ZMP

PDGFD

Ensembl ID:

ENSDARG00000077677

Description:

platelet derived growth factor D [Source:HGNC Symbol;Acc:30620]

Human Orthologue:

PDGFD

Human Description:

platelet derived growth factor D [Source:HGNC Symbol;Acc:30620]

Mouse Orthologue:

Pdgfd

Mouse Description:

platelet-derived growth factor, D polypeptide Gene [Source:MGI Symbol;Acc:MGI:1919035]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22727	Essential Splice Site	Available for shipment	Available now
sa24998	Nonsense	Mutation detected in F1 DNA	Not yet available
sa42627	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa22727

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
ENSDART00000111373	Essential Splice Site	54	372	1	7

Genomic Location (Zv9):

Chromosome 15 (position 43740747)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	44910117
GRCz11	15	44929658

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGGTGATGTCCTCCAGAGTCATGAGGGCTTCAAACATACGCAGCAATGG[T/A]GAGTTTGAACGATAAAGTGATTTAAAAAAATGCTAGGATGAGTGACAGTT

Long Flanking Sequence:

CGGTATTTCCTCGTCCTGACTGGATGAAAGGGGTCCAGCCCTCATAGGCTTCCTTTCTCCCTCCATCCATCCATCCATGCGCACCAAGGCGATCTTTCAGCGGGAGTTTGACGCGTGATCTCCGGGGAGCCGTCATCACCGCCAACTTTTACGCGCGTCCTTTCGCTAAATGTTCAAGGAATGGAAAGTATTCTTGTGGAATTATAAGCTCGGGGTCAAACGGGACAGAAGCAGATAAAGTTGGAAGTCTTTGAATTCCGTGGCTTGGTGTATATATACGGCGTCAACCTGTTCTCTGGATCCGAGGACGCGCGGCGCTGCGGTGGAAACTCCGGGTCCATGTGGCGCTTCTGGGTCGCGGATCAGCGGACGGTTGGGTTCCAGATGATGTGGCTGCTCGTGTGCTCCTTCATCGCGGTGTTGAGTGGTGAGAATTACCCCACACAGGCCCAGGTGATGTCCTCCAGAGTCATGAGGGCTTCAAACATACGCAGCAATGG[T/A]GAGTTTGAACGATAAAGTGATTTAAAAAAATGCTAGGATGAGTGACAGTTATGGATCAAACACGAGCTCTTGTTTTTGTTGACGTTTTAATGTACTTTCATCAGTTTAATATCTGTGGTGAATGTCACTAAGTCAGGTGTCCTAGCAGGTGTAGATGATCAAATTAAAGGGACAGTTCACCCCAACAATCATTTATTTATTCTCCCTCAAGTGATTGCAAACCTTTATGTGTCTTTATTCTGTTGAACAGAAAAGAAGATACTTTGAAGAATGTTTAAAACATTTAAAAATTGCAAGTCAGTGTTTCAACATTTTTCAAAATAACTGTGTTCTACAAAGAGTATCATGTTTTTACCAAAGTAAGAGTGTCGAAATCATGTTTTTGGCAAAGTTAAAGGTTGTAATACACCACAAACACCATGTTTTATTGTAGCAAAGCCACAATTAATTTGTTTTTACCATGTTTTAACAAAGAAATATCCAGTTAAACACAGAAAAAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa24998

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111373	Nonsense	106	372	2	7

Genomic Location (Zv9):

Chromosome 15 (position 43846895)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	44939502
GRCz11	15	44959043

KASP Assay ID:

554-7502.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TACTGTCGCCGCCGCACACACGCATCCTGCTGGAGTTTGATGCTCAGTTT[G/T]GACTGGAAGAGGCCGAGAATGGAGTCTGCAGGTGAGGGCGGAGCTTTGAA

Long Flanking Sequence:

