ZMP
fam184a
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5SPS1]
Human Orthologue:
FAM184A
Human Description:
family with sequence similarity 184, member A [Source:HGNC Symbol;Acc:20991]
Mouse Orthologue:
Fam184a
Mouse Description:
family with sequence similarity 184, member A Gene [Source:MGI Symbol;Acc:MGI:1923156]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17922 | Nonsense | Available for shipment | Available now |
sa43511 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13959 | Nonsense | Available for shipment | Available now |
sa12300 | Essential Splice Site | Available for shipment | Available now |
sa32314 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17922
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005258 | Nonsense | 22 | 1051 | 1 | 18 |
ENSDART00000135715 | None | None | 1085 | None | 18 |
ENSDART00000138686 | None | None | 1036 | None | 17 |
Genomic Location (Zv9):
Chromosome 20 (position 41581531)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 41652690 |
GRCz11 | 20 | 41549800 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCTGGCAGCACTATTACAACCCCGCTGGCAGCGCWTCGACGGGGAAATA[T/G]AACAGCACCTCCACTTCAACATCCACCAGCACGTCCTTCCCRTCCGGTTT
Long Flanking Sequence:
GCAACACCGCTCGACACACACACACACAGACAGACACACACACGGGATCCGACAGATATGCCTCGGTCCTGGATCACACCTGCACCGGCTCTCGCTTCCCAAATACGAGCGGCGTCTGGACGCGCGCCGTCGGCCATTTAAACGCGACGCACCTGCCGGGGATCCAAAAAACATTTGATGTATTCCTCAAATAAATCAACTGTCAGTTCAGAAGAAGCGACGAAATGTGTGGTTAAACTGCCTCTCATCTCTTCCCACCTTCTTTCTCACAGACACATTTTTAATCCGGATGAAATAATGACTATTGTGGATTAACGTCTATTTTTTATTCTTCCTCTTCTTCTTCGCTTTATCGGGATCGGAGGATCATCTGCCTTTTACCCATTTGCCGTTACAGTCTTTATATTACAGGCATAGTAATATAATATCGTGAAGATGGCGACTGGAGCGGGCTGGCAGCACTATTACAACCCCGCTGGCAGCGCATCGACGGGGAAATA[T/G]AACAGCACCTCCACTTCAACATCCACCAGCACGTCCTTCCCGTCCGGTTTAACCCTCGAGTACACGCAGGACCTGCATCTGAAGATGAGCAAGAAGATCGCGCAGCTGACCAAGGTAATTTTGAGCGCCTTTTGGGGATGCGTAATGCCATGTGTGCTGGCTGAGCGATGCGCATTGGAGGTGCCGGAGACCCCGGTCAAAATGACAACAGGCTGGCCTTCAGTTCAGATTAACTCCAGAATGCGTAGATGAGGTCAAAATAGGCTGATTTGGGCGAATGTTTTATTAAAATAAACATTTGAATTACTTGTTTTCCTCAAAAACGTTGGAGAATTTCAATTATTGCGTTGTCAATTGAGAATTTATCATTACATTTTAACGATATTTTATGAAAAATAATCATATTAAATTTGTATTTAATGTTTGTGATTAAAATATACTGCTAAGACATAAAAATAAATCAAAATTGTCCGATTTGGTTAAGTATTTTACTAAAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43511
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005258 | Essential Splice Site | 345 | 1051 | 3 | 18 |
ENSDART00000135715 | Essential Splice Site | 285 | 1085 | 2 | 18 |
ENSDART00000138686 | Essential Splice Site | 285 | 1036 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 20 (position 41675529)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 41746688 |
GRCz11 | 20 | 41643798 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCCACAAACTACAGGCCTCCCTCATGACTGCTGAGAACAACATAAAGG[T/A]AAGGAAACAACACTTTCATTTGTTCTAGAATTAAACTATAGAGGTTACAC
Long Flanking Sequence:
ACATTTTTTACAGTGCATATTAAATATAATTTTCATATCCACCATGAACGCCCTTCCCTAAATGTTGCTTTTACAGGTTCAGGAACTGCTTCGTTCACACCAAAGCCAGAATGCAAACTACAGCAAAGACCAGGAGAAACTGGGCCAGCTTCACAAAGCCGAGGTGGATTCGCTGAACGAGCGGGTGGAGGAATTGAAACAGGACAAGAAGCGTCTGGTGGAGGAGTACGAGGCCAAGCTAAATAAAGCCCAGGCTTTCTACGAGCGCGAGCTGGAGGCCATGAAGCGCACGCAGCAGATGACGGCCGAGAACCTGCTGGCCTGGAAGAAGACCGAGGCTGAGCTTCGCAAAGAGTTCCAGGCGCAGGAGGCGGCGTTGCAGAAAACTCTGGGGAAGCTGCGCAGCGAACTACAGCGCGTGCAGGACGAGGCCAGAGAGAGCAGGGAGAAATCCCACAAACTACAGGCCTCCCTCATGACTGCTGAGAACAACATAAAGG[T/A]AAGGAAACAACACTTTCATTTGTTCTAGAATTAAACTATAGAGGTTACACATTGTGTGTGCACTTTATTAGGGACTTCTATGATCTTTATTTTCTATTTGTCATGCTTTTTTAGTGTTAATGTTTTTATATATATAGTTTTTTACTGTTTTGTTCTAGGGTCCGTTCTTCTTACGTGGATTACTCAGTTAGCTGGATTTGGTTATTGACGATTTGATTTGACCATAATCCAGGATCGTTTCGTTCTTCAAAACTGATCTGAGAGTTGTTGTCATAGCAACTGTTCTGCTAGCTCAAACCTGGTCGGAAGCAGGTTTAATTCATATAAACAAGATTAGATCGGCTCAGTTCAAGCAAAGATAATACAGAAAGTATGTACCGGATTCTGATATTTTCTTACAGTAGTAGTTATATACACTTGGGAAAATACTACATTTTTTAAAACTATATATTATAGTTATAGTTGTAGTTATTAATAAAATAAATAAAGTTATATATTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13959
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 |
---|---|---|---|---|---|
ENSDART00000005258 | Nonsense | 744 | 1051 | 11 | 18 |
ENSDART00000135715 | Nonsense | 684 | 1085 | 10 | 18 |
ENSDART00000138686 | Nonsense | 684 | 1036 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 20 (position 41736649)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 41807808 |
GRCz11 | 20 | 41704918 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGAGCGGGAACACCTGGGCCAGCAGCTGGAGGAGATGGAGATGGAGCAC[C/T]AGCACAGACAGCAGCGGCTRCAGGAGGCTCACTGCTGYGCCATACAGGAC
Long Flanking Sequence:
ATCTGCTGACTAACTCTCTTCGTTCTTAAGCTGAGCAATATTATATGAACATTTATTTATTTTTTTATTAATTTATTTATCTTTATTATTATTATTATTATTATTATACATTTTTGACGTTAATTATGTTTATTTAGCTTTTTCAATGGGAAGTTATAGGCTGTTGAGGGAGGAAAGTGTGTATTTGGGGTAGTGTCAACAACAACATGGAAGGATAATTATAAAAAGAATGTTGTAATTGGTGTTTCGTGTAAAAAACCTAATAAAATAATTTTGACATAAAACAAAAACCACCAACATCCCATTCATTAAGATGTTTACGATAGTATTCCTTTTTTATCTTCATTATTCATTATCTGTGTGTGCAGATCTCGCTGCTGAAGCAGAGTCTGGAGATGCAGCTCTCGCAGTCGCAGCACTCTCTGCAGCAGCTGCAGGCTCAGTTCAGTCAGGAGCGGGAACACCTGGGCCAGCAGCTGGAGGAGATGGAGATGGAGCAC[C/T]AGCACAGACAGCAGCGGCTGCAGGAGGCTCACTGCTGTGCCATACAGGACATGCAGGAGGCCCGTAAGCATGACCTCAAGGTAACACTTTATCTATTCAGTCATTTCTCGTGGTTTATTTTTGTCTTATGTACAGCACTTTTGGTCTTGTGACTGTTTTTAGATGTGCTTCATAAATAAATGGACTTGAACACTTATGTTAACACATATTAAATGAACACTTGCAGAAATGTCCAGACAGTCTGTGAACCAATGGCTTAGAATAGTGCATAGGTATGCAATTTGGAATGCGTCTCATTTTTTCATACTGACACCTGTCATTGTTAGACGGTTAACAACAGTAGCTAAGGGCGAGTGGTGCATACCAGTTCAGTAGGTCAGCAAATCTTCATCAAATACACTTGTATTATACACAAAGACATCTCTTTTTGGAAAGGACACAACTCCTCAACGTTTCTGTTTTTGACTGTAATGTAATAGCGTGCATCTTTCGTAAAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12300
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005258 | Essential Splice Site | 822 | 1051 | 13 | 18 |
ENSDART00000135715 | Essential Splice Site | 762 | 1085 | 12 | 18 |
ENSDART00000138686 | Essential Splice Site | 762 | 1036 | 12 | 17 |
Genomic Location (Zv9):
Chromosome 20 (position 41766012)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 41837171 |
GRCz11 | 20 | 41734281 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAATAGTCTTGTTTGTCATTTTTCTCTGTCTCTCTCTTTTTCTMGTCTTC[A/C]GCGTCGCTTCGTTCTGAGCTCWACCATCTCCACGCATCAGCCATTGAACA
Long Flanking Sequence:
ATTCGGATGTTATCTTAGAGCATGCTCAAATTTCACAAAAAAGCCATATATTGTGGGAAAGTGAAAGTAAAGTTGAATGTCTACTTAAAATTTGTCGTTTTGTGAAGTGATTTTTGGCTACAGTAACATGTAGAAATCAAAATGAATTACTGAGCAACATCAATAAGTACATTTGCATTAGCTTTTCTTACCAAGCAATGCTGGTACAAGATGTTCAATGTAAAACCTGATACAAAACCAGTTCTGCAGCTCTAATTATAGCTTAATGTCATTGGGAAAAAACCCATAATTGTCAAAAACTGGAAAGCAGCATGATGAGGGAGAGCTGGCAGGAAATTGCAGGTGGAGGAACGAGTGTCATTTCCATTTCCACCTGTGACGTTTATGCTTTAGGGAGAGTTGGAGATGAATGGTTTTTAATTCAGCTCCAGACAGCGGTTCGTCTCTCTGGAATAGTCTTGTTTGTCATTTTTCTCTGTCTCTCTCTTTTTCTCGTCTTC[A/C]GCGTCGCTTCGTTCTGAGCTCAACCATCTCCACGCATCAGCCATTGAACACATGCGTCAGACCCATCAACAGGAAACAGCAGCTGCCAAACAGGAACTGGAAAACGCTTTGGAGCAGAGCAGAGTACAGGTAAACTTCCTCCACCGCAACATCGTTATATAGTTTATGCAGATTTTTTTTATATATTGTGGTGACATCAGTTTAAGATTTTCTTGCCCATGCATGTCACAAATGACAAAAATCTGCTGTAATTTGGCAGCTCTATTTAACAGAAACTGCACATTATCTTTCAAAAGTTTGGGGTCGGGAGGAGTTTTCAATAGTTTTTGAAAGAAGACTCAGTAATTCTACATTTATTCATTCATCTTTTCAATTCATCTTTAATTCTGTTGTGCTTTTTACACTGTTAACAATTTCCAGTAGAATCTACTGTTACTTACTGGCCGCAGTTTGCCAGCAACTTACTGTAAATCAATTACAGCAAAAATACTGTATTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32314
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 |
---|---|---|---|---|---|
ENSDART00000005258 | Essential Splice Site | 975 | 1051 | 15 | 18 |
ENSDART00000135715 | Essential Splice Site | 915 | 1085 | 14 | 18 |
ENSDART00000138686 | None | None | 1036 | None | 17 |
Genomic Location (Zv9):
Chromosome 20 (position 41796888)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 41868047 |
GRCz11 | 20 | 41765157 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAAGCCCAGGAGCTGCTGAAGGACAAGATCTCCGCTCTTCAGATCCTG[T/C]GAGTACATGCAAAACAGTTTGTATAAGATATACAGCATGTGCATTTTGAA
Long Flanking Sequence:
ATTCAACATAAAACAATAAGGATGTCCCAAGAACAACTTAAGAATTGTGTTGTTTTAACAAGTAGCAAAAGTCTTTTTTTTTAAGTGCAGTATGAAACATAATAGATCATAATGTTTCATAATGTCTCTTTTAAACAAATGTTTTCTGTTTTCTTTACACTCTGTCTTAAAGATTTCCTATTTCTCTCTGGAGAAAATACCTGGCTATCTTTCTTCCAGAACGTTCCTGTTGTGTTGTATTGTGTGTTTGTGTAGGATGTGTCCTTCAAGCCTGCAGTTGCAGCACTGTAAGTTCAGCCTGCATTTAACAGGTTCATGGAGAGATTTTTTTTTTATATTTGTATGTTTTCAGAGCTCACGAACAGGACCTGTGTAAGAAACACGAGCGAGAGATGGCAGAGCTCAATGCTCTTCACCACAGAGAAACACAAAACATGCTGTCCGACTTTAACAAAGCCCAGGAGCTGCTGAAGGACAAGATCTCCGCTCTTCAGATCCTG[T/C]GAGTACATGCAAAACAGTTTGTATAAGATATACAGCATGTGCATTTTGAAGGAGGAAAGGGCTGGAACTTGTGTTTTGCTGTTTGTTTATATCCAATTGGCTATTGAGGTTATGAAAAAGCCTGAATGCTAACTCTGAAACATTCAGGCAGCTGTCTTGTTAGTGACTTTGAAGGCAGTGTTTGTGCATGAAGGCATCTTGCAAAATGGATTTCTGAGACAGCCTAATGATTTAATCATGTACAGCTAAATATAGAAAGAGCTTTGGTAATTACCAGGGCCAGACAGAATTTATAAAAAAAATTTCTGCTCAGAAGTTTGTAAAAAATCTGTGGATTTATGCAGAATGATTTTGAGAGTAAAGAAACTGATAATGTTAATAACACATGAAATAACACATTAAATAATAAAATAAAAAACTGTTTAAATTGCGTTTAAGGTTTACAATGCAAATCCAATTAGAACCACTTGTTTAGTAAACAAAGCTACAGTACAGTATAT
Associated Phenotype:
Not determined