ZMP
zgc:162472
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC553495 [Source:RefSeq peptide;Acc:NP_001077289]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44959 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23864 | Essential Splice Site | Available for shipment | Available now |
sa23863 | Nonsense | Available for shipment | Available now |
sa17899 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44959
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 |
---|---|---|---|---|---|
ENSDART00000124635 | Nonsense | 603 | 1627 | 10 | 27 |
ENSDART00000125487 | None | None | 562 | None | 11 |
Genomic Location (Zv9):
Chromosome 21 (position 9778004)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 11261367 |
GRCz11 | 21 | 11353995 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTTTCAAATGATGGAGAAAGTGATGTCACTCCAAAGAGACGCAGGGGA[C/T]GAGCAGCGAAAAATACAGACAGGGACATTAAGAGGATATATGAAGAGGGT
Long Flanking Sequence:
GGATCTAGATTTCTTCAAAAAGTTAATGGAGCAGATTCTAAATGACGAGGAAGAGAAAAAGAACAAAAGCAAAGAGCATTTCAAGTTGGCAAAAGCAAAAAGGAAAGTGAGAGGTCAGTTTGTTTGTTTTTTTGGATTTTTTGTTGTTTGTTGAGTTTTTTTTGACAAGCTGTTATAAACACTTGAACTCTTTTTTTTTTTTTGTGATCAACTTTTTATTGTTTTCAGAGATTAACAAAATTACATCTTATGAGACAAATGTGTAATAGACACATTATTGTTAACTTGAGTTAAAAGAAGAACAGGAAAATGCATTTAAATAATAATAATAAATAAATAAACATATATATATATATATATATATATCTGATCCAGTGGCTAAAAGAAAGGGAATGGACTCTTCAGAGGATTCAGACAGTGATGTGGTGGCAGGAGAAAAGGAGAATGAAGATCTTTCAAATGATGGAGAAAGTGATGTCACTCCAAAGAGACGCAGGGGA[C/T]GAGCAGCGAAAAATACAGACAGGGACATTAAGAGGATATATGAAGAGGGTATGCTTTTAATGTATTTTCTATTTTAAGGGGACCTATTATGCTTGTTTTTACAAGATGTAACATAAGTCTGTGATGTTTCCCCATAGTGTGTATGTGAAGTTTCAGCTTAAAGTACTCCACAAATAATGTTTTAGAACTCTTTGAAACTGACCCTTTTAGGCTTTGATCCTAATTGTGCTATTTTGGTGACTGTCGCTTTAAATTCAAATGACATTGTGCTCTTTTCAAAAGAGGGTAGAGCTACATATGCCTGTGTGTCAGCATAGTGGCAGATACAAAAACAAGACTAACGTCCTATGCTAATGAGGGAGAGATTGTCACTAATGAATGGGACTTTCCCCCTCTGAGGACACATACAAAGGGAGAATGTCAACCAAAGTGTTTCTGCAAAATGAATACATTTTTACCATTACAAGCTGGTTATATTCACATACTGTTGCCAAACAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23864
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124635 | Essential Splice Site | 908 | 1627 | 16 | 27 |
ENSDART00000125487 | None | None | 562 | None | 11 |
Genomic Location (Zv9):
Chromosome 21 (position 9768966)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 11252329 |
GRCz11 | 21 | 11344957 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATCTAGTTGTATTGGATGGGATGGTACTAATTTGTGTCTCGTTTTGTA[G/T]GATGTCATTGAGTTTCTTGACCCAGAACACATGGAAGGTGAGGAGAAACT
Long Flanking Sequence:
CCCCGCTGTATGCTTGAATGGTACTGTATGGCCTACATCCATGTACTAAATATACTATCCATGTTTCTGAGCAAAGCGATGTTCAGTCTTGCTTCATCATTCAAATTAATTTCTGCATGTCATGTCCAAGCTTTCATTGTCCTTCCCTTTTCTTTTACTCGTTCCCATTGGCTCCCAGCTGGACATTTCAGCGAATGTGCCTGATATCTTGAGCGCGTCCCACAATGCTTTGTGCCCCGAGTCTGCATGTGAGCAGGCCGTATTTCCTGCTGGTCCTGTCTCGTATGAACATCAGTTGGACCTTCTCGTTGTAAGTCTTCCCATCGTCGGTTGTGGCTCTTTTTCACATCTGATGCTTCCTCCATTCACTGTCCATCATAAACACTGACTTATCACTTAATGTCTTTTTTTATTTCTTTATTTGCACTTGATGTCAGCTGCAGTGAACATAAATCTAGTTGTATTGGATGGGATGGTACTAATTTGTGTCTCGTTTTGTA[G/T]GATGTCATTGAGTTTCTTGACCCAGAACACATGGAAGGTGAGGAGAAACTCTCTCAGGCTTATTTGAGTGAACTATCGCCTGATATACAGTAGTCAACATTTAAAGTGGATCAAAATGTTTTCCTAAGACAAGAATGGGTGTTGATCAATAGTATTAGGATACTTTGAACGTTTTGATCCACTTTAAATGTTGACTACTGTATTTATATCCATCAAGTAGTATATTATATAGTCATAAACTTTTCCACTATTCAATAACATGTAACAGATGCACAGATTTTATTTAGATTTAAAACTGTTATAGTGTTTATTTATTCAAACACTAACCTAAATGAATAGGTTAAACTATAATTCTTATTACACATGCAAACAAATGTATTACATGTAGATATATTAATACCGCAGGGTGTCCGGAGGGTTGTAAAAAGTCTTACAATGTCTTAAATTTCAAACACTAAACTTAAATTTCCTGAAATATTGTGTTGTAGGTCCTTGATCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23863
