ZMP
Q08BP2_DANRE
Ensembl ID:
Description:
LOC562403 protein [Source:UniProtKB/TrEMBL;Acc:Q08BP2]
Human Orthologue:
KIAA1598
Human Description:
KIAA1598 [Source:HGNC Symbol;Acc:29319]
Mouse Orthologue:
4930506M07Rik
Mouse Description:
RIKEN cDNA 4930506M07 gene Gene [Source:MGI Symbol;Acc:MGI:1918903]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20861 | Essential Splice Site | Available for shipment | Available now |
| sa26886 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa26885 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa9626 | Nonsense | Available for shipment | Available now |
| sa15465 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20861
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102567 | Essential Splice Site | 59 | 574 | 4 | 17 |
Genomic Location (Zv9):
Chromosome 7 (position 9560791)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 8508156 |
| GRCz11 | 7 | 8754114 |
KASP Assay ID:
2259-8443.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATCTGCTTAAAGTGTCAATGCATGTTTGATTTATACAAGTACTTTCAC[A/G]GCCTCTTCTCATCTGCTGAAGGAGCTGGACGTGTTAGAAATGCAGTTTCA
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGTAAATACTGTAAATATTTCCTTGGTCTATTAAACATGATGCGGGAAATATTTTAAAAGAAAAACAAATTTCACAGGAGGGCTAATCATTTTTACTTCAACTTATTATGCAAGTGTATGCATAAGAAATATTAAAGTGCTTCTACTACATTTACCTTTATATAATCTGCTACACAGTGCCAGATTCTGGAGAAAGAGCGAGATGAGGCGAATGAAAAGCTGTCAAGGATGGAGGAGGGTGAGACACCTCTGGGAGTCTTTAGTATTGCAATATGCTCATAACAACTTAACTACTGTGAAGGATAAAGTAGCCTCACTGTGAAAGACCTTAAATAACATTTACTGTATGCCTAAACCTTGGCATAACTCGCTGCAAAAGTATCTGCTTAAAGTGTCAATGCATGTTTGATTTATACAAGTACTTTCAC[A/G]GCCTCTTCTCATCTGCTGAAGGAGCTGGACGTGTTAGAAATGCAGTTTCAGATCGAGCGCTCCTGTAGAGAGACCGCAGAGGCCTACGCACTGAAGGTACACACACTTCTCTTTTCCCACAAGGCTATCAGTGTCTGTTTGTTTTTCTTGCTTATTTCACATCCCCATATGGTTGCAAGCTCTACACTGAACAAAAAAGATTCATTGCATTTACTATATTTTTTCAAGGAAGTGTTTGGGCTGAATTTAAGCAAACAAATTAAATTTAGTAATGTTCAACTTAATTTATTTCTGTAAATTTAGCCCATAAAAATAGTTTGCAACCACTTACCTTACAAAAAAAAATAGTAAACCTAATAAATCTTTTTTATAGAGTATGATGCTCTTCAAATAGAGTCAAATTTACAACAGTAAATTCATTCATTTTCCTTCCTCTTAGTCTCAGGTTTATCAAAGGTCGCCACAGGGGAATGAACCACCAATTATTCCAGCATGTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26886
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102567 | Essential Splice Site | 91 | 574 | 5 | 17 |
Genomic Location (Zv9):
Chromosome 7 (position 9554729)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 8502094 |
| GRCz11 | 7 | 8748052 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAAAATAGAATTTATTATGTTATATAATGTCACTCTGTCTCACCCCAC[A/C]GGTGTCAAAAGACTTCAAGGTATTAAAGAGGCAAAGCCAAGCTCTACTTC
Long Flanking Sequence:
CTACTTCGAACTAAGTGAAAGATCACTTTTTTGTCAGACGGCTCGTCGGTCAGATATACATCCACACAGAAATGCCAACTGACCCAGCTGAGACTCAAACCAGTGACCTTCTTGCTGTGAGCGACAGCGTTTCCCACTGAGCCTTCAATCACCAAGCTTTTAAAACTACTTTAAACTTTCAAGTCAAGACTAACTAGTCAAAATCAACAGTGTAAAGAGCTGAATTGTTCAGGGAAATGTTCTTTGGGGAACCAAAAGTGGTTCCTTCATGCTATTGCCTTGTAAGAAACTGACTACTGAAATCAGAAATGAGAAGAGAGAAAGATGCTAATTTTGCACACAGACACTCCCACAGCCGTTGCATTAGAAACACTTATACAAGTAGCGTTAATTACTTACACAAAGTATTGTTTGAATCTTTGGATTGCATTGCTGAAACAATCCGAGTCTGTGAAAATAGAATTTATTATGTTATATAATGTCACTCTGTCTCACCCCAC[A/C]GGTGTCAAAAGACTTCAAGGTATTAAAGAGGCAAAGCCAAGCTCTACTTCCTCTAATTCAAGATATGCCAGAAAATCTCTCCGCCCTGAACCTGGACTCTGAGGCTGATCTGAGCTCTGACTCAGTCCCTGCGGAAGACAGCAGTGAAGATCCACTTCTGATGAGCCAGAACCAAATTAGAGGTGGGACTCACTCGACAAATCACTTCTAAATAGCACAAGTCTCAACAATGGCTGAGGGCACAGTATGTAATTTTCACCACTAGAGGGTGTGTATTAACAACAAACAAAGGTGTAATTTGATGATGGCATGACTGACTGTGGGGGTTCGAGTTGTGGTTAACATTACAACCTGCAAGACTCCTGCAGAAATCATGTGGTTGGATGAGCTAAAGTAATCAACACTTATCATCAGTATGAAGCAGAGTAAAGGTATGTCATTTCCGCACTTTAAAAAATAAATTTGACCTCAGGTTGTGTCAGTCATATAGACACGCTGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26885
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102567 | Essential Splice Site | 183 | 574 | 6 | 17 |
Genomic Location (Zv9):
Chromosome 7 (position 9550983)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 8498348 |
| GRCz11 | 7 | 8744306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCGCAGGTGGACCTCCTTAAGAAAGAGAAGGAGGATCTGAAAGAGAAG[G/A]TATATAAGCGTCTGCAAATGAGACTCCATGACTAAACTACAGTCATGCTG
Long Flanking Sequence:
GCTAGAAATCTAGGTTTTGTGAAATCATTAGCATAACACACAGCACACGCTCCGTCTTACTGGTTAAAATTGCTTATTTCTCTGGATTTAATTTTTTTTTTAAACATATGGGATAATAAGTGCACAATTTGTCAGTGTCAATAGCCTAGTGGTCAGAGTGTAGACAAATAGCACTGAGGTGCTCGTGGCGACCTAAGTTCGATTCCTGGCTCAAGGTCTTTTGCTGATCCTTCCTTATCTCTGCATAATTGAGTTTAATTTATAACACTGCTCTAGTGGGTTTTGAATATTTAAATGAAACAATTATTACATACTGTGCCTTCTGAAGTTTAAAACATGTATTTCATGAAGTCTGTCTAAAAACTGTCTTATTTTTTTTCACTTTGTTTGAAATATGTTTAGAACTTCAGTCATCTGTGGATCGGTTGCTTGGGGAGAAAATTCAACTCTGTGCGCAGGTGGACCTCCTTAAGAAAGAGAAGGAGGATCTGAAAGAGAAG[G/A]TATATAAGCGTCTGCAAATGAGACTCCATGACTAAACTACAGTCATGCTGGACATTCATACAGGTCATAGATTATACATCTTAGAGAATCTGAAAAAAGTTAATCTTTTTTAAATAGAACAGCAATAATGATTTATGAAAATTGCCATTTAAAAGTTTAAATAAAACTGTTTCAATATCTGGATAACTGAAGAAAATTTAATTAATAGTAAATAATTACATATATTTTAAGAAAATTAAAAAATTAAAATTTTTAGCAAATGTGGTATGACTGTTTGTTCATATGGGTGATTATAGAATTGCGGGTACATTTTGCATCTCCAAGATAAACCTTCTTAAACTAAACTTTAACGAAACTTTTTTCATTAATAGCAGAAACAATATTGAATTATCTCTAAAAATAATGTTTGTAAATGTATTACCTTAAAGGCTACCGTTATACCTAATATTTGTCTCTGCCTCTTGAATAGCTTCAATTATCACAAATAACTAAGTGTAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9626
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102567 | Nonsense | 300 | 574 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 7 (position 9540771)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 8488136 |
| GRCz11 | 7 | 8734094 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGTGATGTATAGATGTCTCWGACAGCAGCRGAGGATCTCAACTCTCTGT[C/A]AGATCTGACAGCTAYAARAACAAAACTGGAGATCAGCGAGAGAGAGAGGA
Long Flanking Sequence:
AGAAACAACTCCAGCAGACTCTGAGTCAAGTGAGTGACATCAGCAGAGCTCTGGAAGAGATACGGCTGTGTTACCAGACGCAGGTGAGTGTGTCAGTGCACATCGTGATCATTCAGTTATCATGCTTAATTAAATCTATCCACCTTTATTTTTTATGCACATTTTGAAATATCGCATGAAATGTATTAACTATATGGAAACACATTTATTGATTATTACATTCATATTCCAGCATGCACATAAAAAAGTCATGTGGTTTTGTTTTAACAGATTATGTGATTATAAAATGAGTTAATTCATGGATGTTAATAGACAAACCAGTATTTTGAGCATATTTTAAAATATTTATATCATCATATTTGTATCATCAGAGTATACTTGTTTTACATAAACACCAAATATGTGGCATTAGAATGTGACCGATTTAATTATGTCTTTGCTTTTAATCTTACGTGATGTATAGATGTCTCAGACAGCAGCAGAGGATCTCAACTCTCTGT[C/A]AGATCTGACAGCTATAAGAACAAAACTGGAGATCAGCGAGAGAGAGAGGAGCGAGACTGAGACTCAGCTGAGAGACTCGCAACAAGCTGTGTCTGCACTTCAGGAGCAAAGTAAGGCTCATAAGTTACATAAGCATCTACGCTATTGACCTTATTCGTCATGTATAGTACAATTTTTTAGTTGGAGACTTCTGTTCTCATTCACTTCTGTTGATTTTTAGAGATTAAAAACAGCCTGTTGTGCTGCTTGATGTTGCAAACTGATATTTTCTCATTAGCAAGTTTTGATGTCAATAAAAGTGTCAATGTCATCAAGATGAAAAGAATATTGTGCTGTCTTGAGCATCTTCAGGAAGTGTCACCAAAACTTGCATTGACTTTTTTGCATTGAAAAAATGTCCAGAGTAAACTGTCATAATGAAAACATGACAAAGCCATTTGACTATCTTGTTTTTAAACAATGGTGTCAGGACTTTTCATCTTGATGACACTGACACTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15465
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 |
|---|---|---|---|---|---|
| ENSDART00000102567 | Essential Splice Site | 460 | 574 | 14 | 17 |
Genomic Location (Zv9):
Chromosome 7 (position 9535871)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 8483236 |
| GRCz11 | 7 | 8729194 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
NNNNNNNNNNAACCTYTGGCTTCTTTTTAGGTTGCATCTGAGGATGAAAATGCATGGAAG[G/T]TTAGTGACGSATCATTTAGTTTTATKTAAATGTATTATATGTGTGTGTGT
Long Flanking Sequence:
CTACATTTTTGCGAATCTGAAATGACGTCACTTAGGGTGTATTTTGTTGTACGCTTCAGATGACAAATCCACTAGAGGGCGCTGTCCACACTTTTATGAATTGGAATTACGCTTCTTAGGGTGTGTTTCCTTGATTGTTTAATATGACAAAATCCACTAAAGGGCGCTGTCTAGAGTTTACAGTTTTGCTAGTTACTATGTTACTATGGGTACATATGTACCTATGTTACCTAAGGTACATTTTGTTGTACGTTTCAGATGACAAATCCCCTAAAGGGCGCTGTCTACATTTTTGTGAATATGAAATATGTTACCTCGGGCATATTTTGTTGTACTTTTCAGACATCCTTCTTGCACACATCTATGAGATAGCAGGGCTTGTCATACAGATCACCTAGCAAACCACTGACCTAAACCCAACAAGCTGAATAAATACCAACTGAAATATATGACCTCTGGCTTCTTTTTAGGTTGCATCTGAGGATGAAAATGCATGGAAG[G/T]TTAGTGACGCATCATTTAGTTTTATTTAAATGTATTATATGTGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATTTCTATATATAAAATCATCTATATTCTTTACCATATGTTTCTACCATGTATTGACATAAACATATTTTTCTCTCAGATGTTTGGTAATGTTTTTTTAATTGTCTATTTTAGTTGATAAAGAGTATGAGGAGTTTTCATGACATGCCTAACCACTTTATAGTTAAAAAAATCTGAATGTGTGTGACAGGAGCAGAGGTCTGAGAACCGGAAATCAGCAGTGCTGGAATTGCAGGAGATGCTGGTAAAGCAAGACCTCTTTAAAAACTTATGACGGCAAATACAGCTTTTACTATTTACAGGCAATTGCCTTAATAAAATAAAAAAATAAACATTGTTTGTGTG
Associated Phenotype:
Not determined