ZMP

pcbp2

Ensembl ID:

ENSDARG00000013184

ZFIN ID:

ZDB-GENE-030131-563

Description:

poly(rC)-binding protein 2 [Source:RefSeq peptide;Acc:NP_957486]

Human Orthologues:

PCBP3, PCBP4

Human Descriptions:

poly(rC) binding protein 3 [Source:HGNC Symbol;Acc:8651]
poly(rC) binding protein 4 [Source:HGNC Symbol;Acc:8652]

Mouse Orthologues:

Pcbp3, Pcbp4

Mouse Descriptions:

poly(rC) binding protein 3 Gene [Source:MGI Symbol;Acc:MGI:1890470]
poly(rC) binding protein 4 Gene [Source:MGI Symbol;Acc:MGI:1890471]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa41325	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa38716	Splice Site, Nonsense	Mutation detected in F1 DNA	Not yet available
sa15679	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa41325

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
ENSDART00000025885	Essential Splice Site	31	318	2	12
ENSDART00000131317	Essential Splice Site	31	179	2	8

The following transcripts of ENSDARG00000013184 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 9 (position 221687)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	262823
GRCz11	9	262456

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCATCCGGCTGCTCATGCATGGCAAAGAAGTGGGCAGCATTATTGGGAAG[G/A]TGTGTTGGAGAAGCTTCAGTTTGTGTGCTCAGTCACATCATCACCACCAC

Long Flanking Sequence:

TGGAGGGCTTTAGGTGTGCTGTGTTGGTGTCGTGTGTTTATTCATTCATACTCCATTACACAAGAAAAATGTTGTCTTCGTCGTGTGGGTTATCTCACTATAACTGGGGTTTATAATCAGCTTTATTATATTATAGTTCTTGCTCTGTTTGTGTGATTCATATTGTAATTTTGAGTTTAGTATGCTTTTGTCGTAGCACCCTGGTCTTTGTGACGGTCAAATTATTATTGCTATTGATATTTAATTGGGTCGACTGCAGTATGTTTGATCTTGTCATTTTAATCTATGTAATGGGTGTGCCTTTTGTTTAATATTATTAATGTGTGGTGTGCTGATGTTCTGTGTTTGTGGGCTGCACAGGTTAATCATCCGTGACCAAAGATCCAGATCTCTGCAGGCTGATCATCATGGACTCTGGAGTGATTGAAGGAGGGCTGAACGTCACGCTGACCATCCGGCTGCTCATGCATGGCAAAGAAGTGGGCAGCATTATTGGGAAG[G/A]TGTGTTGGAGAAGCTTCAGTTTGTGTGCTCAGTCACATCATCACCACCACCACCATCATTATTATTGTCTACCGATACCAAAACCCGATCTGAAACCTCTATAATACATTAAGAAAATAGAGTGAATAAACAGATCCAGGATGTTCCTTATTTTTTCATTTCACCTTACTTTATCATTCCACAACTCTCTTAACAAACACAGCGCTTCTGTGAGGGAGCTCAAACAATCAAGTGATAAATAACAACATTTCTTCGCTTGGACTTAAGTGCAGGAGAAAATATATACAAACAAACAGCACCTGAACTTAAAATACCCTGCAGGCAATCCCAGGTTTACATATCTCACAGTTAGCTATGGCGATGTTGTCATCATCAGCTTTATAATACTTCCAGACCACAGACACACTTGCGCTTTCTTCTTCAATCTGCTTCTGTGCTCTACTTTGCCGGCATTCAACTAATAGTGCCTCTGCAACAAAGTGGTTGCTACGTTGCTGTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38716

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000025885	Splice Site, Nonsense	193	318	7	12
ENSDART00000131317	Splice Site, Nonsense	154	179	6	8

The following transcripts of ENSDARG00000013184 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 9 (position 228218)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	256292
GRCz11	9	255925

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCCCTTACCGACCCAAACCCTCAGGATCGCCTGTCATTTTTGCAGGAGGA[C/T]AGGTGGGTGTGTGTTTGTTCGTGTGGGTGTGTGTGCATGCACATCCATAT

Long Flanking Sequence:

TCATCCCCTCTGTGCTGATCTGGAGTCTTGATATGGCCTCAAGTTTCTCTGTTTCAGCAAATGTGATGATGATTTTTGCTGAAAGAGAGAACACACTCTGTTCACACTGACTCTCCTTTGGTGAGGTTGGTGCTGTGTTTGCTCCATTGACTTCCATTATAATCACATTGTTTGATACTGCCATGACCACGAATGCATGATTATACACTGCCAATCAATAAATGTGATTATAATGGAAGTCAGTGGGGACTTCAGCACTGGACAGCACTCAAGGGTTAATCATGCACTTGATCAATTAACTTTTGATTCATTGTAAGGCCAGAGTTAAGTGTTTTGTTGAATCTGTGTTCAGGTGTGCGTTTAAACATCAGTACTCTGCTAGATGTGCGGAGAGACGGTGTGTGTTTACTGTGTGCTTCTGCTTTCAGTCTCCTCCTAAAGGTGTGACCATCCCTTACCGACCCAAACCCTCAGGATCGCCTGTCATTTTTGCAGGAGGA[C/T]AGGTGGGTGTGTGTTTGTTCGTGTGGGTGTGTGTGCATGCACATCCATATATTTGCCTGTCTGTATGCAGTCGTGTGTGTGTGTTGTGTATTTGATATGTGTGTAATCCTAAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTGCAGGCATACGCGGTGCAGGGACAACATGCCATTCCTCAGCCTGATGTAAGAAGCAGACTTAAAGCAGTTTTTGCGTGTGCGTGCGTGCGTGCGTGTGTGTGTGTGACGGTTGTGTTGTGTCTCCACAGCTTACGAAGCTCCACCAGTTGGCGATGCAGCAGAGCCCGTTTCCTCTGGCCCCCAGTAGCCAAGGGTTCACAGGTGTGTGTGTGTGAGACGAGTGTGTGATGTAGGGCTGTCAATATGTCTGAACCCTTATTATTATTATTATTTTGTTGTTGTTTGTTTGTTTTTTAATAAGAAAGATTGTGCAATTATATTTGAATTCTTAAGGTAATCCTATATGTTAGAGGGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa15679

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000025885	Essential Splice Site	307	318	11	12
ENSDART00000131317	None	None	179	None	8

The following transcripts of ENSDARG00000013184 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 9 (position 229753)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	254757
GRCz11	9	254390

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCGGCTCACCCGCCAGCATCAGCCTGGCCGAATACCTGATCAATGCACGG[T/G]AAACRCACGCCAGCCAGCACCACAMTATCMTAACCGGGTCTTCATAACCA

Long Flanking Sequence:

TATGTTTATTTCTTTATATAGCTCTGTAGAAATACAACTGGGTTGAGCAAAGTGCTTTACGGGAAACAGTTTCCTATTTTCTTTTTCTTTTCTAACATCCCACACATTTTAACAATAAACCAAGTTAAAAGTAAACGTATAAGCCTAAAATATCAGAAGCAATTTTTAAAATGGCCTTGAGAGTGTTGGTGAGGGTTAAAGTGCATGAATGTAAGAGAGAAATGAATGAAGGTTTGAGTGTTTGAGAAATGTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTTTGTTTGTTTGTTAATGGTGTGTGTGTGTGTTCTTGTACTCTTGCAGTTGATTGGCTGCATCATCGGCCGTCAAGGTGCCAAGATTAACGAGATCCGTCAGATGTCGGGCGCTCAGATCAAGATTGCTAACCCAGTGGAGGGATCGAGCGACCGGCAGGTCACCATCACCGGCTCACCCGCCAGCATCAGCCTGGCCGAATACCTGATCAATGCACGG[T/G]AAACACACGCCAGCCAGCACCACACTATCCTAACCGGGTCTTCATAACCAGCGCCTTCTGAAAACAGCACACTCATGTGCAATACAGGGCTCCCACGCCTCCTGACAGTACTTTAATTTCAGACATACACATTCAAGATCTGGAAAATACTCAGTGAAGTGTGCTCCGCACTCCATTAGATGAGTTTGGTGCATTAATCAGATTAACAAAACTCAAAAGATCATGATATGCAGTCGTTGCAGTTATCGTTGCTATATATATATATATATATATTTATACACACCCACACACACACATACTTAATGAATAAGTGCTTAAAAAAAACAGCGTTCCTTGAATGTGCTTGATATTTTCTTTTATTCTTTAGATATATTTTGGATATCTTATTTTGGATTTATTGTTAATTAACCTTTGCCCAGCACTAGTAATCTTCGAATAGAGATATTGATATCAGTATTTATACAAAACATCATCATCATGTCAGTGTTGCCAGTGTCCCG

Associated Phenotype:

Not determined