ZMP

Ensembl ID:

ZFIN ID:

Description:

Novel protein similar to human and mouse SH2 domain containing 4B (SH2D4B) [Source:UniProtKB/TrEMBL;

Human Orthologue:

SH2D4B

Human Description:

SH2 domain containing 4B [Source:HGNC Symbol;Acc:31440]

Mouse Orthologue:

Sh2d4b

Mouse Description:

SH2 domain containing 4B Gene [Source:MGI Symbol;Acc:MGI:1925182]

Allele Name:

sa31920

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
ENSDART00000100895	Nonsense	100	450	2	8
ENSDART00000144045	Nonsense	100	441	2	7

The following transcripts of ENSDARG00000069374 do not overlap with this mutation:

• ENSDART00000146998

Genomic Location (Zv9):

Chromosome 13 (position 21744042)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	21473380
GRCz11	13	21603830

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa2711

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:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000100895	Nonsense	136	450	3	8
ENSDART00000144045	Nonsense	136	441	3	7

The following transcripts of ENSDARG00000069374 do not overlap with this mutation:

• ENSDART00000146998

Genomic Location (Zv9):

Chromosome 13 (position 21744440)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	21473778
GRCz11	13	21604228

KASP Assay ID:

554-3316.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa11975

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000100895	Nonsense	236	450	5	8
ENSDART00000144045	Nonsense	236	441	5	7

The following transcripts of ENSDARG00000069374 do not overlap with this mutation:

• ENSDART00000146998

Genomic Location (Zv9):

Chromosome 13 (position 21753063)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	21482401
GRCz11	13	21612851

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa7371

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:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000100895	Missense	360	450	7	8
ENSDART00000144045	Missense	360	441	7	7

The following transcripts of ENSDARG00000069374 do not overlap with this mutation:

• ENSDART00000146998

Genomic Location (Zv9):

Chromosome 13 (position 21761818)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	21491156
GRCz11	13	21621606

KASP Assay ID:

554-4027.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: