ZMP
si:ch1073-459j12.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similat to H.sapiens AEBP1, AE binding protein 1 (AEBP1) [Source:UniProtKB/TrEMBL;Acc:
Human Orthologue:
AEBP1
Human Description:
AE binding protein 1 [Source:HGNC Symbol;Acc:303]
Mouse Orthologue:
Aebp1
Mouse Description:
AE binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:1197012]
Alleles
There are 11 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21368 | Nonsense | Available for shipment | Available now |
| sa10660 | Essential Splice Site | Available for shipment | Available now |
| sa31673 | Nonsense | Available for shipment | Available now |
| sa34477 | Nonsense | Available for shipment | Available now |
| sa34476 | Nonsense | Available for shipment | Available now |
| sa31672 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21368
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 |
|---|---|---|---|---|---|
| ENSDART00000025875 | None | None | 842 | None | 12 |
| ENSDART00000114912 | Nonsense | 68 | 351 | 2 | 8 |
| ENSDART00000132115 | Nonsense | 68 | 1247 | 2 | 22 |
Genomic Location (Zv9):
Chromosome 8 (position 46771664)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 44775418 |
| GRCz11 | 8 | 44769324 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTTTTAGATCTTCTGCAAGTGAAAATAATTCCACCCTATGCAACGATC[G/T]AAGTTGGACAACACAAACAATTGCTCTGCAAAGGTGAGATGCCAGTTAAA
Long Flanking Sequence:
TTTTGGAAGAATCCCCCCTTCCACCCCATCTCCTCCTTTTTCTCCCCTTCTAAAGGGGGAGCGATCGAGACCTACCTTATCTCGGTTCTCCTGATATGCTTCTAGACCGGGCGGGAGCCCTGGGCTCAAATATCTCCGAGCTCAGGGTTCTCTCCCGGGACAGCATGCCAAACCTGCTATAAGTGCCAAGCATATCTAAGTGGAAACTCTTGAAGTGGGCATTCTATAAGAAAGAGAAAGAAACATTTTAGTCTTTAATCAGTCAATACCCAATAGCTATATTATTTAGCAAGTGTGCACGTATTCTGGCTCTGTTTTAGTATTCTTTTTTTAACTTTTTTTTTTTAAATCACTCAGTTCCAAGTGAACAATTTATATTCACATAGCACATTATGACAAGTTGACAAGGTGTGAAAAAAATGTTGATATGAAATACCAAATATTGTTTGTTTCTTTTAGATCTTCTGCAAGTGAAAATAATTCCACCCTATGCAACGATC[G/T]AAGTTGGACAACACAAACAATTGCTCTGCAAAGGTGAGATGCCAGTTAAAATATTAAAGAATTTAATTATTTTCGTGTCATTATAACTTTTTTATATGGATAATTCTGGCTAATATTTTAATTAAAATTTTAGGAAATTATTTTAAATTTTCTTTTGGCTTTGAAGAAAAAAAAATGATATTCCAGTTTGGAACAACATGAGGATGAATAATAAAAACAAAAGGCAGTGTTATATTTGGTTATTTGGGTATATTTTGGTTTTTACCTCAGATGCTAAAGCTACAAATTCAATCTCCTTTCTCTGTTCTTTCTTAGTTTCCAGTGATGCAAAGAATATCAACTGGGTTTCTCCTAATGGTGAGAAAGTTCTGACAAAACACGGCAATCTCAAGGTCCACAATCATGGCAGTGTCTTGTCTTCTCTTACTGTTCTGAATGCCAATTTAAACAATGCTGGAATATACAAATGTGTGGCCACAAATGGAGACACAGAATCACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10660
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000025875 | Essential Splice Site | 106 | 842 | 3 | 12 |
| ENSDART00000114912 | None | None | 351 | None | 8 |
