Busch Lab

ZMP

abcg8

Ensembl ID:
ENSDARG00000063059
ZFIN ID:
ZDB-GENE-050517-41
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
sa38923 Nonsense Mutation detected in F1 DNA Not yet available
sa35429 Essential Splice Site Available for shipment Available now
sa42149 Nonsense Mutation detected in F1 DNA Not yet available

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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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:
sa38923
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091773 Nonsense 235 256 8 9
ENSDART00000114315 Nonsense 313 332 6 6
ENSDART00000128765 Nonsense 290 654 5 13
ENSDART00000147541 Nonsense 291 654 5 12
Genomic Location (Zv9):
Chromosome 13 (position 10502017)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 10804346
GRCz11 13 10936821
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACATGGTGTCTTACTTCACCACTCTCGGGTACCCGTGTCCACGCTATTG[C/A]AACCCGTCCGACTACTACGGTGAGTGGGACTCTAAAGTGATGACTGATCA
Long Flanking Sequence:
GCGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAAATTGATCAGACTTACTGTGAAAATGTCCTTGTTCTGTTAAACATCATTTGGGAAGTATATATGTATATACACAATTAATAAAACGACTACAACATACAAAAGAAAAAGAAAACCTATATTAAGGAATCAAAATGTCAGTTAAACAAATTTGATTATCAATAATACTAAAATAACACTTTGTTTATAGGCTTTTCATTTTGTGTGTTTTCAGGTATACTCATTCTAGATGAGCCTACTTCAGGTCTGGACAGTTTCACGGCTCATAATTTGGTCATCACATTATATCGTCTGGCTCGAGGGAACCGGCTAGTGTTGCTGTCAGTGCATCAGCCTCGCTCAGATATCTTTCAGCTCTTTGACCTTGTGGTGCTGCTGTCCTCTGGTTCAGCCGTGTACTGTGGTCAGGCCAAAGACATGGTGTCTTACTTCACCACTCTCGGGTACCCGTGTCCACGCTATTG[C/A]AACCCGTCCGACTACTACGGTGAGTGGGACTCTAAAGTGATGACTGATCACTTTAGCTGATCCTGCTGTTTGGTTATTGTTTCTTAACTGTGAACTTCTAATGCAGTGGACTTGATAAGCATTGATCGGCGCACTCCTGAAAAAGAAGCACAGTGTTTGGAGAAAGCCAGCATGTTGGCGGCCCAGTTTTTAGAGAAGGTGAAGAACAATGAAGATTTCATGTGGAAATCGGAAGTCTGTGGTCCTCCGGCACTGGAAGCCCCTCAAAGGTAGCCTATAGAGTTTCAAATTTATATTGTTGTTACATCATGAAGTTTTTTTTTTTCCTTTGTTTTTTTCATTTCTCCACGAAATGCGTGAACTGTCATAATAAATTTTCTGTGAAGTCTTATTTTTGTGTCTATAAATAGATGTAGCGTTTCCTCATGTCTGAATTCTGTATGCAAGTTACATGAATTTATTTACTTATTTATATTTCAGAGTACTATTATTAATAATGT
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.
Availability:
Order Allele From ZIRC
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

Mutation Details

Allele Name:
sa42149
Status:
Mutation detected in F1 DNA
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
ENSDART00000091773 None None 256 None 9
ENSDART00000114315 None None 332 None 6
ENSDART00000128765 Nonsense 359 654 8 13
ENSDART00000147541 Nonsense 361 654 7 12
Genomic Location (Zv9):
Chromosome 13 (position 10499046)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 10801375
GRCz11 13 10933850
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTATGCTTTTTTTCTACACCAGCAGTGTTCCTTCTGTCTCAATGAAA[G/T]AATCAGTGATCACAGTTTCCAAACAGAAGGATCAGCTGCCGGGAAAAGTG
Long Flanking Sequence:
CTTTTTTAGATCAGAATGCCTATGGCCGCACATATGAGCGCAAATGCAAGCTGAAACTAGCAAACAACAATAGCGTCGCGCCTTTCGCCACATTGCGCCGGGTGTATGATAGGGCTCCTTGTATGTATATATACACTGAAAAAAGTGTTGCATGCAGAACTGTTGTAAACAATTTACTTGTGTTGAATTTAAACAAACAAATTAAGTTTAATGATGTTCAACTTAATTTGTTTGTTTAATTTCAGCCCAAATAAATTGTTTACAACCACTTAACGTATACAAATTGAATAAATACAAGGAATCATCTTTAAATAATTTTTTTAGTGTAGTGTATGTATAGTAAGTTTATCAGGCACAACAAAAACATGTTTTATTACATTTCTGGTCAAAATAGACCAAAAATGTGTTTGAAAATCTTATATATTATAAGAGAGATTTTTGATCCTATGTTTTCTATGCTTTTTTTCTACACCAGCAGTGTTCCTTCTGTCTCAATGAAA[G/T]AATCAGTGATCACAGTTTCCAAACAGAAGGATCAGCTGCCGGGAAAAGTGCATCAGTTCACAACCTTAATCAGGTAAAAAACCACAACAGCTTTTAAAAAGACTAAATAAAGGCACTTTAACATTCATAGAACTTTGGCATTCCACAAAAGACTATTTAAAGTGGAAAAGGTTAAAATAATGTTCTTCTATAATAATAATTTTATGAACTTAACGAATTCTTTAGGTAACGCAGAATAATTGTACTATGGCAACTCAGTAAAAAAAAAAAAACATTAAAATGAAGCACTTTTTTTAAAGAGTATCTCAAAATTGTCACCTGATAGCTGTTTGCCAAGACATTCCTGTATTTTTTTCTCAGACGGCAGGTATTTAATGACTACCGGGACCTGGTGACACTGGTGGTTCATGGTTTAGAAGCTTTGCTGATGTCATTGCTCATCGGTTTCCTATATTTCGGGTGCACAGAGGAAGGTCTTTCCATCCAAGATACAGTGGCTT
Associated Phenotype:
Not determined