ZMP
si:ch211-260p9.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human c-Maf-inducing protein (CMIP) [Source:UniProtKB/TrEMBL;Acc:Q1LWW3]
Human Orthologue:
AC099480.1
Human Description:
C-Maf-inducing protein [Source:UniProtKB/Swiss-Prot;Acc:Q8IY22]
Mouse Orthologue:
4933407C03Rik
Mouse Description:
RIKEN cDNA 4933407C03 gene Gene [Source:MGI Symbol;Acc:MGI:1921690]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36594 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43067 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32192 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36594
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091512 | Essential Splice Site | 127 | 679 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 12830342)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 13385154 |
GRCz11 | 18 | 13353666 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCCAGAACACTAACCTCAGCGCTCAGGACCACGAAAACATCATTGTGG[T/G]GAGTAGGGCTGCTTTTAGTTTTTTTTTTTTTTGTAACTTAGAAAATATGA
Long Flanking Sequence:
GCAGCGTTCTGTTTTTCTTTTCATTATGAGTGTCATTTGTGAATTGAGGTGTACATTGCATCTCATTTTGAGTTTAATTAATTTATAAAAGTTACCTCTGCATGCGTGTGCGTGTGTGTGTGTGTGTAGCTGTGGTTTAGCTAGACTTTCTTTTTCACATGGCAATGCTGTGATCTTCTTCAGAACAAAGACCTCCAGTGTTTGCATATAGGGAAATATCGGTTGCATCTGCACTCTGGTTTGCAGATGAAGATTATATCTTTGAATCCCACCTATAGCGAGCATGTGAATCTTTTAAAAAGGACTTCCAGTCAAATGGCTGATGTATCCTTGAATCACACAGGCTTTCCCAAAAAGAGTTTGAACGTTTTAAAAACAGGGATTGAGCTATTTAGCTATGGCATTGCTGGCCAATGAATTCTCAACCATTTTTTTTGTCGTGTCATTTCCTTCCCAGAACACTAACCTCAGCGCTCAGGACCACGAAAACATCATTGTGG[T/G]GAGTAGGGCTGCTTTTAGTTTTTTTTTTTTTTGTAACTTAGAAAATATGAAGATGCATGTTGCATTCAAATAAGAGCCTGTTAAACTGCATTGCTAACAAGGCAGGGTTACGTAATATATCTTGAGGCTCATGCTCTGGAATAAAATTGATTTGAAAGTGGAGCGAACTCCCATAGAAACAGGGCTTGAATGCCTAGATGTGCTGGATGGGGCGCTGAAGGTTGCGCACTTCCTTAAAGCATGGCTGAAAAAGCAGCAAGACTCTTCATGTCTGTGGGGAAGGTGACTAATGGGTCAAATCTGTCTGTAGGCCATCGCACCCCTGCTGGAGAATAACCACCCTCCCCCTGACCTGTGCGAATTCTTCTGCAAGGTAAATACAAGTGTTCATAATTATTATTACTATTAGTTTTATTTAACAAATAGATTTTTTATTGCTGGTTGTAATTTTTCATTTTTGTATAAATGAGGGCTGCGCAATATATCGTTTCTTCATTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43067
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091512 | Nonsense | 192 | 679 | 7 | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 12827688)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 13382500 |
GRCz11 | 18 | 13351012 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACTTCGGGAAATGCCCCAGACTCCGTCTCTTTACTCAGGAGTATATTT[T/A]AGCTCTGAATGAGCTTAACGCCGGCATGGAAGTGGTCAAGAAGTTCATTC
Long Flanking Sequence:
TAGTAAAAATATTGTATAATAATAATAATAAATATAATAAATATTCCAAAATATAGTAATAAATATTCCAATTTTTATTATATTTTATATGTAATCAAGTAAATGCAGCCTTGTGAATGTAAGAGACTCAAAAAAATAAAAACAAATCTGACTGACCCCAGACATATGAATGATAGTGCATTGTGTAATGTTATTGTTTGATATCATCCGTCTCTCAAGTAATTTCTTCTAATGGTTTACATATATTAATATGAAATGTGTTCCTCTGTGCAGCACTGTAGAGAGCGTCCTCGGTCAATGGTGGTGATTGAAGTGTTCACTCCTGTGGTTCAGAGAATCCTCAAACACAACATGGTGGGTGCTCAAATTTCACTAGCCATACTCTTGAATTCACACATACTGTATCTGCTCCCTCGTCTTCTAACTCTCCTTGTCTTTTGTTTTGTTCCAGGACTTCGGGAAATGCCCCAGACTCCGTCTCTTTACTCAGGAGTATATTT[T/A]AGCTCTGAATGAGCTTAACGCCGGCATGGAAGTGGTCAAGAAGTTCATTCACAGGTGAGTGACAATTTTTTTTCGTTTCCTTTTTCAAACAGACTCCTGCCAGCAAAACAGTGTATTAATGAAAACAAATGTGTGCTTTAACCCTTATAACAACCCAGTAATATGAGTGGCTTTTTTAAAATGGCTTGTTGTGGTATATTATCACCAAATACAAGATTCAATGTTTTAATCTAGTTTTCCGTCTATTACGACTGATTTTGTTTTTATTTTTGAACCTGCTTGGTCATAGATATCATTGATTTGAAACTGATGCTCCTCAGTTCTTTGAATAACAAGAAAAGAAAACCATTTGTCAACAAGTTTGTCAGTTTAAAATAAAATATAAACTTTATTATCAATATTTTTAATGTTTATCATTTTTAGCAGAAATCGTGATTCTTGTTGACTTATTTGAGTTAATGTAAGTATCAAATACAAAAAATATTCACAGGGTGTCTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32192
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091512 | Nonsense | 240 | 679 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 12824327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 13379139 |
GRCz11 | 18 | 13347651 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCCCAAATCTCGTAGCGGTTTGCCTGGCTGCCATCTACTCCTGCTAC[G/T]AAGAGTTCATCAACAGGTGCGTCCGATTCTCTGTTTACCCCATGTGTTTA
Long Flanking Sequence:
TAAAATCGGCATATGCCACATGTCTTAATGCGGCAATGTCTGAACATGTCTTAATTGTTTGGTTCAATTATGACTTTATTCGGATTAAGATAATCAAAAATGGCTGTTTACATGGTAGATTCTAATTCAGAATATTGTCTTGATCATGTTAAAATCAGATTATTGGTGTCCATGTAAACATACTCAGTGTTACCTAATTTTAGCTCCACCTTGCTTATGTACAACGAACAGGGCTTCATATTATGTACACAAACGAACATCTTTTAATGCATCAGTTTGTGTCAGTTTAGTGGTCTGTTTAGGACCAAACCCTGTGCAGACTTCCTGCGTAAGCTTTGTTTTCTTTCAGCTGTCATTCTCAAACACAGAAGCTATGCTAACCTGACCTTTTCTTCACATGTTGTGATTGCAGCATGCACGGTCCCACCGGACAGTGCCCTCATCCTCGGGTTCTCCCAAATCTCGTAGCGGTTTGCCTGGCTGCCATCTACTCCTGCTAC[G/T]AAGAGTTCATCAACAGGTGCGTCCGATTCTCTGTTTACCCCATGTGTTTACCCCAGAGACTTGAGCTCAAAACATTTCCCTGAATCATGTTTGCCAATTCAACTGCATCATATCTACCTAAAATACTCGCACTTTAATTTCCATTAGCTTGTATTTGTCTGGATGTTTGGCGACAAACAATAGTGACGTGGTTGAAATGACATTATTCGGTCTCACTTGTCCTGTTTGTGTGATCATTTTGGGCCTCTGGGCCGCGGTTCACCCACCTGAGAGGAATAAGGCACTATTTTCAAACGATTCCATGATTCATGATGACTCAAGAGAATGAGACGTGTCTAAAATCACTCCCCAGGCTTCCTTGCACCACTTTTTTTATTGCTCTCATTCACTCTCTAATGGCTTAAATTTCCATAACTACAGTTTAGGCATGTTTTAAAGGCGCACATTTACAGGTGTGGCCATTTCGTGTGTCATTTGTCATCTCTTCTGAATCAGATGAC
Associated Phenotype:
Not determined