ZMP
GOLGA4
Ensembl ID:
Description:
golgin A4 [Source:HGNC Symbol;Acc:4427]
Human Orthologue:
GOLGA4
Human Description:
golgin A4 [Source:HGNC Symbol;Acc:4427]
Mouse Orthologue:
Golga4
Mouse Description:
golgi autoantigen, golgin subfamily a, 4 Gene [Source:MGI Symbol;Acc:MGI:1859646]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13806 | Essential Splice Site | Available for shipment | Available now |
sa10793 | Nonsense | Available for shipment | Available now |
sa14408 | Nonsense | Available for shipment | Available now |
sa22381 | Nonsense | Available for shipment | Available now |
sa15392 | Nonsense | Available for shipment | Available now |
sa13611 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13806
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109469 | Essential Splice Site | 355 | 2037 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 49099762)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 47838144 |
GRCz11 | 13 | 48129174 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTACAGCAGCAGCTGCAGGAGAGACTGCAGGAGCTGGAGAAGATGAAGG[T/C]ACACAAACATCAACYATYACAAKACATGGAGAACAGTGCTGTRGAGCTTT
Long Flanking Sequence:
TGAGGATTAGCAGGCTAGTGCAGAAACTCTATTTAAAATACTGAGGTAAAATAAATTTTCATATTTTAAAGACATGGCTTGGAAAAATGGAGCTTATTGCAGTGCTTCTTGTCTAGTCTGAGACCCACTTTATATTGTATCTCAATCAGGCAGTGAAGGTCACTGATTTTTAAAGAAATCAGATCATGGAGATTTTGTAATGCTGGGAGTGCTTGACTAAAAATTAAACGTCTGTGTGAATATTCACCTTTGCAATTTCCCAACCCCTAGTTGACAGAAGTGCTGTGTGTGCATGTGTCCAACAGAGGGCAGTGTTGACTCGGGCAGCGCTGTGGATGTGGAGAGTCTCCAGAAGCGGGTCACAAGGCAGGAGTCTCTCCTCCAGAGGTGTAAAGAGATGATTCGCAGCAGTAAAGAGCGCTCCGCTCAGCTGAGCAGTGAGAGCGAGGTCTTACAGCAGCAGCTGCAGGAGAGACTGCAGGAGCTGGAGAAGATGAAGG[T/C]ACACAAACATCAACTATTACAAGACATGGAGAACAGTGCTGTGGAGCTTTCCTTTTATTTACATCTTACACATGCATATTTTATACATGATTTTTTATTTATACATGCACAGCTCTTTAGGTATTATGTACATTTTTTTAGTATTTTAATTTTTTTTTTAAAGTTTAAAACTCGCAGTGTGATTTTTACAGATTTTTATAACTTTTTAATTGTATTATTTTTTTCATTTGCAGTTTTTTTAATTATATACAAAAATTTTAAGCTAATTTATTTTAATGTATTTTTATTACATTTTTAGTATTTAGTTTAATTTTTTTCATGCATGGTATATTTTATTCTATATTTTATTTAACGTTTTTAAATTTTAACTTTTTATTTTTAATATCTACCTCTGTTTTGTGCTTAGCATTGTGCATGGCTTCAGCATCTGCTTTTCTGGGTGTGTGAACAGTCAGAGCAGAGGTTAACAGCTGACCTCAAATACACATTACTCCCCCTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10793
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 |
---|---|---|---|---|---|
ENSDART00000109469 | Nonsense | 878 | 2037 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 49078779)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 47817161 |
GRCz11 | 13 | 48108191 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAAGATCTATCTGAGAAAGAGAATTTGCATGCTGCAACTTGTAAAACAT[T/A]GCAAGAGGAGCAAAACCGGTTGAGGAAGCAGCTAGATGACCAGAAGAGTT
Long Flanking Sequence:
CAGTGAAACCTTAAGACAAGAGTTTGAGGAAAGGATCAAGAAAGAGCAAGCAAAACATCAGGCTGAGATTGAGGCTGCTAATAAAAATGAACAGTCATTTGCAGGAGTGGAGAAGATGCTGAAAGAAGAGATAAATCATCTGAAGATTGCGCTGGAGGAGAAGGAAAAAGTATTAGAGGAACATGTGCTCAGGGAAAAGTCTTTGCTGGAAGATGGAAGTGCGCAATTGGAGGAACTTTGGCTCAGGGCACAGTTAAATAAAGAGGCACTTGAGGAATCAAGATCACAGGTTAGCACACTTACAGATGAACTCCAACAAGCCAGGGATCAAGTAAAAAATCTTGAGGAAACCCTTGAGGCAGTGCGTAATGACTGTAAGGAGAAAGAAGTGTGTCTTGAAGAAAAGACAAATGAACTTCAGGAACTAGTTCAGAAGATTGAGCATATCAAGAAAGATCTATCTGAGAAAGAGAATTTGCATGCTGCAACTTGTAAAACAT[T/A]GCAAGAGGAGCAAAACCGGTTGAGGAAGCAGCTAGATGACCAGAAGAGTTCTCAAGAGAAGAAACTTGAGAATATTAGAAAAGACATGGATTGCAAGCTGAAATCCCAGGAAAACAAACTGGAGAAATTCAAGCAGAAAGCCAAAGAAGCACAGGATAAGATGAAGAAGAAGCTTCAGGATCAGGAAGAGAGTGCAAAAGTGGAGTTATCAAAGAAGATTCAAGAGTTGGAACTGAAAGACCAGCAGCTAAAGGAGAAGATCCTTGAGATGGCACAAACAAGTTCTGAGGGCCTCAGCACTGCCATGTCTGATTTGGAGGCCAATCACAAGGAGCACTTAGACAAGCTTCAGGTGAACCATAAACAAGAGCTAGAAGACCTTGTTCGTCATTGGCAGGAGAAACTCAACCAGAATGAAGAGGAGATGCAAGAAAAGCATAGTCAAACTTTGCAAGATAAAGCCCAGGAGTTGGAGGAGATCTCACGTTTGCTTTCATCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14408
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 |
---|---|---|---|---|---|
ENSDART00000109469 | Nonsense | 1427 | 2037 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 49077133)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 47815515 |
GRCz11 | 13 | 48106545 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAAGATAAACTTGCAGACATGGAGAGGCAAATTGCWGAGAAGGATGRA[C/T]AGCTTCAGAYGCTCACTGCCAGCGTTGACAATCACTCCATTAGTAAGTCC
Long Flanking Sequence:
GCTCTCTTGATGAGATTACTCTGCAGTTTGGGGAAAGTTCAGAGACTCTTAAAGCCTTACAAACTGAACGGGAATCTCTGCAAACTGATGCAGAGAGTCGCTTCCAGGTACTTTCTGAGAAAGACCTTCACATTAAGCAGCTATGTGAAGAAAAACAAAACGTATCAGAAAATCTCAAAGCAAATATTTTGCAAATCAGCGATCTAGAATCTGCAATAAATGACTTGAAGACCCAGTTAGCAAGTAGCATAACTGAGAAAGAGGAAGCCATATCTCTGCTGAATCAGCAACACAGTAAGGACAAAGAGAGGGTGACGTCCCAAATGGGGGAAACTGTAGAAAAGCTAGAAAAAGAGAAGACCTTGCTTCAAGAGCAGGTAGACTCACTCAGGAATAAGTTCTCTGAGCTGAAAAAGAAGTTCAGTCAGAGTCACAGCACTGTTAAATCTCTTCAAGATAAACTTGCAGACATGGAGAGGCAAATTGCAGAGAAGGATGGA[C/T]AGCTTCAGACGCTCACTGCCAGCGTTGACAATCACTCCATTAGTAAGTCCGAGATGGACCAGGCTCTTAGTGAGAAAGATCAGAGAGTTCATGCCTTGACCTCAGAGCTGGAAAGTTGCTCAAAGAAAGTTTGTGATTTGGAGGAGCAGTTACAGTTAAGGGTAAAAGAACGGGATCAGCTTGCAGCTGATTTGCAGCAGCATCATAACATAAGGGAGAGTGAAAAGACAGAGTTGATGAAACAGGTGCAGGAAGCTCAGGACCAAAGCTCTCAAAACGGTGCCCTAATGCAAAAAACTGAGGAAAGTCTTCAGTCTTTGAGGAAAGATATTGAATCAGCCAAGCAGGAGCTGGAATCCCAGAGGAAGGATTTCGAGAGGGAGAAGGCTGAGATTCTTAAAGAGAAAAAGGAGGCTGTAAAAGCTGCCCAGGTAAAGGCATCCTCTGAGACTGGTGTTAAAGTGGCTGAGTTGAAGAAAAAGGCAGAGCAGAAGATTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22381
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 |
---|---|---|---|---|---|
ENSDART00000109469 | Nonsense | 1735 | 2037 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 49076209)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 47814591 |
GRCz11 | 13 | 48105621 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGCCAACTACCAAAATGAGGTGAGTCGCCTTAAAGAAGATCTGATTGAA[C/T]AGACATCTAGAGTGCAAGAGCTTCAACAGACATGCTCTGATCTTCGAGAA
Long Flanking Sequence:
CTGCCCAGGTAAAGGCATCCTCTGAGACTGGTGTTAAAGTGGCTGAGTTGAAGAAAAAGGCAGAGCAGAAGATTGGCATGATTCGTAAACAATTGACTTCACAAATTGAGGAGAAGGAGCAGGTCATCAAAGACCTGCATGTGCAGTTGGAAACTATCAAGCAATCCCAGATTGAAAAAGAAGAACATATAAAATCACTCGAGAAAACGATGCAAGAAACCACTGCGAAATTAAATGAGGACCACGCAAAGCATCTACAAGAATTGCAGGAGAAGGAGAAAGATGAAAGACTGACCTCTTTGCAAAATTTACAAGAAATGTACGAGGAGAAGCTTGCTTGTCTTCATAAAGACATATCTGCGAAGGAGGAGCACTCTGCTGCTGCTGCTAGAGAAACGTCTTCAAGACTTGTAGATCTTGAGACCAAACTCTCAGAATCTAATGAGCAGATCGCCAACTACCAAAATGAGGTGAGTCGCCTTAAAGAAGATCTGATTGAA[C/T]AGACATCTAGAGTGCAAGAGCTTCAACAGACATGCTCTGATCTTCGAGAACAGATTAAGCAGAAACAGATTGATGAAGTTGAGAGGGAACAGGTTTGTGAGGTGCAAATAAACAGTAATAGGTTAGGAATGGAGCCTGCAATGTTAGTAGCAAAGGAAAACATGGACACTGTTGGGAACCAGGATGACTGGTTGAGTCAAAAGAATTTATTGGTGAAAGAATACGAAGAGAAGCTGCTAGATTTACAGCAGAGGCTAGAAGATAAAGAAAACGAGTTAAAAGCACAACAAAGTTCGCCTCAAAGAAACGGGGAGAGTGATGGGGAGTGCCTAATCAACAATACAAACACCTCAGAGAATGATCTTCAGAGAAAGCTGGTGGAAGCCGAGAATGAAAAGCAGAAGATCCACAAAGATTATAGCAGACTGCAAAAAGATCTCCGTTCTCTAAGGAAAGAGCATGAGAAGGAGTTGGAGTTCCTGAAAAAAGAGATGGCTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15392
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 |
---|---|---|---|---|---|
ENSDART00000109469 | Nonsense | 1757 | 2037 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 49076143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 47814525 |
GRCz11 | 13 | 48105555 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AARAGCTTCAACAGACATGCTCTGAKCTTSGAGAACAGATTAAGCAGAAA[C/T]AGATTGATGAARTTGAGAGGGAACAGGTTTGTGARGTGCAAATAAACAGT
Long Flanking Sequence:
AGAAGATTGGCATGATTCGTAAACAATTGACTTCACAAATTGAGGAGAAGGAGCAGGTCATCAAAGACCTGCATGTGCAGTTGGAAACTATCAAGCAATCCCAGATTGAAAAAGAAGAACATATAAAATCACTCGAGAAAACGATGCAAGAAACCACTGCGAAATTAAATGAGGACCACGCAAAGCATCTACAAGAATTGCAGGAGAAGGAGAAAGATGAAAGACTGACCTCTTTGCAAAATTTACAAGAAATGTACGAGGAGAAGCTTGCTTGTCTTCATAAAGACATATCTGCGAAGGAGGAGCACTCTGCTGCTGCTGCTAGAGAAACGTCTTCAAGACTTGTAGATCTTGAGACCAAACTCTCAGAATCTAATGAGCAGATCGCCAACTACCAAAATGAGGTGAGTCGCCTTAAAGAAGATCTGATTGAACAGACATCTAGAGTGCAAGAGCTTCAACAGACATGCTCTGATCTTCGAGAACAGATTAAGCAGAAA[C/T]AGATTGATGAAGTTGAGAGGGAACAGGTTTGTGAGGTGCAAATAAACAGTAATAGGTTAGGAATGGAGCCTGCAATGTTAGTAGCAAAGGAAAACATGGACACTGTTGGGAACCAGGATGACTGGTTGAGTCAAAAGAATTTATTGGTGAAAGAATACGAAGAGAAGCTGCTAGATTTACAGCAGAGGCTAGAAGATAAAGAAAACGAGTTAAAAGCACAACAAAGTTCGCCTCAAAGAAACGGGGAGAGTGATGGGGAGTGCCTAATCAACAATACAAACACCTCAGAGAATGATCTTCAGAGAAAGCTGGTGGAAGCCGAGAATGAAAAGCAGAAGATCCACAAAGATTATAGCAGACTGCAAAAAGATCTCCGTTCTCTAAGGAAAGAGCATGAGAAGGAGTTGGAGTTCCTGAAAAAAGAGATGGCTGAGGAAAATGAGAAGAAGCTCAAGTAAGATTTATGTGACTTTTTTTTCTCTTTCATTTTAGAAACAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13611
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 |
---|---|---|---|---|---|
ENSDART00000109469 | Nonsense | 1963 | 2037 | 17 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 49071758)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 47810140 |
GRCz11 | 13 | 48101170 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCACGCAGAGAAAGCTCAGTGTGTTGAAACGGAGCTTATAGAAAGCCAT[C/T]GAGATGAAGTCAGTCAGCTTCAGAAAATAATCTCTCAGAAGGAAGAAGAC
Long Flanking Sequence:
TGCTTTGACACAGTCTACATTGTAAAAGCGCTATACAAATAAAGCTGAATTAAATTGAATTGAATATTAAAATGAGCATTATGAACACTCTGCTTGTCTTCTTTTGTGTTTCACACATTAATAACCGTATGAATTTCTTTCGTTTGTGGAAGTACAAGAGTTTACAATCTTGAATGAAGTATTCCTTTGAGTAAAATTTAAAAAAAATCTTGTTAAAGATACCGAATAAAATCTTGGAAAGCATTGTTGACATGAACAAAAAACGTTTTCATAGTTGGTCTCATTTTCTGATTTACTGACCTTCAGGAAATGTGAGAGATGGAATTCATAACTGATTCACCATGTGTTTTCAATCCTGCCATGTTTTCCTTTCAGTCTGGAAATGAGTGTTGTACACTCACTTTATGGTGACCTTCATGTCTTCTTACTGTACTTTTTTTGTTTGTTATATCCACGCAGAGAAAGCTCAGTGTGTTGAAACGGAGCTTATAGAAAGCCAT[C/T]GAGATGAAGTCAGTCAGCTTCAGAAAATAATCTCTCAGAAGGAAGAAGACCTAAACAGAACGGTTCAACGCTACGAGCAGGTCCTTCAGGTACAGCCAAATAAAGTGAAACCGTAGCTTTGTGTTTAACTGTGAGATACCTGATAAATGGCTAGCAGATGCTTCAGATAATACAACTTTATAGAAAGACATTGGCACTAGAGGAATTCTCTGAGGAGTTTATTGCCTTTTGCTTAATTCCAGCACATAGTCTGTAAGTTCAAGTTTCAGCTAATAGTTTGTTTATCATCAGGAAACACTTACCTCAGTCACCTAGCACCTCAAACCCCTCCGAGAGCTGTAGTGAATGATACAGACCGTATGCTGATGCTTACATCCAGCCTGATAGAGAAGCACACTAACTATTTGTCATAGGATTATTTCCGCATTCTCTAGATCTAATTGTTTACCTGTGCATTTTATGACCCAAGTTTATTAGCTGAAAATGAACTAGTATGGCAG
Associated Phenotype:
Not determined