ZMP
golga5
Ensembl ID:
ZFIN ID:
Description:
Golgin subfamily A member 5 [Source:UniProtKB/Swiss-Prot;Acc:Q7SXE4]
Human Orthologue:
GOLGA5
Human Description:
golgin A5 [Source:HGNC Symbol;Acc:4428]
Mouse Orthologue:
Golga5
Mouse Description:
golgi autoantigen, golgin subfamily a, 5 Gene [Source:MGI Symbol;Acc:MGI:1351475]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22341 | Nonsense | Available for shipment | Available now |
sa4516 | Nonsense | F2 line generated | Not yet available |
sa9432 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22341
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 |
---|---|---|---|---|---|
ENSDART00000057386 | Nonsense | 135 | 760 | 2 | 13 |
ENSDART00000129806 | Nonsense | 135 | 760 | 1 | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 33448392)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33094340 |
GRCz11 | 13 | 33224790 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTGAACGACGATTTGCTTTTTGACTTCTTAAACAGTTCAGATCCACCA[C/T]AGAGCGAGAAAAAGGAAGTCAGGAGAGAAACCGTGTCGAAAGCTTTTCGC
Long Flanking Sequence:
CAGAAGCCACTGTCTCAATTCTGTTTTCCACATATTTTTATCATCGAGATCTCTTAAACATCTCATCATGCATGATTTCCATTCCAGAGGATCTCAGGATGTCTTGGTTTGTTGATCTTGCCGGGAAGGCAGAGGACTTCCTGAATAAAGTGGACCAGGGTGCAGCCACTGCTTTGACAAAACCCAATCAGAAGTCCTCTCTGTCCTACAATAGCCCAGATGCTACCGATTCAACCCAGTATAATGCTGCAGCTTACAGCTCCACCCAGCAGCACCGAGACTCCATCTCTGCCTCGTCCCAAGGAACTTCCACATTCATCTCCGCAGCTGCTGGGAACATAAAGAAATCCAAAGCTACGGTTTTGGCTGGAACAGCAAACGTTTCCAGCACCACACCTTTGGGTTCCAGCAGCAAGGCGTCATCCAATTTTGTGAGGCCTAGAAAGAGTGAAGTGAACGACGATTTGCTTTTTGACTTCTTAAACAGTTCAGATCCACCA[C/T]AGAGCGAGAAAAAGGAAGTCAGGAGAGAAACCGTGTCGAAAGCTTTTCGCCCTACAGGGGTGTCAGCACAGAGCCAGATGCCCACTGTCTCTTTGGCCAGTGATCTGCACACAGGCCCATCGGTCACTCCGACCCCGTCGTCCACACAGGGTCTGTCCAGAAACTCTAGCCTCGGCTCTCTCTCCAACAGCTCGCACAGCGTTAAAACCGAGGACAGCTCCACTCGCGACCAAAGCCAAGGTACAAAGATACATCATGTCCTTTGAGTTTTTGGTTAATCATTTGTTATGATGGTCACAATTTTTGTTGTACGCTCCTCTTTGGCTGTTACAGAGAGGCAATGTGGCGACAAGTTTAACAGAAAAATTTAGATTTTGTATTATTCCTCTCAAGATATTAAATGAATGAATTATATGCAACGTGCTGTGTTTTTATGAGGAACAAGGTGCTGTAGATCACAAATGTCTAACTCATATCCTGGAGGGCCAGAGCTCTGCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa4516
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000057386 | Nonsense | 325 | 760 | 4 | 13 |
ENSDART00000129806 | Nonsense | 325 | 760 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 33443842)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33089790 |
GRCz11 | 13 | 33220240 |
KASP Assay ID:
554-3524.1 (used for ordering genotyping assays)
KASP Sequence:
TCGCACGGTTCGAGAACTTAGCTCWCAGGTCGATGACCTCACAGAAGCCT[T/A]GTCAGCAAAAGACGGTCAGTTGGCGGTCTTGAAAGTGCGACTGGACGAAG
Long Flanking Sequence:
ATGCTGAACCATACTACAGGATGCCAGGGTTAAACCACTTCTCTTTTCGAAGGACGTCCGGGATTTTAAACAACCACAGACTCAGGATCTCAGTTTAACATCTCATCCAAAAGTCGGCCCTCACTGAGGAATATATAGAGTCCCCTTTACTATACTGGTGCGTTAGGACCCACACAGACCACAGGTTGAGCCTCACTAACACCACTTCCAGCAGCAACCAAGCTCTTCCATGTGGTCTACCATCCAGGTACTGCTTAGCTTCAGTGGGCGACCATGTAAGAGTTGCAGAGAGCTAGCTGCTGGCAATTTCAGTTAATGACAGCTATTTTAATTGTTCTAGTTTTCATTACCAACAACACTCCAATTAATACATCATTGCTTCTCCTTTTTAGAGGTGAATCTCGGCAGAGCTCGTGCTGACAAGTGGAATTCGGACCAGTCTCGGGTTGATCGCACGGTTCGAGAACTTAGCTCACAGGTCGATGACCTCACAGAAGCCT[T/A]GTCAGCAAAAGACGGTCAGTTGGCGGTCTTGAAAGTGCGACTGGACGAAGCAGATCAGTTACTGAAGGCCCGAAGTTCTGCTCTTGAAGAAGCACAGAACGAGAGAGTCAGGTGGGTCTTTTTGACATCTCAAGAGCAGAAAGGCAATCCAGCTTTAGTTGACCTTCTAAAATTAATCAATATTATCTATGAATGAAAATTGTGTGTTTTAGGATTCTTCAGGACCACAGTGAGGGCAGCAGTCTTCACTCGCAGGCTGTACAGACACTACAGGATAGGTTAAGAGACGCAGAGGCTGCAGTGAAGAGAGAACAGGAGAGCTACAGACAGATACAGGTGACTAATTAGGGCCATAGACTCTCAGGATGCTTTCACACCTACAGATCGATTGTTTTGTTCCGAAATGGGGATTAAAATAGGGTATATGCCGAAGCATGTTAATAGGACTTTTAATTTGCCAGTAACCTGGGTTAATCGTTTCCGGCGAATTGTATGTCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9432
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057386 | Nonsense | 541 | 760 | 8 | 13 |
ENSDART00000129806 | Nonsense | 541 | 760 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 33439975)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33085923 |
GRCz11 | 13 | 33216373 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGGAYTTTAGGATCTGGAAACCCAAGCGCTCACTGAGAACGAGAGCTGG[A/T]GAGAACAGCTGGCAGAGGTACAGGAACAACAYGCACAGCAGATCAGAGCC
Long Flanking Sequence:
TTTGCCAATGCTTAATAGTTGATTCTTAGTGTGTAGTTATTATAAAGTGTTATTTTATATATAAAAGGTTTATTTTTCGGGTGAACTATCTTTTTTTAAATGTCTTCATGGTCTGTTGCTTTGAGGAAAAACATAAAACAGCAAAAATGTAGTTAGAAAACATGCATTAGGTCATCTAATAAAATAAATAGCAAAACTAAACATTTGTGATACATTTTGTTTAATGTAAAAAAATCCTCAGATTAAAATCCTCCATTTTATTTACTTATGTTTTAATAATCAATAATGGTCATTATAAAGGTATAGATTACAATAATTTATACATTATAGAAATGTATGCTTTAGTTAATCTAATGTAAATTAGCACAACTAAACATTTGTGATGCATTTGTTTAATGTAAAAAAATCCTCAGATTAAAATCCTCCATTTTATTTACTTCAATTGCAAATTTGGATTTTAGGATCTGGAAACCCAAGCGCTCACTGAGAACGAGAGCTGG[A/T]GAGAACAGCTGGCAGAGGTACAGGAACAACACGCACAGCAGATCAGAGCCAAACAGGAAATAGAGGCAGAACTGGAGAGATCCAAACAGGTACGTCATTGCGAGAGAGATGAAAGCACACAGGTTTTCAGAGACGGACAGTATAATGTGCATTGCTACATTTCAGTTTTTAATAAAAACTGATTGTTGATAAATGTTGAGATGCAAGATGTAAGAACATTCAAGGTACCTTTTCTTTCAAAGAGCAAGCAGTAGGTGGCTTACTTGCCAGTTGCCTGCAAATGTCTGACTAAAGTTTGTTTTAGGTTCGCACATTAAGACGTTCTCCTTAATATTATAATTTCAAAAAAGGCTTCTCTGCAAATTCTAAATCAGGAAATTATATTAGCAGCCAAAGACTATCAAAGTACAACATTGTTCACAGTCAATTAACCAGTACTAATGTTGTTTTGAAGTCATACTTGTCTTGCATGCTATTTCTGACCGAATATTCATAGTAAG
Associated Phenotype:
Not determined