3 36,885,408 (GRCm38) missense probably damaging 1.00
R7830:Bltp1 UTSW 3 36,964,932 (GRCm38) frame shift probably null
R7849:Bltp1 UTSW 3 37,026,328 (GRCm38) missense
R7912:Bltp1 UTSW 3 37,007,069 (GRCm38) missense probably damaging 0.99
R7914:Bltp1 UTSW 3 36,946,283 (GRCm38) missense probably benign 0.13
R7945:Bltp1 UTSW 3 36,965,893 (GRCm38) missense probably benign 0.03
R8039:Bltp1 UTSW 3 36,943,214 (GRCm38) missense probably benign 0.12
R8101:Bltp1 UTSW 3 37,008,502 (GRCm38) missense probably damaging 1.00
R8143:Bltp1 UTSW 3 36,946,508 (GRCm38) critical splice donor site probably null
R8145:Bltp1 UTSW 3 36,998,267 (GRCm38) missense probably damaging 1.00
R8171:Bltp1 UTSW 3 36,975,713 (GRCm38) missense probably benign 0.00
R8210:Bltp1 UTSW 3 37,012,881 (GRCm38) missense
R8250:Bltp1 UTSW 3 36,917,662 (GRCm38) missense probably damaging 0.99
R8369:Bltp1 UTSW 3 37,011,603 (GRCm38) missense
R8478:Bltp1 UTSW 3 37,033,277 (GRCm38) missense possibly damaging 0.74
R8558:Bltp1 UTSW 3 37,048,601 (GRCm38) missense
R8688:Bltp1 UTSW 3 37,035,917 (GRCm38) missense
R8724:Bltp1 UTSW 3 36,890,893 (GRCm38) missense probably damaging 0.99
R8818:Bltp1 UTSW 3 36,996,548 (GRCm38) missense possibly damaging 0.60
R8869:Bltp1 UTSW 3 36,958,858 (GRCm38) missense probably damaging 0.99
R8887:Bltp1 UTSW 3 37,033,354 (GRCm38) missense possibly damaging 0.95
R8899:Bltp1 UTSW 3 36,988,280 (GRCm38) missense probably damaging 1.00
R8907:Bltp1 UTSW 3 36,948,146 (GRCm38) nonsense probably null
R8960:Bltp1 UTSW 3 37,012,983 (GRCm38) missense probably damaging 1.00
R8990:Bltp1 UTSW 3 36,921,221 (GRCm38) missense possibly damaging 0.60
R9021:Bltp1 UTSW 3 36,998,344 (GRCm38) missense probably benign 0.00
R9048:Bltp1 UTSW 3 37,011,777 (GRCm38) missense
R9100:Bltp1 UTSW 3 37,044,758 (GRCm38) missense
R9166:Bltp1 UTSW 3 36,987,367 (GRCm38) missense probably damaging 1.00
R9176:Bltp1 UTSW 3 36,956,703 (GRCm38) missense possibly damaging 0.82
R9202:Bltp1 UTSW 3 36,890,821 (GRCm38) missense probably benign
R9303:Bltp1 UTSW 3 37,044,820 (GRCm38) missense
R9305:Bltp1 UTSW 3 37,044,820 (GRCm38) missense
R9332:Bltp1 UTSW 3 37,050,840 (GRCm38) missense
R9362:Bltp1 UTSW 3 36,957,013 (GRCm38) missense probably benign
R9493:Bltp1 UTSW 3 37,011,736 (GRCm38) missense
R9534:Bltp1 UTSW 3 36,998,270 (GRCm38) missense probably benign 0.01
R9569:Bltp1 UTSW 3 37,012,621 (GRCm38) missense
R9593:Bltp1 UTSW 3 36,947,941 (GRCm38) missense probably damaging 1.00
R9600:Bltp1 UTSW 3 37,041,416 (GRCm38) nonsense probably null
R9733:Bltp1 UTSW 3 37,048,583 (GRCm38) missense
R9751:Bltp1 UTSW 3 37,011,740 (GRCm38) missense
RF013:Bltp1 UTSW 3 37,050,757 (GRCm38) critical splice acceptor site probably benign
RF015:Bltp1 UTSW 3 37,050,748 (GRCm38) critical splice acceptor site probably benign
RF021:Bltp1 UTSW 3 37,050,748 (GRCm38) critical splice acceptor site probably benign
RF023:Bltp1 UTSW 3 37,050,760 (GRCm38) critical splice acceptor site probably benign
RF034:Bltp1 UTSW 3 37,050,760 (GRCm38) critical splice acceptor site probably benign
RF035:Bltp1 UTSW 3 37,050,758 (GRCm38) critical splice acceptor site probably benign
RF055:Bltp1 UTSW 3 37,050,757 (GRCm38) critical splice acceptor site probably benign
X0050:Bltp1 UTSW 3 36,957,128 (GRCm38) missense probably damaging 1.00
Z1088:Bltp1 UTSW 3 36,987,567 (GRCm38) missense probably damaging 1.00
Z1177:Bltp1 UTSW 3 36,983,440 (GRCm38) missense possibly damaging 0.88
Z1177:Bltp1 UTSW 3 36,919,950 (GRCm38) missense probably benign
Z1177:Bltp1 UTSW 3 37,036,707 (GRCm38) missense
Predicted Primers PCR Primer
(F):5'- CAGTATCAAGAGTAGAATGCATGCTG -3'
(R):5'- TAGTGGCATGCAAGCTGAAG -3'

Sequencing Primer
(F):5'- GAAGCTACCATCTCTGGACTTGG -3'
(R):5'- GCTATCTAATTACTGCTGAGGTAAAC -3'
Posted On 2016-06-15