ZMP
fkbp10
Ensembl ID:
ZFIN ID:
Description:
peptidyl-prolyl cis-trans isomerase FKBP10 [Source:RefSeq peptide;Acc:NP_001122138]
Human Orthologue:
FKBP10
Human Description:
FK506 binding protein 10, 65 kDa [Source:HGNC Symbol;Acc:18169]
Mouse Orthologue:
Fkbp10
Mouse Description:
FK506 binding protein 10 Gene [Source:MGI Symbol;Acc:MGI:104769]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13780 | Nonsense | Available for shipment | Available now |
sa38876 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13780
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066367 | Nonsense | 142 | 614 | 2 | 10 |
The following transcripts of ENSDARG00000045129 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 15016504)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13872157 |
GRCz11 | 12 | 13910460 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTCAAAGATGGCAAATTGCTGGTGTGGACAAGGGCATTCTGGGTATGTG[T/A]ATAAATGAACGCAGAAAGATCACGGTGCCTCCTCATCTGGCCCACGGTAG
Long Flanking Sequence:
CTTGTGTAAAATTAATATTTTGGGATTTACAAAGCTCTGTTTGAGTGTGCGTGCATATGCAGCAATAGTGTATTTGTCTGTCTGTGTGTGTATGTGCGTGCATATGCACCTGGTATAGTAATACCAGTAGTTATTGACCTGGTGGGAAAATTGTTTGGTCCTCAAAAGGAAAACAGTTAAATTATACATAATGAATATGAGAATCTAAAAATGCTGAATGTTTTCTGTGAATGTAGGATTTAGGAGTAGGGTTTGGGAAAGGGGAAAGAATATGTACTGTCTGTAGCCTACAATACAAATAGTTACATCAATGGGAAGTCATAAAAACATGAAACATAAAACATAAAAAGCCAATGTATATGTGTGTGTTGTTTTTTCAATTAAATTAAAATTGGTTTTGTCTGTTTTAATTGCAGCTATGAGAGAGGTACTGCATTCTTTGGACAGGTGGGTCAAAGATGGCAAATTGCTGGTGTGGACAAGGGCATTCTGGGTATGTG[T/A]ATAAATGAACGCAGAAAGATCACGGTGCCTCCTCATCTGGCCCACGGTAGCAAAGGAGCAGGTACTGTATTATACCCAAACATACATTATACATTCATCTAAAGGAATGTGCATACTAGCTAGAGGCCCAAAACACTTAAGTCATAAAATGGCTTAATATTATATAATTAAATATAAAAGCAAGCATCATTAAAAAAACAAATGTTGTTAGAACTTCACTTTCAACTTCCTCTTTTTCGTTGTGAAATGCTTTACTTCATGTTTTGCATGATCATATTTCTATTTTCAGTATACAGAGCTTAAAACTACTATACACTCACTGGCCACTTTATTAGGTACCACTTGTCCAACTGCTCACTGATGCAAATTTCTAATCAGGCGATCAAATGGCAGCAACTCAATGCAGTTAGACATCTAGACATTTTCAAGAGGATTTGTTGCAGCTCAAACAGAGCATCGAAATGAGGACGAAAGGTGATTTAAGTGACTTTAAACGTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38876
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066367 | Nonsense | 341 | 614 | 6 | 10 |
The following transcripts of ENSDARG00000045129 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 15031130)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13886783 |
GRCz11 | 12 | 13925086 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGCTTTTAAATTCTACTGTATATCACTTTTAAAATCACAGTTATCAA[C/T]AAAACCAGACGTACAACACTTACATCGGAATGGGCTACATGATCGCCGGC
Long Flanking Sequence:
CTACATTAAAAAACATTTTTTGTACCTTGGATGAAGTAACCTTATTAGGATTGGAATAGTATTTAATTAGGGTATGGTATCTGTACTTATACTCAAATTTTTATATTGTATACTTCAACCACCAGCACCACATAACCAGCAAGAAGATTAAGTCAGTTTTCTTTATTTGTTTATCTTTAATTCATCTTTCTCTTGTGTCTCTTTCCCTCAGGTACAGGCATTCCTCCTCATGCATCTGTAGAATATCACATTCTCCTGGAAGACCTGCACAACCCTAAAGATGACATCATTGTGGAGACCCTGAAATTGCCTGAACCATGTGCTCGCAAGTCTGTTGCAGGCGATTTCATTCGTTACCATTACAATGCTTCCTTCCTCAATGGCATCATGTTTGACTCTAGGTATTTTGTTGGTTTGTTAGCTTTTTTAACAATTTGTGGATGCTGTTGGTGTTGCTTTTAAATTCTACTGTATATCACTTTTAAAATCACAGTTATCAA[C/T]AAAACCAGACGTACAACACTTACATCGGAATGGGCTACATGATCGCCGGCATAGATAAAGGCTTGCAGGGTGTTTGTGCAGGAGAGTGGAGAAGAATCATCTTGCCGCCTCACCTTGCCTATGGCCAGCAGGGGGCAGGTTAGATCATTTCAAAGCTTATTTAAAGATAAGTTAGCCAATCAAGATCCAAGCAAGATCCAAGTTTCAATGGCATGATGCAGAAGTACTAAGGGCATGTCTGAATTCTTTTTTGCTATTTAAAGAGTTAGAAAAAAATGGTCCGTGTGCCAGGGCCATGGTCTAAAAGTGTTGTCCTTATTTTATTAATAAGTATATTTTAGGCATAATGTGCATTAAACCAATCAGAGTCTCATCTCCTGTCAGTTGCATTGCACAATGGTGCATTCACTATTAACATGGCAAACTTTGTAAGCAGAAAAACTAAAGGCTTCACTAGTAAGAAAATGGTTGAAGACTATCTGCGCAACCAATGAAAGACC
Associated Phenotype:
Not determined