ZMP

Ensembl ID:

ZFIN ID:

Description:

Novel protein [Source:UniProtKB/TrEMBL;Acc:B0S5K1]

Human Orthologue:

RNF31

Human Description:

ring finger protein 31 [Source:HGNC Symbol;Acc:16031]

Mouse Orthologue:

Rnf31

Mouse Description:

ring finger protein 31 Gene [Source:MGI Symbol;Acc:MGI:1934704]

Allele Name:

sa2051

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 > C

Consequence:

Essential Splice Site, Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112873	Missense	169	867	5	21
ENSDART00000148110	Essential Splice Site	168	633	5	16

The following transcripts of ENSDARG00000078267 do not overlap with this mutation:

• ENSDART00000145183

Genomic Location (Zv9):

Chromosome 2 (position 26864242)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	27060438
GRCz11	2	26716072

KASP Assay ID:

554-3007.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa16893

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112873	Nonsense	497	867	12	21
ENSDART00000148110	Nonsense	263	633	7	16

The following transcripts of ENSDARG00000078267 do not overlap with this mutation:

• ENSDART00000145183

Genomic Location (Zv9):

Chromosome 2 (position 26852849)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	27049045
GRCz11	2	26704679

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa19773

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
ENSDART00000112873	Nonsense	541	867	13	21
ENSDART00000148110	Nonsense	307	633	8	16

The following transcripts of ENSDARG00000078267 do not overlap with this mutation:

• ENSDART00000145183

Genomic Location (Zv9):

Chromosome 2 (position 26852389)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	27048585
GRCz11	2	26704219

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa6845

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
ENSDART00000112873	Nonsense	861	867	21	21
ENSDART00000148110	Nonsense	627	633	16	16

The following transcripts of ENSDARG00000078267 do not overlap with this mutation:

• ENSDART00000145183

Genomic Location (Zv9):

Chromosome 2 (position 26840551)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	27036747
GRCz11	2	26692381

KASP Assay ID:

554-4646.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: