acin1a

Ensembl ID:

ENSDARG00000054290

ZFIN ID:

ZDB-GENE-030616-583

Description:

apoptotic chromatin condensation inducer 1a [Source:RefSeq peptide;Acc:NP_001007106]

Human Orthologue:

ACIN1

Human Description:

apoptotic chromatin condensation inducer 1 [Source:HGNC Symbol;Acc:17066]

Mouse Orthologue:

Acin1

Mouse Description:

apoptotic chromatin condensation inducer 1 Gene [Source:MGI Symbol;Acc:MGI:1891824]

Allele Name	Consequence	Status	Availability
sa19828	Essential Splice Site, Missense	Available for shipment	Available now
sa12080	Nonsense	Available for shipment	Available now
sa16806	Nonsense	Available for shipment	Available now
sa18032	Essential Splice Site	Available for shipment	Available now

Allele Name:

sa19828

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

G > A

Consequence:

Essential Splice Site, Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000040357	Missense	225	631	5	5
ENSDART00000076459	None	None	548	None	12
ENSDART00000128043	Essential Splice Site	224	857	5	18
ENSDART00000136082	None	None	572	None	12
ENSDART00000137395	None	None	149	None	6
ENSDART00000142342	None	None	260	None	6
ENSDART00000144518	None	None	548	None	12
ENSDART00000146485	None	None	345	None	4

The following transcripts of ENSDARG00000054290 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 2 (position 37919112)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	38234026
GRCz11	2	38216354

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACGCCAGACCTCAACGGAGTCGTCGAGCACAGCCGCCAAAAAGTCAACCG[G/A]TGAGGACAAGATCCAGTGGCTCGCAGCAACAGCAGCAGCCACCCCCCCAA

Long Flanking Sequence:

CAACATGGTAAACCGTGACAATGCTGACTGTTGAATTGATTTAAATAAATATAAATACTTGGCAGCAATGTATTAGCAATATTGCGATAAATCGTCATATCAATATTTTGTCCCACCACTAGTATGAATTTGTGTTTGTTTATATATTTCTCTGGTTATGAATTCATTACTAAGTTGTCTTTAATCTCATATTTTTCCGCTAGGATGTTGCTTCTTCCTTAGTCGATCAGAACCAGGGAAGTGCAGCAGTTGCTGGGGGATTTGGGGTCACAGAAAGCGAAAGTGAAAAAGAAATGCCTGGACAACCGTCCCTTTCTACAGCTGCCCATTCCCGTCCAAGAGCTTCATCTGTGCGGCTTCGTGGTAAAGGAGAGCCGACTTCAAGTCATGTACCAGCAGAAAGTGATGATGACAGTGAAGCTGGGGATGATGAGGAGGAGGAGGAGTGGAACGCCAGACCTCAACGGAGTCGTCGAGCACAGCCGCCAAAAAGTCAACCG[G/A]TGAGGACAAGATCCAGTGGCTCGCAGCAACAGCAGCAGCCACCCCCCCAACACATACCTTTACTGTCACAGCAGCTCAGACATCCAACTCCTCCCCCATCCCCTCCTCCTGAACTTTCTTTCCCACTCCCAGACACCCCTAAACAGAGTCCTCCTAGTCCTGGAGAGTCCCCGTCTAGGCAGCGTATATCTAGCTCTTCGAGTTCTGGTAGTTCCAGTAGTGACAGTCGTAGCAGTAGTCCTGAACCAGCAAGTGACACCACAGAACGCAGACCAGGTCCGTTAACCTTACTGGCACGCAAGATGGCATCTGAGAGGGCTTGTTCTGGAGCAGGAAAGCGTGATAGGGAAGGAGTGGATTTACAAAGAAGCCACCAAGAGGGAGTTGTATCCGCAATTACACACACAGCCAATGCAGCATCAGTTCTCTCACACCCTAGTTCAGTCATCTCCAACCAAGGTGTTAGTGTCGTTAGAGCCGCTGTGATGGAAGCGAGCGAT

Associated Phenotype:

Not determined

Allele Name:

sa12080

Status:

Available for shipment
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Availability:

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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000040357	Nonsense	473	631	5	5
ENSDART00000076459	None	None	548	None	12
ENSDART00000128043	None	None	857	None	18
ENSDART00000136082	None	None	572	None	12
ENSDART00000137395	None	None	149	None	6
ENSDART00000142342	None	None	260	None	6
ENSDART00000144518	None	None	548	None	12
ENSDART00000146485	None	None	345	None	4

The following transcripts of ENSDARG00000054290 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 2 (position 37918368)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	38233282
GRCz11	2	38215610

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GACTGGAGAGGGAACAAGCTTTAGAAAGAGAGAGAGCATTAGAGCAAGAA[C/T]GACTCGAAYGAGAGAGGCAAGAAAAAGAGAGGGTGGAGAAGGAAAGACAA

Long Flanking Sequence:

AACCAGCAAGTGACACCACAGAACGCAGACCAGGTCCGTTAACCTTACTGGCACGCAAGATGGCATCTGAGAGGGCTTGTTCTGGAGCAGGAAAGCGTGATAGGGAAGGAGTGGATTTACAAAGAAGCCACCAAGAGGGAGTTGTATCCGCAATTACACACACAGCCAATGCAGCATCAGTTCTCTCACACCCTAGTTCAGTCATCTCCAACCAAGGTGTTAGTGTCGTTAGAGCCGCTGTGATGGAAGCGAGCGATGGCATAAAGCAGGATGAAGGTGTTTTATGGGAGCAAGAACAAGAGAGGCTGAAAGCCCTAGAGAAAGAGGAGGAGGAAAGGGAGAAGGCATTGGAAAAGGAGCGAGCACAAGCTTTGGAACGGAAAAGACTTGAAGCTGCTTCGAAACGTGAGAAGGAGAGGGCTTTACAGCGAGAAAGGGAAGAGAAGGAGAGACTGGAGAGGGAACAAGCTTTAGAAAGAGAGAGAGCATTAGAGCAAGAA[C/T]GACTCGAACGAGAGAGGCAAGAAAAAGAGAGGGTGGAGAAGGAAAGACAAGAAAAAGAGCAAGCTTTAGAGAGGGAGAGACTCAAGCAGGAAAGACTTGAGAAAGAAAGACAAGAACGAGAAGAAGCTCTAGAGAGGGAGAGATTAGAAAGAGAACGGCTTGAAAAGGAAAGACAAGAACGAGAAGAAGCTCTAGAAAAGGAGAGATTGGAGAGAGAGCGGCTTGAGAAGGAAAGAAGAGAAAAAGAAGCTGCTCTAGAGAGGGAGAGATTGGAGAAAGAGCGTCTTGAGAAGGAAAAAAAAGAAAAAGAAGCTGCTCTAGAAAGGGAGAGATTGGAAAAAGAGCGTATTGAGAAGGAAAAAAGAGAAAAAGAAGAAGCTCTAGAGAGGGAGAGATTGGAGAAAGAGCGTCTTGAGAAGGAAAAAAGAGAAAAAGAGGAAGCTCAAGAGAGGGAGAGATTGAAGAAAGAGCGTCTTGAGAAAGAAAAAAAAGAAGCTCTT

Associated Phenotype:

Not determined

Allele Name:

sa16806

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000040357	Nonsense	563	631	5	5
ENSDART00000076459	None	None	548	None	12
ENSDART00000128043	None	None	857	None	18
ENSDART00000136082	None	None	572	None	12
ENSDART00000137395	None	None	149	None	6
ENSDART00000142342	None	None	260	None	6
ENSDART00000144518	None	None	548	None	12
ENSDART00000146485	None	None	345	None	4

The following transcripts of ENSDARG00000054290 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 2 (position 37918097)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	38233011
GRCz11	2	38215339

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCTTGAGAAGGAAAGAAGAGAAAAAGAAGCTGCTCTAGAGAGGGAGAGAT[T/A]GGAGAAAGARCGTCTTGAGAAGGAAAAAAAAGAAAAAGAAGCTGCTCTAG

Long Flanking Sequence:

TGAAGGTGTTTTATGGGAGCAAGAACAAGAGAGGCTGAAAGCCCTAGAGAAAGAGGAGGAGGAAAGGGAGAAGGCATTGGAAAAGGAGCGAGCACAAGCTTTGGAACGGAAAAGACTTGAAGCTGCTTCGAAACGTGAGAAGGAGAGGGCTTTACAGCGAGAAAGGGAAGAGAAGGAGAGACTGGAGAGGGAACAAGCTTTAGAAAGAGAGAGAGCATTAGAGCAAGAACGACTCGAACGAGAGAGGCAAGAAAAAGAGAGGGTGGAGAAGGAAAGACAAGAAAAAGAGCAAGCTTTAGAGAGGGAGAGACTCAAGCAGGAAAGACTTGAGAAAGAAAGACAAGAACGAGAAGAAGCTCTAGAGAGGGAGAGATTAGAAAGAGAACGGCTTGAAAAGGAAAGACAAGAACGAGAAGAAGCTCTAGAAAAGGAGAGATTGGAGAGAGAGCGGCTTGAGAAGGAAAGAAGAGAAAAAGAAGCTGCTCTAGAGAGGGAGAGAT[T/A]GGAGAAAGAGCGTCTTGAGAAGGAAAAAAAAGAAAAAGAAGCTGCTCTAGAAAGGGAGAGATTGGAAAAAGAGCGTATTGAGAAGGAAAAAAGAGAAAAAGAAGAAGCTCTAGAGAGGGAGAGATTGGAGAAAGAGCGTCTTGAGAAGGAAAAAAGAGAAAAAGAGGAAGCTCAAGAGAGGGAGAGATTGAAGAAAGAGCGTCTTGAGAAAGAAAAAAAAGAAGCTCTTGAGAAAGAGCGCCTTGAGAAGGAAAGACAAGAAAAAGAAGCTGTAGAGAGGGAGAGATTGGAGAAAGAGCGTCTTGAGAAGGAAAAAAGAGAAAAAGAAGCTGCTCTAGAAAGGGAGAGATTGGAAAAAGAGCGTATTGAGAAGGAAAAAAGAGAAAAAGAAGAAGCTCTAGAGAGGGAGAGATTGGAGAAAGAGCGTCTGGAGAAGGAAAAAAGAGAAAAAGAAGAAGCTCTAGAGAGGGAGAGATTGGAGAAAGAGCGTCTTGAGAAGG

Associated Phenotype:

Not determined

Allele Name:

sa18032

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000040357	None	None	631	None	5
ENSDART00000076459	Essential Splice Site	413	548	10	12
ENSDART00000128043	Essential Splice Site	722	857	16	18
ENSDART00000136082	Essential Splice Site	437	572	10	12
ENSDART00000137395	None	None	149	None	6
ENSDART00000142342	None	None	260	None	6
ENSDART00000144518	Essential Splice Site	413	548	10	12
ENSDART00000146485	None	None	345	None	4

The following transcripts of ENSDARG00000054290 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 2 (position 37902879)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	38217793
GRCz11	2	38200121

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CGGCGTAAAGARAGGGGGAAGAGCAAAGAGAGGAAAGCTGATAAAAAGGG[T/G]AAGGAAAAWTTTAATGTACAYGGACTACTTTTGTGCATTGGAGTAATGTT

Long Flanking Sequence:

TATGGCCACGCGTACAGCACTGCATGGTGTAAAATGGCCCCAGAGTAACCCTAAATTCCTCAGTGTTGACTTCTGTACGCAAGATGAGGTAAGCATTTCGTTTGATGGTATAGGATATTAGGTTTAAATCTTTTCCACAGTCTTTTTATTCCTTTGGAAACTAATTCTGCGTCATCCCATTAGTTGGACTTCCACAGGGGTTTGGGTCCAGCAGGAGAAAAGCCACCAGAGGATGCCCGTGGGGCTGCAGCTGCTGGGCCTGGCCGTCCTATGCCAGTGCCGCTCCTGCCAGAGCGTGACCAGTGGGCAGAACGTGAACGGGAAATGGAAAGGCGAGAGAGAGCACGTGCAGAAAGAGAGTGGGACAGAGATAAGGTCAGAGACTTCAGCAAACCTGGAGAGGACCGGGAACCTGGAGCCAGAAGATCACGCTCACGAGATCGTGAAAGGCGGCGTAAAGAAAGGGGGAAGAGCAAAGAGAGGAAAGCTGATAAAAAGGG[T/G]AAGGAAAAATTTAATGTACATGGACTACTTTTGTGCATTGGAGTAATGTTGTTTTTGGGATTATTGTAGTTTTTTATTGTATTGCTATACATGGCTTTGTTTTGGTCAAATGTATTTGTAAGTTTGTTCTTAATGCAATTATTTTATATAATTGCTGTATTAATTAAATGTCTGTTGGAATATTATGATAGTTTTGTATATTTTTGCATTGAAAAAACATGACGTGTGTATTTTGTGTTTTTACTTTTATTATTCCAGTGCTGCCGTAAACACAAAGGGATGTAAACACAAAAGCATTTTATTTTTAAAATTAAATTTTATTAACTTCCTCCCTCTTCCTTTTTAGAAAAAGGGCCCGAGGAGCCACCTGCTAAACTTCTGGATGACCTCTTCCGTAAAACCAAAGCTGCTCCGTGTATATACTGGCTCCCCCTCACTGAGGAGCAGGTACAGTTCTTTGGACATTTTAGTTATTTAGGCCCAATCCCAATTCTATTTTT

Associated Phenotype:

Not determined

ZMP

Alleles

Mutation Details

Mutation Details

Mutation Details

Mutation Details