ZMP
lims1
Ensembl ID:
ZFIN ID:
Description:
LIM and senescent cell antigen-like-containing domain protein 1 [Source:RefSeq peptide;Acc:NP_00101
Human Orthologues:
AC108938.4, LIMS1, LIMS3
Human Descriptions:
LIM and senescent cell antigen-like domains 1 [Source:HGNC Symbol;Acc:6616]
LIM and senescent cell antigen-like domains 3 [Source:HGNC Symbol;Acc:30047]
LIM and senescent cell antigen-like-containing domain protein 3 [Source:UniProtKB/Swiss-Prot;Acc:Q9H
LIM and senescent cell antigen-like domains 3 [Source:HGNC Symbol;Acc:30047]
LIM and senescent cell antigen-like-containing domain protein 3 [Source:UniProtKB/Swiss-Prot;Acc:Q9H
Mouse Orthologue:
Lims1
Mouse Description:
LIM and senescent cell antigen-like domains 1 Gene [Source:MGI Symbol;Acc:MGI:1195263]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41878 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18028 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41878
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033980 | Nonsense | 68 | 336 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 34446483)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33347420 |
GRCz11 | 11 | 33610222 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAATGTTATGTTTGATTTTCCTTTCTTCTGTCCATAGTTTGAGGGAAGG[A/T]AGTACTGTGAGCATGATTTCCAGATGTTGTTTGCTCCCTGTTGTCACCAG
Long Flanking Sequence:
TATCATTTAATTTAATCATTTAATCCAGTGATTTTAATGATGAATTTTCAGCTTCATTACTCTAGTCTTCAGTCACATGATCCTTCAGAAATCACTCTAAAATTAATTATTATTATTATTATTATTATTATTATTATTATTATTTTTATTTTATTTTATTTTATTTATTTTTTACATTTAATAAATGCTGCCTTGATAAATAAAATAAATGATAAAAAAAATCTGACACAAGAATAGTGTATATTTCAATTTCAATACATGTTCTCTGCTCTGTAAGATTAATTGAGTTTGAAATACATTTTTTTAATGTATATAAATATGTAAAATAATGAACTTCTATCACTTAAGTTCAAATTCACCTTTAAATTACATTTTTAATTTTAAAACGTGTTCTCTGTTCGGTGTTAATAACATGCAATGGATTGACTTTGAAACATATTCCCACTTGAGCCAATGTTATGTTTGATTTTCCTTTCTTCTGTCCATAGTTTGAGGGAAGG[A/T]AGTACTGTGAGCATGATTTCCAGATGTTGTTTGCTCCCTGTTGTCACCAGTGTGGTAAGAGATTCACATGGATAAACACACAAACAGGTGATGTTAGTGCCTGTGCTGACTGTGAATTGTGTCCCTCATAATCCCTCAGGAGAGTTTATAATTGGGCGTGTGATTAAGGCCATGAATAACAGCTGGCACCCGGACTGTTTCTGCTGTGATATCTGCCAAGCGGTGCTCGCCGATGTTGGATTCGTCAAGAACGCCGGCCGGTAAGTTTGTGGCCAACCGAGCGGTTACCGTAGAATTGTGACTGACAGGCCGCATGTGTTTTTTTTTGGAGCGGAAACTAATTCATTAATGAAATAAGGTGTCCATATCAGCAAACATTCCAACAATGTCCACGCTATTGTACATGCCGCATGCTTTCCTGTTAATAAGCTCATGAGACAAAATGACAGCAGTAGCTATGTTTCAGTTCACTTATTTTTAACACATTCTGGATTATAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18028
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 |
---|---|---|---|---|---|
ENSDART00000033980 | Nonsense | 311 | 336 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 34437603)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33338540 |
GRCz11 | 11 | 33601342 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCTTGTGTTTTAGGAACAAGTTTGTGGAGTTTGACATGAAGCCGGTGTG[T/A]AAGAAATGCTACGAGAAGTTTCCTCTGGAGCTGAAGAAGAGGCTGAAGAA
Long Flanking Sequence:
CGTCAGAAGCAGCTTTACAAGGTAAAAGACAGATAAAAAAAAATAAATAAATAAATTGGTAAGAAATGACTAACAATAATTCAGGGGAGCTTATAATTCTGACTTCAACTTTGTATGTGTAGCTCGCTTTCTGATATGATCATTTTAGTTCATTAATTTATTTCTAACCATTTCTAATTTCCATTAATAAATGTATTTATTATGCCATTTTTTATATAGTTTTAATTTATTTGTATTTGTTTTAACAAAGATTTTGTTTTTTTAAATGTTTAAACCATTTCAGTCAATTGCAAAGGTAAAATTTGTTTTTTGTTGCACTGCCTCATTCATTTCTAAAAATAAATAAAAGTTAAAAGCATTTAACAGTAAACTGTTAGTAGAATTAACTGCATACTTGCATAGCTAGCTCATGTTTTTGGCCTAAATGCATGAGAAAGCACATTTATGCAAATCTTGTGTTTTAGGAACAAGTTTGTGGAGTTTGACATGAAGCCGGTGTG[T/A]AAGAAATGCTACGAGAAGTTTCCTCTGGAGCTGAAGAAGAGGCTGAAGAAGCTGGCCGAGACTTTGGGCCGCAAGTAAAACTCATCGTAATCATCATCTGTGCTCAAATCAACAGACCAAACCAAACCAAAGCGCAGATCATCTTGGAATAGTTGTCTTACTTTATCCTACTTAAACTTTAAGTGTGTTTTTCTACCACAGAAAGTATTGCAGGCAGATTTTTACTGGTTTCACGCTAATGGATGCGCACGTGTCTTAAAAAAACCTGCAAACTAATCAAAACAGTTACCTTTATATTGTTAATGATAAATATACAGTCGTGGAAAAAGGAGACTAATAAATCTTGAGAAACTGAGTATGGATTTGAGGAAAATGTTATTTGTTTTATTCAATAAAGGATTTCTGATAACATTTCTTTTAAACGTTAAATCAAAATATTGTAAATAGCAAATTGCTAAGTGGTTAGAAAAAAATAATGTCTTATTTTGTTGTCTAAAATT
Associated Phenotype:
Not determined