| ENSDART00000132115 | Essential Splice Site | 511 | 1247 | 13 | 22 |
Genomic Location (Zv9):
Chromosome 8 (position 46750959)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 44796123 |
| GRCz11 | 8 | 44790029 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTAATGATAGCAGAGAGTGGACTTTYCTTCATGATGGRTATGCTGAATGG[G/A]TAGGTTGCCAGATTAGAGACCACAATCATTTTTNCTCCATATCTATTTTTT
Long Flanking Sequence:
GACCAGTTACTAACATCCTCTGTTTTTCAACATCGGTATGGGTCACACAGAGCTCGTCTTAATATTCAGGTACAAACATGTGGAGAGATATGCACTTCTACACTTTTACTGGCAGCTGGACCTTTGATTTCATGTCAGTGTGAGCATTTTACTTTATTTAACAGGCATCTGGGGATGACGATGATATGAATGGTGGAGCATGGTGTGCTAACCCTGAAGAGAAGGTCCACTGGATTGAAGTGGATGCACGTACACTAACAGAGTTCACAGGGGTGATCACTCAAGGACGAGATGACCCCTTAGAGTAAGGCAGATCCTAAAAACCTAGAAGCCATGTGGTTAAGTGAACTGTCAAATCAAAATCTAATCTAAACATTGTACAAATACATTGCTTGTTAATGTTTTGTTGTTTCAGGAGTGACTATGTGTCTACCTACTATGTGGCATTTAGTAATGATAGCAGAGAGTGGACTTTCCTTCATGATGGGTATGCTGAATGG[G/A]TAGGTTGCCAGATTAGAGACCACAATCATTTTTCTCCATATCTATTTTTTATGTACACAGTTATTATTTGATCTCAAAGTCATGTGAAATATGAGGAACACATTAAACATGTAAAAAGGGGGTTGGGGAAATGTACATGTAAAATCCATGGGATCACATTTGAACTAAAATGTGGACAGGTGGAAAAAAAATATAATGGAATGGTGTCACATGAAAAAATTCCAAAACCAAATCTTTCATGAGTTGCAAATATTAAATATGTCAAACTGCACAAGATTATGTGAAAGCAAAGTTGTTTTTTATCTGTAGGGGAAAGCTAAATCTCACCTAAATATTAAAAATATCACTAAATACAAAAACACTCATATTAAACTATATAAATACATTGACGATTAGTTTCAGTTGAAATGTACTCATGTTCTGCTTTCTCTCTGTCCTCAGTTATTCTTTGGTAACTCAGATAAAAACACCCCAGTATTGTCTCAGTTTATGGAGCCGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31673
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000025875 | Nonsense | 236 | 842 | 7 | 12 |
| ENSDART00000114912 | None | None | 351 | None | 8 |
| ENSDART00000132115 | Nonsense | 641 | 1247 | 17 | 22 |
Genomic Location (Zv9):
Chromosome 8 (position 46745710)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 44801372 |
| GRCz11 | 8 | 44795278 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTAATATGTTTCCTCAGGAGAGCCAGAATTCAGGTACACAGCTGGCTA[T/G]CATGGTAATGAGGCTTTGGGACGAGAGCTGCTTCTAATGTTCATGCAGTA
Long Flanking Sequence:
CCTAGACATGGAGAAGGTGATGGAAAGCAGCATGAAGTCTCAAGAGTTCATAAGTGGCCAAAAGGGGGGGAAAAAGGCATTTTTAAAAGAGAAAATGCAAAACATTAATATTTGCAGCACAAAATATTTGAAACATAGAATTAGTTAAAACTTTAAGTAGACTTAGAGATTAAAAAAGGGAGATAATCACTTCAAAATTGTCTCTTTTTTGTCACAGCTAATGAAATCCATTTCTGATGAGTGTCCCAACATCACCAGATTCTACAGTTTGGGCAAGAGCTTTAAAGGTCTGGAAATTTATGCCATGGAGATTACTGATAACCCTGGGGTCCACGAAACAGGTATGGAACAACAGAGTAGTTATGAACACATTTTTTTCCCTTTTTGTTTAATTACATAAAAAAGGACAACCAAGCATTGCAAGTGTGCGCATCATTCAGTTGATGAACATATTAATATGTTTCCTCAGGAGAGCCAGAATTCAGGTACACAGCTGGCTA[T/G]CATGGTAATGAGGCTTTGGGACGAGAGCTGCTTCTAATGTTCATGCAGTATTTGTGTAAAGAATATAAAGATGGCAACCCTCGAGTTCGCCACCTAGTGGATGAAACACGAATCCATCTGGTTCCATCAGTCAATCCTGATGGCCATGTGAAAGCTTTTGAGAAGGTGCGTTTAAAATATGTATACGGTAAAAATTTTAAAAGTGCATGTAATTTCAGCAATTAGGAATTGCTCAAATAATGACTATGATAATGACTTTCCTAAATCTTGCATTTTACAATTAACAGGCTATTGAATTTAGCATTTAGGAACTGAGCATTTAGAAAGTGAGCTATTTACTTAAAATTGAGTTAATATATTTAATGCTAATAATGCATAAAAAGGTCATTCTGGTCAATTAGCCAAGGTCAGGTAAATAAAGGTTAGGTAAACTAGTAAATCCCCGCTAAATGGCTTAATACAGATAGTCAAACTCAAAGCTAAGCATGAATAGTGAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34477
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 |
|---|---|---|---|---|---|
| ENSDART00000025875 | Nonsense | 254 | 842 | 7 | 12 |
| ENSDART00000114912 | None | None | 351 | None | 8 |
| ENSDART00000132115 | Nonsense | 659 | 1247 | 17 | 22 |
Genomic Location (Zv9):
Chromosome 8 (position 46745657)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 44801425 |
| GRCz11 | 8 | 44795331 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTAATGAGGCTTTGGGACGAGAGCTGCTTCTAATGTTCATGCAGTATT[T/A]GTGTAAAGAATATAAAGATGGCAACCCTCGAGTTCGCCACCTAGTGGATG
Long Flanking Sequence:
GTGGCCAAAAGGGGGGGAAAAAGGCATTTTTAAAAGAGAAAATGCAAAACATTAATATTTGCAGCACAAAATATTTGAAACATAGAATTAGTTAAAACTTTAAGTAGACTTAGAGATTAAAAAAGGGAGATAATCACTTCAAAATTGTCTCTTTTTTGTCACAGCTAATGAAATCCATTTCTGATGAGTGTCCCAACATCACCAGATTCTACAGTTTGGGCAAGAGCTTTAAAGGTCTGGAAATTTATGCCATGGAGATTACTGATAACCCTGGGGTCCACGAAACAGGTATGGAACAACAGAGTAGTTATGAACACATTTTTTTCCCTTTTTGTTTAATTACATAAAAAAGGACAACCAAGCATTGCAAGTGTGCGCATCATTCAGTTGATGAACATATTAATATGTTTCCTCAGGAGAGCCAGAATTCAGGTACACAGCTGGCTATCATGGTAATGAGGCTTTGGGACGAGAGCTGCTTCTAATGTTCATGCAGTATT[T/A]GTGTAAAGAATATAAAGATGGCAACCCTCGAGTTCGCCACCTAGTGGATGAAACACGAATCCATCTGGTTCCATCAGTCAATCCTGATGGCCATGTGAAAGCTTTTGAGAAGGTGCGTTTAAAATATGTATACGGTAAAAATTTTAAAAGTGCATGTAATTTCAGCAATTAGGAATTGCTCAAATAATGACTATGATAATGACTTTCCTAAATCTTGCATTTTACAATTAACAGGCTATTGAATTTAGCATTTAGGAACTGAGCATTTAGAAAGTGAGCTATTTACTTAAAATTGAGTTAATATATTTAATGCTAATAATGCATAAAAAGGTCATTCTGGTCAATTAGCCAAGGTCAGGTAAATAAAGGTTAGGTAAACTAGTAAATCCCCGCTAAATGGCTTAATACAGATAGTCAAACTCAAAGCTAAGCATGAATAGTGAAAATTTGATATGCCAGACATTTAAACCAACAAAACAATATTTTGATAGTTTCAGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34476
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 |
|---|---|---|---|---|---|
| ENSDART00000025875 | Nonsense | 333 | 842 | 8 | 12 |
| ENSDART00000114912 | None | None | 351 | None | 8 |
| ENSDART00000132115 | Nonsense | 738 | 1247 | 18 | 22 |
Genomic Location (Zv9):
Chromosome 8 (position 46743771)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 44803311 |
| GRCz11 | 8 | 44797217 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTAAATAACATTTATTGGGATTCAGAGGATAAAGGCATGGTGCCCAAAT[T/A]GACACCAAATCACCATATTCCCATTCCTGAGGGTATTCTCTCAAGCAATG
Long Flanking Sequence:
ATAATTTACTATTAATGAATGTGAATCTGAAAGAGAGGCATATGCATGGGTTTACACTAACTAAATAAACACTGCATACAGTCATCTGTTGAGAATGGAATTCTCTGAAATTAGTAGAAGCCTGGCGTGGAAAGCATTCCTTAAATTGCAAAGTAATAAGTGCACTACTTTCATGAGCCCTATTCATCAATAGCAGACTTTAAAATCTGATCTCAACGTTTAAACCCAGAGAGATCATAATTTCATCTGGACAGGTTTAATTCCTAGTAAACATTATCAATAATAGACAGATCAGTGTGGATAAAACAGCTAACCAAATGTTCAAATATGAATGGTGTTGTGACACTAATGTAAGTAACATCACATTGTTTCACAGGGTTCAGAGTTGGGCAGCTGGACATTAGGACACTGGACTGAAGATGGCCATGATATCTTCCAGAACTTTCCAGACTTAAATAACATTTATTGGGATTCAGAGGATAAAGGCATGGTGCCCAAAT[T/A]GACACCAAATCACCATATTCCCATTCCTGAGGGTATTCTCTCAAGCAATGGCTCAGTGAGGAAATAATCATGTGCTATTTATAAATTAAACCGCCACTTGCATACAGTAGCCTTGAGCTCAACTTTTCAGAACAGATTTGTTTTATAATGTTCTTTATGTTCTACCTTTCAGATTGCAATGGAGACTCTGGCCCTCATCTCATGGATGGAAAGCCATCCATTTGTGCTTGGTGCCAACCTGCAGGGTGGTGAGAAACTAGTGACATACCCGTTTGACATGCGCCGTCTAACCAAAGAGTCTGAGGCTATGGAGAAAAAACTTGGCTCCAGAGCAAACCGACGTAAGCGACAGTATGAGGAAGAGGAAGAAGAACCCAACCCTTACCTTCACATAGGATACCATCAGGAGAGCTACAGCGGACCCCAGGAAAACCACGCATATGATCATGAGAGCTATGGGTATCATCAAGAAAGTTATGGGTATCACCATCAGAGTCAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31672
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 |
|---|---|---|---|---|---|
| ENSDART00000025875 | Nonsense | 398 | 842 | 9 | 12 |
| ENSDART00000114912 | None | None | 351 | None | 8 |
| ENSDART00000132115 | Nonsense | 803 | 1247 | 19 | 22 |
Genomic Location (Zv9):
Chromosome 8 (position 46743460)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 44803622 |
| GRCz11 | 8 | 44797528 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACATACCCGTTTGACATGCGCCGTCTAACCAAAGAGTCTGAGGCTATG[G/T]AGAAAAAACTTGGCTCCAGAGCAAACCGACGTAAGCGACAGTATGAGGAA
Long Flanking Sequence:
AACCAAATGTTCAAATATGAATGGTGTTGTGACACTAATGTAAGTAACATCACATTGTTTCACAGGGTTCAGAGTTGGGCAGCTGGACATTAGGACACTGGACTGAAGATGGCCATGATATCTTCCAGAACTTTCCAGACTTAAATAACATTTATTGGGATTCAGAGGATAAAGGCATGGTGCCCAAATTGACACCAAATCACCATATTCCCATTCCTGAGGGTATTCTCTCAAGCAATGGCTCAGTGAGGAAATAATCATGTGCTATTTATAAATTAAACCGCCACTTGCATACAGTAGCCTTGAGCTCAACTTTTCAGAACAGATTTGTTTTATAATGTTCTTTATGTTCTACCTTTCAGATTGCAATGGAGACTCTGGCCCTCATCTCATGGATGGAAAGCCATCCATTTGTGCTTGGTGCCAACCTGCAGGGTGGTGAGAAACTAGTGACATACCCGTTTGACATGCGCCGTCTAACCAAAGAGTCTGAGGCTATG[G/T]AGAAAAAACTTGGCTCCAGAGCAAACCGACGTAAGCGACAGTATGAGGAAGAGGAAGAAGAACCCAACCCTTACCTTCACATAGGATACCATCAGGAGAGCTACAGCGGACCCCAGGAAAACCACGCATATGATCATGAGAGCTATGGGTATCATCAAGAAAGTTATGGGTATCACCATCAGAGTCAAGGGTACCATGAGGAAACACAAGGGTATCACGATGAGACCCAAGGCTATCATAATGAAAACCAAGGGTATCATAATGAAAACCAAGGATATCACAATGAGAACCAAAGGTACCACCATGAGGGTTACTCTGAAGGGTACAATGAGGGATATCAAGAGGGATACCCAGAGGGATATAGGGGGGGTTATGGAGAGGGTGAACAAGAGGAAGAAATCAGAATGGTTGAGGACCAATCTTTGTTCCGCTGGCTGGCCATATCATATGCATCTACTCACCGCACCATGACTCAATCATATCAAAGAGGATGCCATAGT
Associated Phenotype:
Not determined