ZMP

Ensembl ID:

ZFIN ID:

Description:

U2-associated SR140 protein-like [Source:RefSeq peptide;Acc:NP_001184003]

Human Orthologue:

AC018450.1

Human Description:

U2-associated protein SR140 [Source:UniProtKB/Swiss-Prot;Acc:O15042]

Mouse Orthologue:

2610101N10Rik

Mouse Description:

RIKEN cDNA 2610101N10 gene Gene [Source:MGI Symbol;Acc:MGI:1915208]

Allele Name:

sa25819

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
ENSDART00000087714	Nonsense	359	750	9	18
ENSDART00000132651	Nonsense	577	923	17	25
ENSDART00000132854	None	None	277	None	9

The following transcripts of ENSDARG00000061490 do not overlap with this mutation:

• ENSDART00000135261

Genomic Location (Zv9):

Chromosome 2 (position 26779217)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	26975413
GRCz11	2	26631047

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa39842

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
ENSDART00000087714	Essential Splice Site	364	750	9	18
ENSDART00000132651	Essential Splice Site	582	923	17	25
ENSDART00000132854	None	None	277	None	9

The following transcripts of ENSDARG00000061490 do not overlap with this mutation:

• ENSDART00000135261

Genomic Location (Zv9):

Chromosome 2 (position 26779199)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	26975395
GRCz11	2	26631029

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa32928

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000087714	Nonsense	547	750	14	18
ENSDART00000132651	Nonsense	765	923	22	25
ENSDART00000132854	None	None	277	None	9

The following transcripts of ENSDARG00000061490 do not overlap with this mutation:

• ENSDART00000135261

Genomic Location (Zv9):

Chromosome 2 (position 26775427)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	26971623
GRCz11	2	26627257

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa1800

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > A

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000087714	Missense	642	750	16	18
ENSDART00000132651	Missense	860	923	24	25
ENSDART00000132854	None	None	277	None	9

The following transcripts of ENSDARG00000061490 do not overlap with this mutation:

• ENSDART00000135261

Genomic Location (Zv9):

Chromosome 2 (position 26772857)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	26969053
GRCz11	2	26624687

KASP Assay ID:

554-1792.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa39841

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000087714	Essential Splice Site	705	750	None	18
ENSDART00000132651	None	None	923	25	25
ENSDART00000132854	None	None	277	None	9
ENSDART00000087714	Essential Splice Site	705	750	None	18
ENSDART00000132651	None	None	923	25	25
ENSDART00000132854	None	None	277	None	9

The following transcripts of ENSDARG00000061490 do not overlap with this mutation:

• ENSDART00000135261

Genomic Location (Zv9):

Chromosome 2 (position 26772043)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	26968239
GRCz11	2	26623873

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa30820

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000087714	Essential Splice Site	705	750	None	18
ENSDART00000132651	None	None	923	25	25
ENSDART00000132854	None	None	277	None	9
ENSDART00000087714	Essential Splice Site	705	750	None	18
ENSDART00000132651	None	None	923	25	25
ENSDART00000132854	None	None	277	None	9

The following transcripts of ENSDARG00000061490 do not overlap with this mutation:

• ENSDART00000135261

Genomic Location (Zv9):

Chromosome 2 (position 26772043)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	26968239
GRCz11	2	26623873

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: