Busch Lab

ZMP

abcg4a

Ensembl ID:
ENSDARG00000061047
ZFIN ID:
ZDB-GENE-050517-39
Description:
Novel protein similar to vertebrate ATP-binding cassette, sub-family G (WHITE), member 1 (ABCG1) [So
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 4 alleles of this gene:

Allele Name Consequence Status Availability
sa40464 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa17138 Nonsense Available for shipment Available now
sa33630 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa40465 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa40464
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
Founder:
SL7_02_E9
KASP Assay Location:
Unknown
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000086610 Essential Splice Site 189 656 5 15
ENSDART00000141444 Essential Splice Site 174 641 5 15

The following transcripts of ENSDARG00000061047 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 5 (position 32297458)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 30058288
GRCz11 5 30658441
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAGCCAACCTTAAACTTAACGAAAATATGGAGGTGAAAAAAGAACTGG[T/C]AAGTGTATACTGTACCTCTATTATCTCTCTATATAATAGGTGAATTTATT
Long Flanking Sequence:
CTGAAGTGGAGATTATGGTTCAGTGCTGGGAAAAAAACATCTTACAAATCTACAGACAGAAATTGATAAAAGATTATCAAAGAAACATTTACAAATATGCTTTGGATGTTTTCTTTCCATTGGACTGAAAACACTTTATTAAAAATCTCAAAATATCAAGCCTGACTAGTGGATGAAAAGCAGTATTTTTCCTGCAGTGTCTCGCCTTCAGTAAACAAGATTTTGCATATAGAGCACTAAGCTGTTCATTTAACCAATTCCCCTGGCAGCCAATCTCACTTTCTGACAAAATATAAAATAATTTCAACTCCGATCAATATTTTATGCACTAAATTGGTCATCATCTCAACATACACCCTCATAATGGTATTGGTTTGTGGATAATGACCGTCTGATTGCACATTACTCCAAACAGTATTCAAATCAATCTTTCTTTTGTTTTGTTTAGGTGTCAGCCAACCTTAAACTTAACGAAAATATGGAGGTGAAAAAAGAACTGG[T/C]AAGTGTATACTGTACCTCTATTATCTCTCTATATAATAGGTGAATTTATTTCTCAAATGAGCTTCCCTCTGCCCTATGCTCACTCTGAAGGGCAGAGCTCTTGAATGGAGCAGATTGGAAAAAGTAATTGCACTAGTATCATACAGTAATTAAGTTGTTTGGGAAAACACTTGGAGAAGCGTGCAGAGAGAGACAACTCTAATCTTCTCATAGAAGGTTACATGAATGTCACCTATCTACTACAAAACACATTTCTTACTAATTAATTTAATTAGATCTTTACTTGAACTCTTCCAGGTTTAAAATTGTTCCAAATGACTTACATCCACGACATATAACAAAACAGACTACTTGAAAGGGTCTTTGGAAATAAATGATTTCATTCACTCCCGTGATTTGTTTCACAGATTTAATTTGGGAAGGAGATGACACATTTTAACACTTCTTCCCTTTCACTCTAGTCTAGAGCAAGGGTTGGTAACCAAGATTTTGTTGATACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17138
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
Founder:
SL4_09_E1
KASP Assay Location:
Unknown
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000086610 Nonsense 214 656 6 15
ENSDART00000141444 Nonsense 199 641 6 15

The following transcripts of ENSDARG00000061047 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 5 (position 32300257)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 30061087
GRCz11 5 30661240
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TRGGACTACAGGAGTGTGCCCAAAYTCGCACCRTCTCTCTGTCCGGTGGC[C/T]ARTGTAAACGCTTGGCGATTGCCTTGGAGCTGGTCAACAACCCTCCAGTC
Long Flanking Sequence:
CATAAATTGGTTTCAGAGCGAAGGTTTAGAGGGCCTTTAAAGTTGGAGTCATGCTTCTGGGCCAATCAACAACCATGTGATCATCACTGGCCACGCTCATCTAGAACAAAGAGTGAGAGACAGAGAAAAGAAAAAAAATAAATAACACAGTCATTGATCAAAACAAAAAACTACAGGTCATAACACAATATACACTTACTTCAAGGTTATCAATAAGCTTCCAAAAATAGCACGATTTTAATTCAGTAGATACATGTATTTAACAGTCTCTCACTTCCAGCCAATAGCAGTCAGCAGTTTTGATGACATCACTTTGCACTTCTACTTTACATTAGATCTTCTGTTCAATCAAATGCTCTCTAAAATCTGTAGTGGCCCTTTCCTTATCCCATAAAGCAGACAGTAAGTACTGGTATGTTGTGTGACAGGTTAATGAGATTCTAACAGCATTAGGACTACAGGAGTGTGCCCAAACTCGCACCATCTCTCTGTCCGGTGGC[C/T]AGTGTAAACGCTTGGCGATTGCCTTGGAGCTGGTCAACAACCCTCCAGTCATGTTTTTTGATGAACCCACCAGGTACACACAGCTTTAACATTACATACTGACACAATTCATCCAGAATTTAATGTTTGCGTCAACATTTCCAATAAAAATCCCCAAATGTGCATGTTTGTCTCTGTGTTTTAGTGGTCTAGACAGCGCATCCTGTTTCCAGGTGGTGTCCTTGATGAAATCTCTGGCTCAAGGAGGAAGAACCATCATCTGTACCATCCACCAGCCCAGCGCAAAACTGTTCGAAATGTTCGACAAGGTAATTTTTGCATTGTAAATTAAAAAAAAACAATTGTAAACATTGGACTTAATAAAAGGCCAGATTAACTAACAGCTTACGTCAGCTCAAAAACTACATGCAGTGAAATGGTGTAGACACCTTTTTTTTTTAATGGCTGACCTGTTCAAAGTATATTTAAACTTTTCAAAAGTCTGTCTAATCTCAATTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33630
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
Founder:
SL6_09_D11
KASP Assay Location:
Unknown
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000086610 Essential Splice Site 238 656 6 15
ENSDART00000141444 Essential Splice Site 223 641 6 15

