ZMP
acin1b
Ensembl ID:
ZFIN ID:
Human Orthologue:
ACIN1
Human Description:
apoptotic chromatin condensation inducer 1 [Source:HGNC Symbol;Acc:17066]
Mouse Orthologue:
Acin1
Mouse Description:
apoptotic chromatin condensation inducer 1 Gene [Source:MGI Symbol;Acc:MGI:1891824]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9490 | Nonsense | Available for shipment | Available now |
sa38607 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40879 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13260 | Nonsense | Available for shipment | Available now |
sa40880 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18154 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9490
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034218 | Nonsense | 332 | 1259 | 5 | 17 |
ENSDART00000141749 | None | None | 604 | None | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 25242818)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23804570 |
GRCz11 | 7 | 24075727 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGTCAGCCCACTCCTCCACCATCTCCACCTCCAGAGCTCTCATTCCCAT[T/G]ACCTGATACTCCCAAACAGAGTCCACATGACCAAGATGAGCCAGCRGGYC
Long Flanking Sequence:
TGACAGTAAAGCTGGGAGGATCTGGCATCCTTCTTTCCCCTCTGGACATGAGGATGTCGCTACACCCTCCCCTCCACGAGCAGTTGCCTCCTTGTCTGTACGTGTGGTTGGACAACCTGAGCGCCAAGGCCTGCCGCCTCGTTCACAAGAAAGAGAGGGAACGGCCCCAGTTGAAGCAGGTCCTGCCCATTCAATGCTGCAGCTCAGTCGTTCTGCAAGGGCAGCAGGTGGTGCTCAAGTTGACAGTGATGATGATGATGATGAAGAGGACGATGATGACAGTGAGGACGATGATGAGTGGGGTCCGGCCTCGCATGGGAAGAAGAACGTACGGGCTCCTCCAGCACGTGCTCCACCAGCCGCTGCCCCCCAACGCTCCCGTCGAAAACTTCAGCCCCCACAACACATCCCTCCCCAGCTTCAGCCAGTCCTCCAGCCACCTCTGCAGCTCCGTCAGCCCACTCCTCCACCATCTCCACCTCCAGAGCTCTCATTCCCAT[T/G]ACCTGATACTCCCAAACAGAGTCCACATGACCAAGATGAGCCAGCGGGCCTAGCGGAAGCTGCTGTTCCAGGGCCAGGCATGGTCTCTCCTCCATCCCTCACACGACAGGAGTCAAGCTCCAGTTCTAGATCTAGCAGCCCAGAACCTCCATCCACACGCAAACCTGGTCCCCTTAGCCTCTTGGTCCGCAAAATGGAGTCTGAAGGTGTGTTTGGTAGTGCACAGAACATAGAGGTGAAGGGTGAAGGGGACATGGAAGTTGAAGAGCAGGAACATAGTGAAGCAGCAGTGCAAGACTCAACTCGGGAGCTTTCTAGGACAGATGTGTCCTCCTCAGTATCCACAATGCCCCCTGATCAACAAGGTATTCAAGATTCTGAGTTGGAGAAAGGGGAAGATGAGCCAAAACCAAGTGAGGAGACGCAAAATGAGAAAGTGGATGAGACTTCTGTACCATTATGTTCGACTTCGACCACCACGCGCTCATCTAGGAGGCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38607
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 |
---|---|---|---|---|---|
ENSDART00000034218 | Nonsense | 644 | 1259 | 6 | 17 |
ENSDART00000141749 | None | None | 604 | None | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 25244026)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23805778 |
GRCz11 | 7 | 24076935 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGAAGTTGTCCTTTCTTTACTCAAACCAGGATGTAGAAGAGAAAGGA[C/T]GAAAAGGTGCTGAAGAAAAGAAGGCTCAGTCTTCAAGGTTAGCAAATGTT
Long Flanking Sequence:
CAGACGAAAATAAAAAGGCCCTAACTTCACCTCATGCTACATCTGAAGAAGAAAAGATGGATAAAACAAGAGACCGTTCAAAGAAAGATAAAAGACGCTCCTCAACATCAAGTCAGTCGTCATCATCTGATGCGGATTCAGAATCATCTTCCTCTCATTCTTCAAGCTCTCCTTCACGTGATAAATCCAGCCCAACCAGCAAAACGAAGGTTTGTATTTGGTGTATCCACACATCAGGCCAGTGTTTTTTAAATTCTGTTTGCTACTTTTGGTGTTTTCTGATGATGAGCCAGCCATGCTAATACTGATGCACCAGTCTGACTGTGTCTCTCTGGGTGTAAGTGAGTTCAACACAACTTCTCACACTCGTGGTGTGATCTGAAGATGAACACAAAAAAGATTTGTTTGTAGGAAAGTTTAAAAGTGCATTGTGGAATAAATTAAATGTCTTGATGAAGTTGTCCTTTCTTTACTCAAACCAGGATGTAGAAGAGAAAGGA[C/T]GAAAAGGTGCTGAAGAAAAGAAGGCTCAGTCTTCAAGGTTAGCAAATGTTCTATACACACACTATTCATTGTACAGGTACAAAAATGCAATGCTTCTAGTGTGTTGCAGTGTACAAATTCAGCTTATTCATTCATCAGCTTTAAACAAAGACATAATAACTAAAGAAAACATGAGTATTTTGTCACTTTTAATTTCATTTGTTTTGCACATCTACCTTTTATGGCAATCGTTTAAAGGGAAACCCCACCCCAAAATGAAAATTCATCATTTACTCACTCTTTACTTGCTCCAAATCAGTTTGTCGAACACAAACTATATTTTGAAGAAGGCTGGAAACTTGTAACAATTAACTTTCATAGTATTTGTTTTTGCTACTATTAAAGTCAATGGTTACAGGTTTCTGTCAGCTTCCTTCAAAATGTATTTTGTGTTCAGCAGAATGAAATAAACTCATTGAGGTTCGAAGGTGAGTAAATTTGAATTTTTTTTGGATGAACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40879
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 |
---|---|---|---|---|---|
ENSDART00000034218 | Nonsense | 793 | 1259 | 10 | 17 |
ENSDART00000141749 | Nonsense | 138 | 604 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 25257883)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23819635 |
GRCz11 | 7 | 24090792 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCAGATGAGGGCCGTCTCTCTGTGGATGAGGACTCCTCTGGCCCTCGT[G/T]AACGAGAGGAACCGGAAGAGGATCAGGGCCTGAAAATCAGACGCACAGTG
Long Flanking Sequence:
ATTACTGCCTGTTTTGACTGCTTGAATAAATGTAATCTAGGTTAAGTGTGGTAGTAATCTGGAAGTCAGATGAACTCAAATTCATACCCAGCAGCCCTAAAAAATAGCCAGTAAAGTATCAGGACATAAAAAGGGTCAAACATATGTATGTCAGTCATTTAACCATTGTTCATGCAGTACATACATAATGTATTTGTACAGGCCATAGAGAACTAGCCTTTTAGCATCATCTCCAAACAGAAGAGGGAAATAAAATCTTATCTAGACAATAGAAACACAGCAATAAATGTTAATACAAAAGGCTTAATCACTGAAATTGTGTATGAATTTAAAAGGTTTGAAAGCTTCAATAGTGCTGCATCGTAGTATTTGTGTATAAATTATGCATTCTGTTTTTTCAGACATTAATTCCAGACATCAAGCCCCTGCAGGAGGCAGTAGTGGATTTGCACCCAGATGAGGGCCGTCTCTCTGTGGATGAGGACTCCTCTGGCCCTCGT[G/T]AACGAGAGGAACCGGAAGAGGATCAGGGCCTGAAAATCAGACGCACAGTGACACAGGTCAGACATGCAGGAGACTGCAGCATAGTACTGCACAGATTACAAACATATGTTTAAATGCATCTCTGTAAACTTTTGTCCAGATTGTTCCATCTGATGGACACGAGAATGGCCAGAAAGAAATGGACGAGAAGGATGAGGAGGAAGATGAAGATGATGAAGAAGAAGAGCAGAAACACTCGGGAGAAGAAAAGGAGAAACCTAGGAAACAGGAAAGCTCACCTGATGCTAGTGTGGAAACACCAGAATGTGATTCTCAAAAAGGTGACTATTCGTCCACATTTTCAGAAATCGCTTGCTAGATTTGCAGAAATCAACTTTCTTTTTTTTGTCAGTCACACCCAGTGATTCTTTAGTAAGGCGCTCCATCAGTCAGCAGAAGTCAGGTGTGTCCATCACTATCGATGACCCCATACGAACGGGCCGCCAGCTTTCTCCTCCTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13260
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 |
---|---|---|---|---|---|
ENSDART00000034218 | Nonsense | 899 | 1259 | 12 | 17 |
ENSDART00000141749 | Nonsense | 244 | 604 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 25258355)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23820107 |
GRCz11 | 7 | 24091264 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATCAGTCAGCAGAAGTCAGGTGTGWCCATCACTRTCGATGACCCCATA[C/T]GAACGGGCCGCCAGCTTTCTCCTCCTCGTGGAAAAACCTCCAACATCATA
Long Flanking Sequence:
TGTGGATGAGGACTCCTCTGGCCCTCGTGAACGAGAGGAACCGGAAGAGGATCAGGGCCTGAAAATCAGACGCACAGTGACACAGGTCAGACATGCAGGAGACTGCAGCATAGTACTGCACAGATTACAAACATATGTTTAAATGCATCTCTGTAAACTTTTGTCCAGATTGTTCCATCTGATGGACACGAGAATGGCCAGAAAGAAATGGACGAGAAGGATGAGGAGGAAGATGAAGATGATGAAGAAGAAGAGCAGAAACACTCGGGAGAAGAAAAGGAGAAACCTAGGAAACAGGAAAGCTCACCTGATGCTAGTGTGGAAACACCAGAATGTGATTCTCAAAAAGGTGACTATTCGTCCACATTTTCAGAAATCGCTTGCTAGATTTGCAGAAATCAACTTTCTTTTTTTTGTCAGTCACACCCAGTGATTCTTTAGTAAGGCGCTCCATCAGTCAGCAGAAGTCAGGTGTGTCCATCACTATCGATGACCCCATA[C/T]GAACGGGCCGCCAGCTTTCTCCTCCTCGTGGAAAAACCTCCAACATCATACATGTCCTTCACCTGGTAGGTACTGGATCACTGCTCACTGTAATGTAGGGATGTCTTAGGGTGCTTTTACATCTAATTCACTTGACTGGGCCGAATCCAAGTTCGATTGTCCTCCCCTTGCCATCTTATCAGCTGGTTTGTGTTCACACCGTCGTCTTTCCTTCTGAACCCCGGTACGCTTGCGTCATCAAGCTGCTGTTTGTGTACAGCTGTTGCTAGGTGATGGCCACTCAAGCAAAGTGGCAAAATGGAAAAACGTACGCTCATCGCGGTCTTTCTGCTGTTACAGAATTTTTTGCTTTTTTTTTTTTTATTTTTTTAGCAAAACCAAAATATAGAGAGCCACCCCAAAAAATAATAAAAATGTTTAGAACATCACGCGATGTTTGCAGAAGTAGTTTTTGGTGGAGACTAGCAGACATTATAACTGTTTGCACTGGATCAGTCTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40880
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 |
---|---|---|---|---|---|
ENSDART00000034218 | Nonsense | 1175 | 1259 | 17 | 17 |
ENSDART00000141749 | Nonsense | 520 | 604 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 25262499)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23824251 |
GRCz11 | 7 | 24095408 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGCGAGAGAAGAGGAGGAAGGAAATCTTTGAGGAAGAAGACAAAAAA[C/T]GAAAAGAAAGAGAGCAAGAGAGAGCAAAAGGCCGCGACCGAGTGGGAGGA
Long Flanking Sequence:
GGTAATCAGAAATTGCTGTTTGGTGCTTGTGTAGGCCGTACAGTTCAAAATTCATGTTTAACTGAATAAACAGTTAGTAAACACAAGTACATCTTATTGAACATCATTTATTTTCATCACCAATTATCATAGTAGAACAGTTTCCCAAGTAGTTTGTGATGCATTTTGGAAACAGGCGATGAGCCCCAGGTCTAATGCACCACCTGGCTCGAGAAACCCGTTCTCAAAGACTTATTATTTGAGTAGCACACATATTCTGAATGCCTTGGGCAGAATTCAGATAAGCCATTTTAATCTAGATCAATTCCAAGATTACAGTGAGATTAATCTAGAGTTAAATAAATCTATGCCCCCCCCCTTGAGTTATGAGTTAACTGGGTGATTTAATCTTCGCTTCTTTTCTCCCTCCTCAGGCAACACAGAGAGATCAGGAGCGAGCCGACCGCATCAAGGAGCGAGAGAAGAGGAGGAAGGAAATCTTTGAGGAAGAAGACAAAAAA[C/T]GAAAAGAAAGAGAGCAAGAGAGAGCAAAAGGCCGCGACCGAGTGGGAGGAAACACAGCAGAAACCAGAGCTGGAGTTCCCAGACGGTCAACCGAAGGGGAGAGAGACCGAGGGAAGGGCGGAGAGAGAGAAAGAGGAAGAGAGGCGGACAAGAGGAAAGATGCACAGAGAGGCCAACGTGACTCCAAAACCACCACAGCAGCGGGCAACAGACGCTCGCAGAGCCACAACAGCACCTCCAGAGACAGACGACACTGAGAGAGGATGGAAGATCAGAGTCGACAGGACCACCATTTCACACAGGATCACGATTCTTCACACAAACTACATTTACTCACTCTCATGTCATTCCAAACCTGTATTTATTTGAAGAACAACAGATTTGTTTTCATAAATGGTTTATACGCCAGATTGGACCCCCTTAACTGCGAAAAATGTTTGATTATGCTTCACAAAATGGTCAGAAATAAGGGATTCTTCACCTAAAAATAAAAATGGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18154
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034218 | Nonsense | 1199 | 1259 | 17 | 17 |
ENSDART00000141749 | Nonsense | 544 | 604 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 25262571)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23824323 |
GRCz11 | 7 | 24095480 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGCAAAAGGCCGCGACCGAGTGGGAGGAAAYACAGCAGAAACCAGAGCT[G/T]KAGTTCCCAGACGGTCAACCGAAGGGGAGAGAGASCGAGGGAAGGGCGGA
Long Flanking Sequence:
GTTAGTAAACACAAGTACATCTTATTGAACATCATTTATTTTCATCACCAATTATCATAGTAGAACAGTTTCCCAAGTAGTTTGTGATGCATTTTGGAAACAGGCGATGAGCCCCAGGTCTAATGCACCACCTGGCTCGAGAAACCCGTTCTCAAAGACTTATTATTTGAGTAGCACACATATTCTGAATGCCTTGGGCAGAATTCAGATAAGCCATTTTAATCTAGATCAATTCCAAGATTACAGTGAGATTAATCTAGAGTTAAATAAATCTATGCCCCCCCCCTTGAGTTATGAGTTAACTGGGTGATTTAATCTTCGCTTCTTTTCTCCCTCCTCAGGCAACACAGAGAGATCAGGAGCGAGCCGACCGCATCAAGGAGCGAGAGAAGAGGAGGAAGGAAATCTTTGAGGAAGAAGACAAAAAACGAAAAGAAAGAGAGCAAGAGAGAGCAAAAGGCCGCGACCGAGTGGGAGGAAACACAGCAGAAACCAGAGCT[G/T]GAGTTCCCAGACGGTCAACCGAAGGGGAGAGAGACCGAGGGAAGGGCGGAGAGAGAGAAAGAGGAAGAGAGGCGGACAAGAGGAAAGATGCACAGAGAGGCCAACGTGACTCCAAAACCACCACAGCAGCGGGCAACAGACGCTCGCAGAGCCACAACAGCACCTCCAGAGACAGACGACACTGAGAGAGGATGGAAGATCAGAGTCGACAGGACCACCATTTCACACAGGATCACGATTCTTCACACAAACTACATTTACTCACTCTCATGTCATTCCAAACCTGTATTTATTTGAAGAACAACAGATTTGTTTTCATAAATGGTTTATACGCCAGATTGGACCCCCTTAACTGCGAAAAATGTTTGATTATGCTTCACAAAATGGTCAGAAATAAGGGATTCTTCACCTAAAAATAAAAATGGTCATCATTTACTCATCCTCCAAACCTGCTTGAGTTTCTTCTGTTGAACACAAAGGAAGAATGCTGACTTCCATAG
Associated Phenotype:
Not determined