ZMP

abcg2b

Ensembl ID:

ENSDARG00000079361

ZFIN ID:

ZDB-GENE-050517-36

Description:

ATP-binding cassette, sub-family G (WHITE), member 2b [Source:RefSeq peptide;Acc:NP_001034155]

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 is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa45063	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa45063

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000091798	Essential Splice Site	470	618	11	17

Genomic Location (Zv9):

Chromosome 1 (position 7755050)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	7994855
GRCz11	1	8678966

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCGCATTGTCCCGATTTTAATCTTCTCCAGCATTTCCTACTACATGATGG[G/A]TAAAACAATCTCTGTTTCACATAAAACTGTGATTAAACGTCAACATCAGC

Long Flanking Sequence:

GGTTTTTGGCAACTTGTCAGCAGTAGAGCTCTTCATTAATGAGCGAGCAATTTTTGTGTGAGTATGATTTTATCTGCCTTGCTTATAATTGTATTTGATGTTTCTAATGTTTCATTGATACAACATTATAGTATATATTAATATTTTGAATTAGCTTTTCATTTCATATTTGATCATTTGGGCATTTCAATTTAAACATTATTTCAGATTTTTTTCAGATTTTTTTTGACAGATTAAATAGAAACAATAACACTTACATTTATGTGTTCGAATTATATGTGCATGTTATGTATGGATGTAAACAAACTTCACTTGTTCATTTGGCTTACTTTTTTAAAAAGTTTTTTTTTTTCTGTATGTCTGTGTCTGTTTTAGGCATGAAAACTCTGGAGGATATTACCGTACATCTGTGTATTTCCTCTCCAAGGTGTTCGTGGATCTGTTACCAAATCGCATTGTCCCGATTTTAATCTTCTCCAGCATTTCCTACTACATGATGG[G/A]TAAAACAATCTCTGTTTCACATAAAACTGTGATTAAACGTCAACATCAGCACATGCTGTTTTCTAAATAAGCATTAATATGCACAGTAATTGAATATATGTATTTGTAAACAGGGTTGAATCCAGCATTCACATCCTTCCTGTGCTTCGCGTTGACCATGTCTCTGGTCAGTCTAGCAGGAGTGAGTTTGGCCTTTCTGGTCAGTGCCAGCGTGAGCACTTTCGCCATGGCCAACATCCTCGTCGTCTTGCCTTTCGTCTTCATGATGGTCAGATTTCAAATGCTTACTTGCTCATAAGCTTTTTACAAGATGTAAAATAAGTCGCTGATGTCCCTAGAACAGGGATGGGCAAACTTGATCCTCGAGGGCCGGTGTCCCTGCAGAGTTTTGTTCCAACACTAGTCAAACACACCTGAGCAAACTAATCAGTGTCTTCAAGATCACTTGAACTCTATAGGGAGGTCTGTTTGAATAGGGTTGGAGCTAAACTATGCAGGAC

Associated Phenotype:

Not determined