ZMP
LOC793832
Ensembl ID:
Human Orthologue:
KIAA1841
Human Description:
KIAA1841 [Source:HGNC Symbol;Acc:29387]
Mouse Orthologue:
0610010F05Rik
Mouse Description:
RIKEN cDNA 0610010F05 gene Gene [Source:MGI Symbol;Acc:MGI:1918925]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36407 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6476 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17898 | Nonsense | Available for shipment | Available now |
sa17464 | Nonsense | Available for shipment | Available now |
sa13546 | Nonsense | Available for shipment | Available now |
sa42930 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45606 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36407
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113276 | Nonsense | 17 | 735 | 1 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 23766072)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23919514 |
GRCz11 | 17 | 23937915 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATGAAAGAAGAGCATTGCTTTCAGAGGAAACCGCGCATCCATCTGGAA[C/T]AGGGTAAACCGGCGGTTGGGTGTTAGCTTAGCATTTCACACGGCGACGTG
Long Flanking Sequence:
GGAAATCGAGAGCACAGAGGCAGAGCGCAGGATGTGGAGCTAATCCTCTTCCACGGGCGGCTTTCAATCGTTTTATCCAGCTCGCTTGATCAGGCTCAGGTCAACGAGCTTTGGCATCACAACAAATCGCAGCAGACAGGCGTAACGTTACAGACAGGCGGCAGAGGGAGGAGGAGGAGGCTCGATCGGGGACACTGCAGCAACATCATCATCAGCAGCACGCTCTCTCTCTTCAACATCTCTGGCATTTTATAACACGAGCAGACACACGGACGTGGGTAGTCATGCCCACCCGATCCTTTGATTTTAACCTTAGTTTTTACTGTTATTTGCATACGCTGAGCGGATGCGAACTTTTCTGGTTTACCCGGATCAAATCAAAGTAAGCCACACAGCATCTCCGTTGATGTTGCTCAAATCCAGCCCGGTGTCTGCAGCCCCGCTCAGCTGGAATGAAAGAAGAGCATTGCTTTCAGAGGAAACCGCGCATCCATCTGGAA[C/T]AGGGTAAACCGGCGGTTGGGTGTTAGCTTAGCATTTCACACGGCGACGTGACACAAAACGCAGGAGTGCCACGATATATTATTCATTATGCTGGCTAAGCACATTTACCTTCACACACACTGAACGTGCTTAGCCCGTCATATCATAAAAATAGTTTTCTTGGCGTTGTCAGCTGTTATTTGTGACATTATGAGCTTTGTGATGCGTCAAATCACAGCTGTCATCCTGTCAAGTTGAGCTTTGGTTCTCTGAAATTCAATACAATGGGACAAAAGAGAGCCAGTAGATGGCATGACTGTCAAGGTTGATTTTATAAATAAATGTTTTATTCAAAAATAGGTGACCGTTTTCTTCTTCCTCCACAGAAATGAATCGTCTTTGCTCTGTTAATAATAACTTTCCGTATGACAACAACCTCCTGGTGCTGGACATTGTGCTGAGCTCACTGTGGGCATCACCTCAGCCAATCAACTGGGAGAATGTTGCCAAGCTAGTGCCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6476
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 |
---|---|---|---|---|---|
ENSDART00000113276 | Essential Splice Site | 163 | 735 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 23770164)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23923606 |
GRCz11 | 17 | 23942007 |
KASP Assay ID:
554-4733.1 (used for ordering genotyping assays)
KASP Sequence:
GAGATTGCAGATCCTGCCAAGAACATTGAGAAAACAGAAGAAAATAAAAG[G/A]TGAGGCACATTTACGTCAATCTAGTCATCCTGTACTAATAATTTCTTCAC
Long Flanking Sequence:
GGTGTCGTAAGGAGCAAAAATACAACATATGGGCTCTAATATTGCTGTTGTGTCATCACATATTGCAAGTCATATCTCCCCAGCCCCTCATTTGGGATGCTTTTCATAAACTGGCCCCCATGACAAACTAATTGAATAGCCGTGTTATATGGTGTCATGGCTTTGCTGTCAAAAATCTCATTATAAAGGAGGTCAATGGGGCAAAACAGCCACCAACATAATGAAAGGGTATAGTAAATTTGAACATTACACTGGGGTTAAATTGTGTTTTTTGGTGTTGAACAAAGGTGGGGATTGGAATTTCATAAAAGTAAGATTTTTGGGTGAACTAATCCGTTAATATGGTGATTTTTGGTATTTTTGGGTAAAAAGAATGTTCTGAAATGGGGCTTTTATCTATTTTTAGGCCTCAATGTTCTCCCTACTGGTCGAGGAGCCTCTATTGAGACTGAGATTGCAGATCCTGCCAAGAACATTGAGAAAACAGAAGAAAATAAAAG[G/A]TGAGGCACATTTACGTCAATCTAGTCATCCTGTACTAATAATTTCTTCACTAAATGCATTTATTTCCTGTCATACAGCCCCAACATGGTCATTCACGTTTGTGACGAGGCCAAAAACCTGAAGCAGGACTTTGTGTGTCCAAGGAACCTTCTAGTGAAAGAGATGCGTTACTTTGAGGAGTATCTATCTGTGGACCCACAGCGCTGGGACGAGGTGGACATTTCCGTTCACTGTGACGTCCAGATCTTCGACTGGCTCATGAACTACGCCAAGAGTCACAACACCGAACAATCACACGGGAAACATACAGAGAAACCGAAACTGGGTAATTGTCTTTTTGCGTTCACCATTGTGTGTTTTACTTCTTTAACCAAATATACCATCAGAGTTGTCGTGTGTACTCTGACCTGGCTGAATGGTGTTTGTAAGTGATGGTGGGTGGTGTTGTAAACAGTTTTGCGTTGGCTGTGAGTTGGACGTTTCGCTGTTTGTGATGTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17898
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113276 | Nonsense | 376 | 735 | 9 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 23773756)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23927198 |
GRCz11 | 17 | 23945599 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACAGAGAGAAAAATCCCTTGTGTTCCAAACAAGAWCAACATAGATGCC[A/T]GAGGAAACATTGTATTCACTCACAGCAGGTTATATAAGACACTATTTCAA
Long Flanking Sequence:
CATTATTGTCGCTTTTGATTTATTAGTTTTTTTGTATTCATTTGTTTTATAAAAAAATATTACTGAAAGAAAACTTTTGGTAATTTAAAGATAATAATAAATTAATACAATATTTTTATTATACAAAACATGTTTAATGATGTTATTAATCATATTTTACTCTCACCTTTTTCAACTTTCCATCAGTAAACTGTTTCAAAAGAAGATTGAGAGAATATTTGATCATGGTTATCAGAATCACGATTCCCCTGGTAATGCATCTACTCTGTACAGGTGAGACATTTGCATTATGCTGGATTGTAGCCTGTTAATATTATGAAAATAATATGATGTGTTTTTGTAGTTTAAACATGCACAATAAATATCATAAATATGGATCTCAAAGTGATAATGTGTTGTTGATGTGGTTCCTCCGCAGATGTGGACTTTGCCTTAAACTTCTAACCAAAGAAACAGAGAGAAAAATCCCTTGTGTTCCAAACAAGATCAACATAGATGCC[A/T]GAGGAAACATTGTATTCACTCACAGCAGGTTATATAAGACACTATTTCAATCACACGAACACGAATAATAAAGTCTTAGATTTAAGTGTTAGGCACACACACACATATGAGGATATATGTTAATAATTGTGCTTGTTTGTGTAGACATAAGGCCTGGGAGGTTCATGAGTATGTGAATTGTCTTTATGAAGAGTTAAAGTCATGGGTTCAGGTCTACTGGAGGATCTGGGGCACTATCAACTTCCTTACATGTTCACGCTGCAAACAGGTAAACAGATAGTCATTTTAGTACAATATGCATATGAACTGTAGTGTGAGAAAGTATTTACCCCTTACTGATTTCTTTTTGTGTTCTTTTTTTTTTTGCTGTTTGTCACACTTTAATGTTTCAGATCAACAAACAAGTTTAAATATTAGTCAAAGGTAACACAGGCTGTATTAACATTGTGCAGTTTTGAAATTAAGGTTTTTAATATTAAGAAAAAACAAAATACAAGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17464
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 |
---|---|---|---|---|---|
ENSDART00000113276 | Nonsense | 397 | 735 | 10 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 23773937)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23927379 |
GRCz11 | 17 | 23945780 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTGTTTGTGTAGACATAAGGCCTGGGAGGTTCATGAGTATGTGAATTG[T/A]CTTTATGAAGAGTTAAAGTCATGGGTTCAGGTCTACTGGAGGATCWGGGG
Long Flanking Sequence:
ATCAGTAAACTGTTTCAAAAGAAGATTGAGAGAATATTTGATCATGGTTATCAGAATCACGATTCCCCTGGTAATGCATCTACTCTGTACAGGTGAGACATTTGCATTATGCTGGATTGTAGCCTGTTAATATTATGAAAATAATATGATGTGTTTTTGTAGTTTAAACATGCACAATAAATATCATAAATATGGATCTCAAAGTGATAATGTGTTGTTGATGTGGTTCCTCCGCAGATGTGGACTTTGCCTTAAACTTCTAACCAAAGAAACAGAGAGAAAAATCCCTTGTGTTCCAAACAAGATCAACATAGATGCCAGAGGAAACATTGTATTCACTCACAGCAGGTTATATAAGACACTATTTCAATCACACGAACACGAATAATAAAGTCTTAGATTTAAGTGTTAGGCACACACACACATATGAGGATATATGTTAATAATTGTGCTTGTTTGTGTAGACATAAGGCCTGGGAGGTTCATGAGTATGTGAATTG[T/A]CTTTATGAAGAGTTAAAGTCATGGGTTCAGGTCTACTGGAGGATCTGGGGCACTATCAACTTCCTTACATGTTCACGCTGCAAACAGGTAAACAGATAGTCATTTTAGTACAATATGCATATGAACTGTAGTGTGAGAAAGTATTTACCCCTTACTGATTTCTTTTTGTGTTCTTTTTTTTTTTGCTGTTTGTCACACTTTAATGTTTCAGATCAACAAACAAGTTTAAATATTAGTCAAAGGTAACACAGGCTGTATTAACATTGTGCAGTTTTGAAATTAAGGTTTTTAATATTAAGAAAAAACAAAATACAAGACTGCATAGCTCATTAGTTCACTCAAAAATTTAAATTCTCTTATTGATTACGCTTATGTCATTTTAATCCTCAGACATTCATTCATCTTTAGAAAACAAATTAAGATATTTTAGATACAATCTGAGAGCTCTCTAACAGCATTCATTCATTTATTTTTCATTCATGTATTTTTCATACACTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13546
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 |
---|---|---|---|---|---|
ENSDART00000113276 | Nonsense | 463 | 735 | 11 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 23776520)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23929962 |
GRCz11 | 17 | 23948363 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCATTGGAGCAGATCATAGAYGGCACGGCCTTGGTGTTTATCCTTGCTG[C/A]ARCCAGAAAGTCCTACGATTTGATCCCTCTTTYATGCCCAAGGTTTGTGT
Long Flanking Sequence:
ACTTTATTCGGAAATTTATAGTATATAATGCAGACTTCTACTACAAGCTTTACATGTTTATATTAGTTTTATATCTCCTAAACATGAAGTTTTGGTGCACACACTCTTCCAGACCATAGTTGCAACTACATTGTCTGAGAGACAAAATGCACATTCATGAGCTGCCATTGAAGATCATTGGCTGACAATATCAAAATCTGTTACAGACCTACATAGATTTGTGCAGAAAGTAAGGTAACTTGTATAATGCAGTTCTTTATTTTGGAAGTACTTTGGAAAGCTCTTTGGAACTTTGCAGACTTAACATTTACAATCAGTTACACTTACATATTACATTAAAGTTAATATCCATAAAAATGTAATATGTGCATGTTCTATGGCCTTTGGCAGGCATTCTTGTGTACCGAATTGGGTCAGTGTAGGTATCACCCAGAGGCAGTTGTGTATCCTGGCATTGGAGCAGATCATAGATGGCACGGCCTTGGTGTTTATCCTTGCTG[C/A]AACCAGAAAGTCCTACGATTTGATCCCTCTTTCATGCCCAAGGTTTGTGTTATTGCTAGAATTTGTCTTTGTGAACTCGTTTGACCTTTAAACCCATCCCACCATGTGTGAATGTCTGTTTTCCTTGTCGCAGGGCTGTAAAATAAGAGACCACATTGTGAGTGCGGCAGATGGTGGTGACTGTAGCGATCACAATGTAAACTCAACCCAGACCAGAATACTCAATGACCTGCTGCTGCACAGAGACGCTGTGTGTGTGGCCGAGAGGTTAGATTATAGCAAAAAAAAATTGTATAAATGATTGGCTTTCTGTTTTATGCATTATTTAAACGGTCTGGTCATTTGTCTAGTCTTTTGATGGTTTTATGCCATTATCTATTTTGTTTTGCTGTAGCTCTGAGGATCTTTCTGTAGGCAGTGAAAATGTGCCAGGATGTGATGTTATGCTTGAGCCAGGGGTGCTTACAGCTCACAGACCCAAGGAAACCACAGCTGTGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42930
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113276 | Nonsense | 596 | 735 | 15 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 23778986)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23932428 |
GRCz11 | 17 | 23950829 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAGGGTCAGAGGTCACCGAGGATGAGGTTGGGGATGAAGAAGACACAT[C/A]AAAAAAACAAGGCAAGCTAAAAAATCTTACATTATTAAAAAAAATCAATA
Long Flanking Sequence:
AACACATATCAGTGATTCAGCTTCTACATTTAATAATATTAATGAATTAATCATTAAAATTAATTAGATCATAAACCATTGTGCTGTACAATGTCCGTTATATTAAATAGATTTATAACTGAGAAAATTTGCATTTATACATTATTATATATAACATTTTATGCTGAGATATAAAGTCATTATTGTGAAATATAAGGACATAATTACCTTTTTTTGCATGTGTGTATTGACTTATTCTCAATCTAAATGTATTTGTCCAGTTTTGAATAATGAAAGCACTTTTCTTCCCTTCTGGTGCAGTTTTCGCTCTTAAAAAATTGGAGTCTTCAGCTGGTAAGAACCGAGCGTTGATGCAACTTCCTACACACCTATAATAAAATCACACATCTCACCCATATTTCTTCTTGTGCAGCGCCAGCAGTCTCTGCTGTCTGAAGATGAGGAGTACACTACAGGGTCAGAGGTCACCGAGGATGAGGTTGGGGATGAAGAAGACACAT[C/A]AAAAAAACAAGGCAAGCTAAAAAATCTTACATTATTAAAAAAAATCAATACATGCTCTTTAATAGGCAGTACCTAATTATGGCCAAGGAGTGGCAGTCATGTTCAATTTCAAGGACACTGCTGATTTTTATATGACTTTGTGTACATAGCTGCAAAGAAAGCAAGAAAATCTGGCAAACCTTTGAAAAGACAAGTGTCTTCTCCCAATTTTCACCGCAAGGAGAAATCTGGTGAAAAGGTGAGTGCAGTTAATTTTTTCCATGAGAGTGACTTTCTCAAAATTATTAGTGCTGGATTTTTTTAAACCATGAAAATAAGAATTGAAAGAAGAACTGCTTAAGAATGAAAAAGATATGTGTAATTTTTCTCTTTTTTTCATATATCCTGTAATTTTAAAGGCACCATCTCGAGATACAACCCCATTCACGTGAGTAACTCCAAAAACCTACTGTTTCTATATAGAGATGTCCGATTAGGTTTTTTTTGCCCTCGAGTCTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45606
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113276 | Essential Splice Site | 629 | 735 | 16 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 23779226)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23932668 |
GRCz11 | 17 | 23951069 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGTGTCTTCTCCCAATTTTCACCGCAAGGAGAAATCTGGTGAAAAGG[T/C]GAGTGCAGTTAATTTTTTCCATGAGAGTGACTTTCTCAAAATTATTAGTG
Long Flanking Sequence:
ATCTAAATGTATTTGTCCAGTTTTGAATAATGAAAGCACTTTTCTTCCCTTCTGGTGCAGTTTTCGCTCTTAAAAAATTGGAGTCTTCAGCTGGTAAGAACCGAGCGTTGATGCAACTTCCTACACACCTATAATAAAATCACACATCTCACCCATATTTCTTCTTGTGCAGCGCCAGCAGTCTCTGCTGTCTGAAGATGAGGAGTACACTACAGGGTCAGAGGTCACCGAGGATGAGGTTGGGGATGAAGAAGACACATCAAAAAAACAAGGCAAGCTAAAAAATCTTACATTATTAAAAAAAATCAATACATGCTCTTTAATAGGCAGTACCTAATTATGGCCAAGGAGTGGCAGTCATGTTCAATTTCAAGGACACTGCTGATTTTTATATGACTTTGTGTACATAGCTGCAAAGAAAGCAAGAAAATCTGGCAAACCTTTGAAAAGACAAGTGTCTTCTCCCAATTTTCACCGCAAGGAGAAATCTGGTGAAAAGG[T/C]GAGTGCAGTTAATTTTTTCCATGAGAGTGACTTTCTCAAAATTATTAGTGCTGGATTTTTTTAAACCATGAAAATAAGAATTGAAAGAAGAACTGCTTAAGAATGAAAAAGATATGTGTAATTTTTCTCTTTTTTTCATATATCCTGTAATTTTAAAGGCACCATCTCGAGATACAACCCCATTCACGTGAGTAACTCCAAAAACCTACTGTTTCTATATAGAGATGTCCGATTAGGTTTTTTTTGCCCTCGAGTCTGAGTCAGAGTCATTTGATTTTGAGTATCTACCGATACCGAAACCCAATCTGATACTTCTATAATATATTTAAAAAAATAAAGAAGAACGAAGAAACGGATCCAGGTCGTTCTGTGTTTTTTATTTATTTATTATTTTACCATTCAACAAATCTGTTAACTAACAGAAAACTTCTGTGAGGTAGCTTGAACAATCAAGTAATAAATAACATTAATTCTTCCTGTTTGGACTTCAGTGTAACAGT
Associated Phenotype:
Not determined