Incidental Mutation 'R3916:Fkbp2'
ID 309783
Institutional Source Beutler Lab
Gene Symbol Fkbp2
Ensembl Gene ENSMUSG00000056629
Gene Name FK506 binding protein 2
Synonyms mFKBP2, mFKBP13, 13kDa
Accession Numbers
Essential gene? Not available question?
Stock # R3916 (G1)
Quality Score 225
Status Not validated
Chromosome 19
Chromosomal Location 6977741-6980461 bp(-) (GRCm38)
Type of Mutation critical splice donor site (1 bp from exon)
DNA Base Change (assembly) C to A at 6978557 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000136438 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025914] [ENSMUST00000070850] [ENSMUST00000070878] [ENSMUST00000130048] [ENSMUST00000177752]
AlphaFold P45878
Predicted Effect probably benign
Transcript: ENSMUST00000025914
SMART Domains Protein: ENSMUSP00000025914
Gene: ENSMUSG00000024962

signal peptide 1 19 N/A INTRINSIC
PDGF 45 126 1.11e-44 SMART
low complexity region 182 207 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000070850
SMART Domains Protein: ENSMUSP00000064129
Gene: ENSMUSG00000056612

low complexity region 2 26 N/A INTRINSIC
Pfam:PP1_inhibitor 36 147 1.1e-40 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000070878
SMART Domains Protein: ENSMUSP00000066839
Gene: ENSMUSG00000056629

low complexity region 6 21 N/A INTRINSIC
Pfam:FKBP_C 40 132 5.6e-37 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000130048
SMART Domains Protein: ENSMUSP00000120860
Gene: ENSMUSG00000024962

signal peptide 1 19 N/A INTRINSIC
PDGF 45 126 1.11e-44 SMART
Pfam:VEGF_C 134 188 1.3e-9 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000177752
SMART Domains Protein: ENSMUSP00000136438
Gene: ENSMUSG00000056629

low complexity region 6 21 N/A INTRINSIC
Pfam:FKBP_C 40 132 4.8e-37 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.4%
Validation Efficiency
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 immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. This encoded protein is a cis-trans prolyl isomerase that binds the immunosuppressants FK506 and rapamycin. It is thought to function as an ER chaperone and may also act as a component of membrane cytoskeletal scaffolds. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2008]
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932414N04Rik T G 2: 68,731,985 (GRCm38) F319V possibly damaging Het
Acad12 A G 5: 121,599,214 (GRCm38) V498A probably damaging Het
Adam19 A G 11: 46,060,935 (GRCm38) E37G probably benign Het
Anks3 A G 16: 4,947,279 (GRCm38) Y423H probably damaging Het
Arfgef1 A T 1: 10,189,443 (GRCm38) V600D probably benign Het
Arhgef18 T C 8: 3,454,197 (GRCm38) F939L probably benign Het
Arhgef2 A G 3: 88,633,033 (GRCm38) N127S probably damaging Het
Arid1b A G 17: 5,342,653 (GRCm38) S2100G probably benign Het
Atp1b2 A G 11: 69,603,075 (GRCm38) V93A probably damaging Het
Atrnl1 T C 19: 57,935,652 (GRCm38) V1283A possibly damaging Het
Bpifb5 A C 2: 154,228,181 (GRCm38) K184Q probably benign Het
Cadps C T 14: 12,457,702 (GRCm38) A1060T probably benign Het
Cant1 A G 11: 118,408,746 (GRCm38) V259A probably damaging Het
Ccdc89 A G 7: 90,426,825 (GRCm38) D81G probably damaging Het
Cntnap4 C G 8: 112,875,533 (GRCm38) P1190A probably benign Het
Colgalt2 T A 1: 152,508,611 (GRCm38) Y567* probably null Het
Cyp4f18 A T 8: 71,996,037 (GRCm38) F256Y probably benign Het
Ddx41 G A 13: 55,534,480 (GRCm38) R205W possibly damaging Het
Dop1a G A 9: 86,521,133 (GRCm38) R1462H probably damaging Het
Dync1i2 A G 2: 71,249,372 (GRCm38) T377A probably damaging Het
F2 G A 2: 91,625,488 (GRCm38) T600M probably damaging Het
Fam91a1 C T 15: 58,430,734 (GRCm38) H308Y probably damaging Het
Gabarapl2 T A 8: 111,952,396 (GRCm38) F115L probably benign Het
Heatr3 T G 8: 88,150,371 (GRCm38) probably null Het
Ifi204 T G 1: 173,755,775 (GRCm38) K292N possibly damaging Het
Itpkc A T 7: 27,228,303 (GRCm38) I62N probably benign Het
Kcnab1 G A 3: 65,304,164 (GRCm38) probably null Het
Krt88 G A 15: 101,452,928 (GRCm38) probably null Het
Larp4 C T 15: 99,990,403 (GRCm38) T107I probably benign Het
Lmo7 T C 14: 101,929,342 (GRCm38) probably benign Het
Lrrc37a T C 11: 103,455,518 (GRCm38) Y3174C possibly damaging Het
Lyzl4 T A 9: 121,583,035 (GRCm38) D105V probably damaging Het
Mst1 A G 9: 108,084,295 (GRCm38) I575V probably benign Het
Myh7 C A 14: 54,974,046 (GRCm38) E1555D probably damaging Het
Nwd1 T A 8: 72,667,811 (GRCm38) C608* probably null Het
Obox3 C A 7: 15,627,226 (GRCm38) C38F probably benign Het
P4ha2 A G 11: 54,126,248 (GRCm38) D441G probably benign Het
Pcdhb14 A T 18: 37,448,545 (GRCm38) I235F possibly damaging Het
Rasgrf2 A G 13: 92,030,788 (GRCm38) V259A probably damaging Het
Scn1a T C 2: 66,277,613 (GRCm38) T1590A probably damaging Het
Sdk1 T A 5: 142,051,244 (GRCm38) D817E probably damaging Het
Sema3b A G 9: 107,600,458 (GRCm38) F482S probably damaging Het
Slc35a5 G C 16: 45,158,158 (GRCm38) probably benign Het
Slc6a3 A G 13: 73,562,308 (GRCm38) I346V probably benign Het
Slu7 G T 11: 43,440,684 (GRCm38) probably null Het
Spns1 A T 7: 126,371,539 (GRCm38) probably null Het
Supv3l1 T C 10: 62,449,420 (GRCm38) D89G possibly damaging Het
Taf1c G A 8: 119,600,505 (GRCm38) R412W probably damaging Het
Tctn3 T A 19: 40,607,649 (GRCm38) T305S possibly damaging Het
Tekt1 A G 11: 72,345,748 (GRCm38) I296T possibly damaging Het
Tet2 T C 3: 133,486,055 (GRCm38) K873E possibly damaging Het
Thada G A 17: 84,441,782 (GRCm38) A587V possibly damaging Het
Tmprss15 T A 16: 78,985,996 (GRCm38) N712Y probably damaging Het
Tnks A G 8: 34,853,361 (GRCm38) S719P probably damaging Het
Tnrc6a A C 7: 123,181,384 (GRCm38) Q1332H probably damaging Het
Trpv3 A G 11: 73,283,734 (GRCm38) D309G possibly damaging Het
Tti2 A G 8: 31,153,519 (GRCm38) K221E possibly damaging Het
Uba5 A T 9: 104,054,190 (GRCm38) C227S probably damaging Het
Ugcg C T 4: 59,207,798 (GRCm38) P46S probably benign Het
Unc80 T C 1: 66,677,495 (GRCm38) C2925R probably benign Het
Vmn2r83 G A 10: 79,478,910 (GRCm38) G331R probably benign Het
Xirp2 G T 2: 67,511,422 (GRCm38) V1336F probably benign Het
Zbed5 T C 5: 129,902,277 (GRCm38) Y356H possibly damaging Het
Other mutations in Fkbp2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03242:Fkbp2 APN 19 6,978,612 (GRCm38) missense probably benign 0.08
R6923:Fkbp2 UTSW 19 6,979,169 (GRCm38)
R9259:Fkbp2 UTSW 19 6,978,592 (GRCm38) missense probably benign 0.07
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2015-04-17