ZMP
si:ch73-19n18.2
Ensembl ID:
ZFIN ID:
Description:
LOC567806 protein [Source:UniProtKB/TrEMBL;Acc:A1L2F9]
Human Orthologue:
UMODL1
Human Description:
uromodulin-like 1 [Source:HGNC Symbol;Acc:12560]
Mouse Orthologue:
Umodl1
Mouse Description:
uromodulin-like 1 Gene [Source:MGI Symbol;Acc:MGI:1929785]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10685 | Essential Splice Site | Available for shipment | Available now |
sa30942 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10242 | Essential Splice Site | Available for shipment | Available now |
sa27634 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18380 | Nonsense | Available for shipment | Available now |
sa41690 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10685
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 |
---|---|---|---|---|---|
ENSDART00000099853 | Essential Splice Site | 106 | 950 | 2 | 17 |
ENSDART00000126952 | Essential Splice Site | 106 | 927 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 10 (position 33590793)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 32692142 |
GRCz11 | 10 | 32636002 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGACATGTTGCCATGGCTAMGAACAAGTTGGTAGTTACTGTGCCTTGC[G/A]TRAGTATKTTCAACTAAATCAGAGTGAAAGTGGAAAGTGAAGGAATGCAA
Long Flanking Sequence:
CATTAGAAGCTGGTTATATTCACAGATTTTGCCACACAACTGTGTTTAAGCCTCTTATAAAAGTGATTTATGCATATTAGGTCCCTATTTTCTAATGATTTATGGCATTATAGTAAAAGCAATAACCATGATGCAATTTTGTTTTTTCCCAAATGCAACATAAGACTGTTTTTGTGCTCCAGGGTCACAAATGTTAAGGAGTGTTGAAACTATTACATTGTATTAAACTGAATATTTAAACTACTTGCATTCTTTAGGATATGAGCAGACACTGTCAGGTTATCATCTCTGTAACATGACTGAGCTAGTGTCGATGACCAGGGTGGTCTCTTATCCCTCCCCATACACCCAGAGGAGAGCGTGTGGCGGTTGGCTGCCATGGAACATGTGTGACGTCACCGTTTATAAGACAGCATATCAAACAGAGGTGTATTACATCTCCCGACAGGTGAAGACATGTTGCCATGGCTACGAACAAGTTGGTAGTTACTGTGCCTTGC[G/A]TGAGTATGTTCAACTAAATCAGAGTGAAAGTGGAAAGTGAAGGAATGCAATTTTATATATTGATTGATATTATTTTTATCTCAGCCTTGAACAGAAGTGCAGAATTCACATCAAAACCAGGACTGTGTCCCTCAGCAAGAGCAACAGGAAATCATTCAGACTCTGGAACTGTGTGCAACTGGGACACAGATTGTCCACAGTGGCAAAAATGCTGTCAGACTGAAAACAACTCCAGCATCTCTCGGTGTTTAGAGCCAGTGCCAGCAGGTAAACACGATCCCATGCAATGAACGCAGAATTTCTATTCATTATAAAATAACATACAATTTTATATAAAAATATAATTTGTGCTCAAGCCAACAGAACCTGGTGCTTCAACGTGACAATAACCGTAAGGACAACCTATGAGCTATTGGCAATCGACAAAGGTCTCTTGAACCACACCAGACTGCTTCACTCTGTGGTTTGTAATCATTTGCTGTATAAAGTGCCTGAGTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30942
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099853 | Nonsense | 198 | 950 | 4 | 17 |
ENSDART00000126952 | Nonsense | 198 | 927 | 4 | 16 |
Genomic Location (Zv9):
Chromosome 10 (position 33590347)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 32691696 |
GRCz11 | 10 | 32635556 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACAACCTATGAGCTATTGGCAATCGACAAAGGTCTCTTGAACCACACC[A/T]GACTGCTTCACTCTGTGGTTTGTAATCATTTGCTGTATAAAGTGCCTGAG
Long Flanking Sequence:
AGGTGAAGACATGTTGCCATGGCTACGAACAAGTTGGTAGTTACTGTGCCTTGCGTGAGTATGTTCAACTAAATCAGAGTGAAAGTGGAAAGTGAAGGAATGCAATTTTATATATTGATTGATATTATTTTTATCTCAGCCTTGAACAGAAGTGCAGAATTCACATCAAAACCAGGACTGTGTCCCTCAGCAAGAGCAACAGGAAATCATTCAGACTCTGGAACTGTGTGCAACTGGGACACAGATTGTCCACAGTGGCAAAAATGCTGTCAGACTGAAAACAACTCCAGCATCTCTCGGTGTTTAGAGCCAGTGCCAGCAGGTAAACACGATCCCATGCAATGAACGCAGAATTTCTATTCATTATAAAATAACATACAATTTTATATAAAAATATAATTTGTGCTCAAGCCAACAGAACCTGGTGCTTCAACGTGACAATAACCGTAAGGACAACCTATGAGCTATTGGCAATCGACAAAGGTCTCTTGAACCACACC[A/T]GACTGCTTCACTCTGTGGTTTGTAATCATTTGCTGTATAAAGTGCCTGAGTCTGAGAGTACATGTAGAAGTCTGCAGCCAGACACTATTAAATCATCTTGCTGTGTTCCAAAACAAAAGAGTTCCCTACCTAGCATACAGTAAAGGGACAGTAATAATGACTTAAAACCACACTGAACTGAGCTAAACTGAACTGAACTTAAACACTAAAAACTGAACTACCCTGATCTAGTTACGATGACCCTTTATGTGAAGCTGCTTTGACACAATCTACATTGTAAAAGCGCTATACAAATAAAGCTGAATTGAACTGAATTGAACAGTTCACCCCAAAAAGTTCTGTTATCATTTACTCACCCTTTACTTGTTTAAAATCTATTTGAGTTTCTATTTGAGTTTTTTTTTGTTGAACACAAAAGATACTTTGAAGAATGCTGATAGCTGGCACCCATTGACTTCTATAGTATTTCATTTTTCCTACAATGGAATACCAGCAGCCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10242
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 |
---|---|---|---|---|---|
ENSDART00000099853 | Essential Splice Site | 569 | 950 | 11 | 17 |
ENSDART00000126952 | Essential Splice Site | 546 | 927 | 10 | 16 |
Genomic Location (Zv9):
Chromosome 10 (position 33580191)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 32681540 |
GRCz11 | 10 | 32625400 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGRATACAYAGACTTGAACCCCAGAAGACCGGGACGCAGCTGTGCAGG[T/C]ACACACTGTGGAAAACGCTACTGTWGAGATTTCATTAGACTGGCACACAC
Long Flanking Sequence:
GTTGGCATTTCTGTGTGGTGTTTGCATGTTCTCCCCATGTTCCTGCGGGTTTCCTTCGGGTGCTCCGGTTTCCCCTACAGTCATGCACTATATGGTCAATTGAATCAATTAAATTGTCCATAGTGTATGAGTGTGTGTGTCAATAAGTGTGTATGCATGTTTCCCAGTAGTGGGTTGCGGCTGGAAGGGCATCAGCTGCATAAAACATATGCTAGAATAGTTGATGGTTTATTCCGCTGTGGGAGACTAAGAGACTAAGCTGAAGGAAAATGAACGAGTTGACATAACATGTACTGTTTCCATCTGTGTTAATGATGTGATATGTTGACTTGAGATGTGATCGGCCTCTTGTTATTTATAGATTTAAATGAGTGTTTGCTGGCTGAGGCGGACTGCTCTCGATGGGCTCATTGTATAAACACTGAGGGCTCGTACAGCTGTGACTGTTGGTCTGGATACATAGACTTGAACCCCAGAAGACCGGGACGCAGCTGTGCAGG[T/C]ACACACTGTGGAAAACGCTACTGTAGAGATTTCATTAGACTGGCACACACTTTGAATAGAGATAAAAAGCTGTTGAGCATACACATAATACACATAATATATTGTTAAATTCATGGGCGCCAGCAGGAATTTACTCCAAGGTACGCACAAATCCAGCACCACCCCGCCCCTTCCCCCAATCGTGTCAAGAAACACTGATGCTTACTGCCAAAGGCTACATTATTTAAGGGCATTCCTTACGACATAATTCATTTCCTTTTTTCATTTTAAAATTTCGATGAAATCTAAATGTAATAAAAGCACATCAGCACCAAGGAAAAATATAACGCAAGACGTAATCTTTAAAGTTATGACATATTAAAAAATTTGCAAATATATGACAGAAAAAACTGTACAAAAGCACGCACGTCTCTCTTAATTCGGTGCTCAGCCAAAACCGCAAAAAGTGCAAATTAAATGTAAATCATGTGATCCGGAAGTGTATAAAAAGGAGCACCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27634
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099853 | Nonsense | 674 | 950 | 12 | 17 |
ENSDART00000126952 | Nonsense | 651 | 927 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 10 (position 33577070)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 32678419 |
GRCz11 | 10 | 32622279 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCGAGATTACCTCAAGGCCAATAACATCTCAGAGACCTCCTTGTATCTT[G/T]GAAATCCTGAATGCGGGCCCGTTGGGTTTGATGATTCTTATTTGTGGCTC
Long Flanking Sequence:
ACACAATAAATGTGCTCTATAAATACACATTACAAACAATGTCATCTTTGCATTTAAAATGAGCGATGACACCCAATGACAGTTGTTATTAGTGTGTCATGTCATGGTTATAAAGGTTAAATGACAGCAAGCAATTTTCCTCTGATATCTCTGTTTGCATCTGTTTGTTTCTGCTCATAACCACAGCTTCATCTAATGCTACAGCATCAACTGTTCATCCAGCCACGAACTATACTGAACTATCAAGCGCTGCAATAACTGGCAACCCATCTGTGAGCAGGACTAATGTTCAGAGCAACCTCACAACAACAACAATGTCTTCAGCTTCCTCGACCTACGCTAACAGACTGATCCAGGCCATCAGTCCTGCAACAACACTCAACATTACTTGCCACTCTGTCTCCTGTATAACTGTTGAATGCAGCCCCTGGTTAATAAAAGTCGACATAAGGCGAGATTACCTCAAGGCCAATAACATCTCAGAGACCTCCTTGTATCTT[G/T]GAAATCCTGAATGCGGGCCCGTTGGGTTTGATGATTCTTATTTGTGGCTCATCACAGCTTGGGATAAGTGTGGCACAACACCAGAACATGTAAGTCCTCCAGTGTTTAAATTGAAGGGATAGTTCACCTGAAAGTCTAAATTGATTTACACTCACGTTATGTTAATTATTTTTAAGGGTGCTTTCACACCTTTGTATCAATTCAGTTGTTCCGAAACAGAGATTACAATTGTTACAATGTTGCTCTTTGCTCTTGGAGCGGTTCGCTTTCACACTGCAAAGTTTCTAATCGGACCAAAAGAGCTAAAACAAGTCACGTGCGAGTAAACTCTCCTTACATTGGTCAGAGTGTCAGGGTTTATTTTGCAGCGTCCCGCTAAGCTGTCAGGAGAGGTGGTGGTTTGGTGGTGATTGACAGGGTGCGCGCATGACGTGTCTGAGGAGAAACGTGGTGGGGAGGGGTGGGAAGGGTGCGCAACGATACCTATTTGAGGACCGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18380
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 |
---|---|---|---|---|---|
ENSDART00000099853 | Nonsense | 900 | 950 | 16 | 17 |
ENSDART00000126952 | Nonsense | 877 | 927 | 15 | 16 |
Genomic Location (Zv9):
Chromosome 10 (position 33568742)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 32670091 |
GRCz11 | 10 | 32613951 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTGTGACCGTCTTCTAAGTGCCAGGTCTTCTAAATTATTTGGACTGACC[C/T]GATCYGTTGGACCCTTAAACAGATTACACACAAGTAAATGCTTYTTATTT
Long Flanking Sequence:
AAATGAAAGAACGAATGAAGGAATGAATGAACGAATCAATAAATGAATAAATGAATGAACAAACAAATGAATCATAAAAAGAATGGACAAATAAATGAAGAAACGAACGAACGAATTAACAAACGAATGATCAAACAAACGAATGAAAGAATTAACGGATGAATGAATGAATAAATAAATGAATAAACGAACAAACTAATGAATGACTGAACAATTGTATGAATAAACGAATATACAAATGATTCAACGGATGAACTAATAATGCAGTACTAACTATTTTAAAAAATGTATTTATATTTCTTTTCAGTTGTCAGTTGTGTCGATCTATATTGTGGATAGATTAAATAAACACCAACTTAATATTAAATTAAACTCAGACAATGTAGGAGGTATAATGTATATGTCATGATAAACACACCTTTTCTTATTTTTTCTATATTTCTTTATAGGCTTGTGACCGTCTTCTAAGTGCCAGGTCTTCTAAATTATTTGGACTGACC[C/T]GATCCGTTGGACCCTTAAACAGATTACACACAAGTAAATGCTTTTTATTTAATGCATGTGAATATCCACAGCCTTCCATGATATCAGTTAGCATCACTAATTCTTTCTCTTTCATTTTCTTAAAGCAACTTTCCAAAGCGACACATCAAATACTGTGCAGGCTGTTGGATTTGTTCTGCTCGGTGTCGGTGTGTTTCTGCTTTCGCTCACTGTCATTGCAGGATTGCTGTATCAGAAAAGAAAAATCGGGAACTACAACTTCCATGTCAGACCACAGCCGGAAAACTTCACCTATAATGTTTTTAACACGTAATCATCTCACTTTAGCCACTAATAGAGGGATAAATCTAACTATTGTTATTACCATTAGGTATAATGTATTGAAAATGGTTTAATTTGATTATATTTTTATACTTAAAACCTACATGTGATGTACTGTAGTTGTCATTCTTAGTTTGTTTTCCTTTTCAGCACTTTATAGGTAATTAAACTGACTGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41690
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099853 | Essential Splice Site | 910 | 950 | 16 | 17 |
ENSDART00000126952 | Essential Splice Site | 887 | 927 | 15 | 16 |
Genomic Location (Zv9):
Chromosome 10 (position 33568708)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 32670057 |
GRCz11 | 10 | 32613917 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTATTTGGACTGACCCGATCCGTTGGACCCTTAAACAGATTACACACAA[G/A]TAAATGCTTTTTATTTAATGCATGTGAATATCCACAGCCTTCCATGATAT
Long Flanking Sequence:
ATCAATAAATGAATAAATGAATGAACAAACAAATGAATCATAAAAAGAATGGACAAATAAATGAAGAAACGAACGAACGAATTAACAAACGAATGATCAAACAAACGAATGAAAGAATTAACGGATGAATGAATGAATAAATAAATGAATAAACGAACAAACTAATGAATGACTGAACAATTGTATGAATAAACGAATATACAAATGATTCAACGGATGAACTAATAATGCAGTACTAACTATTTTAAAAAATGTATTTATATTTCTTTTCAGTTGTCAGTTGTGTCGATCTATATTGTGGATAGATTAAATAAACACCAACTTAATATTAAATTAAACTCAGACAATGTAGGAGGTATAATGTATATGTCATGATAAACACACCTTTTCTTATTTTTTCTATATTTCTTTATAGGCTTGTGACCGTCTTCTAAGTGCCAGGTCTTCTAAATTATTTGGACTGACCCGATCCGTTGGACCCTTAAACAGATTACACACAA[G/A]TAAATGCTTTTTATTTAATGCATGTGAATATCCACAGCCTTCCATGATATCAGTTAGCATCACTAATTCTTTCTCTTTCATTTTCTTAAAGCAACTTTCCAAAGCGACACATCAAATACTGTGCAGGCTGTTGGATTTGTTCTGCTCGGTGTCGGTGTGTTTCTGCTTTCGCTCACTGTCATTGCAGGATTGCTGTATCAGAAAAGAAAAATCGGGAACTACAACTTCCATGTCAGACCACAGCCGGAAAACTTCACCTATAATGTTTTTAACACGTAATCATCTCACTTTAGCCACTAATAGAGGGATAAATCTAACTATTGTTATTACCATTAGGTATAATGTATTGAAAATGGTTTAATTTGATTATATTTTTATACTTAAAACCTACATGTGATGTACTGTAGTTGTCATTCTTAGTTTGTTTTCCTTTTCAGCACTTTATAGGTAATTAAACTGACTGATTGTGTTACTTAAAGGGATAGTTGACCCAAAAATGA
Associated Phenotype:
Not determined