Busch Lab

ZMP

abca1a

Ensembl ID:
ENSDARG00000074635
ZFIN ID:
ZDB-GENE-031006-12
Description:
ATP-binding cassette sub-family A member 1 [Source:RefSeq peptide;Acc:NP_001139161]
Human Orthologue:
ABCA1
Human Description:
ATP-binding cassette, sub-family A (ABC1), member 1 [Source:HGNC Symbol;Acc:29]
Mouse Orthologue:
Abca1
Mouse Description:
ATP-binding cassette, sub-family A (ABC1), member 1 Gene [Source:MGI Symbol;Acc:MGI:99607]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa5800 Essential Splice Site F2 line generated Not yet available
sa2010 Essential Splice Site F2 line generated Not yet available
sa15548 Essential Splice Site Available for shipment Available now
sa39699 Nonsense Mutation detected in F1 DNA Not yet available
sa928 Essential Splice Site F2 line generated Not yet available
sa12376 Essential Splice Site Available for shipment Available now
sa9624 Essential Splice Site Available for shipment Available now
sa13007 Essential Splice Site Available for shipment Available now
sa32775 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa5800
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051558 Essential Splice Site 507 2268 11 49
ENSDART00000142465 Essential Splice Site 507 2268 11 49
ENSDART00000051558 Essential Splice Site 507 2268 11 49
ENSDART00000142465 Essential Splice Site 507 2268 11 49

The following transcripts of ENSDARG00000074635 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 53089837)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 51960436
GRCz11 1 52595174
KASP Assay ID:
554-3387.1 (used for ordering genotyping assays)
KASP Sequence:
GTTCAACGAGACTGAYCAGGCCATACAGACCATCTCCCGCTTCATGGAGG[T/C]ACACAGTTTTATCTTCCTTAACGTCCTATTATCATTATCWTCATATGCAT
Long Flanking Sequence:
TCGTATGACTTCATGTAAGGTCATGCTGACAAATAGAAATAGTCACAACAGTCATTTAAATTTGACAGAAAGTGCATTTAATTAATATAGAAAGTAATATTTTTTCACAGTATACATGTATGAATGGGATATAATAGAAAAGGCTTCACAGCATATTTCACAGCTGCATGAATGCATTAATTAATCTGATTAATTCACTAAATTATAATATAGCATCATATCATAATATTATAATATAGTCTTTTACGACTACAGGAGATGCATGGTATTTCTGATATTAAACCAATTGTTTTTTCCTCAACAGACGCTGCTCCAGAATAACGCCAGCGCTCGTTTCTTCAATGCTAAGCTGAGCGGGACAGAATGGCGCGTGGAGGATGTGTCCCGCTTCTTGTCCAAGTCTTCAGAGGACACTCGTCCACATGGGACAGCGTACACATGGAGAGAAGTGTTCAACGAGACTGACCAGGCCATACAGACCATCTCCCGCTTCATGGAGG[T/C]ACACAGTTTTATCTTCCTTAACGTCCTATTATCATTATCATCATATGCATGGTGCGAGACATTAATTGGAGATGCAGTTTTATCGTCTTTAGCTTTCTCATTGTGATCAACTTCAAGTAGATAATGTAAGACACTTCTGGTAAATAAGGTTAAAAAAAAACAATTTTTTTTTACTATGCATTGATATTTTTTGGATTACAAGTTTCTGAAATGCTAAGAATAAATATGCAAACGAGGCGATGCTTATTTAAATATGTGCTATTTGCATATATCTCTTTTAAATTTTGGAGTTTCTGAAATTGTGTTTTAAATATCTAAATGAGACATTGTTTATTTAAATATGTGCTAATTTGCATATATTTGCATATATCTGATAAAAAAGATTGGATATATTTTGTAGTATTACTATTTCTGAAATATGCAAATGAGCCAATGTTTATTTACATATTTGCTAATTTACATACATTTGCATATATCTAAAATTTTATAGTTAAATATGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2010
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051558 Essential Splice Site 507 2268 11 49
ENSDART00000142465 Essential Splice Site 507 2268 11 49
ENSDART00000051558 Essential Splice Site 507 2268 11 49
ENSDART00000142465 Essential Splice Site 507 2268 11 49

The following transcripts of ENSDARG00000074635 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 53089837)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 51960436
GRCz11 1 52595174
KASP Assay ID:
554-3387.1 (used for ordering genotyping assays)
KASP Sequence:
GTTCAACGAGACTGAYCAGGCCATACAGACCATCTCCCGCTTCATGGAGG[T/C]ACACAGTTTTATCTTCCTTAACGTCCTATTATCATTATCWTCATATGCAT
Long Flanking Sequence:
TCGTATGACTTCATGTAAGGTCATGCTGACAAATAGAAATAGTCACAACAGTCATTTAAATTTGACAGAAAGTGCATTTAATTAATATAGAAAGTAATATTTTTTCACAGTATACATGTATGAATGGGATATAATAGAAAAGGCTTCACAGCATATTTCACAGCTGCATGAATGCATTAATTAATCTGATTAATTCACTAAATTATAATATAGCATCATATCATAATATTATAATATAGTCTTTTACGACTACAGGAGATGCATGGTATTTCTGATATTAAACCAATTGTTTTTTCCTCAACAGACGCTGCTCCAGAATAACGCCAGCGCTCGTTTCTTCAATGCTAAGCTGAGCGGGACAGAATGGCGCGTGGAGGATGTGTCCCGCTTCTTGTCCAAGTCTTCAGAGGACACTCGTCCACATGGGACAGCGTACACATGGAGAGAAGTGTTCAACGAGACTGACCAGGCCATACAGACCATCTCCCGCTTCATGGAGG[T/C]ACACAGTTTTATCTTCCTTAACGTCCTATTATCATTATCATCATATGCATGGTGCGAGACATTAATTGGAGATGCAGTTTTATCGTCTTTAGCTTTCTCATTGTGATCAACTTCAAGTAGATAATGTAAGACACTTCTGGTAAATAAGGTTAAAAAAAAACAATTTTTTTTTACTATGCATTGATATTTTTTGGATTACAAGTTTCTGAAATGCTAAGAATAAATATGCAAACGAGGCGATGCTTATTTAAATATGTGCTATTTGCATATATCTCTTTTAAATTTTGGAGTTTCTGAAATTGTGTTTTAAATATCTAAATGAGACATTGTTTATTTAAATATGTGCTAATTTGCATATATTTGCATATATCTGATAAAAAAGATTGGATATATTTTGTAGTATTACTATTTCTGAAATATGCAAATGAGCCAATGTTTATTTACATATTTGCTAATTTACATACATTTGCATATATCTAAAATTTTATAGTTAAATATGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15548
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
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051558 Essential Splice Site 507 2268 11 49
ENSDART00000142465 Essential Splice Site 507 2268 11 49
ENSDART00000051558 Essential Splice Site 507 2268 11 49
ENSDART00000142465 Essential Splice Site 507 2268 11 49

The following transcripts of ENSDARG00000074635 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 53089837)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 51960436
GRCz11 1 52595174
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTCAACGAGACTGAYCAGGCCATACAGACCATCTCMCGCTTCATGGAGG[T/C]ACACAGTTTTATCTTCCTTAACGWCCTATTATCATTATCWTCATAKGCAT
Long Flanking Sequence:
TCGTATGACTTCATGTAAGGTCATGCTGACAAATAGAAATAGTCACAACAGTCATTTAAATTTGACAGAAAGTGCATTTAATTAATATAGAAAGTAATATTTTTTCACAGTATACATGTATGAATGGGATATAATAGAAAAGGCTTCACAGCATATTTCACAGCTGCATGAATGCATTAATTAATCTGATTAATTCACTAAATTATAATATAGCATCATATCATAATATTATAATATAGTCTTTTACGACTACAGGAGATGCATGGTATTTCTGATATTAAACCAATTGTTTTTTCCTCAACAGACGCTGCTCCAGAATAACGCCAGCGCTCGTTTCTTCAATGCTAAGCTGAGCGGGACAGAATGGCGCGTGGAGGATGTGTCCCGCTTCTTGTCCAAGTCTTCAGAGGACACTCGTCCACATGGGACAGCGTACACATGGAGAGAAGTGTTCAACGAGACTGACCAGGCCATACAGACCATCTCCCGCTTCATGGAGG[T/C]ACACAGTTTTATCTTCCTTAACGTCCTATTATCATTATCATCATATGCATGGTGCGAGACATTAATTGGAGATGCAGTTTTATCGTCTTTAGCTTTCTCATTGTGATCAACTTCAAGTAGATAATGTAAGACACTTCTGGTAAATAAGGTTAAAAAAAAACAATTTTTTTTTACTATGCATTGATATTTTTTGGATTACAAGTTTCTGAAATGCTAAGAATAAATATGCAAACGAGGCGATGCTTATTTAAATATGTGCTATTTGCATATATCTCTTTTAAATTTTGGAGTTTCTGAAATTGTGTTTTAAATATCTAAATGAGACATTGTTTATTTAAATATGTGCTAATTTGCATATATTTGCATATATCTGATAAAAAAGATTGGATATATTTTGTAGTATTACTATTTCTGAAATATGCAAATGAGCCAATGTTTATTTACATATTTGCTAATTTACATACATTTGCATATATCTAAAATTTTATAGTTAAATATGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39699
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051558 Nonsense 672 2268 14 49
ENSDART00000142465 Nonsense 672 2268 14 49

The following transcripts of ENSDARG00000074635 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 53094263)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 51964862
GRCz11 1 52599600
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGTGGCCATCATCATCAAGGGTGTGGTGTATGAAAAAGAGGCCCGACTC[A/T]AGGAGACCATGCGGATCATGGGTCTGGATAACGGCATCTTGTGGCTGAGC
Long Flanking Sequence:
ACATACCTGCAGGACGTGATTGAGCACGGGATCATCAGAGCTCTGACCGGCAGCAAGGAAAAAACCGGAGTCTACATCCAGCAGATGCCGTATCCCTGCTATGTGGATGACATGTAAGAGAGATCATCACCATTTACAGCCTTTATATTCATATGCAGATTTCAGTCACAATTAGAACAGAGTGACATGTAAGCCCTGTTATTGAAATACAGTGGCATATAAGCTTTGTTTTTTTAAATATAGTGATCTATATGCTTTGTTTTTGAAAAATAGTTGTAAATATATAAGCTCTATGTTTTAAAAATAAAAAAACAGTACTCCTGCATGTTTTAATAAAAATAAATCAGCCATTTTAGTGATTGTGTGACCCCTGCTTTCTCCTGTTGTCCAGTTTCCTGCGGGTCATGAGCCGCTCCATGCCTCTCTTCATGACTCTGGCCTGGATGTACTCGGTGGCCATCATCATCAAGGGTGTGGTGTATGAAAAAGAGGCCCGACTC[A/T]AGGAGACCATGCGGATCATGGGTCTGGATAACGGCATCTTGTGGCTGAGCTGGTTCATCAGCAGCCTGATACCACTGCTCATCAGCGCCGCCCTGCTGGTGCTCATCCTGAAGGTGTGCATCTCTCGGTTTCTCTGTCCAAATATGACCAAGCAACATTAATGGACACATTTCCGTATGTCTCAGTACACTAACAATGCTGGGTTCCACGCAATTCATTCATGTTGTCTGAACATAAATCGATTAAGTTGGCTTGACAAGTTTAAACAGTATAGAGAAACACTTTGATTGACATTTTCCCTTTGTACGTGTCATCTGAGGGGAAAGCCCTGCCCACTAGTGATGATCTTTCCCTCATTAGCATAGGACGCTAGTATTGTTTTTGATTCTGCCACTATGCTGATACATAGGCATTTATAGCTCCGCCCTCTATTTAAAAAGTGCACAATCTCATTTGCATTTAAAGCGGCAGTCACCAAAACGACACAATTAGGACCAAAG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa5665
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051558 Nonsense 771 2268 15 49
ENSDART00000142465 Nonsense 771 2268 15 49

The following transcripts of ENSDARG00000074635 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 53095107)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 51965706
GRCz11 1 52600444
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCATCATTTACTTCACGCTTTACCTGCCCTATGTGCTCTGCGTYGCCTG[G/A]CAGAACTACGTRGGCTTCGGTGCCAAAATAGTAGTGGTGAGTGCAAGTAA
Long Flanking Sequence:
GATCTTTCCCTCATTAGCATAGGACGCTAGTATTGTTTTTGATTCTGCCACTATGCTGATACATAGGCATTTATAGCTCCGCCCTCTATTTAAAAAGTGCACAATCTCATTTGCATTTAAAGCGGCAGTCACCAAAACGACACAATTAGGACCAAAGCCTAAAAAGGGTACGTTTCCGAGAGTAGAAAAACATTACTTGTGTGGTACTACAAGCTGAAACTTCACACACACTCTCTAGGAACACCAGAGACATGTTTTTTCTTCTTTTTCTTGTAAAAAGGCATAGGTCCCCTTTAACACCAAATTTTTTTTCAGATGGGGAATCTCCTGCCGTACAGCGACCCCGGCGTCATCTACTTGTTCTTGTCCTCTTTTGCGGTGGTGACCATCATGCAGTGTTTCCTGATCAGCACACTCTTCTCTCGTGCCAATCTTGCCGCCGCCTGCGGAGGCATCATTTACTTCACGCTTTACCTGCCCTATGTGCTCTGCGTCGCCTG[G/A]CAGAACTACGTGGGCTTCGGTGCCAAAATAGTAGTGGTGAGTGCAAGTAATACGCTGACATGTCATCTGATCTGCCTTTTTAGTGACTTCACGTGTCAGTGTTTTTAATATTATTTTAAATGCAATGACAACCCCAAATTTATTTAAGAAGTATTTCCAATTTGGGGTTTGGAAATTGTTCAGTATTTTATTTATTTATTTTATATATTTTTATTTCATTTAATATTAGGTTGTACTGTGGTTTTAGCTGTATTATATATGTATTTATTAATTAGAACAAACATGTATTTATTTACTTTAATTGTACTGAACTTAAATCTCATTTGACTTTAATCAAATTTTTAAAAATGTATTCTCACTTTGTATTTATGTATTTATTTGAATATATTTTTTGAATTTGTTTATGTAATTTTTTATCACATTCACATAACACATTGATATACACATTATATTATACTTGTACTTTATATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa928
Status:
F2 line generated
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
ENSDART00000051558 Essential Splice Site 991 2268 19 49
ENSDART00000142465 Essential Splice Site 991 2268 19 49

The following transcripts of ENSDARG00000074635 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 53098062)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 51968661
GRCz11 1 52603399
KASP Assay ID:
554-0833.1 (used for ordering genotyping assays)
KASP Sequence:
ATCCGCCAAAACCTGGGCGTCTGTCCTCAGCATAACGTCCTGTTCAGCAT[G/A]TACGTCCACAACACACCTTTTTACACATTTTACACACTCTTTCATGGGAA
Long Flanking Sequence:
TTGGCCACAACGGCGCTGGAAAAACCACAACCATGTAAGAAAACTCAGAAAAACATCTTAAGACAATTCAATCCACTTGAATTTGTAAAAACGGTTAAGTTAAAGAATTGTGTGGAACCCAGTTTTTTTACAGTGAACTTTTTAAGGAAAGGAATGTGAAAGTATTTGTTATGTTATTATTGTTTATAAAGTGAGTGCATATTTAATAAAACAATCCTTTGTTTGCATATTCAGAAAATTATAAAATATTTAGAAAACTTTTTTTTAAAAAGCTGGGAAAATAAGAGAAATTATATTGTTAAATGTGAATATAACAGTGTAATTTTATTTCTGGTGTCAAAACGAGTTGCATTTTCTTGCTTTTTCAGGTCAATCCTCACCGGCCTGTTTCCACCGACTTCTGGCACTGCGTACATCCAGGGCAAAGACATCCGCACAGACCTGAATGCCATCCGCCAAAACCTGGGCGTCTGTCCTCAGCATAACGTCCTGTTCAGCAT[G/A]TACGTCCACAACACACCTTTTTACACATTTTACACACTCTTTCATGGGAATCTGCAATGCAAAAGAACTCTGTCCATAAAAAATATGGACGCACAATATGTCAATATTTTTTTATGCCATACATGACAGCCTACAAGCTCATATTTGGATTTTATATATGCATAATAAATATGTCATATATCCAACAAATATTGCAAAAATAATTATAGAATTACCATTGGAATTACTAATATGTACATATATGTTCAAATATGTTAGATGCAATTTGATTAGATATACATATGTTCATATATGGCCATTATATTCACGCTATAGCAAATATATTTGAATATATTTACATATTTGTTGATTGGCATTTATCAGATTTCTATGTGAGTGCCTCTAGACTGAGTTTGTGTGTGTGCATGTATTTCAGGCTGACCGTGGAGGAGCACATCTGGTTTTATGCGCGTCTGAAGGGTTTGTCTGCGGAGAAGGTGAAGTCTGAGATGGAGCAGATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12376
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
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051558 Essential Splice Site 1083 2268 21 49
ENSDART00000142465 Essential Splice Site 1083 2268 21 49

The following transcripts of ENSDARG00000074635 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 53099554)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 51970153
GRCz11 1 52604891
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTTACGCCCGCCGTGGCATCTGGGACCTGCTGCTGAAATACCGCCAAG[G/A]TAAACATCTGCAATAAAAAACAGCCTWTAATTACAWTAAATATGTCATGC
Long Flanking Sequence:
TTGTTTTTCTATTTTTTGCATTGCTAAATTTCCATCAAAAGCTCAAAGTAGCTTTATATGCTTTTCCTTAGTAGTTTAATCACATGTGAAGGTAAAAGATTCTATCAAAATATTTAAAATATCTAACCTTGTAACATAATAAATAATTTACTGTCATTTTCTTATTAATTTAATGCATTCCAGGTGTAAAGAAATAAAAATATTTAATATTTTGGGTATTAGTATTGATCTTGCTGATCATTTTTTCTAGTTTTTGCATTGCTCAATTTCCATCAAATGCTCAGAGTAGCTTTATATGCTTTTCGTAAATAATTTAAGCACATGTGAAATGTCAAATTATTTAAAAAGATCTAACCTTGCAGGAGGAATGCAGAGGAAGTTATCAGTCGCGCTGGCCTTCGTCGGAGGCTCAAAAGTGGTGATTCTGGATGAACCGACTGCTGGAGTTGATCCTTACGCCCGCCGTGGCATCTGGGACCTGCTGCTGAAATACCGCCAAG[G/A]TAAACATCTGCAATAAAAAACAGCCTTTAATTACAATAAATATGTCATGCAAAAAAAAATGTTATCCAAGTGCACATACAGTAAGATAAATACAATAAATGTCATATAAACCAAATAAATTAAGGCATTGCTTGTAACAGATCTGCTTATAACAAAACCATCATCATGTAATGCACTTTAAAAGATGCACCAAGATGTCTCTGATGTCCCCAGAGTGTTTTTGTGAAGTTTCAGCTCAAAATACCACACATAATGTTTTAAAACTCTTTTAAGGCTCTCTTTTAGGCTTTGATCCTAATTCTGCTTTAAATTCAAATGAGATTGTGCTCTTTTCAGAAGAGGGCGGAGCTACAAATGCCTGTGTGTCAGCATAGTGGCAGATTCAAAAACCAGACTAATGTTATATGCTAATGAGGGAGCATATCTGACAACATTCAGATCATAAAATCCGGGAGATTTTATCCGGGGCTGTGCGTGAAGTGAATAGCGGGGTGGGGGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9624
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
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051558 Essential Splice Site 1432 2268 30 49
ENSDART00000142465 Essential Splice Site 1432 2268 30 49

