ZMP
LOC797812
Ensembl ID:
Human Orthologue:
LRFN2
Human Description:
leucine rich repeat and fibronectin type III domain containing 2 [Source:HGNC Symbol;Acc:21226]
Mouse Orthologue:
Lrfn2
Mouse Description:
leucine rich repeat and fibronectin type III domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:191
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa864 | Nonsense | Available for shipment | Available now |
sa42983 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28909 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa864
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085218 | Nonsense | 251 | 780 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 40388751)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 40273367 |
GRCz11 | 17 | 40223023 |
KASP Assay ID:
554-0766.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGTCTCTCAGCTTTGGTGGGAATCCTCTTCACTGTAATTGTGAGATTT[T/A]ATGGTTGCGACGCCTAGAGAGGGAGGATGATATGGAAACCTGTGCCTCCC
Long Flanking Sequence:
AAGAAACACCATCAGCTTCATTCAGCCATTCTCCTTTGTGGATCTTGAAACTCTGCGTTCGTTGCACCTGGATAGCAACCGTTTGACAGAGCTGGGTCCAGATGTCTTACGAGGCTTAGTAAACTTGCAACACCTCATCCTGAACAACAACCAGCTTACACATATCTCCAAAGAAACTTTCGATGACCTGCTGCTCACCTTGGAGGACCTAGACCTCTCCTACAACAACCTGCGGGGCATTCCCTGGGACGCCATACGCAAGATGCTCAACCTACACCAGCTGAGTCTTGACCACAATCTCATCAACCACATTGCTGAGGGCACTTTCACTGATCTTGAAAAGCTAGCAAGGCTGGATCTTACATCAAACCGTCTCCAGAAGCTTCCACCAGATCCTATTTTTGCTCGATCGCAGAGCAACATCGTTCTCAGTACACCATTTGCCCCTGTTCTGTCTCTCAGCTTTGGTGGGAATCCTCTTCACTGTAATTGTGAGATTT[T/A]ATGGTTGCGACGCCTAGAGAGGGAGGATGATATGGAAACCTGTGCCTCCCCTCCAAGCCTCAAAGGTCGTTACTTTTGGTATGTTCGAGAGGAAGAGTTTGTCTGTGAACCACCATTAATTACTCAACACACCCATAAGCTTTTGGTCCTGGAAGGACAGACGGCTAGTTTACGCTGCAAAGCTGTTGGTGACCCTATGCCTTTTATACACTGGATTGCACCAGATGACAGGCTAATAAGCAACTCATCCAGAGCTACTGTGTATGAAAATGGTACTTTAGACATTGCAATCACCACATCAAAGGATTATGGGACATTTACTTGCATTGCTGCAAATGCAGCAGGAGAATCAACAGCCTCAATTGAACTCTCCATCATCCAGCTTCCTCATCTCAGCAATGGAACTAACCGCACATCTCAGCCCAAGTCCAGACTATCTGACATCACCAGCTCCACTAAAACCAGTAAAGGCGAGACCAAAGCCCAGCCAGAGCAAGTCG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa42983
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 |
---|---|---|---|---|---|
ENSDART00000085218 | Essential Splice Site | 459 | 780 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 40388126)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 40272742 |
GRCz11 | 17 | 40222398 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTACCAGCTGCAATACAACTGTTCGGAGGATGATGTCCTGATTTATAG[G/A]TAAATATTCTATGTTTCCTTTCCTTTAAACAACTGGAGACTGATTAGGCA
Long Flanking Sequence:
CAACACACCCATAAGCTTTTGGTCCTGGAAGGACAGACGGCTAGTTTACGCTGCAAAGCTGTTGGTGACCCTATGCCTTTTATACACTGGATTGCACCAGATGACAGGCTAATAAGCAACTCATCCAGAGCTACTGTGTATGAAAATGGTACTTTAGACATTGCAATCACCACATCAAAGGATTATGGGACATTTACTTGCATTGCTGCAAATGCAGCAGGAGAATCAACAGCCTCAATTGAACTCTCCATCATCCAGCTTCCTCATCTCAGCAATGGAACTAACCGCACATCTCAGCCCAAGTCCAGACTATCTGACATCACCAGCTCCACTAAAACCAGTAAAGGCGAGACCAAAGCCCAGCCAGAGCAAGTCGTTTCAGTGTCAGAGGTCACTGGAGTCTCTGCTCTAATCAAGTGGATGGTTAGCAAAGTATCGCCCAAAGTAAAAATGTACCAGCTGCAATACAACTGTTCGGAGGATGATGTCCTGATTTATAG[G/A]TAAATATTCTATGTTTCCTTTCCTTTAAACAACTGGAGACTGATTAGGCACATACTTTAGGCACAAGTTCTTTTAGTTTCTCATTGAATATATGTTGGAATTAGACAAATAGATTGTATCTCAATTTAAAAAATGGCCGTAAAAATTCTGGTTAACTGGTTAAGAGTAAGTTTTCATAATATATACAATAAACAACTGTTAATGGACTTCTCCATAATTCCTCACTTTTTATGCTTTTTTTTTAATTGCTATGCTTTTTTTACTTATCGGTTATGTACATTAGAGTTTTATGTTACATCTAATTTCGATAAACAATTTTTATTGCATTACTTTAATTTTATGCAGCAAATATACTGGACTTTAACTCCATGTAGGAGTTGTTGACGGGGCCCCCCGCTACACCACTGATTGTATATTTGTTACCATGATGTTTTTTTACTAGTTTTTTAATAGTAGAGTTTTTTTTCTAACAAGAATAGGTATTATTGGCAACCACTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28909
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 |
---|---|---|---|---|---|
ENSDART00000085218 | Nonsense | 625 | 780 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 40382021)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 40266637 |
GRCz11 | 17 | 40216293 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAGTAGCATCTCTTCCTCTTCATCCTCCTCAGCAGACACACTTGGATG[T/A]GAGAAAGTAGAGTCCTACAACCGGCATGGCGATTCAAACACCTTGCCTCA
Long Flanking Sequence:
AGAATGATTCCGGCAATCAGCAGATCCTTTTTGGTCAACAACCTGATGCCAGGGATGCAGTATGATCTATGTGTGTTAGCCATCTGGGAAGACACTGCCACCACACTTACTGCAACCAACATAGTGGGCTGTGTGCAATTCGAGACACGTGATGAGTTTCCTCGCTGCCAGTCACTTCACAGTCAGTTTCTAGGAGGAACCATGATCTTAGTGATTGGTGGAGTGATTGTGGCCACTTTGTTGGTTTTTATTGTCATCCTTATGGTTCGCTACAAAGTGAACAGCGGTTTGCAAGTTGCAAAGTTAGTGACTGTGAGCAACACCTACTCCCAGACCAATGGGAGACCACAAGCTCCGCAACGTCTAAACAATGGTGCTCCTACACCACAGACACCAAAAACTGTAGTGGTGATGCGAGATGAAGTGGTGGAGTTTAAGTGTGGCTCCTTGCAGAGTAGCATCTCTTCCTCTTCATCCTCCTCAGCAGACACACTTGGATG[T/A]GAGAAAGTAGAGTCCTACAACCGGCATGGCGATTCAAACACCTTGCCTCATAGGTGGAAGCAGTCGTCAGCCAAAGCGCGGCCAAACTTGGATAACCTTCTTGGGGCATTTGCCTCTCTGGATTTGAGAGCTCCCACAAGAGATCCAGGAGGACCATCTTCCTCTGGGACCATGGCAATGGCCATGAGACCCCCCACTGACAAGGAGCCTCTGCTAGGCCGAGGAGATTCTAAGCTTGGAAAGCTTGTGATGCTGCCATCAGAGAACAAGCCCAAGCGCAGCCACTCATTCGACATGGGGGACTTTGGTGCTTCACAGTGCCTTAGCTACCCACGGCGCATCAGTAACATTTGGACTAAGAGGAGTCTCTCAGTTAATGGCATGCTCCTGCAGTGTGACGAGAGTGAGGGGGAAGGCGATAAAGCGACATTTGATAGCTCTGAGTGGGTCATGGAGAGTACAGTCTGACAGGGACATTGGATTAGCTCTGCCAAAAGAGA
Associated Phenotype:
Not determined