ZMP
fhl2b
Ensembl ID:
ZFIN ID:
Description:
four and a half LIM domains 2b [Source:RefSeq peptide;Acc:NP_001006028]
Human Orthologue:
FHL2
Human Description:
four and a half LIM domains 2 [Source:HGNC Symbol;Acc:3703]
Mouse Orthologue:
Fhl2
Mouse Description:
four and a half LIM domains 2 Gene [Source:MGI Symbol;Acc:MGI:1338762]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20673 | Essential Splice Site | Available for shipment | Available now |
sa20672 | Nonsense | Available for shipment | Available now |
sa141 | Nonsense | Available for shipment | Available now |
sa26710 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20673
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003898 | Essential Splice Site | None | 279 | 1 | 7 |
ENSDART00000124132 | Essential Splice Site | None | 279 | 1 | 6 |
The following transcripts of ENSDARG00000003991 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 15001238)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 14974470 |
GRCz11 | 6 | 15101410 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGCATAGCACATCACATCACACCACTCCTCTCCTCTCCACGGGACAGG[C/A]AAGTTAAGCATCGCAACAATTATAACCTCTTCTCTTCTCTTCTCTTCTCT
Long Flanking Sequence:
TAGATAAGTTGGCAATTCATTCTGCTGTGGCGACCTCAGATGAATAAAGGGACTAAGCCAAAAGGAAAATTAATGAATGAGTGTAGCTTGTGACATCAACTTCATTATGAATAGGTGAGCACCTTATATGCACTAATTTGCACTGTGGTCAGAACTAGATGAATGTCAGCTCATACAACATGTATACTGTATAATACTGTATACATCTAAATGTTCTTTCAATTACGCACTATGGATTCGGTGGAAACAAACACTTCTTGCAAAGTTATATAAGAGCATGTATGGTCAAGTACTGGGTGCACAGTTGATTTCATGACTTAGTGGTGTCTGTGTATTTATAGTTCCTGATAAAGTGTCCAACCCATTTCAATCACCCCATTGCCCAACACAGGGGGAGTAATCCAATAAAGAGGAGCACAAGAGTCGCTCCTCCATCTCTCAAGAACTAAAGACGCATAGCACATCACATCACACCACTCCTCTCCTCTCCACGGGACAGG[C/A]AAGTTAAGCATCGCAACAATTATAACCTCTTCTCTTCTCTTCTCTTCTCTTCTCTTCTCTTCTCTTCTCTTCTCAATGGTTCTCTATCATGTTCTTTTCTGTACATTGTATTTAAGTGCATAGGAAGCCATTTCACATAGTCTCTGTTCTGTCAGTTTTATATCCTGTGTATTCCAAAAAAAATTGTTTCAGGTTTTTATTTAAAAAGAATATTCTATATATAAATGTACAGATGGTTTACTTTTATACAATATATATTAATTTCAATGACTCAACCATATTTGATCAATTAAAATGAATGTAAGAATGAACAATTGCTTCAGAGTAAGGAGCTGAAAATAGCCTGTATTTAAAAAATATCAACATGATCACTGTTGCTTAAATGCAATTGTGGACATCCCAGGGTTTTGTAAAACACATTTAGTACAAGTACATTTTCGTTTTGAGATTACATTTGTAAGAAACGTCCTTTTTTGGCTTCTTTACAACCACCTGTCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20672
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003898 | Nonsense | 70 | 279 | 3 | 7 |
ENSDART00000124132 | Nonsense | 70 | 279 | 3 | 6 |
The following transcripts of ENSDARG00000003991 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 14984259)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 14957491 |
GRCz11 | 6 | 15084431 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTGTCTTATAAAGACCGGCACTGGCACGACGACTGCTTCCACTGCTTC[A/T]AATGTCACCGTTCTCTTGTGGACAAGCCATTTTCTACCAAGGACGAGCAG
Long Flanking Sequence:
TGGTCTGGAGGACAGGCCTGAGGTGTTGCCACATCTGTGTGCCACGTCCTTGGCCCAGTTCCCCGTCGCTCCCCCATAGCAGCCCATCAGCATGACCTCATATCACCCTGGGCCAGCAATTTAACGAGCACACACACACACACACTCTCTCCCTCTCAAACATTGGTGGATAATTAAACCACCGGTGTCATACACTCCTCCTGAGGCTCAGTACCGACTCTCACTAACACACTCCAATTGGCAGATCACACTGGGCTCCAGCACCTGCGGCTCTCATTGGCGAGTGACCCGCTGTGAAGCTGACATTGAGGAACCCTTTACCCTCTCGCTTTCCCTAATTAGATGTTCAAAAGCTGAAAAAGGCCACTGAGGCAAAGCACATTCGGTTTAATGCAGGTGTGACAGAATGTAGGTTCAAAGTCTTTACCTTTATGCGTTTCTCTACTCAGGATCTGTCTTATAAAGACCGGCACTGGCACGACGACTGCTTCCACTGCTTC[A/T]AATGTCACCGTTCTCTTGTGGACAAGCCATTTTCTACCAAGGACGAGCAGCTACTGTGTACCGAGTGCTACTCCAATGAGTATTCCTCTAAATGTTTCGAATGCAAGAAGACAATCATGCCAGGTGAGTGAACACATTTGCTTGGCCTGATTCTCACACATTATCTTATTTCGACCTTGTCACAGTCACCAAGTTAAGCGCCCACCAGACACTCTAGAGGGAACTCTACACTTCCGCTACTGAACCGGACTACATACTCCATCATGCACTTCAAACACACCAGTTCCAGTTTACCACTGATTACAATCACATAGCTGAATTTCATGAGGACTGACATTCAGGACTGTGGGGTATATGCCGAAGCATGCTAATAGGACTTTTAATTTGCCAGTAACCTGGGTTAAGTGCTTCCGGCGAATTGAATGCCAATGCAAAATCCGGTGCATTTAAGGTCTGTTTTCTTTAAAAATCAGCGATCTCCACTAGCTGAGTGATGTCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa141
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 |
---|---|---|---|---|---|
ENSDART00000003898 | Nonsense | 97 | 279 | 3 | 7 |
ENSDART00000124132 | Nonsense | 97 | 279 | 3 | 6 |
The following transcripts of ENSDARG00000003991 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 14984176)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 14957408 |
GRCz11 | 6 | 15084348 |
KASP Assay ID:
554-1340.1 (used for ordering genotyping assays)
KASP Sequence:
TCTACCAAGGACGAGCAGCTACTGTGTACCGAGTGCTACTCCAATGAGTA[T/G]TCCTCTAAATGTTTCGAATGCAAGAAGACAATCATGCCAGGTGAGTGAAC
Long Flanking Sequence:
CCATCAGCATGACCTCATATCACCCTGGGCCAGCAATTTAACGAGCACACACACACACACACTCTCTCCCTCTCAAACATTGGTGGATAATTAAACCACCGGTGTCATACACTCCTCCTGAGGCTCAGTACCGACTCTCACTAACACACTCCAATTGGCAGATCACACTGGGCTCCAGCACCTGCGGCTCTCATTGGCGAGTGACCCGCTGTGAAGCTGACATTGAGGAACCCTTTACCCTCTCGCTTTCCCTAATTAGATGTTCAAAAGCTGAAAAAGGCCACTGAGGCAAAGCACATTCGGTTTAATGCAGGTGTGACAGAATGTAGGTTCAAAGTCTTTACCTTTATGCGTTTCTCTACTCAGGATCTGTCTTATAAAGACCGGCACTGGCACGACGACTGCTTCCACTGCTTCAAATGTCACCGTTCTCTTGTGGACAAGCCATTTTCTACCAAGGACGAGCAGCTACTGTGTACCGAGTGCTACTCCAATGAGTA[T/G]TCCTCTAAATGTTTCGAATGCAAGAAGACAATCATGCCAGGTGAGTGAACACATTTGCTTGGCCTGATTCTCACACATTATCTTATTTCGACCTTGTCACAGTCACCAAGTTAAGCGCCCACCAGACACTCTAGAGGGAACTCTACACTTCCGCTACTGAACCGGACTACATACTCCATCATGCACTTCAAACACACCAGTTCCAGTTTACCACTGATTACAATCACATAGCTGAATTTCATGAGGACTGACATTCAGGACTGTGGGGTATATGCCGAAGCATGCTAATAGGACTTTTAATTTGCCAGTAACCTGGGTTAAGTGCTTCCGGCGAATTGAATGCCAATGCAAAATCCGGTGCATTTAAGGTCTGTTTTCTTTAAAAATCAGCGATCTCCACTAGCTGAGTGATGTCCGATTTAAAGTGGATCTCAGACTGTATAGGAAGCACTGCATTAAATTACATTTCCCCCGCCATATCTTTATAATATGAGCATTTA
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:
sa26710
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003898 | Nonsense | 181 | 279 | 5 | 7 |
ENSDART00000124132 | Nonsense | 181 | 279 | 5 | 6 |
The following transcripts of ENSDARG00000003991 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 14980134)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 14953366 |
GRCz11 | 6 | 15080306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACTCTCAGCCAATCACCACCGGGGGCGTGACCTATCACGACCAGCCCT[G/A]GCATAAAGACTGCTTCCTGTGTACTGGCTGTAAGCAGCAGCTGTCTGGCC
Long Flanking Sequence:
CGAGAAGCAGTTTGCTCTGCAGTGTGTGCAATGCAAGAAGGTAACAGCTGGAACACAACTTGACACGTTAAATATGTAAAAAGTAATAAATGACATCAAACCTCAATCAAATATTGTGTAGTTCTGAGTGTGCTTCATGTAGGTGAGTGGGCTTGACAAACCACCTGTCGGATGTGCTTTCTCTCTATGCACTAGGCACTTTATTAAAAACACTTCTATGTTCTCTACGTTTGTTTGTAAAGCTAAGTTTTTTTTATATTTATTTTGTTATATAGCTATAACTTATAATTATATATTCCAGAATTTTGTTTGTATTTATACTCCATAATTTATAAACTTAATGATAATATATTTATGATAATAATATAACCTTTTTTGAAGGTCACTGGTGGTTGTATAAGCATTTTACTGCATATAATGTGTATTGTGACAAATAAAATTTAAATTTGTTCACTCTCAGCCAATCACCACCGGGGGCGTGACCTATCACGACCAGCCCT[G/A]GCATAAAGACTGCTTCCTGTGTACTGGCTGTAAGCAGCAGCTGTCTGGCCAGCGCTTCACCTCTCGTGATGACTTTCCCTATTGCCTCAACTGCTTCTGCAATCTGTATGCCAAGAAGTGTGCTGCCTGCACCACCCCGATCAGCGGTATGAACAACCAAAACTTTTACATCTCCTTATTTTTGTGCGTCCTTATTGTTGAAAGTGCTTATAAGCACCAAATGCAAGCCTATGAAGAATAAGCACAATTTACTTTTTTTGAAACAGAAGTTCTCTTCTGTATTGTTAAAGGGATAGTTGACCTCAAATTACTAACCCTTAAGTGATTTTAAACCTTTATTAATTTTTTTTAACACAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTGTAGAATGTTGGAAATCATGAGGCATTGACATC
Associated Phenotype:
Not determined