| Primary Identifier | MGI:3841297 | Allele Type | Targeted |
| Attribute String | Conditional ready, No functional change | Gene | Bptf |
| Transmission | Germline | Strain of Origin | 129S1/Sv-Oca2<+> Tyr<+> Kitl<+> |
| Is Recombinase | false | Is Wild Type | false |
| description | Phenotypic Similarity to Human Syndrome in Orthologous Human Gene: NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL (OMIM:617755) in conditional knockout mice homozygous for Bptftm1.1Cwu and heterozygous for Emx1tm1(cre)Krj (J:334252). |
| molecularNote | A loxP site was inserted upstream of exon 2, and a frt-flanked neomycin cassette and a downstream loxP was inserted downstream of exon 2. Flpe expression removed the neomycin cassette leaving exon 2 floxed. |