The following transcripts of ENSDARG00000074635 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 53106281)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 51976880
GRCz11 1 52611618
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAAGTTGTTTGTTTTCAWATATTTGTTTGTGTGTGTTTTGTTTGTTACA[G/A]TAGCAGATCGTGTCCGATTAAAGATGGAGAATGGCTGGTTCCAGAGGTTA
Long Flanking Sequence:
TTTTGTTATAAAATAATAAATAAGTAATGTTTATTAACTTAAATATTTAATCAAATATTAAAAGTATTTTTGTTGGTTTTTATATGTGTTGTTGTTGGAATAATTAAATGTCTTATTATTACAACAGCAACATTTATAGAAAACAAAACAAAAAAAAATATATATATATATGTATATATATATATTTTTTTTTTTTTAAATCCGCAAATATTATTAAGGATTTAGTTTTTGTAAGGACTTTATTTTTTATTATTATTATTTTTTTAAGATAAACAGTTGCATATTTTGTCCAGTAATATCAGAGTGGATATTTTCAGTCGCAGATCATTAATAATATATTGATTTTACTTAATTTTTTATTTTATTTTTTTCAAATAGTAGAGCATTTTTTCCAACAAAAGATGAGCTTATGATATTCCCATTAGTGGATTGTTAATATTTTAGATTTTTTTAAGTTGTTTGTTTTCATATATTTGTTTGTGTGTGTTTTGTTTGTTACA[G/A]TAGCAGATCGTGTCCGATTAAAGATGGAGAATGGCTGGTTCCAGAGGTTACCGAGAGCATTGAGGCAATATTCCTGAATGGAAACTGGAGTATGGAAAACCCTTCTCCTCTGTGTGAGTGCAGCTGTGAAGGACGGAAAAAGATGCTTCCGGAGTGTCCGCCTGGAGCAGGAGGCCTTCCACCGCCTCAGGTACACATATTCACCAAATACTGTAATATCTGGTTTTATCTTAATATTTAGGCAGCAGAACGTATGACTTTCTCTTCTTTCCTCAGATTAAAGTCACCCATGATGAAACCCTGCAGAATCTGTCTGGAAGAAACATTTCAGACTATTTGGTGAAAACATACGCACAGATTATTGGGAAAAGGTGAGTTGAGACAGTCCACAATATAAATAAGCCAACTGAAATAAAATGTTCCTGGTTTTCATTCTAACTTTGTCCTGTTTTATCTGTTCAGTTTGAAGAACAAGCTCTGGGTCAACGAATTCAGGTACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13007
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
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051558 Essential Splice Site 1886 2268 40 49
ENSDART00000142465 Essential Splice Site 1886 2268 40 49

The following transcripts of ENSDARG00000074635 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 53111123)
Other Location(s):
Assembly Chromosome Position
GRCz11 1 52616460
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTCAGCATCACCGTCCTCATCCARYACCGCTTCTGCATTAAGGCCAG[G/A]TGAGGATACYTTTGTCAATACATTTGTGTGTGTGTGTGTGTGTGTGTGTG
Long Flanking Sequence:
TCGACAGAAGTAGATCAAAAATATTACTCATGATTATCCGCGTCTGTATTTAAGTGTCTATTGTGACTATATTGTATAAAATATTTGTTTGTAATTCCTGTAATCATACAATAAATCCAAAATAATACATACATTTAAAAATGTTTTCAGAGCATGTGACATTTTAACCACGCAGAAGTACTTCAGACTAATTAAACTTAGCATTTAGGTTTTTTCAATTGTTATTTATGGGTGGAGGGCGGGGCTTGGAGGCTAGAATTGATTAGATGTGAATGGCAGATTGATCCCGCCCTCAAATCTGTGAGCACCAATCAGAGAGGACATGAGAGTATCAGCTTCCGCTGATGTGCTGTTTTCTGAATGTTTTCAGGAGAGAATCGTTTCCGCTCTCCTCTGGCGTGGGACATGGTGGGCAAGAATCTGTTCGCTATGGCCATCGAGGGCGTGATTTTCTTCAGCATCACCGTCCTCATCCAGTACCGCTTCTGCATTAAGGCCAG[G/A]TGAGGATACTTTTGTCAATACATTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGATTATTTTGAAATGCATGTGATTTAATTTTTATACAATCTTCTGTGTTGGTGTTTATAGGTCACTTAGCACTAAGCTGAAGCCAATCGGAGAGGAGGATGAGGACGTAGCCCGAGAGAGGCAAAGGATTCTGGGAGGAGGAGGACAGACTGATATCCTGGAGCTCAGGCAGCTCACCAAGGTGTGTATTTGAGACACTGGAGAAATAAATGTATCATAGACAGACAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32775
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051558 Nonsense 1915 2268 41 49
ENSDART00000142465 Nonsense 1915 2268 41 49

