ZMP
fam169b
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1LWJ5]
Human Orthologue:
FAM169B
Human Description:
family with sequence similarity 169, member B [Source:HGNC Symbol;Acc:26835]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23290 | Nonsense | Available for shipment | Available now |
sa43095 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11717 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23290
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 |
---|---|---|---|---|---|
ENSDART00000100776 | Nonsense | 148 | 344 | 5 | 9 |
ENSDART00000141739 | Nonsense | 89 | 220 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 20842385)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21072608 |
GRCz11 | 18 | 21061674 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTATTCCTGCTCAGCCAAGTTATATTTGGGATTCTGGAAAGGCCTCTT[G/T]AAGATGACCTATATTTTTCTGCCTATTCTTTGAGGGAACATGGCAAAATC
Long Flanking Sequence:
TAATTTAAATTCCTCATTAAAGAGTAATATTTGTGTTTACAGGTGAAAGTAAGCAGTGAGAACATTGGTCAGCTCTTGTTTCTGAATGATGGTGATTTATCACATTTTATTCTTGCTCTTCACACACCCGAGGATGAATCTCAAGGTCTGACTCCACACAATATAACACTATCCTTCCTATGCCACTTTTGAGTCATACGGTCTATTTAGATAATAATATAAACCCTGTTATTTTAGTGGTTGCCATGTTCCTGCAAGGCAAATGGTGGCCTGTTGGTGATGTTTTAAAGACGTCAAACAAATCCAGATGTGGACTTTTGTTAGTGAGTAACACAGTCTGACAGACTACATTTTAGTCTGCAATGTTTTGAGCAGAAATAAAATCATCATTTCCACGATAGCCATGACAGATATTGTCATCCCAGGTGGAGTCTCTGATGGAGAGAGTCGTGCTATTCCTGCTCAGCCAAGTTATATTTGGGATTCTGGAAAGGCCTCTT[G/T]AAGATGACCTATATTTTTCTGCCTATTCTTTGAGGGAACATGGCAAAATCCTGTGGCAAGATGGTGAAGCTGTTGGGTTTTATACTGTCAAGAAAAAGGGTAATGTGTTTGGAAATAAGGTTGTAGTATTTTTAGAAATTTATGGTGGATTTAAAAAATTGTTTTCATTATTTTTCTGTTTTTTATAGGCAGTCTGTGTAATGGCAGCACTGGCCAGAGTTATCGGCTCCCTGTGTTGGATACTGTGTTTGTTCGCCCTCGCTGGAGAAGGACTGGACTTGCTTTACAGATGCTGGAAGATTTCTGCTCATCTCAGCCTTTTGAGTGCATTCTGGGAATTAGCTTTCCTATGTCTCCTAGCATGTATGGAGGTAGGTGTACATTAGGATTAAAAATATGCTGATTTTGTGCTCAAGAACCTTTTTTTTTGTATCATCAGTGTTGAAAACAGTTGTTCAAGATGTTTTTGTGGAAAATATGATATGTTTTTTAGTATTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43095
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 |
---|---|---|---|---|---|
ENSDART00000100776 | Nonsense | 246 | 344 | 7 | 9 |
ENSDART00000141739 | Nonsense | 187 | 220 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 20843991)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21074214 |
GRCz11 | 18 | 21063280 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGGTTTACACGACTTGTTAAAATAATGGTTTACAGTGTGCAAGAAGTA[T/A]CTTGAGGTCCATGAAAAAGAAAGAGAGCGTCTCTATGAAGTGGAAGCCCC
Long Flanking Sequence:
ACGAGTAGCAGAGCGATATGGCTCTATATCGTCACTGGTGGGACAATGAGGCGCACGCCTCCCACCAGTGCCGATATACAGCCATATCGCACTGCTACTCATGTGATATTGCTCATATATTGCTATATCTCTTTAATGAATAGAAACAAACATTTATCTGACATGAAAATCTATTTTAACATTATAAATGTCTTAATTTTTGATCAATGTAATGCATAATTTCTGAATAAAAAATATAAATTTCTTTAGAAAACAGATTCAATATAATATGTCATAGTACAAGGTTTAGGAGTGATGACACCATTTAAGTATCAGAATAAATCCTTTAAATGATTATACCATATGTGTGCAGAAAACACAAACCACTCCTATTTCCCTCATTGGTTTACATTGACTGTTTATTAAACAACTCTTATCTGTTATTATAAGTGCAATGAAGGCCTGTGACCACAAGGTTTACACGACTTGTTAAAATAATGGTTTACAGTGTGCAAGAAGTA[T/A]CTTGAGGTCCATGAAAAAGAAAGAGAGCGTCTCTATGAAGTGGAAGCCCCTGGTGAATGGCCTCAGAGACGTAATGTGTGGTTGAATATCCAGCTTCGGGACCTCCCAAAACACTGTAAGATTAATATAGCAACATACTCATAGCACGTGAGCAAGGAGCTCTGATTAGAATAGCTTACTGCACTTGTGTTTTATTGCACCATATAGGACAGTTTATCTCTGAGGTGTTGTTTTTTATAGGTGGAAACTCAGAGCAAGGTCCACACTGCTCATCTAGTCACGAAAGAAGCCATGCTGATTTAAAAGAGGAGGTATGACATTTATTATCTTGCATTTATTTAAGCTTATCTAGAAACTGTTTACTGCCTATTACCGTAAGTTTGTCTTGGTATGTCATGCTTGTATCTGTAAAATTTTACATAATGAATTACAGTTGAAGTCAGAATTATTAGCCGCCCTGAATTATTCGCCCCCCTGTTTATTTTTTTCCAAATTTCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11717
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 |
---|---|---|---|---|---|
ENSDART00000100776 | Nonsense | 258 | 344 | 7 | 9 |
ENSDART00000141739 | Nonsense | 199 | 220 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 20844027)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21074250 |
GRCz11 | 18 | 21063316 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGCAAGAAGTATCTTGAGSTCCATGAAAAAGAAARAGAGCGTCTCTA[T/G]GAAGTGGAAGCCCCTGGTGAATGGCCTCAGAGAYGTAATGTGTGGTTGAA
Long Flanking Sequence:
GGTGGGACAATGAGGCGCACGCCTCCCACCAGTGCCGATATACAGCCATATCGCACTGCTACTCATGTGATATTGCTCATATATTGCTATATCTCTTTAATGAATAGAAACAAACATTTATCTGACATGAAAATCTATTTTAACATTATAAATGTCTTAATTTTTGATCAATGTAATGCATAATTTCTGAATAAAAAATATAAATTTCTTTAGAAAACAGATTCAATATAATATGTCATAGTACAAGGTTTAGGAGTGATGACACCATTTAAGTATCAGAATAAATCCTTTAAATGATTATACCATATGTGTGCAGAAAACACAAACCACTCCTATTTCCCTCATTGGTTTACATTGACTGTTTATTAAACAACTCTTATCTGTTATTATAAGTGCAATGAAGGCCTGTGACCACAAGGTTTACACGACTTGTTAAAATAATGGTTTACAGTGTGCAAGAAGTATCTTGAGGTCCATGAAAAAGAAAGAGAGCGTCTCTA[T/G]GAAGTGGAAGCCCCTGGTGAATGGCCTCAGAGACGTAATGTGTGGTTGAATATCCAGCTTCGGGACCTCCCAAAACACTGTAAGATTAATATAGCAACATACTCATAGCACGTGAGCAAGGAGCTCTGATTAGAATAGCTTACTGCACTTGTGTTTTATTGCACCATATAGGACAGTTTATCTCTGAGGTGTTGTTTTTTATAGGTGGAAACTCAGAGCAAGGTCCACACTGCTCATCTAGTCACGAAAGAAGCCATGCTGATTTAAAAGAGGAGGTATGACATTTATTATCTTGCATTTATTTAAGCTTATCTAGAAACTGTTTACTGCCTATTACCGTAAGTTTGTCTTGGTATGTCATGCTTGTATCTGTAAAATTTTACATAATGAATTACAGTTGAAGTCAGAATTATTAGCCGCCCTGAATTATTCGCCCCCCTGTTTATTTTTTTCCAAATTTCTGTTTAATGGAGAAAAGATTGTTTCAACACATTTATATA
Associated Phenotype:
Not determined