ZMP
si:ch211-13k12.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein (Si:ch211-13k12.1) [Source:UniProtKB/TrEMBL;Acc:A2BI98]
Human Orthologue:
FKBP8
Human Description:
FK506 binding protein 8, 38kDa [Source:HGNC Symbol;Acc:3724]
Mouse Orthologue:
Fkbp8
Mouse Description:
FK506 binding protein 8 Gene [Source:MGI Symbol;Acc:MGI:1341070]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23310 | Nonsense | Available for shipment | Available now |
sa36654 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23310
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007856 | None | None | 430 | None | 8 |
ENSDART00000097167 | Nonsense | 30 | 504 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 25437158)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 25666931 |
GRCz11 | 18 | 25653463 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTGGAGATCCAGAGGAGACAACATTGGAAACTGAGATGTTTGCGAAAT[C/A]AGAAGAGCTGAAAAGTGAAGAAAGTGTTTTGCAGCCCTGGGAGGAACCAA
Long Flanking Sequence:
TTAGATTTTGCTCTTCTAATCCAACAGATTATCAGTGCACACAACTCTACTGACCAGTAGGGCTTCACATTTTAACACAATGCTCATGCACTGATCATTTCTTGCATCTTTCGATAACAGAACATCTCTCGAATCAACACATTTCCTGCAAAACATTCATAAAAGGACTGTTTCATCAGTGCTGCAGGAGATGGACTGGCTACAGATGGGATTTATGTCATGCGGAGATGCACTTCCATGACAATTCTATTAGAGTCCATGTGGACACACCATGCTTTAGAAAATACTACACGCTGTTACTAATGGATGCAGGTGCTCATCGGTTTGGCAGTTGAGCAGCAGGGACATCAATTTTTACAGACTTGGCGTTTATCGTGTGCTTGGAAGATATTCAACACTTTTAGGAAAATAAATGGTATCCTTAGCACCGTGTGGGGACATGGAGCCAGAAGCTGGAGATCCAGAGGAGACAACATTGGAAACTGAGATGTTTGCGAAAT[C/A]AGAAGAGCTGAAAAGTGAAGAAAGTGTTTTGCAGCCCTGGGAGGAACCAATAATGGAGTTGCAGAAAATGAATATCACTGAAAAGGAGGTTGAGAGGAAAATAGCAGAAGAAGGAAGTGAGGAGAGAGATGAAATGGAGAATAAAGAGGCAGAAGAGAGTGAAGAAGAGTTTGCTGAAAGCTTTACAGATGCTAATGCCTCCACCAGTTACCCAACAAATGAGCCCATTACTTCAAAAACCCACATCGGCCCACCTAAATCCATTGAATCCAATCCAATGGAGGACAGAGGAAAACTGTCTAAGACTCCCAGCTTTGGGAAAATGGTTCGGTTTAAGGAAATTGAAGTAGTGGAGGAAAGGGACACCTCAGACGACACTCTTTTTCCAGACTTTGACATGGAAGAGTGGACCACCAGCAGGTTTGAGGAGCTTTTTCTGGCAGACGACTGGAAGAACATTACAGGTGAGATGTTCAAGTGATCATATGAAACCCTAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36654
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007856 | Essential Splice Site | 270 | 430 | 5 | 8 |
ENSDART00000097167 | Essential Splice Site | 344 | 504 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 25524388)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 25754161 |
GRCz11 | 18 | 25740693 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGATAATTGTTTGGGGTTATACAACGAGGCTGTAAAATTGTCCTCCTAC[A/T]GATGGTCAAAACTGTGTGGCAGAGGAAGAAGAAGAAGTGAACGATTATCG
Long Flanking Sequence:
TTATATTATCTGCTAATTAGTAACCTCATGTGGAACTGCGTCTCATTTCGGAGTCTGCTACTGTCCACCGGAGGTCGCATTCCAGTCAAGGATGCAAGCTTTGAGAGCCTTCCTGAATGAATGAATGAATGAAATGTGCTGTTTTGAAGCAACCCGAGGTGCTAATATTTTTGGCAGTTTAAAAGAACCAAAAAAGTCAGCGTTCCGGCACGGAAAACACATTTTCAAAGCAGAATATCTGACTTCAGCATTGTGTTTCAGATAAACAAGAATGTTCACTTGCATGTTTCTTGAATATCTACAAACATATTAGGGTGTTTATATGCTTTAGAAGAGTAAAAAACTTACATACAGCACCTTTAAACAAGAAAAGTATTGTATTATTCAGTTACGATAAATGAAACTGAATGTTAATAATAAACACACTTTTAAATGTCTTTATATTTCCTTGAGATAATTGTTTGGGGTTATACAACGAGGCTGTAAAATTGTCCTCCTAC[A/T]GATGGTCAAAACTGTGTGGCAGAGGAAGAAGAAGAAGTGAACGATTATCGAGTGAAATGTCTGAATAATCTGGCAGCAGCACAGCTGAAGCTTGGACATTTCGATGAGGCGCTGCACACCAGTCAAGATGTGCTGTTTCTGGATCCCCAGAACGTCAAAGCATTGTTCAGGAAAGGAAAGGTATGGGCTGCATGTTATTCAGCAAACTAGGCACTGAAACTAGGAATGTTTGTCTTTTACACTTGGATTGTGCTCAACTGTAAATGTACAATATGTATGCAGCTTTTATCAGACAAGGGCGAGTATGAGGAGGCCATGGAGACCTTGAAGAAGGCTTTGAAACTGGAGCCATCAACCAAGGTGAGAGAGAGACGTAACCGTATCTCCTGGACACATCTACATTTCACGTGAACTGGCAACAGACAATCCCATTAGCAGCTATTTACAGATCAACCAAGGCCTTTATGAAACACCTGGCCTGACTGCTGCACTGCTGTTAT
Associated Phenotype:
Not determined