ZMP
manea
Ensembl ID:
ZFIN ID:
Description:
mannosidase, endo-alpha [Source:RefSeq peptide;Acc:NP_001004566]
Human Orthologue:
MANEA
Human Description:
mannosidase, endo-alpha [Source:HGNC Symbol;Acc:21072]
Mouse Orthologue:
Manea
Mouse Description:
mannosidase, endo-alpha Gene [Source:MGI Symbol;Acc:MGI:2444484]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa42897 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa23028 | Nonsense | Available for shipment | Available now |
| sa28827 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42897
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 |
|---|---|---|---|---|---|
| ENSDART00000040605 | None | None | 148 | 2 | 3 |
| ENSDART00000124672 | Nonsense | 27 | 438 | 1 | 4 |
| ENSDART00000132571 | Nonsense | 27 | 219 | 2 | 3 |
| ENSDART00000142972 | Nonsense | 27 | 438 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 15504876)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 15655704 |
| GRCz11 | 17 | 15663637 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCAGTCATCGTTTTAGCCTTAGCTGTGTTCATTATAACAGTCATCCTT[A/T]AGTCTCTAAGCCCTGAAGATAACATTTCCGGCAGCCATTTTGCAGTAAAA
Long Flanking Sequence:
TTCGACAGTTTAATTCAAGTAGTTATCTATAGTATGCTTCCAAACACTAGTATTTATTATAGTATTTTTCATTTAACGTAATAGCTTATAGAGTATCTATAACCTCGAAGACAGGCAAACATATTTTAGTTCAGCAGAAAACTCTGTCCTCTTTATGATATAAAGAACAAATGTGCTTATTTTCTGTTTGTATCTCCTTTGAAATATAGTTTAAATCGCGTAAATACACTTTTCTCTGTCTCCCATTCAGTTTTTTACTTCCTACCCTCCATCTGAATTTCACTCGTCACCAGAACCATGTGATTGTAAACAACCTTTTATTTTTATTTTTACAGCTATCCAGCGGTTACCTAAAGATGATCACATCTGTTCCATCTCCTGAAGATCTTGGCTGGAATGGACTGTAACCGTCCACCAGAGTAATGGCACGGTTTCGGCGGAAATCATGTTGTGCAGTCATCGTTTTAGCCTTAGCTGTGTTCATTATAACAGTCATCCTT[A/T]AGTCTCTAAGCCCTGAAGATAACATTTCCGGCAGCCATTTTGCAGTAAAACTTATTCCCTTTCCAAAAGAAAACACCAACCTCATTTTATCCCCCAAACCCGTGCTGATGATACCATTAGAAAAGCCTGAGAAAATGGAGAATGAATTGCAAGATTTCCCTGAACCAAATTACAATGTGCACGCTTTCTACTACGTCTGGTATGGAAGCCCTCAGTTTGATGGAAAGTACGTCCACTGGGATCATCCACTTTTACCACATTGGGACCCCAAAGTGGCCTCAAGTTATTCAACGGGACGACACCAACCTCCTGAGGACATCGGGGCAAATTTCTACCCTGCGTTGGGTCCGTACAGCTCCAGAGATCCAGCGGTTTTAGAGGAACACATGAGACAGCTGAGAATGGCTGCTGTTGGTGAGGAAATGTATTTAAGCAAATGTATATTATACAGTTAAAGTCAAAATAATTCGCCCTTCTGTGACTTTTGTTTTCTTTTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23028
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000040605 | None | None | 148 | 3 | 3 |
| ENSDART00000124672 | Nonsense | 212 | 438 | 3 | 4 |
| ENSDART00000132571 | None | None | 219 | 3 | 3 |
| ENSDART00000142972 | Nonsense | 212 | 438 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 15501406)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 15652234 |
| GRCz11 | 17 | 15660167 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTGTTCCTCCATGACAGGTTGTGTTTCATATTGAACCATACAAAGGA[C/T]GAGACGATGCAAATATGCGTGAAAATATTCAGTATATTGTGGATCGGTAT
Long Flanking Sequence:
TCCTTACTGGGTTGCAGCTGGAAGGGGATCCGGTGCGTAAAACATATGCTGGATCAGTTGGCAGTTTATTCCACAGTGGCAACCCCTGATGAATAAAGAGACTAAGCTGAAAAGAAAATAAATAAATAAAACTAGAACATATAAAAATTAATTTAGTTTAACTTGATTTATTCAAATGTTAAAACAATAAATTATTTTCAAAATTATTAATTTATTTATTAAGAAAACTATTTAAAGATCCTTCAATAATACAGAACTACTTAAACTTTGATTACAAAATTTTAAGATACCAAATTAAAATATAATACAGTAATAAAATGTAATTTTTTTTTCCTCAACATTTTATAAATAACAATTTTCCCATTTCTTTTGTAATTGTTTATACAACAACTTTTTTTCTGTGTCATTATTTGGTTGAAATTCATAGGTGTTTTGGTGTCCTATATAAACTATTTGTTCCTCCATGACAGGTTGTGTTTCATATTGAACCATACAAAGGA[C/T]GAGACGATGCAAATATGCGTGAAAATATTCAGTATATTGTGGATCGGTATGTTTAATCCATTTTATTAAGCTCTCACTATTTATCTACTTCATACAAGTGTACAAATACAAATAATACTCAGATTTGTAATGTTAGACAAGCCTGTTCAAGATCAAGAATAAAATACTTTGCCTATAATTTTCTAAATATACTAATAAATCATTAACAAACTCTTGTTTTTTTATTTATAATTTAGGAAATTAATCTCTAATTATTCTCTAGCTAATCTAAATCATCTGTAGCTACTTTAACAGAAACACATGATCAATACACATTTTATTTAATATCCCTTATTCTCTTTTTATACTAGCTATGGAAACCATCCTGCTTTTTATAAATACAAAACAAGCACAGGCAAACTTCTTCCTCTCTACTACATATACGACTCCTACTTACAGACTCCTGATGTTTGGGCACAACTGCTAAAGCCGAACGGCATATCGACCGTCAGAAACACACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28827
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000040605 | None | None | 148 | 3 | 3 |
| ENSDART00000124672 | Nonsense | 436 | 438 | 4 | 4 |
| ENSDART00000132571 | None | None | 219 | 3 | 3 |
| ENSDART00000142972 | Nonsense | 436 | 438 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 15500429)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 15651257 |
| GRCz11 | 17 | 15659190 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGATAACGCAAAGGTGGGCTAGAAAGTTTAGCGACGAGCAGAAGAAGT[G/A]GCTGGAGTAGTTTTATTGGTCATCCTGGAAAAACAACTGTTGGGGCTTGT
Long Flanking Sequence:
CATATCGACCGTCAGAAACACACCATATGACGGCATCTTCATCGCCCTTCTTGTGGAAGAAAGACACAAGAAGGACATCCTGACTGCAGGATTTGATGGACTTTACACTTATTTTGCAACCAACGGCTTTACATACGGCTCTTCACATCATAACTGGAGAACCATCAAAACCTTCTGCGACTATAATGACTTGGTGTTTATTCCAAGCGTAGGGCCAGGTTATATCGATACTAGTATCCGGCCCTGGAATGCACAGAATACAAGAAACCGCATTAACGGAAAATATTATGAAACCGCTTTTAATGCTGCAGTGGATGCGAGACCACAGATCATCTCCATAACGTCATTCAATGAATGGCATGAAGGAACGCAGATTGAAAAGGCCATCCCTAAAACATGGGGTAAAACCGTGTATCTTGACTACCTGCCACATAAACCCACCGTTTACCTGGAGATAACGCAAAGGTGGGCTAGAAAGTTTAGCGACGAGCAGAAGAAGT[G/A]GCTGGAGTAGTTTTATTGGTCATCCTGGAAAAACAACTGTTGGGGCTTGTTTTAATCTGATTTATTGTAGGTTTTGGGTGTTTTTTGTTTTACTTACATGCCTTTTACTACTGTATATGACAATCTTACTTGAATGAACTTTTAAAACGCTATTAATGATGATATATTCTGGCTGGATGCTGTAAATATAACAAATCCTGCTTTATGCTAGGTGTTTTTAAGTATGCTATAATTAAAATATGTAAAGTATGTTTACTTTTAAGCTGTGAGTCAATTTCCCATCAAGTTTTTTTATTAAATAATAAAAAAATTGACATTCAAAACTGTGTTTCTGTTTATAAAACACTCACATCTCACATTTTTTATTAATAACAGCAATTCTTTTTTGTTTACAATGTGTTCCCCACTCCAAGTATACTATTACTTTAAATTTCAATGTGCATTAAAGGGCACCTATGATGAAAATCTTCTTTTGTAAGCTGTTTGGACCGAACTGTGCG
Associated Phenotype:
Not determined