ZMP
si:ch211-276k2.5
Ensembl ID:
ZFIN ID:
Human Orthologue:
NMUR1
Human Description:
neuromedin U receptor 1 [Source:HGNC Symbol;Acc:4518]
Mouse Orthologue:
Nmur1
Mouse Description:
neuromedin U receptor 1 Gene [Source:MGI Symbol;Acc:MGI:1341898]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11726 | Nonsense | Available for shipment | Available now |
sa12218 | Nonsense | Available for shipment | Available now |
sa15050 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11726
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086243 | Nonsense | 64 | 395 | 1 | 2 |
ENSDART00000131469 | Nonsense | 54 | 360 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 22 (position 38365040)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 35513461 |
GRCz11 | 22 | 35489210 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCATWGTCATYGCTAAAAACAAAGTCATGMGGACGCCGACCAACTTCTA[C/A]CTGTTCAGCCTGGCCATTTCAGATCTTCTAGTGCTTCTCCTGGGAATGCC
Long Flanking Sequence:
GTTTTTTTAATACCAAGTACTGGGTTGTGGCCGGAAGGGCATTCACTGCGTAAAAGATATGCTGGAAAAGTTCGATTAGGGCAACCCCTGATAAATAGGAGACTAATCCGAAGGAAAATGAATGAATGAATTTTTAAAAAATCATCAAACAAGCTTGTTCCTCACCCATAATCTCCAACCCTTTCTTCTTCTCCCATCCGCAGGTCCGGAATGATCCCCAAACCCAACTGCTCCTCGACCGATTCCTCAACGCCAAAATGCATCCAAGACCTATTATGCAACACCAGTGTGGCATTAAACCTCACCGAGATGGAGATTGAAGACTTCTGCCTTGACCAAGACGAGTATCTGGAGAAATACCTCGGGCCAAGACGATCCCCAGTGTTCCTGCCTGTATGCCTGACCTACCTCCTGATCTTCCTGGTGGGAGCGGTGGGAAACATCCTTACCTGCATTGTCATTGCTAAAAACAAAGTCATGCGGACGCCGACCAACTTCTA[C/A]CTGTTCAGCCTGGCCATTTCAGATCTTCTAGTGCTTCTCCTGGGAATGCCTTTGGAGCTTTATGAAATGTGGAGCAACTATCCGTTCCTTTTAGGCAAGGGCGGTTGTTACTTCAAGACTCTTCTCTTCGAGACTGTTTGCTTTGCGTCGATCTTGAACGTAACTGCTTTGAGCGTTGAACGCTACATTGCTGTGATTCACCCACTCCGAGCCAAATACGTAGTAACCCGCACTCATGCAAAGCGCCTGATATTGAGCGTCTGGAGCATTTCCGTGCTTTGCGCCATTCCCAACACGATCCTCCACGGTATATTTACTCTCCCGCCTCCTAAAGGGAAAGCAGCAGGAGTCATGCTCGACTCCGCCACATGCATGCTCGTGAAACCGCGCTGGATGTACAACCTGATCATCCAAATCACGACTCTGCTATTCTTCCTGTTGCCCATGTTGACCATCAGCGTTTTGTATCTGCTCATCGGCATGCAGCTGAAGCGGGAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12218
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 |
---|---|---|---|---|---|
ENSDART00000086243 | Nonsense | 220 | 395 | 1 | 2 |
ENSDART00000131469 | Nonsense | 210 | 360 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 22 (position 38364572)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 35512993 |
GRCz11 | 22 | 35488742 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGASTCTGCTATTCTTCCTGTTGCCCATGTTGACCATMAGCGTTTTGTA[T/A]CTGCTCATCGGCATGCAGCTGAAGCGGGAGAAGATGCTGCAGGTCCTGGA
Long Flanking Sequence:
AACAAAGTCATGCGGACGCCGACCAACTTCTACCTGTTCAGCCTGGCCATTTCAGATCTTCTAGTGCTTCTCCTGGGAATGCCTTTGGAGCTTTATGAAATGTGGAGCAACTATCCGTTCCTTTTAGGCAAGGGCGGTTGTTACTTCAAGACTCTTCTCTTCGAGACTGTTTGCTTTGCGTCGATCTTGAACGTAACTGCTTTGAGCGTTGAACGCTACATTGCTGTGATTCACCCACTCCGAGCCAAATACGTAGTAACCCGCACTCATGCAAAGCGCCTGATATTGAGCGTCTGGAGCATTTCCGTGCTTTGCGCCATTCCCAACACGATCCTCCACGGTATATTTACTCTCCCGCCTCCTAAAGGGAAAGCAGCAGGAGTCATGCTCGACTCCGCCACATGCATGCTCGTGAAACCGCGCTGGATGTACAACCTGATCATCCAAATCACGACTCTGCTATTCTTCCTGTTGCCCATGTTGACCATCAGCGTTTTGTA[T/A]CTGCTCATCGGCATGCAGCTGAAGCGGGAGAAGATGCTGCAGGTCCTGGAGGCCAAAGCCAGTTCGGGCCTGGACAGCTCATCTAATGTGCGCAGTCAGCAGCAGAAAACCCGTCGCCAGCAGGTGACCAAGATGTTGTGTAAGTAGGCCGACTGTTACACTCTGGCAGACTGCTTTGAATCACATTACACTGCAAGCGTATTCATAACATATGAAGCCTGCTCCGTCACTTTGAGTCATCTTTTGGTTTCGCGTGCAGTCTTGGCAGCCTAATGGCATCATTATTATGTTTACGCTCCAAACAGTTGTTGACGAGCAATCGTTTTGTAGATGGCGGGCTGTCATAAAGACAGAAATTGGAGGAAATAGCCTCTAACCATTGGTAGATGAAGAAGTTTATTTATATACATCGTGAAGACACGAGGGAAAGGGTGTTTTTGGAGAGGAACAACAAATAATTGTGTGCATTTTTCTAATAAGCGTAAGTTTTTATCTCAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15050
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086243 | Essential Splice Site | 267 | 395 | None | 2 |
ENSDART00000131469 | Essential Splice Site | 257 | 360 | None | 2 |
Genomic Location (Zv9):
Chromosome 22 (position 38364431)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 35512852 |
GRCz11 | 22 | 35488601 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCAGTCAGCAGCAGAAAAYCCGTCRCCAGCAGGTGACCAAGATGTTGTG[T/C]AAGTAGGCCGACTGTTACACWCTGGCAGACTGCTTTGAATCAYATTACAC
Long Flanking Sequence:
TACTTCAAGACTCTTCTCTTCGAGACTGTTTGCTTTGCGTCGATCTTGAACGTAACTGCTTTGAGCGTTGAACGCTACATTGCTGTGATTCACCCACTCCGAGCCAAATACGTAGTAACCCGCACTCATGCAAAGCGCCTGATATTGAGCGTCTGGAGCATTTCCGTGCTTTGCGCCATTCCCAACACGATCCTCCACGGTATATTTACTCTCCCGCCTCCTAAAGGGAAAGCAGCAGGAGTCATGCTCGACTCCGCCACATGCATGCTCGTGAAACCGCGCTGGATGTACAACCTGATCATCCAAATCACGACTCTGCTATTCTTCCTGTTGCCCATGTTGACCATCAGCGTTTTGTATCTGCTCATCGGCATGCAGCTGAAGCGGGAGAAGATGCTGCAGGTCCTGGAGGCCAAAGCCAGTTCGGGCCTGGACAGCTCATCTAATGTGCGCAGTCAGCAGCAGAAAACCCGTCGCCAGCAGGTGACCAAGATGTTGTG[T/C]AAGTAGGCCGACTGTTACACTCTGGCAGACTGCTTTGAATCACATTACACTGCAAGCGTATTCATAACATATGAAGCCTGCTCCGTCACTTTGAGTCATCTTTTGGTTTCGCGTGCAGTCTTGGCAGCCTAATGGCATCATTATTATGTTTACGCTCCAAACAGTTGTTGACGAGCAATCGTTTTGTAGATGGCGGGCTGTCATAAAGACAGAAATTGGAGGAAATAGCCTCTAACCATTGGTAGATGAAGAAGTTTATTTATATACATCGTGAAGACACGAGGGAAAGGGTGTTTTTGGAGAGGAACAACAAATAATTGTGTGCATTTTTCTAATAAGCGTAAGTTTTTATCTCAGTTTTGAGGGGTTTTTCTGAATTGGAAGAATATTGTCATTGTGTTTTTTTACATTGTGAAAGGTAAAATCTCTTTTTTGTCAGACTATTAGCATCTGCAAGCTTTTTCGCAAGTTCTATATTTTGTCTTGAAAATTCAGAGAGA
Associated Phenotype:
Not determined