ZMP
zgc:165655
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100073343 [Source:RefSeq peptide;Acc:NP_001092249]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16233 | Essential Splice Site | Available for shipment | Available now |
sa2850 | Nonsense | Available for shipment | Available now |
sa32084 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16233
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115263 | Essential Splice Site | 198 | 341 | None | 10 |
ENSDART00000137107 | None | None | 138 | None | 6 |
ENSDART00000139943 | Essential Splice Site | 69 | 260 | None | 9 |
The following transcripts of ENSDARG00000094071 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 21000933)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 19237688 |
GRCz11 | 16 | 19043327 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTTCAGCTGGTCCCACAYGAGCAGCTCTGTRGTGGAACCCAGAGGCGG[T/C]GAGCACATGGTTACACATAAAGCTTAATAATGGTGTTTTTTYCAAGGTCC
Long Flanking Sequence:
TGGCTGATGGACCATTGCGAATTCATCCAAAACAGGGAAATAGCTTCCAAAATCTGGAATGTTCTCCTAGATTTGGGCATTCTGCTTTCAGGTACACAACCAATGCTGGGGAAGAACAAAGCAGACACACAAGTTTGGATGATTTATATAAAATGTTTGATTAATATTTTTATTATTATTATGTTATAAGGTACTATATACATTTGCAGTTTGCATAACAGCCGATTTCATCCAATGTGGTGCCTAAACAGAACATACATTTACATAAGCTTTGTCTAGATATAGCTTTATGTTGGATGTTTAACCCCAATGTGCTTCTGTTGTGTCCAGTGGAGCAGAACAATATATTTGAGGACTCCAGGTCTTTATACCAGTTCACCTTTAAGGAATGTGAGGCCCAGAGCTGTGATTTCAGAAATCAGGTCAACTGGCGGAGTGCAGTGCATCTGCTCCTTCAGCTGGTCCCACACGAGCAGCTCTGTGGTGGAACCCAGAGGCGG[T/C]GAGCACATGGTTACACATAAAGCTTAATAATGGTGTTTTTTTCAAGGTCCAAGGTCTTTAAACATCTTGTCCTACAAGGGTGTAAAACTTAATAGCTTTTTATTTACCATCCATTGCTAACAGAACGTGCCCATACGCATCAACAGTCTTTACTGATTACCTAAGTAGAGCTAAACGTATTTAAAATGGGTATTAATTACCCTGTAAGTAGAGCGACAGGTAGAGTAAGTTGTTAGCATTTACTACTTGAAGTTTTTTCTGGCTTGCATCCCAAAGGAGGCTAAAGATTTACTTTCATTCTATAATCAGCGTTGATCCAGTTAACCCAGAATGTTTTGTTTGTATTTTTTTCATTTTATATATATATATATATATATATATTGTTTTACATTTTACTTAGTTTCCTGTGTCCCCATAATTGGAGTTTTAAGATTAAATTTTATCTCAAATTACAACATTGTTTAATTATATAGTGTTGGGCAACGATGTTTCTGTGACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2850
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 |
---|---|---|---|---|---|
ENSDART00000115263 | Nonsense | 210 | 341 | 6 | 10 |
ENSDART00000137107 | None | None | 138 | None | 6 |
ENSDART00000139943 | Nonsense | 81 | 260 | 3 | 9 |
The following transcripts of ENSDARG00000094071 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 21006327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 19243082 |
GRCz11 | 16 | 19048721 |
KASP Assay ID:
554-2883.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTTGCTTTGTAGCTGTAAAGAAGATAAACAGAAAACACCTGATGCTTG[T/A]AATCCAGTTCTTCAAATGAGGGCATTGGAGCATTTCACCTCAACAGTAAG
Long Flanking Sequence:
GTATCTATATATTACGATTTTCGTGAGTTTTGTAATTATTATAGACCTTACAATCAGTGTCGTGCAGAATATTTTATTATATTAAGTTAATGTTTATGAATTTTGGACGGTTTTATTTTAGGGGTTCTCTTTATGATGTTTTTTCCTCTGTGCATGTTATTTACATCAATAAACTTCAATACATCAATAAGTTTTGTACACATATATTTTTGATATATATTGACGTATAAAATGGCATTTTTTAATTTCTTTAAGAAAAGAGTTATCCCCTTAATATTACATTATTATTACTGTAATATTACCTTTTATTCTCAGTACAGTTTTGATATTTCTAAATGAATGTCTCCTAAAAATATTAAAATACATTTAAAAACTATTTTATCATAGAATTATATTATTTGTGTTATTGTCAATGTGGAAATGTAAATGTAGTAAACAAAACAACATTATTTTTTGCTTTGTAGCTGTAAAGAAGATAAACAGAAAACACCTGATGCTTG[T/A]AATCCAGTTCTTCAAATGAGGGCATTGGAGCATTTCACCTCAACAGTAAGTCAATTACATTGCATTTTTTGCATCTTCTATCATTTCCCTCAATTTTAAATGGATTCACACAAAACAATAATCATGTCAGTAACTAAGCCTCCACTTGCTCCAAACACTAAAGAAGATATTTTGAAGAATGTTGCCAACCAGTAATCATTGACGTCCGTAGTATTTGTTTTCCTGCTATAAATGTCAGTGGCTACAAGTAATCAACACAAAATAAATAATATTTGTATTTTAGTTTATTTTAGAATGCTTTAACACCTGTAGATCGATTGTTTTGTTCCGAAACAGGGATTAAAATTCTAACAATGTTGGACTTTGTTCTTGTTGCGGGTCACTTTTAAAGTTTCTAAACGGACCAAAATGGCTACAATAAGTTGCATGCCAGTAAACTCTTCCCACATTGCACAGATTGAGTTCCATGGTTTATTTGTTTTATACATCCTGCCATAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32084
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 |
---|---|---|---|---|---|
ENSDART00000115263 | None | None | 341 | None | 10 |
ENSDART00000137107 | Essential Splice Site | None | 138 | 5 | 6 |
ENSDART00000139943 | Essential Splice Site | 251 | 260 | 9 | 9 |
The following transcripts of ENSDARG00000094071 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 21081987)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 19318742 |
GRCz11 | 16 | 19124381 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTCATTGGATCGTCTAATGTGTGTGTTACATGTTATGTTTATTTTCA[G/T]ATAGTCTGCTGGATGATTTTCTTCTGACGTACCCAGTGTTCATGTCTACT
Long Flanking Sequence:
TGAGCCACTTGTACATCCAGGAAGTGTTCAGGAAAAGCAAAACAGCAGCGAAGAAACTTGACACAGAGGAACATTTACACCTCATTGCCAACTAGCGTTTCGGAAGTGTTATTGCAAACCAACAGAGACAGCGCACAGAAGTATAAATGCATAGCTACGTGCGTTGCATGTGCCGTGGGTTACGCCGGTCACTTGACGCAGAAGTATAAACCAGGCTTAACCCATTGTCATCAGAAAAGTTTGTTTACATAATGAACCAAGAAAACACGGTTATTCTTTCTGCACATTAAGAGCCACCAATTGGAACCAATTAGCATTTTTATTTAGCATACACTACTTTGTATTACTTTGTTTTGTACTTGTGTTTTTATATATACACAGCAATTTAAAAATGAAAACAATAGATGTAATTCTAGTTGAAAACTTCAGACTTTTCCATTTCCAGTCAGTTTTCTCATTGGATCGTCTAATGTGTGTGTTACATGTTATGTTTATTTTCA[G/T]ATAGTCTGCTGGATGATTTTCTTCTGACGTACCCAGTGTTCATGTCTACTAGTGACCTGTGTCAAGCTCTACTTGGTCAATATCCTTCAGAACACAAACACGCACTGTCTAAAAATATGTTTTAAACCCATTTACAAATTATTAATTTGTCACTATGTAAATATACAAGAAACATTATAAACCTAATTGACATTTTAAGATTGATATTTCTCACAGAAGTTTGATCATATTTGATGGGCCATGACACCTAAACGATTGAAAACCCTTGCATTAAAGGATAAGTTCACCAAAAATGAATATTCCATTGTTAATTACTCACCTTCATGTCACTTCAAACCCCTAAGGACTTCGTTTATCTTCTGGATGCTAAGTAAAAAATTGTTCATGAAATCTAAGAGCTCTCTTATTCATAGACAGCAACAGCCAGTCATTCAACTCTAATTATATGAAGTTTTAAGAGCACTTTTGTATTTCAAAATTAGATTTTCTACATGGAATAT
Associated Phenotype:
Not determined