ZMP
si:ch211-88n13.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate ABI gene family, member 3 (NESH) binding protein (ABI3BP) [Sourc
Human Orthologue:
ABI3BP
Human Description:
ABI family, member 3 (NESH) binding protein [Source:HGNC Symbol;Acc:17265]
Mouse Orthologue:
Abi3bp
Mouse Description:
ABI gene family, member 3 (NESH) binding protein Gene [Source:MGI Symbol;Acc:MGI:2444583]
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12479 | Essential Splice Site | Available for shipment | Available now |
sa31723 | Nonsense | Available for shipment | Available now |
sa21504 | Nonsense | Available for shipment | Available now |
sa18355 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12479
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089543 | Essential Splice Site | 57 | 1072 | None | 26 |
ENSDART00000133746 | None | None | 290 | None | 8 |
ENSDART00000143986 | Essential Splice Site | 61 | 128 | None | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 31194024)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 30349970 |
GRCz11 | 9 | 30160716 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAATTCATCCARCTGCCGGAGGATGGACAACCWTATGAGACTGAGATAGG[T/A]AMTGTCGTTCTTCTACTCTTTAAAWAAYTTTAGTGCTTTTTAAAACTGAT
Long Flanking Sequence:
CCACAGGAGTCTTACACTGGTATTCTTCTTTTGTGTGTTTTCATGTTGTCATAGTTCACAAAACAAGGTAATTATAATGGCAGAACGTGATGTTTGTGTGGGAGGAATGAGAGCTTGAGCAAAACACTTTCGGTTACACTGTAAAAGCATTTCAGAAAGAGGAAAATATGACACCAGACTGATTGTTATTCCGAATCTCTTGGCTAAAATGTTGTAGATACAGTCACATGATTTCTTGTATTCGTAGCTGAAGTCATTGTGTAAATCTAAGGGACCTAAGTAAATCTGACATTAGTTTTCCTGTGTATTTGCATCTCAGTGCCAACACAAAACATGAGGGTCCGGATCAGCGCTGTTGGAGACACCGTCGTCTTCAAGTTCATCAGGCCTCATGTGGACTCCAGACTGGGAGGGTATATCCTGGGCTATGGCAGCAGCATGTTCTCCAAACAATTCATCCAGCTGCCGGAGGATGGACAACCTTATGAGACTGAGATAGG[T/A]AATGTCGTTCTTCTACTCTTTAAATAACTTTAGTGCTTTTTAAAACTGATTCTCCTCCTTTCTCTAGATGCTGAACCCAAATATCTGCTCGCGATACAATCAAATAAACCAGAAGAACCTAAGAAACAGTGTGCAGGTAAGCAGCTTTGTGAAAGAAAACATCTGTCCATACAGTGGACCCTAAGTAGTTGTGCACAAAACCACACTTTATTTTTTTGATAAAACAGTTAAACAATTAATACAAAGTTATTTTGTCTGTCTTTGCTTTTCCAATGAAAATAGTTCCAAACAAGTCAAAGTCAGTCTTTCACCAAGGATACGGTATGGCGTTTTGTCCCTGAGTCAATCAGTGCTTTGAATGAACCAGCAGGGTAAAAGTTAAAATAAAGTTCTCAATTAGATATTAGAATTAGTTGAGTAAGCTTGTCAATTAAACAATTTAACACTACAAGTCAAGTACACTTCAAATATTTAATTAGTATAATTAGAGGCCTGTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31723
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 |
