ZMP
heatr3
Ensembl ID:
ZFIN ID:
Description:
HEAT repeat-containing protein 3 [Source:RefSeq peptide;Acc:NP_957183]
Human Orthologue:
HEATR3
Human Description:
HEAT repeat containing 3 [Source:HGNC Symbol;Acc:26087]
Mouse Orthologue:
Heatr3
Mouse Description:
HEAT repeat containing 3 Gene [Source:MGI Symbol;Acc:MGI:2444491]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34126 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1194 | Nonsense | Available for shipment | Available now |
sa14921 | Nonsense | Available for shipment | Available now |
sa34125 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34126
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052368 | Nonsense | 71 | 682 | 2 | 15 |
The following transcripts of ENSDARG00000036076 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 39309682)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 37646322 |
GRCz11 | 7 | 37917580 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAGTATGCCTGTGCCAGTATCTCTCGGATTGTCCAGGAGAATCAAACCT[T/G]ACCAGGATTCCTCCAAAGAGATGCAGTGAGGAAAATTGGACCTTTATTGC
Long Flanking Sequence:
AGAGTTGTTGTTTTTTTCTATTTCTGTACCTGTTTTCACCATTTCATATGATGTTGTGATAGTATCATGCACCATGATTAAATCTTCAGTGAAAATGTGATGCCCTCACATGCGCAAGTGTGTCTGCTCTTTGAATGATGGGATGAATGGATAGTAGCAAGTTGAATAGAGGAAACGAGTCAGCAAGCTTCCAGTTCACAGCTTAACTGACTAGTGTATCTGTTAAGCAAGCTGTAGACGACTCTTCAGCTTTGAAACAGCCAGTTTTTCCTCAGCCCCTATTGAGGTATTCCGATATATCTTAATTTAAATGTGACTCTCATAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTATTTATTTGTTTGTTTGTTTGTTTGTTTCTAGTTGCAGAGTCCCTCAGCAGATGTGCGCGAGTATGCCTGTGCCAGTATCTCTCGGATTGTCCAGGAGAATCAAACCT[T/G]ACCAGGATTCCTCCAAAGAGATGCAGTGAGGAAAATTGGACCTTTATTGCTTGATCACAGCCTGACGGTCAGAGAAACTGCTACAGGAGCGCTCAGGTACATGCACAAATGACACTGACTCTAGATCTGAACTGTGAATTGAAGGTGACATATGTAGATGTAAATGTCTGAGTATTCTCTCTCAAAGATTTTAAAGTTTCTTAACTGTTTTAAAGGTTTTTGTAATTAAAAAAAAAAAACAGAAATGATTAGAATGACAATGTACATGCATTTGATATACAGTAAGGCCAAGTTCAGACTGCAACATTTTCAAAGTAGTCATGTCACAGGTGTTTTCACAATACATGACTATCTGCACTAGTGTTGAGTCACTGCTGTGTTAACACTGCAAGATGGATTGGCGACAGGGGGTTTCACACCGCATGACTTTATGATAGGAAGAATCGCAGACAACTTTGTCTCTGTCCAAAAACTACATCTTACAACCAAACACACGCGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1194
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 |
---|---|---|---|---|---|
ENSDART00000052368 | Nonsense | 187 | 682 | 5 | 15 |
The following transcripts of ENSDARG00000036076 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 39304725)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 37641365 |
GRCz11 | 7 | 37912623 |
KASP Assay ID:
554-1103.1 (used for ordering genotyping assays)
KASP Sequence:
GCACAGCAGTGTCCGTGTTTAACAAGGCTGGACTTGTGGATGTTCTTCTA[C/T]AATGTCTACAAAAGCACCCTCAGAATATGGAGCTGGCAATATCAGCAGGT
Long Flanking Sequence:
TGTGTCTGTGTTGTGTGTTTTTGTGGAGAACAGTGCTGTGCAGGCTTTGGCGTGAACTCTCCTTCTAAGAAAGGACAGAAAACCTCAGTGGAAGATGTCGCCAATGAAGCAGTCAATTTACTTTGGAACCTCTGGTAAGAATGAACTTAAACTGAAAGCAAGGACCAAGTCACAAATAGGTGGTCAACACTGATTGATGTTTACACCTCACATGTATATTAACAAAATTAGTTAATATTAGCTTTAACATTTTTTTTTTCATGTATGTGTATTTTGTCACCACCTGTGATATGACAGCATATCATCATGCTTTATTTATTGGCTGTATTTTGCAAGGTGAAAATGACACTTATAGTTAGTTTGATCAATTGCCACATTTAAAAAGTACCAATTCATGTTATCTGTGTTTCTGTCTTTTTTTGTTTGTTTGGTTGTGTAGTGAGAGCAGCAGCACAGCAGTGTCCGTGTTTAACAAGGCTGGACTTGTGGATGTTCTTCTA[C/T]AATGTCTACAAAAGCACCCTCAGAATATGGAGCTGGCAATATCAGCAGGTGACACACACTATTATGGTCATCTATTCAAACTTTAAAGGTCCAGGAGCACAACTTTTTAACATTGTTTTTAGCTCTGATAAATTAGAATTCAAAAGCACCAAATCAGCAACAAGATCATGTGATTGTGAAAACTGCAATAATGACTGCTGAAATAATTCTGTTTCGCCATCTCAGAAATAAAAATATGTATAAATAACATGTATACATTTTAAGATATATTCAGTTATGTTTGCAGATGTCTGAGTGGAGTATGAAAATGTTTTGTTTGGATTTTTTGTCTGAGCACTTTGACTGATGTTTGTTTTAATCAAGATTGCTTCTTTGAACAAAACTTGCTGTTTTTTATATGCTCACTATGAATTTATGTAGACATAACATATTGATATTACCTGTGCCCTTCAAACTAATAACTACATTGTCTTTACTTGCTATGTAAAATGTCATTTAAA
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:
sa14921
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 |
---|---|---|---|---|---|
ENSDART00000052368 | Nonsense | 356 | 682 | 8 | 15 |
The following transcripts of ENSDARG00000036076 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 39297838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 37634478 |
GRCz11 | 7 | 37905736 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCCTCARCAAATACTTTTNGTTTGTGTGCCTGTGGGTTTCTAGCGAGAC[C/T]RACTGGAGTTGCGAGAGGCYAAAGCACTGCTGTCAGCACAGCAAACGTCT
Long Flanking Sequence:
GTGCGTGATGTGCTCAAATATGGATACTGGTCCTTAAAGGTGGAACTCACAATAGTGGGACTGCATATACAGTAGCATCTCTTTCATGAGTCAGTACTGGGCCGTGACCTATTCACATTGCTGAATCACTCATTTAAAAGGAGAGTTAACCCAAAAAAAAAATTAATAATAATTGTCTTCATTTAGTTATCCTCCATTTGTTCCAAACCTGTTTGAACTTCTGTCTTCGGTTGAACACAAAGAAGGACATACTGAAGGATGCTGGAAAAGCAGCCTATTGTTCCTATTATGAAAGTCTATGGCTTGATTTTTTTTTTTCAGCAGAAGAAAGAAATTTACTGGAAATTTGTCTGGAACCAGTATATGTTGAGGACATCTATATATTTGCATAAACTATCCCTTTAAATGTTTAAAAAATTCAACCATCACTATATGTGTTTATTACTGGTGACCCTCAACAAATACTTTTTGTTTGTGTGCCTGTGGGTTTCTAGCGAGAC[C/T]GACTGGAGTTGCGAGAGGCTAAAGCACTGCTGTCAGCACAGCAAACGTCTCTGGAGATCATCGTCAACATGTGCTGCTCTGATGGTGAGTGTGTGTGTGTGTGTTCATATGTGAGCTGGTGCTTGAGGCAAGACATGAATATTGTAGCCAGTAAATGTGCTAAAATTGGAGGAATGATTTCATTGTATGTGTCGGCAAAGATGAGGCAGAGGATAATGTGACAGGATATTGGCTCTTTCTCTCTTTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTGTCTATGTGTCTGTATTTTTGTGTGTACAGAGCCCTCTGATGATGAATGGGAGGAGATGTCCAGCAGCGATGAGAGCGAAATGTGTGCTGATGGGATGTCAGACACTAATTCCAGCTTGTTCTCTCCTCTCTGTCTGTCTGCTGAACTTCACACAGTCCTGCTCAACCACAGCATGCCTCAACAGGTACATTGTTAATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34125
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052368 | Nonsense | 449 | 682 | 10 | 15 |
The following transcripts of ENSDARG00000036076 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 39296791)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 37633431 |
GRCz11 | 7 | 37904689 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTATTTCAGGTGTTGAAGAAGGCTGAGTTCCCTAGTGCTGCTGCACTT[G/T]AGCTCTGTAGCAAAGATTCTTCTTGGAAATGCCTCTTGAAAAAGTAATGT
Long Flanking Sequence:
CAAAACAAAATTGATAATAAATTATCTCATTATTTTTACAATGTAACCAGAGGGTACAGTAAGAGTTATTTCCATATTCTGTATTTGGGAACAGAGTTATTTAAACCTTTATTTATTTTTATCCAGTGAATAAAAAATAATGAGAACCCGTACAAAACATTGAAGTGTTGCTAAAACATTGTTTCACCTACAAATTCACATTGAGAGAATGCATCAACCTTTTGTGTTCTCTTCAAATTATGTGTTCACTTTCCTTCACTTGTCCCTTAACTTTGCCTTTATAAACCTGCAGAAACCCTGTAAGTCGACCTTGGGTGGGGAATCCGTAATTTTATTCTACAACCCCTTGAAATACACAAAGAGTTGTCAAAAACACAAAAAGCCGCCTGTATAATACATTTAAGTTGCTGTTCTTGTGTCAAAGATAAGTGCATTTACTTCACTAAATGATTTTATTTCAGGTGTTGAAGAAGGCTGAGTTCCCTAGTGCTGCTGCACTT[G/T]AGCTCTGTAGCAAAGATTCTTCTTGGAAATGCCTCTTGAAAAAGTAATGTACACTTATTTTTTAAAATAGTTTGTAGACTTTAGACACACCTTCTCATTCAAAGAGTTTTCTTTATTTCTTGACTATGAAAATTGTAGATTCACACTGAAGGCATCAAAGTTATGAATTAACACATGTGAAATTATATACATAACAAAAAAGTGTGAAACAACTGAAAGTATGTCATATTCTAGGTTCTTCAAAGTAGCCACCTTTTGCTTTGATTACTGCTTTGCACACTCTTGGCATTTTCTTCACCTGAAATGGTCTTCCAATAGTCTTGAAGGAGTTCCCAGAGATTCTTAGCACTTGTTGGCCGTTTTGCCTTCACTCTGCAGTCCAACTCACCCCAAACCATCTTGATTGGGTTCAGGTCATCTGGCGCAGCATCCCATCACTCTCCTTGGTCAAATTGCCCTTACACAGCCTGGAGGTGTGGTTGGATTCATGTTCCTGTTGA
Associated Phenotype:
Not determined