ZMP
si:ch211-223p9.3
Ensembl ID:
ZFIN IDs:
Description:
Novel protein similar to vertebrate UNC-112 related protein 2 (URP2) [Source:UniProtKB/TrEMBL;Acc:B8
Human Orthologue:
FERMT3
Human Description:
fermitin family member 3 [Source:HGNC Symbol;Acc:23151]
Mouse Orthologue:
Fermt3
Mouse Description:
fermitin family homolog 3 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2147790]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa40594 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31489 | Essential Splice Site | Available for shipment | Available now |
| sa31488 | Essential Splice Site | Available for shipment | Available now |
| sa33766 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa45237 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa11472 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40594
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 |
|---|---|---|---|---|---|
| ENSDART00000113077 | Nonsense | 40 | 641 | 1 | 14 |
| ENSDART00000141095 | None | None | 349 | None | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 69792467)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 66119508 |
| GRCz11 | 5 | 66798612 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTCACTTCAGATTTACACATCGGCGGAGTCATCCTCAAAGTTGTGGAA[A/T]AGTCACGTGAGTTTCTAGTGGCTGATTTGAAGAGGCTGTTAATCATACTT
Long Flanking Sequence:
TTATCTTTAAATTTCTAAAAATGTTTGGTGACTAAAATATTATTTTAATAAATATATCTGTTCAATAAATCTGTTTTGTTTAAATGCACCAAAATACACAGCCTATATTCACAGAGAAATGGATCAAAACATTCATTTTCAAAATAGGGTGTACTCAATTATGTATATGCATCAAACTAATGTGAAAGAATGTGAGTGCTGGGAAAGTCAAATAAAAGAAGAAGAAACTTTTTTTTTTACACAAAGTAATTTCACTAAAGCCTAAATTTAAATAAAAACTGATAACTAAGCATGCTAAGCACATTAAATACAAACTATCAAAGGGGAAATGAGTGAGATTGTGGAAGCATGAAGTCTAATGGCATCTCTTTCTGCGAATCAGAATGGCAGCGTGGGACCTGTCCATCATGGTAGAGGAACTGGGACCACAGGCTCCTCCTCTAAAAATCAGTGTCACTTCAGATTTACACATCGGCGGAGTCATCCTCAAAGTTGTGGAA[A/T]AGTCACGTGAGTTTCTAGTGGCTGATTTGAAGAGGCTGTTAATCATACTTTCACACTACATTTCACTAAATATAATGTTCATGTTATGATAAGTGTAATGTAGTGCACAAAATGTGAGAAAATAATTCAAAGGTCTTTTTTTTAAGGAATAGCCCAGCCAAAATTGATCATACTATTTTCTCACCATGCTGTGTCAGTATTTCATGCATTTTTGTTTGTTTTTTTTTTGTCATTCTCTGCAATTTTTTTGTGATATTTGCTGACATTTATTATATTGTAAAAAACAGTCTAAATAAACATTCTTCATTCTTCAGAAGAAAGATACAATTAGACCAACATTGGAAATTCTTCTTCTATATACATCGTTAGCCCTTATGTGAAATTCTTTTTCAAATATCTCTCTAGCTTTGTTAAATGGAGACAAGGTTTTTTTTCAATGCATTTTAAACATAATAGTTTTAATATAATCTAATTATTTTCCATCGGCTTAGTTTCTGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31489
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113077 | Essential Splice Site | 285 | 641 | 6 | 14 |
