ZMP
si:ch211-241p10.1
Ensembl ID:
ZFIN ID:
Description:
UPF0623 protein [Source:UniProtKB/Swiss-Prot;Acc:Q5PNP6]
Mouse Orthologue:
Mei4
Mouse Description:
meiosis-specific, MEI4 homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1922283]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1540 | Nonsense | F2 line generated | Not yet available |
| sa36932 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1540
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 |
|---|---|---|---|---|---|
| ENSDART00000064483 | Nonsense | 191 | 366 | 3 | 5 |
| ENSDART00000137135 | Nonsense | 188 | 363 | 3 | 5 |
| ENSDART00000148301 | Nonsense | 112 | 151 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 839260)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 795125 |
| GRCz11 | 20 | 815951 |
KASP Assay ID:
554-1463.1 (used for ordering genotyping assays)
KASP Sequence:
TGCAGCTGCTGGATTGTGTGGTGGAGGACTTCAGGCAGGCGCACACTGGA[C/T]AGCCTTTACGTCACCCAGAGCAGCTGCATAACGCCATTCAGGTGGTGGCA
Long Flanking Sequence:
CAATTAATAAATTCACCATCCAATCAACCAGCAAATAACCAATTAATAAATAAACCATCCAATCAGTGAATCTATCAACTAACCAATTAACCAATTGATAAATCAACCAGCCAATCAATCTTTATTTATATGTACCCATCGAAAAAAGGTGGACAGGAACATGACTAATGTCACAGAAGGATGCAGATATTCTGTGTTTTGCATTCACAGGTCAAGAGATTGCCAAAGTGCTCTCTCAGGATGACACACGGGAGGTCAACTCTGGCACTTTACAGACATGCCTGCCTCCGACCCCTCCAAACAGCCAGAAGGTTCCTCCGAAAGATCGGCAGTGGCGCCAGGACCACAGACTGACCAAACACGTGCAGTTCCTTCAGCGTCTGAGTGGCTTACGCAGCGGTTTCGAGGAGTCTCTGTGTCAGGATGGTGATGTGGTTTGGGATTCAGTAGTGCAGCTGCTGGATTGTGTGGTGGAGGACTTCAGGCAGGCGCACACTGGA[C/T]AGCCTTTACGTCACCCAGAGCAGCTGCATAACGCCATTCAGGTGGTGGCACAGACCCTGAGTCCAGGAGGAGCACGCCAGGGGTTTCCAGTGCAGCACTTCAGCAGAGTGGAGGATCTGTTGAAGGAGATGGTCAACCTACTGCTAACCAACCAACAACTCAATGCGGTAAGAGAAACATTACCACGATATCATGCTTCATATCATTCGATTATTACTGACTATTTTTTGAGAATGCATTTAGGAATATTAGGATGTTTTAACCATTTAATTTCACCAACATCACCAAGGCAAATAGCTTTAATAGACGAAAACAAAAATATTTAAAATAAATATCTGATCTCTTGATAATAAAATAAACAGAAGTGTTAAAGAGACTCTTAAACCTGACTTGAATGTTACAAAGTGTGTGCAATGGTAAAGGCAGATCAACATCTGTAAGGTGTGAATACTAATGATACAGTAAACCTCAAACATTGTCAACAACACATAATCAAATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36932
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 |
|---|---|---|---|---|---|
| ENSDART00000064483 | Nonsense | 208 | 366 | 3 | 5 |
| ENSDART00000137135 | Nonsense | 205 | 363 | 3 | 5 |
| ENSDART00000148301 | Nonsense | 129 | 151 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 839311)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 795176 |
| GRCz11 | 20 | 816002 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCTTTACGTCACCCAGAGCAGCTGCATAACGCCATTCAGGTGGTGGCA[C/T]AGACCCTGAGTCCAGGAGGAGCACGCCAGGGGTTTCCAGTGCAGCACTTC
Long Flanking Sequence:
AAACCATCCAATCAGTGAATCTATCAACTAACCAATTAACCAATTGATAAATCAACCAGCCAATCAATCTTTATTTATATGTACCCATCGAAAAAAGGTGGACAGGAACATGACTAATGTCACAGAAGGATGCAGATATTCTGTGTTTTGCATTCACAGGTCAAGAGATTGCCAAAGTGCTCTCTCAGGATGACACACGGGAGGTCAACTCTGGCACTTTACAGACATGCCTGCCTCCGACCCCTCCAAACAGCCAGAAGGTTCCTCCGAAAGATCGGCAGTGGCGCCAGGACCACAGACTGACCAAACACGTGCAGTTCCTTCAGCGTCTGAGTGGCTTACGCAGCGGTTTCGAGGAGTCTCTGTGTCAGGATGGTGATGTGGTTTGGGATTCAGTAGTGCAGCTGCTGGATTGTGTGGTGGAGGACTTCAGGCAGGCGCACACTGGACAGCCTTTACGTCACCCAGAGCAGCTGCATAACGCCATTCAGGTGGTGGCA[C/T]AGACCCTGAGTCCAGGAGGAGCACGCCAGGGGTTTCCAGTGCAGCACTTCAGCAGAGTGGAGGATCTGTTGAAGGAGATGGTCAACCTACTGCTAACCAACCAACAACTCAATGCGGTAAGAGAAACATTACCACGATATCATGCTTCATATCATTCGATTATTACTGACTATTTTTTGAGAATGCATTTAGGAATATTAGGATGTTTTAACCATTTAATTTCACCAACATCACCAAGGCAAATAGCTTTAATAGACGAAAACAAAAATATTTAAAATAAATATCTGATCTCTTGATAATAAAATAAACAGAAGTGTTAAAGAGACTCTTAAACCTGACTTGAATGTTACAAAGTGTGTGCAATGGTAAAGGCAGATCAACATCTGTAAGGTGTGAATACTAATGATACAGTAAACCTCAAACATTGTCAACAACACATAATCAAATCTGAGCTTTAAGTAAAGGAACCAGCCATCATTATACACATACATCCTGCAGCA
Associated Phenotype:
Not determined