ZMP

Ensembl ID:

ZFIN ID:

Description:

CLIP-associating protein 2 [Source:UniProtKB/Swiss-Prot;Acc:Q6NYW6]

Human Orthologue:

CLASP2

Human Description:

cytoplasmic linker associated protein 2 [Source:HGNC Symbol;Acc:17078]

Mouse Orthologue:

Clasp2

Mouse Description:

CLIP associating protein 2 Gene [Source:MGI Symbol;Acc:MGI:1923749]

Allele Name:

sa36908

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:

T > A

Consequence:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000039871	Splice Site, Nonsense	128	1529	4	41
ENSDART00000076668	None	None	1287	None	35
ENSDART00000102499	None	None	1288	None	36
ENSDART00000136873	Splice Site, Nonsense	128	1476	4	37
ENSDART00000139109	None	None	1250	None	30
ENSDART00000144557	None	None	1288	None	36

The following transcripts of ENSDARG00000020345 do not overlap with this mutation:

• ENSDART00000133711
• ENSDART00000138735

Genomic Location (Zv9):

Chromosome 19 (position 44303807)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	43131575
GRCz11	19	42701012

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa13291

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000039871	Nonsense	174	1529	5	41
ENSDART00000076668	None	None	1287	None	35
ENSDART00000102499	None	None	1288	None	36
ENSDART00000136873	Nonsense	174	1476	5	37
ENSDART00000139109	None	None	1250	None	30
ENSDART00000144557	None	None	1288	None	36

The following transcripts of ENSDARG00000020345 do not overlap with this mutation:

• ENSDART00000133711
• ENSDART00000138735

Genomic Location (Zv9):

Chromosome 19 (position 44308343)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	43136111
GRCz11	19	42705548

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa36909

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
ENSDART00000039871	Nonsense	360	1529	11	41
ENSDART00000076668	Nonsense	128	1287	6	35
ENSDART00000102499	Nonsense	128	1288	6	36
ENSDART00000136873	Nonsense	360	1476	11	37
ENSDART00000139109	Nonsense	121	1250	4	30
ENSDART00000144557	Nonsense	128	1288	6	36

The following transcripts of ENSDARG00000020345 do not overlap with this mutation:

• ENSDART00000133711
• ENSDART00000138735

Genomic Location (Zv9):

Chromosome 19 (position 44345869)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	43173637
GRCz11	19	42743074

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa16627

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
Order Allele From EZRC

Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000039871	Nonsense	469	1529	14	41
ENSDART00000076668	Nonsense	237	1287	9	35
ENSDART00000102499	Nonsense	237	1288	9	36
ENSDART00000136873	Nonsense	469	1476	14	37
ENSDART00000139109	Nonsense	230	1250	7	30
ENSDART00000144557	Nonsense	237	1288	9	36

The following transcripts of ENSDARG00000020345 do not overlap with this mutation:

• ENSDART00000133711
• ENSDART00000138735

Genomic Location (Zv9):

Chromosome 19 (position 44347361)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	43175129
GRCz11	19	42744566

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa43337

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000039871	Nonsense	512	1529	16	41
ENSDART00000076668	Nonsense	280	1287	11	35
ENSDART00000102499	Nonsense	280	1288	11	36
ENSDART00000136873	Nonsense	512	1476	16	37
ENSDART00000139109	Nonsense	273	1250	9	30
ENSDART00000144557	Nonsense	280	1288	11	36

The following transcripts of ENSDARG00000020345 do not overlap with this mutation:

• ENSDART00000133711
• ENSDART00000138735

Genomic Location (Zv9):

Chromosome 19 (position 44349926)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	43177694
GRCz11	19	42747131

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa36910

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000039871	Essential Splice Site	686	1529	21	41
ENSDART00000076668	Essential Splice Site	454	1287	16	35
ENSDART00000102499	Essential Splice Site	454	1288	16	36
ENSDART00000136873	None	None	1476	None	37
ENSDART00000139109	None	None	1250	None	30
ENSDART00000144557	Essential Splice Site	454	1288	16	36

The following transcripts of ENSDARG00000020345 do not overlap with this mutation:

• ENSDART00000133711
• ENSDART00000138735

Genomic Location (Zv9):

Chromosome 19 (position 44365192)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	43192960
GRCz11	19	42762397

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa29259

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
ENSDART00000039871	Nonsense	928	1529	28	41
ENSDART00000076668	Nonsense	667	1287	21	35
ENSDART00000102499	Nonsense	667	1288	21	36
ENSDART00000136873	Nonsense	875	1476	24	37
ENSDART00000139109	Nonsense	649	1250	17	30
ENSDART00000144557	Nonsense	667	1288	21	36

The following transcripts of ENSDARG00000020345 do not overlap with this mutation:

• ENSDART00000133711
• ENSDART00000138735

Genomic Location (Zv9):

Chromosome 19 (position 44376455)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	43204223
GRCz11	19	42773660

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa18570

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
Order Allele From EZRC

Mutation:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000039871	Essential Splice Site	938	1529	29	41
ENSDART00000076668	Essential Splice Site	677	1287	22	35
ENSDART00000102499	Essential Splice Site	677	1288	22	36
ENSDART00000136873	Essential Splice Site	885	1476	25	37
ENSDART00000139109	Essential Splice Site	659	1250	18	30
ENSDART00000144557	Essential Splice Site	677	1288	22	36

The following transcripts of ENSDARG00000020345 do not overlap with this mutation:

• ENSDART00000133711
• ENSDART00000138735

Genomic Location (Zv9):

Chromosome 19 (position 44377533)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	43205301
GRCz11	19	42774738

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa12804

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
Order Allele From EZRC

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000039871	Nonsense	1003	1529	30	41
ENSDART00000076668	Nonsense	761	1287	24	35
ENSDART00000102499	Nonsense	762	1288	25	36
ENSDART00000136873	Nonsense	950	1476	26	37
ENSDART00000139109	Nonsense	724	1250	19	30
ENSDART00000144557	Nonsense	762	1288	25	36

The following transcripts of ENSDARG00000020345 do not overlap with this mutation:

• ENSDART00000133711
• ENSDART00000138735

Genomic Location (Zv9):

Chromosome 19 (position 44385111)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	43212879
GRCz11	19	42782316

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: