ZMP

Ensembl ID:

ZFIN ID:

Description:

Novel protein similar to mouse silencing mediator of retinoic acid and thyroid hormone receptor (SMR

Human Orthologue:

NCOR2

Human Description:

nuclear receptor corepressor 2 [Source:HGNC Symbol;Acc:7673]

Mouse Orthologue:

Ncor2

Mouse Description:

nuclear receptor co-repressor 2 Gene [Source:MGI Symbol;Acc:MGI:1337080]

Allele Name:

sa21362

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
ENSDART00000001092	None	None	1999	None	35
ENSDART00000051139	Nonsense	103	2325	3	44
ENSDART00000140618	None	None	1989	None	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45544262)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43495198
GRCz11	8	43501985

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa7154

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
ENSDART00000001092	None	None	1999	None	35
ENSDART00000051139	Nonsense	196	2325	4	44
ENSDART00000140618	None	None	1989	None	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45528922)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43479858
GRCz11	8	43486645

KASP Assay ID:

554-5459.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa13457

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000001092	None	None	1999	None	35
ENSDART00000051139	Essential Splice Site	196	2325	4	44
ENSDART00000140618	None	None	1989	None	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45528918)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43479854
GRCz11	8	43486641

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa14103

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000001092	Essential Splice Site	462	1999	9	35
ENSDART00000051139	Essential Splice Site	842	2325	19	44
ENSDART00000140618	Essential Splice Site	462	1989	9	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45460088)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43412870
GRCz11	8	43419657

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa34468

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000001092	Nonsense	696	1999	15	35
ENSDART00000051139	Nonsense	1060	2325	24	44
ENSDART00000140618	Nonsense	686	1989	15	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45448974)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43401756
GRCz11	8	43408543

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa41279

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
ENSDART00000001092	Nonsense	724	1999	16	35
ENSDART00000051139	Nonsense	1088	2325	25	44
ENSDART00000140618	Nonsense	714	1989	16	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45448816)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43401598
GRCz11	8	43408385

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa41278

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
ENSDART00000001092	Essential Splice Site	786	1999	17	35
ENSDART00000051139	Essential Splice Site	1150	2325	26	44
ENSDART00000140618	Essential Splice Site	776	1989	17	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45448503)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43401285
GRCz11	8	43408072

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa15996

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000001092	Essential Splice Site	1159	1999	23	35
ENSDART00000051139	Essential Splice Site	1523	2325	32	44
ENSDART00000140618	Essential Splice Site	1149	1989	23	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45441548)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43394330
GRCz11	8	43401117

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa11868

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
ENSDART00000001092	Nonsense	1177	1999	24	35
ENSDART00000051139	Nonsense	1541	2325	33	44
ENSDART00000140618	Nonsense	1167	1989	24	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45441362)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43394144
GRCz11	8	43400931

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa15101

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:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000001092	Nonsense	1211	1999	24	35
ENSDART00000051139	Nonsense	1575	2325	33	44
ENSDART00000140618	Nonsense	1201	1989	24	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45441260)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43394042
GRCz11	8	43400829

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa1781

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000001092	Nonsense	1321	1999	26	35
ENSDART00000051139	Nonsense	1685	2325	35	44
ENSDART00000140618	Nonsense	1311	1989	26	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45440637)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43393419
GRCz11	8	43400206

KASP Assay ID:

554-1774.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Stage	Entity	Quality	Tag
Larval:Day 5 ZFS:0000037	whole organism ZFA:0001094	quality PATO:0000001	normal PATO:0000461

Allele Name:

sa21361

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000001092	Nonsense	1437	1999	28	35
ENSDART00000051139	Nonsense	1801	2325	37	44
ENSDART00000140618	Nonsense	1427	1989	28	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45439868)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43392650
GRCz11	8	43399437

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa34467

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
ENSDART00000001092	Nonsense	1490	1999	28	35
ENSDART00000051139	Nonsense	1854	2325	37	44
ENSDART00000140618	Nonsense	1480	1989	28	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45439709)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43392491
GRCz11	8	43399278

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa12530

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000001092	Nonsense	1687	1999	30	35
ENSDART00000051139	Nonsense	2013	2325	39	44
ENSDART00000140618	Nonsense	1677	1989	30	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45430694)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43383476
GRCz11	8	43390263

KASP Assay ID:

2260-0990.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa38706

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
ENSDART00000001092	Essential Splice Site	1788	1999	None	35
ENSDART00000051139	Essential Splice Site	2114	2325	None	44
ENSDART00000140618	Essential Splice Site	1778	1989	None	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45427048)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43379830
GRCz11	8	43386617

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa34466

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
ENSDART00000001092	Nonsense	1972	1999	35	35
ENSDART00000051139	Nonsense	2298	2325	44	44
ENSDART00000140618	Nonsense	1962	1989	35	35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

• ENSDART00000133292

Genomic Location (Zv9):

Chromosome 8 (position 45422458)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	43375240
GRCz11	8	43382027

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: