ZMP
si:ch211-136i24.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate bicaudal D homolog 1 (Drosophila) (BICD1) [Source:UniProtKB/TrEM
Human Orthologue:
BICD1
Human Description:
bicaudal D homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:1049]
Mouse Orthologue:
Bicd1
Mouse Description:
bicaudal D homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1101760]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17748 | Nonsense | Available for shipment | Available now |
sa16298 | Nonsense | Available for shipment | Available now |
sa14781 | Nonsense | Available for shipment | Available now |
sa390 | Nonsense | Available for shipment | Available now |
sa36586 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17748
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 |
---|---|---|---|---|---|
ENSDART00000112671 | None | 222 | 854 | 4 | 8 |
ENSDART00000140854 | Nonsense | 222 | 820 | 4 | 7 |
ENSDART00000112671 | Nonsense | 222 | 854 | 4 | 8 |
ENSDART00000140854 | Nonsense | 222 | 820 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 11553609)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12136539 |
GRCz11 | 18 | 12105257 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGCTTGAAGAAGAAACGGTGCTGCTCAACAGTCAATTAGAAGAYGCTT[T/A]ACGGTTAAAAGACATTTCCCAAGGCCAGTTGGAGGAAGCGTTGGATTCTC
Long Flanking Sequence:
ACAGTCTTTAGAAAATGTAAAGATGGAATATTGTTTTTTTTTTTTTGGTATTAAAAAGACTCCTTACAATAATTTTTCTTAATTTATATATTTATTTTATGGCTATAATTATTGGAATTGTAATGACTTTTATTTGAAATGAGTGACAGTGTGTCTTATTTTATTATTTTTATTTATTTTTATAAGTATTTATGTATTTGTTTGTTTGTTTATTTCTTTTATTATTATCATAATAATAATAATAATAATAATTATTATTATTATTATTATTAACTATAATAATAATAATAATAATAATATAATCATTATTATCATCATCATCATTATTAATATTATTATATTTTTTATTATCATCATTATTATTATCATTATTATGATTATTATATTCCACAGTTGAGTGTCCATTTATTTCTCACAGGTGGAATATGAGGGTCTAAAGCATGAAATCAAAGTGCTTGAAGAAGAAACGGTGCTGCTCAACAGTCAATTAGAAGATGCTT[T/A]ACGGTTAAAAGACATTTCCCAAGGCCAGTTGGAGGAAGCGTTGGATTCTCTGAAGAGCGAACGAGAGCAGAAGAACAATCTGAGAAAAGAGCTGGCTCATCATCTCAGCCTGACTGACAGTGTTTATGGAGCCAGCACTCACCTGGCCATCTCTGCCGTGGAGGGTCTGAAGTTTGCAGAGGAGGCTGCGACCAATGGCACGTCTGCTTCCGGGACCAGTCCTAACAACGAGGACAGCAACCGGTGTAATAATGAGTGTAATGGACATGGACCAAAAGGAGAATACCATCGCAGGAAGACAGAGATGCTCCCGGTGTCTGATCTCTTCAGTGAACTCAACCTGTCTGAGATACAGAAACTCAAGCAGCAGCTCATACAGGTCAGTCGAAAAAGATGGGATAATCTGATTATAATATACAGTTTAAGTCTGAATTATTAGCCCCCTCTATATTTTTGTCACCAATTTCTGTTTAATGAAGAGAAGATTTTCTTTAATACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16298
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 |
---|---|---|---|---|---|
ENSDART00000112671 | None | 222 | 854 | 4 | 8 |
ENSDART00000140854 | Nonsense | 222 | 820 | 4 | 7 |
ENSDART00000112671 | Nonsense | 222 | 854 | 4 | 8 |
ENSDART00000140854 | Nonsense | 222 | 820 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 11553609)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12136539 |
GRCz11 | 18 | 12105257 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGCTTGAAGAAGAAACGGTGCTGCTCAACAGTCAATTAGAAGAYGCTT[T/A]ACGGTTAAAAGACATTTCCCAAGGCCAGTTGGAGGAAGCGTTGGATTCTC
Long Flanking Sequence:
ACAGTCTTTAGAAAATGTAAAGATGGAATATTGTTTTTTTTTTTTTGGTATTAAAAAGACTCCTTACAATAATTTTTCTTAATTTATATATTTATTTTATGGCTATAATTATTGGAATTGTAATGACTTTTATTTGAAATGAGTGACAGTGTGTCTTATTTTATTATTTTTATTTATTTTTATAAGTATTTATGTATTTGTTTGTTTGTTTATTTCTTTTATTATTATCATAATAATAATAATAATAATAATTATTATTATTATTATTATTAACTATAATAATAATAATAATAATAATATAATCATTATTATCATCATCATCATTATTAATATTATTATATTTTTTATTATCATCATTATTATTATCATTATTATGATTATTATATTCCACAGTTGAGTGTCCATTTATTTCTCACAGGTGGAATATGAGGGTCTAAAGCATGAAATCAAAGTGCTTGAAGAAGAAACGGTGCTGCTCAACAGTCAATTAGAAGATGCTT[T/A]ACGGTTAAAAGACATTTCCCAAGGCCAGTTGGAGGAAGCGTTGGATTCTCTGAAGAGCGAACGAGAGCAGAAGAACAATCTGAGAAAAGAGCTGGCTCATCATCTCAGCCTGACTGACAGTGTTTATGGAGCCAGCACTCACCTGGCCATCTCTGCCGTGGAGGGTCTGAAGTTTGCAGAGGAGGCTGCGACCAATGGCACGTCTGCTTCCGGGACCAGTCCTAACAACGAGGACAGCAACCGGTGTAATAATGAGTGTAATGGACATGGACCAAAAGGAGAATACCATCGCAGGAAGACAGAGATGCTCCCGGTGTCTGATCTCTTCAGTGAACTCAACCTGTCTGAGATACAGAAACTCAAGCAGCAGCTCATACAGGTCAGTCGAAAAAGATGGGATAATCTGATTATAATATACAGTTTAAGTCTGAATTATTAGCCCCCTCTATATTTTTGTCACCAATTTCTGTTTAATGAAGAGAAGATTTTCTTTAATACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14781
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112671 | Nonsense | 431 | 854 | 5 | 8 |
ENSDART00000140854 | Nonsense | 431 | 820 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 11560011)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12142941 |
GRCz11 | 18 | 12111659 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTGCTGTGAGTTTGARACWGACATCAATGGAATAGAGCTTYTAGAGTGC[A/T]AATACAGAGYTGCCGTGACTGAGGTCATTGACTTGAAGGCGGAGCTTAAG
Long Flanking Sequence:
ATAATGCATGTTTGTTTGTGTTGGAGACGTTTCTGGGATTAGGGGACTTAAATAAACCTGCAATGTTTGGAAATGTAAAAGAACTTAATGGATAAATAAATAAATGTATTTTTGTTCATTTAACTAAAATAAATTATTACATAAATACAAATTATTTATTTAAATGTTTATGTATTATTAAATTAATAAATACTTGTATTTTATTAAATATGTATTAGTTTTTATGTGTTCACTTTTATATTTTTTTCCACCAGGTTGAGCGAGAGAAAGCAATTCTACTTACCAACCTGCAGGAGTCTCAAACTCAACTGCAGCACACGCAGGGTGCTTTAACTGAGCAGCACAGACGTGTTCACCGCCTTACGGAACGTGTTAATGCTATGAAACGCCTCCACAATGACAAGGAGTTTGACACAGAAGAGTCCGAGAAGGGCGACGGTCCTATTAACGGTTGCTGTGAGTTTGAAACAGACATCAATGGAATAGAGCTTCTAGAGTGC[A/T]AATACAGAGTTGCCGTGACTGAGGTCATTGACTTGAAGGCGGAGCTTAAGGTGTTGAAGGAAAAGTATAACCAGTCTTTGGAGAGCCAATCAGAAGAGAGCAACCACAGCGAAGGGAAGGTCCAGGCGCTTGAAGAACAGGTGAAACAACTGGAGAAAAGCTGTCGTGAGGCACGTGAGCGGGTCAGCAGTCTGGAAGCTGAGCTTCGGTGTGCTTCTGGAATGGCCAGCGAAAGTAACGGCATGCTGAATGCAGCTCAAGATGAGCTGGTTACATTTAGCGAGGAACTTGCTCAGCTCTACCACCACGTCTGCTTGTGCAACAATGAAACGCCAAATCGTGTCATGCTGGACTACTACCGTCAGAGTCGGGTCACACGTAGTGGCAGTCTCAAAGGCCCAGAAGACCCACGAGCCCTGCTTTCTCCACGTTTAGCTCGGCGTCTTGCAGCTGTGAACTCCTCAGACATGTCCAAGAGTCCTCAAGACTCTCCTTCGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa390
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112671 | Nonsense | 613 | 854 | 5 | 8 |
ENSDART00000140854 | Nonsense | 613 | 820 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 11560557)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12143487 |
GRCz11 | 18 | 12112205 |
KASP Assay ID:
554-0252.1 (used for ordering genotyping assays)
KASP Sequence:
CGAAGGAACCCCTTGGAGACGGAATTAAAGGGGAAGGAGGAAGTCCCAAT[A/T]GAACCCCATTTGGCTCACCAATCAATGGTTCATCTCTCTCATCCTCCACA
Long Flanking Sequence:
TTAAGGTGTTGAAGGAAAAGTATAACCAGTCTTTGGAGAGCCAATCAGAAGAGAGCAACCACAGCGAAGGGAAGGTCCAGGCGCTTGAAGAACAGGTGAAACAACTGGAGAAAAGCTGTCGTGAGGCACGTGAGCGGGTCAGCAGTCTGGAAGCTGAGCTTCGGTGTGCTTCTGGAATGGCCAGCGAAAGTAACGGCATGCTGAATGCAGCTCAAGATGAGCTGGTTACATTTAGCGAGGAACTTGCTCAGCTCTACCACCACGTCTGCTTGTGCAACAATGAAACGCCAAATCGTGTCATGCTGGACTACTACCGTCAGAGTCGGGTCACACGTAGTGGCAGTCTCAAAGGCCCAGAAGACCCACGAGCCCTGCTTTCTCCACGTTTAGCTCGGCGTCTTGCAGCTGTGAACTCCTCAGACATGTCCAAGAGTCCTCAAGACTCTCCTTCGAAGGAACCCCTTGGAGACGGAATTAAAGGGGAAGGAGGAAGTCCCAAT[A/T]GAACCCCATTTGGCTCACCAATCAATGGTTCATCTCTCTCATCCTCCACAATTCCAGAGACAGGTGATCTCCGCAGGGAGCCCATGAACATCTATAACCTCAACGCCATCATCCGTGACCAAATCAAGCACCTGCAGAAGGCTGTAGACCGCTCTCTCCAGTTGTCCAGGCAGAGGGCTGCTGCTAGAGAGTTGGCGCCTATCCTCGATAAGGACAAGGAGGCCTGCATGGAGGAGATCCTGAAACTCAAATCGCTCCTGAGCACCAAAAGAGAGCAGATCGCCACCTTACGTCTTGTCCTAAAAGCCAACAAACAGGTAGAAGACCAAGTCTTTGCAAGAACTACTTTTAAATTGAGTAATAAAAGCAAACCTAAAAGAACATTATATCTTTGTCATATTTGTTTCTAGACTGCTGAGGTGGCCCTGGCAAACCTCAAGAGCAAGTATGAAAATGAGAAATGCATGGTGACGGAGACAATGATGAAGCTTAGGAATGAA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa36586
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112671 | Splice Site, Nonsense | 718 | 854 | 5 | 8 |
ENSDART00000140854 | Splice Site, Nonsense | 718 | 820 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 11560872)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12143802 |
GRCz11 | 18 | 12112520 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAAAGAGAGCAGATCGCCACCTTACGTCTTGTCCTAAAAGCCAACAAA[C/T]AGGTAGAAGACCAAGTCTTTGCAAGAACTACTTTTAAATTGAGTAATAAA
Long Flanking Sequence:
GTCAGAGTCGGGTCACACGTAGTGGCAGTCTCAAAGGCCCAGAAGACCCACGAGCCCTGCTTTCTCCACGTTTAGCTCGGCGTCTTGCAGCTGTGAACTCCTCAGACATGTCCAAGAGTCCTCAAGACTCTCCTTCGAAGGAACCCCTTGGAGACGGAATTAAAGGGGAAGGAGGAAGTCCCAATAGAACCCCATTTGGCTCACCAATCAATGGTTCATCTCTCTCATCCTCCACAATTCCAGAGACAGGTGATCTCCGCAGGGAGCCCATGAACATCTATAACCTCAACGCCATCATCCGTGACCAAATCAAGCACCTGCAGAAGGCTGTAGACCGCTCTCTCCAGTTGTCCAGGCAGAGGGCTGCTGCTAGAGAGTTGGCGCCTATCCTCGATAAGGACAAGGAGGCCTGCATGGAGGAGATCCTGAAACTCAAATCGCTCCTGAGCACCAAAAGAGAGCAGATCGCCACCTTACGTCTTGTCCTAAAAGCCAACAAA[C/T]AGGTAGAAGACCAAGTCTTTGCAAGAACTACTTTTAAATTGAGTAATAAAAGCAAACCTAAAAGAACATTATATCTTTGTCATATTTGTTTCTAGACTGCTGAGGTGGCCCTGGCAAACCTCAAGAGCAAGTATGAAAATGAGAAATGCATGGTGACGGAGACAATGATGAAGCTTAGGAATGAACTCAAGGCTCTCAAAGAAGACGCAGCCACCTTTTCCTCACTGAGGGCAATGTTTGCAACAAGGTACATTTTTAGCTCTTGTCTGCAGTTAACATTATATACATTTTCTGCCGCTCTCCTCCAACTTAAAAGGTCTTCTGATGTAGTTCAAATGCTATGTTTCCATCCAAAGATGTTAATCAAAATTATGTGTTAAACTGGAATATCGCATAAAACATTTGCGAATAAAGCATTGTTTCAATCCGATGAGTTAAAGAGTACACAATCATCATTTCCTGATAAACTGATGCCAAATATTAAAAAGAAAATGGTTGAA
Associated Phenotype:
Not determined