Busch Lab

ZMP

kirrel3a

Ensembl ID:
ENSDARG00000075806
ZFIN ID:
ZDB-GENE-091117-44
Human Orthologue:
KIRREL3
Human Description:
kin of IRRE like 3 (Drosophila) [Source:HGNC Symbol;Acc:23204]
Mouse Orthologue:
Kirrel3
Mouse Description:
kin of IRRE like 3 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1914953]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa34970 Nonsense Mutation detected in F1 DNA Not yet available
sa38811 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa4391 Nonsense F2 line generated Not yet available

Mutation Details

Allele Name:
sa34970
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113414 Nonsense 110 774 3 16
ENSDART00000135756 Nonsense 110 564 3 13

The following transcripts of ENSDARG00000075806 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 10 (position 41056347)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 39770973
GRCz11 10 39692460
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATGACGGAAGCTTTGAGTGTCAAGCCATCCAGGTTGCTGGCAGATCT[C/T]GACCCGCTCAACTCACTGTGCTAGGTCAGTGTAATCTTCAAGAAAAACCC
Long Flanking Sequence:
TGTGTGCTGTAAGCTTTAATTCCAGTCATTCCACAGATTTTGTTATTTCACGACTGAAGTAAACACAACTGAGATCATTCAAGGTTACCTCTGAATGGGTCCCGTCTCCTATTGTGTGGTGAAATATTGGTATTTTTGTATGTTTCACCCATTTGAGCAACTTTCATAGAATTTAACAATACCACAGCACAAAGAGTAAAAACCAACAACTCTCTCTACAGTAAACACACTGAGCAAACCCGCATTTTTCATATAACAAATATGCTCGGGGTAACTTAAATGCTTGAAGGCAGAAGAAAATAATGTCACGCTTGCAATTAAGATATGTTAATGGTGTAATGCTTCCTTTGTTTAATGCTAAACTTTGTGTTCCAGGCTATCCACGCTATGATGTGATCGGGGACCACAGTAAAGGAGAATATCATCTGCTCATCGAGCGGACTGAACTGGTGGATGACGGAAGCTTTGAGTGTCAAGCCATCCAGGTTGCTGGCAGATCT[C/T]GACCCGCTCAACTCACTGTGCTAGGTCAGTGTAATCTTCAAGAAAAACCCACACACAAGACAGAAAGAGGCAGATAGATGGATGGACAAATGAGTAGACATATGGGTGGATGTGTGGATGGATGGACAGATGGGCAAACAGACAGATGAACAGATAAATGAATGAATGAATGGATGGATAGGTGCATGTATGGATGGATGGATGGGTGGATGAATGGATGGGTGGGTGAATGGGAAGATTAAAAGAAGGGCAGAAAATCAGATAGACAGGTGAATAGGTAAATAAATAGATGGATAAATGGGCAGATGAATGGACATGTAGAAGGATTGATGGACAGAGGGACAAACAGGTTGATAGACTGACAAGAGCTGGCTGGCTGGCTGGCTGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGATGAAAGGATGGATGGATGGAATGGGTAGGTTGATGGATGAATAGATGGATGGATGGATAAATAGACAGATGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38811
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113414 Essential Splice Site 554 774 13 16
ENSDART00000135756 None None 564 None 13

The following transcripts of ENSDARG00000075806 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 10 (position 41172408)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 39887034
GRCz11 10 39808521
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCCTCTCTTCTAGACAGAGAGAGATATCCGGCACAGTAAAAAGCGAAA[G/T]TAAGCTCGTCTCACTTCTTGCACACTTCCCTTTAAAAATCATACATCTGG
Long Flanking Sequence:
GTATATTGTATATGTAAAGAGTGTGTTTAAATATACTTGAATCAAAAATCTAGCCAATCAGAAACTGTTTCATGTTGAAATGTAAATGTCTGAAATTGCATGCCAACCTGTAATGCTGCGTGTAGAAAAAGTCAACTTGACAGTAGTTTAAGGCATCAGTGTCTTGTAGCCCAGCAAGCCACATTTCCTGAGTAGTTCTTCAACACTGTAGCGCACGATGATAAGAGCACACCCACACCTTCCTCACGTCTTCCTCTATCTGAGGTCTTTATTGTCTTATCTTGCCTTTCGCAAATTGCCTCCATTAGCGGCCAGCTCCCGCTCCTCAGCCTGACTTTATCTGAGCGCGACTGTAAAGACCTCATTTTTTAACAAGTGATCTTACTTCCTTTGCATGTTGTGACCGTGCGCCACAGAGGACATGCACCTGGTGATGTCTTCACTCCCAGTGTCCCTCTCTTCTAGACAGAGAGAGATATCCGGCACAGTAAAAAGCGAAA[G/T]TAAGCTCGTCTCACTTCTTGCACACTTCCCTTTAAAAATCATACATCTGGCAATATATGCTAATTATATACATGACAAACAAGTTCATATTTGTATTGCATATGTATAGACTGTATAAAGCAAATGCAACATATGTTTCAAAATATTGCAAAAATGCTGATTTACTTACAGTGGTGTGAAAAAGTATTTGCCCCCCTATTGATTTCTTTTCTTTGCATGTTTGTCACTCTTGAATGTTTCAGATCATCAAATAAATTCAAACATTAGTCAAAGATAAAGTTGAAATGAAGGTTTTTTTATTATTAGGGGGAAACAACACAACATAGCCTTGTGTAAAAGTATTTGCCTCCTAAGCCAAATAACGTTCGAGGTTACTAAAGTAACCCTTCGTTCCCCGAGGAGGGGAACGGAAGCACTATAAGTGGATTTGATTTGTAAAATCCACGCATTGGGAGGATTCGGATCAGAAGCCGCTTGTCTGGAGAGTATTGAACGGGCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa4391
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113414 Nonsense 634 774 16 16
ENSDART00000135756 None None 564 None 13

The following transcripts of ENSDARG00000075806 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 10 (position 41201788)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 39916414
GRCz11 10 39837901
KASP Assay ID:
554-3565.1 (used for ordering genotyping assays)
KASP Sequence:
ATGTCTTGTAGGATCCAACCAACGGCTATTACAGCRTGAACACCTTTAAA[G/T]AACAGCCAACCCCGACCATTTCTYTYACAGCCAATCAGAACGCTGAGGTG
Long Flanking Sequence:
TTTATGAAACTTCACTTTAAGAGTTCACACTTAGATATGCTTAGCATTATAGCAGGTTTGTCATGCTGTCCCGGGAGAGACCCCTAAGCTCGGAGATATTTGAGCCCAGGGCTCCCGCCCAGTGAATAAGCATATAAGAGGATACGAGATCAGGAAGGTCTCGATAGTTCTCCCTTTTAGAAAGGGGAGAAAAAGGAGGAGGTGGTGTGGAAGGGGGGATTCTTCCGAAATGAAGATAGGGAAAAAGGTTAGAAAGTGATCCATTTATAGTAGGCTAGGATCACTCGGATTGGATTATTACTGATTATGAATGAGCGGCCAGCTGTGCTCAATCATATCACGTGCTCCTCTCGAAATTAGTTTATGAAACTTCACTTTGTGGTCTGTACGAATCACGGATCAGCCGTGATCCGCTACACCCCTAATTAATTGTATTAATTCTAATCTCTTATGTCTTGTAGGATCCAACCAACGGCTATTACAGCGTGAACACCTTTAAA[G/T]AACAGCCAACCCCGACCATTTCTCTCACAGCCAATCAGAACGCTGAGGTGCGAAACCCTGCCACGGCGACCCTCGGAAAGCATCGTGTCCCCACCGGCATGTCCTACACCAACATCTACAACACACTGGGCGCCGGACCCAACCGCCTTTACGACTACAGCCAGCGATTCGTGCTGGGCATGGGCAGCAGCTCCATCGAGCTCTGCGAACGCGAGTTCCAGCGAGGATCCCTGAGCGACTCCAGCTCCTTCCAGGACACGCAGTGCGACAGCAGCGTCAGCAGCTACAGCAAGCAGGACGGATACGTGCAGTTCGACAAAGCCAGCAAAGCCTCAGTGTCGTCTTCATCCCACTACTCGCAGTCCTCGTCTCAAAACTCAGACCTGACCCGACCACTGCAGAAACGGATGCAGACGCACGTTTAACAAGGTGTGCTTATAAACAAACACTGAAGGTGAGTCGCTCCCGCATCATTCCTCAACACGCTCAAGCATCACTAG
Associated Phenotype:
Not determined