ZMP
zgc:136930
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC563946 [Source:RefSeq peptide;Acc:NP_001034908]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15439 | Essential Splice Site | Available for shipment | Available now |
sa45106 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15439
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 |
---|---|---|---|---|---|
ENSDART00000077514 | Essential Splice Site | 200 | 465 | 1 | 9 |
ENSDART00000082250 | Essential Splice Site | 211 | 476 | 1 | 9 |
The following transcripts of ENSDARG00000055192 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 32498683)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 32797590 |
GRCz11 | 2 | 32780808 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGATTGAGCTGGACAAYGTCAGGGGAACTGCWCAYGAGCTGAAGGCTAA[G/A]TGAGTGGTTTCTTTTTATTATTAAATCTGATTGTTTTCNNTTTTTTTAGC
Long Flanking Sequence:
GGAGGACTTGGATATGGTGCAGGTGGAGGTTTTGGACTTGGCCTTGGTGGAGGTGCAGGGGCAGGTGCGGGATTGGCACTGGGTGGTGGTGGTGGTGGTGCACTGGTTGCCAGTCCTGCATTTGCTATGGGTCGTGCTGTTGCTGCTGGAGGAGTCGGTGGAAGCTCTGCATTCGCTGCTGGTCCTGCAACCGCTGCTGTAGCCCCCATCCTTTCCAGAGCGGCTGAAAAGCACACACTGTCTGGGCTGAATGACCGCTTTTCCACATACATGGCCAAAGTGAGGGCGCTCCAGCAGGAGAACGCAGCTCTGGAGGCCAAACTGTCCCAGCTAACCGGGGGGGCAGATGTGTCTCCAGAATCCTCAGTGGCTGCAACGGTGGAGTACGAGGCTCAGCTGAGCGAATATCGCAGCACCCTGGAAACTCTCACCATCGACACTGTCAAACTAGAGATTGAGCTGGACAACGTCAGGGGAACTGCTCATGAGCTGAAGGCTAA[G/A]TGAGTGGTTTCTTTTTATTATTAAATCTGATTGTTTTCTTTTTTTTTAGCAATAATTCTTGTGGAAATGTTTCAATATGATAATGAAAGTTAGCTGAAACACTTGAAAAATACAAATAGTTTTTTGTTCTGATTTTCACTAAGGCTTGACTTTGAGCAAGGAGTGAAGTTTCAGCTTGAGTCTGATATCGCTGCCATGAAAAAGGTGAGCAGGATGACATTTAGTCACAGTATAAATATCGAATCAGTACTTTTAGTAAATAAAATGCTATATGTTGTTTGTGGTTTTCTGTTTCCTTTTTCAGGACATTGAACTGGCTTCTGATCTAAGAATTGACCTGGATGCTAAATACTCTAGCTTGAAAGATGAGCTGGACTATGTGAGCAAAACACAAGAACAGGTACAGAATTAGACAAAAATCTCTCTACTGCACGCATTATGATAGATCTTTGAAATATTTGACTGTTTTTCTAGAAAGGCTAACCTTGAAGTGAAGGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45106
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 |
---|---|---|---|---|---|
ENSDART00000077514 | Essential Splice Site | 313 | 465 | 5 | 9 |
ENSDART00000082250 | Essential Splice Site | 324 | 476 | 5 | 9 |
The following transcripts of ENSDARG00000055192 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 32501096)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 32800003 |
GRCz11 | 2 | 32783221 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCCTGCATTCCAAACTAACAGATCCTATACTGTCTACTTATGACTGCA[G/A]ATGGATGAGATGCAGACGGTCACGGCCAAAAACACAGAGGCTGTGTCGTT
Long Flanking Sequence:
CTAAATAAAAACAAAAGATACTACGGTAGTCAGTGGCTGGAGGTTTTTTCCAACATTGTTTAAAATAAATCCCCTTGTGTTCAACTGAAGAAACTCAAACATGTTTTTAAAAAGTGGAGAAAGACTAAATATTGACAGAGTGAACTATCCTTTTAGCTTCCATAAAAAAATATTTGTGGCTGTATTTTTCTTACTTATTTTTGTGACTTTGTTTTGTCTATCACTGTAGGAACTATCATCTCTGCAGTCTAAACTGGGCACATCAACAATGGACACTTCAGTTTCAATGATTGAAGTAGACACCGGGAAGTCCTTTGACATTGCTACAGCACTCAACAAGATGCGAATGGAATATGAGAAAACTGTACAGCAAAACAGAGAGGAGGCAGAGGCATATTACAAACTCAAGGTCTGCAAACATGAAACACTCAGTGTCTAAACACTTTAATAATTCCTGCATTCCAAACTAACAGATCCTATACTGTCTACTTATGACTGCA[G/A]ATGGATGAGATGCAGACGGTCACGGCCAAAAACACAGAGGCTGTGTCGTTGACTAAAGCAGAGATCACATCAGCCAGGAAAGAGCTGCAGACACTGAGTTTAGAGCTTCAAGGGCTTGCAGCTGCAGTAAGTGTTGGCCTTATGAAATGAATTAAGAGATTAATGTGTGATACTTAAATGAACTGCCATTTAATGAGTGTTCAGAAGACTTTAAGCAGTGTTCAGATGGTAATGGTGCTCAAGAGTTGTAAGTCTCGAGAGAAACCATATTGTCAGCAGTGTGAAATGCTTCAGTGCAGATTCTCAGGCATACAATCAACACTTCTGAATAAATCACAGCTGTCTGAGACAGGAAGCAGATGACATAGGAAGTGGTTTATTGATCTCAGCCGTTTCATATCGACACTAAAAGCCCCAATGCCACAAGAAGTAGTTTTGCTGCTGCAAAAGAATCAGTTTCCCAAAACAACTTGGGCACTTCAAGTGTTTGACATCATTTA
Associated Phenotype:
Not determined