ZMP
midn
Ensembl ID:
ZFIN ID:
Description:
Midnolin [Source:UniProtKB/Swiss-Prot;Acc:Q6NYU6]
Human Orthologue:
MIDN
Human Description:
midnolin [Source:HGNC Symbol;Acc:16298]
Mouse Orthologue:
Midn
Mouse Description:
midnolin Gene [Source:MGI Symbol;Acc:MGI:1890222]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37493 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37493
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 |
|---|---|---|---|---|---|
| ENSDART00000003929 | Essential Splice Site | 320 | 509 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 18960522)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 18711457 |
| GRCz11 | 22 | 18736435 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAAAGTTTTGTGAATCATGCCCCTGGAGTCTTCTCTGGGACATTTTCTG[G/A]TAAATTTTACAAGTTTGATAATTTGTTGATTGACAAATCATATAATCAAA
Long Flanking Sequence:
ATCACCCACACCAACATCCTCACCATCCAAACACAACGCTTCCATCTAATCCAGCAGCCTTCCCACCTTCCCCCTCTATCCCATCCATTCCTCCCATGTACTCCACCTCAGCCTCAGGGCATTGTAGCCCTCCACCACAACCCTCTCAACTCCCTGGAAGTTTTCTTCACTCTCAACAGCCGTCTTCGGCCTGCGCCCCTTCTCCAAGCAGCCCCAGCCCCGCAGCTTCCTGTCCAGAGGTAAGCCACTGTTTGTCCTACATGATTTGATGCAGTATGTTTTGTTTCATAATACATATTTATCAGTTAGATTTGAAAGATGTACAAACTATGATTAGTTATTCATAACTAGTTTGAAAACTCATTCATGTTTTTCACAGGCCAGTTGCTCAGCAAAGACTTCCGGCAACTGTAATACTCCCTTGCGATCTCGCAAACCTGGCGCTATCATCGAAAGTTTTGTGAATCATGCCCCTGGAGTCTTCTCTGGGACATTTTCTG[G/A]TAAATTTTACAAGTTTGATAATTTGTTGATTGACAAATCATATAATCAAAATCTATTCTACATTTATAATCTATGTGAATTGATAACTGAACCTCTTCCTTTAGGCACTTTGCATCCCAACTGTCAGGACAGCACCGGACGTCCCAGACGGGATATAGGCACCATCCTTCAAATTTTGAATGACCTTTTGAGTGCCACCCGACATTATCAAGGCATGCCCCCATCGCTTACACAGCTTCGCTATCAGACCCAGTGCACCAGCCCCAACTCACCAGCACCATCACCACCACCCTCACCTCCCCACACCACTGGACTAACAGGCCTGCCTACCACAGTGCCCTCAGAGACCCAACCAACTCTTCACCCACTTGTGCAGTGCCAAAGCCAGATCCGAATGTGCAAACCTCCCGGTAAGTTTTGTTGTATTTGCCAGATTTTGCACTTGCAGTGATGCATTTCCTGAAGCACTGACTGTAGCTAAAGTATTTTGAAAGCTACCA
Associated Phenotype:
Not determined