ZMP

Ensembl ID:

ZFIN ID:

Description:

Novel protein similar to H.sapiens ANAPC1, anaphase promoting complex subunit 1 (ANAPC1) [Source:Uni

Human Orthologue:

ANAPC1

Human Description:

anaphase promoting complex subunit 1 [Source:HGNC Symbol;Acc:19988]

Mouse Orthologue:

Anapc1

Mouse Description:

anaphase promoting complex subunit 1 Gene [Source:MGI Symbol;Acc:MGI:103097]

Allele Name:

sa38973

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109247	Nonsense	245	1932	7	47
ENSDART00000133146	Nonsense	245	500	8	13
ENSDART00000140045	None	None	1336	None	33

The following transcripts of ENSDARG00000075687 do not overlap with this mutation:

• ENSDART00000133503
• ENSDART00000141381

Genomic Location (Zv9):

Chromosome 13 (position 47488724)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	46740729
GRCz11	13	47030564

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa2701

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109247	Nonsense	977	1932	24	47
ENSDART00000133146	None	None	500	None	13
ENSDART00000140045	Nonsense	381	1336	10	33
ENSDART00000109247	Nonsense	977	1932	24	47
ENSDART00000133146	None	None	500	None	13
ENSDART00000140045	Nonsense	381	1336	10	33

The following transcripts of ENSDARG00000075687 do not overlap with this mutation:

• ENSDART00000133503
• ENSDART00000141381

Genomic Location (Zv9):

Chromosome 13 (position 47555698)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	46807703
GRCz11	13	47097538

KASP Assay ID:

554-3051.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa5608

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109247	Nonsense	977	1932	24	47
ENSDART00000133146	None	None	500	None	13
ENSDART00000140045	Nonsense	381	1336	10	33
ENSDART00000109247	Nonsense	977	1932	24	47
ENSDART00000133146	None	None	500	None	13
ENSDART00000140045	Nonsense	381	1336	10	33

The following transcripts of ENSDARG00000075687 do not overlap with this mutation:

• ENSDART00000133503
• ENSDART00000141381

Genomic Location (Zv9):

Chromosome 13 (position 47555698)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	46807703
GRCz11	13	47097538

KASP Assay ID:

554-3051.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: