si:dkey-85g17.2

Ensembl ID:

ENSDARG00000074759

ZFIN ID:

ZDB-GENE-030131-146

Description:

cell division cycle and apoptosis regulator protein 1 [Source:RefSeq peptide;Acc:NP_001139071]

Human Orthologue:

CCAR1

Human Description:

cell division cycle and apoptosis regulator 1 [Source:HGNC Symbol;Acc:24236]

Mouse Orthologue:

Ccar1

Mouse Description:

cell division cycle and apoptosis regulator 1 Gene [Source:MGI Symbol;Acc:MGI:1914750]

Allele Name	Consequence	Status	Availability
sa8754	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa22266	Nonsense	Available for shipment	Available now
sa22267	Nonsense	Available for shipment	Available now
sa35455	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Allele Name:

sa8754

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
ENSDART00000109579	Essential Splice Site	488	1194	10	24
ENSDART00000111129	Essential Splice Site	532	1238	11	25
ENSDART00000133057	Essential Splice Site	488	1194	11	25
ENSDART00000138172	None	None	282	None	7

The following transcripts of ENSDARG00000074759 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 13 (position 18450100)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	18270135
GRCz11	13	18401127

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACACAGCAGTGCTGGACCCGCCTGATGCCAATCACACCTACAGTGCAAAG[G/A]TAGAGTCAGCATAATACTTACTTCCACTTCAGAGGATTTTTGACAATCAT

Long Flanking Sequence:

GACGGATCCTAAAGGTGTGTGTACAAGCGTACCTGTTTCAGACAAAATCTCTTCAAAGTGTTTCATATTCAATTTAAATCAAATAGGGCGTCTCAAAAAATGCTAAAAAAAATCATGTTGCGCGCACCCAAAGCAAACCTCCGCAAACACATCGATAACGTCACATTCGCCGTGCGCACTCAAGTGAACTAGCGGATGCATCAAGTATAAACTAGGCTTCATGCCTATTCAGGACTATATTCAGTTAATGATTGCCTTTCTCTGTTTTCGACAGATACAATTGTGATATGATGGAGTTGCGGCGGAGGTATCAGAGCCTCTACATCCCTAGTGACTTCTTTAACGCTGTGTTTACTTGGGTGGATGCCTTCCCCTTATCAAGACCTTTTACTTTCGGAAACTACTGTAACTTCCACATCATGCATAAAGAGGTGGACTCGTTGGTCAAAAACACAGCAGTGCTGGACCCGCCTGATGCCAATCACACCTACAGTGCAAAG[G/A]TAGAGTCAGCATAATACTTACTTCCACTTCAGAGGATTTTTGACAATCATTATTTTTTTGGTAATGGTTATAGGTGATGCTGTTGGCCAACCCCAGTCTAGATGAGCTGTATCATAAGTCATGTGCTCTGTCAGAAGATCCAGCCGAGCTCAGAGACTCGTTCCAGCACCCTGCCCGCCTCATCAAGGTACGGCTCTCCAGATTACTCCTCTAAATGCAGCTGGGTTTGTGCAATAAGCTTGCATTATATGTAATCACTAACTTGTGGGCTTTTTAATGGCATTTGCTTTGCACTTCAGTGGTAGCAGTTTCACAGGAATGGACAACATTGTTTTTTATTACTTTTGTGGTTTTCTGCTGTTATTTAGCTATTAGAGCACAGCATTGACTGCTAGTATCCCATTGAGTTTCTTCATCAGTTATTTGACAGAGATTCCTCCATAATGAGAACTAAGCCTTGGCTTGAACTGAGCCAAAGCAGCCAGCTTTGAAATAAATAA

Associated Phenotype:

Not determined

Allele Name:

sa22266

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109579	Nonsense	850	1194	17	24
ENSDART00000111129	Nonsense	894	1238	18	25
ENSDART00000133057	Nonsense	850	1194	18	25
ENSDART00000138172	None	None	282	None	7

The following transcripts of ENSDARG00000074759 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 13 (position 18467305)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	18287340
GRCz11	13	18418332

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCTTCCAACCAAGGATGAGAAGAAGGACAAAAAAGAGAGAGCTAAAAAA[G/T]AGGCCGAAAGAAGGGATATAAAGAAAGAAAGAGATGAAGACAATGGAGAG

Long Flanking Sequence:

GTTGTCTTTCCTTGTCTATGGCTAGGCAGAACCTCGGTTTTTAGCACTACAAAGTTTTGAATGTGGTAATCATGGAACATTTTCTTGCACATGACCACACAGAACAAACTTGTTGGCATCCAAAGACTTGTAGGCTTTTAACTTCTCTTGAAAAATCACTTGAAGTTTCAATGAGGTAGTTTTATGTTTCTTATCCAATATCCATTGGGAGGGTGCTAGCGCAAATGGACCTGTCAGACGAACGCGGCTCACTTTAACGTTAATTTTGCTTATCTGTGCTTTACTTCACTGTGCTTATCACTGGGTGAGAAAACAATTGTTAATATCTGGCCGCGACGAGGCATAAACAGCACTGGTCATTTGTTCTGTTTCAGGTGTCATTGTTTGCTGAATTGTTCAACGAAATGCTTCAACGAGACTTCGGCTACAGGATTTACAAAGCTCTCGCTTCTCTTCCAACCAAGGATGAGAAGAAGGACAAAAAAGAGAGAGCTAAAAAA[G/T]AGGCCGAAAGAAGGGATATAAAGAAAGAAAGAGATGAAGACAATGGAGAGCCGGTCGCAAAGAGAATAAGAGAGGAAGATGACAAGAGGAAGGTGAGGACGTACTTCAGTGTGAATTGGATCTTTAGGTGTTATCTTAAATGAATGTAAAAGTAAGCCACTCAATTTGTGTTTCCGGGATAAAGGATGAGGAAAAGGAGAGAGGAATAAAGAGAGAAGAATCCAAAGATGACGACGATAATGAAGATGGAAGCAGCAACAACAATGCAGATGAATACGATCCTTTGGAGGCAGAAGATGCAGACGATTATGATGACGATGGTAGGGCTGTTGAAATAATATAGCTGAATTCAAAGAAAAGTTTTGATTAGGGATAAATGTGTTTTATTTTATATTACATTTAAATATTTAAACAAATAATTTTTGTTTAAATTAGGTTTTATGAGAAGTACGTTATCTATAAATAAGGCATTATTCTTTGATAATATTTCTATATGCATT

Associated Phenotype:

Not determined

Allele Name:

sa22267

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109579	Nonsense	1020	1194	21	24
ENSDART00000111129	Nonsense	1064	1238	22	25
ENSDART00000133057	Nonsense	1020	1194	22	25
ENSDART00000138172	None	None	282	None	7

The following transcripts of ENSDARG00000074759 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 13 (position 18476756)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	18296791
GRCz11	13	18427783

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGGTGAAGAAGTTGTTAAACAAACCTTTGGTTAAAGAGTCGTGCCATTA[T/A]CGAAAGCTGACGGACAGGCCTAAAGATGAGCCTTGCCCCGCACTGATCTC

Long Flanking Sequence:

CTGTATTATTATTATTACCATTTCAAACTAATATTCATGTAATAATAATGCTTAAAATAACTTTCATATTTTGTAAAAAAAAAAAAAATAATAATAATATATATATATATATATATATATATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATGTATGTATGTATATGTATGTATCATTTATGTATCAAAGTAATTGATTAAAAGGAAAAGATGTTTGTTGCATCATGCCTGATCACAATATAATGTGTTACTAGTAATTTTCTAATTGAACGCAATGTAGCATATTTATTAAAAGACTGTTTTTTTTCTATCTTTTCAGGTGAAGAAGTTGTTAAACAAACCTTTGGTTAAAGAGTCGTGCCATTA[T/A]CGAAAGCTGACGGACAGGCCTAAAGATGAGCCTTGCCCCGCACTGATCTCTGAGGCTCACATAGACAACCTTTTAGGTGTGCAAAGAGGAGGATGACTGAAACTGAGAAGCTCATTTGTAACAATAGAGCACATATCAATGACAAACTCTCTGTGCCCACAGGTAACCAGATTTTACTGACCAGCCAGAAGATCAAGCGAGAGCCAGATGAGAGCGGTGAGTCAGGGAGTCTAATCGTCTACAAGGGAGCTCTGGTGGATGTGGGAAGTATGATGCAGAAGCTGGAGAAGAGCGAGAAAACACGAGAGGACATTGAGCAAAAGCTCATGCAGCAAGATGTTAAAATGGGTAACACTTTTTTTATTACATTCAAATGACTGTCATGAGCAGTTTGATTTGTGGTCAGTGAACCTTAGTGACCCATTATGTTTATTTTTTTGATGGGATAATAATAGTTGCTCCTTTTTAGATCCAGGTTGTAGCACATTTTGTCTTCACAA

Associated Phenotype:

Not determined

Allele Name:

sa35455

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109579	Essential Splice Site	1046	1194	22	24
ENSDART00000111129	Essential Splice Site	1090	1238	23	25
ENSDART00000133057	Essential Splice Site	1046	1194	23	25
ENSDART00000138172	None	None	282	None	7

The following transcripts of ENSDARG00000074759 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 13 (position 18476917)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	18296952
GRCz11	13	18427944

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCATTTGTAACAATAGAGCACATATCAATGACAAACTCTCTGTGCCCAC[A/C]GGTAACCAGATTTTACTGACCAGCCAGAAGATCAAGCGAGAGCCAGATGA

Long Flanking Sequence:

TGTATGTATGTATGTATGTATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATGTATGTATGTATATGTATGTATCATTTATGTATCAAAGTAATTGATTAAAAGGAAAAGATGTTTGTTGCATCATGCCTGATCACAATATAATGTGTTACTAGTAATTTTCTAATTGAACGCAATGTAGCATATTTATTAAAAGACTGTTTTTTTTCTATCTTTTCAGGTGAAGAAGTTGTTAAACAAACCTTTGGTTAAAGAGTCGTGCCATTATCGAAAGCTGACGGACAGGCCTAAAGATGAGCCTTGCCCCGCACTGATCTCTGAGGCTCACATAGACAACCTTTTAGGTGTGCAAAGAGGAGGATGACTGAAACTGAGAAGCTCATTTGTAACAATAGAGCACATATCAATGACAAACTCTCTGTGCCCAC[A/C]GGTAACCAGATTTTACTGACCAGCCAGAAGATCAAGCGAGAGCCAGATGAGAGCGGTGAGTCAGGGAGTCTAATCGTCTACAAGGGAGCTCTGGTGGATGTGGGAAGTATGATGCAGAAGCTGGAGAAGAGCGAGAAAACACGAGAGGACATTGAGCAAAAGCTCATGCAGCAAGATGTTAAAATGGGTAACACTTTTTTTATTACATTCAAATGACTGTCATGAGCAGTTTGATTTGTGGTCAGTGAACCTTAGTGACCCATTATGTTTATTTTTTTGATGGGATAATAATAGTTGCTCCTTTTTAGATCCAGGTTGTAGCACATTTTGTCTTCACAATGAGTAGAGGTGTGAACCTACATTAGTTTCATAGTTTGGTTTGGTCACGATTATCATGCCATCGATTCGGTTTAATTCGATATCTCGTAGCTTCACGGTGCATTGACAATGCTTTCTATAAACAATTGAATATTTTACTTCACAGCACAACATTTTATATA

Associated Phenotype:

Not determined

ZMP

Alleles

Mutation Details

Mutation Details

Mutation Details

Mutation Details