ZMP
LOC557383
Ensembl ID:
Human Orthologue:
BICD2
Human Description:
bicaudal D homolog 2 (Drosophila) [Source:HGNC Symbol;Acc:17208]
Mouse Orthologue:
Bicd2
Mouse Description:
bicaudal D homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1924145]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35141 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa5846 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12439 | Nonsense | Available for shipment | Available now |
sa41891 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1692 | Nonsense | Available for shipment | Available now |
sa38858 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35141
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 |
---|---|---|---|---|---|
ENSDART00000109235 | Nonsense | 127 | 836 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 37910186)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 36802673 |
GRCz11 | 11 | 37070216 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAGGCGTACTATGAGCAGAGGGTGCAGGAGCTGCAGTCGGACCTACGA[C/T]AAGCTAAAAACACCCTCACCGGCACCCAGGCGGAGAACGAGCGCCTGGCC
Long Flanking Sequence:
CGGTTTTGCTTTACGTGTGGTCGGTTTTTAGAGTTTATAAAGGACGCGGACCAGACGGAAACACCAGTCATACTGCATTAATGTGTTGAATATTTTTATGAGATCCACTCGTATGCTGTAATCATAATTGTAAATTTAATTGTAAATTTGTTTCTGAAGTGTCTGAATAACATTTGGTTTGACTGTACATTCCATAACATCCATTTAGTAGTGTTGTACAAGTGCTTTAAACTTCAAACCTCCACCCCCATCCATCCTCCACCCTACAAGACAAGTAATTAGCTTGTAAACCACAGAGCTAGATCTTACTAGACTTTTTACAGAATTTAACCCTCAATCTCTCTCCTATCATGTTCCCACAGGCCTATGGCCAGGTTCACTCAACCCACAGAAAGGTGGCTGCGGACGGCGAGAGCAGGGAGGAGTCGCTCATCCTGGAGTCGGCATCTAAAGAGGCGTACTATGAGCAGAGGGTGCAGGAGCTGCAGTCGGACCTACGA[C/T]AAGCTAAAAACACCCTCACCGGCACCCAGGCGGAGAACGAGCGCCTGGCCACCCTTGCCCTCGAGCTGAGAGAGGTCTGTGAATGCCACCACATAAAATGTATTCAACAGCAAATGTTGCTTGAAAAAAAGTTACAAGTACAAAAATATTAATAATTATACAAGTAATACAGTACAATACTAATTGTAATACTTATCTAATACAAACTAAAGCCAGTGGATCGCTCCTCCAATGAAATGTTAAGCTATTATTTAGGAATATCGATTTCCACGTTTCCATCACCCAAAAATGAAAATCGCTCATAAAAGAAATCAAAACTGTAAATTTCCTCACTTATTACTCACAATCAAGTAGTTTTGTTTGCCAAGGTAAATACTATTAGATTCAAAAGATTCATTGGTAATATCAATTATTACAATGAAAATGATCCATATCCTGTTTTAAACCCTGTTTTATTTATTTGTAATTGATTAATTCATCCATTCAATAATTAATTCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5846
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 |
---|---|---|---|---|---|
ENSDART00000109235 | Nonsense | 267 | 836 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 37914769)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 36807256 |
