ZMP

abcg2a

Ensembl ID:

ENSDARG00000043037

ZFIN ID:

ZDB-GENE-050517-35

Description:

ATP-binding cassette transporter sub-family G member 2a [Source:RefSeq peptide;Acc:NP_001036240]

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 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa44064	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa44064

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000063180	Essential Splice Site	450	644	10	18

Genomic Location (Zv9):

Chromosome 23 (position 46094689)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	46087198
GRCz11	23	45929993

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGCTCTGTTTCAGCAGCTGAACTCTTCATCGCAGAGAGGAAACTGTTTGT[G/T]TAAGTTTTTCAAATACAATAAAAATGGAGGATTTTCACAAGGTTTAGTTG

Long Flanking Sequence:

GTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCAGCTAGAATAAAAGCAGTTTTTAATAGTTATAAAGTCATGTTAAGCTCAATATTATTGGCCCCTTCTCCAGAATAAACCACTGTTATACAATGACTTGCCTAATTACCCTAACTTTACCCTGATTACCCTAGTGAAGCCTTTACATGTCTCTTTAAGCTGAATACTAGTGTCTTGAAGAATATCTAGTCTAATATTATTTACTGTCATCATGATGAAGAGGAAATAAATCAGTTATTAGAGATGAGTTATTAACACTGTTATGATTAGAAATGTGTTGAAGAAATCTGCTCTCCGTTACACAGAAAAATGAGGAAAAATAAACAGGGGGGTGAATAATTCTGACTTTAACTATATTAATGTGTGTGTGTGTTTCAGGATGGGGGCTCTGTTCTTCATCACCACTAATCAGTGCTTTAGCTCTGTTTCAGCAGCTGAACTCTTCATCGCAGAGAGGAAACTGTTTGT[G/T]TAAGTTTTTCAAATACAATAAAAATGGAGGATTTTCACAAGGTTTAGTTGCATTAACGGCTCTTAAACATCCTGAATGACTAATTATGTGTTAATTATCTAAACTAATCTCTTTTCTTGGTGAAAAGCATTGATTAAATATATTAATGTAGACTAAAGAATTATTTTAGGTCACATGAACAATAATAATGTATAACGGTTAGTAGTTAACGTAATTAACAGGATTATTGTTATAATCTAAACAGAATAGTTTTGTCGTGTGCATCTGTAGAGTGTGTTTGACAGATGTTGTGTGTTTGTCTGGTCAGACATGAGTACATCAGCGGATACTACAGAGTGTCTGTCTACTTCCTGTCCAAGATCCTGTCTGACATCCTGACGCTGCGCACCATTCCAGCGGTCATCTTCAGCTGCGTGGCTTACTTTATGATCGGTCAGAGAATAACACGATCCTTATTCCATATTTATCACACCATCAAACCAACATTATTCAGACACATT

Associated Phenotype:

Not determined