ZMP

Ensembl ID:

ZFIN ID:

Description:

Novel protein similar to H.sapiens CNTLN, centlein, centrosomal protein (CNTLN) [Source:UniProtKB/Tr

Human Orthologue:

CNTLN

Human Description:

centlein, centrosomal protein [Source:HGNC Symbol;Acc:23432]

Mouse Orthologue:

Cntln

Mouse Description:

centlein, centrosomal protein Gene [Source:MGI Symbol;Acc:MGI:2443104]

Allele Name:

sa16056

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
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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000044234	Nonsense	74	1120	3	25
ENSDART00000147414	Nonsense	100	428	4	11

The following transcripts of ENSDARG00000033345 do not overlap with this mutation:

• ENSDART00000134032
• ENSDART00000147727

Genomic Location (Zv9):

Chromosome 1 (position 25973789)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	26314006
GRCz11	1	27007720

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa32688

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
ENSDART00000044234	Essential Splice Site	130	1120	4	25
ENSDART00000147414	Essential Splice Site	156	428	5	11

The following transcripts of ENSDARG00000033345 do not overlap with this mutation:

• ENSDART00000134032
• ENSDART00000147727

Genomic Location (Zv9):

Chromosome 1 (position 25966761)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	26306978
GRCz11	1	27000692

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa39622

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000044234	Nonsense	212	1120	6	25
ENSDART00000147414	Nonsense	238	428	7	11

The following transcripts of ENSDARG00000033345 do not overlap with this mutation:

• ENSDART00000134032
• ENSDART00000147727

Genomic Location (Zv9):

Chromosome 1 (position 25960334)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	26300551
GRCz11	1	26994265

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa24847

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
ENSDART00000044234	Essential Splice Site	465	1120	12	25
ENSDART00000147414	None	None	428	None	11

The following transcripts of ENSDARG00000033345 do not overlap with this mutation:

• ENSDART00000134032
• ENSDART00000147727

Genomic Location (Zv9):

Chromosome 1 (position 25857692)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	26197909
GRCz11	1	26891623

KASP Assay ID:

554-7454.1 (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa39621

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000044234	Nonsense	712	1120	17	25
ENSDART00000147414	None	None	428	None	11

The following transcripts of ENSDARG00000033345 do not overlap with this mutation:

• ENSDART00000134032
• ENSDART00000147727

The following genes are also affected by this mutation:

• ENSDARG00000092860

Genomic Location (Zv9):

Chromosome 1 (position 25836125)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	26176342
GRCz11	1	26870056

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa30583

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000044234	Nonsense	927	1120	21	25
ENSDART00000147414	None	None	428	None	11

The following transcripts of ENSDARG00000033345 do not overlap with this mutation:

• ENSDART00000134032
• ENSDART00000147727

The following genes are also affected by this mutation:

• ENSDARG00000092860

Genomic Location (Zv9):

Chromosome 1 (position 25810075)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	26150292
GRCz11	1	26844006

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: