ZMP
si:dkey-11f4.4
Ensembl ID:
ZFIN ID:
Human Orthologue:
BPIL2
Human Description:
bactericidal/permeability-increasing protein-like 2 [Source:HGNC Symbol;Acc:16503]
Mouse Orthologue:
Bpil2
Mouse Description:
bactericidal/permeability-increasing protein-like 2 Gene [Source:MGI Symbol;Acc:MGI:3026884]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12773 | Essential Splice Site | Available for shipment | Available now |
sa7167 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27302 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12773
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121749 | Essential Splice Site | 32 | 472 | None | 15 |
ENSDART00000134093 | None | None | 98 | None | 3 |
ENSDART00000138006 | Essential Splice Site | 32 | 197 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 140922)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 343588 |
GRCz11 | 9 | 343221 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATAATCCAGCATTCAAAGCTCTTCTGTCAGAGAAGGCTCTCACAGACTG[T/C]AAGTTTGCTKTATTTATTCAGTTAGAGGACACGTTTAGCTTTAATCCTGT
Long Flanking Sequence:
TTCTTATAGTTTTTGCTTGGTTTGTTGTCAAGACTAGGAGTTTCTCTGACATGCAAAGCTTTTACACACTGAGAAATCTAAATGTGCAGAGATGTGAATGTTCTCTGTTCCCCACACATTTACTTCCCAGCATTGTTAAAAAAGCAAAAACACACTCTTTAGAAGATAAGCAAGACAAAGATAAACATGAGACAGCTAAATATACACACACATGCATCTGAGCAGGCCCTCAGATAAGCAGATGTGTGCTGCTGTGGGTATCACTTCTCTATAATTTAAGGAAGTGAGCTGAATGGAGGCATTGTGCACCGATATTATAAGCTCTACATGCAGCGTGAGCATCAGTCAGACGCTCAGACAGAAGCAGATGAAGTTCATTAGTTCATTACTGCTGTAATTTGCAGGATGCAGAGGCTGATGTTCCTCCTGATGTTGACGCAGTCATGTGCGGATAATCCAGCATTCAAAGCTCTTCTGTCAGAGAAGGCTCTCACAGACTG[T/C]AAGTTTGCTTTATTTATTCAGTTAGAGGACACGTTTAGCTTTAATCCTGTCTGTTTTATGCAGACTACATTAGATTCAAGATGCCAAAGAGATTTACCATTAGAAAAAATGTTAGAGTATTTGGTGTTGGGTCATTTTCATCCACTCTGGGCTGATTTTGAGTCTTAATTTGGCCTCAACTTTCTCTGTTTCAGATAGCAGAATGATTTTTGGTGACAAATCTTATTTTGACATACAGTTGAAGTCAGAATTATTAGCGCCCCTGTTTATTTCCCCCCCCTGATTTCTGTTTAATGTAGGGAAGATTGTTTCAGCACATTTCTAAGCATAATAGTTTTACAAACTCATCTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTACATAATATTTTACTTGATATTCTTCAAGTCACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTTATAAGGTGAACTAGGCAGGTTTGTGTAATTAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7167
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121749 | Nonsense | 117 | 472 | 4 | 15 |
ENSDART00000134093 | None | None | 98 | None | 3 |
ENSDART00000138006 | Nonsense | 117 | 197 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 136184)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 348326 |
GRCz11 | 9 | 347959 |
KASP Assay ID:
554-4571.1 (used for ordering genotyping assays)
KASP Sequence:
TTATKAGTAATGCTYATGCCTGTTCTCTGACTGCAGCACMGACAGCGGCT[C/A]RTTTGATGTGGAGGKCTACAATATATACATCYGTGTGGTCCTGGGGGTCG