GRCz11 | 11 | 37074799 |
KASP Assay ID:
554-3861.1 (used for ordering genotyping assays)
KASP Sequence:
ACGGGAGCAGAAAGCAGCCCTTCGGAAAGARCTGACGCATCACATGACCT[T/A]GGGAGACTCCCTTCTCGCCAGCTCATTGGACGGACTCAAATTGAGTGCAG
Long Flanking Sequence:
CAAAAGCCCCCTTTCATGCTTAAATATACAAGCGTGGCTGTTTAGTGTTCATTTTTTGGTTAATTATGTCAGAATTTACTGGTATTTTGGAAAGGATGTGTGAATAGTGTTTTCCAGAAAATTTCGTAACGTCCTTTTATTAATTTATCGGTAAAGTTGTTCCTGAAATTTTCCGGATATTTACCAATTTCACTGTGTAAAAGGGGCTATTGTGGATGCATGAAAATTTCTGATTAACTTCCACAAAGTTGCATGTGTACAATTGCTGTATTTGTTTTGGCTTAAAAATCTTTCGCCTCTTTCAAAGGTGGAGTTCGAGGGACTCAAACATGAAAATCGGCGATTGGAAGAGGAAGTGCAGTACTTAAACAGCCAACTAGAGGATGCCATTCGGTTACGGGAAATCGCAGATCGTCAGCTAACGGAGGCTCTAGAAACCGTCAAGACCGAACGGGAGCAGAAAGCAGCCCTTCGGAAAGAGCTGACGCATCACATGACCT[T/A]GGGAGACTCCCTTCTCGCCAGCTCATTGGACGGACTCAAATTGAGTGCAGATGAACCTAATAATGACGATGCCATTCTGACTCTTGAAAACGGATTTGCTAAAGTCTGTGAAGGTAATGATGAAGATAACAGATTGTCTTCACCCAAGAGAGATGAAAATTTCCGTCCCGCACCAAGTCTGGTAGATGACTTGTTGACCGAATTGAACATCTCTGAGATCCAGAAACTCAAGCAACAGCTCTTACAGGTATGCTAATGTACAATTCTACAAATGCAGGCTTCAAGTCCAATGGTTCTTGTTAAAAATATATATTAAAAACGATTTAAAATTAGATAAAAATGAAATTTTACAGCAAATCTCAAACAATGAAGCAAATAATGGCATACAAATCAGTCATTTTAGGACACATGATTAGATTAGACATGTCAATATTCAGTAATTTATTAAGTCAGTATATCACAATATTGATATCATGAGCACTTCATAATACCATGAGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12439
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 |
---|---|---|---|---|---|
ENSDART00000109235 | Nonsense | 303 | 836 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 37914878)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 36807365 |
GRCz11 | 11 | 37074908 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATAATGAMGATGCCATTCTGACTCTTGAAAACGGATTTGCTAAAGTCTG[T/A]GAAGRTAATGATGAAGATAACAGATTGTCTTCACCCAAGAGAGATGAAAA
Long Flanking Sequence:
TTTTCCAGAAAATTTCGTAACGTCCTTTTATTAATTTATCGGTAAAGTTGTTCCTGAAATTTTCCGGATATTTACCAATTTCACTGTGTAAAAGGGGCTATTGTGGATGCATGAAAATTTCTGATTAACTTCCACAAAGTTGCATGTGTACAATTGCTGTATTTGTTTTGGCTTAAAAATCTTTCGCCTCTTTCAAAGGTGGAGTTCGAGGGACTCAAACATGAAAATCGGCGATTGGAAGAGGAAGTGCAGTACTTAAACAGCCAACTAGAGGATGCCATTCGGTTACGGGAAATCGCAGATCGTCAGCTAACGGAGGCTCTAGAAACCGTCAAGACCGAACGGGAGCAGAAAGCAGCCCTTCGGAAAGAGCTGACGCATCACATGACCTTGGGAGACTCCCTTCTCGCCAGCTCATTGGACGGACTCAAATTGAGTGCAGATGAACCTAATAATGACGATGCCATTCTGACTCTTGAAAACGGATTTGCTAAAGTCTG[T/A]GAAGGTAATGATGAAGATAACAGATTGTCTTCACCCAAGAGAGATGAAAATTTCCGTCCCGCACCAAGTCTGGTAGATGACTTGTTGACCGAATTGAACATCTCTGAGATCCAGAAACTCAAGCAACAGCTCTTACAGGTATGCTAATGTACAATTCTACAAATGCAGGCTTCAAGTCCAATGGTTCTTGTTAAAAATATATATTAAAAACGATTTAAAATTAGATAAAAATGAAATTTTACAGCAAATCTCAAACAATGAAGCAAATAATGGCATACAAATCAGTCATTTTAGGACACATGATTAGATTAGACATGTCAATATTCAGTAATTTATTAAGTCAGTATATCACAATATTGATATCATGAGCACTTCATAATACCATGAGTATTTAATTAATACTAAAACTTTTAGAGTTAAGATTTTAGAGTTAAAATTTTGAATTAATCAGGTTTATTTAAAAAATATATATATTTAAAATAAAACATTTTTACATTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41891
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 |
---|---|---|---|---|---|
ENSDART00000109235 | Nonsense | 332 | 836 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 37914964)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 36807451 |
GRCz11 | 11 | 37074994 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGAGAGATGAAAATTTCCGTCCCGCACCAAGTCTGGTAGATGACTTGT[T/A]GACCGAATTGAACATCTCTGAGATCCAGAAACTCAAGCAACAGCTCTTAC
Long Flanking Sequence:
TGTAAAAGGGGCTATTGTGGATGCATGAAAATTTCTGATTAACTTCCACAAAGTTGCATGTGTACAATTGCTGTATTTGTTTTGGCTTAAAAATCTTTCGCCTCTTTCAAAGGTGGAGTTCGAGGGACTCAAACATGAAAATCGGCGATTGGAAGAGGAAGTGCAGTACTTAAACAGCCAACTAGAGGATGCCATTCGGTTACGGGAAATCGCAGATCGTCAGCTAACGGAGGCTCTAGAAACCGTCAAGACCGAACGGGAGCAGAAAGCAGCCCTTCGGAAAGAGCTGACGCATCACATGACCTTGGGAGACTCCCTTCTCGCCAGCTCATTGGACGGACTCAAATTGAGTGCAGATGAACCTAATAATGACGATGCCATTCTGACTCTTGAAAACGGATTTGCTAAAGTCTGTGAAGGTAATGATGAAGATAACAGATTGTCTTCACCCAAGAGAGATGAAAATTTCCGTCCCGCACCAAGTCTGGTAGATGACTTGT[T/A]GACCGAATTGAACATCTCTGAGATCCAGAAACTCAAGCAACAGCTCTTACAGGTATGCTAATGTACAATTCTACAAATGCAGGCTTCAAGTCCAATGGTTCTTGTTAAAAATATATATTAAAAACGATTTAAAATTAGATAAAAATGAAATTTTACAGCAAATCTCAAACAATGAAGCAAATAATGGCATACAAATCAGTCATTTTAGGACACATGATTAGATTAGACATGTCAATATTCAGTAATTTATTAAGTCAGTATATCACAATATTGATATCATGAGCACTTCATAATACCATGAGTATTTAATTAATACTAAAACTTTTAGAGTTAAGATTTTAGAGTTAAAATTTTGAATTAATCAGGTTTATTTAAAAAATATATATATTTAAAATAAAACATTTTTACATTAATCTGGCCTATTAAATGGACAAATTCTGTGACTATGTATAGGCCTTTATGCAAGTTTTTATTAGTAGCATCTGTTAATTTACTAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1692
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109235 | Nonsense | 663 | 836 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 37921101)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 36813588 |
GRCz11 | 11 | 37081131 |
KASP Assay ID:
554-1638.1 (used for ordering genotyping assays)
KASP Sequence:
GCATGGAGGAGATTTTGAAGCTCAAGTCCTTRCTGAGCACCAAGCGTGAA[C/T]AGATTGCCACRCTCAGGACTGTGCTCAAGGCCAACAAGCAGGTGAGAGTA
Long Flanking Sequence:
TCGCTAAGCTAGAAAAGGAACTGAAGGAAGTGAGCGCAGTTGCAGGCGAGACCGAAGGAAGTCTCAGTGTCGCCCAGGATGAGCTTGTTGCATTTAGCGAAGAGCTGGCAAACCTCTACCATCATGTCTGCATGTGCAACAATGAAACCCCGAATCGTGTCATGCTCGATTTTTACAAAGAGGGTAAAGGAAGCAAGACGGAAACTAAAGATCGGCAGTCTACATTAACGCAAACTAATGAAAGTAAAGCCCAGACGTCAAGGTCAAACTCAATCCCTGTTGACAGAGAAGAGCCACGTCCCGAACCGATGGACGTCTACAACCTGGTTGCAATCATTCGGGATCAGATACGCCACTTGCAGAAGGCTGTGGACCGCACCACAGAACTGTCCCGGCAGAGAGTCGCCTCTTTAGAGTTGGCTGCAGTTGCGGATAAAGACCAAGCTGCTTGCATGGAGGAGATTTTGAAGCTCAAGTCCTTACTGAGCACCAAGCGTGAA[C/T]AGATTGCCACACTCAGGACTGTGCTCAAGGCCAACAAGCAGGTGAGAGTAAAAAAGATTACCTTGGCATGAATGTAAATGACGTCAGAATGTTGAGCTGGTCGTAGGACATAGGTCTCAAACTCAATGGAGGACGGCAGCTCTGCACAGTTTTGCTCCAACCCTAATCAGGCACACCTGGTCTAACTCATCAAGGTGTTCAAGACTACTCTTGAACACCTTGATTATTTGGATCAGCTGAGTTTGAATCCACATTCACATGGGGCGTCAGCATCAACGCTTCCTAATCACTTTGAATGGGTGACATCAGGCGTTGCCGAACTGCATTGTGGATCCATCGGCGCCGCTTCAGAGGCATTGCTCGCTGCAGAAGTCGGGAGTAGCTCAACTTTTCAAGAGCCGATGGAAGTGTCAGCCAATCAGATCACTGTATGCAAATACACCAGCTAGACAGTGGCCTATTGCTGACTGAATTTCATTGGCTGAGGCTGCTCTGACGAT
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:
sa38858
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109235 | Essential Splice Site | 677 | 836 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 37921957)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 36814444 |
GRCz11 | 11 | 37081987 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAGAATGAATGGTCTTTCTGAACAGTGGTGTATGGTTGCTTTTCTTTC[A/G]GACAGCTGAGGTCGCCCTGGCAAACTTGAAGAGCAAATATGAGAATGAAA
Long Flanking Sequence:
ATTGCTCGCTGCAGAAGTCGGGAGTAGCTCAACTTTTCAAGAGCCGATGGAAGTGTCAGCCAATCAGATCACTGTATGCAAATACACCAGCTAGACAGTGGCCTATTGCTGACTGAATTTCATTGGCTGAGGCTGCTCTGACGATCGCTTCAGCCCTAACTTCAGACACGCCTTCAGTCAAGCGTTGACGCTGAAGCCCCGTGTGAATAGGGCGTGAGACCTACTGTATGTTGCAGAGCAGGGGTGTCCAATCTCAGTCCTGGGGGGCTGGTGTCCTGCAGTTTTGTTCCAGCCCCAATCAGACACACCTGGTCTAGCTAATCAAGCACTTAATAGGCTTTCTAGAAACATCCCTGCAAGGTGTGTTGAGGCAAGTTGGAGCTAAAATCTGCAACACATGGCTGTCCAGGACTGAGTTTGGACACCCCTGTTGTAGATCATCCAAATGGATTGAGAATGAATGGTCTTTCTGAACAGTGGTGTATGGTTGCTTTTCTTTC[A/G]GACAGCTGAGGTCGCCCTGGCAAACTTGAAGAGCAAATATGAGAATGAAAAGGCCATGGTCACTGAAACCATGATGAAGTTACGAAATGAGCTTAAGGCTCTTAAAGAAGATGCCGCCACTTTCTCCTCTCTCAGGGCAATGTTCGCCACCAGGTATGGTGTCGATGTTTCTGTCTGACTCGCAATAACCAACCCAGTTGTTATTCCTGATACCTTCCAGAATACTGTAGGCTAACTAGTGTTGTGGTGATCACCAGTTTTCAGGTAAAACGCATGGGACGATAACAGGTTTCAAGGTCTACTGTGGTTTGGAAAAGTCGAAAGGTTTTAAAACTGCAAAAAAATGATGTTATACAATTCCTACAGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTACATGTTTTTTATTACTTTTTAGTTTTTTAAGGCAACAGTATT
Associated Phenotype:
Not determined