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 |
---|---|---|---|---|---|
ENSDART00000124635 | Nonsense | 1561 | 1627 | 26 | 27 |
ENSDART00000125487 | None | None | 562 | None | 11 |
Genomic Location (Zv9):
Chromosome 21 (position 9754899)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 11238262 |
GRCz11 | 21 | 11330890 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTATCCTTCATTTCAACAAAAAGTACACAAGGAGCACCAACACGTCAT[C/T]GAGGATCCAAACCAGGAGTCAACACTGCCCGTCCTGACAGAAAACAGGTA
Long Flanking Sequence:
CTTTTTTTTCCTTCTCTTCGCCTTAACACCCCCACCATTCCCAATACTAATGCTAGTAATAATAATAATAATAATAAATATATTGATAATAGTTGGCTACTGACAATTCCAGCTGTGCACAACCCTGGGGCAAAAAAGGCATCTGGGAAGAAATAAAGAATATACAGTCGAGCCCAAAATTATTCATACCCCTGGAAAAGTTGTGAAGTTTTTGTTCAAATGTAAATAAAAGCTGAGAAATATTTTTTTTCCACAATGACACCTTTTGTACATTGTCTTATTATTTTTTGGGAGAAGCCTGGTGTCATTTCCAGTGAAAACTATTTTGCTGGTTGAATAAAAGAACTTTAAGTCAGAATTTGCCAAGGGTATGAATAATTTCGGACTTGACTGTGTATATATTTGGTAAATTTCACGTCTTTTTCAGGCCTGGTAGAAAACCCAAAGGCTTCTTATCCTTCATTTCAACAAAAAGTACACAAGGAGCACCAACACGTCAT[C/T]GAGGATCCAAACCAGGAGTCAACACTGCCCGTCCTGACAGAAAACAGGTAGCGAGTGCATCAGCAAACCTTGGAGTAAAGCGAGCTTTACCAACTCCTGCTTCCACCACTGAGGTATCACACAGTCTCCTGTTTCACTGCATGTTTTTAGAAGCATATTGTGTATTTCTAATTATAAATTGGATTTCATTCCTCCCTCTTATCAGCAGCGCTCAGAAGAAGAGCCCACCAGTGTCTCCAAGTACTTTTTCAGCGACATCTTTACTGAAGTTGATGAATTAGAGGACATGGATTAAAGCAAACGGTTGGAATAATGAAGCAGGCACAACACGCAAATATCAATTGGCTGAATAAACATGTAAATATGTACATTTGTTAATAAGGACAGTTTCATTTTGGGAAAACTAAATGACAGCGAAAACACAACTCAATTTAAAAGGTTGTACCTTTCATCTTGTTTTATTTTTGTAAAGAAAATAGTTTTGAATTTGAGTGTTAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17899
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 |
---|---|---|---|---|---|
ENSDART00000124635 | Nonsense | 1564 | 1627 | 26 | 27 |
ENSDART00000125487 | None | None | 562 | None | 11 |
Genomic Location (Zv9):
Chromosome 21 (position 9754890)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 11238253 |
GRCz11 | 21 | 11330881 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATTTCAACAAAAAGTACACAAGGAGCMCCAACACGTCATCGAGGATCC[A/T]AACCAGSAGTCAACACTGCCCRTCCTGACAGAAMACAGGTAGCGAGTGCA
Long Flanking Sequence:
CCTTCTCTTCGCCTTAACACCCCCACCATTCCCAATACTAATGCTAGTAATAATAATAATAATAATAAATATATTGATAATAGTTGGCTACTGACAATTCCAGCTGTGCACAACCCTGGGGCAAAAAAGGCATCTGGGAAGAAATAAAGAATATACAGTCGAGCCCAAAATTATTCATACCCCTGGAAAAGTTGTGAAGTTTTTGTTCAAATGTAAATAAAAGCTGAGAAATATTTTTTTTCCACAATGACACCTTTTGTACATTGTCTTATTATTTTTTGGGAGAAGCCTGGTGTCATTTCCAGTGAAAACTATTTTGCTGGTTGAATAAAAGAACTTTAAGTCAGAATTTGCCAAGGGTATGAATAATTTCGGACTTGACTGTGTATATATTTGGTAAATTTCACGTCTTTTTCAGGCCTGGTAGAAAACCCAAAGGCTTCTTATCCTTCATTTCAACAAAAAGTACACAAGGAGCACCAACACGTCATCGAGGATCC[A/T]AACCAGGAGTCAACACTGCCCGTCCTGACAGAAAACAGGTAGCGAGTGCATCAGCAAACCTTGGAGTAAAGCGAGCTTTACCAACTCCTGCTTCCACCACTGAGGTATCACACAGTCTCCTGTTTCACTGCATGTTTTTAGAAGCATATTGTGTATTTCTAATTATAAATTGGATTTCATTCCTCCCTCTTATCAGCAGCGCTCAGAAGAAGAGCCCACCAGTGTCTCCAAGTACTTTTTCAGCGACATCTTTACTGAAGTTGATGAATTAGAGGACATGGATTAAAGCAAACGGTTGGAATAATGAAGCAGGCACAACACGCAAATATCAATTGGCTGAATAAACATGTAAATATGTACATTTGTTAATAAGGACAGTTTCATTTTGGGAAAACTAAATGACAGCGAAAACACAACTCAATTTAAAAGGTTGTACCTTTCATCTTGTTTTATTTTTGTAAAGAAAATAGTTTTGAATTTGAGTGTTAATTGCTATCAAA
Associated Phenotype:
Not determined