ZMP
abcg5
Ensembl ID:
ZFIN ID:
Description:
ATP-binding cassette sub-family G member 5 [Source:RefSeq peptide;Acc:NP_001122162]
Human Orthologue:
ABCG5
Human Description:
ATP-binding cassette, sub-family G (WHITE), member 5 [Source:HGNC Symbol;Acc:13886]
Mouse Orthologue:
Abcg5
Mouse Description:
ATP-binding cassette, sub-family G (WHITE), member 5 Gene [Source:MGI Symbol;Acc:MGI:1351659]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22240 | Essential Splice Site | Available for shipment | Available now |
sa17622 | Nonsense | Available for shipment | Available now |
sa2683 | Nonsense | F2 line generated | Not yet available |
sa42150 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22240
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 |
---|---|---|---|---|---|
ENSDART00000091845 | Essential Splice Site | 92 | 652 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 13 (position 10513080)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10815409 |
GRCz11 | 13 | 10947884 |
KASP Assay ID:
2260-6109.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCATTTCATTTGGACAGTGGCCAGATAATGGGAATTCTTGGAAACTCAG[G/A]TAAATGTCTTAAAATCTGTGAGAAAAAGAATGACTGCAATGCTTTCAATT
Long Flanking Sequence:
AGCTGGAACTGTTTACAGGTAACGATTAAAATAAAATTCAATTCATGTTTATTTCTATAGCACTTTTACAATGTAGATCGCGTCAAAGCAGCTTAAGATAGAAGTTTAGTAAATTGAATCTGTGTCAGTCCAGTTTTCAGAGTTTAAGTTCAGTTTAGTTCATTTCAGTGTGGTTTTAATCTCACAGCTGAAAGTCCAAACACTGTTGAGCAAATCCACCGATACGCAGCTTAACAAGTCCCAAAACAATTAAGCCAGTGGCGAGGAACAAACTTCACCAGTTGACTAAAGTGAAGGGAAAAAAATATTGTCCAAAATATTGATAAGCTAACATTTTTATGCTCATATCATATACATTTTATTTTTTCACTGTTACAGTGAACGTGTAGGACCCTGGTGGGATCTTTCATCTTTTCGAAAAAAATGGACAAGGCAAATATTAAACGAAGTGTCATTTCATTTGGACAGTGGCCAGATAATGGGAATTCTTGGAAACTCAG[G/A]TAAATGTCTTAAAATCTGTGAGAAAAAGAATGACTGCAATGCTTTCAATTATAACACATTGTTAGAACAGAGCCTAGCTAACATGCTATTGACTTATAAATATGTTCATTTGTGAAATTTACTGTGATATTTCACTCAAAGATGAACATTTAAAGTGTTTATTTCTCCCTCAAGTGGTTGCAAACCCTTATGAGTTTCTTTATTCTGTTAAACAAACAAGATCTTTTGAAGAAAGCTGAAAACTGATAACCCCTGACATTCATAGCAGGAAAAATAATAATACTAATATGTAAGTCAGTGGTTACAGGTTTCCAACTCTTTTTAAATGATCTTCATCTGTGTTCAACAGAAGAATTACAAATAGATTTGGAAGGAGTGGAGGATGAGTAAAAGATGACAAGGTTAAAATTTTTGGGTGAACTCTCCCTTTAACTAAATACAATTTAATATAAGATGTTTTAAAATATAACAAAAAATAATAATATTTACAAATCTTTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17622
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 |
---|---|---|---|---|---|
ENSDART00000091845 | Nonsense | 128 | 652 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 13 (position 10513850)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10816179 |
GRCz11 | 13 | 10948654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCWACCTYCAGGGAGAAGTGTTTGTGAATGGACGAAAGCTRAAAAGAGAA[C/T]AGTTTCAAGACTGTTTCTCTTMCGTTCTGCAGGTGAGATTAAWTGTTATT
Long Flanking Sequence:
AAAAATAATAATACTAATATGTAAGTCAGTGGTTACAGGTTTCCAACTCTTTTTAAATGATCTTCATCTGTGTTCAACAGAAGAATTACAAATAGATTTGGAAGGAGTGGAGGATGAGTAAAAGATGACAAGGTTAAAATTTTTGGGTGAACTCTCCCTTTAACTAAATACAATTTAATATAAGATGTTTTAAAATATAACAAAAAATAATAATATTTACAAATCTTTCCCAGTATTGTTAAACGTATATGGATTAGAACATGACAATAAGCAATAATAAAGAATGAACCTGGAAATGTATTATACACTTATATTACATTTACAATACATAATAGTTTCTTTAAAAGTCAGATGATATCCTCATATGGTAATAAACGTTTTGATCTTCTCCTTAAGGTTCTGGAAAGACCACTCTGTTAGATGCTATAGCAGGGCGCATTGGGAATTCTGGCAACCTCCAGGGAGAAGTGTTTGTGAATGGACGAAAGCTAAAAAGAGAA[C/T]AGTTTCAAGACTGTTTCTCTTACGTTCTGCAGGTGAGATTAATTGTTATTAAAGGTAAAATTCCCCCAAAATGACAATTTACTGAGTATTTACTCAACTGCAGGTGCTTATAAACCTTTATGAGTTTCTTTCTTCTGTTAAACACAAAAAGAAAGTTGAAAACCAGTAACTATTGATTCCCATATAGAAAAAAATAAATGCATGTCAATAGTTATAGGTTTTCAACTTTCTTCAAAATATCTTACTTTGTATATAAAAGAAGAGAGAAACTCATTATGTGTGCATGCTTCAAGTATAAATGTCAAGATGCATTTAACTGAACTCTGGCCAACAGTAGTGTACAGTATACATATGAAAAGCGATTGACTGACTGGAGGTCGCGTCTGCTGTGACCAAACTTAAGCAAATACAGTAAAGTTTGTAGAAAAGTTCATCTGTAGAGTCCGCTCTGAAATTGGCCGTTACACATGAGTTGGTTATAATATTCTTCTGAGCTACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2683
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000091845 | Nonsense | 436 | 652 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 13 (position 10525121)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10827450 |
GRCz11 | 13 | 10959925 |
KASP Assay ID:
554-2577.1 (used for ordering genotyping assays)
KASP Sequence:
GTACAGGACCGAATCGGCCTAATCTACCAATCCATGGGTGCATCTCCCTA[T/A]ACCGGAATGCTGAATGCTGTGGCTCTATGTAAGTATACAGATAACAATCG
Long Flanking Sequence:
GTACAAGTATTGTTTATTTTTAGTTTACTCATCCTCCACTTGCTTCAAACCTGTTTGAGCTTCTTTCTTCTGTTGAACTGTGGATATTAAAGATGTCAATGGCTGTTTTTTTTCCCCTGATCATCTTCATAATATTGTGCTTTGTGTTCAACGGAAAAAATAAATTCATAGTTAATGAGTTAATGTTGAGACAATTTTCATCTCTTTAACTAAAATGAACTAACGGAACCTTGTTTTAAAATGTGACTAGATTATCTTAATAGTCCATAATGTTAATGCTATATTTATTCATACATTTTTTGCTCCTTTACATGCACACATAGACGGACCTTTCGCAACGTGTCCCGTGACAGGATGGGTATTCTCATGCGTCTCTCTCAGAATCTCATCTACGGCCTCTTCATTGCTTTTTTCCTCATGAGGCTTGGTAAGGATGTGACAAAAGGTGCCGTACAGGACCGAATCGGCCTAATCTACCAATCCATGGGTGCATCTCCCTA[T/A]ACCGGAATGCTGAATGCTGTGGCTCTATGTAAGTATACAGATAACAATCGATGTATTGTTCTATGCAGCCTGCAATCTGAGTGAAATCATTTTCCATCATGATTTACAAGAACAGCATATAATTCTTTTACCTGTATTTACTAAAATATGTAAAATGTTAATCATACAAATTTTTATTTTTGTTTTGGGTAAATGGGTAAATCTAGTGGTTTAAGGCAGGTTTTATCAAACTTTTCAGCTTGCGAACCCCAAAATAATTCCAGTGACTCGTGACCCCCACTATTCATGGAGGTGGTTTCAAACATGCAAACATTGCACAGACACACTAATAGAAACTATATAAGCAAGCTTATTGACAACACAAAATCATGCAACGGAATAAAAACCATATAATTTTTTATAGTCGTTATTCATTAGTTTAGTTTAATATTAACCTCACCTAATGAGAATGGTAGGCATAATAATTACAGCACAAGATTCTTGGTTTAATTTTAGAGAAA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa42150
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 |
---|---|---|---|---|---|
ENSDART00000091845 | Nonsense | 612 | 652 | 13 | 13 |
Genomic Location (Zv9):
Chromosome 13 (position 10533341)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10835670 |
GRCz11 | 13 | 10968145 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCTTGCCAGGAGAGTGTCTGGTAGACAGTGGGAATATGATCATAGAT[C/T]AGGGTTATCCTGGAGCTCTGTCCCGTTACACTCAAGACTTCCTGTTGCTC
Long Flanking Sequence:
GCGGTGTAGGTGAATTGGGTTGGCTAAATTGTCCGTTGTGTATAAATGTGTGAATGGGGGTTTCCCAGTGATGTGTTGAGGCTAAAAGGGCATCCACTGCATAAAACATATGCTGTATAAGTTGGCGGTTCATTCTGCTGTGGCGACCCTAGATTAATAAAGAGACTAAGCCGAAAATAAAAAAAAATGAATGAATGAATGAATGCTTACAAAATAATGGTGCACAAACATCGTTTATAACAAGCACTACTAAATACATATGAAAATAAGAAGTCTATTTTGATTTCATTCTGACTTTAAGTGCATCACTGCAGAATAAAAGATATTTTTGAACAAATTTTTTATATCACTTTTGCCTGAATCTTATTTCGATTCACTGTTTTTAACAGATATAATGCATACGTTTTCCAGACTAACCACTTTTCTCTCTCTCACTCTCAGCCCCTATAGCTGGCTTGCCAGGAGAGTGTCTGGTAGACAGTGGGAATATGATCATAGAT[C/T]AGGGTTATCCTGGAGCTCTGTCCCGTTACACTCAAGACTTCCTGTTGCTCTATGCCTTCCTGCCCGCTCTTGTGATCCTGGGCATCATCAGCTTCAAGATACGAGACCACCTCGTCAGACGCTGAGCCTCCATGTGTGTGCACATGTGTGTGTGTTATTGTGTACAGAATGCTATGTTCTTTATTTGTATTTTTGTAGATCATATATTGTAGGTTATATCCAGACAACATCACCATGGGAGCTAATGCTTTTCCAATGAAACACATCAATTTTCTTCGTAAAGTTTTGTACTATAATGTGATTTTAAATGTGACTGAACAAATAATCTATTATTATAAGACACCTGTTTTGTCTTTGCTGGTCATTAGTGCATATTATTGCAGCCACATTTCTTTATACAAGATGTTATGTTTCATTCTGCTGGCTGTAACATGTAACCTAATAAACAACTTTGCCTGCTTTAAGGCTTTGAGATTTATTCTCTTTCTCAATTATGATAA
Associated Phenotype:
Not determined