ZMP
xirp1
Ensembl ID:
ZFIN ID:
Description:
Xin actin-binding repeat-containing protein 1 [Source:UniProtKB/Swiss-Prot;Acc:Q5PZ43]
Human Orthologue:
XIRP1
Human Description:
xin actin-binding repeat containing 1 [Source:HGNC Symbol;Acc:14301]
Mouse Orthologue:
Xirp1
Mouse Description:
xin actin-binding repeat containing 1 Gene [Source:MGI Symbol;Acc:MGI:1333878]
Alleles
There are 14 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14052 | Nonsense | Available for shipment | Available now |
sa12194 | Nonsense | Available for shipment | Available now |
sa16645 | Nonsense | Available for shipment | Available now |
sa46 | Nonsense | Available for shipment | Available now |
sa32919 | Nonsense | Available for shipment | Available now |
sa32920 | Nonsense | Available for shipment | Available now |
sa32921 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14052
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 |
---|---|---|---|---|---|
ENSDART00000042413 | Nonsense | 61 | 2297 | 1 | 1 |
The following transcripts of ENSDARG00000030722 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 24107141)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24101354 |
GRCz11 | 2 | 23757005 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTCCCCGTACCACCTCCAAAAGAAACCTTCTCAGAGATCTACCAACAR[C/T]GAYAAAAAAGTGAACTGAAGCGCCTTTTTAAACACATCCACCCTGAACTG
Long Flanking Sequence:
AATGTAGCTACACATTACATATTCTTGTAGTTATAGAACAAATCAAATATTGTCCTGTTCTGTCAAGCTCCAAAAATATCTGCAAATGTGAAGCTTTTGTTGTGGTGAATGAATCTTTGAACTAATGAAGCTGAAAATCATCATAAATGAAGTCAAACCTGAATAGGTGTGCAGTGAACTAACTCAACTATCCCCAGCTAAACACGGAAAAAGGTAAAGTATTTCAGCTTAATCATACTAACATTTTAACAATGTTTCAATTTATTAAATCATTGCATTGTGGAGAGTAACGTGAGCCTTCATACTTCTTTGCCCCCAAGATGGCAGAAGTAGCCAAACAGAAAAAAGCTACAGAAGCAGTCTGTGGAGATGAGGATTTCCCTCCACCTCCACCTCCTCTTCCAAGACCTCAGGTTCTGGAGTCACTTCAAAAAGATCTAAGCCAGAACTTCCTCCCCGTACCACCTCCAAAAGAAACCTTCTCAGAGATCTACCAACAA[C/T]GACAAAAAAGTGAACTGAAGCGCCTTTTTAAACACATCCACCCTGAACTGAAGATGACTGTTGATGACGTTGTAGATGACGAACTAATTGATGCAATAAATCCTCAAGCAGCAGATGCAGCATATCAGGGAGAAGTCCAATCCATGCGGTGGATCTTTGAGAACTGGACTCTTGATAATATTGGAGACCCACATGAAACTAAAAAACTACTCTGTGAGGAAAATCCTCAAGGTGGGGATGTGAAGGGCAAATCCTCTTTGTTTGAGCATTCAACATTCGACAGTCAGCATGCAGCAGGTGCCGAGAGAGCAGGTGTAGTCAGAGGAGATGTTCGCACAGCCACCTGGTTGTTTGAAACACAGCCTCTAGATTCAATCAGCAAGTCAAAGATAGAGGATGAGGAAATTGTGGAGGTCGTCTTGAAGGAACCTGTTCAGAAGGGTGATGTGACCGGCGCACGTCGTCTGTTTGAAACCAAACCACTGGATTCTTTAGGTCGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12194
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 |
---|---|---|---|---|---|
ENSDART00000042413 | Nonsense | 62 | 2297 | 1 | 1 |
The following transcripts of ENSDARG00000030722 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 24107144)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24101351 |
GRCz11 | 2 | 23757002 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCCCGTACCACCTCCAAAAGAAACCTTCTCAGAGATCTACCAACARYGA[C/T]AAAAAAGTGAACTGAAGCGCCTTTTTAAACACATCCACCCTGAACTGAAG
Long Flanking Sequence:
GTAGCTACACATTACATATTCTTGTAGTTATAGAACAAATCAAATATTGTCCTGTTCTGTCAAGCTCCAAAAATATCTGCAAATGTGAAGCTTTTGTTGTGGTGAATGAATCTTTGAACTAATGAAGCTGAAAATCATCATAAATGAAGTCAAACCTGAATAGGTGTGCAGTGAACTAACTCAACTATCCCCAGCTAAACACGGAAAAAGGTAAAGTATTTCAGCTTAATCATACTAACATTTTAACAATGTTTCAATTTATTAAATCATTGCATTGTGGAGAGTAACGTGAGCCTTCATACTTCTTTGCCCCCAAGATGGCAGAAGTAGCCAAACAGAAAAAAGCTACAGAAGCAGTCTGTGGAGATGAGGATTTCCCTCCACCTCCACCTCCTCTTCCAAGACCTCAGGTTCTGGAGTCACTTCAAAAAGATCTAAGCCAGAACTTCCTCCCCGTACCACCTCCAAAAGAAACCTTCTCAGAGATCTACCAACAACGA[C/T]AAAAAAGTGAACTGAAGCGCCTTTTTAAACACATCCACCCTGAACTGAAGATGACTGTTGATGACGTTGTAGATGACGAACTAATTGATGCAATAAATCCTCAAGCAGCAGATGCAGCATATCAGGGAGAAGTCCAATCCATGCGGTGGATCTTTGAGAACTGGACTCTTGATAATATTGGAGACCCACATGAAACTAAAAAACTACTCTGTGAGGAAAATCCTCAAGGTGGGGATGTGAAGGGCAAATCCTCTTTGTTTGAGCATTCAACATTCGACAGTCAGCATGCAGCAGGTGCCGAGAGAGCAGGTGTAGTCAGAGGAGATGTTCGCACAGCCACCTGGTTGTTTGAAACACAGCCTCTAGATTCAATCAGCAAGTCAAAGATAGAGGATGAGGAAATTGTGGAGGTCGTCTTGAAGGAACCTGTTCAGAAGGGTGATGTGACCGGCGCACGTCGTCTGTTTGAAACCAAACCACTGGATTCTTTAGGTCGCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16645
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 |
---|---|---|---|---|---|
ENSDART00000042413 | Nonsense | 239 | 2297 | 1 | 1 |
The following transcripts of ENSDARG00000030722 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 24107676)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24100819 |
GRCz11 | 2 | 23756470 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATTCTTTAGGTCGCKGCTGCTCTRTCGAAGACCAACATTTCCTAACAT[T/A]AAAATCAGAACTCCAAGAGAACAAAGGAGATGTGAAGAAAACAGTCAAAC
Long Flanking Sequence:
