ZMP
ap1g1
Ensembl ID:
ZFIN ID:
Description:
AP-1 complex subunit gamma-1 [Source:RefSeq peptide;Acc:NP_955976]
Human Orthologue:
AP1G1
Human Description:
adaptor-related protein complex 1, gamma 1 subunit [Source:HGNC Symbol;Acc:555]
Mouse Orthologue:
Ap1g1
Mouse Description:
adaptor protein complex AP-1, gamma 1 subunit Gene [Source:MGI Symbol;Acc:MGI:101919]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12746 | Nonsense | Available for shipment | Available now |
sa21138 | Nonsense | Available for shipment | Available now |
sa34235 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13042 | Essential Splice Site | Available for shipment | Available now |
sa7103 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34234 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa25376 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12746
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 |
---|---|---|---|---|---|
ENSDART00000006455 | Nonsense | 77 | 819 | 2 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 70430771)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 69027544 |
GRCz11 | 7 | 69336264 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATGGACAAAATGTCAATTTCAGCTGGAGTGCCTGAAACTGATTGCATCA[C/T]AGAAGTTCACAGATAAAAGGATAGGATACCTGGGAGCCATGCTGCTTCTT
Long Flanking Sequence:
TTCCCCGCTGATTGCAGAGCCGTCTTTATAGACAATCCCATGTGATTTATCGTTCAGCCCTACTTCAAATGTTGCTTTGGCAAACGGCAGTACTGCATAAATCTTCATTTGTCTTTGTGGCACTTATATTGCAGCTTGTGTGACCCTCCACTGGCTGACATTGTGCTTTTATTACAGAGGATGCCAGCTCCGATCAGACTGCGGGAGCTGATCCGGACCATCCGGACGGCTCGAACCCAGGCAGAGGAGCGGGAGATGATCCAGAAAGAGTGTGCTGCCATCAGGTCATCCTTCAGAGAAGAGGACAACACATACCGCTGTAGAAATGTGGCTAAGCTTCTTTATATGCACATGTTGGGCTACCCAGCACACTTTGGCCAGGTGAGGAAAAAAGAGTACTTCAGAATTGTTTTAATCTTCAAAAGGAGTGCATGGAGTTTTCCAGTATTTAATGGACAAAATGTCAATTTCAGCTGGAGTGCCTGAAACTGATTGCATCA[C/T]AGAAGTTCACAGATAAAAGGATAGGATACCTGGGAGCCATGCTGCTTCTTGATGAGAGGCAGGACGTCCATCTATTAATGACAAACTGCATCAAGAAGTGAGTGTGCAGATGATCTCATCTCGTCTCAACGCTTCCATCCATCACAGCTGGTTGTGTTGATTGGTGGGAGTTTAATGTGACTGTTGTAGGTGGCGAGTGTAAAGTGCAGACTGATTGGGAGCTGCTTCCTGAGTGTGATGGCATTTTAATTCACATCTCCTTTTTTTGTTCCATTAAGTGTGCCTCAAGCTGATCATTTTACATTTTCGGTTCTAAAAAGCTTGTTGTTTATTGTTTGCTGGAGATCTAATGTGATATTAAACTATGAACAAAAACTTACAATTCTGTTTTTTTAAGGAGCTTGTGAATTTCATGCTCTCATTATTGACTAGACATGCATTGAGGGTGGTGTGAACCATTTGTTTTTGTTTTTCTTTTGACAGTAACATTTAGTTAAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21138
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 |
---|---|---|---|---|---|
ENSDART00000006455 | Nonsense | 221 | 819 | 6 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 70425152)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 69021925 |
GRCz11 | 7 | 69330645 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTCTTTTCTCCCAATTATGTATCTTTTTAGCTGGTTCCACAACTTGTG[C/T]GAATCCTGAAGAACCTGATCATGTCAGGCTACTCTCCTGAGCATGATGTG
Long Flanking Sequence:
TTCTTTTTTTTTTTGGTTTTGACGTACTGTTTATTTTGCAATTGTTGTCATTTAAGTGTTTTCTTTTGATTATACAGGATTATGTAGACCTCATATGCATTCTCACCTGTCCTGCGTTCACCTTTAGATTAATTTTTAATGGTTCTCCTTTCATACGGTCACTATTGGGTTGTGGTTTTTCCAATATGTACAGTATTGTGGGGGGTACAAATGAAGACATTTGCTAAATTAACAAGAATTCTGGTTATAAACACACAAACAATTATAGCAAACGCTGACATGATGATATCCATGTCTTAAATACCAAATCAGCTGTGTAGTGAAACCAATCTATTGGAAGATGATCAACTCAGGGTGCCTATGTGTATTGACTCTTACTGACCCCTTTTTTTGTGCTGTCCTCTTAAGACCTCAGTGACCCTGCTGTGACCTTGCTCATTATTGCTCTATCATTCTTTTCTCCCAATTATGTATCTTTTTAGCTGGTTCCACAACTTGTG[C/T]GAATCCTGAAGAACCTGATCATGTCAGGCTACTCTCCTGAGCATGATGTGTCCGGCATCAGTGACCCTTTCCTGCAGGTATAGACGCATCGTTTTCTGTCAGTGGTGCATAAAAGTGCATTGGATGATGTTAGTGTTATGAAAATTTCTTCAACATATTGAAACAACAGTCTTTGACTTTAATTTGGTTAAAGTATGATGTACTTTCATCTAAATTGGAATATTGAGTAGGGGTAGGGCTTTTGCACATTCCCTTGTAGCAAACTAACAGTTTTGTTAAGACCACAGAAGCACCGCTACTCTAAATGCGGAAACAAATGATCAGATTGTGATTTAAAACAAGGCAAAACCTTTTTTTTTTTTTTCTGTAGATTAATTTTTCACTAAATGAATAACAATGTGCACTAGCAAAATAAAGATTGTAGATTTTGAATTCATACAGACTTTAAACACTCCCAGTTAGGGCTGCAGAATAAATAGATCACTCATCAGCGATACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34235
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006455 | Essential Splice Site | 363 | 819 | 10 | 22 |
ENSDART00000006455 | Essential Splice Site | 363 | 819 | 10 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 70420150)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 69016923 |
GRCz11 | 7 | 69325643 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGCACTATCGTGGACTGCTTAAAAGACCTTGACGTGTCCATTAAAAGG[T/C]AATTTATGTGCACTCTATGGATATTTATGCATGCCGCGACATCCTCCTCC
Long Flanking Sequence:
TGTGGTGGTAATTCCCAGAAAGTTGAAGACAATTTTGCGTAAAAACAATTATATAATTTATATATATATATATATATATATATATATATATATATATATATAAATATATACACTGCTCGGAGGTATAACTGCTGAAGAGTGAACAGACACTTAAAAATATCATTTCCAAAGCAGTAGGCCAATCAGAAGTATTTAGAGGCATAAAAGACATTGCAAGCTTCTGGTGCTTCTTTCAACCATTCCTGAGAGCTATCTCACGTTTTTAACCACAAAGATGCTTTCTGTGTGACCGGCTCCTCGCTGTGAAATAAACTAATTGATTTCACGTGCTTTCTTGATAGTCTAAATGACAGGGGTTTTACATGTATTACTATTTTTTTATCAGATATGTGGCATTGACATCTCTACTGAAGACGGTTCAGACAGACCACAATGCTGTGCAGAGACATCGAAGCACTATCGTGGACTGCTTAAAAGACCTTGACGTGTCCATTAAAAGG[T/C]AATTTATGTGCACTCTATGGATATTTATGCATGCCGCGACATCCTCCTCCTAACATGTGTCCTTCAACAGGCGTGCAATGGAGCTGAGCTTTGCCCTCGTCAATGGCAACAACATCCGGGGCATGATGAAGGAGCTTCTGTATTTCCTGGACTCCTGTGACCCCGAGTTCAAAGCGGACTGCGCATCGGGGATCTTCCTGGCTGCTGAGAAGTAAGGCTGTTTAGTGAAGAAATCATAAGAGGAAGAGCCAAGGATTTCTATATCAAGTGGCTCTTTTTGCATGTCCTTGTAGCTTCTGTTGAGATTTTAAAACTGTAAAAGCCTAGCAGAAAAAAATCAGATCAAATGCTATAAGCAAATCCTTGAAGAACAAAGAGGGTTTTTTAGCTGAGTTGTTTGAGTGAGTTGTGAAGTGGCTGTGTGATGATAAAATGAGTGATCCATCGGCAGAAGATGATTCTGTTGACACTTTTATATCTGACAGCACTAAAAGGAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13042
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006455 | Essential Splice Site | 363 | 819 | 10 | 22 |
ENSDART00000006455 | Essential Splice Site | 363 | 819 | 10 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 70420150)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 69016923 |
GRCz11 | 7 | 69325643 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGYACTATCGTGGACTGCTTAAAAGACCTTGACGTGTCCATTAAAAGG[T/A]AATTTATGTGCACTCTATGGATATTTATGCATGCCGCGACATCNTCCTMC
Long Flanking Sequence:
TGTGGTGGTAATTCCCAGAAAGTTGAAGACAATTTTGCGTAAAAACAATTATATAATTTATATATATATATATATATATATATATATATATATATATATATAAATATATACACTGCTCGGAGGTATAACTGCTGAAGAGTGAACAGACACTTAAAAATATCATTTCCAAAGCAGTAGGCCAATCAGAAGTATTTAGAGGCATAAAAGACATTGCAAGCTTCTGGTGCTTCTTTCAACCATTCCTGAGAGCTATCTCACGTTTTTAACCACAAAGATGCTTTCTGTGTGACCGGCTCCTCGCTGTGAAATAAACTAATTGATTTCACGTGCTTTCTTGATAGTCTAAATGACAGGGGTTTTACATGTATTACTATTTTTTTATCAGATATGTGGCATTGACATCTCTACTGAAGACGGTTCAGACAGACCACAATGCTGTGCAGAGACATCGAAGCACTATCGTGGACTGCTTAAAAGACCTTGACGTGTCCATTAAAAGG[T/A]AATTTATGTGCACTCTATGGATATTTATGCATGCCGCGACATCCTCCTCCTAACATGTGTCCTTCAACAGGCGTGCAATGGAGCTGAGCTTTGCCCTCGTCAATGGCAACAACATCCGGGGCATGATGAAGGAGCTTCTGTATTTCCTGGACTCCTGTGACCCCGAGTTCAAAGCGGACTGCGCATCGGGGATCTTCCTGGCTGCTGAGAAGTAAGGCTGTTTAGTGAAGAAATCATAAGAGGAAGAGCCAAGGATTTCTATATCAAGTGGCTCTTTTTGCATGTCCTTGTAGCTTCTGTTGAGATTTTAAAACTGTAAAAGCCTAGCAGAAAAAAATCAGATCAAATGCTATAAGCAAATCCTTGAAGAACAAAGAGGGTTTTTTAGCTGAGTTGTTTGAGTGAGTTGTGAAGTGGCTGTGTGATGATAAAATGAGTGATCCATCGGCAGAAGATGATTCTGTTGACACTTTTATATCTGACAGCACTAAAAGGAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7103
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 |
---|---|---|---|---|---|
ENSDART00000006455 | Nonsense | 411 | 819 | 12 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 70417748)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 69014521 |
GRCz11 | 7 | 69323241 |
KASP Assay ID:
554-5212.1 (used for ordering genotyping assays)
KASP Sequence:
AAGTGTTTATTTGGTTTGCTGATGTMACTAATGATTGTTTGTTGCAGGTA[T/A]GCGCCTTCCAAAAGATGGCACATAGACACCATTATGAGGGTTCTGACCAC
Long Flanking Sequence:
TAATTAAACCGTCATTTCTCCTTTTTAGCCAAAAAGCCTGATAGATTAATTGTTGTGCAATGAAATATACTTACTAACCGACAAGGAAACACGCATGGAGAGTGCTTCTCCATCATTCATTCATAGAAAGAACAGCCAGGATGGGGAAATTGATGGATTTGGGATCACTGTATACCTAGTTTGCTTGCTTTGACACGTTATTTAGGAAATGTGGCTAAGACATAACTTGAAATTTTTTAATTTTGAATGGGGCTAGTAAAAAATCTTTTCCACTGGCCATTAGAAACAATCCTTAGTGTTTAGCACCATATAATTCTGAAATTTCATTCATAATGGTCTTCAAAAAGGTCTTAAAGTCCTAAATTTGACTTGGTGAAGCCTGAAGAAACCCTGATTGAAGCAATCACACTCAGGTGTGCACCAAAAGAGGACCAGGTGTGAAAGCATCTCAAGTGTTTATTTGGTTTGCTGATGTCACTAATGATTGTTTGTTGCAGGTA[T/A]GCGCCTTCCAAAAGATGGCACATAGACACCATTATGAGGGTTCTGACCACGGTAAACAATACATTTATTTTCTTCCCTTTTTTTATTCTGCTTAAATTTCCACTTTTTGTTGGACTAGATAACATTAATGATCATTTTAGTTGATCACCTGAAGTCTTTTCAAAGCACACATTAGAATAAACAATGTTTTTAATAGATGCTGTTGACTTGATCTTGGTTGTAGATTTTAGATCCTATAATTTGACAACAGCTTTTTCTAATCTTTTTGTTTGTCATATAATACATTTTTTCACCTAAATTGGTGCTGAAGCCAGTAGTTGGCAGACCTCTTGCAAAACCAGTTTGCATTTTTGCTAACTTGAGCCAAATGATGACATAAGCAGCCCACGAACACAACAAAATGAGTTCTGAGGACAGTTTAACAACCACAATAATTTACATCAGTCTTTTTTTTAATTATTATTCTGATTGATTGGCAGATATGTTGTGAACACTTACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34234
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006455 | Essential Splice Site | 623 | 819 | 17 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 70412217)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 69008990 |
GRCz11 | 7 | 69317710 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTCTGGACACAAAACATCCGCCCAACATCCCTCAGCCAATCAGTCAGG[T/A]GAGTTTTTCTTTTTTTTTACATCTACATTTTTCAGTTCAAACAAATGCAC
Long Flanking Sequence:
TCTAACTGCTATCATGAAGCTGTCGACCCGTTTCAGCAGTGTGAAGTAAGCACATCTCTTCTGATACAAATATGAGGATATACTTCCCTGAAATGAGTTTGAGTCCCCGAGTGGATGAGGTCCTGATCTTCTATTTATTTTCATTTGCCCTGTAGTCGAATCAAGAAAGTGGTCTCGATATATGGCAGCAGCATAGATGTGGAGCTACAGCAGAGAGCTGTGGAATATAACGCACTTTTCAAAAAATATGATCACATGAGGTAAGAGCTGACCTACTTGTGCTACCGTTTTCGACTATTTTTGGTTCACTCCTAGCTTTGGTTTTCTCATCCTCACTCTTTCTGTTCCCCCATGTAGACCTGCATTACTAGAGCGAATGCCTATCATGGAGAAAAGCGCCACCAACGGCCCAGCAGAGATTGTACAGACCAATGGAGAAACAGATGCACCCATTCTGGACACAAAACATCCGCCCAACATCCCTCAGCCAATCAGTCAGG[T/A]GAGTTTTTCTTTTTTTTTACATCTACATTTTTCAGTTCAAACAAATGCACATTAGCAGACCTCAAGGCTTCTCAGTATCTTCATAAAGCTGCGTTCACACCAGACGCGGATGAAGCGTCAAGCCTGAGGGATTTACATGTTAAGTCAATGCAAATAGACATCTTGTGGCATGTTTCGTGCGAATGATGCGATTTGCACAAATAAAGTAGCTCACCGCATTAACCAATCAGGAGCTTGCTTTTGTGGGGGCATGATTATGACGTAGCGCCTGTTGTTGGTGTCCCAAAGGGAAATCCTCTTGCTGACACTGGACAATAGTTCATCAAACAGGGCTGGGCTCAGTCTGAAGCACTGCTGAAAGCCTCCATCCAAGTACAGTTTCTCAAGGAGTTGATGAACTCACAGAGCTGGGTGCACCTCTGAAAGGATCTAGCGGACTCAGACATGGCGCCGAATGAATCCACGCTGTTTTTCAGTCTTCCTTAAGCACATAGAGCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25376
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006455 | Nonsense | 691 | 819 | 19 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 70407804)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 69004577 |
GRCz11 | 7 | 69313297 |
KASP Assay ID:
554-7710.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCTGTGCCCATGTCCCAGCCCCCTTTCCTTTTGGACGGTCTCACTTCA[C/T]AGCCCCTCTTCAATGACATTGGAGCGGGTGAGCTTACAGTCAATTTCATC
Long Flanking Sequence:
GCCCAGAACTAATTAAAATATTTGAAGTAGGTAATTATATCTTCAAGTTTTTCTTAATAAGGTTTAGTTATTAATATTATTAATTTATAAACATATTTTATGTGCAATTTTATGTTTGAATACAAATAAATAGTCAGATTTAATGTCTAATATTATAGTCAGAGTTCCATACAGTATGCTGCATTAGTTGAGAAGGGTACATATACTTGAGAGAAACTGTATCTGACATATCTCCAAATGAATCAGTGTCAAGTCAATTTGACTGTGTCACTGAATTGAAAGGCATGCTAGTGAACTGCTTCAAATCATGCCAAGCCCTAGATATCCTCTTTCTAATTTCAGACTAGTATGAGTTTCCTTTACCAGTGATTCATTTTTGGGTGAATCCCTGCTCACGCCATTATGTTGCTGCTTCTCACCCCTTAGGCGGTCCGGCCCCCACCCCTGCTCCCTCTGTGCCCATGTCCCAGCCCCCTTTCCTTTTGGACGGTCTCACTTCA[C/T]AGCCCCTCTTCAATGACATTGGAGCGGGTGAGCTTACAGTCAATTTCATCATGATGGTTCCTGCAAATTAGCGCAGACAATTAGCACGAGTTTCTCTTGCAGGCATTCCACCAATGACGGCGTACAATAAAAATGGATTGAAAATCGAGTTCACGTTTGAACGCTCCAACCCCAATCCCAATATAGCGGTAATCACCATCCACGCCACCAACACCACAGAGGTGGACATGACAGAATTTGTGTTCCAGGCTGCAGTACCAAAGGTTTGTCTGGTTTTTACAGTTTTCAGACAGTGATTATTTTCATTATACAGAGGTTTTTTTTTTAATTAAAAGTAACGACAACAACAATCTTTATTTATAAAGCACCAATAAAAATAACGAAACAAAAACTATTGTAGACCAAGATGCTGTACAATCAAAAAAAAAGAAACGTTAACACCAAGGACAACAAATTACACCACAAAATGATCCCTGACAAATCACAACTAACTATAATTA
Associated Phenotype:
Not determined