ZMP
si:ch211-149k23.9
Ensembl ID:
ZFIN ID:
Human Orthologue:
AC027045.1
Human Description:
Putative germ cell-specific gene 1-like protein 2 [Source:UniProtKB/Swiss-Prot;Acc:A8MUP6]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa28610 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa802 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa28610
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 |
---|---|---|---|---|---|
ENSDART00000055465 | Essential Splice Site | 81 | 246 | 4 | 8 |
ENSDART00000140946 | None | 4 | 260 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 15649831)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 14008290 |
GRCz11 | 16 | 13898410 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGAGGAACTTGCCAGGATTCGCCAAAGGCAATTAGCCAATGCAGTGCA[G/A]TACATCTGGGAGACGGGAGAAGACAAGTACACCTTCAGATATTTCCACAC
Long Flanking Sequence:
TAAGCAAATGGTTAAAAGTGAAAGTTAGTTACCCAAACTAAAAAGTTACAACAATTTTTGAAGACATTGGTTGAGTGAAAGAATCAATGACTTGTGATTTATAAAATGGTGGCTGCTTATTGGTGAAATAATGTAGCCTGCAGAAACAGTAAAAAGGCAAATATTTTGAATGATGTGATTAAGTGCATGACTCAATTCATATTTCTTCATAAAACAAGATTTGTTTATAAAACAAGACAATGAAATAGAAATTGTCTGACTAATGCTCAGTCATCTTTGTGGATTCTGTAATTTGTATGTAGAGAAGCAAAGCAGTTCAAACAAATAATGAACTTCCCCAAGCAACAACCCACTCATTCAGGTGGCTATCTTGTTTATTGGTTATCTTTTTTCTCAGAAAGCCCCACTCCGGACCCACGGGGCCCATTACCAACATTATCAACAAAGCGGAGAGAGGAACTTGCCAGGATTCGCCAAAGGCAATTAGCCAATGCAGTGCA[G/A]TACATCTGGGAGACGGGAGAAGACAAGTACACCTTCAGATATTTCCACACAGGATTCTGGCAGTCTTGCGAAAAACATGCTGATGGTAAGAAAAAGTCTCATGAAGAGAATTAAAATGAAAGAGTCTGTCCCTTTGCCATTGTCTTTTATAACTTCTCATCTTTTCATGCATCGACTGCAAAAAGAAATAGGCTTGACGTTTATGTTGCTCTTTCCTATACACTAGCTACTATAAAAACTGCAAGCTTAAATGAATTTGCAAAGTGCTACCATATCCACCTCATTGCCAACCACCCAAAAAATCTGAACAGCAGGTTGCCATAAAATTTAAGGTTCAGTCAATATTTTAGTTGTATAGGACAAAAATATCAAAGTAGTGATTTTATACGCATAATGTGAACAGCCATTATGCTGCTGAACAACCGAACCTTATATTGTGTAATCATAAACCGTGAGATTTGGGTTTACAATGCACACAATCTTCCGGTAGATTGTGAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa802
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000055465 | Nonsense | 101 | 246 | 4 | 8 |
ENSDART00000140946 | Nonsense | 25 | 260 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 15649892)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 14008351 |
GRCz11 | 16 | 13898471 |
KASP Assay ID:
554-0707.1 (used for ordering genotyping assays)
KASP Sequence:
AGACGGGAGAAGACAAGTACACCTTCAGATATTTCCACACAGGATTCTGG[C/T]AGTCTTGCGAAAAACATGCTGATGGTAAGAAAAAGTCTCATGAAGAGAAT
Long Flanking Sequence:
AGACATTGGTTGAGTGAAAGAATCAATGACTTGTGATTTATAAAATGGTGGCTGCTTATTGGTGAAATAATGTAGCCTGCAGAAACAGTAAAAAGGCAAATATTTTGAATGATGTGATTAAGTGCATGACTCAATTCATATTTCTTCATAAAACAAGATTTGTTTATAAAACAAGACAATGAAATAGAAATTGTCTGACTAATGCTCAGTCATCTTTGTGGATTCTGTAATTTGTATGTAGAGAAGCAAAGCAGTTCAAACAAATAATGAACTTCCCCAAGCAACAACCCACTCATTCAGGTGGCTATCTTGTTTATTGGTTATCTTTTTTCTCAGAAAGCCCCACTCCGGACCCACGGGGCCCATTACCAACATTATCAACAAAGCGGAGAGAGGAACTTGCCAGGATTCGCCAAAGGCAATTAGCCAATGCAGTGCAGTACATCTGGGAGACGGGAGAAGACAAGTACACCTTCAGATATTTCCACACAGGATTCTGG[C/T]AGTCTTGCGAAAAACATGCTGATGGTAAGAAAAAGTCTCATGAAGAGAATTAAAATGAAAGAGTCTGTCCCTTTGCCATTGTCTTTTATAACTTCTCATCTTTTCATGCATCGACTGCAAAAAGAAATAGGCTTGACGTTTATGTTGCTCTTTCCTATACACTAGCTACTATAAAAACTGCAAGCTTAAATGAATTTGCAAAGTGCTACCATATCCACCTCATTGCCAACCACCCAAAAAATCTGAACAGCAGGTTGCCATAAAATTTAAGGTTCAGTCAATATTTTAGTTGTATAGGACAAAAATATCAAAGTAGTGATTTTATACGCATAATGTGAACAGCCATTATGCTGCTGAACAACCGAACCTTATATTGTGTAATCATAAACCGTGAGATTTGGGTTTACAATGCACACAATCTTCCGGTAGATTGTGAATTGGTACCTTGCTAAAATAGTATAGAAATCGCACAGTGCTTACCCTAGGGATACCTAGGGAGA
Associated Phenotype:
Not determined