ZMP
si:ch211-191j22.8
Ensembl ID:
ZFIN ID:
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15661 | Essential Splice Site | Available for shipment | Available now |
sa37290 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15661
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 |
---|---|---|---|---|---|
ENSDART00000065596 | Essential Splice Site | 33 | 553 | 1 | 9 |
ENSDART00000132174 | None | None | 150 | None | 5 |
Genomic Location (Zv9):
Chromosome 21 (position 20131521)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21267010 |
GRCz11 | 21 | 21303646 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGAGGGTCTGCAGGACCAGAGGAAGGGGTCTTACAACAGCTTGCCAAGA[G/A]TGAGTTTGAAATCMATGTTTTTAATTTTATTTTGAATAATCTGTCTTTTA
Long Flanking Sequence:
ATATATGGAGTCCAGGAAGATGGCTGCATTGTTTTGGGACTTGGATGATGCTACTACTCCTCCAAAGACTCCACCTCTACACTTCGGCTCTGAGTTCAGGAATACTAGCTCTGCGAGGTGAGATTTTGTCTTTTACCATATTTAATTATCATTTGACCTGGTGAAAAAAGACCATCTTTTTCAGTTCCTATGGTGGTTCACCAGTGCTAGGCAGTTTCGACTGGGCTTCATCTGAGCAAGTGGAGTTCTCAACATTAAACCCCTCCAGAACTAAAGACAAACAAGGTCTGCTAGCAGGTTATGCATGCTTTTATTAGCAACATCATTTAGTTTGTATTTCATTTTGCTTAATGTCATTTGCCTCTGCAATTTTATCCTTCATTTCAGAAGGAGAGTGGCATATGATAATGTCTACTCGCCCTTTAATTGGATGGGAAAAAGCAGCCCAAAGGGAGGGTCTGCAGGACCAGAGGAAGGGGTCTTACAACAGCTTGCCAAGA[G/A]TGAGTTTGAAATCCATGTTTTTAATTTTATTTTGAATAATCTGTCTTTTATATCTAATAAAGACATAAGATTACAAAAAATTTAGTCTAGTGTTGGTTAGAATTGATTTGACCCCAAAATGAGAATGACAACATTAACCATGCATTCACACAATGCTTTAGCCTCAACGCTTGACATGGGTGTAGCTGATGTAATTGTCAAAGCAGCATCAGCCAATGAAATTAACCCGCAAACGGTGACTGTCTGAGCTGCGGTATTTGCATAAACTGATCTGATTGGCTGACACTTCCGTTGGCGCTTGAAAAGGTGAGAATTTCCTAACTTCTGCAGTGAGCAATGACACTAAAGCAGCGCTGACGGATCTACAATGCAGTTCGGCAACGCCTGACGTCACCCATTCAAAGTGAATTGGAAGCGTTGATGCTGACGCCCTGTATGAATGGGGTGCAATTGTTTTCACTCATGAGGTTTAAAACCTTCTATCTACCATAAAACACAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37290
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065596 | Nonsense | 314 | 553 | 4 | 9 |
ENSDART00000132174 | Nonsense | 48 | 150 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 21 (position 20141415)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21276904 |
GRCz11 | 21 | 21313540 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTGAGCTCAAAGAATGTGTTTGGTCAGCCCCGAGTTGTTGCGTCTCTG[C/T]GAGCAGCTTGTTCACCGCGGCCCGTTCGCAAAAGCACAGTGGTGGAGGAC
Long Flanking Sequence:
TATGAGTTTAAATGAGAGATTTGTAAGGGGTTTACTTATGTATGCTGAGCACTGTATATATATATTTTTTTTATTTATTTATTTTTTTCCTTTACTTTTTAAAGTCAATATTATTACCCAGCTTGATCAAAAAAAAATTTCGATTGGCTACCGAACAAACCACTGTTATACAATGACTTGCCTAAGTACCCTAACTTGCCAAGTTACCCTAGTTAAGCTTCTAAATTGCACTTTAATCTGAATATTATTATCTTGAAAAATATCTAGTCAAATATTATGTACCGTTATCGTGGCAAAGATAAGATGAATCAGTTATTATTAAAACTGTTTTAGTAAGGAATGTGTTCAAAAATCTTTTCTTCATTAACTTAGGGGAAAATATAAAAGAATTGAAATGTAACTGGAGGGCTAATAATTGTGACTTGAACTGTATATTTTTCAGTCAGGTGGATGTGAGCTCAAAGAATGTGTTTGGTCAGCCCCGAGTTGTTGCGTCTCTG[C/T]GAGCAGCTTGTTCACCGCGGCCCGTTCGCAAAAGCACAGTGGTGGAGGACCTGAAAAAACTCATTGTGATGGATGACACCGAGGACAGCGCTCGGGGGGATTCAGTACGTGAGGTGAAATATGTGCAGTATGACCCTGAACAAGGACAATAATGTAAAAAAAGCAGGTATTGTTCTACTGAGGGTTGGTATGTGTGCAGTGTTACCATGTTGCAATGTGTCTCTTTCTAGTCGACAAATCAACAAAAAGTGCCAGAGCTTTGCAGTAGTTCGCCAATGTCAGCTTCATGTGCCAGTCCATCATTATTCAGTCCTACTCCAGCGCTCACACCAGTCCATCTTCACCTGCAAACATGTCAATCAGGCAAGGGTTTTTTCTTTATGAGTGATTTATGCTATGGACTGTTTATAGTATCCGTTTGCATTCACTGGTTGTCTTTTTCTAGAATGTGATGTTTTGCCTGAGCAGGCTGAATCTGACCTGTGGGAACATCCTGACAC
Associated Phenotype:
Not determined