ZMP
fam184b
Ensembl ID:
ZFIN ID:
Human Orthologue:
FAM184B
Human Description:
family with sequence similarity 184, member B [Source:HGNC Symbol;Acc:29235]
Mouse Orthologue:
Fam184b
Mouse Description:
family with sequence similarity 184, member B Gene [Source:MGI Symbol;Acc:MGI:2442958]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32672 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa24844 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa16579 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32672
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077394 | Essential Splice Site | 114 | 1165 | 3 | 19 |
| ENSDART00000145942 | Essential Splice Site | 54 | 1105 | 2 | 18 |
Genomic Location (Zv9):
Chromosome 1 (position 22310332)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 22845499 |
| GRCz11 | 1 | 23536238 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAAGATGAATAGATTCACTTTCTTTAACCTGGCAAATGTATCCATCTT[A/C]GGTGGAGGAGCGTGGACAGAGGGCTGAAATAGAGTATGCAGAGCGCATAG
Long Flanking Sequence:
TGCACCAATACACACATCAAGACTGGTGACAGAGTGGTTTGATCAACATGAAAGTGAATTCTCCCATGTCCTGCACAGGTCTAAACATTATTGAGTGTACTGAATGATTGAGTCAGGAAACATTTTCCTCCACCTGGCCACTTTTCTGCAAAAAGAATGACTCAAAATCCCTCTCGCCACTGTGCAGGACTGGATCTGCCTAGACAAATTGAATTTTACTAATGAATTATTGTGGTCCAAAACCAGGCAATTTTCTTTAATAGTCCTCTTTGTGTGTGTTTTGTTGTGAATGTCAGTGTTTTGTTTTGTTTTTTAACAGAAGAAAGAAACTCATAAACATTTAGAAACACATCAGTGAGTAGATTTAGGTTTTTGAGTGAACTTTCCTTTTAAATGCAGTGTGAAAAGCCCTACACTTTATCTTGTTTGTATGGATTTAAGTAAGTTATATACAAGATGAATAGATTCACTTTCTTTAACCTGGCAAATGTATCCATCTT[A/C]GGTGGAGGAGCGTGGACAGAGGGCTGAAATAGAGTATGCAGAGCGCATAGCTGTGTTGACCCAAGAGACATCAGATCTGCGCAGAGACTACCAGAATCTGCAAACAGATAGAGACAACCAACACAAATTACTGCAACAAACACAGGATGAAAAAAAGCACTTGGAAAACGAGTGCCAAGAGCTACGGAGAGCCAGAGATGAAGAGAGAAAGCGAGAAGAGGAGGAAAAGATGCAAAGAGTGGAGGAGGAGAGGAAGAAAGAGATGGAGGAGAAGAACAGAGAAACGGAGGAAAGGAATAGAGTGTCACAGGAAAGAAAAAGAGTAGAAGAAGAATATGAGGTAAAGTTGAAAACGGCGAGAAAGGAGGTACAGGTTCTGAGGGAGGAGAAGGAGAGCATGGAGAAACAACTTAAGAGCGACATGGAGGAGTGGAAGAAGAGAGTGAAGGAGATGGAAGACGAGAGGAAGGACGAGCAAGAAGCGGCAAAGAAGGCACTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24844
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077394 | Nonsense | 548 | 1165 | 7 | 19 |
| ENSDART00000145942 | Nonsense | 488 | 1105 | 6 | 18 |
Genomic Location (Zv9):
Chromosome 1 (position 22300740)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 22835907 |
| GRCz11 | 1 | 23526646 |
KASP Assay ID:
554-7814.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCACTGAAGAAGACAGAAAGCTTTTAGAGACAGAGAGGGAAGAGCTGTG[C/A]AACCAGCTACAACTGTCCAAAACAGAGGTAAGTTATCACAATGTATGCCA
Long Flanking Sequence:
TGAACTGAAAAAGGTAGACACTTTAAACAAGATTTAATTTATTAAGATTAATCGGTGCAAATGTAGTGGTTAGTGCGTCGATACATGCAGTCTGGTGGCGACCAGAGTTTGATTCAGCCTCGCGGTCCTATGCCGATCCTTCCGATATATATCTATAGCTCATTGTTAATTTATAATTGATATATGATAATACCAGAAGAATCTTACTGTAAAGTGTTACAGAATTGTATACATAAATGCAACATCAGTTTTGGATGAAAGCAATTAATGATAAGAATGTAAAGATAGGCTATATGCCCCTTAAAACAGGATAGAATAAAATAAAATAATAACATGCTAAATCATTATTTAAAATATTTGATGTTATCATCTACTAATTTTGTTATTATGGAGATAAAAAGCACTTGTATTTCGATGTTGGTTTGAATACAGGCTGAGGAGCAGATGAAAAGCACTGAAGAAGACAGAAAGCTTTTAGAGACAGAGAGGGAAGAGCTGTG[C/A]AACCAGCTACAACTGTCCAAAACAGAGGTAAGTTATCACAATGTATGCCACACACAAACAGACATCTTCCTTTGCTTTTTCTCTCAAAAACCACAACAGTCTTGGAGATATTGCAAAACATTGTTGACCTACTACTGAATCGGGTCACCATTAAGAAGATCTATATACATATCAAGCTCAGGCTAAGAGAACAGACTCAGTCCTTCTGCTTAAATACACAGAGACAGACTGAGAGGCCCAGAGCTCTCCACATGACCATGATAAATGAGAAAACAAAAGGAACATTTGTAGTGCCCAAGGCACAGGGCTTCATGTAATGCATCATCTAATCTGCCAGCAGGCTTGGAACTAGGTTATGATTACAGAGCACTACTTAATAAGTGATAGATAAGAAAAAGAGTGTTTTTTTCAGTGCTCAGTTGCAGCAGTGAAGAAAATCATTACAGTTCCTTCTCTATATAAGAAAACTGTGTGCTACAGCCTAATTTGCTTACTTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16579
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077394 | Nonsense | 793 | 1165 | 12 | 19 |
| ENSDART00000145942 | Nonsense | 733 | 1105 | 11 | 18 |
Genomic Location (Zv9):
Chromosome 1 (position 22295819)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 22830986 |
| GRCz11 | 1 | 23521725 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAGCGGGGGTGGCGTGAGCGAGAGGAGGAGCTGTTGCGTGTGGAGAGGT[T/A]AAATCACCAGCGAGCTCTTCAGRTCCTGRAAACACAAGCCAATGAAGAAC
Long Flanking Sequence:
AGAAGGCTTATAAAGCACTAAATTAAATGAAACATGAGCATGTATTTCAGTTCCCAACACTTCACAACAAACCCTTTGAATTAAATATTGTCACAGAATAACATAAAGAAAAAAGTATGAACGTATAAAACAAAGATACATTTTTTCTGACATTTTTTATAAACAAAATCATTTGTAAATGTCAGACCTAAACAAATGTATTTTAAAAGCTAGTGGGAAATGTGCTTTACAAATACCCATCCAAATGTGTGTGTTCTTTACAGGTGTTTGAACCCCATTGGTTTTTATTGTTTGGATAAAAGAAGTTGAACTGATGACAGAAGACATTTCTGTGGAAAGACCTCTTTATATCAGCAATTTGTGTTGTCTCTCTGTATTGCAGGTAGTAAAAGAGGAAGATGAGGACGAGGAGGATGGAAAGAGTACAAGAGAGAGGGAAGAGGAGAGGGACAAGCGGGGGTGGCGTGAGCGAGAGGAGGAGCTGTTGCGTGTGGAGAGGT[T/A]AAATCACCAGCGAGCTCTTCAGGTCCTGGAAACACAAGCCAATGAAGAACTTCAGGCAGAAAGACAACGCTTGCTCACACAGCACAAACTCCAGCTGGGTAATCGTCACTGCTCATACAGAATGCTTTTTTTAATCTCAGCAAGATATCTAGTCCTCTAAAAAAAAACTAAAAACTAGTCGCTTTATATCAAGGAAAGAAAATATGCTGATTGGCCTATGGAAGTAGTTTTCCATATGAGGGCCGAAACACACTAGGGGGCTTCGTCACACTATTCAACGGGCTGCAAGTTAGCTAAAATAAGTTTTAAACAGGAAAAAGTCAAGATAAATTGGGTTCTATAATCTATAATGGGTTCATACGGTCATGGAAAATTCATGGAATTTTTACATGACATTTTCCAAGCCTGAAAACGTTTGGGTAAATCAGAAAAGTTATGGAGAACCAATATCTATATACTTAAATATGGGTTAGTTGTCTTTATTTATTTTCTGTCCTTGG
Associated Phenotype:
Not determined