ZMP
GGA3 (1 of 2)
Ensembl ID:
Description:
golgi-associated, gamma adaptin ear containing, ARF binding protein 3 [Source:HGNC Symbol;Acc:17079]
Human Orthologue:
GGA3
Human Description:
golgi-associated, gamma adaptin ear containing, ARF binding protein 3 [Source:HGNC Symbol;Acc:17079]
Mouse Orthologue:
Gga3
Mouse Description:
golgi associated, gamma adaptin ear containing, ARF binding protein 3 Gene [Source:MGI Symbol;Acc:MG
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33086 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45128 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16740 | Nonsense | Available for shipment | Available now |
sa38371 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33086
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 |
---|---|---|---|---|---|
ENSDART00000081977 | Nonsense | 242 | 686 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 3 (position 6903043)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 6622194 |
GRCz11 | 3 | 6508302 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACGTCAAGCTCCTGACTGAAATGCTGAGTCAATATGACAGAGAGCGAT[C/A]GTCAGACGCCGACCGTGAGCTCATCAAGGTGAGAGCACACAAATAGCACT
Long Flanking Sequence:
CACATTACAGCTCCGTATCACTACGCTGAATGATTTCATCAGTCAACAAAACACATCAAACACACAACAGAATGCTTTGGAGGAGATGTGTGAGAAACACAAGGAGCAGGTTGAGGACAAAAACCTGACGAATGTCTCAAATACATCATCTAAACCATAGCTTTAGGGGTGAGAAGCAGCGTATAAGCAGAATAATTCACACCAGACTGTTGAATTATTAGAAAATAATGCATAACCACCACCTCAGGTTGTGGTTTGAATTATTTAAAAAATAACGTGCAATAATCATCAATTCTTCCTCGCATTATGCATTTGAATGTTGTGCAGATGAAACTGAACTGTGATTTAGATTAATTGTGAAGTCTGAATGTGTGCTGTTAATGATGTTAAGGATGACGCCCGCGTGCACAAGCTGACCAAGCGCATCAACACGCTGGAGGAAGTGAACAACAACGTCAAGCTCCTGACTGAAATGCTGAGTCAATATGACAGAGAGCGAT[C/A]GTCAGACGCCGACCGTGAGCTCATCAAGGTGAGAGCACACAAATAGCACTCATACATGAACAGAAAATGACTAGACTGATATGAGTGAAGAGTTTCTAAAGTGTATAAGCCTCACGTCTTTCCAAAACCTTCATTTATCATCAGCGCTCCAGTGCCTGAAAACTCTTCAGCACTTTAAAATGATCATAAAAACAGCACACGTGAATAAAGTGGGTTAATACACGTTTTCAGAAGACACAGATTTAATTTAGCCCGTGGCATTTTTATTTTGAGTTTATTATTAATATTTCAAGAGTTCACAATTAGCTATAACTTAATACCAGTTGCAGGTTTGACATGCTGTCCCGAGAGAGAACCCTGAGCTCGCAGATATTTGAGCCCAGGGCTCCTGCCTGGTTGATGAGCATGTGAGGGGGTCAGAGATCAGGTAGGTCTCGAGAGCTCCCCCTAATAAAGGAGGAAAGAGGGAGGTGGGGTGGAAGGGGGGATTCTTCAAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45128
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081977 | Nonsense | 320 | 686 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 3 (position 6909251)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 6615986 |
GRCz11 | 3 | 6502094 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGTCTGATAATGCCGTTGATGTTCTTCATGGTTTTTCTCCAGCATGT[G/T]AGAGCGGCACTGGCACACTCATTGATCTGGCTGGACTGGATGAACCTTCC
Long Flanking Sequence:
AACTTGCCTAATTACCCTAACCTGCCTAGTTACCCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAAAATATCTTTTAAAATATTATTTACTGTCATCATGACAAAAAATAAATAAATCAATTATTAGAAATAAGTTTTTAAAACTATTATGCTTAGAAATGTGCTAAAACAATCCTTCCTCCATTAAACAGAAATTGGGGGAAAAATAAACAGGGGGACTAATAATTCTGACTTCAACTGTACAAGCTTTACATGTTTATATCAGGTTTAAATCTTCTAAATGTGAATTTTGTCACTGTTTTGGTGCACAGTAGCTTATAGATATCCTAAAAACTAACAATACTGATTCTAACATCTAAAAAAACTTTATTTCAATTTTACAGGACCTTTAATAGCAGGTGTAAACAGAGCTACATATCCTCCTTTTGTCTGATAATGCCGTTGATGTTCTTCATGGTTTTTCTCCAGCATGT[G/T]AGAGCGGCACTGGCACACTCATTGATCTGGCTGGACTGGATGAACCTTCCTCTCCTCCTCCACCTCCTCCTCCAGCTCCAGCTCCAACTTTAGCTCCAGCTCCAGCTCCTCAGATTTCCTTAGCCACTCAGAAGGCCTCCTCCATTCCTGTGTTGCCACCTCCTCCTCGCCGATTGGCCGGTGCTCACGGCAGTCAGACGAGCAGCCCCAATCACAAAGCAGCAGAGCATCAGAGCTCTCTCTCCCTGCTGGACGACGAGCTCCTGTCTCTCGGTAAAACTGACGGGTTTTTCTTATCTGCTTGTTAAGTGTGATGTCACGTGAAGTGGCTTATGAGTTCAAGCGCTCTATCAAACTGTATGAGGAGACTCAACAAATGGTAGTAATAAATGTTTACAAAGTGATGTAATACTTTCCAAAAGCATGCTCGCAATCTATATATCCATGCCAGAAAGTGTATCCGATAGCCAGAAAGTGACGACTAAAAAGTGGTCACTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16740
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081977 | Nonsense | 431 | 686 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 3 (position 6911562)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 6613674 |
GRCz11 | 3 | 6499782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTCCCTCTGTGCCAAACAGACCAAAGCTGGATGATTTATCTGCTCAGTG[G/A]ACGTCTCTACAGGTAGCACACACTAAACTCCAGATCTTCAGAGCGTATGC
Long Flanking Sequence:
TTAATAAAATATTAATAATAATGATCTTAACCATAATATGAATCTTGCAACTTATTATTATTCAAAATTCTTTTTTTTATTAAATAATAATTTGGAAAATAATAGATTTGATTATTATTATAATTAGGTGGTTCAGTCCGCTGATAAATATCAGGGCAACCCCTTTTAAATAAGGGATTAAGCTGAAGGAAAATTAATGGATAAATTACTATTTATTATTAATAATAATATTATAAAAGATAATATAAACAACCTTCATATTAATCATGCATTTCCCTTTTTTATAATAATCATTATAAATGAAAATAAAAAACATAATTTTAATATTTTTTATGAATAATACAAATATTTTATTAATAATAAAAAAATAAGTATTAGTTAATGTATTTTTTAAATTATTGCACTAATTAAATGTAACATATTATTGTTTTATTTTCAGGACTGAACGACCCTCCCTCTGTGCCAAACAGACCAAAGCTGGATGATTTATCTGCTCAGTG[G/A]ACGTCTCTACAGGTAGCACACACTAAACTCCAGATCTTCAGAGCGTATGCAGAACATTAATAATAATCCTCAGTATAATGTCTGTATTTGGCCATCAGGCTCCTGATCCGGGCCTGGACCTGTTTGGGAGCATCTCAGCTCCGAGTGCCGTCTTTCCGTCAACACACACTCCTGCACCGACCTCACACACACTCACACACGCTCAGGGCCTGCAGGAACTCTCCGTGTTGGACTTTGGAGGTGAAAAGAGGTAAACTTTCACTCTGAAACACCTCAGATGGACACAAAGGGCTGATGTTCTGATGCTCAATATTTGACTGAATGACAGGATCACTATAGGGTTTGTGCAGCTGCTGGAAATCCTTCAAAATGCTTGAATTTTAGTTTATTGTTTTAATGGTTTTATTTTTGAGTTTTATTTATGAGTTTTAGATTTTTAATAATAATAAAAATACATGCATCATTTTATTTTTATGGTTATTATTTATAGTAATAATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38371
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081977 | Splice Site, Nonsense | 636 | 686 | 15 | 16 |
Genomic Location (Zv9):
Chromosome 3 (position 6916477)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 6608755 |
GRCz11 | 3 | 6494863 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACGGCACCGCTGCCCGTGAGGAATGTAGTTCTGCAAGCAGCCGTGCCC[A/T]AGGTAAAACACTTGCGCCTGCAACACACACATTCACACAGAGTCAGATTC
Long Flanking Sequence:
TGTATTATACTGTTATATTCCCCTGGAAACCTTTTTAGTTTTGCTCTGTTGTATTTATATACGCATGTAGTTAATTATATTTTATGCAGATGCACTGCCTAGAAAATGACTTGAAAATACCAGTCAGTTTAAAATAATCAAATCATCTGGTGAATTATATATCACAGCAAAACAAAACATTGCAGTATTATGCAGCCCTACTATGCATTTCTTATACTTATTCTTCTGTCAATTTTGGGATCCACCAGTAGAGTGATATAGATCTACTGCCAGGTTGGCGGCCATTAGATGTTTTTAAGTGTGTGTGATGTTTCTGTGGGTGTTTGTGTGCAGGTAAAGTCTTACCCGTGACGATGTATGATAAGGATGGAGTTCGAGTTCTCCTGCACTTTGCGATGGACTGTCCGCCGGGTCGACCGGACGTCCTGGTCATGGTGGTGTCGCTGCTTAACACGGCACCGCTGCCCGTGAGGAATGTAGTTCTGCAAGCAGCCGTGCCC[A/T]AGGTAAAACACTTGCGCCTGCAACACACACATTCACACAGAGTCAGATTCTGAATGATTCACTTGAGTCAAGTAATCTATCTATAAGCCCAACCCTGGAATACAGAAAACAGTGGCTGAGAGAGCTTAACGAGCTACAATTTAAGAAAACACATACAATAAAAAACATCAGCAAATTAAGAAACACAAACATATGAAGAAAACGCCTGCATTTACTCACAACACATGCAAATAGCACAGAACACAATGGAAATGATTCAGGGGGACCCTAAAATGTGACATGTAAATTTTGAATGAGTTTGACCTGTGCTTGACCTGTGCTGTTGTGTTTGTGTCAGTCTATGCGAGTGAAGCTTCAGCCTCCGTCTGGTACAGAGATCTGTCCCTTTAACCCCATCCTGCCCCCCGCATCCATCACTCAGGTCATGTTGCTCGCAAACCCGCTGAAGGTGAGCGCACACACATACGTACACACATACATTCACACATAACCACACTCAA
Associated Phenotype:
Not determined