ZMP

Ensembl ID:

ZFIN ID:

Description:

Novel protein similar to vertebrate centrosomal protein 350kDa (CEP350) [Source:UniProtKB/TrEMBL;Acc

Human Orthologue:

CEP350

Human Description:

centrosomal protein 350kDa [Source:HGNC Symbol;Acc:24238]

Mouse Orthologue:

Cep350

Mouse Description:

centrosomal protein 350 Gene [Source:MGI Symbol;Acc:MGI:1921331]

Allele Name:

sa15445

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
ENSDART00000090254	Nonsense	1677	3018	25	37
ENSDART00000132327	None	None	1078	None	15
ENSDART00000146175	Nonsense	495	1836	11	23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

• ENSDART00000137871

Genomic Location (Zv9):

Chromosome 8 (position 15093002)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	14538346
GRCz11	8	14576051

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa31635

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
ENSDART00000090254	Essential Splice Site	1999	3018	30	37
ENSDART00000132327	None	None	1078	None	15
ENSDART00000146175	Essential Splice Site	817	1836	16	23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

• ENSDART00000137871

Genomic Location (Zv9):

Chromosome 8 (position 15083510)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	14528854
GRCz11	8	14566559

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa21227

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
ENSDART00000090254	Nonsense	2513	3018	33	37
ENSDART00000132327	None	None	1078	None	15
ENSDART00000146175	Nonsense	1331	1836	19	23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

• ENSDART00000137871

Genomic Location (Zv9):

Chromosome 8 (position 15081622)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	14526966
GRCz11	8	14564671

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: