ZMP
si:ch211-204c21.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate disabled homolog 2, mitogen-responsive phosphoprotein (Drosophil
Human Orthologue:
BDP1
Human Description:
B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB [Source:HGNC Sy
Mouse Orthologue:
Bdp1
Mouse Description:
B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB Gene [Source:MG
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6060 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa26556 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33686 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6060
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 |
---|---|---|---|---|---|
ENSDART00000122353 | None | None | 636 | None | 15 |
ENSDART00000123943 | None | None | 485 | None | 11 |
ENSDART00000128763 | None | None | 2342 | None | 43 |
ENSDART00000142271 | Nonsense | 143 | 491 | 5 | 12 |
ENSDART00000147252 | None | None | 202 | None | 3 |
Genomic Location (Zv9):
Chromosome 5 (position 45512076)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 43293341 |
GRCz11 | 5 | 43893494 |
KASP Assay ID:
554-3922.1 (used for ordering genotyping assays)
KASP Sequence:
GGGATGTCACTGACAGCAGAGCTTTCGGCTACGTGTGTGGCGCGGAGGGC[C/T]AGCACCAGTTCTTCGCTATTAAAACAGCACAGCAGGTACAGAGAGATTTT
Long Flanking Sequence:
TGCTCACTTGGCATGTTTCTTGAATCTATACTTTAGATAAGTCAAAAAACGTACATACAGCACCTTTACATTTAGAAATTTATCTTACTGAAATGTTAACCGTTAAATTCCAGCAACCACATCTACTGTTTTTAGCGTGAATTTTAAAGGTTTGTTTACAGTATATTTATTTAGGAGGACACTGTCCTAGTTAATCATTCATTTGTGTTTGTTCACAGGGCAAGGCGGTGGCAGCTCGCTCTCAGGGCAAGCACAAGCAGAGAGTCTGGGTGAACATCTCTCTTTCGGGAATCACTGTCACTGATGAGAAAACTGGGGTGTGTGTGTGTTTTATTTTTCTTCTCACTGTCAGTTTAAATGATATATCAACATGCAGTATTCATTGTCACTTTTGTCTTCTCCAGGCAGCAATACTGGAGCATGCAGTAAATAAGATCTCCTTCATAGCCCGGGATGTCACTGACAGCAGAGCTTTCGGCTACGTGTGTGGCGCGGAGGGC[C/T]AGCACCAGTTCTTCGCTATTAAAACAGCACAGCAGGTACAGAGAGATTTTTTTTACTTTGCAAATCTCTTTACTCCTTCACACACTCCTGCCTTAGGCACACACAGATGCTCACATTCCCTCTCTGTGTAGATCTGTTACACATTTTTCCCAGAAGTGCGTTTTTCTACAAGCATACCCACAAAAACACATTCCTGCCGCTCACAAACATTCACCCATAAACCTGCAGGAGACACGCTTTTAACACGCTGCTTGTGTTTTCACTCAGGCGGAGCCTCTTGTCATTGACCTGAAGGATCTTTTCCAGTTAATCTTCAATATGAAGAAAAAAGAAGTCGAGGGGTCGAAGAAGGTGCGAGACATAAACGATTTTTTTAAATCCATCTAGACTGTGCACACACATACCTGTAATGTTCTGTTAATGCTTAAAATTTCAACAAATGCCAAGTTCAGATTGCAGGATTTTCAAAGTGGTGTTGTCACGGATGTTCTCACACAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26556
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 |
---|---|---|---|---|---|
ENSDART00000122353 | Nonsense | 280 | 636 | 3 | 15 |
ENSDART00000123943 | Nonsense | 280 | 485 | 4 | 11 |
ENSDART00000128763 | Nonsense | 329 | 2342 | 4 | 43 |
ENSDART00000142271 | None | None | 491 | None | 12 |
ENSDART00000147252 | None | None | 202 | None | 3 |
Genomic Location (Zv9):
Chromosome 5 (position 45473255)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 43254520 |
GRCz11 | 5 | 43854673 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACTTCTAATGCAGCAACGGCGCGGACGGCATAAGCGCGAACATGTCTA[T/A]GAGATGGATCCTGATAAAATGACTTTAGCTGACTTCATTTATTACATCCC
Long Flanking Sequence:
GATGTTTCTCAAAACTCTAAATTTTCTGGCTCTACTGCAGCAGCCCATTGCCCTCCATCATCACCATGTCTTCTATCCATCTCTGGCTGCCCAGAATCTCCATCCTTCACATCATCTCATCAAGAGCCCTGCAAATCTCCCCTGAAAATCCAAAGCAAGGACGTTGGACTCCTAGAAGGAGGTGCTCCAGCTCCCTCCACATTCTCTCCGTATGTGAAGCTGTCACGTGTTGATGGACCTGGTTCTCCTCTCAGGGAGAAAATCCTCTCGGACAAGGAGCGAGTCTTAAGGGCCCTCAAACTGAAAGAACTGATGAAGATGGAGAGGTCAAAGGAAAGAATGGTAAAGTCAATATACTTAAACATGGTTGGATTAGGAAAGTCATAATGGTTGTTAGAATATAAGTGATCTATCAAAAATTAAGCTTTGTTTATTTATTTTTTTGCGGGACCACTTCTAATGCAGCAACGGCGCGGACGGCATAAGCGCGAACATGTCTA[T/A]GAGATGGATCCTGATAAAATGACTTTAGCTGACTTCATTTATTACATCCCAGATACTAATCCTATGAAGTAAGTTGATAATAAATATCATCATAGTACATTGTACACACTAACACTTTTGGATTGTCCATGTGTATGCAAACTGTGATCATGATCACTAGTATATTATTATACTGAACATAATTTCCTTTCTAAGTGAATGTTTTCTAACTAATGTCTTTTAATATGTGGTTGTTCACTTCTAAAAGCTCTTTCATTTCATTGGTCGTGTTTTTGTTACAGGTCTTCCCTTTCAACAGAGGAGGTTCAGACAGCACCTACTGCTACTGCTATTTCTCCATCTCCCTTGTAAGTCAAATCTAATGTGCAAAGTGAAATTGACTTTGTTTTAGATTATTTAAACTTCTGTGCATATTGTGAAGTGGAGCCGGAAGTGTCCATGTTTTATGGGTTTCATTTGTTCTGAAATAATGTACATACCTCAGGTGGTCGTGACAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33686
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122353 | None | None | 636 | None | 15 |
ENSDART00000123943 | Nonsense | 333 | 485 | 6 | 11 |
ENSDART00000128763 | Nonsense | 382 | 2342 | 6 | 43 |
ENSDART00000142271 | None | None | 491 | None | 12 |
ENSDART00000147252 | None | None | 202 | None | 3 |
Genomic Location (Zv9):
Chromosome 5 (position 45470265)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 43251530 |
GRCz11 | 5 | 43851683 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTCTCTCTCTCTCTCTCTCTCTCAGGGTGCAGAAATACATGGCAGAT[G/T]AGGATGATGATGATGCAGATGATGATATGCTGGTTCCTAAAGTGAGGGTG
Long Flanking Sequence:
TAAGTTTTGTAACAATGTCACACCGACACAGCTAAAGATTTCTTTCCAATATGATTCATTTGAACCAATCTGAGTCTACTCTTATTGATAAATCAATAATTTTAAACACGGGGCACTTTCAGATTTAAGTCACTTCACTTACAGTAGAGCTGTTACTGTGTCATTTTCAAAAACCCATGACAGGGTCTCTTTAAATGTTTCTTTGTTGTTAAAAAGCTAGTTTATAAAACACACGTTTGGTAAGGAACTCCCAGGGTTTGCGTAGATGTCCAACTTGTGTGTTAACATCATTGCATTCCAATATTTTGTCTTATGTTTTGACTTTTTATTTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCCCTCTCTCTCTCCCTCTCTCTCTCCCTCTCTCTATCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCAGGGTGCAGAAATACATGGCAGAT[G/T]AGGATGATGATGATGCAGATGATGATATGCTGGTTCCTAAAGTGAGGGTGGCAGAGGACGGCTCACTAATTTTGGATGAAGAAAGGTACAGTGGTCTTTCACCTTTGCATTCAAGTTTGATCTTTGCTCAAAGTGGAATTCAAAGTTTGAAAAGGTCATGTGATTTAAGATGGCGTTTAAGGCCCTGGCATTCGCTTGTTGTTATGTGACTCATTGCTTCTTGAATAACGAATGTTTATTGATACTTTCACTCTACATGCATTTTATGCAGGGTAACAAATGAAAAGATATGATTTAGCACACACAGAAACACATGAACTTTTTGAGTCTTGTATAATGCAAAAGATCAGTAAATTAATTTATTGCTGTTTAGTTTGACAGTGCGTGTTCAGAGGGCATCTGATACAGTTATCGACAATACAAATCTACTGTTTGAACGAGGCTCTACTACAACATACAGCAGTTTCAGGAAAAATTACCATGTGAAGAACTGGTCTGTC
Associated Phenotype:
Not determined