ZMP
abcg1
Ensembl ID:
ZFIN ID:
Description:
ATP-binding cassette sub-family G member 1 [Source:RefSeq peptide;Acc:NP_001103924]
Human Orthologue:
ABCG1
Human Description:
ATP-binding cassette, sub-family G (WHITE), member 1 [Source:HGNC Symbol;Acc:73]
Mouse Orthologue:
Abcg1
Mouse Description:
ATP-binding cassette, sub-family G (WHITE), member 1 Gene [Source:MGI Symbol;Acc:MGI:107704]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22581 | Essential Splice Site | Available for shipment | Available now |
sa35797 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35798 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35799 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22581
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 |
---|---|---|---|---|---|
ENSDART00000092809 | Essential Splice Site | 102 | 673 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 15 (position 4892471)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 5042524 |
GRCz11 | 15 | 5033671 |
KASP Assay ID:
2260-8102.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAAGACCTCTCGTATTCCGTTCCTGAAGGACCATGGTGGAGGAAAAAAG[G/A]TAACGTGTGACCTTTTAAATGGCATTCTGAGGTAAATAAAAGTATTAGTA
Long Flanking Sequence:
GACTGAAACAACCCTTTGAATGTTTTACTCATTCATTTTGAATAACATTTATTACAACATCTACGTATTATATGTTATTTTTATTATCATTTGCTGTTATTATATGTTATTTTGCCATCTTCGAACACTGTATGACTGCAAACTTCTGCACACGTGAATTTTTCCGACAGAGCTTTAATCCTCAGGGCGAATGCTTCAGGGTTTTTCCCTCAAGGCTGCAGCGCATTACATAACCGTGCTGTCTCTCCTTCCCCAGAATACAAATGGACCTCCTGATCTCATGCTTGACCCCAGAACCGTGTGTGTTTCCATTGATGAAATGATGTCCAACCATGTCAGCAGTCAACAAACACCACTGTTACATGCACACCTGAAAAAAGTGGAGAACAATCTGACCGAGGCGCAGAGGTTCTCATACCTGCCTCGCAGACCCGCAGTCAACATCGAATTCAAAGACCTCTCGTATTCCGTTCCTGAAGGACCATGGTGGAGGAAAAAAG[G/A]TAACGTGTGACCTTTTAAATGGCATTCTGAGGTAAATAAAAGTATTAGTAGCATTAGAGATTCAGTGTACTCGTGATTTATCTTCTGTAGAAACCTGTTCTGACACTCAATAGCAACAAGTATGTGTCTATGATTTTACCAATGCAATACTGGTTATGTTTGAACACAGTATTGGTTTAATGCTCTAAAAAAAAAAATCTACACGCTGTAAAAAATCAACAAAATCTGTTCATTACCACTTATCGTATTTTGTGATTCTAAGGTGTTTTCCTTAATTTATGGACATGGATTTTGCATATTGGGACCTTGATCTCTACTCTGTAGACTTTTGATGTTGAAAATACATCTCTGCTGTTTAATAGGGTGAATTATTGACATTTTAGTATAAAAAACCATGTATAATATAATAAATGCAATAATAAACACAACTCAACGGTGAAGAATGGTTCCAAAAAGTGGGTAGGAAAAAAACAGAATCCAAAAGTAAACAAGTAAATAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35797
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 |
---|---|---|---|---|---|
ENSDART00000092809 | Nonsense | 282 | 673 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 15 (position 4922023)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 5072076 |
GRCz11 | 15 | 5063223 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGAAGGCTCTCGCTCAGGGTGGAAGAACCGTCATCTGCACAATACAC[C/T]AGCCCAGCGCTAAAGTCTTCGAGCTCTTCGACAAGGTGATAGTTGTGTTT
Long Flanking Sequence:
AGATGTTTTGAAAGATATTTTGAAAAATGTTTGAATGGCTGTAACCATTGACTTGTATAGTGAGATAAACAAGTACTATGAATGTTAGTGGTTGCAACATTTTTCAGAATATCTTCTTTTGTGTCCAACAGAAAAAAAGGGATTTAAATGATGACAGAATTATAATTTTTTGGTGAGCTGTCCCTTTAAGATGATCTAAGGTGTTTCTAATAAACATTTTCATATTTTACAATTAAAGCTACAGCCTCTAATTGTCCTCAGCAATGGACATACAGCATCAGTGTGAAGAGGCCTTAGAATGCAAAGTTCTAATACACGAGGTTTTATAGAAGAATGGTTGATGTAAGCCAGTTTGAAACGTTTTCTTTTTACCAGTGTAGTGATGCTTTTCTTCTTTTTTTTCCTCATGAAGTGGCCTGGACTCGTCCTCCTGCTTTCAGGTGGTGTCTCTGATGAAGGCTCTCGCTCAGGGTGGAAGAACCGTCATCTGCACAATACAC[C/T]AGCCCAGCGCTAAAGTCTTCGAGCTCTTCGACAAGGTGATAGTTGTGTTTGAAGTGTGTAAATGTAAATTTTCTCCACTAGAGGGCGCATGTTGCCAACAAACAAAGGCGTAATTTGATGAGTGTGGATTCATTGGTGCTGTGATCTTTATTACATCCTATAGATTGATTTCACGCGGCCTCCATTTTTAAAAGCGAAGTCGAGGCTGTGGTTGGAAGAAACACAGAAGTATCGTTGGGAGTTGCATAGGAACGTTGTGCACTTGGCTGTATATCTTAGCAGTGAAGATAAAGTGACACAAATGTATTATTCCACCGCCTTCCGAGTGACCTCAAGGTTCGTTCTGAATGAATGGTGAAAATAAAAAGGAATATCAGAGCTCCTTTTCAGCTAAGTTAAGGGAAATGGCACTAGTTAGCTAACGTTTTCTTTCCCAAACACACATTTTAGATGCCATTTATTAAACTCTAGTTAATAAACTGATTCTTTCACTATATTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35798
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092809 | Nonsense | 361 | 673 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 15 (position 4926122)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 5076175 |
GRCz11 | 15 | 5067322 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTCGTCTGGTGAAAGCTGTGCAGGAGCACAAGTGCGAGAAAGACTAC[A/T]AAACTGAAATGAATGGCAACGGAGTCCACAATCCATTCCTGTGGCATAGA
Long Flanking Sequence:
TTATTATCAGCATCATCATCATTATAACAATAATAATAATAATATTTTTTATAATTATGCATTGTTAAATATTGTTTTTAGCTACTTATTAAATAATGTAATATAATCAGTGTGCTTTAATGATGATAATAATGATGATAATAATAATAATAACAACAATTATTATTGTTGTTGTTGTTGTTATAATACTGCTACTACTAATAATAATTACAACAACACTTATAATTGTTGTTATTGTTATAATACTGCTACTACTACTACTACTACTACTACTACTACTACTACTACTGCTACTACTACTAATATTAATTTTGAAAACATTTTATTTATTTATAATTATATAATTATATTTAACAAAAAACATGAAAATGTGAGTTCTCTCAGACTCAGTGTGTGTTTGTGTTGTGTTGTCAGTAATGGAGGTGGCGTCTGGTGAATACGGTGATCAGACAGCTCGTCTGGTGAAAGCTGTGCAGGAGCACAAGTGCGAGAAAGACTAC[A/T]AAACTGAAATGAATGGCAACGGAGTCCACAATCCATTCCTGTGGCATAGACCATCCGATGAGGTGTGTATACAGAAACGCCATTTTACAGAGAATTAAACAACAAGCAGACAGTAATGAAGGCTGTTTTTCCTGCAGGACTCTTCATCTTCAGAGGGATGCCACAGCTTCTCTGCCAGCTGTTTGACGCAGTTCTGCATCCTCTTCAAGAGAACTTTCCTCAGCATCATGAGAGATTCGGTAAACAACACTGACACCTGCTGGACGACTTCAGGCTTTGTAGGCCAGATTCATGTGAAAATGTTAATGTTTTGAAAATAAAGTCGGCCTTTTATTCCTGCGATGAACAACTACACAATTATCTGAAAATACTTAAAAAGCACTTTGAAAATGTCAATAATAAATCATTATTTGTGGTATTTTTAAGTGTTCAGGATATCAATATTGTGATGTAGTAAATATATTAGTATACGTCCACTTATAATATAATGTACAGAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35799
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092809 | Nonsense | 491 | 673 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 15 (position 4927802)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 5077855 |
GRCz11 | 15 | 5069002 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAGATGGGTGTGTTTTTGAGAGAGCATCTAAATTACTGGTACAGTCTG[A/T]AGGCTTACTACTTAGCCAAAACAATGGCGGACGTCCCGTTTCAGGTAAGA
Long Flanking Sequence:
GATTTGTAGCCGATCGAGAAAAAAAGGGAATTAAGGAAACTAATAGTATTCACCTTAAAATTAATGATAATAAAAAAAATTAACTGCTATTATTCCACTCAAACTGAAAGAAAGAAGGCTTTCTATTTCAGAAAAAAATTATACTATACATAAATACATTATGATCTTCTGTGTTTAGGTGTTGACTCACTTGCGGATCATGTCTCATCTTGGCATCGGGATTCTGATCGGGCTTTTGTATCTGGGCATCGGCAACGAGGCCAAGAAAGTCCTCAGCAACTCCGGCTTCCTGTTCTTTTCCATGCTGTTCCTCATGTTTGCAGCTTTGATGCCCACCGTTCTCACCTGTGAGTCTGGTGAAAAAAACAAACAAACATCATATTCTTTCTAGAGACAAGCATCTGACGAATACTTTCTATCTAATTGTTCTTGCTGTTTTTGCAGTTCCACTTGAGATGGGTGTGTTTTTGAGAGAGCATCTAAATTACTGGTACAGTCTG[A/T]AGGCTTACTACTTAGCCAAAACAATGGCGGACGTCCCGTTTCAGGTAAGAGAACAAATAAAACATGGGGTTTTCTCCTGAAAAAAAGTTGATAGTTTGGTTCTGCTGCTAAGAAGAATTATTCACAATTCTATTCCTTTATTATAAGAACACAGTAAAGTGAATGTGAAACATAGTTTTGAAACAATTTCAATTAAATAAAGGTATTTTCATGCGTGTTTCACTTACGATTTTAACATGTTCATTTTAAATGTGTAAAATCGATTTTTCGAGGCTGATCTTTTTTTTTAAATTTTTGGCAATTTTGACTTGTAATGAAGTAATTTGTACAGTAAGGTATCTGTACTTTTACTCAAGTATGGTTTTCGGGTACTCTTTACACCACTGGTTGGAACTAAACTGTGCAGGGCTGCGGTCTTCTAGGAATTGAGTTTGACATCCCTGATCTAGATCTTGTCTACAAGCCAATGTTAGGGTTAAATATTTGATTATTAGAAATCT
Associated Phenotype:
Not determined