CATCCACCCTGAACTGAAGATGACTGTTGATGACGTTGTAGATGACGAACTAATTGATGCAATAAATCCTCAAGCAGCAGATGCAGCATATCAGGGAGAAGTCCAATCCATGCGGTGGATCTTTGAGAACTGGACTCTTGATAATATTGGAGACCCACATGAAACTAAAAAACTACTCTGTGAGGAAAATCCTCAAGGTGGGGATGTGAAGGGCAAATCCTCTTTGTTTGAGCATTCAACATTCGACAGTCAGCATGCAGCAGGTGCCGAGAGAGCAGGTGTAGTCAGAGGAGATGTTCGCACAGCCACCTGGTTGTTTGAAACACAGCCTCTAGATTCAATCAGCAAGTCAAAGATAGAGGATGAGGAAATTGTGGAGGTCGTCTTGAAGGAACCTGTTCAGAAGGGTGATGTGACCGGCGCACGTCGTCTGTTTGAAACCAAACCACTGGATTCTTTAGGTCGCTGCTGCTCTGTCGAAGACCAACATTTCCTAACAT[T/A]AAAATCAGAACTCCAAGAGAACAAAGGAGATGTGAAGAAAACAGTCAAACTTTTTCAAGCAGATCCCTGTTGTGCGCTTAGGGATAGCAATGGTAAAATCCATGAAATCAAATCAATCTGCAGAGAAGAAATCATGAGCAGTGACTTTAAAACTGCACGTTGGCTTTTTGAAACTCAACCCTTAGATCACATTAATGAAGGAGCTCATGTTCAGATAATTCGAGGGATATCTCTTGAAGAAGCTCAGAGAGGCGGTGTTGATAAGAAAAAGTGGATGTTTGAGACGCAGCCGCTTGATGCAATTCACGAAGGTGTTGTGGAAGAGCAAAAGTTTCAAGGAACAGCAGTGGAGGGTTTCTCTGGAGCAGCAGATGTTCATAACAAACTACAGCTGTTTGAAAACCAGCCCCTGTCATCCCTTAAAGGAGATTCTGAGGGTGACGTTTTAGAGAAGGAGGCAATTGTTGGAGGAAATGTTGGATCCACCCTATGGCTTTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa46
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 |
---|---|---|---|---|---|
ENSDART00000042413 | Nonsense | 271 | 2297 | 1 | 1 |
The following transcripts of ENSDARG00000030722 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 24107771)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24100724 |
GRCz11 | 2 | 23756375 |
KASP Assay ID:
554-0064.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAACTTTTTCAAGCAGATCCCTGTTGTGCGCTTAGGGATAGCAATGGT[A/T]AAATCCATGAAATCAAATCAATCTGCAGAGAAGAAATCATGAGCAGTGAC
Long Flanking Sequence:
GAGAAGTCCAATCCATGCGGTGGATCTTTGAGAACTGGACTCTTGATAATATTGGAGACCCACATGAAACTAAAAAACTACTCTGTGAGGAAAATCCTCAAGGTGGGGATGTGAAGGGCAAATCCTCTTTGTTTGAGCATTCAACATTCGACAGTCAGCATGCAGCAGGTGCCGAGAGAGCAGGTGTAGTCAGAGGAGATGTTCGCACAGCCACCTGGTTGTTTGAAACACAGCCTCTAGATTCAATCAGCAAGTCAAAGATAGAGGATGAGGAAATTGTGGAGGTCGTCTTGAAGGAACCTGTTCAGAAGGGTGATGTGACCGGCGCACGTCGTCTGTTTGAAACCAAACCACTGGATTCTTTAGGTCGCTGCTGCTCTGTCGAAGACCAACATTTCCTAACATTAAAATCAGAACTCCAAGAGAACAAAGGAGATGTGAAGAAAACAGTCAAACTTTTTCAAGCAGATCCCTGTTGTGCGCTTAGGGATAGCAATGGT[A/T]AAATCCATGAAATCAAATCAATCTGCAGAGAAGAAATCATGAGCAGTGACTTTAAAACTGCACGTTGGCTTTTTGAAACTCAACCCTTAGATCACATTAATGAAGGAGCTCATGTTCAGATAATTCGAGGGATATCTCTTGAAGAAGCTCAGAGAGGCGGTGTTGATAAGAAAAAGTGGATGTTTGAGACGCAGCCGCTTGATGCAATTCACGAAGGTGTTGTGGAAGAGCAAAAGTTTCAAGGAACAGCAGTGGAGGGTTTCTCTGGAGCAGCAGATGTTCATAACAAACTACAGCTGTTTGAAAACCAGCCCCTGTCATCCCTTAAAGGAGATTCTGAGGGTGACGTTTTAGAGAAGGAGGCAATTGTTGGAGGAAATGTTGGATCCACCCTATGGCTTTTTGAGACTCAGCCCATGGACACTCTGAAAGATAGCTACGAGGTGGGACGTCTCCAGAAGGTTATGGTATCAAGTGATGAAAAAGGAGAAGTTCAAGAC
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:
sa32919
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 |
---|---|---|---|---|---|
ENSDART00000042413 | Nonsense | 991 | 2297 | 1 | 1 |
The following transcripts of ENSDARG00000030722 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 24109931)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24098564 |
GRCz11 | 2 | 23754215 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACTCTAAAAGGTGAACCAGATGAGCAGAACAACTTGACAGCTGTACAT[A/T]GAGAAGATAACACTAAGGGAGATGTGAAACGCTGCACTTGGTTGTTTGAA
Long Flanking Sequence:
CAATGCTTTTTGAATCCCAGCCATTGTATGCTATAAGAGACAAGGATGGGCAGTTTCATGAAGTTACCACTGTAATGAAGGAGGAAGTCATGAGAGGAGATGTCAGGGGTGCAAGATGGATGTTTGAAACCAAGCCACTGGATACTATTCAAGCAGACAAGGAAATCTACGTCATCCGTGCAGTTACGCAGGAGGACGTGCACAAAGGAGATGTGAAATCTGCGCGATGGAAGTTTGAGACTCAGCCTCTTGACTCATTTACACCTCACGAAGGGCCCTCTGTGCGTGTTGTTGAAGATATAGGCAATGAAAAGTGTGTGCAACAAAGCAGGCAGCTTTTTGAGACAGAGCAAGCATCCCAAAAGAAGTTTGTGCGAATGGTGAGCGTTACAGATGTTCAACAAGGTGATGTACGTACCTCAACCTGGCTTTTTGAGAATCAGCCTATTGATACTCTAAAAGGTGAACCAGATGAGCAGAACAACTTGACAGCTGTACAT[A/T]GAGAAGATAACACTAAGGGAGATGTGAAACGCTGCACTTGGTTGTTTGAATCACAGTCCTTAGATAAAATAAAGGACAATAAGCCAACTGAAGAGTTGGTTTCATCAAGGGAAGAAATTCCCAAAGCTGATGTCAAAAGTACAACCTGGTTATTTGAGACCACACCACTTGACAAAATCACTGTTGAAAGTGTGACAGACATACTATACAGACTTTGTCATAATTCCTTCATTCATTCCAGCGGAATCATCATCCAAGCAAATGATTACAAGTATGTAAACATGGCAAAATATCAGATTATGAAGGATGAGGGGCCCAAAGTCCTAAAGGAAGAAGTTGTTGAAGGAAACATCAGGAACCTAATGTTGCAGTTACTGTTCAAACCCAATATTAAACCTATGGTTGTCCTCCTTAAAGAAGACGAACAAGGCAAGATGCACAGTACAGTACTTGAAATCCCATTTCAACAGCCAGGATCTGCAACCAACCCTGAGGCGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32920
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 |
---|---|---|---|---|---|
ENSDART00000042413 | Nonsense | 1865 | 2297 | 1 | 1 |
The following transcripts of ENSDARG00000030722 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 24112553)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24095942 |
GRCz11 | 2 | 23751593 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACAACTACAGACACAGGCTCACCTTTCCCGAAGAAAATTAAAGTTGTG[C/T]AAAAAGAAAACATTCAGGAACAGGCTAAAACCTCCAATAAAGATGAGTTA
Long Flanking Sequence:
