Busch Lab

ZMP

abcg2c

Ensembl ID:
ENSDARG00000058574
ZFIN ID:
ZDB-GENE-050517-37
Description:
ATP-binding cassette, sub-family G (WHITE), member 2c [Source:RefSeq peptide;Acc:NP_001034728]
Human Orthologue:
ABCG2
Human Description:
ATP-binding cassette, sub-family G (WHITE), member 2 [Source:HGNC Symbol;Acc:74]
Mouse Orthologues:
Abcg2, Abcg3
Mouse Descriptions:
ATP-binding cassette, sub-family G (WHITE), member 2 Gene [Source:MGI Symbol;Acc:MGI:1347061]
ATP-binding cassette, sub-family G (WHITE), member 3 Gene [Source:MGI Symbol;Acc:MGI:1351624]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa7378 Missense Mutation detected in F1 DNA Not yet available
sa22207 Nonsense Available for shipment Available now
sa7377 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa7378
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:
T > A
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000032322 None 1 634 2 16
ENSDART00000091806 None 1 263 2 7
ENSDART00000141790 Missense 15 185 2 5
Genomic Location (Zv9):
Chromosome 13 (position 4738954)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 4933732
GRCz11 13 5062318
KASP Assay ID:
554-4319.1 (used for ordering genotyping assays)
KASP Sequence:
TGAGATTTTATTTTTGTTCATTTCAATCTTCCTTCAGGCAGAGGAAGGCA[T/A]CATGCTGGATGAGGTGGTTGTGAATGAGCAGTCGTCCACAGATGCGGAWG
Long Flanking Sequence:
TATTATAACATTTTAAAAGTTATATATATATATATATATATATATATATATATATATATATATATATGCGCCAGGGGGTAAGCATAAATCACATACAAATATACATATGTTGTAATCAAATAAATACATTGTAGAGTTGACAAAGTTTTAAAGTGCGTAAAGCTTTCTTATTTAGAGAATCTTTGATACTACTAATATATAAGCATAAATCCATCACCAACACCTTAAAGTTGGGTTTCTTATTGGTAAATTTACATTTATGAATGTAAAATTTTGTTTCTTTTTCTGAAAGTCTTGATAACAAGTCTTGAGGTTGTCTTTTATTATTTCAGCAAACAGGATTGTAAAAAAAAATCTTTGTTGTACTCTCCCATTCATTGCACTCTAAGTTTACCCAACTATCATGACTTCCACTACTAATAAACCTGGAAATGTGAAAAATTTGTGCTATGAGATTTTATTTTTGTTCATTTCAATCTTCCTTCAGGCAGAGGAAGGCA[T/A]CATGCTGGATGAGGTGGTTGTGAATGAGCAGTCGTCCACAGATGCGGATGAGTCAGTGCCATGTTTCCAGACTCCAGGACCCACCGTCACCTTCCATCAAATCCGATACCGCATCAAGGAACGATTAGGAATGTTTAGCTGCCAATGGCGTGAAAAGGACATCCTTAAAGATGTCAGGTGATGGTTTAACATAGACTGATAATTAAAACAATGGATAAACTCTCTTGATCTTTAAGCTTGTAGTCATAAACCTGTAGCTTACTGTACGTTGTAAAAAATTGTCACACAGGTTTGATTTATTTATTTCAAAGAGTTTGTGATTGTGCCAAAACTAATATAGGTATAGATGGCCGTAGCTACATATTATGGTAAAATAGTTTTATACTATTTTTTACTTCTTTTAAGTGTTTCCTAAACTCAAAGGCTACTTTTGTCTTTACATATTGTGAAATATTATTACAGTTCAGTTTATTTCTAATGCATAAAAATTTAATTTATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22207
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000032322 None None 634 None 16
ENSDART00000091806 Nonsense 228 263 6 7
ENSDART00000141790 None None 185 None 5
Genomic Location (Zv9):
Chromosome 13 (position 4724825)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 4919603
GRCz11 13 5048189
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACACTGCCAACTCCATCATGGAGCTCCTGCAGAAGTACAAAATCTCATA[T/A]CAAATATACCTGCCTCCCGCTGCAAGCAATAATAAAGTATGCCTTTTAAA
Long Flanking Sequence:
ACCCATAATAGGGGCTCTTTAAAAAAGTAATGTGTATCTAATTCCTAACCCCAACTGTAAATTATTCCCAAAATCAGAGGGCATTAATAATTCCAACGTTGCCAATGTTACCGGTTGAAACCTAAAGTGGCGATGAAGTCTTAAAATGTATGGAAAGTGTCTTAAAGGTATTGAATTTCATTCTCTGATTCCTGTACATACTAAGATGTTGATGCAGGAACATGTCCTGCTTGGTGAAATCAAACTAAACATCCCTATATTGTGAGTGGTGGAATGAAAATGTCCATTTAAAGTGATATTGCTTTGTTTGGGCTTGTTGTCTCTCAGATCGGTACAATGTTTTTACGAGGTGTTTCTGGTGGGGAGAAGAAAAGGTGCAGCATTGGCATGGAGCTCATCACTTCCCCGTCGCTCCTGTTCCTGGATGAGCCCACCACAGGCCTGGATGCCAACACTGCCAACTCCATCATGGAGCTCCTGCAGAAGTACAAAATCTCATA[T/A]CAAATATACCTGCCTCCCGCTGCAAGCAATAATAAAGTATGCCTTTTAAAAACACTTTCTTCCAGCATAACCTTGTGAAGCCTCACATAATGAAGGGATGGTTCACCCAAATCGAATTTACTCGCACACAAGTGGTTCTAAACGTTTATGAATTTCTGTCTTCTGTTGAATGCAATAGAAGATATTCTGAAGAATGTAGCCAGTAGCTATGTTTCTATCCAAAAATGTGAACGAAAATTAATGCGCAAAACTCAAATATCCCATAAAAGATGTGCAATTAAAGCAGCGTTGAGTCAAAGAGAACAAAATCGTCACTTCATGATTATCTGGCACCAAATATTAACAGTAAAAACGGAATTTGCTGTGATAGGAGAAGCTGCGTGAATCTTTTCTTCATTTAATAAATTACTACCTCAGAACACAATGCCGACACGCAATGAATGCGTGGTGACGTTTGAAGGCGTGAGATGCGGCACACAAAAACTCTTGACTATTTTAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7377
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 > T
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000032322 None None 634 None 16
ENSDART00000091806 Missense 233 263 6 7
ENSDART00000141790 None None 185 None 5
Genomic Location (Zv9):
Chromosome 13 (position 4724812)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 4919590
GRCz11 13 5048176
KASP Assay ID:
554-4318.1 (used for ordering genotyping assays)
KASP Sequence:
CCATCATGGAGCTCCTGCAGAAGTACAAAATCTCATATCAAATATWCCTG[C/T]CTCCCGCTGCAAGCAATAATAAAGTATGCCTTTTAAAAACACTTTCTTCC
Long Flanking Sequence:
GCTCTTTAAAAAAGTAATGTGTATCTAATTCCTAACCCCAACTGTAAATTATTCCCAAAATCAGAGGGCATTAATAATTCCAACGTTGCCAATGTTACCGGTTGAAACCTAAAGTGGCGATGAAGTCTTAAAATGTATGGAAAGTGTCTTAAAGGTATTGAATTTCATTCTCTGATTCCTGTACATACTAAGATGTTGATGCAGGAACATGTCCTGCTTGGTGAAATCAAACTAAACATCCCTATATTGTGAGTGGTGGAATGAAAATGTCCATTTAAAGTGATATTGCTTTGTTTGGGCTTGTTGTCTCTCAGATCGGTACAATGTTTTTACGAGGTGTTTCTGGTGGGGAGAAGAAAAGGTGCAGCATTGGCATGGAGCTCATCACTTCCCCGTCGCTCCTGTTCCTGGATGAGCCCACCACAGGCCTGGATGCCAACACTGCCAACTCCATCATGGAGCTCCTGCAGAAGTACAAAATCTCATATCAAATATACCTG[C/T]CTCCCGCTGCAAGCAATAATAAAGTATGCCTTTTAAAAACACTTTCTTCCAGCATAACCTTGTGAAGCCTCACATAATGAAGGGATGGTTCACCCAAATCGAATTTACTCGCACACAAGTGGTTCTAAACGTTTATGAATTTCTGTCTTCTGTTGAATGCAATAGAAGATATTCTGAAGAATGTAGCCAGTAGCTATGTTTCTATCCAAAAATGTGAACGAAAATTAATGCGCAAAACTCAAATATCCCATAAAAGATGTGCAATTAAAGCAGCGTTGAGTCAAAGAGAACAAAATCGTCACTTCATGATTATCTGGCACCAAATATTAACAGTAAAAACGGAATTTGCTGTGATAGGAGAAGCTGCGTGAATCTTTTCTTCATTTAATAAATTACTACCTCAGAACACAATGCCGACACGCAATGAATGCGTGGTGACGTTTGAAGGCGTGAGATGCGGCACACAAAAACTCTTGACTATTTTAGTAATTAATAATATT
Associated Phenotype:
Not determined