ZMP
abcg8
Ensembl ID:
ZFIN ID:
Description:
ATP-binding cassette sub-family G member 8 [Source:RefSeq peptide;Acc:NP_001108041]
Human Orthologue:
ABCG8
Human Description:
ATP-binding cassette, sub-family G (WHITE), member 8 [Source:HGNC Symbol;Acc:13887]
Mouse Orthologue:
Abcg8
Mouse Description:
ATP-binding cassette, sub-family G (WHITE), member 8 Gene [Source:MGI Symbol;Acc:MGI:1914720]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22239 | Nonsense | Available for shipment | Available now |
sa22238 | Nonsense | Available for shipment | Available now |
sa35429 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22239
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 |
---|---|---|---|---|---|
ENSDART00000091773 | None | None | 256 | 2 | 9 |
ENSDART00000114315 | Nonsense | 55 | 332 | 2 | 6 |
ENSDART00000128765 | Nonsense | 32 | 654 | 1 | 13 |
ENSDART00000147541 | Nonsense | 33 | 654 | 1 | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 10509212)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10811541 |
GRCz11 | 13 | 10944016 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACTTACAGCGGAGGCCGCAATGAACTGGAAGTCCGCAATCTCAACTA[T/G]GAGGTCAGACACTTCGGTCCACATTTTTGGTCTTTATTCTTTCCACTGCC
Long Flanking Sequence:
CACCCCTCACAGCAAGAAGGTCGTTGGTTCGAGCCTCGGCTGCGTCATTTGGCATTTCTGTCTGGAGTTTGCATGTTCTCCCCTCGTTTGCGTGGGTTTTCTTCGGGTGCTTCGGTTTCCACCACAAGTCCAAAGACATGCAGGTTAGGTGAATTGGGTAAGCTAAATTGTCCATAGTGTATGTAAGTGAATGAGTGTGTGTGGATGTTTCCCAGTGATGGGTTGCAGCTAGAAGGGCATCAGCTGCGTAAAACATTTACTAGATAAGTTTGCAGTTCATTCTGCTGTGGCAATCCCAGATTAATAAAGGGACTAAGCGGAATGAATGAATTAATGAGTGGATATTTACTTATTGGCTTTGGCACTAACTAATCTTATGTTGCTCTGCCTCAAAACACGCAGGGTCGAGATATTCTTTTTTCATCTCCAGAGGAGGACAGCAGTCTGTATTTTACTTACAGCGGAGGCCGCAATGAACTGGAAGTCCGCAATCTCAACTA[T/G]GAGGTCAGACACTTCGGTCCACATTTTTGGTCTTTATTCTTTCCACTGCCTTCAATCAAAGCCTTTCCGAAAGCTTACATCAAATGTAAATTTCAACCAAAACATCGTTTTACCCACCCTCCATTTGTTCTGTTTTCTGTGTAAATAAATTAAGAAACCAATAGCCATTGTCACCAATATCAAAAAATATATATATTATGGAAGTCAGTGGCTACAACATTCTTTTAAAAAACTAGTTAAAATCTTCTTTAGTGTTCAACAGAAGAACAAAGCACAAATAGGTTTGAAAGTGGGGGTTGAGTGAATGATGCCTGAATTCAAAACTGAAACAATGTACCAATTCTGGCCTGCACTTAAACGTTAAAATAAATATATAAAAGAATATTTATGATATTTTATGTTACATGATTAATAACTTGGCTGATAAGTGAGTAAAATTCAGTGCTTTGAAGAATAGTGGCAACATATAAAGGTTCAAAATGACAATTAATTAATAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22238
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091773 | Nonsense | 229 | 256 | 8 | 9 |
ENSDART00000114315 | Nonsense | 307 | 332 | 6 | 6 |
ENSDART00000128765 | Nonsense | 284 | 654 | 5 | 13 |
ENSDART00000147541 | Nonsense | 285 | 654 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 10502035)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10804364 |
GRCz11 | 13 | 10936839 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTGTGGTCAGGCCAAAGACATGGTGTCTTACTTCACCACTCTCGGGTA[C/A]CCGTGTCCACGCTATTGCAACCCGTCCGACTACTACGGTGAGTGGGACTC
Long Flanking Sequence:
AAACTGCTTTTATTCTAGGCGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAAATTGATCAGACTTACTGTGAAAATGTCCTTGTTCTGTTAAACATCATTTGGGAAGTATATATGTATATACACAATTAATAAAACGACTACAACATACAAAAGAAAAAGAAAACCTATATTAAGGAATCAAAATGTCAGTTAAACAAATTTGATTATCAATAATACTAAAATAACACTTTGTTTATAGGCTTTTCATTTTGTGTGTTTTCAGGTATACTCATTCTAGATGAGCCTACTTCAGGTCTGGACAGTTTCACGGCTCATAATTTGGTCATCACATTATATCGTCTGGCTCGAGGGAACCGGCTAGTGTTGCTGTCAGTGCATCAGCCTCGCTCAGATATCTTTCAGCTCTTTGACCTTGTGGTGCTGCTGTCCTCTGGTTCAGCCGTGTACTGTGGTCAGGCCAAAGACATGGTGTCTTACTTCACCACTCTCGGGTA[C/A]CCGTGTCCACGCTATTGCAACCCGTCCGACTACTACGGTGAGTGGGACTCTAAAGTGATGACTGATCACTTTAGCTGATCCTGCTGTTTGGTTATTGTTTCTTAACTGTGAACTTCTAATGCAGTGGACTTGATAAGCATTGATCGGCGCACTCCTGAAAAAGAAGCACAGTGTTTGGAGAAAGCCAGCATGTTGGCGGCCCAGTTTTTAGAGAAGGTGAAGAACAATGAAGATTTCATGTGGAAATCGGAAGTCTGTGGTCCTCCGGCACTGGAAGCCCCTCAAAGGTAGCCTATAGAGTTTCAAATTTATATTGTTGTTACATCATGAAGTTTTTTTTTTTCCTTTGTTTTTTTCATTTCTCCACGAAATGCGTGAACTGTCATAATAAATTTTCTGTGAAGTCTTATTTTTGTGTCTATAAATAGATGTAGCGTTTCCTCATGTCTGAATTCTGTATGCAAGTTACATGAATTTATTTACTTATTTATATTTCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35429
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091773 | Essential Splice Site | 242 | 256 | 9 | 9 |
ENSDART00000114315 | None | None | 332 | 6 | 6 |
ENSDART00000128765 | Essential Splice Site | 297 | 654 | 6 | 13 |
ENSDART00000147541 | Essential Splice Site | 298 | 654 | 6 | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 10501911)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10804240 |
GRCz11 | 13 | 10936715 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGATCCTGCTGTTTGGTTATTGTTTCTTAACTGTGAACTTCTAATGCA[G/A]TGGACTTGATAAGCATTGATCGGCGCACTCCTGAAAAAGAAGCACAGTGT
Long Flanking Sequence:
TACACAATTAATAAAACGACTACAACATACAAAAGAAAAAGAAAACCTATATTAAGGAATCAAAATGTCAGTTAAACAAATTTGATTATCAATAATACTAAAATAACACTTTGTTTATAGGCTTTTCATTTTGTGTGTTTTCAGGTATACTCATTCTAGATGAGCCTACTTCAGGTCTGGACAGTTTCACGGCTCATAATTTGGTCATCACATTATATCGTCTGGCTCGAGGGAACCGGCTAGTGTTGCTGTCAGTGCATCAGCCTCGCTCAGATATCTTTCAGCTCTTTGACCTTGTGGTGCTGCTGTCCTCTGGTTCAGCCGTGTACTGTGGTCAGGCCAAAGACATGGTGTCTTACTTCACCACTCTCGGGTACCCGTGTCCACGCTATTGCAACCCGTCCGACTACTACGGTGAGTGGGACTCTAAAGTGATGACTGATCACTTTAGCTGATCCTGCTGTTTGGTTATTGTTTCTTAACTGTGAACTTCTAATGCA[G/A]TGGACTTGATAAGCATTGATCGGCGCACTCCTGAAAAAGAAGCACAGTGTTTGGAGAAAGCCAGCATGTTGGCGGCCCAGTTTTTAGAGAAGGTGAAGAACAATGAAGATTTCATGTGGAAATCGGAAGTCTGTGGTCCTCCGGCACTGGAAGCCCCTCAAAGGTAGCCTATAGAGTTTCAAATTTATATTGTTGTTACATCATGAAGTTTTTTTTTTTCCTTTGTTTTTTTCATTTCTCCACGAAATGCGTGAACTGTCATAATAAATTTTCTGTGAAGTCTTATTTTTGTGTCTATAAATAGATGTAGCGTTTCCTCATGTCTGAATTCTGTATGCAAGTTACATGAATTTATTTACTTATTTATATTTCAGAGTACTATTATTAATAATGTGTTTGAAAAAAAAAATCAAGTTTTTTTGAGGAAAGGAATTCAAAGGAATATCAAATATTATGGCTCAGTTGTTTGCACTGTCGCCTCACAGCAAGAAAGTTGCTGG
Associated Phenotype:
Not determined