ZMP

Ensembl ID:

ZFIN ID:

Description:

Si:ch211-245g11.2 protein [Source:UniProtKB/TrEMBL;Acc:A8WFY7]

Human Orthologue:

SFRS15

Human Description:

splicing factor, arginine/serine-rich 15 [Source:HGNC Symbol;Acc:19304]

Mouse Orthologue:

Srsf15

Mouse Description:

serine/arginine-rich splicing factor 15 Gene [Source:MGI Symbol;Acc:MGI:2146350]

Allele Name:

sa19125

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000016273	Essential Splice Site	53	722	3	17
ENSDART00000099234	Essential Splice Site	55	729	3	16

The following transcripts of ENSDARG00000018854 do not overlap with this mutation:

• ENSDART00000129218
• ENSDART00000130404

Genomic Location (Zv9):

Chromosome 15 (position 40822317)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	42338713
GRCz11	15	42295065

KASP Assay ID:

2260-8960.1 (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa17523

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000016273	Splice Site, Nonsense	54	722	4	17
ENSDART00000099234	Splice Site, Nonsense	56	729	4	16

The following transcripts of ENSDARG00000018854 do not overlap with this mutation:

• ENSDART00000129218
• ENSDART00000130404

Genomic Location (Zv9):

Chromosome 15 (position 40822415)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	42338811
GRCz11	15	42295163

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa2824

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000016273	Nonsense	413	722	12	17
ENSDART00000099234	Nonsense	421	729	11	16

The following transcripts of ENSDARG00000018854 do not overlap with this mutation:

• ENSDART00000129218
• ENSDART00000130404

Genomic Location (Zv9):

Chromosome 15 (position 40828379)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	42344775
GRCz11	15	42301127

KASP Assay ID:

554-3397.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa35985

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
ENSDART00000016273	Nonsense	463	722	13	17
ENSDART00000099234	Nonsense	471	729	12	16

The following transcripts of ENSDARG00000018854 do not overlap with this mutation:

• ENSDART00000129218
• ENSDART00000130404

Genomic Location (Zv9):

Chromosome 15 (position 40830183)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	42346579
GRCz11	15	42302931

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: