ZMP

RASSF7 (1 of 3)

Ensembl ID:

ENSDARG00000094325

Description:

Ras association (RalGDS/AF-6) domain family (N-terminal) member 7 [Source:HGNC Symbol;Acc:1166]

Human Orthologue:

RASSF7

Human Description:

Ras association (RalGDS/AF-6) domain family (N-terminal) member 7 [Source:HGNC Symbol;Acc:1166]

Mouse Orthologue:

Rassf7

Mouse Description:

Ras association (RalGDS/AF-6) domain family (N-terminal) member 7 Gene [Source:MGI Symbol;Acc:MGI:19

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa45022	Nonsense	Mutation detected in F1 DNA	Not yet available
sa30265	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa45022

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000136169	Nonsense	268	415	2	4

Genomic Location (Zv9):

Chromosome 25 (position 26353379)

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTTGCATGAATTCAACAATCGTGCCATACAACTGGAGAAGGACATTCAG[A/T]GAGAAATGCTACGAGTTGACATTTTACCTGTTCAGTCCGATTCAAAAGAC

Long Flanking Sequence:

CAATATCAGAGTCCAAGCAGGGTTTACCTAGGAAATCTTTCACTTTTAACTTGGGTCCTTCCAGTTCTCCTCGTTCAAAACCTAAGGATTCAAATAAAACACCCTCTTTTGAACAGAGGGCTTCACCTGTTCCACATGTAGCATATCTTCCAGGGCCATCTAAAGAGGAGGTGTTCAGTCATGTTCTTCAGCAGCAGGAGCAGCTTCATTCCCTTGAGACCCAGCTGGTGGCTGTAGACAAGGAATGTGAAACTTGGGAAAAGTCATCAGCTAAGGAGACATCGCTGCAGGCAGAGATGGAAGCTTTGGAAAAGATGCTGTGGAAGAATCAGCAAGAGTTGGTGGATGAGGAGTTTTGGCAGGAGGAACTAAGGTTAGAGACAGAGAGGGAACGTGGGATGAAGCGGCGGGTGGGAGAGCTGCATGCTAAACTGGATGACTGTGGGCAAAAGTTGCATGAATTCAACAATCGTGCCATACAACTGGAGAAGGACATTCAG[A/T]GAGAAATGCTACGAGTTGACATTTTACCTGTTCAGTCCGATTCAAAAGACTCTTTAGAGGTAGTCAAGGCAGATCTTCAAAGTCGACAAAAGCAGGGGGAGGAGATGGAGGCAGAACTTAAAGAGCTTGAGAAGACTTTGGGGAGGGCTGAGACTTTGTTAAAGGTAAGTAGAGAGGGCCTGGCTCAAGAGAGAAGCTTGTAGGGGTTGACTGCAAATGTTGAACGGTATCGTGGTCCCCTTGTTGGAGTTGTATTGGCAATTAACGGAAAGATCAAAAGTGAACAGAGGAAACCACTTCACTTCTTGAAATATTTCATAAATACAAATGTTTTTTCATTTGGTCCTTCTTACATTTATTTATTTTCTTGTGAATTTTATGACTTGTGATAATAAAAGTGTACCACTATTTAATGAGTTTTTTTTACCTGCTAGGAATGCATGAAATTTATATTGCACCTAAATATGCATAACCTCAGTTTTATAACAGCATTTCAGAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa30265

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
ENSDART00000136169	Essential Splice Site	322	415	2	4

Genomic Location (Zv9):

Chromosome 25 (position 26353544)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	25393858
GRCz11	25	25488936

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AACTTAAAGAGCTTGAGAAGACTTTGGGGAGGGCTGAGACTTTGTTAAAG[G/A]TAAGTAGAGAGGGCCTGGCTCAAGAGAGAAGCTTGTAGGGGTTGACTGCA

Long Flanking Sequence:

AGGAGGTGTTCAGTCATGTTCTTCAGCAGCAGGAGCAGCTTCATTCCCTTGAGACCCAGCTGGTGGCTGTAGACAAGGAATGTGAAACTTGGGAAAAGTCATCAGCTAAGGAGACATCGCTGCAGGCAGAGATGGAAGCTTTGGAAAAGATGCTGTGGAAGAATCAGCAAGAGTTGGTGGATGAGGAGTTTTGGCAGGAGGAACTAAGGTTAGAGACAGAGAGGGAACGTGGGATGAAGCGGCGGGTGGGAGAGCTGCATGCTAAACTGGATGACTGTGGGCAAAAGTTGCATGAATTCAACAATCGTGCCATACAACTGGAGAAGGACATTCAGAGAGAAATGCTACGAGTTGACATTTTACCTGTTCAGTCCGATTCAAAAGACTCTTTAGAGGTAGTCAAGGCAGATCTTCAAAGTCGACAAAAGCAGGGGGAGGAGATGGAGGCAGAACTTAAAGAGCTTGAGAAGACTTTGGGGAGGGCTGAGACTTTGTTAAAG[G/A]TAAGTAGAGAGGGCCTGGCTCAAGAGAGAAGCTTGTAGGGGTTGACTGCAAATGTTGAACGGTATCGTGGTCCCCTTGTTGGAGTTGTATTGGCAATTAACGGAAAGATCAAAAGTGAACAGAGGAAACCACTTCACTTCTTGAAATATTTCATAAATACAAATGTTTTTTCATTTGGTCCTTCTTACATTTATTTATTTTCTTGTGAATTTTATGACTTGTGATAATAAAAGTGTACCACTATTTAATGAGTTTTTTTTACCTGCTAGGAATGCATGAAATTTATATTGCACCTAAATATGCATAACCTCAGTTTTATAACAGCATTTCAGAATTCCTGTGACAAAGCAAAAACTTAGGGCACTATCATACAACCGGCACAATACAAGTATGGCGCAATTTGTTGCTATCTTCAGACCAAAATAAACCTAATTTTTACATTTTCTGTCATGTTGTTTAAATAGCAATTCCAATTACACCTCTCTGTGGACTCATGGGCA

Associated Phenotype:

Not determined