ZMP
si:dkey-161m5.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate MON1 homolog B (Yeast) (MON1B) [Source:UniProtKB/TrEMBL;Acc:B0UY
Human Orthologue:
MON1B
Human Description:
MON1 homolog B (yeast) [Source:HGNC Symbol;Acc:25020]
Mouse Orthologue:
Mon1b
Mouse Description:
MON1 homolog b (yeast) Gene [Source:MGI Symbol;Acc:MGI:1923231]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34311 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41127 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34311
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051756 | Nonsense | 170 | 502 | 2 | 4 |
ENSDART00000132031 | Nonsense | 170 | 474 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 10234766)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 9651348 |
GRCz11 | 8 | 9689933 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCTTACACAGGCCAGCATAAAACGCATCTTTGAGCACCGCAAGAACTA[T/G]GACCTGCGGCGCCTGCTGTTTGGCTCTGAGAGGGTCCTGGACAGCCTTCT
Long Flanking Sequence:
TCTTCAAGGAGAATAACGTTGCTCTTTTGGACCATCCTGCATGCTCCCCTGATTTATATCCCATTAAGAACATTTGGGGATGGATGGCAAAGGTTTACAAAATTGCCCCCCCAAAAAAAACGCCAGGTACAGACAGTGGGTGACCTTCCTGAAGCCATCTTAACCACGTGGAGCACTTAAAGAGGAATAAGTTAGTAAATTTTCATTTTTTGGTGAACTATAGCTTCAATGCAGACACTTAAAAGATGTGTCTTGTCTTTGTCCTGTGTATATATAATGCATACAGCTAACAGCTAATATAATGCTACTTTTTGTCTCTTTCCCTCAGATGAGCACACGGTGGTGTTTTTACAGCAGGGCCCTCTGGTGTTTGTTTCTGTCTCCACAACTCATCAATCAGAGCAGCAGCTGCGCGGTGAACTCCTCCATGTCTATCATCAGATAGTCAGCATGCTTACACAGGCCAGCATAAAACGCATCTTTGAGCACCGCAAGAACTA[T/G]GACCTGCGGCGCCTGCTGTTTGGCTCTGAGAGGGTCCTGGACAGCCTTCTGGACGTCATGGACTTTGATCCCAGCTTCATGTTATCAGCAGTCCAGTGTTTACCCCTGCCGTCTTCTTCAAGAGACATCCTCAGTAACATCCTACAGAAATCCATCACCCCCAATCTGGTATTCTCCTTTCTCATTGCACAAAACCGGCTTGTGTCCATCGTTCAGGAGAAGACAGTCGCGGAGGACACTAGACTAAAACCCAGTGACCTTCATCTTCTCTTAAACCTCATCAGGGCATCTTCTGCTTTTCAGGCCGGAGAGATTTGGATGCCCATCTGCCTGCCCCTGTTCAATCATGACTGCTACTTTTATGCCTACGTGGCGAATCTAGACCCTCCTGAATGCACCATATGCCTTGTGCTTCTTTCAACAGATAAAGAAGCTTTTTATGCCATGGCAGAGTGCAAACGGAAAATCGAGCAAGCTTTCATGTCTCAGAATGCCTTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41127
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 |
---|---|---|---|---|---|
ENSDART00000051756 | Nonsense | 338 | 502 | 2 | 4 |
ENSDART00000132031 | Nonsense | 338 | 474 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 10235270)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 9651852 |
GRCz11 | 8 | 9690437 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAAACGGAAAATCGAGCAAGCTTTCATGTCTCAGAATGCCTTGGAGTG[T/A]GTGGCAAACAGTCAGATGTACTGTGTTGAGGATGTCGGTGTAAATAATCT
Long Flanking Sequence:
CTGCGGCGCCTGCTGTTTGGCTCTGAGAGGGTCCTGGACAGCCTTCTGGACGTCATGGACTTTGATCCCAGCTTCATGTTATCAGCAGTCCAGTGTTTACCCCTGCCGTCTTCTTCAAGAGACATCCTCAGTAACATCCTACAGAAATCCATCACCCCCAATCTGGTATTCTCCTTTCTCATTGCACAAAACCGGCTTGTGTCCATCGTTCAGGAGAAGACAGTCGCGGAGGACACTAGACTAAAACCCAGTGACCTTCATCTTCTCTTAAACCTCATCAGGGCATCTTCTGCTTTTCAGGCCGGAGAGATTTGGATGCCCATCTGCCTGCCCCTGTTCAATCATGACTGCTACTTTTATGCCTACGTGGCGAATCTAGACCCTCCTGAATGCACCATATGCCTTGTGCTTCTTTCAACAGATAAAGAAGCTTTTTATGCCATGGCAGAGTGCAAACGGAAAATCGAGCAAGCTTTCATGTCTCAGAATGCCTTGGAGTG[T/A]GTGGCAAACAGTCAGATGTACTGTGTTGAGGATGTCGGTGTAAATAATCTCAGACACTTTTTGTACAAGCCTTCAAATGTGATGGAACATCATCGCCAGCTCCCACAGTTTACATGGTAAGGCCCTAAAGGAAATGTGCATTTTTTAATTCAAAATTTTATGTGTACTTAACTGAAACATGAAGAGAGGGCGGGAAATATAGTAGCTCCTCCCCTTTATAAAAAAAACAGCCAATAGCGTTTTGTTTTTATCACAGCTCTGCTACCAAGGTCAAGTGGATCAAATGAAAAGCAAATGAGAAGTGTCTTGAAGTGGGCGGGGCATGTCAGATAAAAAAAGCATTTGATTGGTCTGAAGTTTTGATGAGTAACTGAAGTATGAGAGAGAGAGGTATCCAGCTGCCAGCTGACAGTCTTATTCTATTTTGTCTTGTTTAATGATTAACCGCTTAGGAATAATTATCGCCACCTACTGAATTTCACAAATATGGCGATCGACAC
Associated Phenotype:
Not determined