ZMP

Ensembl ID:

ZFIN ID:

Description:

zgc:153898 (zgc:153898), mRNA [Source:RefSeq DNA;Acc:NM_001077555]

Human Orthologue:

RAP1GAP2

Human Description:

RAP1 GTPase activating protein 2 [Source:HGNC Symbol;Acc:29176]

Mouse Orthologue:

Rap1gap2

Mouse Description:

RAP1 GTPase activating protein 2 Gene [Source:MGI Symbol;Acc:MGI:3028623]

Allele Name:

sa32040

Status:

Available for shipment
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Availability:

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Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000099895	Nonsense	71	472	4	15
ENSDART00000126559	Nonsense	122	700	6	23
ENSDART00000137817	Nonsense	65	629	2	19

The following transcripts of ENSDARG00000061551 do not overlap with this mutation:

• ENSDART00000128973

Genomic Location (Zv9):

Chromosome 15 (position 28643594)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	29361624
GRCz11	15	29294500

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa22667

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000099895	Nonsense	85	472	4	15
ENSDART00000126559	Nonsense	136	700	6	23
ENSDART00000137817	Nonsense	79	629	2	19

The following transcripts of ENSDARG00000061551 do not overlap with this mutation:

• ENSDART00000128973

Genomic Location (Zv9):

Chromosome 15 (position 28643636)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	29361666
GRCz11	15	29294542

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa18310

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

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000099895	Essential Splice Site	354	472	12	15
ENSDART00000126559	Essential Splice Site	405	700	14	23
ENSDART00000137817	Essential Splice Site	348	629	10	19

The following transcripts of ENSDARG00000061551 do not overlap with this mutation:

• ENSDART00000128973

Genomic Location (Zv9):

Chromosome 15 (position 28650830)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	29368860
GRCz11	15	29301736

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: