ZMP
morc3b
Ensembl ID:
ZFIN ID:
Description:
MORC family CW-type zinc finger 3b [Source:RefSeq peptide;Acc:NP_001003579]
Human Orthologue:
MORC3
Human Description:
MORC family CW-type zinc finger 3 [Source:HGNC Symbol;Acc:23572]
Mouse Orthologue:
Morc3
Mouse Description:
microrchidia 3 Gene [Source:MGI Symbol;Acc:MGI:2136841]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa25653 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa19564 | Nonsense | Available for shipment | Available now |
| sa32755 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39677 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25653
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 |
|---|---|---|---|---|---|
| ENSDART00000074450 | Nonsense | 243 | 763 | 6 | 17 |
| ENSDART00000137448 | None | None | 173 | None | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 47684971)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46496632 |
| GRCz11 | 1 | 47187864 |
KASP Assay ID:
2259-1021.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGAGAAGCAACGGTGACCTCGCCATGATCCCAGAAAGTGAATACTCAT[T/A]ACGGGTGAGCGGAAATATCTTCTAGATAGAGTTGATGGTAGAAACTAGAG
Long Flanking Sequence:
TATGTGTAAAAGACAGACTGAGAGATTCTCTCTTGAGTTTTCCAGCTGTTGTTTCTAACAATATAGTCTGTCTTCTTGCATCAAAACATTAAGACTTTTTCACAGAAGAAGCAGACTCCACATCACTTTTTGCTGACATTACAGGACATGTTGTTAAAACAGATGGCCATCTAAAATGATAAGTTTGCTAAAAACTAAATTACATTTCAAAACATATATTTTAGAAACAAAATTTCAGCTTATTGCTCTTTATTGTGTTTAAAATCTAATAAATACAGCCTTGGTGAGCATTAGGGACTTTAAATATTAGATAAACGCTTGTGAACTTTTTTTGTATAATTTGAGTTTTAATAATGACCCATAACTTGTGTTTTATAGGACAACAAATGGCGAGACTGAGTTTGACTTTAACACCAGTAAATATGACATTCTGATCAGGTGGAACATCAGTGAGAGAAGCAACGGTGACCTCGCCATGATCCCAGAAAGTGAATACTCAT[T/A]ACGGGTGAGCGGAAATATCTTCTAGATAGAGTTGATGGTAGAAACTAGAGTTGAATAATATATCGTTTGATCATCGATATCACAATGTGAGTATCCGCAATAGTCACATCGCAGGATTAGATTATTTATCAAAGATTAAAAGATAAAGATATTATTATATAATATGTATATATTATTGTATAAAATTAGTTATACAATGACAACCATGTCCTTTTACTATTGATTTTTTAAAGTCTTTGTATTTGAATACAGTTAGACTCCAAAGAAAACCGTAAAGCACTGTTTATTTGACTTTTTTTATTTGTTTATTTTTGCTTGTAATTTACTATATTTCATGCAGATGCACCGCATAAAAAAGGTCAAAATAATTAACTCCTTTCAAATCAAGCTATTCAAATGATCTGATAAAATTTATATTCATATCACAATATACAGTTGAAGTCAGAATTATTAGCCCCCCTCTGTTTATTTTTTCCCCATTTTCTGTTTAACGTAGAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19564
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000074450 | Nonsense | 282 | 763 | 7 | 17 |
| ENSDART00000137448 | None | None | 173 | None | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 47687174)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46498835 |
| GRCz11 | 1 | 47190067 |
KASP Assay ID:
2259-1022.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAGTCAACTGATATCCAAAAGTCTGGCTCATATTGCGCAGGACAACTA[C/A]AGGCCGTCATTCCTTGTATCCTTTCAAAACATATTATGCTTGTTTGTTGT
Long Flanking Sequence:
AGCTGCAATCCATCCCTGGGAAACACCCATACACTCCCATTCACACTCATACACTACAGACAATTGTAGCTCACCTAATTCACCTGTACCGCATGTCTTTGGACTGTGGAGGAAACCGGAGCACCCAGAGGAAACCCACGCCAACACAGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGGCCCTGCCAAGGCTTGAATCAGCGACCTTCTTGCTGTGAGGTGACAGTGCTACCCACTGCACCACTCATATTGATCATTATAGTCTTTTAACTCATGGTGTTAATTGCAATTTATTCACCTGCAAAATATTTAAGCAATTAAAACTCTTCATAGTTGGTGCGAGATTAATTATTTTTTATTATTATTGTTATTTTCCTATAGGCATACTGTAGCATCTTATACCTGAAACCTCGCATGCAGATCATCATACGTGGACAAAGAGTGAAGAGTCAACTGATATCCAAAAGTCTGGCTCATATTGCGCAGGACAACTA[C/A]AGGCCGTCATTCCTTGTATCCTTTCAAAACATATTATGCTTGTTTGTTGTTGTTCTTTGGAGTCCACACACACACATAACCATCATCCGGATGTTGACATTTCTTAACCCCTCCTTCAGAATAAGCGTTTGCGCATCACTTTCGGATACAACACCAAAAGCAAAGAGCATTATGGGATTATGATGTACCATAAGAACAGACTTATAAAGCCATACGTGAAAGTGAGCTGCCAATGTAAGGTAACCTGAAACGATCGTGTGTTGCTTCAGCTTCTTTATTCCCATAAATCCAATCCTGAAAGCGGCGGTTTTGCGTTTCTAACAGGCCGAGAGGAGAGGCGTGGGCGTTATTGGTGTTATAGAGTGCAATTTTCTTCAGCCCACTCACAACAAACAAGACTTTGATGACACCGATAAATACAGGTGCGCTGTTTATCACTCTGCTGCTATTTACTCTAAATCATGCCCTTGGGTTGCTTTGATAGAAAGGCACTATTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32755
