ZMP
FARP2
Ensembl ID:
Description:
FERM, RhoGEF and pleckstrin domain protein 2 [Source:HGNC Symbol;Acc:16460]
Human Orthologue:
FARP2
Human Description:
FERM, RhoGEF and pleckstrin domain protein 2 [Source:HGNC Symbol;Acc:16460]
Mouse Orthologue:
Farp2
Mouse Description:
FERM, RhoGEF and pleckstrin domain protein 2 Gene [Source:MGI Symbol;Acc:MGI:2385126]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40695 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15550 | Nonsense | Available for shipment | Available now |
sa40696 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38550 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa26745 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40695
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000013400 | Nonsense | 162 | 1044 | 5 | 26 |
Genomic Location (Zv9):
Chromosome 6 (position 26704527)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 27005738 |
GRCz11 | 6 | 26996299 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTTTCTCTGCAGATAAAGAGGGATCTATTAGATGGCCGACTGAGCTG[T/A]ACAGAAAACACTGCTGCCCTGCTTGCCTCTCATTTGGTGCAATGTATGTC
Long Flanking Sequence:
CAAGTCATAAAAATGTGAAAGACTTTTTTTTCACAGTAAATGTTAGCATCCATGTATCAAAAGGAAACGATTGTTTACCGTATCATGTTTTACAAGCTTTTTCTACGGTTAGGCTGTTTTTCAGTGCCATTTTATTTATTTCCCGCTTGTTAGCTGGCAGCCACCAAGCTGTACCTCTTAATTAAAACAAACATGCCTGGAAAATGTTCATTTCAAGAGCTTTGTCTACAAAATGACCTCTTCAAATAATAGGTGTTAGACTGCATGCTCTCTTTTCGGTTATTTTCAAATTCTTAGGTAAATTATCCAACATTGATCTCCTTATGGCTTTTAAATTTGTGAAAAGGACATTCAAGCTTGGACAATTTTAATATTATGCAAAGCACAACAGCACCATGTTTTGAACAGAACTGTTCTAATCCTCTAATGATATGCTTTTTCTCCAGGTACTTGTTTTCTCTGCAGATAAAGAGGGATCTATTAGATGGCCGACTGAGCTG[T/A]ACAGAAAACACTGCTGCCCTGCTTGCCTCTCATTTGGTGCAATGTATGTCATTTGAGATCAGTTGGTGTAACAGTTAGTTATTGTGTATTGTCTCTGCTTTCATTGGCTTATTTCTTTCCCGATCTAATAATAAGTTTTTAATTGCATTACAATGGAATTCATACATTAAGTGACTTTACAAATGGAGCAATAAGCATTAGGTGATTTAACCTTTTTTATATTGCAAGAATATTGTATGTATACTGCCCAATTGTAAAGATTTGTTCTCTGTTTGGGGTACGTAGGATTTGGAGTGTTCTTTTGGTCACCAAGGGTTCATTTATTTGATTAGAAAATACAGTTAAATATTAATATAGTAATGTTTTGTGTAAATATCTATACTAAAATATTATTTATTAGACATGTGTCCATGTATACATGTGTCCATATATGTTTGAGTGTTTACATGTGTATATAATTGAAATTATATTTTGGTCTTTTTTTTTTTTGGTTTTTCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15550
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013400 | Nonsense | 382 | 1044 | 11 | 26 |
Genomic Location (Zv9):
Chromosome 6 (position 26713480)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 27014691 |
GRCz11 | 6 | 27005252 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTWGTATTGATTATTCKATTTTTACAGGAGRAACAGTAAGATTCGCATGT[C/A]GAYGCGTTCCTTGGCTTCTGATGTGCCAAAACAGGTCAGCAGAGTTTAAG
Long Flanking Sequence:
CAACAGCAGCTTGATGACGCAAACATACCAGAAGGAATAAAGACAGTGTGAACACAAACCAATTGAGAAGGTGGCAAGGGGGGACAATCGAACTTGGGTTCGGTCCAGGCAATTGAACCAAGAGTGAAAGAACCTTAAATCAAATGTTATAAACCATGACACATTTGATTAATAAAGGCTGTTGTTTTGTTGTTTTTAACCTTCCACCTCTATGTATTTGTGCTAGATCTGTTTGACTTGATTTGTCATAAAACCTTATATTTCAATTTATATTTAACAGTGGGAGGACACAGAAACAGCTTGTTGAGTATGTGAGGGACAGCGGGTTGAGAAGAACTCCTTACCAGAGGTAAAACTTTTGAAGTCTCACAAGAAACTAGTTTAATTCTCTATAATTGACCTTTTTAAGCCTCTTATTTTGATGGTGCATTTCTCTGCATGTTGTGCATCTTAGTATTGATTATTCTATTTTTACAGGAGAAACAGTAAGATTCGCATGT[C/A]GACGCGTTCCTTGGCTTCTGATGTGCCAAAACAGGTCAGCAGAGTTTAAGATCCAACCCAACTAATACCAATAATAACAATAATAACTGACCTTTTCATCCTCTTTATTTACTTTTCCCATTCGTTTCAGAATCTGTCTTTTAACGACAGCCTGAGGACTCACATACCTCCTTCCTCCATCACCGCCTCCTTCCAGTCTCTGCATGCCCCCAGCGTTTCTATGAGGGCCGAGACCCCAAACCAGCTTTTGCATCTTCATCAGACGCAGCACCAGCCTCTCAGAGCCCCCAGCCCAATGAAGCAGGACCCCATCAAGACCAACTCCCAATCCACCTACGCCTTCCCAGGTGCCACTCATATCCCGGCAGCAGGAAACTGCAGCCCCTCGTTTGTGTGTGTAGAGAGTAGTTCCTCTAGTGTACGACCCTCCCAAAATGGCAATGAGGATAGCGAGCAAGTAGGGGTGGGTGGCGTGATTGGCGGGGTGCAGAAGGGTTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40696
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000013400 | Nonsense | 529 | 1044 | 14 | 26 |
Genomic Location (Zv9):
Chromosome 6 (position 26724668)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 27025879 |
GRCz11 | 6 | 27016440 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATAACTCATCAAAGAGTGGTTTTAAGTCTGCTTTCTTTTTTCAGAGATA[T/A]CCAACAGACAAAGCCTACTTCATTGCAAAAGAGATTCTGACAACAGAGCG
Long Flanking Sequence:
AGATTTTGATGATCCCCTTAAAACCCAGAAGTTACATAATAACCAGTGCTTTATATTGATGGTTCAATCTTTTGATTGCAAGGTACTTTGCAACTTCATGCCTATTAACTCTTATTACAGTATTAATAAAGTAGTAGAGAGTTAAATTTAGTAGAATAAGCTGGCCTGCACTCACAAAGTTATTTGTAATCATTAAAATGAATTCTGGGCGACCATCAAAATGAAGTGTTAGCGAATATTAAGCAGACAATGTACTTATGTTCTAGTGACTGCTAGCTGACACTTTCTATGTGGTCACAACAGATACTTATTTTTGTTTACTGCCCCTTCCCCCTTTTTTCTAATACATATTGAACAAGCAGGCCTTTTTCGTACCTAAAATTTTTAGATCTTTGAGTTAAGTTTATATGTTTGAGTGTAAATAATATTAATGAACTTATGTGCAGAGAACATAACTCATCAAAGAGTGGTTTTAAGTCTGCTTTCTTTTTTCAGAGATA[T/A]CCAACAGACAAAGCCTACTTCATTGCAAAAGAGATTCTGACAACAGAGCGGACTTACCTGAAGGATTTGGAGGTCATCACAGTGGTGAGCAGAGCTGATTGCTTTCATGACTCACGACTATAACAAGTTTACCTTGTGAGGCTTGTCTGGAAATGCACACTGTGGTGTCTGTACAATGTGTACTGTTTGCTGTGTCATTTAAGAGGTCTTTGTTTGTCTTTAGATGTGCTTAATGTGTGTCTGTTAGAGGATTTCTGGCTTTGAGCTCTATCTAATCACTTTGGTGTGTGTCTGTCTCTCCTGTCAGTGGTTCCGCAGTGCAGTGATTAAAGAAAATGCAATGCCTGAGGGACTCATGACCCTCCTGTTCTCCAACATCGACCCAATCTATGAGTTCCACCGAGGCTTTCTCAAAGAAATTGACCAAAGGCTGGCGCTCTGGTACCAGACCCTCTCATTAGTTACAATACATCTTGGCGTATATTTTCTTTAAATTGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38550
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000013400 | Essential Splice Site | 708 | 1044 | 17 | 26 |
Genomic Location (Zv9):
Chromosome 6 (position 26727051)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 27028262 |
GRCz11 | 6 | 27018823 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTGTAAACATTATTCACCCCAGCACAGAGACTACGATGACTGCAAAG[G/A]TAGACCTTATTCACATAAATATCACATTTTTTTGTTCTGAAAATCTGCGG
Long Flanking Sequence:
AGAAACATCTATATATTTTTTTTGTTGGGTGAGAAATCACTTTAATGAAGGGTTTGTTTGATTGACGTTTTTGATTTTCACAGGGAGGGGCGCTCTAACGCTCATGTAAAAGGAGATTACCAACGAATCGGAGATGTAATGCTGCGCAACATGTGTTCTTTGAAGGTAAGATGATAATTCAGAAAAACAACGTTTGACTTCAATTTGATTTTTGAGCTAATCCATAATTCATTTAATGTCTTTGCTGCTTTTGTCTCCTCAGGAGTTCACCGGTTACCTGCAGAAGCACGATGAGGTGTTAACCGAGCTGGAGAAGGCAACCAAGCGTGTGAAGAAGCTGGAGACCGTGTATAAGGAGTTTGAGCTGCAGAAGGTTTGCTACCTGCCGCTAAACACCTTCCTGCTGAAACCCATCCAGAGGCTCATGCACTACAAACTGATCCTGGAGCGTCTGTGTAAACATTATTCACCCCAGCACAGAGACTACGATGACTGCAAAG[G/A]TAGACCTTATTCACATAAATATCACATTTTTTTGTTCTGAAAATCTGCGGATGGTGATGTATTGTTATTTCTCCAGAGGCCCTGAAAGAGGTTGCAGAGATCGCTACACAGTTACAGAGCAGTCTGATTCGACTGGAAAACTTCCAGAAGCTGACAGAACTTCAGAGAGACCTGATTGGCATTGAGAACCTTACAGCTCCTGGAAGAGTGAGTGTGACTGTTTTAAGTGCTGTTTTCTGTTAAGGTTATTGCACACTGAATCCAAAATTTACGTCCATAATTTATTTAACTCATGATACTTCACATTGAAAAATAAATTTGATCTCATGTTGTGTAAATCGCCTTGTCACACTGCCTCCGAAACCTTTGCCCATCATAAAAAAAAATCAAACCAGGTTAAATTTTTTTGGTTTGTTTTTCTTATCTTTATTTTCTTATAAAATTCGCTTTTGAGAGGTGTTTTAACAGTTAAGAGCCACTGTACAAGCGAAAAGCTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26745
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000013400 | Nonsense | 948 | 1044 | 24 | 26 |
Genomic Location (Zv9):
Chromosome 6 (position 26741246)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 27042457 |
GRCz11 | 6 | 27033018 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTTATCTTCTGAGGAAGTTCAAGAACAGCAACGGCTGGCAGAAACTAT[G/A]GGTTGTCTTCACCAACTTCTGCCTGTTCTTCTATAAGACGCACCAGGTAC
Long Flanking Sequence:
TAGTTTATTTATTTCTTTGTTTATTTATTTTTCACTTTAATTTATATGATGAAGTAATAAACAGAATAGTAAATTAATAATCAAAAACATGATTAAAATCTCTAATATATTTGAAAAACATTTAAAAATACATTTGCAATTACAGCTTTATTTTTCATGATTCTACAGCTCTGTGCTTGTCACGTTTGTTGTTGTAAAAAGTGCTATACAAATAAACTGCAGTCATTAAGCAGTTCCCTTTTAGGATCTATTTCTCACCACTAATCTGTGTAGAGCGTATGAATTCTATCCGCTAAATTGGAAAATCCTCACTCTCTCGCGCTCAGCTCTTTGTACAGCTGAACTCCTCTACCGCTGTACCAGTGGTCCTTTGTAAATGAGTTCTCTCTGTGCTCTTCTCTTTTGTGAGTTTTAACAGTCATGTTCTCCCACTTTACAGAACCAGCTGTCTGGTTATCTTCTGAGGAAGTTCAAGAACAGCAACGGCTGGCAGAAACTAT[G/A]GGTTGTCTTCACCAACTTCTGCCTGTTCTTCTATAAGACGCACCAGGTACTGAAATATGAATCAAATTCACGGGCTTGAACTTCCTGCATGAGATCTGGATCATTTCTAAAGGGTTTGTGTTTTTGCTGCAGGATGATTTCCCTCTGGCCAGTCTGCCTTTGCTGGGATACACAGTCAGCACTCCTGGGGAATCAGACAGCATTCATAAAGAATACGTCTTCAAGCTCCAGTTCAAATCCCATGTTTACTTCTTCAGGGCAGAGAGCGAGTACACATTTGAAAGGTGATGTTTGTGGATTTGAAAATCGTTCTCTTTTCATGTTTTGGTTATTCTTGGTTTCTTATCAGTTAATTTTGGTGTCGTCAGTTGTTTTAATTTGATCATTTTCATAATTCGGATATGTGTTGAATTAGTGTACGATTGAAGACATATTTTCTCTGCTGTGACATAAAAAAAATTGAATAGATTTTTGCACATAATAGTTGTAATGACTAATTT
Associated Phenotype:
Not determined