ZMP
acvr1b
Ensembl ID:
ZFIN ID:
Description:
activin receptor type-1B [Source:RefSeq peptide;Acc:NP_571065]
Human Orthologue:
ACVR1B
Human Description:
activin A receptor, type IB [Source:HGNC Symbol;Acc:172]
Mouse Orthologue:
Acvr1b
Mouse Description:
activin A receptor, type 1B Gene [Source:MGI Symbol;Acc:MGI:1338944]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
hu3520 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa12061 | Nonsense | Available for shipment | Available now |
sa12247 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
hu3520
Status:
Confirmed mutation in F2 line
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 |
---|---|---|---|---|---|
ENSDART00000023094 | Nonsense | 179 | 505 | 3 | 9 |
The following transcripts of ENSDARG00000018968 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 28048191)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 27881013 |
GRCz11 | 23 | 27807554 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGAGGATCCATCCTGTGATCACCTGTACTTGGCCAAAGACAAGACCT[T/A]ACAGGATCTCATCTTCGATCTGTCCACCTCTGGTTCAGGGTCTGGTAAGT
Long Flanking Sequence:
TTGTTTAATCCCACTCCTTTTCGCTGCGCGATACGACAGAATTTTGCAAGCTCACTCGAGTGTGACCGCAGTATTAGTGTGTTAAAGCAGGGTTGGAACTAAACTGTGGAGGGCTGCGACCCTCCGGGAACTGGCTTTGACACCTGTGCTTTATAACTTGTATTTTGTATAAATTCAACAGAATTCTTTTTTTTCAATGTTGTTTTTAGTGTTAAAATATAGTAGTCTAGAGAAGTTGACCATTTGTCTCTTTTTAGCCATAACATGAAAATGATCTTCCTTTTACCTGCCTCTTTCAGGGATTGCTGATGGTAAAGGAGGTAGTTGGGGTCCGGTAGAGCTGGTGGCAGTGATAGCAGGCCCGGTCTTCCTCTTTTGCCTGCTGCTTATCGTGGGAGTGCTCCTTTTCCAGCACCACCAACGAAACTATAACCACCGGCAGCGACTGGATGTTGAGGATCCATCCTGTGATCACCTGTACTTGGCCAAAGACAAGACCT[T/A]ACAGGATCTCATCTTCGATCTGTCCACCTCTGGTTCAGGGTCTGGTAAGTTGCATGTTTATCCTTCTCCTGCATGTCTGAAAAGTGTTTTGCCTGTGTGCTGATTTCTCTCTCTCTCTCTGTCTCTCTGCAGGGCTGCCCTTGTTCGTTCAGAGGACTGTGGCCAGGACAATTGTACTGCAGGAGATCATAGGAAAAGGTCGCTTTGGGGAAGTGTGGAGGGGGAGATGGAGAGGAGGTGATGTGGCTGTGAAGATCTTTTCATCCAGGGAGGAACGTTCCTGGTTCCGTGAAGCTGAGATTTACCAAACCATCATGCTCCGCCATGAAAACATCTTGGGCTTCATTGCTGCTGATAATAAAGGTAAGACAAGTCATGTTACATGTCATTATGTTCACCCAATAAGTTGTTAAAATAAAATATGTAATTAATAATTTAAGGTCTGAATGAAATGTAAATTATGGTTATTTAAACATTCATTTTAATAACTTTGTAATTGT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa12061
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 |
---|---|---|---|---|---|
ENSDART00000023094 | Nonsense | 308 | 505 | 5 | 9 |
ENSDART00000023094 | Nonsense | 308 | 505 | 5 | 9 |
The following transcripts of ENSDARG00000018968 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 28046301)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 27879123 |
GRCz11 | 23 | 27805664 |
KASP Assay ID:
554-4621.1 (used for ordering genotyping assays)
KASP Sequence:
TGACTATCTCAACCACTACTCCGTCACAATCGAGGGGATGATCAAGTTAT[C/T]GCTTTCAGCCGCCAGCGGTCTGGCACATCTGCACATGGAGATCCTGGGCA
Long Flanking Sequence:
ATTTTATTCATAATGGTATTTTAAAAAGTCTTAAAGTCTTAAATTTGACTCGATGAAACCTGTAGAAACCCTGCTCTAGTCTGTCCTTGGCCAATCACATGCCCTCACATTAGTAGTGCTGTGTAAGCATTATTTAAATACATTTTACATAGATTTGGTGTTTTATGATATGGTGTAAAACATTTGAACGTGCATTGTTTTGTTTTTTTATCGTTTACCACGTATACGTAGATATTACAATAAAACATCAGGTCATGAAAATGTACTTAACTCATGGAATTTTAGTAGTAAAAAAATGTGTATGAACTGCTTTAAGTGATCAAACATTCAGAGTAATTTTGTTTCATTTTTTAATATCTTTTTGGTTTAAATATGTTTCTGTTTCTTAGACAATGGCACATGGACACAGCTGTGGCTAGTGTCAGACTACCATGAGCATGGCTCATTATTTGACTATCTCAACCACTACTCCGTCACAATCGAGGGGATGATCAAGTTAT[C/T]GCTTTCAGCCGCCAGCGGTCTGGCACATCTGCACATGGAGATCCTGGGCACACAGGGTGATTAACAAAATAATATTCTCCAGACTATAATAATTTACAATTTGTCAATTCCTGGACTCACTAAACCATTATGATCTCCTACAGGGAAACCAGGCATCGCACATCGTGACCTCAAATCCAAAAACATCTTGGTGAAAAAGAATGGTACTTGCGCCATAGCAGATCTAGGGCTCGCTGTACGGCACGAGTCTATCACTGATACTATAGACATTGCACCCAATCAGAGGGTGGGCACTAAAAGGTACATCTGGCCCTGTCATTATTAATACAAATGGCTGCTTGTCTTTAAATGTAACTATGAAAACTTTAATGTAAGTTGTTGCTTTTTCCCCTTTCTTAGATATATGGCCCCAGAGGTACTAGATGAAACGATCAACATGAAGCATTTTGATTCTTTCAAGTGTGCTGATATCTATGCTTTGGGACTGGTATATTGGGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12247
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 |
---|---|---|---|---|---|
ENSDART00000023094 | Nonsense | 415 | 505 | 7 | 9 |
The following transcripts of ENSDARG00000018968 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 28045795)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 27878617 |
GRCz11 | 23 | 27805158 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAAGTGTGCTGATAWCTATGCTTTGGGACTGGTATATTGGGAGATTRCA[C/T]GACGGTGTAATGCTGGAGGTGAGGAAAAATGAGACCCATCTTACACCCAC
Long Flanking Sequence:
CAGCCGCCAGCGGTCTGGCACATCTGCACATGGAGATCCTGGGCACACAGGGTGATTAACAAAATAATATTCTCCAGACTATAATAATTTACAATTTGTCAATTCCTGGACTCACTAAACCATTATGATCTCCTACAGGGAAACCAGGCATCGCACATCGTGACCTCAAATCCAAAAACATCTTGGTGAAAAAGAATGGTACTTGCGCCATAGCAGATCTAGGGCTCGCTGTACGGCACGAGTCTATCACTGATACTATAGACATTGCACCCAATCAGAGGGTGGGCACTAAAAGGTACATCTGGCCCTGTCATTATTAATACAAATGGCTGCTTGTCTTTAAATGTAACTATGAAAACTTTAATGTAAGTTGTTGCTTTTTCCCCTTTCTTAGATATATGGCCCCAGAGGTACTAGATGAAACGATCAACATGAAGCATTTTGATTCTTTCAAGTGTGCTGATATCTATGCTTTGGGACTGGTATATTGGGAGATTGCA[C/T]GACGGTGTAATGCTGGAGGTGAGGAAAAATGAGACCCATCTTACACCCACTGCATCTTAACAGATTAAGCCTGCAATTAATGTCAGTTTTTTCACAGGTTGCATAGAACTCCTATAATAGTGGTCTATCATTATGAGCTTCTCTTTAAGATTTTAAAATGAGTAGAGAGTACACTGCCTCTGTAAAATAAAAAAAATCTTTCTTTTGAATTTCTTTTTATTAAAGAACCTGTAAATTAAGTCCAAGGCATTTGAAAAATGTGGAAAAAATATTAAAAAGCCTTTATTGACATGGCTATTCCTTAAAACTGCCTACGCATCAACGTTACCCTGATGAAGGTAAGTGTTTGCCATGTCAATAAAGGCTTAATATTTTTTTTCACATTTTTCGAGTGTCTTGACCTGACTTTTGCTGTTTATTCTAATGAATCCCTTACCCAAAGTGCACTGATCTGTTGTTTAAGCTAGGACTGAGCACTTTGATTTTTAAATATGGAAAGT
Associated Phenotype:
Not determined