ZMP

Ensembl ID:

ZFIN ID:

Description:

hypothetical protein LOC799868 [Source:RefSeq peptide;Acc:NP_001076403]

Human Orthologue:

ST6GALNAC1

Human Description:

ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltran

Mouse Orthologues:

Gm11735, St6galnac1

Mouse Descriptions:

ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltran
predicted gene 11735 Gene [Source:MGI Symbol;Acc:MGI:3713525]

Allele Name:

sa24910

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
ENSDART00000064335	Essential Splice Site	36	427	1	9
ENSDART00000112847	Essential Splice Site	36	270	1	10

The following transcripts of ENSDARG00000043816 do not overlap with this mutation:

• ENSDART00000141804

Genomic Location (Zv9):

Chromosome 12 (position 22044240)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	20569821
GRCz11	12	20691695

KASP Assay ID:

554-7537.1 (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa14861

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
ENSDART00000064335	Nonsense	108	427	2	9
ENSDART00000112847	Nonsense	108	270	2	10

The following transcripts of ENSDARG00000043816 do not overlap with this mutation:

• ENSDART00000141804

Genomic Location (Zv9):

Chromosome 12 (position 22044532)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	20570113
GRCz11	12	20691987

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa2629

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000064335	Nonsense	247	427	5	9
ENSDART00000112847	Nonsense	247	270	5	10

The following transcripts of ENSDARG00000043816 do not overlap with this mutation:

• ENSDART00000141804

Genomic Location (Zv9):

Chromosome 12 (position 22049186)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	20574767
GRCz11	12	20696641

KASP Assay ID:

554-2558.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa2651

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
ENSDART00000064335	Nonsense	307	427	6	9
ENSDART00000112847	None	None	270	7	10

The following transcripts of ENSDARG00000043816 do not overlap with this mutation:

• ENSDART00000141804

Genomic Location (Zv9):

Chromosome 12 (position 22049434)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	20575015
GRCz11	12	20696889

KASP Assay ID:

554-3169.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa22086

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000064335	Essential Splice Site	336	427	None	9
ENSDART00000112847	Essential Splice Site	None	270	None	10

The following transcripts of ENSDARG00000043816 do not overlap with this mutation:

• ENSDART00000141804

Genomic Location (Zv9):

Chromosome 12 (position 22050933)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	20576514
GRCz11	12	20698388

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: