ZMP
arl13b
Ensembl ID:
ZFIN ID:
Description:
ADP-ribosylation factor-like protein 13B [Source:UniProtKB/Swiss-Prot;Acc:Q8JHI3]
Human Orthologue:
ARL13B
Human Description:
ADP-ribosylation factor-like 13B [Source:HGNC Symbol;Acc:25419]
Mouse Orthologue:
Arl13b
Mouse Description:
ADP-ribosylation factor-like 13B Gene [Source:MGI Symbol;Acc:MGI:1915396]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25614 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17422 | Nonsense | Available for shipment | Available now |
sa25615 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25614
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 |
---|---|---|---|---|---|
ENSDART00000102184 | Essential Splice Site | 162 | 407 | 4 | 10 |
ENSDART00000122316 | Essential Splice Site | 162 | 261 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 33315606)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 32950357 |
GRCz11 | 1 | 33682925 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGTCATTGGAGAAGCTAGTCAACGAAAATAAATGCCTTTGCCAGATTG[T/A]AAGTTAATATTTCATCACAATTTATTATAACCGGAGTCTGGTTTGATAAT
Long Flanking Sequence:
AAAAAATGTTGTTTAGAGATAAGACCTTGAGTTTACTGATGAGCCTAGAGGGTTTGATGAATGCCGAGCTGTAATCAGTGAAGAGCATCCTCATATCAACAGGCCCTGCCTGCAATCCAAGTGGAATGGGGCGGTGTGCAGTAAATGTGCAATACATCATCTGTATATCTGTTGGGTTGTTAGACAAGCTACAGTGGGTCCAATTAACTGAGGTAGTGAGGAGCAGATGAAGTCCTTGACTAAATAAAGCTTAAGTGTGCTAATAAGTCAAGAGCGCTCTGTGACACAAGGCTAATTATTCTGTCCACCTCAAGTTTAGATCTCAGGTCATTTGTTTGTGACAGCTTACCAAATGACCTTCACATGCTTTTTTTTCTTCTGATTGGCTTACAGACTGGCTAATAAACAGGACCAAGATGGGGCAATGGCTGAAGCAGATATCATTGAGACCCTGTCATTGGAGAAGCTAGTCAACGAAAATAAATGCCTTTGCCAGATTG[T/A]AAGTTAATATTTCATCACAATTTATTATAACCGGAGTCTGGTTTGATAATTAAATCTTGATTCTTAGTAAGGTGAAAAATTAATTAGAAAAAATTGATCTATGTTCACACACTTTTTTTTTAATCACTAAATTAATTGACGGAAATGTATTTAAATGTTGTTTCATTTACTTTCAGGAGCCCTGTTCAGCTGTCTTGGGTTATGGTAAGAAGGTTGACAAATCCATCAAAAATGGCCTTAACTGGCTCCTAAATAACATTGCCAAGGACTATGAGGCAATTTCAGAACGTGTGCAAAAAGATACAGCCGAACAGAAGGCTCAGGAAGAACAAGACAAGAAAGAAAGAGCAGAGAGAGTTCGGCGGATCAGAGAAGAGAGGTCAGTGAGCTTACAAAACTTCAGATTGTTGCTGCTTAACGCCTGGTTTATACTCTACGCGCCAGCTAGTTCGCTTGAGTGCGTGCAGCGAATGTGACGTCATCACAGAGTTTGAGGAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17422
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102184 | None | None | 407 | None | 10 |
ENSDART00000122316 | Nonsense | 249 | 261 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 33316043)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 32950794 |
GRCz11 | 1 | 33683362 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTTACWAAACTKCAGATTGTTGCTGCTTAAMGCCTGGTTTATRCTCTA[C/A]GYGCCAGCTWGTTYGCTTGAGTGCGTGCAGCGAATGTGACGTCATCRCAG
Long Flanking Sequence:
ATATCATTGAGACCCTGTCATTGGAGAAGCTAGTCAACGAAAATAAATGCCTTTGCCAGATTGTAAGTTAATATTTCATCACAATTTATTATAACCGGAGTCTGGTTTGATAATTAAATCTTGATTCTTAGTAAGGTGAAAAATTAATTAGAAAAAATTGATCTATGTTCACACACTTTTTTTTTAATCACTAAATTAATTGACGGAAATGTATTTAAATGTTGTTTCATTTACTTTCAGGAGCCCTGTTCAGCTGTCTTGGGTTATGGTAAGAAGGTTGACAAATCCATCAAAAATGGCCTTAACTGGCTCCTAAATAACATTGCCAAGGACTATGAGGCAATTTCAGAACGTGTGCAAAAAGATACAGCCGAACAGAAGGCTCAGGAAGAACAAGACAAGAAAGAAAGAGCAGAGAGAGTTCGGCGGATCAGAGAAGAGAGGTCAGTGAGCTTACAAAACTTCAGATTGTTGCTGCTTAACGCCTGGTTTATACTCTA[C/A]GCGCCAGCTAGTTCGCTTGAGTGCGTGCAGCGAATGTGACGTCATCACAGAGTTTGAGGAGGTTCACTTTGGGTGCGTGCGATATGATTTCGGCCAGCGAATCGCATGATTTTTTTGAGACTCGAGCACAGTTTGAGCGGCACCGCAACTGATTTGAATTGAGTATGAAACACTTTAAAGAGATTTTGTCTGAAACAGTATGCCTGTACAGACATCTTTATGATCCGTGATCATAGAGATAACCAGATGACCAATAATTATTGGCTAGAAATTGCAACAGTCGCGGTAAAGGAGAAAGTTTTTGTTTAAAGGTTTTGTAAAAACCCGAGGGATAAGTTTGGTAAAGCAAAAAAAAGGCCTTAGCTAAAGTGGAGACGCAGGTACACAATTACAGAATATGTTTTTCCACCCTTCATAGGTTTAACACTGGTGTATATGTTTAATTTTGAATTTAAAACAATTTATTAGTTACAAATATAAAATTAAGGAGCAAATTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25615
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102184 | Nonsense | 270 | 407 | 7 | 10 |
ENSDART00000122316 | None | None | 261 | None | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 33319787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 32954538 |
GRCz11 | 1 | 33687106 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCGAACTCATTAGAATGCAAATACTCACTTTATATAAAAATTCCAGAAC[C/T]AAGACAGACTAAACAGAGAAAAAGAGATGCAAAGACAGAGGGAAAATGGC
Long Flanking Sequence:
TACACTACCTTTCAAATGTTTGGGGTCAGTATGATTTTTAAATGTTCAAGTACAAAATTGTAAAATTGTGAAATGTTATTGCACTATAAAATAACTGTTCAAAAGTAGTTTATCATTTAATTTAATAATTTATTCCAGTGACTTTAATGATGAATGTTCCGCTTCATAACTCCAGTTTTCAGAGTCGCATGATCCTTTAGAAATCACTCTAATATTATTAATAATAATAATAATAATAATAATAATAATAATAATAATTATTATTATTATTAACGTAATAGTAATCAAAGCAATAGTGACTAGAGTTATCATTTCATTTGAAACTTCATACAATAAAGAAGCAGTTATTTAAAATTAATAAATATTTAACTTTTTTTTATTTAATAAATGTTGCCTTGATGAGCAGTATAATTTTCTTTAAAAAAAAAAAAAACTGACCCTAAACTTTTGGGCGAACTCATTAGAATGCAAATACTCACTTTATATAAAAATTCCAGAAC[C/T]AAGACAGACTAAACAGAGAAAAAGAGATGCAAAGACAGAGGGAAAATGGCCAGCAGGGCAGTGTGCAAGAACAGATAGCACTTCAAGATGAGGAGGAAGAAGAGGAAGATGAAGAGAGTGAGAGACAGACTCCAGAAAGCACAGAATCAGGTAGGACCTCTAAAATCTCAAAAGGCCTCCATCATATTGAAAGAAATATATATGTATAAAAAAATCTTAGAATTGTTCGTTAAATTTAAGCTTTTTCTATTATATTATATAAAGAACCTATTTGCTGCTGTAGTTTCTGCATGAAAGGAAGTGAGTGTTTTTCATCTTCGATCAGGAGCAGTGGACCAGACCAAAAAGAAAACTAGGAAACTACGGTTGAAACGCAAACACAGAGTCGACCCTCTTAGGATGGAAGAAGCAGCACCCAAAAGCCCCACGCCTCCTCCTCTGCCAGGTATGAATGGCTCTTTTACAAGGTGTCAATGGGGTCTTACAAGTATTAAAAAGTC
Associated Phenotype:
Not determined