---|---|---|---|---|---|
ENSDART00000089543 | Nonsense | 144 | 1072 | 4 | 26 |
ENSDART00000133746 | None | None | 290 | None | 8 |
ENSDART00000143986 | None | None | 128 | None | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 31191064)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 30347010 |
GRCz11 | 9 | 30157756 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCGCTACAGAGAACAAGAGCCCAGCAATACCTGGAACTATCAAACCTG[T/A]CCATCCTCCAGCACAGTCATCGACAACCTCAAACCAGATGTGTTGTATGA
Long Flanking Sequence:
AATGATATCGTCTATATGTTTTAGTGTTTACTTTGCTCTTAGATACATATTTAAGTTGTTACTGTGTTTGTGGGGACATATGGTCTGCAAAATGTATTCAAAAGCTGACCAACACACACTCTCCTTGGACAAGTTAGTGGAAAGCTTGACCTCAGCCCTCTATAAAACAACCAATTTGATCCTTCTATTCCATAAAAATCTTATAAATACCAGAAAGAGAAGGAGATACTGATATAAAAATATAATAAAGAGTAAGAAGGGCCATCTTTAAAGTTAAATAACATCTGGGTTTAGCCCATTAGTCTCTTGTACTGCTAGGTTATTGAAGCCAAAGGTCTATTTTTTATTATCTGATTGTTAATGCTGCCATTTTAAATCAAGTTATTGCTATTACAGTGTGTGTGTGTGCGTTTTTTTTTTTTTTTTTGGTCTGCTCGCAGACATTTCACAGTGCGCTACAGAGAACAAGAGCCCAGCAATACCTGGAACTATCAAACCTG[T/A]CCATCCTCCAGCACAGTCATCGACAACCTCAAACCAGATGTGTTGTATGAATTTGGGGTTCGAGCAGAAACTGACAGCAAATGTGGAGCCTGGAGTCCACCTGTCATCCATAACACAGATGGTGTGTCTCACATTTTGTGCAAAGCAGTTGTTTTACCACAGTAGAATGAATTCATACTGGTATACTTGAGGGAAGGAATAATTATAACTGAGGTTTCTTTTATACCTCAATTGTTTCTCCTAGACATCAATGCTCAGACAGCAGATTCTGAGCTGAGCTTTTTATATTAGCTTTATGGTTAAATAATCTTATTTTGTTGCAGATTATCTCATTCATTTGTATTTCTTTATTTTCCTGTTCACAGATCAAATAATAAGGCCATTTAAAGAACTGAACCAGGCAAAGCCTAAAGTAAGTACTGTAACTGCTGTAAGGACCAAACCTTTTTTTCCTGCTCTGCTTTATTTTTCTGTAACCTTGGGTGTTTCTTTCTAAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21504
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 |
---|---|---|---|---|---|
ENSDART00000089543 | Nonsense | 471 | 1072 | 9 | 26 |
ENSDART00000133746 | None | None | 290 | None | 8 |
ENSDART00000143986 | None | None | 128 | None | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 31187925)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 30343871 |
GRCz11 | 9 | 30154617 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTAGCAGACAACCAGTATTTAGCACTACTGCATCCACCTATACCAAATA[T/A]TCTATATTCCATATTCCCACAACTGAAGATCCTCCTCTTAACAAAAGTGA
Long Flanking Sequence:
CAAGAATATATCAAAACACAGATTTCAACTAAAGACCCACCATATACAGCCAAACAACAGTTTAGTGAAACAACATCTCCTGTTTCGACAACTTCTCCTATTCCAACTACAACCAAACCACAACAAACCACAACTAAGGAACCAGACACCACAACTCAGGAGAACCTCTATACAAGAAAAACCCAGCCTAGAAACAAGATGCAACGATTGAGACCATTCCGTTTCCGAGGCACGTCTAAACAACAAACCACTCACACTTACCCTCTGCCAAAAACCACTTCTTACTACCAGTCAAGCACAATCACGCTTTCAGAATATGCAAACACCAAACCACCAACAACCACGGTGAGCTGGTCCACAAACAGCCATTCTGTGACAAACACAGCTTTGACTTCCACCACTACTATCACAAACATTCAGGATGACGTAACATCACAACAGACTACTGATGTTAGCAGACAACCAGTATTTAGCACTACTGCATCCACCTATACCAAATA[T/A]TCTATATTCCATATTCCCACAACTGAAGATCCTCCTCTTAACAAAAGTGAACAGGAACTGACTCGACAACCTGTAAATCTACCCATAACATTTGGGTACAAGCCCCAACCCAGTACTGCAACACAGCAGTCCAACACCCCAAAACAGCGAGCTAGCACTGCTAAATTCGTCCTAAAACAGCATATCCAGGATGAAAGCCAATCACATAACCCTGAAGAACGGTTGCCAGGTACCCAAAAACCACTATTAAACCAAACAGCTTTCATCAAATTCGATGCCATTCAAAACTCACCTGTGACGGAGAAGGTAACAGTGAGGACAAGTCAACAAAGCCAACCAACTGGTAACTTCTCCCCTAGCCATTTACTATTAAAAAAGATTAAATATAGTTAATTGAATTGTTGCAATCTGGCAAACCAAAATGTATAATTTTAGACAGATGTGTCCAGTCCTGCACCTGGAGCTCAGATTCTAATTAAAGGCAGCTGAATGAACTAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18355
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089543 | Essential Splice Site | 676 | 1072 | 14 | 26 |
ENSDART00000133746 | None | None | 290 | None | 8 |
ENSDART00000143986 | None | None | 128 | None | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 31181644)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 30337590 |
GRCz11 | 9 | 30148336 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTGCTTACAGGTTTAATGTGGTGTTTCAGATAGATGTCCCTGTTTTGT[T/A]GAAAACAWCTCCTGTGCAGAAAACGATTCCCAWGCAGCTGGATTTCATGA
Long Flanking Sequence:
CAGCTGATTACTCCTGTGACACCTGATACTACAACTGAACACTTTTTGTCATTTAAGTGCACAGTTTCCCTTTAAATCTGGTTTCTTACTCTAATTTTATCAAATGCAAACCTCCATGTGCTTACATTGCTTTATGTTTCTTGAATGTTCACATGTGTTTTGGAGAGATTTGAACTTGAAATGGGTTTGATTATAGCAATCTTTTCTATCCTGACAGGGCCTCATGGTGAGGGTCACATAGGCCTTCATGGAAACAAGCCTAGAAAACAACCTGGTAAACTCTTTTATGGATTATTTTTGAAGATTATTTAGTAAGGGAATTCAGATCTCATTCTCCTTACAATCCATGTGATGTTACTTTAGTTTCAAAGCCTGGTTTTATGTTATTCCGTTGAGTGATTTTGTAGTCCATGTACCAGAAAACCGTGAATCCAATTGTGCACAGTGCTAGTTTGCTTACAGGTTTAATGTGGTGTTTCAGATAGATGTCCCTGTTTTGT[T/A]GAAAACATCTCCTGTGCAGAAAACGATTCCCATGCAGCTGGATTTCATGACAAATCTAGGCCAAAGCAAATATTTATGTGCTGTTCATGTCATAATGGATTTTCAGAGCTTATGCTTCTTTGGAAAAGCATGACAGATCAGCCATTGATAAACTCTGCCAACTGCTCATGAGAACACAGGACTCGTCTCACTTTCTCCATCATCCTCTCCCAACCAAAGACAACATAGCAGCTGAATAATGAAGAATCAAAATTGAATCCCTCTGTCCATACCCAATAGCTCATTCCATCCATCCCATCCGACTTTTATTAGAAAATATACAGCCCTGAACACATTTGGCCGACATGTGATTACTTAAGGAAAATCTGAGAGCATTACTCATCCAGATTTTCTTAAAAAACATCCATTCGAGCTAAATTAGATTCCTGATAATGTTCCAGAATGTTTCACGAGTTGCATAATGGAATATTAGAGAGATGGCTGTTGGAAATAATTATGTT
Associated Phenotype:
Not determined