Busch Lab

ZMP

igsf21a

Ensembl ID:
ENSDARG00000031049
ZFIN ID:
ZDB-GENE-050809-118
Description:
immunoglobin superfamily, member 21a [Source:RefSeq peptide;Acc:NP_001029356]
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 5 alleles of this gene:

Allele Name Consequence Status Availability
sa41859 Nonsense Mutation detected in F1 DNA Not yet available
sa13436 Nonsense Available for shipment Available now
sa21932 Essential Splice Site Available for shipment Available now
sa41858 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa30948 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa41859
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041443 None None 375 None 7
ENSDART00000123245 Nonsense 22 494 1 10
ENSDART00000140871 Nonsense 22 84 1 2
Genomic Location (Zv9):
Chromosome 11 (position 29958765)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 28834751
GRCz11 11 29081925
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGGCGAGCTGCCGGAGAGCATGTAAACGCAAATGGAGTTTGGGATTTAT[T/A]GCAAAATATGGGAAAGATGACCGTCTTGTCTTTGTGTTTTCTCTTGTGCG
Long Flanking Sequence:
GAAAAAAATCCAGCAGGAATAAATCGGCTTAGTGGACAGAATTAGAGGGGAAGGGTTTGGAGCCAGGGTAGGATTAAGGAAAATTGTGTGAAATAAAAAGCGAGTGATCACGAGTGACTCTGTTCGTGTCTGTTTCTGGAGGGAGGGAGGAGAGAGAGAGAGAGAGAAAGAGAGAGAGAGAAAGACAGAGTGTGTGTGTGAGAAAGATTTTCATCCAAATCCATATCTATTTTTTAATCCTCGTCTGTGCGTAAACGCTGGTTACAGCCTTCGCGAGGAGACTATTTCGCAATGCAACGCTTTTAATAATCTTTACGCAATCTTCACGCAATCATCTTTGCATCCGTTGAAGTGCGCATTTGTTTTAAACTTCAATCTTCCCTCCGACACACTTGGACAGCATCATGACCAGTTTGTGGGATCGCATCCCGTTGGAATGGTGGGAATTACGCGGCGAGCTGCCGGAGAGCATGTAAACGCAAATGGAGTTTGGGATTTAT[T/A]GCAAAATATGGGAAAGATGACCGTCTTGTCTTTGTGTTTTCTCTTGTGCGCTGATCTACTGCAAGTAGCTGTTGGTAAGTAATTCTTATGTTGTGTGTTTTATCACTCGAATGAGCTGTTTATCAGAAAACGCGCGTTTCGGATTCCACGCACACGCGCGCATCCCCATAAGAAAGCGCTGCGTGCATATATTGAGTCGTCTTTCATATTTACTTAGATCAAGTTTGCTCGTTTTATGCGAGACGCCGCTTAGCGTGGATTTCCCAAGAATACCAACGGCTCAGCCGCGGCACTTTGGGGTATAGTGCTGGCTGGGTAAAAGAGCAGACACCGGGTGAATGTCATTTTTCATACGGTACATTGTGAAACAGCAGGACGCTTGAACATTCTGACGCCCAGGAATAAATGAGGCTGAACGGATTAATGCCAAGAGCTATTGACTTTAACCCTGACCGTATTTATTGTTGCATAGTCAAATCTCATGCATACAGATGCATCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13436
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041443 None None 375 None 7
ENSDART00000123245 Nonsense 37 494 1 10
ENSDART00000140871 Nonsense 37 84 1 2
Genomic Location (Zv9):
Chromosome 11 (position 29958720)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 28834706
GRCz11 11 29081880
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTATTGCAAAATATGGGAAAGATGACCGTYTTGTCTTTGTGTTTTCTCT[T/A]GTGCGCTGATCTACTGCAAGTAGCTGTTGGTAAGTAATTCTTATGTTGTG
Long Flanking Sequence:
AGGGGAAGGGTTTGGAGCCAGGGTAGGATTAAGGAAAATTGTGTGAAATAAAAAGCGAGTGATCACGAGTGACTCTGTTCGTGTCTGTTTCTGGAGGGAGGGAGGAGAGAGAGAGAGAGAGAAAGAGAGAGAGAGAAAGACAGAGTGTGTGTGTGAGAAAGATTTTCATCCAAATCCATATCTATTTTTTAATCCTCGTCTGTGCGTAAACGCTGGTTACAGCCTTCGCGAGGAGACTATTTCGCAATGCAACGCTTTTAATAATCTTTACGCAATCTTCACGCAATCATCTTTGCATCCGTTGAAGTGCGCATTTGTTTTAAACTTCAATCTTCCCTCCGACACACTTGGACAGCATCATGACCAGTTTGTGGGATCGCATCCCGTTGGAATGGTGGGAATTACGCGGCGAGCTGCCGGAGAGCATGTAAACGCAAATGGAGTTTGGGATTTATTGCAAAATATGGGAAAGATGACCGTCTTGTCTTTGTGTTTTCTCT[T/A]GTGCGCTGATCTACTGCAAGTAGCTGTTGGTAAGTAATTCTTATGTTGTGTGTTTTATCACTCGAATGAGCTGTTTATCAGAAAACGCGCGTTTCGGATTCCACGCACACGCGCGCATCCCCATAAGAAAGCGCTGCGTGCATATATTGAGTCGTCTTTCATATTTACTTAGATCAAGTTTGCTCGTTTTATGCGAGACGCCGCTTAGCGTGGATTTCCCAAGAATACCAACGGCTCAGCCGCGGCACTTTGGGGTATAGTGCTGGCTGGGTAAAAGAGCAGACACCGGGTGAATGTCATTTTTCATACGGTACATTGTGAAACAGCAGGACGCTTGAACATTCTGACGCCCAGGAATAAATGAGGCTGAACGGATTAATGCCAAGAGCTATTGACTTTAACCCTGACCGTATTTATTGTTGCATAGTCAAATCTCATGCATACAGATGCATCATTTAATTACTTCTCTTGGAATTTGTACAGTCACACATTTGGGCTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21932
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041443 None None 375 None 7
ENSDART00000123245 Essential Splice Site 84 494 None 10
ENSDART00000140871 None 84 84 None 2
Genomic Location (Zv9):
Chromosome 11 (position 29787891)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 28663877
GRCz11 11 28911051
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCAACTTCAAGACAGATGGAAGATTACGAGAGATCGTATGGTACAGGG[T/A]AAGTTGCAGTTTACTCTTAATTTATCATCATTGTTTAAGTTCATAATTTG
Long Flanking Sequence:
ATGCATATATATTAATTTAGTTATTGGAAATATTATTTTACTTGACTAAAACTATTTGCCTTGTTATATACATTTTATCATGGAATATTTTGATAATTTTTTTCACTTTATAGATTTTTTATTCAGTGTACAAAAAAGGCTTTTGTTTTGTTGAAGCCAAAGCCTTAGTTTCCTTAGCAACGACATCGTTTTGAGCTGGCATGTTAACTTGTGTCAATTAGTTCCAATTCATTCTGTAATCAGTTCATAATTCTGAATAATATGATCAATTATATCATGAAGTGGTCTGATTTATGATAAGCTTTTCAGTCTGCACCTCATGTATCACCATCTGGCTATTTGGCTTATATTTTTAATAAAAGTGATGTCTTGTTTTGCCTCTGCAGGATATCTAACTGTAACGATAGAGCCATTGCTACCTGTTGTTGTGGGAGAAGCGGTGACTCTAAAGTGCAACTTCAAGACAGATGGAAGATTACGAGAGATCGTATGGTACAGGG[T/A]AAGTTGCAGTTTACTCTTAATTTATCATCATTGTTTAAGTTCATAATTTGTTCTGTTTTGAAACTGTTAGTGTGTTAATGTTCAGACTTTTTTAATTGTGTGATCTTGAGGCTGCTCTATTGTTTAATATTAAACATTTCAATGGAATTCTTTCTTGTTATTGATCGTCTGTGGCATTATGTGGTCAAATCTTTAACTGCTGTAAATTAAAGTTGTGAGCCGCCACTTTCATAGCTCTTGTATTTTGCTCTGGACTCAGTTGAGTGATTGCTCTTGTACACAAACCCAATTATTTATTAATGATCTCAGAGGCTGATTGTTTTGCTCAGTGCTGTGGACTTGAATTGTTCAGTTTGTATTATAGTGGAAGTTTCCAGGTACTTAAGTGGTGGGATTTGGTACACAGAGGATACAAAAGGATCGGATAAAGTCCAAAATAAATGAAAAATTGAGGAGAAAGATCATTTAGGTAACTTTGAATGTGGAAATTAGCAAGGGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41858
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041443 None None 375 None 7
ENSDART00000123245 Essential Splice Site 125 494 3 10
ENSDART00000140871 None None 84 None 2
ENSDART00000041443 None None 375 None 7
ENSDART00000123245 Essential Splice Site 125 494 3 10
ENSDART00000140871 None None 84 None 2
Genomic Location (Zv9):
Chromosome 11 (position 29685724)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 28561710
GRCz11 11 28808884
