ZMP

zfr2

Ensembl ID:

ENSDARG00000071683

ZFIN ID:

ZDB-GENE-070705-184

Description:

Novel protein [Source:UniProtKB/TrEMBL;Acc:A5WV30]

Human Orthologue:

ZFR2

Human Description:

zinc finger RNA binding protein 2 [Source:HGNC Symbol;Acc:29189]

Mouse Orthologue:

Zfr2

Mouse Description:

zinc finger RNA binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:2143792]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa13178	Essential Splice Site	Available for shipment	Available now
sa37419	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa13178

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000106164	Essential Splice Site	387	1004	6	19
ENSDART00000122341	Essential Splice Site	393	1010	6	19
ENSDART00000128916	Essential Splice Site	386	558	6	10

The following transcripts of ENSDARG00000071683 do not overlap with this mutation:

ENSDART00000144889

Genomic Location (Zv9):

Chromosome 22 (position 4725206)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	4699620
GRCz11	22	5083995

KASP Assay ID:

2261-6327.1 (used for ordering genotyping assays)

KASP Sequence:

CCGGCGCCGACGCTTACGCTGCGCACATTCGCGGATCCAAACACCAAAAG[G/A]TTTGTTTAATGTTTMATTTCAAYACTCTTCATCTYTTCAACATGTTTTTG

Long Flanking Sequence:

CGATCAGCCCTTCACAGTCATTTCTGTTGAGCATGTTCGCATGATGGAGTTTCTGCAACCGCCTGCTGCTCCTGATGGCGCTTGCATTTAAACTGACTTTCATTTTGTTTTACTCTTACACAACTAAATGAATTTTTTGGTCTATTTAAAAGACTGTATTTTAATTCCGTTACATCATCAATGCTTTAACAGGAACTTTATGAAATTAGTCATATCAGTCTTTCACCTGAAGTTTATACGTGGCCATAAAAACTCTTGACGCTGGTTTTCATAAAACATATTGCTTTATTTAATGTTGTTACTTTGCTGTCCCGCAGACTTATCGGGAACATCTGGAAGGGCAGAAGCACAAGAAGAAAGAGGCGGCTCAGAAGAGCGGCAGTCAGGTGACCAATGGCCCCCGTGGCGTCCAGACACAGTTGCGCTGTGAACTGTGCGACGTCTCGTGCACCGGCGCCGACGCTTACGCTGCGCACATTCGCGGATCCAAACACCAAAAG[G/A]TTTGTTTAATGTTTCATTTCAACACTCTTCATCTTTTCAACATGTTTTTGTATTGCAGCTTCTTTTTTTAAGTGTTGTCAATTATTTAGTTGAAATTAGGGCCGGACAATATATCAAAATAATCACAAATGTAGGAAATATTGCATGATTGAAGAATCTGAGCATTTGTATATGCAACAATAGAAGTACAAAATACACATGCAAATATTAATCAAAACATATTTCATTAGCATATTCTTATAATCTGTAGACATTTTGTGAAATACGAAAAAAAAGATTTTGTTATAATACGGTGGGAAATTACACATACTGTAAGTGTTGTAGTAATGTTTATTTTAATAAGAATTATTTGACAATTTTTTGATAATTAAACAAATTCTGTACTTTTTATTGTGAACATTTTTTAATTATTTTAGTATATGCTGTATTTTGCTAAATTTAGGGCTAGATAATAAATCAAAATTATCAAAATTTTGCAAATGTTTTTTTTTCCAGAAAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37419

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000106164	Nonsense	931	1004	18	19
ENSDART00000122341	Nonsense	937	1010	18	19
ENSDART00000128916	None	None	558	None	10

The following transcripts of ENSDARG00000071683 do not overlap with this mutation:

ENSDART00000144889

Genomic Location (Zv9):

Chromosome 22 (position 4699141)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	4673555
GRCz11	22	5057930

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGATGGTCCTGGTCTTCTCGACCCATGTGAGAAAGGTCAGACAGATGCTT[T/A]GGGAACCATGTCGAAACAGGCTCGTGAAGACGTAACCGCTAACGCACAGG

Long Flanking Sequence:

TCAATATTCAAATCGACATGGTCACTGAGTATATTGTAGAATTTAATGGCCATGTTTTTTAGTATTGGCTGATACATGCTATTTTCAATGTTATCGGTATTAAAGCTGATATAGCCACCAATATATTGTTAGCATTTAATGGGCAAATTTTTGCATTAACCGATACCTGCTAATTTCAATGTCATCAGTATTGAAACCGATATAGCCACTCTTTATATTGTAGAATTTAATGGCCATGTTTTTTAGTATTGGCCAATACATGCTAATATAAATGTTATCGGTACTGAAACCGATATCGCAAGCAGTATTTATTGGCTTTATTTATTAAAATAGACTAATAAATGTTACGCTTTTTAAGTGTTATCATGTCAAATCAATATTTCCACTAATATATTGTGCATTATAATAAAATATCTCTCAATATATTGACTATTTTTGGGTCTGTCCCTCAGATGGTCCTGGTCTTCTCGACCCATGTGAGAAAGGTCAGACAGATGCTT[T/A]GGGAACCATGTCGAAACAGGCTCGTGAAGACGTAACCGCTAACGCACAGGTACTAAACTAATGTGACTAGTCAAGTTTTTCAACTATTTTATATGAGCTGTTCTGTAAGGGACGTATCTTCGTTTTCCAGCATGCACTACGTCTGCTGGCTTTCCGTCAGATCCATAAAGTCCTCGGCATGGGCTCATTGCCGGTGTCCAAAGCTGCCGCTAGAAACCGCAAAAGACGACGTGACGGCAGCGACGTCGGTGAAGGAGAAGCAGACGGAAAAAAGGACAAAAAAGATGATTCCAACGACCCCTGAGACGTCTGCGTAATCTCAGCAACCTTTCAAAATGTATAAATATCCCTCAAAAGAGGAAAGAAACAAAGCAACACCCAATGGTTCTGTTTTTTGAAAATGACAAGTGACGGAAATAACTTGTATTCGTTCCCCTTTTATGATGTAATACCTTTTTATTACATCTGAGATGAAAATACGCTCCCAAAATTGGACTTAG

Associated Phenotype:

Not determined