ZMP

abcg4b

Ensembl ID:

ENSDARG00000078068

ZFIN ID:

ZDB-GENE-080215-10

Description:

ATP-binding cassette, sub-family G (WHITE), member 4b [Source:RefSeq peptide;Acc:NP_001104682]

Human Orthologue:

ABCG4

Human Description:

ATP-binding cassette, sub-family G (WHITE), member 4 [Source:HGNC Symbol;Acc:13884]

Mouse Orthologue:

Abcg4

Mouse Description:

ATP-binding cassette, sub-family G (WHITE), member 4 Gene [Source:MGI Symbol;Acc:MGI:1890594]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42544	Nonsense	Mutation detected in F1 DNA	Not yet available
sa7405	Missense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa42544

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115051	Nonsense	124	644	4	15

Genomic Location (Zv9):

Chromosome 15 (position 22853727)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	23564914
GRCz11	15	23500179

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACATTTAAAAATCTTGTTATGTGCTTTATAGGGAAACAGGGATGACTGGA[C/T]AGATCCTAGTAAATGGAAAGCTCCGAGACCCCCGAACCTTTCGTAAAATG

Long Flanking Sequence:

AGCACCCAGAGGAAACCCACGCGAACACAGGGAGAACATGCAAACTCCACACAGAAACGCCAACGGACCCAACCGAGGCTTGAGTTAGCGACTGTCTTGCTGTGAGGCGAACATGCTACCAACTGTGCCACCGTGCAGCAATTGCAAATTTAGATTAAATTGAAAAATAAATTGTTCTTTGATCAAATTTAATATAAAGAAAATTTAAATAAATTATCACTTTCTACATTTAACAAAAAAATTAAATCGTAAAAATAGATATAGTATAGGAAAAATAGATATAGTAGAATATAGTAATGCATTAAAATAATTACACTAAAAAAGGATAAATTAAATTCAGTTCAAATTTTAATCACAAATGTAATCTAAAATAAATTTTAAAATAGTTTTCTCAATAATATTTAATATTAAATATAAACTAAATTAAATCTATCTTGATTCAAATCTTGAACATTTAAAAATCTTGTTATGTGCTTTATAGGGAAACAGGGATGACTGGA[C/T]AGATCCTAGTAAATGGAAAGCTCCGAGACCCCCGAACCTTTCGTAAAATGTCCTGTTACATTATGCAAGAAGACAAATTGCTGCCTCACTTGTCAGTTCAAGAAGCAATGATGGTGAGTCTCCAGGGTGAATAATGTGGTAAAGGATGCCCCCTAGTGCTGATTTGATGCTAATGCTTATAATACAGTCACATGCAAAAGAAAATGACTGATTTCTCCACTGTTTGTAAGGTATCAGCCAACCTGAAGCTGAATGAAAGCTCAGAGGTGAAAAAAGAGCTGGTAGGTGAAGCTTATCTCCTTGGAAGCTGCACCGGTATGCTTGCTTGCCTTTAAAATTCAGCTCCTTCCTTTGTGTTTATGCTGACCTGTAGATAAAAGAAATCCTGACAGCACTGGGACTTCATGAATGTGTCCACACTCGTACCGTGTCTCTGTCTGGTGGTCAGTGTAAGAGACTGGCTATTGCCCTTGAGCTAGTAAACAACCCTCCAGTCATGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7405

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:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115051	Missense	138	644	4	15

Genomic Location (Zv9):

Chromosome 15 (position 22853684)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	23564871
GRCz11	15	23500136

KASP Assay ID:

554-4030.1 (used for ordering genotyping assays)

KASP Sequence:

GACTGGACAGATCCTAGTAAATGGAAAGCTCCGAGACCCCCGRACCTTTC[G/T]TAAAATGTCCTGTTACATTATGCAAGAAGACAAATTGCTGCCTCAYTTGT

Long Flanking Sequence:

ACTCCACACAGAAACGCCAACGGACCCAACCGAGGCTTGAGTTAGCGACTGTCTTGCTGTGAGGCGAACATGCTACCAACTGTGCCACCGTGCAGCAATTGCAAATTTAGATTAAATTGAAAAATAAATTGTTCTTTGATCAAATTTAATATAAAGAAAATTTAAATAAATTATCACTTTCTACATTTAACAAAAAAATTAAATCGTAAAAATAGATATAGTATAGGAAAAATAGATATAGTAGAATATAGTAATGCATTAAAATAATTACACTAAAAAAGGATAAATTAAATTCAGTTCAAATTTTAATCACAAATGTAATCTAAAATAAATTTTAAAATAGTTTTCTCAATAATATTTAATATTAAATATAAACTAAATTAAATCTATCTTGATTCAAATCTTGAACATTTAAAAATCTTGTTATGTGCTTTATAGGGAAACAGGGATGACTGGACAGATCCTAGTAAATGGAAAGCTCCGAGACCCCCGAACCTTTC[G/T]TAAAATGTCCTGTTACATTATGCAAGAAGACAAATTGCTGCCTCACTTGTCAGTTCAAGAAGCAATGATGGTGAGTCTCCAGGGTGAATAATGTGGTAAAGGATGCCCCCTAGTGCTGATTTGATGCTAATGCTTATAATACAGTCACATGCAAAAGAAAATGACTGATTTCTCCACTGTTTGTAAGGTATCAGCCAACCTGAAGCTGAATGAAAGCTCAGAGGTGAAAAAAGAGCTGGTAGGTGAAGCTTATCTCCTTGGAAGCTGCACCGGTATGCTTGCTTGCCTTTAAAATTCAGCTCCTTCCTTTGTGTTTATGCTGACCTGTAGATAAAAGAAATCCTGACAGCACTGGGACTTCATGAATGTGTCCACACTCGTACCGTGTCTCTGTCTGGTGGTCAGTGTAAGAGACTGGCTATTGCCCTTGAGCTAGTAAACAACCCTCCAGTCATGTTCTTTGATGAACCCACTAGGTAATGATACACTCAGACATGCAT

Associated Phenotype:

Not determined