ZMP
gmds
Ensembl ID:
ZFIN ID:
Description:
GDP-mannose 4,6 dehydratase isoform 1 [Source:RefSeq peptide;Acc:NP_001095945]
Human Orthologue:
GMDS
Human Description:
GDP-mannose 4,6-dehydratase [Source:HGNC Symbol;Acc:4369]
Mouse Orthologue:
Gmds
Mouse Description:
GDP-mannose 4, 6-dehydratase Gene [Source:MGI Symbol;Acc:MGI:1891112]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6636 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6635 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43452 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37043 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6636
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 |
---|---|---|---|---|---|
ENSDART00000046764 | Nonsense | 4 | 370 | 1 | 11 |
ENSDART00000103234 | Nonsense | 4 | 377 | 1 | 12 |
ENSDART00000143267 | Nonsense | 4 | 91 | 1 | 3 |
ENSDART00000146326 | Nonsense | 4 | 257 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 26852011)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 26923314 |
GRCz11 | 20 | 26822404 |
KASP Assay ID:
554-5317.1 (used for ordering genotyping assays)
KASP Sequence:
CCACAYACACTCGGTCAGAACAGAAACCCGCTCCAGAGAATGGCTCAGTG[T/A]ACAGCAACGACGACTGGTGGCGGTATGAACGGAGACAGCAAGAGGAAGAG
Long Flanking Sequence:
AAAATTCAAATATTATTCATGTTTGTTATTTATGTAAAATCTAATAAAACATCTAATAATTAATTATATAAATTTAATTATTAAAATATAAAATTTGTAGGTAATAATTATTATTATATTTTTTATTATTATCATTAATAATTATATTTTAATTATACTTGTTATATATATTTAATTATTCACTTTGTAAATGAAAATTAAGAGAGAGAGAGAGTAAAAAATAGTGTCCAACTCCTCCTGCACATTTAAACCTTAAGCTGGCGCTGTGACGCATCTTCACCATGAGCCAGCATGATTCCTCTCCTCTTCGTTCTGTGGTGTACACGTCACTGGCGCTCTGCTCTGTGATTGGCTGCCGACTGCAGGTTTCTGATGTGTCTCTCCAGCAGCTGGAGTTTCGGATGTGTTTGCATCCGTAGTTGATAAACGAACGCACACAGCGGAACCAAACCACATACACTCGGTCAGAACAGAAACCCGCTCCAGAGAATGGCTCAGTG[T/A]ACAGCAACGACGACTGGTGGCGGTATGAACGGAGACAGCAAGAGGAAGAGGAAAGTGGCTATCATTACAGGCATAACCGGTCAGGTAACGTGAAGTATTGTCTCAACAATTCCGACACGGTAGCCGAGACGCGTCGATGGTCCAAAAAACAACCATTTAGTCAGTCATACGCTGCTCTGAACCGTTGTGTTTTTGTGCGGAAAACTGAAGGATGTGTGATGCAGAATGACTGATTCGCTCACTGTTTAGTCTCATTAGAGTTTAAAAATATATCTTTAATAGTAACCGAAGCTGTCAGCTCTTAAAATAACGTTAGGGAGACGATGACAGACTTTTGTGGGGTGGTTTTATCTTGCACGTTTCTACGCAGACTGAGTGCAGGACTCTGTTACCTATTTTGGTAGCCATGACAACTATAATTTTAGCTCAAATCCAATATTTAGTGTACATGTAACGTTAGTTATTTCGGTAGCATCTTATTTTACATCCCAGTTTCAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6635
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 |
---|---|---|---|---|---|
ENSDART00000046764 | Nonsense | 46 | 370 | 2 | 11 |
ENSDART00000103234 | Nonsense | 46 | 377 | 2 | 12 |
ENSDART00000143267 | Nonsense | 46 | 91 | 2 | 3 |
ENSDART00000146326 | Nonsense | 46 | 257 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 26839203)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 26910506 |
GRCz11 | 20 | 26809596 |
KASP Assay ID:
554-4864.1 (used for ordering genotyping assays)
KASP Sequence:
TGGTTTCAGGATGGGTCCTACCTGGCAGAGTTGCTCTTGGCTAAAGGTTA[T/A]GAGGTGGGTAAATCAACACAACCCTGAAAGACTTCCTACAAACAAGTCCG
Long Flanking Sequence:
TTAACCCACCCTTAAACCTACCCATACCACCAAACCTTTCTCTAACACTACTATATCCCACCTCAAGTGCGGTGCAAGTGTTCTGCAATACATTATAAAAACAGTAAGTACATTGTATTTATTTTTTGATGGAAATACATAGTAGTTACGGCCACCTAATATGAAGTGGGAACATTATTTTCTTAGGCAAGTGCATGTGTTAAGTACATGTACTGTAATATAAAGTGCATCATCCAACTACAGAACGACATGAGGGTGAATCTCAACATGAATGAGTGTGTACGTGTGCAAAAAAGCCTATTAGTGTAATGTAGGCGTGTTTTCACTGTGGTCTGGCGCATGATATTCAGAAAGAAATGGTCATTGTGTTGCATACTCTCTTGGGTAATGCTTGCCGTAAATGTGTGTGTTTGCGTTTCTCAAAAGTTGAAATATAATTCTCCCTCTATGTGGTTTCAGGATGGGTCCTACCTGGCAGAGTTGCTCTTGGCTAAAGGTTA[T/A]GAGGTGGGTAAATCAACACAACCCTGAAAGACTTCCTACAAACAAGTCCGAAAGCTTTCTCGCTTTTATCTAATGCAAATCTGTCCCGCTGTCTGTTAAGTCCGATTTTCATGAGATTCAAATTTAAATTGGATGCATCTCATTTAAAGGTGCCCTGTACATTTTGTTATTTATAATATAAATTGTAGAAAAACAGAGGTATTTCAACTTATTTTGTGTCAAATAAATTTCTTGATTTTTTTTGTGTATTATTTTCTATTAATTTATTTTTTAAACAAATCAAAAGTTCAAAATGACAGCATTAATTTGAAATTGTTTGTCACATTTTAAATATCTTATATAACTCATGAGCATTTAAATGCATCCTTATTGCATCAATATTATGTTCTAATGCTCTAACCTATTCAACAGTATCATGTTTTAAGTCTGTTTGAAAATGTGCAGTTTGCTGAGATTGAGTGTCTTTGGTGTTTTGGACAGGTTCACGGTATCCTCCGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43452
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 |
---|---|---|---|---|---|
ENSDART00000046764 | Nonsense | 195 | 370 | 6 | 11 |
ENSDART00000103234 | Nonsense | 202 | 377 | 7 | 12 |
ENSDART00000143267 | None | None | 91 | None | 3 |
ENSDART00000146326 | Nonsense | 202 | 257 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 26813187)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 26884490 |
GRCz11 | 20 | 26783580 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGCTAAGCTCTATGCATACTGGATCGTTATAAACTTCAGGGAAGCCTA[T/A]AACCTCTTTGCTGTGAATGGGATCTTGTTCAATCATGAGAGTCCTAGAAG
Long Flanking Sequence:
TTATTGTATAATCGATTGTTTGTTCTGTAGACTATCGAAAAAAATTAGCTTAAAGGGGCTAATAATTTTGTCCCTAAAATGTTTTTTATAAATGCTTTTATTCTAGCCAAAAGAAGACAAATAAGACTTTCTCCAGAAAAATAAATTATCAGACACACTGTGAAAATATCCTTGCTCTGTTTAACATCGTTTAGGAAATATTTAAAAAAGAAAAAAAAGTCAAAGGGGGGCTAATAATTCTGACTTCAACTGTATATATTCACTGAGAAATGGATAAAAATATTCATTTTCAAAATTGAGTGTACTCGGTTATGATGAGCACTGTATAGGAAATCAGATTTGGGTGTTAAATGTGTGTTTGACACCAATATCATGTCTTTTTATAAAATTTCTTAAAGCGGTATTTCAACTGTCTATCTCTTTCTTTTTGTTTTGTTTTTTCTTGCAGGTGCTGCTAAGCTCTATGCATACTGGATCGTTATAAACTTCAGGGAAGCCTA[T/A]AACCTCTTTGCTGTGAATGGGATCTTGTTCAATCATGAGAGTCCTAGAAGAGGTCAGACACACACCACACACACACACGATTCATAGTCTGGTGCAGAGATATTGCAGTTACTTTCACTTGGGGGCACTTTCTGGTAAAAGTAGGCCTGATTGGGTTTCATTTGGTTTTGAAAAATGCAGTAACCAGCAGCCACTGCTACGTGTCAGACCTCACATTTTCAGCACCTCATTCATCAAAACAGTCATAAGTGCTGGTCAATCTTAACAAGTCAACCTATTTTTTTTAACGCTCATGCCAAAAGGAGAGTAATGAAGTTTGAGAATGTCACCCATTCACTTAAATACCTTATAATTCATAAATGCTTTTTAATGTGTAATACATCATTCCTGTATGTTAATGGTTACATTCTTTTGTTGTACTCAAAGCAACATATTCTGAAGGGTTCGAATTTTGTACATGAACCAAATAATGGCAAATTCGTCAGTTGGTCCAGTGTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37043
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 |
---|---|---|---|---|---|
ENSDART00000046764 | Nonsense | 307 | 370 | 9 | 11 |
ENSDART00000103234 | Nonsense | 314 | 377 | 10 | 12 |
ENSDART00000143267 | None | None | 91 | None | 3 |
ENSDART00000146326 | None | None | 257 | None | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 26758037)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 26829340 |
GRCz11 | 20 | 26728430 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCTTGTTTTCAGCTGGGAGGGGAAGGATGAGAAGGAGGTGGGCCGCTG[T/A]CAGGAGACAGGAGTCATTCATGTGAGGGTTGATCCGAAATACTACCGGCC
Long Flanking Sequence:
TGATATTTGCCACAGGAACCACACTCACAGGTTTTGCATAATGATATCACTTACATTATCTCAGAAGCAATAATAATAATAATGATATTGATTTTTGTGTTTGTCTCACAGGCGATGTGGCTGATGTTGCAGCAGGAGGAGCCTGTGGATTTTGTCATTGCAACCGGGGAAGTACACAGTGTTCGAGAGTTTGTGGAGAGAGCCTTCAAACACGTGGGCAAAACCATTGTGTGAGTGCTCGCGCGCACACACACACACACACACACACACACACACACACACACATCCACCTCAGATTAAGCCCATCTGGTTAATCTGGCACATCTGGTGTTGATTCGTGGACAAGCTCTACAAGACCGCAAAACAACACGCAAGCACACCATAAATATCGCAAATTTGTAACACATATGCTGACAGCCGAATTGGGAAACAAATAAGATGAAAGAATGTGTTCTTGTTTTCAGCTGGGAGGGGAAGGATGAGAAGGAGGTGGGCCGCTG[T/A]CAGGAGACAGGAGTCATTCATGTGAGGGTTGATCCGAAATACTACCGGCCAACTGAAGTGGTGAGTTCAGTGTCTTTGTTTTATCCCATGTAGTCAAAGGTTTAATACACGACACTTCTTTTGCTGAGTTTTCCTGCTCTGATTTAGAATTCAATATATTAAAAGTCAGAGATATTCTACAGATTTAAAGGCATAGAATGTCATTTTTGCCACTAGTGGGCCTGTATTCACCTAAAAATTATTGCAGTTAATTATTGCAGGTATCATGGGAGTTATCGTCATCATTACATTCCACAGGTGTCTTCAGAAATCATGTCTTTTGAGCTAAATTATTCAAAACTTGTAGTAGTATAATGCAGAGAAGCTGGAATTCATCAAAGAGAAAGTAGACCACCAAAGCAATTGCTAAGAGATGAGCATGGTGCAGCAGAGCTTTTATTATGCCATAGTCAATCACTTTTGGTTATGATCCCATGCTAACGACGCAGCGCTGTTTTATT
Associated Phenotype:
Not determined