ZMP
igsf21b
Ensembl ID:
ZFIN ID:
Description:
immunoglobin superfamily, member 21b [Source:RefSeq peptide;Acc:NP_001103943]
Human Orthologue:
IGSF21
Human Description:
immunoglobin superfamily, member 21 [Source:HGNC Symbol;Acc:28246]
Mouse Orthologue:
Igsf21
Mouse Description:
immunoglobin superfamily, member 21 Gene [Source:MGI Symbol;Acc:MGI:2681842]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa45797 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa1517 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45797
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000104188 | Nonsense | 42 | 473 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 23 (position 21939736)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 21719043 |
| GRCz11 | 23 | 21645594 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGAGCCTCTGCCTCCTGTGGTTATGGGGGACACTGTGACTTTGAAGTG[C/A]AATTTCAGGACGGATGGCAACTTACGAGAGATTGTGTGGTTTCGGGTAAG
Long Flanking Sequence:
TTGCTAAATAATGAATAATCAGGGATATATCTGTCAGGTAAACTCAGAAAAAAGTTGTTTCTTGCAGCGAGAAGATTAAAAATGAATGAATTGGAGCACTGATACTGTGTGGTCTTCTCACAACATTCATTAATAGCGTTTTTTTGCAATCATACTTTTTCATCTAAAATATTCACAAGTTGAATCAAAAGCTCATTATGTGCTATAATTCCACTGTCATTGCAGTATGACTTCTCTTGGGGCAAGCTTTATATTGGGTTCTTCAAGAGCACGTCATTTTACTTACTTATGACTTAATGCTTTCAGAAATGAGGAGAGCACTGTAATTTTGCCAGGGCTCATTGCTGGTAATTTGGATGAGATTGTTAAAGAGGCTGTGCAATTTGCGGATGTAATAAAGCATTGAAGAAATGACACTGCTATCTTCTTCCAGGTTATTTAACAGTCACCATTGAGCCTCTGCCTCCTGTGGTTATGGGGGACACTGTGACTTTGAAGTG[C/A]AATTTCAGGACGGATGGCAACTTACGAGAGATTGTGTGGTTTCGGGTAAGTGGGGTCCGAGCTTTATCTTTCCGTGATACGGCATTTATTTCAGAATCCTGGAAAAAATAATCACTTGTTTTTCACTGTGCTAGTTTTTGTCTTCTTTCAAACTCTTTTAGGTTGTTTTTCTGTTGGCAAACTGACGTTGTGAGAACTGAAGCTGTCAAAAAATATGAAAATATATTCAGGATTAAGAGTGAACGGCTCAGTGATTTTAGGACAAGCGGTTTTCATTTTGTCGTCACACCAAGCCATAAGTGTGGCAGGATTGATGAGCTATCGGATAAAATATTCCATTAAAAAACATATCAGTTTGCTGACAGATTTCCGTGACATTTTAAATAAAACTCTACTGTGCAATGCGTCACATATTACTTAGCCATAAATTTGCCATTTTTCTGTCCCTCTATTGAAAATCAAACAAAGGTCACATAATGATAGTGGCCACAAAAGCTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1517
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000104188 | Essential Splice Site | 434 | 473 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 23 (position 21948120)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 21727427 |
| GRCz11 | 23 | 21653978 |
KASP Assay ID:
554-1441.1 (used for ordering genotyping assays)
KASP Sequence:
CCAAAACCCTTTGGGATCCACCAACACACACACCCGCCTCATAGTGTTCG[G/A]TCAGTATACCASATGCATCACATGCACATGCCAATATTCATATCCNNCTCAT
Long Flanking Sequence:
ATGTTGAATATAAATTATTCAGGTGCTTTTGATGTCGTATAGTAGACCTTAAATGTTTAAAAGCTTCTTTTAAAAAATAGTTTAATATTCTCTGTACAGTATATAATCTAAGAACAAATGGATACTGCTAGTGCCAACAGTGTTTAGTAAATGTATATAAATTATTAAAAAGAGGTCTCCTAAGCAGTTCCTCATAAATATAGCTTTTTAGTTTTTGCACAAAGATGTACATTATTTCAGTATTATCATACTCAGTATTATAAATGTCTGCTGTGTTAATATTTTGTTTTTTATATTTCTGCCGCAGAATGAAGTGTTTCCTGAGCCTCTGTTCACATGGACACGTGTGGGAGGACCTCTGCTGGATGGAAGTGAAGAGAGATTTGGGAAAGAACTGGTTCTGGAGAGAGTCCCGGCAGAGCTCAACGGCTCGATGTACCGCTGCACTGTCCAAAACCCTTTGGGATCCACCAACACACACACCCGCCTCATAGTGTTCG[G/A]TCAGTATACCAGATGCATCACATGCACATGCCAATATTCATATCCCTCATTGTGTTCAGCTTCCACCTGTGTGCACTTCATAAACCTGGATCCACATCTGACGCTCAGAGTGTTTAGTCTTTATCCAGCACTCGCATAACTTAAAATGTTTAAACCATTCCCAAACATCCTTATTTTCATGCAGTGTTTGTTTTGTATCCAGTAATTAAATGCCCCATACTGTTTACTAAGATTCAATCGCAGTAAGCTGTTTGTTTCCAAAAGCTACTGCAGTGTTGGAACAGTAGGCAAGAAAACATGTAGCACTCATAATGTCTAGTCAATTGAAGTACCAGGAGGCATAAATATCAATCATAAATCAACCAATGAAATAAATGAAGAAAACAACCATTTAATGATTTAAAGAGACCGTTTACTACAAAATAAAATAAAATAAAAATGTTAATTTACTCACCTTCAGGTACTCACAAACGTGTTTTTTTGGGAAGATTTGTGGCCTT
Associated Phenotype:
Not determined