TTACAGAAACATCAAATATGTGTCCAAACTCAACTGTGAGCATTAATGATACACAACAGACTCCAGCAATACCTCTGAAAGTGACTCCCAGCAATAAAATGTTTACACATGAAACAGAAATTGCAAAAACTTCAAACAAAATTAAAGACAAGGAATCCAAAATTCATGAACAAGTTCAAAGGACAAACTTAACTGATCCTACGGATTTTCAGAGGATGCAGTACACTGAACAATGGGTCCAGAATTCCCACATGCAAATTACAGACACTCCATCAGTCAATAAAACAGATTCTTTTAAAAATGGTTCCTTTCCTGGTGATTCAATTGGAATGGAGAAAAATGTGGTTCAGAGAATAAATGCTGCAGAAGAGATCAGGATGTGTTATTCAAAGGATAATGATGAACTAAACAAGGGTTTTAAGGCTGTACTTCAGAATTTTGGAGAAAAGAAGACAACTACAGACACAGGCTCACCTTTCCCGAAGAAAATTAAAGTTGTG[C/T]AAAAAGAAAACATTCAGGAACAGGCTAAAACCTCCAATAAAGATGAGTTACACTTCACCAGCAGAGACACCTCTTCAACACCTAACAAACATGAAGTTCCTTCAATTCACAATAATTCTGAGAACAAGGTAGTTTTGAGAGAAAAGAAAGCAAAGAGGGAGACAGAAGATGAGCGCCGACAGAGGCTCTCCATCCACAGAGATGAGATAATGAGGGGCAACGTAAAAGCAGCCATGGAGATCTTTGAAAATCTTATGAGACGAGAAGAACTGAAGGTCATTTTGTCAAAGGTTCAAGAAATAGAGGGGGAGACTTTTGAGGTGGATGTCAGATCTCTCAAGACTTTATTTGAAAATGTGCCTGCTTGGATTACCAATCCAAAAGAAAATACCAAACGCAGACATCGTCCGAGAGTTGCCAAAGAGACGGAGGGCTTAAGAGATGATCTAGAGAGCATATCTTCAGTTGAGGCTGCATTTGAGGACCTAGAAAAAGCAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32921
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 |
---|---|---|---|---|---|
ENSDART00000042413 | Nonsense | 1874 | 2297 | 1 | 1 |
The following transcripts of ENSDARG00000030722 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 24112580)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24095915 |
GRCz11 | 2 | 23751566 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCGAAGAAAATTAAAGTTGTGCAAAAAGAAAACATTCAGGAACAGGCT[A/T]AAACCTCCAATAAAGATGAGTTACACTTCACCAGCAGAGACACCTCTTCA
Long Flanking Sequence:
ACTCAACTGTGAGCATTAATGATACACAACAGACTCCAGCAATACCTCTGAAAGTGACTCCCAGCAATAAAATGTTTACACATGAAACAGAAATTGCAAAAACTTCAAACAAAATTAAAGACAAGGAATCCAAAATTCATGAACAAGTTCAAAGGACAAACTTAACTGATCCTACGGATTTTCAGAGGATGCAGTACACTGAACAATGGGTCCAGAATTCCCACATGCAAATTACAGACACTCCATCAGTCAATAAAACAGATTCTTTTAAAAATGGTTCCTTTCCTGGTGATTCAATTGGAATGGAGAAAAATGTGGTTCAGAGAATAAATGCTGCAGAAGAGATCAGGATGTGTTATTCAAAGGATAATGATGAACTAAACAAGGGTTTTAAGGCTGTACTTCAGAATTTTGGAGAAAAGAAGACAACTACAGACACAGGCTCACCTTTCCCGAAGAAAATTAAAGTTGTGCAAAAAGAAAACATTCAGGAACAGGCT[A/T]AAACCTCCAATAAAGATGAGTTACACTTCACCAGCAGAGACACCTCTTCAACACCTAACAAACATGAAGTTCCTTCAATTCACAATAATTCTGAGAACAAGGTAGTTTTGAGAGAAAAGAAAGCAAAGAGGGAGACAGAAGATGAGCGCCGACAGAGGCTCTCCATCCACAGAGATGAGATAATGAGGGGCAACGTAAAAGCAGCCATGGAGATCTTTGAAAATCTTATGAGACGAGAAGAACTGAAGGTCATTTTGTCAAAGGTTCAAGAAATAGAGGGGGAGACTTTTGAGGTGGATGTCAGATCTCTCAAGACTTTATTTGAAAATGTGCCTGCTTGGATTACCAATCCAAAAGAAAATACCAAACGCAGACATCGTCCGAGAGTTGCCAAAGAGACGGAGGGCTTAAGAGATGATCTAGAGAGCATATCTTCAGTTGAGGCTGCATTTGAGGACCTAGAAAAAGCAAGTATGGACATTGTCAATTTGAAAGAACAG
Associated Phenotype:
Not determined