ZMP
lrrc40
Ensembl ID:
ZFIN ID:
Description:
Leucine-rich repeat-containing protein 40 [Source:UniProtKB/Swiss-Prot;Acc:Q7SXW3]
Human Orthologue:
LRRC40
Human Description:
leucine rich repeat containing 40 [Source:HGNC Symbol;Acc:26004]
Mouse Orthologue:
Lrrc40
Mouse Description:
leucine rich repeat containing 40 Gene [Source:MGI Symbol;Acc:MGI:1914394]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14971 | Essential Splice Site | Available for shipment | Available now |
sa10669 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14971
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022586 | Essential Splice Site | 49 | 601 | 2 | 15 |
The following transcripts of ENSDARG00000017708 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 29828043)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30123686 |
GRCz11 | 6 | 30114247 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GNNNNNNTAATCATGATATTTTGGTGATKGTTATTAATGGTATTTGTTCA[G/A]TTCCTGCTAGTGTATGGAGGTTGAACTTAGACACACCYCAGGAAGCCAGNNNNNN
Long Flanking Sequence:
TGTTTACAATTGTTTACTTCACAACACTACAACCTCATTCAAGTATACAGGTGCTTTAACATCGCATTGATGTCTCGTTTTAAAAGAGGAGCACACGTGGACTCCAGAGCAGGATTCAGACAAGAGAAGGAAGACTGTCCTGTTCCGTATGGCTTACTGAAAGCTGCTAGAAAGAGCGGGCAGCTCAATCTGTCCGGGCGCGGTCTAACCGAAGGTAAGTTAACGTTACTGTAACGGTAACAGTCCTGGAGCAACACTTCAAACACACTTCAGTGACAAAATGTTAAACTTTATGCAGTAACTATCATTTGAGGCCTCGGAACAGCACATAACAGATATAAACGTTGACTTCGACGTGATTTAAATTCCAAAGATGTTTCTGAAAGAGACATCTGTCTCCTAAACTTTGAAATGTCGTGGCTTACCGTAATAACAATAATTGCTGTAGGGGTAACGTTAATCATGATATTTTGGTGATTGTTATTAATGGTATTTGTTCA[G/A]TTCCTGCTAGTGTATGGAGGTTGAACTTAGACACACCTCAGGAAGCCAAGCAAAATGTGTCTTTTGGAGCTGAAGATCGGTGGTGGGAACAGACTGATCTGACCAAACTGCTTCTGTCCTCCAACAAACTCCAGAGCATCCCTGATGATGTTAAACTTCTGCCTGCCCTGGTGGTCCTTGATGTAGGTTTCTCTATTCTATTCTATTCTATTCTATTCTATTCTATTCTATTCTATTCATTAAAATGAATATAAAAATAAACAACTAAATATTAAATGAAATTACAATAGTTATTAACAATTTTGACTCCCCAATATGTAGATATGAATTGTGGTGCATTTCATTGTTTTTTATTTATTTATACGACTCTTTTTTTTGTTTAGCCTTTAATTAAAAAAAAAGAAAAAAAATATGTAGTGTGTGTGTGTGTGTGTGTATCGATGTATAATGTCAAACACATTAGAATATAAAATATATTTTGTATATGTTCTGTTAACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10669
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022586 | Nonsense | 79 | 601 | 2 | 15 |
The following transcripts of ENSDARG00000017708 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 29828133)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30123776 |
GRCz11 | 6 | 30114337 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGAAGCCAAGCAAAATRTKTCTTTTGGAGCTGAAGATCGGTGGTGGGAA[C/T]AGACTGATCTGACCAAACTGCTTCTGTCCTCCAACAAACTCCAGAGCATC
Long Flanking Sequence:
GCACACGTGGACTCCAGAGCAGGATTCAGACAAGAGAAGGAAGACTGTCCTGTTCCGTATGGCTTACTGAAAGCTGCTAGAAAGAGCGGGCAGCTCAATCTGTCCGGGCGCGGTCTAACCGAAGGTAAGTTAACGTTACTGTAACGGTAACAGTCCTGGAGCAACACTTCAAACACACTTCAGTGACAAAATGTTAAACTTTATGCAGTAACTATCATTTGAGGCCTCGGAACAGCACATAACAGATATAAACGTTGACTTCGACGTGATTTAAATTCCAAAGATGTTTCTGAAAGAGACATCTGTCTCCTAAACTTTGAAATGTCGTGGCTTACCGTAATAACAATAATTGCTGTAGGGGTAACGTTAATCATGATATTTTGGTGATTGTTATTAATGGTATTTGTTCAGTTCCTGCTAGTGTATGGAGGTTGAACTTAGACACACCTCAGGAAGCCAAGCAAAATGTGTCTTTTGGAGCTGAAGATCGGTGGTGGGAA[C/T]AGACTGATCTGACCAAACTGCTTCTGTCCTCCAACAAACTCCAGAGCATCCCTGATGATGTTAAACTTCTGCCTGCCCTGGTGGTCCTTGATGTAGGTTTCTCTATTCTATTCTATTCTATTCTATTCTATTCTATTCTATTCTATTCATTAAAATGAATATAAAAATAAACAACTAAATATTAAATGAAATTACAATAGTTATTAACAATTTTGACTCCCCAATATGTAGATATGAATTGTGGTGCATTTCATTGTTTTTTATTTATTTATACGACTCTTTTTTTTGTTTAGCCTTTAATTAAAAAAAAAGAAAAAAAATATGTAGTGTGTGTGTGTGTGTGTGTATCGATGTATAATGTCAAACACATTAGAATATAAAATATATTTTGTATATGTTCTGTTAACATAATACAAATCACTTTATAATTAGTAATGTCTATTTCAGTTAATTTGGACAACTTTAAAGGCAAATTTCTTCGTATTTAGATATTTTAGATT
Associated Phenotype:
Not determined