GAGACGCATTCACGCCAGAAGTGAACTAGGTTTGTTTATTATGAAGACAGAAGTGAATTCAGATTATTTCGCCTAGAGTCTGCAGAGACTGAAAAGCAACTTAATGCTTATTTTCTCAATTGATCAGAAATAAACGTATAAATTAAGATGAAATTTATTATCTGAGCTGAATCTATGCTCTTCCCCGACCTGAACTGTGTTAAACTGAAATGAAGCAAATTCTGTCCTTTTATATGTGTTGTTTCTGTATATATCTGTGTGTGTATGCGTGTGTGTTTGTTTCCGAGAATAAACGCACTAACCTGTCCAAGTTGTGACCAGTAACAGACAGCAATCGCCTCACAGACTTGTACCGGAAGGAAGAGGTCATAATGATCAAGGGCGGAGGTCACGTCCAGAGCCCGCGCTTCCCCAGCTCGTACCCGCGCAACCTGCTGCTGTCATGGAAACTACTGTCGCCGCCGCACACACGCATCCTGCTGGAGTTTGATGCTCAGTTT[G/T]GACTGGAAGAGGCCGAGAATGGAGTCTGCAGGTGAGGGCGGAGCTTTGAATGTTTGAGTTCATGAATAATCAATCAGATCTGTTTAAGTGGAGGTGGAGAATGGAGTCTCCAAGTGAGGGCGGAGCTTTGAATGCATTCTTACATGAATAATTAATCAGATCTGTTTAAGTGGAGGTGGAGAATGGAGTCTGCAGGTGAGGGCGGGGCTTTGAATGCATTCTTACATGAATAATTAATCTGATCTGTTTAAGTGGAGGTGGAGAATGAAGTCTGCAGGTGAGGGCGGAGTTTTAAATGCATTCTTACATGAATAATTAATCAGATCTGTTTAAGTGGAGGTGGAGAATGCAGTCTGCAAGTGAGGGCGGAGCCTTGAATGCATTCTTACATGAATAATTAATCAGATCTGTTTAAGTGGAGGTGGAGAATGGAGTCTGCAGGTGAGGGCGGAGTTTTAAATGCATTCTTACATGAATAATTAATCAGATCTGTTTAAGTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42627

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
ENSDART00000111373	Nonsense	366	372	7	7

Genomic Location (Zv9):

Chromosome 15 (position 43880763)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	44973370
GRCz11	15	44992911

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACTCTGGAGGAGATTTACCTGCAGCATCACGAGAGATGTGACTGTGTGTG[T/A]CAATCCAGACCACCACGATAAACACACACACACTAGAGTCCAAACCACCA

Long Flanking Sequence:

GTATAGAAGTGTCTTGAAGAATATCAAGTCTAATATTATTTACTGTCATCATGGCAAAGATAAAATAAATCAGTAATTAGAAATTAGTTATTAAAACTATTATGTTTAGAAATGTGCTGAAAAAAAAAAACATCTCTCCGTTAAACAGAAAGTGGGGGGAAAGAAACAGGGAGGCTCATAATTCAGGACGGCTAATAATTCTGTCTTCAACTGTATATATTAATTTTGGATTTTTAATATTTAATTTTTGCAAGATCAGATGAAGTAGATAGTGTGCGGGACATTTTTCTAGTTTAGATTAGGTTTTGAAATCTATTTAAATCTATAGATTATTGTCTCTAATGTATTTGTGTGTGTGTGTGTTTGTGTGTATGTGTGTGTGTGTGTTGTCAGGTGCTGAAGTTTTCTCCTGGTGCCAGTTTCTACAGGAAGAAAAGCAGAGCGCGGTGGACTCTGGAGGAGATTTACCTGCAGCATCACGAGAGATGTGACTGTGTGTG[T/A]CAATCCAGACCACCACGATAAACACACACACACTAGAGTCCAAACCACCACAGTGAATACATACATACATACATACACACACACACACAGAGTCCAGATCACCACAATGAATAAATATAAACACACACAACACACACATAGTCCACATAATCAAGATAAACTCACACATACACACACACACACACACACACACACACTAGAGTCCAAACCACCACAATGAATACACATACACATACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCCGTGATTCTTGATAGCCACGATTAACACACACATCCAGACCACCAGTTAACACACACACAGATTCTAGATTGCCAC

Associated Phenotype:

Not determined