ZMP
fam125bb
Ensembl ID:
ZFIN ID:
Description:
family with sequence similarity 125, member B [Source:RefSeq peptide;Acc:NP_001129949]
Human Orthologue:
FAM125B
Human Description:
family with sequence similarity 125, member B [Source:HGNC Symbol;Acc:23368]
Mouse Orthologue:
Fam125b
Mouse Description:
family with sequence similarity 125, member B Gene [Source:MGI Symbol;Acc:MGI:1919793]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa45330 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa11811 | Nonsense | Available for shipment | Available now |
| sa21338 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45330
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 |
|---|---|---|---|---|---|
| ENSDART00000109600 | Essential Splice Site | 105 | 273 | 3 | 9 |
| ENSDART00000138921 | Essential Splice Site | 124 | 292 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 34377010)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 33519736 |
| GRCz11 | 8 | 33528968 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACTGTTTGCCAGAGGGCTTCACTCCCATCCAAGACACCATGGATACCC[G/A]TAAGCATGGTTTCCTTCAGAAAATTCTGTTTTCTTTTTCATCCACTTTCT
Long Flanking Sequence:
CCTACTGGCCCATATCTATCAGCTGATAACCACTGATAATGCTCATTAAATCGAGTGATAACATTCAAAGCGGGTGCCATAGTAAAAATCTGTCCTTAAACTAAATTTAAAAAAAAAAATTGCCATATAAAACTACAAATAATAACACTTTTGTGAGTGAAAATGTATGCTAGATAAAAAACAAATATCTATAATTAAATCAGGACAGACACTGAAAAAGAAATGAAAACTAAATCAGTATTACAGTTGAATTGTTTTGATGCTTAAAATCCACTTTTGGTCTCAGACCCAGGTGTGATTCATGCATAATTGAAACACGCCTGGTTTCAAACAGTCTTTGAAAAGTGCTTTCATTGGCATAATGCTGGTATAATCATGATTATATCCCTACATTTTGTGGCAGAAGCAATTATGCAACGTGGTGGTGGATATGAAGCTGATGGACCTGAAGGACTGTTTGCCAGAGGGCTTCACTCCCATCCAAGACACCATGGATACCC[G/A]TAAGCATGGTTTCCTTCAGAAAATTCTGTTTTCTTTTTCATCCACTTTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTTCTCTGTAGTCATCCTGAGGGAGCGCTTCTCCAGAGCTTGTGAATGTGAATGTTTCATGGGCTCAGGTTTAGCTTAATTTATGATAGCGCGAGCGAGTAAAATAAACATTTTGCCCCGGAGGAAGGAGGAGAGGAGAACGATGAGTCATTGTTTATCTCTGCCAGAACCCAGCTTTTTCTTTATGATGTGCTTATTTATTTATGTATTTATTTGTGCAGAGCGGGAGTGGATGGTGGTTATCTAATATTAATGAAATGCATTCCCTTGATGCTTTAGTGCTTTTTGAGTGCTACGTATTTCTCCCCTTCTCGTCTTCTCTCTTCTCCTCTCACCGCAATATTCTTTTGGCATCGGGAGTGAGGGCAGCATGTTTATTATTTTCATTATTATTGCATTTACACAGCCCTCGCCCCTGACGCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11811
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109600 | Nonsense | 157 | 273 | 5 | 9 |
| ENSDART00000138921 | Nonsense | 176 | 292 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 34369263)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 33511989 |
| GRCz11 | 8 | 33521221 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACATATACATATTTATTTTCCACAGAGAGCTGAATGGTTTGGGGATTTG[G/A]TACCAGCTGGGAAAAGTCCCTAAGTCGCAKGACACAACACAGAAAACATT
Long Flanking Sequence:
CACATTGGTTCAATGGTTCATTTTGTCTTCCTATTCTGTTTACCATGCTACTCTAAATATTTGCTCTGAAATAGCATGTAAGTGTGCCTTAGTAATAAATGTAATTCCTGCACGCCGCCGGGCGGCCAAACATTAACTAACTGGCGAATGACATGAACTAGTGGGTTGTCTGCTGTTGTGCGGGATGCACGCGTTCGCAATTTCAGGAGGCGTGGCTTTGAATCACAGTCCCTCCCCGCCGTACAAAGATAATATGCTAAGCGGCTAGCATTTTGGCAGATCACCTACTGCACCTTTAACTAGGCAGGATAGGGTTATCAGGCAAAAATATTATCAGACATACTGTGAAAATTTCCTTGCTCTGCTAAACATCATTTGGAAAAAAATTTTAAAAGAAAAAATTAAAGGGGGGTGAATAATTCTGACTTCAAATTTATACAGTAGTATTATAACATATACATATTTATTTTCCACAGAGAGCTGAATGGTTTGGGGATTTG[G/A]TACCAGCTGGGAAAAGTCCCTAAGTCGCATGACACAACACAGAAAACATTGCCTACCTCTACAAGTATTTGTAGCATTGCCAGGTAAGTCACTTCACTAACAAAAAGACATAAGCTATATTGGCTATTTTAACAGGATGATCCTTAAACAGGAGGAATTGCTCATTTTCAAGGAGACTTCCTCAGCTGTGAGATACACTCAAGACAATTGCTTTTGCTGCTTATTGAAACTGCTTGCTTAATATGAGTTGAACCAACACAATTCTTAAGTTTTTTTTTGTGAACAACTTCATTCTTTTATGTTCTATCTACTTAAGATTGTTAACATGATTAATTTAACTTAATTAATATGTGTTGGGACAAAATGAAGAAATTGTGTGGAACCCAGCATTTTTACAGTGCACTCAACAATCAAAAAATTGGATGTCCAATTTCATGCTGAGCAGAATGTAGCATAAGAGAACTCAGTGTATTTCCATGGATAAGCTAGAGTTCGGCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21338
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109600 | Essential Splice Site | 215 | 273 | 6 | 9 |
| ENSDART00000138921 | Essential Splice Site | 234 | 292 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 34325744)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 33468470 |
| GRCz11 | 8 | 33477702 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTGTCAAGCCAGATTATGACGAAATCTACAACATCTACACCAAATCAG[G/A]TCAGTCCTTTTTTAAATATGACTAAACATTAGCTTATCAGCAATTGCAGC
Long Flanking Sequence:
CCTACAATCCCTAACATCATATTATATTAATATCACATTTATATTCCATCGCTTGAAAGAGTATTAAGAACTCCAGCTAATTCAGGTGTGATTTTGTACAGACCCAGTAAAGACAGATTTCAGACTGTTTGCTTCATTGTTCACAACTTAGCACTTTGAGTAGCAATGTGCAAAGTGTTCATGGTGGGGTTTTTTTAAGGCATGCAGGTTTGTGTTGTTATTGATTTGCATAATTCCTACGGTACATAATTATGCAGAAATTGTGTACAGAAAGAACATTGGAATTTTAGAAAGCAAAACGCTCATGTTGAATTGTTGCATGTTAATATTGTAATTAAATAAAAGTATTATTCTAATTATTTCTTATGCGTTTGCACAATACCAATGAGTTCTGCCTGTCTTCCCTAGACAAGCCCCAAAGTCTCCGGTCTCTAGTCCTACTAAAAAGAACATTGTCAAGCCAGATTATGACGAAATCTACAACATCTACACCAAATCAG[G/A]TCAGTCCTTTTTTAAATATGACTAAACATTAGCTTATCAGCAATTGCAGCAAAACTATGGTGTTGTACTTACAGCATGTTTGTCATTGAGGCATTCAAGTGAATAATTAAAAACGCTGATTCATCCAGTAATGAAGCAAGTGAAATGTCTTTTAATGAGTGAGTCATTGAATAATTCATTTAAAAAAGATTCATTCAAAACACTGACTCATTCAGTGCAGTAAGTGAATGATTAATTCAAAAACTTTGTTCAAAAACACAAATAATTCCAGTTATCAAAAGTCTTTACAAGTGAACACACATGCACACACGCATACAAGTATACGTTTAAAACATTGCAGCAATAAACATTTTGTGAGAACTTTTAGTAAGCTGCATAGCGTTCAGTTATTTTTTCAGAGTCATGGGAGAATCATGATCTCTAGTTATCTGAATAAGTGCATCTGTAAGTATCATTGCACTGACATCCATAGTGGATGTCTTTATTATCATCCTAATTAA
Associated Phenotype:
Not determined