ZMP

PGF (1 of 2)

Ensembl ID:

ENSDARG00000076767

Description:

placental growth factor [Source:HGNC Symbol;Acc:8893]

Human Orthologue:

PGF

Human Description:

placental growth factor [Source:HGNC Symbol;Acc:8893]

Mouse Orthologue:

Pgf

Mouse Description:

placental growth factor Gene [Source:MGI Symbol;Acc:MGI:105095]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa7440	Missense	Mutation detected in F1 DNA	Not yet available
sa14929	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa7440

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 > C

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114220	Missense	92	131	2	5

Genomic Location (Zv9):

Chromosome 17 (position 44915154)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	44635027
GRCz11	17	44748792

KASP Assay ID:

554-4275.1 (used for ordering genotyping assays)

KASP Sequence:

AGGGCCAGGAATATGTGGAGATGACCTTTGTGGAGCACAAAGCCTGTGAA[T/C]GTAGGTAAGGGAAAACATCYATTCAGTTTATKTAASCACTGTGYTTTGCA

Long Flanking Sequence:

CACTGTTGACCATCCCTTACACCTTAACCCACCCTTAAACCTACCCATGCCACCAAACCTGTCCATAACCCAACCTCTATCCCAACTCAAAAGCACCACAAGTGTTCTCAAATACATTATAAACACAGTAAGTACATTGTATTTATTTTTTTGATGTAAGTACATAGTAGTTAGGGACACTTAATATAAATTGGGACCGTACTTCCAACTGAAACAGAATATTGAGTAGGGGGCGGGGCTTTCTTTTTGCACATCATTGGCTCGAGTAAACCAACACAAAAATACAGTCATATAAATTACAGGAAATGTGGAAATATAAATAAAAATTGCATCACTGATGTTGGATGGGTTTTCACTAAATTCAAAAACTTTGTTTGTCAAGCACGTAGTTGGGGTGGATATTAATAATATTATGACTTTTTCAGTTATTAAAGATTAAGCCAGCAGAGCAGGGCCAGGAATATGTGGAGATGACCTTTGTGGAGCACAAAGCCTGTGAA[T/C]GTAGGTAAGGGAAAACATCTATTCAGTTTATGTAAGCACTGTGTTTTGCATTGCGATGCAGCTTTGGGTTGTCATTATAAATAAAAGTATTAAACATAAATGAGGAATAAACTGCATGCTGAACGGAAATAGAGGTGTTTTAATAGTCCCTTTGCTTTCTTTTCTTTTACATTGTGATTCCAAGACTAAGAAAACCTACAACAAAACAAGACAGGTAACAAGTTGTGCTACACTTACGCATTTTTGTTAATATAGGATATAGACTAAATGGAGTAATTGTTTCTTTTGTTGTAGATGGAAACCCAGAAATAGAGGGAGAAAAAGGAAGGAGAAGCAGAAAGCCAAAGACTGTGACCGGTAAGTAAAGCGTCTGCTAATAGTTTACCGTATATTAGCATTCAGCTAAGCTAACAATGCTTATCACACTTACTGACCTTTCAAAATATCCAAGGATATAAATAACATTTCTACAATTTTCATGAATAAAAGAAATATAATAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa14929

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114220	Nonsense	101	131	3	5

Genomic Location (Zv9):

Chromosome 17 (position 44915361)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	44635234
GRCz11	17	44748999

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

KTCTTTTCTTTYACATTGTGATTCCAAGACTAAGAAAACCTACAACAAAA[C/T]AAGACAGGTAACAAGTTGTGCTACACTTACGCATTTTTGTTAATATAGGA

Long Flanking Sequence:

ACTGAAACAGAATATTGAGTAGGGGGCGGGGCTTTCTTTTTGCACATCATTGGCTCGAGTAAACCAACACAAAAATACAGTCATATAAATTACAGGAAATGTGGAAATATAAATAAAAATTGCATCACTGATGTTGGATGGGTTTTCACTAAATTCAAAAACTTTGTTTGTCAAGCACGTAGTTGGGGTGGATATTAATAATATTATGACTTTTTCAGTTATTAAAGATTAAGCCAGCAGAGCAGGGCCAGGAATATGTGGAGATGACCTTTGTGGAGCACAAAGCCTGTGAATGTAGGTAAGGGAAAACATCTATTCAGTTTATGTAAGCACTGTGTTTTGCATTGCGATGCAGCTTTGGGTTGTCATTATAAATAAAAGTATTAAACATAAATGAGGAATAAACTGCATGCTGAACGGAAATAGAGGTGTTTTAATAGTCCCTTTGCTTTCTTTTCTTTTACATTGTGATTCCAAGACTAAGAAAACCTACAACAAAA[C/T]AAGACAGGTAACAAGTTGTGCTACACTTACGCATTTTTGTTAATATAGGATATAGACTAAATGGAGTAATTGTTTCTTTTGTTGTAGATGGAAACCCAGAAATAGAGGGAGAAAAAGGAAGGAGAAGCAGAAAGCCAAAGACTGTGACCGGTAAGTAAAGCGTCTGCTAATAGTTTACCGTATATTAGCATTCAGCTAAGCTAACAATGCTTATCACACTTACTGACCTTTCAAAATATCCAAGGATATAAATAACATTTCTACAATTTTCATGAATAAAAGAAATATAATATGTTATTCATTTAAAGTTATTGTGCTGTACATCTTGGTCTGTTGTTTTAGACTATTTTAATGTTTATGTTGTCTTCATTTTAAAAAAAATGGCGGTCCCCTAAGAAGTTTACTGATGCCTTTGTTGTGAATGAAAGAAGAGACAAACCAGGAGAAAATTTTGGGTATTTTCAAAGCAGAATCTTTTATAACAACTCGCTATCTGTGTC

Associated Phenotype:

Not determined