The following transcripts of ENSDARG00000074635 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 53111411)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 51982010
GRCz11 1 52616748
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGATGAGGACGTAGCCCGAGAGAGGCAAAGGATTCTGGGAGGAGGAGGA[C/T]AGACTGATATCCTGGAGCTCAGGCAGCTCACCAAGGTGTGTATTTGAGAC
Long Flanking Sequence:
GCCCTCAAATCTGTGAGCACCAATCAGAGAGGACATGAGAGTATCAGCTTCCGCTGATGTGCTGTTTTCTGAATGTTTTCAGGAGAGAATCGTTTCCGCTCTCCTCTGGCGTGGGACATGGTGGGCAAGAATCTGTTCGCTATGGCCATCGAGGGCGTGATTTTCTTCAGCATCACCGTCCTCATCCAGTACCGCTTCTGCATTAAGGCCAGGTGAGGATACTTTTGTCAATACATTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGATTATTTTGAAATGCATGTGATTTAATTTTTATACAATCTTCTGTGTTGGTGTTTATAGGTCACTTAGCACTAAGCTGAAGCCAATCGGAGAGGAGGATGAGGACGTAGCCCGAGAGAGGCAAAGGATTCTGGGAGGAGGAGGA[C/T]AGACTGATATCCTGGAGCTCAGGCAGCTCACCAAGGTGTGTATTTGAGACACTGGAGAAATAAATGTATCATAGACAGACAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGAAAGATAGATAGACAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGACAGACACACAGACAGACAGACAGACAGACACAGACAGACAGATAGACAGACAGACAGACAGACAGACAGACAG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa4868
Status:
Allele not cryopreserved
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Availability:
n/a
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051558 Nonsense 2093 2268 46 49
ENSDART00000142465 Nonsense 2093 2268 46 49

The following transcripts of ENSDARG00000074635 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 53116175)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 51986774
GRCz11 1 52621512
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAACCCACCACTGGGATGGACCCCAAAGCACGGCGGGCCCTGTGGAACTG[C/A]ATCCTCAGCATCATTAAAGAGGGACGCTCCGTCGTGCTGACCTCACACAG
Long Flanking Sequence:
AAAAGCATCAATAAACAAAACTGCTAGAGACTAAAGGACCAAAATATATTTTCATTCTCTCCAAAACACGCACAGATCTGCATATGGGTGTATTTAGGTCACCTCCATTTCATGAAAAGATCTTGTGACACTCGCTCCAGTTTAGTTCAGTGCTGTTGTGTAACAGTCCTCCAGTTGACGGCCTGCCAGACCTCTTTTTCCCAGAACAAAAGCACAAAAAAAATGTCAAAATCCCACACGGCGTTTAGCTCTTGCCACATTTTTAATACGGCGTGAAGCGTTTAACTCTCAGAGGAGCATGCTTGTGTTGAGCAGTCGAGCTGTTGAGCAGAGGCAGCGCAGACGCCAGGATCATGATCACTCTTTTCCCACTCTTCATGGTTTTCTGCCTGTGTTTTCTGCTCAATCTGTGGGCCACGGTTAACCTGGCTGTTATTGTGGTTACAGGACGAACCCACCACTGGGATGGACCCCAAAGCACGGCGGGCCCTGTGGAACTG[C/A]ATCCTCAGCATCATTAAAGAGGGACGCTCCGTCGTGCTGACCTCACACAGGTGAGACAGATACATGCAACATTATAAGCCCGCCTATGCAATATTCACTCTTTTTGTGATGTTTAACAGATTTTCACAGTATTTTCTATAAAGTTTTTTTCTTCTGGAGAAAGTCTTACTTCTTTTATTTCAGCTAGAATAAAAGCAGTTTTTAATAATATTTAAAAAAAAAAAACATTTTAGATCAATATCATTAGCCCCCTTCAGCAAATTTCCTTTTGCCTTGGCTACCATTTATATCATTTTGATTTTCTTGTGATTTTTAACTTGACGCTTGTTTTGTTCTGCAGTATGGAGGAATGTGAAGCTCTTTGCACTCGGATGGCCATCATGGTGAACGGCAGGTTCCGCTGTCTGGGCAGTGTGCAGCATTTAAAGAACAAGTAAGTTTATTGAGTTCAGATGGTGCTTTATTCTTAAATGAACTCCATTTGATGCCTATTAAATACC
Associated Phenotype:
Not determined