ZMP

Ensembl ID:

ZFIN ID:

Description:

Novel protein similar to vertebrate MCF.2 cell line derived transforming sequence-like (MCF2L) [Sour

Human Orthologue:

MCF2L

Human Description:

MCF.2 cell line derived transforming sequence-like [Source:HGNC Symbol;Acc:14576]

Mouse Orthologue:

Mcf2l

Mouse Description:

mcf.2 transforming sequence-like Gene [Source:MGI Symbol;Acc:MGI:103263]

Allele Name:

sa32745

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
ENSDART00000114083	Essential Splice Site	121	1166	4	31
ENSDART00000144821	None	None	213	None	7

The following transcripts of ENSDARG00000075859 do not overlap with this mutation:

• ENSDART00000134291

Genomic Location (Zv9):

Chromosome 1 (position 47032386)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	45844047
GRCz11	1	46535279

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa9961

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
ENSDART00000114083	Nonsense	704	1166	19	31
ENSDART00000144821	None	None	213	None	7
ENSDART00000114083	Nonsense	704	1166	19	31
ENSDART00000144821	None	None	213	None	7

The following transcripts of ENSDARG00000075859 do not overlap with this mutation:

• ENSDART00000134291

Genomic Location (Zv9):

Chromosome 1 (position 47073771)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	45885432
GRCz11	1	46576664

KASP Assay ID:

2259-0994.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa18705

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
ENSDART00000114083	Nonsense	704	1166	19	31
ENSDART00000144821	None	None	213	None	7
ENSDART00000114083	Nonsense	704	1166	19	31
ENSDART00000144821	None	None	213	None	7

The following transcripts of ENSDARG00000075859 do not overlap with this mutation:

• ENSDART00000134291

Genomic Location (Zv9):

Chromosome 1 (position 47073771)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	45885432
GRCz11	1	46576664

KASP Assay ID:

2259-0994.1 (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa31232

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114083	Essential Splice Site	743	1166	20	31
ENSDART00000144821	None	None	213	None	7

The following transcripts of ENSDARG00000075859 do not overlap with this mutation:

• ENSDART00000134291

Genomic Location (Zv9):

Chromosome 1 (position 47075579)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	45887240
GRCz11	1	46578472

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: