ZMP
LOC559131
Ensembl ID:
Human Orthologue:
AC114947.1
Human Description:
Serine/threonine-protein kinase NIM1 [Source:UniProtKB/Swiss-Prot;Acc:Q8IY84]
Mouse Orthologues:
E130304F04Rik, E130304F04Rik
Mouse Descriptions:
RIKEN cDNA E130304F04 gene Gene [Source:MGI Symbol;Acc:MGI:2442399]
RIKEN cDNA E130304F04 gene Gene [Source:MGI Symbol;Acc:MGI:2442399]
RIKEN cDNA E130304F04 gene Gene [Source:MGI Symbol;Acc:MGI:2442399]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35015 | Missense | Mutation detected in F1 DNA | Not yet available |
sa45421 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6190 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35015
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111841 | Missense | 18 | 445 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 11 (position 6248578)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 6216761 |
GRCz11 | 11 | 6214016 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTAATTTGACTTCACTGGTAATTTCCTTTTTTTTTTTGTCTTATCCAA[G/A]GTACCAAAACACTAAATATCTGGGCAAAGCGGCACGCAAAGAAAGGAAAG
Long Flanking Sequence:
ATTTTTTATTTGTATTAAACCACAGGTTTTCATTGGTTTACAAAACAAAAAAATGAGCTGTTCCATATTATCAGTATAAAAAATAACAAAAAACATCAGTGTGTGGACATAAAAAAAAAAAAAAACATCATTAGTGTGGAAAAATTGAGTTATCAACCCAATTTCTTTGGGTTGCTACAAGTTAAATATTGTTTTAAAGTAACTAACAGATATATTTGCCTTTAAATTAGCCACATTTTTTAATTGTTGTAATTATTAATAATTTTCTGTTTCGAAAACTTAATAAAATTATTCTGGTAACTTAAAAGTTTTAATTTAATAAGCATTTTAGAATTTTTAAGTTACAATAATGTGTTAAACTGTGTAGTGGTAACAGCCTTCTTGAGTTTTTATTTAGAGTGACCCAAAAACAGTGTTCACCACTGTTATTACATACATTTTTATTAACAGAAGTAATTTGACTTCACTGGTAATTTCCTTTTTTTTTTTGTCTTATCCAA[G/A]GTACCAAAACACTAAATATCTGGGCAAAGCGGCACGCAAAGAAAGGAAAGAATGAGGCAGCAGCACAACCCGTTCAGAAAGAGGCAGAAGCACGAAAGCCTCCGGTTCTCACACCCGAACAACGAGCAAAGCAGACAGCCTTCGAGAGGGTCCTCTATGACATGTCCCACAACGACCGGGTCATCAATGACATCATTCTGGGCCGCAGGATAGGTTTCTACGATCTCAGAGGAGAAATAGGGACTGGAAATTTCTCCCAGGTCAAACTTGCTGTTCATGAGTTGACCAAAGGTAAGAAAATCAGAAGTCAGTTTCAGTGAGTTAATAATGTATTTTAACAGTCGTGCCACAATGTCTGAATGGAAATATTATAAATGCAATAAAACCTGTGAAAGTTCTCACTTCTCAGCAAACTAATTGTTTTAAAAGATGTTTTGGAAAATTTAAATGACACATTGTCAATTTCATTCCAATTACAGTTAATCATATAGGATTTAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45421
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 |
---|---|---|---|---|---|
ENSDART00000111841 | Essential Splice Site | 34 | 445 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 11 (position 6248628)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 6216811 |
GRCz11 | 11 | 6214066 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTACCAAAACACTAAATATCTGGGCAAAGCGGCACGCAAAGAAAGGAAA[G/A]AATGAGGCAGCAGCACAACCCGTTCAGAAAGAGGCAGAAGCACGAAAGCC
Long Flanking Sequence:
AAATGAGCTGTTCCATATTATCAGTATAAAAAATAACAAAAAACATCAGTGTGTGGACATAAAAAAAAAAAAAAACATCATTAGTGTGGAAAAATTGAGTTATCAACCCAATTTCTTTGGGTTGCTACAAGTTAAATATTGTTTTAAAGTAACTAACAGATATATTTGCCTTTAAATTAGCCACATTTTTTAATTGTTGTAATTATTAATAATTTTCTGTTTCGAAAACTTAATAAAATTATTCTGGTAACTTAAAAGTTTTAATTTAATAAGCATTTTAGAATTTTTAAGTTACAATAATGTGTTAAACTGTGTAGTGGTAACAGCCTTCTTGAGTTTTTATTTAGAGTGACCCAAAAACAGTGTTCACCACTGTTATTACATACATTTTTATTAACAGAAGTAATTTGACTTCACTGGTAATTTCCTTTTTTTTTTTGTCTTATCCAAGGTACCAAAACACTAAATATCTGGGCAAAGCGGCACGCAAAGAAAGGAAA[G/A]AATGAGGCAGCAGCACAACCCGTTCAGAAAGAGGCAGAAGCACGAAAGCCTCCGGTTCTCACACCCGAACAACGAGCAAAGCAGACAGCCTTCGAGAGGGTCCTCTATGACATGTCCCACAACGACCGGGTCATCAATGACATCATTCTGGGCCGCAGGATAGGTTTCTACGATCTCAGAGGAGAAATAGGGACTGGAAATTTCTCCCAGGTCAAACTTGCTGTTCATGAGTTGACCAAAGGTAAGAAAATCAGAAGTCAGTTTCAGTGAGTTAATAATGTATTTTAACAGTCGTGCCACAATGTCTGAATGGAAATATTATAAATGCAATAAAACCTGTGAAAGTTCTCACTTCTCAGCAAACTAATTGTTTTAAAAGATGTTTTGGAAAATTTAAATGACACATTGTCAATTTCATTCCAATTACAGTTAATCATATAGGATTTAGAAAATGTAATTGTTTAATGCAGTGATGATTTAGTAAAAAATTTAAATTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6190
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 |
---|---|---|---|---|---|
ENSDART00000111841 | Nonsense | 337 | 445 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 11 (position 6257532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 6225715 |
GRCz11 | 11 | 6222970 |
KASP Assay ID:
554-5067.1 (used for ordering genotyping assays)
KASP Sequence:
ACCGCAGCACACTGTCACAGCTGATGATCTGCTCCTGGATGCAGTGCATC[G/T]AATACCCCAAACCYTACCCCACATTCAGCGGGACACCCGGCTATCTGGCT
Long Flanking Sequence:
ACACATTTTCACATCATATTTTATTTACTACACATTGTAATCGAGTCTAACTTGTTTATGTCATCCTGTGTTTTCAGCATGAAATCAACATCATCCACCGTGACCTGAAAGCCGAAAATATTTTTTACACCACATGCTACTGCATCAAAGTGGGCGACTTTGGTTTTAGTGTGTTTAGTGAGCCCGGCGAAACTCTCACCACGTTTTGTGGTTCCCCTCCATATGCAGCTCCCGAGCTGTTCAGGGACAAGAGCTACATGGGCCGTTATGTGGACGTCTGGGCGCTGGGCGTCCTCCTCTACTTCATGGTAACCGCCACCATGCCTTTCTTCGCTGACAACTTAGGCCGACTGAAGCGCTGCATCCTGCAGGGGGCATACAGCATCCCGTCCTATGTCCCGGACTCCTGCCAGCTGGCCATCAAGGGGATGCTGAGACCTGTACCTGTGGACCGCAGCACACTGTCACAGCTGATGATCTGCTCCTGGATGCAGTGCATC[G/T]AATACCCCAAACCTTACCCCACATTCAGCGGGACACCCGGCTATCTGGCTGACCCTGCCAAGAGCCTGTGTGTGGAGGAGCAGGAGGTAAAGTCAGCTCTAAGCGAGCTGGGTTTAAGCGGGACACATCTGCAGAATAACACCTGCACTGACTGCCGCAGCCCGATCACAGGAGCCTACCGTATCCTGCTGCACCGCATCCAGAAGAGGAGATCCGTGGAGGCAGTGGGATATTCAGGTCTCTACCCAGAGGATTTCAGTAGCAAGAAATACTGGGCCAACAGCCCGACGGCAAAACACAATCCTTCCGCAGTGTGTAATGTCCTGTGAAGACCTTATTTTGAAACGGATTATGTGAATGAGGCCACATTACAGGAACTGGTGAATTGAAATTCATGCAATTATTTCCAGTTTAAGGGTTAGTTCAACCAAAATTTACATTTCTGTAATTAATTACTCTCCATCTTGTCGTTTTCATCCAATGAGACCTTTATTTAACTT
Associated Phenotype:
Not determined