Busch Lab

ZMP

LOC100333421

Ensembl ID:
ENSDARG00000039500
Human Orthologues:
LRFN1, LRFN2, LRFN4, LRFN5
Human Descriptions:
leucine rich repeat and fibronectin type III domain containing 1 [Source:HGNC Symbol;Acc:29290]
leucine rich repeat and fibronectin type III domain containing 2 [Source:HGNC Symbol;Acc:21226]
leucine rich repeat and fibronectin type III domain containing 4 [Source:HGNC Symbol;Acc:28456]
leucine rich repeat and fibronectin type III domain containing 5 [Source:HGNC Symbol;Acc:20360]
Mouse Orthologues:
Lrfn1, Lrfn2, Lrfn4, Lrfn5
Mouse Descriptions:
leucine rich repeat and fibronectin type III domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:213
leucine rich repeat and fibronectin type III domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:191
leucine rich repeat and fibronectin type III domain containing 4 Gene [Source:MGI Symbol;Acc:MGI:238
leucine rich repeat and fibronectin type III domain containing 5 Gene [Source:MGI Symbol;Acc:MGI:214

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa18342 Nonsense Available for shipment Available now
sa14275 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa18342
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
ENSDART00000028944 Nonsense 246 639 1 2
Genomic Location (Zv9):
Chromosome 18 (position 48266236)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 49417397
GRCz11 18 49412174
KASP Assay ID:
2261-2650.1 (used for ordering genotyping assays)
KASP Sequence:
GAAGGGATCACCGCTGACYGCACTKGTGCTCAGTTTCGGGGGGAATCCGT[T/A]GCATTGTAATTGCGAGTTGGTTTGGTTGAGACGTCTTACTCGTGAGGATG
Long Flanking Sequence:
CCTGATCCACCTCACACTCTCCCGAAACACCATCAGCCAGATCCGACCCTACGCATTCGCAGACCTCCAGGATCTACACGCATTGCATCTGGACGCAAACCGGCTGACGGTTCTAGATGACACACACTTACAAGGCCTGGTTAATCTCCGCCATCTAATACTAGCCAACAATCAAATCCACAGCATCTCAGAAGGAGCCTTTCAGGACTTCCTGGAAACTCTTGAAGATCTCGATCTGTCGTATAATAATCTGGTGGACTTACCGTGGGACACCATTGCGATGCTAGCCAGCGTCAACACCTTGAGTTTGGATCATAACCTGATTGAGTTCGTTCCTGAGGGGATATTTTCAAATCTGCATAAACTAGCTAGACTTGATATGACGTCCAATAAGCTGAAGAAGATTCCTCCGGATCCTTTATTTCTGCGTATTCCTGTATACGCCAAGATGAAGGGATCACCGCTGACCGCACTGGTGCTCAGTTTCGGGGGGAATCCGT[T/A]GCATTGTAATTGCGAGTTGGTTTGGTTGAGACGTCTTACTCGTGAGGATGATCTGGAGACCTGTGCATCTCCGAGAGAGCTTGCTGGGAAGTATTTCTGGACGATTCGGGAGGAGGAGTTTGTTTGCGAGCCGCCGATGATCACTCGACACACTTCTAAGATGTTTGTGATGGAGGGTCAGGAGGTCAGCCTGCGCTGTCGGTCCGTCGGCGACCCTGAACCCATCGTGCATTGGATCAGTCCTGATGGGAAGCTAATCGCTAACACTTCACGTACAGTATGCTATGATAACGGCTCTCTGGATATCCTGACCGCCACAGTGAAGGATTCTGGCGTGTTTACATGCATCGCTTCTAATGCAGCCGGTGAGGCTACGGCGCCGGTGGAGTTGGTTGTGAATCCTTCACCGCATTATGATCCCAAACTGGAGCCTGAGCCGGGACCCTCGGATATGCCCACGTCTATAAAGTCCAACAGCAGCGGCAGCGGAGGGCAGAATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14275
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028944 Nonsense 432 639 1 2
Genomic Location (Zv9):
Chromosome 18 (position 48266795)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 49417956
GRCz11 18 49412733
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCGRGTCACGGTTTCAGAAATTACRCCCAGCTCTGCTATGATCCGCTG[G/A]CCTCMACAAAGCCAGATTCCTGGAGTGCGCATGTACCAGRTCCAGTACAA
Long Flanking Sequence:
ACCTGTGCATCTCCGAGAGAGCTTGCTGGGAAGTATTTCTGGACGATTCGGGAGGAGGAGTTTGTTTGCGAGCCGCCGATGATCACTCGACACACTTCTAAGATGTTTGTGATGGAGGGTCAGGAGGTCAGCCTGCGCTGTCGGTCCGTCGGCGACCCTGAACCCATCGTGCATTGGATCAGTCCTGATGGGAAGCTAATCGCTAACACTTCACGTACAGTATGCTATGATAACGGCTCTCTGGATATCCTGACCGCCACAGTGAAGGATTCTGGCGTGTTTACATGCATCGCTTCTAATGCAGCCGGTGAGGCTACGGCGCCGGTGGAGTTGGTTGTGAATCCTTCACCGCATTATGATCCCAAACTGGAGCCTGAGCCGGGACCCTCGGATATGCCCACGTCTATAAAGTCCAACAGCAGCGGCAGCGGAGGGCAGAATCGAGCTGATCAGCGGGTCACGGTTTCAGAAATTACGCCCAGCTCTGCTATGATCCGCTG[G/A]CCTCCACAAAGCCAGATTCCTGGAGTGCGCATGTACCAGGTCCAGTACAACAGCTCCACTGATGACATCCTCATCTACAGGTGAGTTCACTGCACGGATTATTACATTCATTTATAAACACATTACATCTTTATTGAACAACATTCACATATAGATATATTTCTAATCAAGTCCATTTATTTATCCATCCATCCATATAAATATTGACCCATTCATCCAAATATCAATCAATCCATCCATCCATTCATATAAATATACATCAATCCATCTAAATATCCATCCATTCATCCTTCCATCCATACATCAAAATACACATCAATCCATCCATTCATCCAACAATCCATCCATCCAAATATACATCAATTCATCCATTCATCCAAATATCTATTCATCCATCCATACATACATCCATTCATACAAATATACATCAATCCATCCAAATATCCATCCATTCAACCATCCCATTATACATCATTTCATCCATTCATCCAAATATCTAT
Associated Phenotype:
Not determined