| ENSDART00000141095 | Essential Splice Site | 36 | 349 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 69763725)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 66088908 |
| GRCz11 | 5 | 66768013 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAATCGAATGCACTGAGGAGGAGATGATGGTCTTTGCTGCATTACAG[G/A]TACAGATGATGGACAGCAGATATCAGCTCATTATATGAATGATAGTTCAC
Long Flanking Sequence:
ACTTCTACTTGAACTTAATGTTGACAGATTTAGATTTTACTATATAATTACTTACGTTTTATATATAAACTAAACCAAAAAAAATACAGTACAGTACAAATAGTATTATACAAATGGTAATATAATCATAAAATGCATATATAACGCATACATACATAAATATTCTCATTTAGATGTTCAATATATGTAATTCTCTGTTTTAATCTTACTTAATTAAATGTTCTTTTTGTCCTTTCGTGTCTGTATGCACCCAGAACTCCTGAAAACCACAACAAACTGATTCTAGTATTTAGCTATTTTTGCTGTATGTTCTAAAAAGCACATTATGGGTAATTTTGTCATTTTTTTCTCACCTAACCTATTAATGAACATCTTGTGAATGTCCCTGGCAGTCGGACGTTGTGCGTCTGACACAGCTGTACGAGCAGGCTAGGTGGGCTATCCTGCTGGAGGAAATCGAATGCACTGAGGAGGAGATGATGGTCTTTGCTGCATTACAG[G/A]TACAGATGATGGACAGCAGATATCAGCTCATTATATGAATGATAGTTCACCCAAAAATGAAACCTCTGCCATCTACACATGTTCAAAAAAAAAGAAAAAAAAAAGTTTCTTTCTTCTGTTAAACACAAAAGATTATTTTTTACTGCTTGTTCAAACTACTTATTTAAAATGAGCTGAATCAACACAATTCCTGAGTTTATTGAGGGACAACTTAATTTTTTAATGTTCAATCTGCTTAAATTTGTAATTGACATGTGTCAGGACAACATGAAGGAATTGTGTGGAACCCAGCATTTTTAACAGTGTATGTTGAAGAATGCTGATAGCTGGTACCCATTGACTTCCATGGTAAATATTTTTCCTGCTATGAATGTCAATGGGCGCCAGCAACCAGCATTCTTTAAAATATCTTCTTTCGTGTTCAGTGGAAGAAAGAAAACACACGAGGGAGAGTAAATGATGAGGTTATTTGGGCGAGTGTCCAAACTCGGGCCTGGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31488
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113077 | Essential Splice Site | 421 | 641 | 10 | 14 |
| ENSDART00000141095 | Essential Splice Site | 129 | 349 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 69757723)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 66082906 |
| GRCz11 | 5 | 66762011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATACCCGGGCCAGAGGGCATGAATGAGGTCTACTTGCGCTGCGAGCATG[T/A]AAGTCAGTTATGTGTAATCTTATGAAGTGCTAATCTTTCAAACTTTCATT
Long Flanking Sequence:
CAGAAATGCCAACTGGCCCAGCCGAGGCACGAACCAGCGATCTTCTTGCTGTGAGGCGACAGTGCTAACCACTGTGCAGCCACATTGTACTTACACTTGATTAACTGCATGCATGTAATAACATTGTTATTAGTTTCTGTACTTACATTTATAATTACACTGTTGACCATCCCTTAGACCATCTCTAAACCTACCCATACCAACTAACTTGTTACTAACCTTGCCCTCAATAGCACTAGAAGTGTTCTGCAATACATTATGAACACAATACGTACATTGTACTTATTTTTAATGTAAATACATGTAGTTAAGGCCCCTTAATATAAAGTGCGACCAAAGCTTATATGTGTGTACAAGACACACAGATGACCACAAATCTTTGACCGACACAGGTTGTGAAGTGGCTCCTGACGTGAGCGTTGCTGGGCAGAAGTTTTGTATCAGGTTGCTGATACCCGGGCCAGAGGGCATGAATGAGGTCTACTTGCGCTGCGAGCATG[T/A]AAGTCAGTTATGTGTAATCTTATGAAGTGCTAATCTTTCAAACTTTCATTTTGGATGCAATTAATCTTTGCGCAGCAGTACTTTTTTTTAAGGTAACTTACCCCTAATTATAGATATATACATTAGATGTCGCCTGGCCTATAGTTTTCTATTGGACGGAATGCGTCAATTGCGCCGCCATCTTGCTACAGGGTAGCGCTCCTTTGAAATGAATGCGGGACCAAGGTACAGTGGAGGACTGTGGCCATGCAAAGCCAGAGATATACACATATACACATATATCTATGATCGGGAGTTTTCCTGGATGTTAGTATGCAATTTTTTTTTCTAATTACGAAAATTATAATTTTACATCACTTTTCTACATTGATGGATCAGTGACATACGGGCATTCCTGACAAAAAGCTTGTGTTTGTGTGTACAGAAATGTACTATTCACCCTCCCTGTTAAATTTAATCTAATCACGTCCTGAAACACAGCTCCTCTCCTGCTTTCACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33766
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113077 | Nonsense | 482 | 641 | 11 | 14 |
| ENSDART00000141095 | Nonsense | 190 | 349 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 69756394)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 66081577 |
| GRCz11 | 5 | 66760682 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATAACACAGCCCAGACGGATGAAAGCATCAACACACACAGCCTCGTCT[C/A]GCCACGCTACCAGAAGAAGTACAAACCCAAACAGGTACCACATATTAAAG
Long Flanking Sequence:
TGTTTGCTCGTTACTAAACCCGTAGACAGCGCTAAAGTCCCGCATCTTCACGTAATAACACTGTCTTGACTAGTGCGGTTGAATGACATCTGTCCTGGGAGCACTGTACCAATGTGGCGGCGCTATTGACGCATGCTCAGGGTCCCTATGCGATATCTAGTGTATATATCTATGAGCCCCAACATTGTTTGTATAGTGATAAAACAGGAACAACAAAGCTGTACATAAAATTAATTAGAATGAATCATTTCTGTTCACATATGAATACCAAATGAATCATTCTGAAGGAAATTGATTGAGACTCTCTGATTTACTGCAGGAGCAGCAGTACAGCCGATGGATGGCAGCATGTCGTTTGGCCTCAAAAGGCAAGACTTTAGCCGACAGCTCGTTCTCTAATGAAGTGCAGAGTATCCAGTCCTTTCTGGCCATGCAGAAAACCACACCTAGCAATAACACAGCCCAGACGGATGAAAGCATCAACACACACAGCCTCGTCT[C/A]GCCACGCTACCAGAAGAAGTACAAACCCAAACAGGTACCACATATTAAAGATGTTAATTAATTACAGCGTTGACTTTAAAGGGTTAGTTCACCCAAATATGAAAGTTTGGTTTCTTTCCCACACTCTTGCTGTCACGTTATGAGGTGAATGGAGAGAAGGCGAGGACCCAAATGCGGGAAATGAAGGATTTATTTAAAAAACAAAACAAAAACAAAACTCAAATCTCCCCATGTGGGGAAAAACATGACATTATATTAAACACTCAACTAGACTTAACTTGATTTGGTTCTTGGCATGACACACTACATTAAACAACTGTTGTAGACCAGACATCCACAGACCTCATACAACAGCAAGAGAAAGCAGACAGTCAACAACGGACCACCACAGAACAGAGCACACTAGGAGAATAAATAGGAAACACAGACCAATAAACAGACAGGCGGAGAGGTGAAAATGATAATTACAAACAGGATAACTAGGTGGGCGGGACAGGACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45237
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 |
|---|---|---|---|---|---|
| ENSDART00000113077 | Nonsense | 503 | 641 | 12 | 14 |
| ENSDART00000141095 | Nonsense | 211 | 349 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 69754562)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 66079745 |
| GRCz11 | 5 | 66758850 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAATCTCATTCTCCTTGTTCAGCTCACACCAAGGATTCTGGAGGCCTAT[C/T]AAAATGTGGCTCAACTCTCATTAACTGATGCCATTCAGAAGTTTCTTCAG
Long Flanking Sequence:
CTCGAATACGTACCTCCTGGGATGTATCTCACGGTCCGCAGAAACGTCCACGGGGCTACGTTTCCACAATGAGCCCGGGTTGCATATGCGATGTGAATGTTCCCTCCCAGCGCCATCCGAAACCGAAACCAACTGAAATGCTGGGAATAAACATCATGCGGCAGACAAAACAAACATGACAAGAGCGCGCACCTATACCATGTCCGGACCTCGCGCGCCCGCATCAAGCTGGAGCGCACATAGTCCAATAGTAACCAGGCAGGCGCTCACACAATGACAAAAAAGAGGTACTCAACCCAAGAAAACTCAAGCTGAGCACCACATATAACACATGACCTGACTAGTGTCTGGAATTTGCCACAAAAACAAGAATTAACAGGACTGGAGTGGCAGAATTCTGACACTTGCTGTCTAATAATATTGTTAGGTGAACTATCCCTTCTTTCTGTTTAAATCTCATTCTCCTTGTTCAGCTCACACCAAGGATTCTGGAGGCCTAT[C/T]AAAATGTGGCTCAACTCTCATTAACTGATGCCATTCAGAAGTTTCTTCAGATCTGGCAGGCTCTTCCTGACTTCGGCCTCTCTTATATTGTAGTCAGGTAAGTTTTGTAAAAGTTGTCAGGGTTGTCATGCAAAGAATGTGATAAAGGGTAATGAGTGTGGCGTGTACCTTTTAGGAGTGTTAGGACTGATTTTGCTCTCAATATTTCTCTTCAGGATCGTAACTGATGTAATTCTCCATATATAAGTTGCTTTAATATTATTATTAATAATAAATATTGATAATGCTGAAAATTGCTTCAATAAAAACACAATAACATGAGTGTAAGGTACACTGTAAACAAATGCTGGGTTCCACACAATTCCGTCATGTTGTCCCAACACAAATCGATTATTCATTCATTAATTTTCTTGTCGGCTTAGTCCCTTTGTTTATCCGGGGTCGCCACAGCGGAATGAACCACCAACTTATCCAGCAGGTTTTTACGCAGCGGATGTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11472
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113077 | Nonsense | 531 | 641 | 12 | 14 |
| ENSDART00000141095 | Nonsense | 239 | 349 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 69754476)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 66079659 |
| GRCz11 | 5 | 66758764 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAAGTTTCTTCAGATCTGGCAGGCTCTTCCTGACTTYGGCCTCTCTTA[T/A]ATTGYAGTCAGGTAAGTTTTGTAAAAGTTGTCAGGGTTGTCATGCAAAGA
Long Flanking Sequence:
TGCGATGTGAATGTTCCCTCCCAGCGCCATCCGAAACCGAAACCAACTGAAATGCTGGGAATAAACATCATGCGGCAGACAAAACAAACATGACAAGAGCGCGCACCTATACCATGTCCGGACCTCGCGCGCCCGCATCAAGCTGGAGCGCACATAGTCCAATAGTAACCAGGCAGGCGCTCACACAATGACAAAAAAGAGGTACTCAACCCAAGAAAACTCAAGCTGAGCACCACATATAACACATGACCTGACTAGTGTCTGGAATTTGCCACAAAAACAAGAATTAACAGGACTGGAGTGGCAGAATTCTGACACTTGCTGTCTAATAATATTGTTAGGTGAACTATCCCTTCTTTCTGTTTAAATCTCATTCTCCTTGTTCAGCTCACACCAAGGATTCTGGAGGCCTATCAAAATGTGGCTCAACTCTCATTAACTGATGCCATTCAGAAGTTTCTTCAGATCTGGCAGGCTCTTCCTGACTTCGGCCTCTCTTA[T/A]ATTGTAGTCAGGTAAGTTTTGTAAAAGTTGTCAGGGTTGTCATGCAAAGAATGTGATAAAGGGTAATGAGTGTGGCGTGTACCTTTTAGGAGTGTTAGGACTGATTTTGCTCTCAATATTTCTCTTCAGGATCGTAACTGATGTAATTCTCCATATATAAGTTGCTTTAATATTATTATTAATAATAAATATTGATAATGCTGAAAATTGCTTCAATAAAAACACAATAACATGAGTGTAAGGTACACTGTAAACAAATGCTGGGTTCCACACAATTCCGTCATGTTGTCCCAACACAAATCGATTATTCATTCATTAATTTTCTTGTCGGCTTAGTCCCTTTGTTTATCCGGGGTCGCCACAGCGGAATGAACCACCAACTTATCCAGCAGGTTTTTACGCAGCGGATGTTCTTCAGCTCCATCTGCAACACACACACACACACACACACACACACGCACACTCATACACTACGGACAATTTAACCTACCCAATTCATC
Associated Phenotype:
Not determined