ZMP

LOC100334116

Ensembl ID:

ENSDARG00000063316

Human Orthologue:

HGF

Human Description:

hepatocyte growth factor (hepapoietin A; scatter factor) [Source:HGNC Symbol;Acc:4893]

Mouse Orthologue:

Hgf

Mouse Description:

hepatocyte growth factor Gene [Source:MGI Symbol;Acc:MGI:96079]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa25053	Nonsense	Mutation detected in F1 DNA	Not yet available
sa18536	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa25053

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000092421	Nonsense	149	377	4	9

Genomic Location (Zv9):

Chromosome 18 (position 9387426)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	9958065
GRCz11	18	10012061

KASP Assay ID:

554-7862.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTACGGGATAATTTATGTCGTAATCCGGACAACACCACAACGGGTCCTT[G/A]GTGTTTTACCACAGACCCCAAACTACGTCACCAAGACTGCAGCATCCCAC

Long Flanking Sequence:

AACCTTTGTACTTTGTGAAAAAAAAAATGAAGAAGCTACATTTTTCCTAGGGCCAAACAGATTCTTGCATCGCAATGAAGTGTGGAATAGCATCTGCATTCTGATGTTGCAGATATAGTTAGTCATACCGCTCTTATTAATCTGCAAATTATTGAGATGTTGTTCTTGGCTGAAATTACAAGAAAAAAAATCTTCCATAAATGATTCTTATGTCATTTGTTTTGAAGCATTTGTTTCGACAAAAAAAAGCTAATACTTGTAGAGGATTGTTTATGTTTCTTTGCCACTGATTTAATGTGGTCATCAGTCTCTACTTTATGGAGCTAAAATGTCAAAGAGTAACAGCGTTTTAACAAAATTGCAGCAATTTAACTTTGTGTTTGATTCTACAAACCTCTCTTTCATATTTCATTTGATCAGTTTCTTACCCCAGAGGCACAAGCATCGAGATCTACGGGATAATTTATGTCGTAATCCGGACAACACCACAACGGGTCCTT[G/A]GTGTTTTACCACAGACCCCAAACTACGTCACCAAGACTGCAGCATCCCACAATGCTCGGAGGGTGAGTTTATTGTTTACCAGCTGTTCTTTCATATGCTGTACAGTTGCTCGATGTTAGGTTTATAAAGAGTGTCAATGTTTTTTTTTTTTTTGGATAGTTTAGGAACAAAATTGTTAACTAAGCTGTTAAGTAAAGAATAAAGTACATCCAAGAGTGTGTTATTGTCAAATAAGACCTGAGAGCAGTGGAATGGAAGGCTGTTGCATTAGACTGATGGACAAAAACAACCTTTTGGATGTACTTTCTACCACTTAATGGCTGCTCGCATTTTTTATTATTTTTTTTGCTAATTCTTAATCACCACAGCAGCATGGTGCCAGTAAATGCTAATATGTGTGTGGAGAGGATTATACTGCATATGGCATTTGTGTGTGACTCATCATTTCAGAAAGGCTTGAAAAACTCCACAACAAATACATGGAATAAACTTGGTATTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa18536

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000092421	Nonsense	180	377	5	9

Genomic Location (Zv9):

Chromosome 18 (position 9385238)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	9955877
GRCz11	18	10014249

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACATGTTCTTTATCCGTAGTGGAATGTATGACGTGTAACGGAGAAAGTTA[T/A]CGTGGACCCTTGGACCACACGGAGAGTGGYCGGGAATGCCAGCGCTGGGA

Long Flanking Sequence:

TTGGTCCTGTAGTGACTAAGCTCTACACTAAGTACTGTAATAATTACATGTTTCTTTAACCTTTGATCGTATGAAATCTGTTAGAAGCATACTTCTGGGGTTAAATACGAGGCCTAATGGGTGGTATGTCTGCGTAGTAAATTGAAGCGTCAGATGATTTATTTTTGGACAATCTAAGGGTCACATGTGGCTTCATAATTGCTTGTCTTCTTGATAAATACGATTACAATCCCTGTGGATATTAGCGTTGGTGATTACTGATTAGGCTACAGTATGTGACACTAACGTGCATTCATTCACTACCAGCATTTTGCCTGGGTTACATTTTTCTAACCGTTTAACACAACAATCAGGGTTGAATTTGAACCCAGTTGACTCATCCTTTACATGCACGCTAATGTCACTCAGATGGGGTCTTTGGGGCATTGTCCTGGTTAACATTCTTACCAGACATGTTCTTTATCCGTAGTGGAATGTATGACGTGTAACGGAGAAAGTTA[T/A]CGTGGACCCTTGGACCACACGGAGAGTGGCCGGGAATGCCAGCGCTGGGACCTTGAGGAACCACATAAACACATTTTCCACCCTAAAAGGTATGAGAACCAACACAAAATTGGAGATATTAGGAGAAAATCATTCAGAAATGTTTATGGTCTGGATTTTTATTTAATCAATATGAGTGTATAAGTGCATCTATAAAATATTTGCAAATTCATTCAATTCTCCTCTTACGTAAGGTTAGGTTCTTACTAAAACAGCCAAAGTAGATCCTTTAGCATAAATTGCAGACATGTTTTGGATATTATGGAGACTTTGGGCCAGTCTGGGGTGTGTTTCCCAAGGAACGACATAACTCGTGGCTGAACTATCATAGTATGATGCATCATTTGGGAAAAGAAGGATGTAGTAACAGTATTTCCCAAAACCATAGTTGCTTTGTTGCAGATTCATCATTTGAACCACGTTAGTTATATCGTAAAACATTAATAATGATATTGTAAACA

Associated Phenotype:

Not determined