ZMP

pdcd4b

Ensembl ID:

ENSDARG00000041022

ZFIN ID:

ZDB-GENE-030131-9847

Description:

programmed cell death protein 4 [Source:RefSeq peptide;Acc:NP_945329]

Human Orthologue:

PDCD4

Human Description:

programmed cell death 4 (neoplastic transformation inhibitor) [Source:HGNC Symbol;Acc:8763]

Mouse Orthologue:

Pdcd4

Mouse Description:

programmed cell death 4 Gene [Source:MGI Symbol;Acc:MGI:107490]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39379	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa32409	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa39379

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000009223	Essential Splice Site	147	470	4	12

Genomic Location (Zv9):

Chromosome 22 (position 32371215)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	29732345
GRCz11	22	29681540

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGCGAAGATGAAGTCGATTATAAAGATCCCAATTACGATGCAGAGCAGG[T/G]ATGACCCACATAATACTATTGCTTTCGTAAAAGTTCGTAACCAATACATT

Long Flanking Sequence:

TATCAGACAATAATATAATGTAGATATTTATACAGATTTGAATTGGCATGGAAGTTTATCTAGTAAAGCCTGTACACTTATAGCTTATTAAGCCTTTCACCAGTTGGTTAGGTTTGGTTTCTGTTTCTCAGCTCAGTATCAGATTAGCTCTTGTGGTCAGAGCCCTGCACGAATCGAGAAATGATGTCATGCTGCTGTGAATTAAAGGGACCTGCCTCTGTTTTGGGGAATTATTTTATACTAGACATAACCCTGTCATATGATGACAATAACATGAACAGTGGCTAAAGCATGAGGCTAAAGAGTCGCACGGTTTCTGTTCTGCCTTTCTTCCTATACATCAGTTTTTTTTTTCATATTTTTTTTTTTTTTTGTGTTCAAAAGTATGTGTTTTGCTTCTGTAGGTGGTGCTGGGGGTAAAGGTGTTTGGGGAACACCTGGAGAAGTTTATGGCGAAGATGAAGTCGATTATAAAGATCCCAATTACGATGCAGAGCAGG[T/G]ATGACCCACATAATACTATTGCTTTCGTAAAAGTTCGTAACCAATACATTTTTCATGTAATCCACAATTTTGTGCTTCCAGGAAAACTGTGTATACGAGACGGTTGTCCTTCCTCTGGATGAAGAGGCGTTCGAGAAGACGGTCACTCCTATCGTGCAGGAGTACTTTGAACACGGAGATGCTAATGAAGTGGCGGTGAGATTGTTATGACCCCTATTGCTCGTTCATATCTAATCATTAAGCTTGTTTACGTGCATGCCAACGTGCTGATAAGCAGCCCAGACAGAATTTGCTGACTTGTTTTGCTATTTCTGTGCAGTGTTTGGTTAAAATATTGATGCAAAATGATTTTTAAAGTATTAGATCTGAAAACTTGACAAATAATTATTAAAAACTTATTATTTTTTTATTTACTTAACTAAAATATTAACATTTACTTAACAGGTTTTATTTAAGCCTTACAATGCAATTCCATTTGCAAACACTTATTTGTAAGCAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa32409

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000009223	Essential Splice Site	185	470	5	12

Genomic Location (Zv9):

Chromosome 22 (position 32371018)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	29732148
GRCz11	22	29681343

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCCTATCGTGCAGGAGTACTTTGAACACGGAGATGCTAATGAAGTGGCGG[T/A]GAGATTGTTATGACCCCTATTGCTCGTTCATATCTAATCATTAAGCTTGT

Long Flanking Sequence:

TGAATTAAAGGGACCTGCCTCTGTTTTGGGGAATTATTTTATACTAGACATAACCCTGTCATATGATGACAATAACATGAACAGTGGCTAAAGCATGAGGCTAAAGAGTCGCACGGTTTCTGTTCTGCCTTTCTTCCTATACATCAGTTTTTTTTTTCATATTTTTTTTTTTTTTTGTGTTCAAAAGTATGTGTTTTGCTTCTGTAGGTGGTGCTGGGGGTAAAGGTGTTTGGGGAACACCTGGAGAAGTTTATGGCGAAGATGAAGTCGATTATAAAGATCCCAATTACGATGCAGAGCAGGTATGACCCACATAATACTATTGCTTTCGTAAAAGTTCGTAACCAATACATTTTTCATGTAATCCACAATTTTGTGCTTCCAGGAAAACTGTGTATACGAGACGGTTGTCCTTCCTCTGGATGAAGAGGCGTTCGAGAAGACGGTCACTCCTATCGTGCAGGAGTACTTTGAACACGGAGATGCTAATGAAGTGGCGG[T/A]GAGATTGTTATGACCCCTATTGCTCGTTCATATCTAATCATTAAGCTTGTTTACGTGCATGCCAACGTGCTGATAAGCAGCCCAGACAGAATTTGCTGACTTGTTTTGCTATTTCTGTGCAGTGTTTGGTTAAAATATTGATGCAAAATGATTTTTAAAGTATTAGATCTGAAAACTTGACAAATAATTATTAAAAACTTATTATTTTTTTATTTACTTAACTAAAATATTAACATTTACTTAACAGGTTTTATTTAAGCCTTACAATGCAATTCCATTTGCAAACACTTATTTGTAAGCAAAGCAGGTCTCTTATATACATGGTGTCAGGTGGGTCTTAAAATGTCTTAAATTTCTATAACTAAAACTAATAGGCCTTAAAAAGTCTTAAATTCACTGAAATATGGTGTTGTATGTCTTAAAGACTTTTAAGCAGGTCTTTATTTTTCTTTTTTTTTCCATATAAAGCTACAATCAAAAATCTATCTGAAATTTACAAA

Associated Phenotype:

Not determined