ZMP
zgc:172302
Ensembl ID:
ZFIN ID:
Description:
Zgc:172302 protein [Source:UniProtKB/TrEMBL;Acc:B5DDZ5]
Human Orthologue:
ABCA7
Human Description:
ATP-binding cassette, sub-family A (ABC1), member 7 [Source:HGNC Symbol;Acc:37]
Mouse Orthologue:
Abca7
Mouse Description:
ATP-binding cassette, sub-family A (ABC1), member 7 Gene [Source:MGI Symbol;Acc:MGI:1351646]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41770 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24886 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45420 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41771 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41770
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113281 | Essential Splice Site | 101 | 1165 | 4 | 46 |
Genomic Location (Zv9):
Chromosome 11 (position 5674884)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 5644340 |
GRCz11 | 11 | 5590646 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTTTTTTTTAACTTCAGCCATTGATGGAGATTTATTTTGTTATTTTC[A/T]GACTTTCTCGACTTTTAGTCGATATGAGGACCGTCCTGACAATCAGTGGC
Long Flanking Sequence:
CACCTGTACCGCATGTCTTTGGACTGTGGGGGAAACCTGAGCACCCGGAGGAAACCCACGCGAATGCAGGGAGACATGCAACATGCAAACTCCAAACAGAAACACCAATTGCTGTGCAATTGCATTCTTGCTGTGAGGCGACAGCACTACCTACTGCACTATTGCCTCAACGCATTTATTATTTACTTAATATTAATATAAATCATTAATTTAATTGATATTATTTTTAATGTTTCACATTAAATGTTGCTGATCTTTTCTCTTTTTATGTTTTAGGTCATTTTCCTAACAAGGCGCTTCCTTCGGCTGGCACACTAGCATGGATTCAGGGCATTATATGCAATGTCAACAACCCCTGTTTTCATCAGCCTACAGCAGGGGAAACACCCGGGCTCGTGAGCAACTTCGACAACTCCATGTGAGAAGTCTTTTTGTTTTATCTCAGACAAATTTCTTTTTTTTAACTTCAGCCATTGATGGAGATTTATTTTGTTATTTTC[A/T]GACTTTCTCGACTTTTAGTCGATATGAGGACCGTCCTGACAATCAGTGGCAACCGAACAACCTTCTCTGGTCTTCAGGACCTGTCAAAGACAATCCAAAGACTCGGGGAAAGACCAGATGCCTGGCCAAGTATATATTCATTAAATATCTCATTTTAGAAGCTGAAAATGCTGTATCGGATGTGTTCAGTAGATTCAGTTAGTATCTCCTTAGCAAGCTCCTTGTACCTTGATGTTGTGTCTCACAGATAGATGAATTGAAGAACTTGGCTTAGTTTTCAGATAACCTCATGTGCCTCATCTAGAACCTCAATGTCTCAGTTTGTACAATACAATACAATACAATACAGTACAATACAATACAATACAATACAATACAATACAATACAATACAATACAATACAGTACAATACAATACAGTACAATACAGTACAGTACAGTACAATACAATACAATACAATACTATACAATACAATACAATACTATACAATACAATACTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24886
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 |
---|---|---|---|---|---|
ENSDART00000113281 | Nonsense | 236 | 1165 | 6 | 46 |
Genomic Location (Zv9):
Chromosome 11 (position 5680622)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 5650078 |
GRCz11 | 11 | 5596384 |
KASP Assay ID:
554-7304.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGGGGGCGCTGTGTGTTGTGCCCTCAGATATTATGCAGAAGGCAGAG[C/T]AAATCTTCCTCTCACAGCTGGACTTCAGCAAGATTGTTACGGTTAGTGAG
Long Flanking Sequence:
TTTCTAAAATGATGCTTGAATGCATCTAAAATGATGGTTAGGGTTGGTACAATTGGAAGTGGGGCAGGGCTTTTCAAAGGGTCAGTTTTTCAATAATTAGGTTTGATTAAATCTTACTCCGACTAGCTTGCATTCATTTCCCTTTTTTGAGCACAACCCTCTAAACTCAATTTCCAATCTAAAATTCAATTAACAAAACCAAGTCTCCACCATGCAATCTTCCGATTTAATGATTCATTATACTCACAATATGGAAGACTAGATCTGTCACTTCTTGTATTACATCATAGATGTGAACACACTGATCATTGTAGCATAGTAAGTTCTAAAGTTCTTTTTTTCTCAAGGTTACCTTAGCAGGAGAAGGAGTGCGTCTGTCTGACATTGTCTGTAATGCTTCACTCTTGAGCCGATACCTCACCGTTGAGGAAGGAGATTCTTTTCCTGAACTGCAGGGGGCGCTGTGTGTTGTGCCCTCAGATATTATGCAGAAGGCAGAG[C/T]AAATCTTCCTCTCACAGCTGGACTTCAGCAAGATTGTTACGGTTAGTGAGTTTACACTCTAATGTCCTGTGTTTATTTTGTTTAGTGTGGCGAGAGACTTTAAAGGGCACCTATGATGCAAAACCAACATCTGTAGGCAGAACTGTGTATAGGTATAGTGTGTCCTCTGTCATATTGCTATAAACACAAGTTTCTTTTTAAAATTTTCTGAAGTTGAAATAAGATAAAAAACCCAGTGATTTTGAGGCCAACTTCAACGTGACGAAGAGTGCGGTTTCCCCACCCACCAAATTGGTGAGGCCTGTATTAACATGTCTTCATAGTAACACATATGCACATTTCCACAGAACTTATTTTGCAAAGAAACTGGGATTAAAAGATCTGTTCAGCTCTCTGTGATCAGCTGCACCTCAAGAATGAGTTTTACAAGTTTAAAACATTTTAAAATCAGAGCATGTTGATAATAAAGACAGTAAAACTGCAATGTAATTCATAACTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45420
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 |
---|---|---|---|---|---|
ENSDART00000113281 | Nonsense | 718 | 1165 | 14 | 46 |
Genomic Location (Zv9):
Chromosome 11 (position 5700990)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 5670446 |
GRCz11 | 11 | 5616752 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTATTAAGCTTTGTGTCTCTCTGCTGTCTCTTGCAGTGGGGAGATATTT[T/A]ACCCTACAGTGACCCGGCTGTTGTGTTCTTCTTCCTGGCTGCGTTTGCTA
Long Flanking Sequence:
GCTGGTTCGACTCCCGGCTGGGCCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTGGTGTGGGTTTCCTTTGGGTGCTCCGGTTTCCCCCACAGTCTAAAGACATGCACTATAGGTGAATTGAATAAACTAAATTGGTCGTAGTTTATGAGTGTGAATGAGTGTGTATGGATGTTTCCCAGTACTGGGTTGCAGCTGGAAGGGCATCCGCTGTGTAAAACATATGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGAACCCTGATTAATAAGGAGACCTAGCCGAAGGAAAATGAATGAATGAATGTATGCAAATATGTAATTTGTCACACTTGTAAAATGGCGGAAACATTTTTAAAATGCATCTGGTAAGTGTTTTAAAAATGCTTGGAAAAGGTTTATAGTTCCTCTTAAATGTTTCTTAAAATTGTTAAAATATGTATTAAGCTTTGTGTCTCTCTGCTGTCTCTTGCAGTGGGGAGATATTT[T/A]ACCCTACAGTGACCCGGCTGTTGTGTTCTTCTTCCTGGCTGCGTTTGCTACAGCCACCATCATGCTTTGCTTCCTCATCAGCACGTTCTTCTCACGCGCTAACCTGGCAGCAGCGTGCGGAGGACTTATTTACTTCACACTTTACCTGCCGTATGTGCTGTGTGTAGCCTGGAGGGAATATCTGACCAGCACACACAGGATCTTAGCGGTGAGATTTTTTCCTCTGCCGGCTTGACTCCACAGATCATATATAGTTGAAGTCAGAATTATTAGCCCTCTTGAATTATTAGCCCATCTGTATATTTTTTTTACCAATTTTTTCAACACATTTCTAAACATAATAGTTTTAAAAATTAATTTCTAATCACTTCAGTTCTTTTATCTTTGCCATGATGACAGTACAGATTATTTGACTAGGTACTAGATACTAGTATTCAGCTTAAAGTTACATTTAAAGGTCCCATGGAATTAAAATAAAGTTTTTTAGATGTTATTATCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41771
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113281 | Essential Splice Site | None | 1165 | 41 | 46 |
Genomic Location (Zv9):
Chromosome 11 (position 5734404)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 5702515 |
GRCz11 | 11 | 5648715 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGTTTTACGCTCGCCTCAGAGGAGTGCCCGAGTCTTATGTTGAAAAG[G/A]TACAGGATGCTCCAAGCACATCATAATAAATATCTGAGTTAGTATTACTA
Long Flanking Sequence:
TTGAGTTGGACATCACAGATCTCTCTTAAGAACAAACATCACTTTATTTTTCTGTTCTGATAGTTTCAACTACAGCAAGTGTTTCTTTTACTGCCGTTTCAGTGTTTTGGGCTTCTTGGTGTTAACGGCGCTGGGAAAACCTCAACCTTCCGTATGCTAACAGGAGACACCCGGATCACATATGGAGAAGCGTTTCTTAGCAACCAAAGGTTAGACCATTAACATGTGGTGAACATTATGCTGATGTTTTTACAATAATTAGGTGCTTATTAATCCCAAAGTCTAATTTCCTTAATATTACTATACACTGGCAAATCGCTGCACCACCCTAATATTACCTACCATATGTTTTACTCAGCGTTCTTACAGAAATGGAGAAGGTTCATCAGCTGATGGGCTACTGTCCTCAGTTTGATGCCATCATTGACCTGCTGACGGGACGAGAGCACTTGGAGTTTTACGCTCGCCTCAGAGGAGTGCCCGAGTCTTATGTTGAAAAG[G/A]TACAGGATGCTCCAAGCACATCATAATAAATATCTGAGTTAGTATTACTACTAATATAAGGACCTGTGCCAGGGTCTGTCTAAGACTTAAGGGGCTGTTTGTAAAAACTGTTGTATATTAGTCACTTTTTAATCAGCAATGTGTGAACAGCTTGTCAATATATAGCTAATCTGCAATGTCCATGTGTTATGCAAAGACATAGGGAAAATGTAATTATAGGTTTACATAGCCAGATCTTGTATAATGTATACTTTCAAACACAACCCCAACTGAGAAAAGGTTTGGACATTTTGCAAAATCCATTGAAATCAAAAATCTGATTTTGTGAACTCTTTTTAACTTTATTTAATTGAAAAAAGTTGATAGAAAAGATTTCCAGTGTTTTCACAGACAAACTAAAATGTATTTTAGAAATAAAAACTTTTTTTTTATTTCGATGGCTTCAGTGCACTAGAACGGTTGAGACAGAAGCAAAATAAAAGTGGGAAGGTTACAGATTA
Associated Phenotype:
Not determined