The following transcripts of ENSDARG00000061047 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 5 (position 32300331)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 30061161
GRCz11 5 30661314
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGAGCTGGTCAACAACCCTCCAGTCATGTTTTTTGATGAACCCACCAG[G/A]TACACACAGCTTTAACATTACATACTGACACAATTCATCCAGAATTTAAT
Long Flanking Sequence:
ATGTGATCATCACTGGCCACGCTCATCTAGAACAAAGAGTGAGAGACAGAGAAAAGAAAAAAAATAAATAACACAGTCATTGATCAAAACAAAAAACTACAGGTCATAACACAATATACACTTACTTCAAGGTTATCAATAAGCTTCCAAAAATAGCACGATTTTAATTCAGTAGATACATGTATTTAACAGTCTCTCACTTCCAGCCAATAGCAGTCAGCAGTTTTGATGACATCACTTTGCACTTCTACTTTACATTAGATCTTCTGTTCAATCAAATGCTCTCTAAAATCTGTAGTGGCCCTTTCCTTATCCCATAAAGCAGACAGTAAGTACTGGTATGTTGTGTGACAGGTTAATGAGATTCTAACAGCATTAGGACTACAGGAGTGTGCCCAAACTCGCACCATCTCTCTGTCCGGTGGCCAGTGTAAACGCTTGGCGATTGCCTTGGAGCTGGTCAACAACCCTCCAGTCATGTTTTTTGATGAACCCACCAG[G/A]TACACACAGCTTTAACATTACATACTGACACAATTCATCCAGAATTTAATGTTTGCGTCAACATTTCCAATAAAAATCCCCAAATGTGCATGTTTGTCTCTGTGTTTTAGTGGTCTAGACAGCGCATCCTGTTTCCAGGTGGTGTCCTTGATGAAATCTCTGGCTCAAGGAGGAAGAACCATCATCTGTACCATCCACCAGCCCAGCGCAAAACTGTTCGAAATGTTCGACAAGGTAATTTTTGCATTGTAAATTAAAAAAAAACAATTGTAAACATTGGACTTAATAAAAGGCCAGATTAACTAACAGCTTACGTCAGCTCAAAAACTACATGCAGTGAAATGGTGTAGACACCTTTTTTTTTTAATGGCTGACCTGTTCAAAGTATATTTAAACTTTTCAAAAGTCTGTCTAATCTCAATTATTAATTAAATAACTCGCACAAAAATGAATCCTTTCATCAATTACTCTCCCACATCATTTTTGCTTATCTTCAAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40465
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
Founder:
SL7_05_D1
KASP Assay Location:
Unknown
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000086610 Essential Splice Site 456 656 None 15
ENSDART00000141444 Essential Splice Site 441 641 None 15

The following transcripts of ENSDARG00000061047 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 5 (position 32308715)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 30069545
GRCz11 5 30669698
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTATGCTGTTTCTCATGTTTGCTGCTCTCATGCCCACCGTCCTAACATG[T/C]AAGTCAACCTACTGGCTTTGCTCAATTCCTCATGAGCATGGAAAATAGAT
Long Flanking Sequence:
TCTAGTTATGTGTGCTGTATGCATCAGACATTCAGCCAATGGTCTGTGAGTGTGGCATCTGTGCTGACATCCGACAAACACCTGTATTTTTAGCATTGTACACTTGGAATAGAATCAGCTAAAATACATCTTAATACCATGTGTAAACAACCTCCTAATTGACTTGTAGCTGCTATGTAAATTAAAGTCAACAGAATATCTAAATTAAACAGGATTCTAAATCAGAAATCAAAATGAAGTGCTAACATAGCTTTTGTATTGTTTGTATCTTTTAACTGTTCAATCAATCTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTTCAGGTATTAACCCACCTGAGAGTGATGTCGCACCTGTGTATCGGCGTGTTGATTGGCCTGCTGTATCTGAACATTGGGAATGATGCCAGCAAAGTGTTCAACAACACTGGCTTCCTGTTCTTCTCTATGCTGTTTCTCATGTTTGCTGCTCTCATGCCCACCGTCCTAACATG[T/C]AAGTCAACCTACTGGCTTTGCTCAATTCCTCATGAGCATGGAAAATAGATTTGATTCGAGTAGTTAGTAAATCCTTTTTTGATTTGTGATGGATTAGAAGCGCTTATTGGCTTGATTGAGGGTTATGGTCTTTACAGAATCTGATTGAATTAAGCACTGAAGCGATGATGTATTTCCTCTTTCAGTTCCACTGGAGATGGGTGTGTTCATAAGAGAGCATCTTAATTACTGGTACAGTTTAAAGGCGTATTACTTGGCTAAGACCATGGCTGACATTCCATTCCAGGTACTTCTGTTTATCTTTCTCATGTGACTTTTTATTTTGAAAAATGTATTCAACCCTATGTGTCCTTTTAGAAGGATCTGAAATGTTCAAATGTGACACATGCAATTAGGTGTGTCATTTTTCTAAGCATACCTGAGCCCCAGGCAAACTTCTTCAGTGTTCTTCTCTCTCTTCCAGGTCATTTGTCCGATTATGTACTGCAGTATAGTGTACT
Associated Phenotype:
Not determined