ZMP
ENSDARG00000088672
Ensembl ID:
Human Orthologues:
IL1R1, IL1RL1, IL1RL2
Human Descriptions:
interleukin 1 receptor, type I [Source:HGNC Symbol;Acc:5993]
interleukin 1 receptor-like 1 [Source:HGNC Symbol;Acc:5998]
interleukin 1 receptor-like 2 [Source:HGNC Symbol;Acc:5999]
interleukin 1 receptor-like 1 [Source:HGNC Symbol;Acc:5998]
interleukin 1 receptor-like 2 [Source:HGNC Symbol;Acc:5999]
Mouse Orthologues:
Il1r1, Il1rl1, Il1rl2
Mouse Descriptions:
interleukin 1 receptor, type I Gene [Source:MGI Symbol;Acc:MGI:96545]
interleukin 1 receptor-like 1 Gene [Source:MGI Symbol;Acc:MGI:98427]
interleukin 1 receptor-like 2 Gene [Source:MGI Symbol;Acc:MGI:1913107]
interleukin 1 receptor-like 1 Gene [Source:MGI Symbol;Acc:MGI:98427]
interleukin 1 receptor-like 2 Gene [Source:MGI Symbol;Acc:MGI:1913107]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31751 | Essential Splice Site | Available for shipment | Available now |
sa10057 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31751
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 |
---|---|---|---|---|---|
ENSDART00000122155 | Essential Splice Site | 345 | 580 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 9 (position 54849227)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 53483978 |
GRCz11 | 9 | 53023485 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCAGCAGTCGAGGACATCTGACCGGCCAGTTCATGCTCATCCCAACAG[G/A]TACATCAAAAGAGTACCTAATCAGAAAATCTTTGCAAACCCTAAATAAGT
Long Flanking Sequence:
CATCCACCTATCTATCTACAGTATCTATCTGTATGTCCCTCTGTCCATCCATCCATCTATCCATCTGTCCATCCGTCCGTCCATCCATCTATCTTTCAATCTGTCTATCCATCTATCTATTTATCTATCCGTCTATCCATCCATCCATCCATGTATATATCCATGTATCTATCAATCTGTCTATCCATCTGTCTATCCGGCCATCCATCCATCCATCCACCCACTGTATCCATCATTATGTATTAATATTTAATGTATATTTGGTTTGTAGAATGCAAAACTAAGCATTCAGATGTTTTACAATATACCCTTATGTTGTTCATTTTTCCCCCTCCATATGTGTTCCTCTTGCAGCGAGAGCGTCACTGCAGATGGTTTCGTGTTTGTGCGAACCCTGTCGGTGTCTCATGTGTCGGAGGATGATTTCTATCTGAACTTCACCTGTCTGGTGTCCAGCAGTCGAGGACATCTGACCGGCCAGTTCATGCTCATCCCAACAG[G/A]TACATCAAAAGAGTACCTAATCAGAAAATCTTTGCAAACCCTAAATAAGTATGCGATATCTATGCAATGTGACCATACGATTGCGATATCGATGCTGAAACTATATATGTTGCAGCCCTTTTATATACACAAATAATATTTTATATAGTGACAATACTGATTGTGATTGTCTGCATGTGCACAGATCCGGATCTGCTGTTGTTTGCTGGTCTTCTCCTGGGTTTGCTGGCTCTGTTCTTCACCAGCGCAGTGTTTCTGTGCTCCGTCTTTAAGGTGGAGCTGGTCTTATGGGTCAGGACTGCGTTTCCATTTCTCTACAAAACCACAGGTGCTCGTATAAACAGGAAACGCACTCTAACAGCTTACTTAACAGTTACTTGGAAACGATGCAGTTGCATTAACGAGAATTAACACCTTTCACAGTGCTGTTTACTTCACTCACTTTATTATTCACACTTTGGGAAATGTGCCTCAGGCTTAACACTTTGTATTAGCTATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10057
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122155 | Nonsense | 400 | 580 | 9 | 11 |
ENSDART00000122155 | Nonsense | 400 | 580 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 9 (position 54845089)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 53479840 |
GRCz11 | 9 | 53019347 |
KASP Assay ID:
2260-2603.1 (used for ordering genotyping assays)
KASP Sequence:
TTATTCTTCACTGTGGTTGTTTTTCCTYTAGATGGCGATGGTAAGCAGTA[T/G]GACGCATATATCGCCTATCCCAGAGTCCTGGAGGGCTCYAGTGAAAAGGC
Long Flanking Sequence:
TTACCTACAGCTACAGTAGATTTATTTTTACTCATTTTATTTATTTCACACCATAATATACTATATATATATATATATATACACACACATATATATATATATATATATATATATATATATATATATATATATACATATACATAATATACAAACATACATAATTATTATTATTATTATACAGTTTATAATTCAATCAATATACAAAAATTAAAATCTGCACAGTAGATTTATATTATATGTATATATATACATATATGTATATATATACATATATGTGTATATATATATATATATATATATATATATATATATATATATATACATATACATAATATACAAACATACATAATTATTATTATTATTATACAGTTTATAATTCAATCAATATACAAAAATTAAAATCTGCACAGTAGATTTATATTAACGCTAAACAGTATTGTTACTGCTCTTTTATTCTTCACTGTGGTTGTTTTTCCTTTAGATGGCGATGGTAAGCAGTA[T/G]GACGCATATATCGCCTATCCCAGAGTCCTGGAGGGCTCTAGTGAAAAGGCGGAGGTTTTTGCCATGAGCACTTTGCCGCAGATTTTGGAGGGTCGATACGGTTATAAACTCTTCATTCTGGGCCGTGACGGGCTGCCTGGGGAAGGTAAAGCATCTCTGAATAAACAAACCACTCTAAACCACCTGTTATGTCCATATATGATCTGTTGAAACTGAATCACATGACTCTTCTGATGTGCATGCTGGAATTTATGCACATTTTCTTTTCAGACAAATTGCGTAATACAAAATGCACATGAGTTTTAATGCATATTTTCAAAATGTACGCACATCAACCGTTTAATATGTGATCATTCAACATGTGCATTAAAGGGTCATGTCACCCCCCGCTTTCGGTTCAGGTCTACCTCAGAATTTTTTCAAAAGATGCATCATAGTGGGCGTGGAGCTCTGCGAGCAGAGGGCAGGAGTGGGCGTGACCAGCAGGGGAGAAGGAGGGG
Associated Phenotype:
Not determined