ZMP
zgc:113293
Ensembl ID:
ZFIN ID:
Description:
Zgc:113293 [Source:UniProtKB/TrEMBL;Acc:Q566N1]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39734 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39735 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39734
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000101071 | Nonsense | 11 | 245 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 250504)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 217172 |
GRCz11 | 2 | 206083 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGTGTGCAGGACCACAATGCATCTCAACACTTTGTGTTTCCTTTATT[T/A]ACTGCTCGGTAAGTTCATTAATCTGTAATTAATTGAGAAAGTGTATTTTA
Long Flanking Sequence:
TTTTAAATGATTTTGAAGGGTTTGTTTAGTTTTATATGGATAACTAACCTTTCTTTCGGTCATCGGCTCTTCTTCTTGTTTACATTTACTGGCAGATCTCAAAGCTCCGCAGCGCCACCTGCAGCCCGCCTCATTTAATCAAACAGTACACTCAATTTACGTAGGAGCGTTTTTCACCTAAACGTCTCCTAATATAACGTTACCCACAGAACACGTGGCGATTTTAATATTGTGGCTATAAAAAGAAAGAAGAAGGGCTTACAAACCGGAAAGCCAGAGAGTAAATAAGATAGTAAATGTTTTCTCGTGATTTAAATGTTCGCTCTTCACTCTTGTTTAACTTTCCAAAATCACTAAACCTTTTTTAAGTTGAATAATTTAGCTTTAATCACTAATCGCGTCTGAACAAACGATTTATTCCACATTTATTCCATATTCTAAGAGACTGTTTGGAGTGTGCAGGACCACAATGCATCTCAACACTTTGTGTTTCCTTTATT[T/A]ACTGCTCGGTAAGTTCATTAATCTGTAATTAATTGAGAAAGTGTATTTTAATTTTGTTGTTTTAAGAATTTAGACTAGTTTGACCAGCTAGCAGTGAGCCAGTCAGCACTGAATCTGAGTACAAATTATAATGTTTGTTTGTTGTATTTGACTTTCAAAACAATGACCAGGACAAAAATCATAACTCTTAAGACTAGTTTAATCAGCTCATGCAGCAGGTCAGATATCTAGTTTTATAATGTTGTAAGTGTTTTTTTCCCATCTCTGTCATACTTTATAAGTCATAGTCATCATAACTCAATATTTTTAACTATATTGTTCTGGTCTGCATCTTTTGAGTTTAGCCTTTTAAATCAGTGCATTTACCCCTTTATAATTTAAATAGTGACAAACTTTACGTGCATTAATATGTTAACATGCAAAAATACACTCATTTAAATACACACAAACTACACAAAAGATAATATACATAAAAACGAAATAAGNNNNNNNNNNNNNNN
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39735
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000101071 | Essential Splice Site | 128 | 245 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 251638)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 218306 |
GRCz11 | 2 | 207217 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGGTAGCAGGAACACCTTCAACAAGAGCTTCAGTCTCAGAGTCTACGG[T/C]GAGCAGAAGCCATCTCACAACTCTATTTGTTTAATGATATGCTTTAAATG
Long Flanking Sequence:
TGTTTCCCAGTACAGGGTTGTAGCTGAAAGGGCATCCGCTGTGTGAAACATATGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCTGACTAAGCTGAAAAGAAAATGAATGAATGATGTGAAACATGCGTGCGTTCGTGTGTGTGTGCAGGTGTGTGTGGTGCGCGCAGTGACCGCTCTGAGCTGGTGTCAGTCTCTGTGGGGGAGTCGGTGACTCTCCGCACCGGTGTGAGCGTGCGCATTAATGATCGTGTGCTCTGGAGGTTTGGGTCTGACCGTGCAGATCCTCCCATCGCCGAGATCCTCCGCCGGTCCTACATGCTGTCTCTGCACGTCGGAGCTCTGGAGCGCTTTCAGGACCGACTGCAGCTCGACCAGCACAGCGGATCTCTGACCATACACAACTGCACATCCCAGCACTCGGGACTCTACAGGCTGACCGTCAGCGGTAGCAGGAACACCTTCAACAAGAGCTTCAGTCTCAGAGTCTACGG[T/C]GAGCAGAAGCCATCTCACAACTCTATTTGTTTAATGATATGCTTTAAATGCGCCTGCAGTCTTATTCAGCCTGTTATATACAAGATATAAACTGCGTCTGTGCGGTGTCCAGAGTGTGTGTGAGCTGAGAATACACACAGGTCATGTCCTCCAGCTCTCTGAAACTGACCCTCTCAGGCTTTCATCCTCATTGTGGTGTTTTGGTGGCTGTCGCTTTAAATGCAAATGAGATTGAGCTCTTTTCAGAAGAGGGCGGAGCTACAGACTGCTACACAATAAGTGTTGTGTGTGTGTGTGTGTTTGTGCAGCTCCTCTGTCCGTCCCCGTCGTCAGGAGTGTGTCGCTGTCCAGCAGATCTGCAGGTCAGAAGTGTGTGTTGGTGTGTTTGCTGAGGAACGCCTCGTGGGCGACGCTGTCCTTCTACAGCAGCGGCGGAGTGTTACTGTCCAGCGTCACACACACCAACAACAACTCGGACCACAGCAGCCTCTCATTACCAC
Associated Phenotype:
Not determined