ZMP
zgc:55418
Ensembl ID:
Description:
hypothetical protein LOC100149890 [Source:RefSeq peptide;Acc:NP_956153]
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 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17654 | Essential Splice Site | Available for shipment | Available now |
sa1628 | Essential Splice Site | Available for shipment | Available now |
sa32407 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17654
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 |
---|---|---|---|---|---|
ENSDART00000030404 | Essential Splice Site | None | 157 | 2 | 19 |
ENSDART00000089546 | Essential Splice Site | 31 | 785 | 2 | 21 |
ENSDART00000128016 | Essential Splice Site | 31 | 807 | 2 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 30122122)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 28504896 |
GRCz11 | 22 | 28455017 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCACTGGTTCATGAGCCAGTAATTCACATTTTGTTTTCCNTTTTTTGCA[G/A]TAAGAAGACAAAATRTGAAGGTTCGCATCAATGCCACYGGAGATACAATT
Long Flanking Sequence:
GCAGGATTGAAAAGATAATGATCAGATTACTTTAAAAGTGTGTCCGTGTTAAATTCCCGAAAACATACAAAGGCTCATAATTCCTCTGGATGTAATGCAGCATAACTAATATTGGAGGTCCATATGCTACTGTGCTTTGAGAGAAGTGAAGAGGAGCTCAACTGTGAAAGCCATTGCCCTTGATTTACCCCAATGGTGATATTTAAAGCACACACTTTTGTACTTCTCAAAAACAGCGCTCCTCCATCCCCCTTTGGTCTCATAAATCAATAAACTCCGTAAATTCACAATCCCCATCCAACACATGGGAAGCATAAAGTCTTACTCTTTACTCTTTAAGTAATTAATCATTTATTCATTGCAGTGTTCTGAAAGTTGCTCTTTTTGTGCAATTACGTCTTACTGCCAATGAATGTCAAACACAGAAACTGAAAACATTAGAAGAGCTGCAGCACTGGTTCATGAGCCAGTAATTCACATTTTGTTTTCCCTTTTTTGCA[G/A]TAAGAAGACAAAATATGAAGGTTCGCATCAATGCCACCGGAGATACAATTGTTTTGAAGTTTGTTCGACCCAACCCTGATGTCAAACTTGAAGGCTACATCTTAGGCTATGGCTCCAGCATGTTCTCCAAACAGTTCATCCAGCTTCCAGAAAACGGAGAACCCTATGAGACAGAGATTGGTAAGTTAGAGCTAAACCACAGGCAGCCGTTATTTCACTTAAGAGCCCGTAGGAAGCCCACAACACAATCGCTAATGTTGTTTTGTGGGTTAGCACAGGGATGAAAAAGTAACCACAAACGGTCGATTTCTTGCCCCATCGAAACCGCGGTCTTGATTTGTACACCTATGTTTGCGCCAATTCTTCCATTATTAGAAAACATAAACTGTAACTCAAGCCCAAATGACTGCTATTTATTAAAGCTTTCTTAACCGCAGTATTTTGTCATCACCAAAAAGTTACAGATCATATTTGACAAGGTTAAGAAAGGTCATATTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1628
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000030404 | Essential Splice Site | 8 | 157 | 4 | 19 |
ENSDART00000089546 | Essential Splice Site | 158 | 785 | 4 | 21 |
ENSDART00000128016 | Essential Splice Site | 158 | 807 | 4 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 30116438)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 28510580 |
GRCz11 | 22 | 28460701 |
KASP Assay ID:
554-1569.1 (used for ordering genotyping assays)
KASP Sequence:
TAAAGACACCCTATGAGGGAAACATCATGAACGACTGCTTGGAGGAAGGG[T/G]GAGTTACACACACAACATCTGGATTTTACTTTTTCCTCCACCAACATGTT
Long Flanking Sequence:
GAACAGCAGGTGCGAATAGCACTCGCAAGAGAAATCTGAGATCTCAAAAAGTGTTTGAACCCTTGAATGAGTTGTGTTGCTTTTCTTCACAGATGCCGAGCCTAAGTACCTTGTGGCTGTTCAGCCAATGCCAACCAATGATGTGAAGAAGCACTGCACAGGTAACATGGAAAATTAATTTAAAAATAAGAAGAATTTGGCAATGGATTACAAATAAAAAAATACTGTGAAACTATTGCTGGAGACGATTGTATATTTAGTGGAAAACGCACAACAGATGTACTATTAAACCAATGGGTACGCTTGAAAACCTCCAAAAAAGTCATATTGCTCTGTTAAATATTAATAACTCTGGGTTTGAAACAGGTAAAGTGAACCTGGAGAAACCTCTTCACCTGGTGATTGATTCTGTCACACCAACATCTGTGCTTTTATCCTGGGGAACCTACTTAAAGACACCCTATGAGGGAAACATCATGAACGACTGCTTGGAGGAAGGG[T/G]GAGTTACACACACAACATCTGGATTTTACTTTTTCCTCCACCAACATGTTCCATATGAGTGCCCTGAATCCCTGAGGAAGACTTAATTTACTTTACTTCATATTTAGGGACCACTTAGCCTGGAAAAAAAACTGGGGAAAAAAAGATAATGAAATATCATGGCACCCTGTCTCCAATATTTAGGGGTCCAGTCCTCAGAAACATTGCAGTGCAGGTTTTTATTCAATATTCTCACTGCACTGACAGGAGGCTGGATTTATGATGCGTAACCGAGAGAGCCATTCAATGAGCGCAATGTTTTTTTCTACACAGACGAAAAAAATGTGTGGGATATGGATCCCTGCCATTGCAGGTGTGGTGTGAGTCTACATGTTTAAATGCTTTTTGAGGATACAGGCACTGTTGGGACGCACTGACATGAGTCTCTAACTCACTCTGGTTTTCATATACAAAAGTATGTGATTTTTTTTTCCTCCATTAAAGGGAGACTTTTGGAAAGG
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:
sa32407
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 |
---|---|---|---|---|---|
ENSDART00000030404 | Essential Splice Site | None | 157 | 13 | 19 |
ENSDART00000089546 | Essential Splice Site | 581 | 785 | 15 | 21 |
ENSDART00000128016 | Essential Splice Site | 603 | 807 | 16 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 30102124)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 28524894 |
GRCz11 | 22 | 28475015 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCTCCTTCATTATTCTCGACTGGGAGAAAACAGATAATGAGACAACAG[G/A]TAGGAAATTCATTATTTAATATCAGTAGACCGGGTGACGCAGTGGCGCAG
Long Flanking Sequence:
GATGCTTTATGATTTTCTAATAGGACATCCTTGCATACATTTCCATATAGTAAATATCCTGATGGAAAGAATTTGTTTCTAACCACATTGTGAAATTATTGACATTTCCCTAGCACCCAAGTATGAGACCTGGGAGAACTCTTCAAGTTTCAGCCCTGTCCCTGCTTCTAAAGTTGATGCCATGGGCAAAGAGCGCTACATTGGTAATAATACTTTCTTATCTATTGTAGACATGCATGCCAAGCACTGTGAATGAAGCTTGTTTTAATCAAGAATGTGTTGTTGGCCAGCTCCACATGTGGTCTACAAGACAGATAAGAAGCCAGATGAACCTTGCTCCATCACCACCTCTCTAACTTACTTCCCCGAAGAGGAGGGTGGAGAACAAAATGTCACCAATCCTCCAAAAACAGCACCATCCAACCTCACCGTTGTAACAGTAGAAGGATGTCCCTCCTTCATTATTCTCGACTGGGAGAAAACAGATAATGAGACAACAG[G/A]TAGGAAATTCATTATTTAATATCAGTAGACCGGGTGACGCAGTGGCGCAGTAGCTAGTGCTGTTGCCTCACAGCAAGAAGGTCGCTGGGTCAAGCCTCTGCGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGTTCGCATGGGTTTCCTCTGGGTGCTGCGGTACAGGTGAATTGAGTAGGGTAAATTGTCCGTAGTGTATGAGCGTGTGTGAATGAGTGTGTGCGGATGGAAGGGCATCCGCTGTGTAAAAACGTGCTGGATAAATTGCCAGTTTATTCCACTGTGGCGACCCCCGATTAATAAAGGGACTAAGCCGACAAGAAAATTAATGAATGGATATCATTTGACCTATTTGTTTCTTAGGAATAAAATATGTAATATATTGTGAGATCAAAGTCAAGGGTTTAGGGTATGACACAAAATCTAAACTGCAACTGTGATTGATTAGGTTGTCTTTAGGGGCGGGCTGATGGCCTGCATAGTTTAGCTCCAACTTG
Associated Phenotype:
Not determined