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAGGATTACCGCAGACGGGAAGACCTGGTGTATCAGTCGACGGTCCG[G/T]TAAGAACCTTTCAGTGTTATTTGATTGCTACTGGATGTAATATTTATGTG
Long Flanking Sequence:
AAATGCAGTGATAATAATCTGAAATATTCTGAAATACAACCCCCCCCCCCCCACACCTTTTTTTTTCCTTCTTCATCTTATTGGTGGCTACTTTATAGTGCACTAAATACCTAATGTCACATATGCAAATTCATCTAATTTCATCATGCTTGGCGGAACTCTTTTAAATGTGTCTCCTCAAGAGCTCTTAAAAAATATACCAATAATAACTCTAAACGGATCAATGGGATCATTTTAAAGTGTGAGAACTAACTTTGCCTGTGGGCACTGAGCTCTTGTACTGTCTCGTCTCATTATTTATGTATAGGGGTCTATGGAATATCCACTTCATTATGAGACACCTCGTTTTATGAATGTTTTATTCTTATTTCCTAACAGGTTACTGACGGGGGCACCATTAAGCAGAGGATTTTTACGTACGATGCTATGTTCAATACAAATTACTCTCATATGGAGGATTACCGCAGACGGGAAGACCTGGTGTATCAGTCGACGGTCCG[G/T]TAAGAACCTTTCAGTGTTATTTGATTGCTACTGGATGTAATATTTATGTGGTCTGAGTGATTGAGGTGCCAGATTTTGTTCATTTCCAATACATCGTTGTTTAATAAGTTGATGTGTGCTGCTAGATGCCATGGCGTATTGGCCCAGTGTGTTCATGTAGGTAATATACCATGTAGTCTGACTTTAAAATATTACTTTATTATATTTTTCCCATCGGATTTAACATTGCTGTGAGAACAAATATTTTGGATATTTGCTAATGCATTTTACAGGAAGGTCAAGATGTTTTCTTGCAGATTTAACGTAAAATTAGTTATCATTGCATATTGTATATAGTTAGCGTTGTATTTGTTTGCGTTATGAAACATTTATATCAAATGTTGGTTATCTTATCAGCCAAAATGTCTGTATCTGTGTATCCCTGATATAGGCTAAACAAGTAATACACATACTATGTCTGATGTCACATGTGCATGACATCAGAAGATTTGTATTTCTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30948
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041443 None None 375 None 7
ENSDART00000123245 Essential Splice Site 125 494 3 10
ENSDART00000140871 None None 84 None 2
ENSDART00000041443 None None 375 None 7
ENSDART00000123245 Essential Splice Site 125 494 3 10
ENSDART00000140871 None None 84 None 2
Genomic Location (Zv9):
Chromosome 11 (position 29685724)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 28561710
GRCz11 11 28808884
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAGGATTACCGCAGACGGGAAGACCTGGTGTATCAGTCGACGGTCCG[G/T]TAAGAACCTTTCAGTGTTATTTGATTGCTACTGGATGTAATATTTATGTG
Long Flanking Sequence:
AAATGCAGTGATAATAATCTGAAATATTCTGAAATACAACCCCCCCCCCCCCACACCTTTTTTTTTCCTTCTTCATCTTATTGGTGGCTACTTTATAGTGCACTAAATACCTAATGTCACATATGCAAATTCATCTAATTTCATCATGCTTGGCGGAACTCTTTTAAATGTGTCTCCTCAAGAGCTCTTAAAAAATATACCAATAATAACTCTAAACGGATCAATGGGATCATTTTAAAGTGTGAGAACTAACTTTGCCTGTGGGCACTGAGCTCTTGTACTGTCTCGTCTCATTATTTATGTATAGGGGTCTATGGAATATCCACTTCATTATGAGACACCTCGTTTTATGAATGTTTTATTCTTATTTCCTAACAGGTTACTGACGGGGGCACCATTAAGCAGAGGATTTTTACGTACGATGCTATGTTCAATACAAATTACTCTCATATGGAGGATTACCGCAGACGGGAAGACCTGGTGTATCAGTCGACGGTCCG[G/T]TAAGAACCTTTCAGTGTTATTTGATTGCTACTGGATGTAATATTTATGTGGTCTGAGTGATTGAGGTGCCAGATTTTGTTCATTTCCAATACATCGTTGTTTAATAAGTTGATGTGTGCTGCTAGATGCCATGGCGTATTGGCCCAGTGTGTTCATGTAGGTAATATACCATGTAGTCTGACTTTAAAATATTACTTTATTATATTTTTCCCATCGGATTTAACATTGCTGTGAGAACAAATATTTTGGATATTTGCTAATGCATTTTACAGGAAGGTCAAGATGTTTTCTTGCAGATTTAACGTAAAATTAGTTATCATTGCATATTGTATATAGTTAGCGTTGTATTTGTTTGCGTTATGAAACATTTATATCAAATGTTGGTTATCTTATCAGCCAAAATGTCTGTATCTGTGTATCCCTGATATAGGCTAAACAAGTAATACACATACTATGTCTGATGTCACATGTGCATGACATCAGAAGATTTGTATTTCTAT
Associated Phenotype:
Not determined