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000074450 | Nonsense | 331 | 763 | 9 | 17 |
| ENSDART00000137448 | None | None | 173 | None | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 47687508)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46499169 |
| GRCz11 | 1 | 47190401 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAATCCAATCCTGAAAGCGGCGGTTTTGCGTTTCTAACAGGCCGAGAGG[A/T]GAGGCGTGGGCGTTATTGGTGTTATAGAGTGCAATTTTCTTCAGCCCACT
Long Flanking Sequence:
CATAGTTGGTGCGAGATTAATTATTTTTTATTATTATTGTTATTTTCCTATAGGCATACTGTAGCATCTTATACCTGAAACCTCGCATGCAGATCATCATACGTGGACAAAGAGTGAAGAGTCAACTGATATCCAAAAGTCTGGCTCATATTGCGCAGGACAACTACAGGCCGTCATTCCTTGTATCCTTTCAAAACATATTATGCTTGTTTGTTGTTGTTCTTTGGAGTCCACACACACACATAACCATCATCCGGATGTTGACATTTCTTAACCCCTCCTTCAGAATAAGCGTTTGCGCATCACTTTCGGATACAACACCAAAAGCAAAGAGCATTATGGGATTATGATGTACCATAAGAACAGACTTATAAAGCCATACGTGAAAGTGAGCTGCCAATGTAAGGTAACCTGAAACGATCGTGTGTTGCTTCAGCTTCTTTATTCCCATAAATCCAATCCTGAAAGCGGCGGTTTTGCGTTTCTAACAGGCCGAGAGG[A/T]GAGGCGTGGGCGTTATTGGTGTTATAGAGTGCAATTTTCTTCAGCCCACTCACAACAAACAAGACTTTGATGACACCGATAAATACAGGTGCGCTGTTTATCACTCTGCTGCTATTTACTCTAAATCATGCCCTTGGGTTGCTTTGATAGAAAGGCACTATTTTGTACAGGAAGATCATGCACAACCTCAGCATAAAGCTGGAGGAGTACTGGAACGAAATCCGCTACAAACGAAAGAAAGAGGATCCAAAGTGCACCGTGGCGGTAGAGGATGTGTTGTGAGTATTGCTGTCAAGAATATGTCAGTAGCCATACAAATCACAAGTTTGTTTGTTTTCTCACTCACTTCTCACTTGTCACAAACCTGTTTGAGCTTTGTTGAACATAAAAGAAGATATTTTGGAAACTTGTGACCATTGACATCCATATTTGTTTTTACTAAGGATGTCAATGGTTACCTTTTTCCAACATCTTCGTTCTCACTCTATTTTGATGGTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39677
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000074450 | Essential Splice Site | 396 | 763 | 10 | 17 |
| ENSDART00000137448 | None | None | 173 | None | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 47687787)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46499448 |
| GRCz11 | 1 | 47190680 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACGAAAGAAAGAGGATCCAAAGTGCACCGTGGCGGTAGAGGATGTGTT[G/T]TGAGTATTGCTGTCAAGAATATGTCAGTAGCCATACAAATCACAAGTTTG
Long Flanking Sequence:
CCTTCAGAATAAGCGTTTGCGCATCACTTTCGGATACAACACCAAAAGCAAAGAGCATTATGGGATTATGATGTACCATAAGAACAGACTTATAAAGCCATACGTGAAAGTGAGCTGCCAATGTAAGGTAACCTGAAACGATCGTGTGTTGCTTCAGCTTCTTTATTCCCATAAATCCAATCCTGAAAGCGGCGGTTTTGCGTTTCTAACAGGCCGAGAGGAGAGGCGTGGGCGTTATTGGTGTTATAGAGTGCAATTTTCTTCAGCCCACTCACAACAAACAAGACTTTGATGACACCGATAAATACAGGTGCGCTGTTTATCACTCTGCTGCTATTTACTCTAAATCATGCCCTTGGGTTGCTTTGATAGAAAGGCACTATTTTGTACAGGAAGATCATGCACAACCTCAGCATAAAGCTGGAGGAGTACTGGAACGAAATCCGCTACAAACGAAAGAAAGAGGATCCAAAGTGCACCGTGGCGGTAGAGGATGTGTT[G/T]TGAGTATTGCTGTCAAGAATATGTCAGTAGCCATACAAATCACAAGTTTGTTTGTTTTCTCACTCACTTCTCACTTGTCACAAACCTGTTTGAGCTTTGTTGAACATAAAAGAAGATATTTTGGAAACTTGTGACCATTGACATCCATATTTGTTTTTACTAAGGATGTCAATGGTTACCTTTTTCCAACATCTTCGTTCTCACTCTATTTTGATGGTCAGTTGGTTGAATTTAAGTTACATTGCAACTAATTGTCATTAGATTATTAGGTTGACTGTTAGGTTGGGGTTAGGGTTGCTGGCTCGTACCCAGGGGGGGTTCGGGTGGTTTGAAAGAACTACCCTGCCCCCACTGACAAACATCCAGAATTTGCCATTGGTCCAGAATTTTTGCCACACTCTCATTTGACCTTTTTTGACTGCTATGTCATTATAAATAGTGGAAAAACCCATCAAATGTTTTAAGAAAACACACAATATGACATAAGTGAAGTCAACTTT
Associated Phenotype:
Not determined