Long Flanking Sequence:
CAGTCAGTCAGTCAGACAGACAGTCGACAGCAGCCTCTGGTGGGTTTACACGAGAACAGCGCGGGCACGAACGGCACTTGGGAGAGAAATTAGAGATATGAAAAAGCACACACAGCGCCCTCTCGTGGATTCGCGAAAACAAAAACTGCCAAAATACGTACCTCCTGGGATGTAATTCGCGGCCTCCAGAAACATCCACGGGACTACGCTTTCAGAATGAGCCTGGGGTTGGTTTTGTGTCATGTGAACATCATTCAGTGACCAGCATTCTGGGTATCTAGAAACAGCCTTTGCCATCTTTAGCTCCCCGTTACCAGCCAATCTGTGCCGACCACACACTGTGATTGGTGGAGAGCAGACAGTGGTGAAGCCATACACACAATACTTTATGAGCACAGAGAGTCCTCACTTTAATATCTGAATGAACGTATAAAGCTAAAATGAATGTGTTTATGAGTAATGCTCATGCCTGTTCTCTGACTGCAGCACAGACAGCGGCT[C/A]GTTTGATGTGGAGGTCTACAATATATACATCCGTGTGGTCCTGGGGGTCGGGGATAAAGACGGTCACCTCTCCATCAGCAGCGAATCCTGCAGTAATGATGTAGGAAATGTCTACATTCAGTTTCACGGAGGAACAAGGTAAAGAACAGAGCGTAAGGTGAGAGACGCCAGTGACTGATGCCATCATAATCACTGTGCTCTTCTGCAGCTTCTTCTATCAGCTGTTTGAAGATTATTTCAGTGGAAAAGCCTCAGACATGATACGCCAGAAGGTTGGTGTAGTCTTCAACAGTCCATCACTGTCACTGTATATCTGCTGCTTCTCAAACACCTCATATTGTCTTTCTTATAGATCTGTCCAGCAATCCAACAAGCAGTCACTAACATGGAGACAATTCTGCAGGAACGAACCGGTGATGAACACAGACACGGCATTGTGTATTTAGCACAATGAAGACTGTTTGTTTTAAAATGTTTTATAAAGCATTGTATAGAGTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27302
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121749 | Nonsense | 437 | 472 | 14 | 15 |
ENSDART00000134093 | None | None | 98 | None | 3 |
ENSDART00000138006 | None | None | 197 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 130901)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 353609 |
GRCz11 | 9 | 353242 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTCTTTGTGATTATCTTGTCTCAGCTCGTCTGAGGTCCGGCTTTCTCT[T/A]GCCCACGCTGCAGGGATTTAGCTTGAGTAACTCTCAACTGCTCATCAAAA
Long Flanking Sequence:
AATGGTTATCTGACAGACAGAGCCTTTTCACTGTAGTAACCCCAAGAAAAAAAGGTGGTAGATTAATGAAACTCTTCCTCTGCGTTTCTCATAAATGCTGCTCCAAGTATAACACTGACTGTGGGATCATCTGAGATTGGAGATTTCAAGGTGAGATTTAATAAGCTGTTATTATTCATATCAAGCGTTCATCATCACTAATGATTTCTCAATTCTTCAATATGTGCAGACTGACACAATTAGGCAAGTGTTAGTGATCGCCGTCAACACCATTATCCTGCCAAAGCTAAACGGTGAGCACTTCTAATTTTTTATAAACCCTTTCCATTATTTCAATTATTCATCATTTTGTAAATTCCTTTGCAACTGAGTAAAGCAAATTTCGAAAACTATAGTTATGTATTTATTTATGAATTATTTTAGGGGAAATCTGGAGGTTATCTGAAGGTTAACTCTTTGTGATTATCTTGTCTCAGCTCGTCTGAGGTCCGGCTTTCTCT[T/A]GCCCACGCTGCAGGGATTTAGCTTGAGTAACTCTCAACTGCTCATCAAAAACGTGAGTATTTTAAATGAATGTTCATGTATTTAATGATGTTTTTGTTAATGTTAGAAACTTGTTGGAAAGCAGCACAATATCAGTGTTAATTCGATCCCTTTATTTCAGGGCTTTGTGGTCATTTTTACCGACATCAGACTCCCTGATGGGCTGAATGCTCCATAACGGCTCACATGTCAACACAAACCACAGGCGCTCGACAGAACTCTGCTGTTCATTATACAGCCAACTGCTTTTGTGTTGTCATGTTTTGTGTGAACAAACTGCTTATACGTTTCCCAGTGCTGGGTTGCTGCAGGAAGGGCATCCACTGCCTAAAAAATACGCTGGAATAGTTGGCGGATGGTTCCGCTGATGAACCAAGGGAAAATGAATGAACTGCTGTCATTGGCTGTATGTGGTTGTCTCTTGTTTTGAGCACACGGCTTTGTTTTGTTTCACTTTCTGC
Associated Phenotype:
Not determined