Busch Lab

ZMP

si:dkey-155f10.1

Ensembl ID:
ENSDARG00000073920
ZFIN ID:
ZDB-GENE-081105-126
Description:
Novel protein similar to vertebrate contactin associated protein family [Source:UniProtKB/TrEMBL;Acc
Human Orthologue:
CNTNAP5
Human Description:
contactin associated protein-like 5 [Source:HGNC Symbol;Acc:18748]
Mouse Orthologues:
Cntnap5a, Cntnap5b, Cntnap5c
Mouse Descriptions:
contactin associated protein-like 5A Gene [Source:MGI Symbol;Acc:MGI:3643623]
contactin associated protein-like 5B Gene [Source:MGI Symbol;Acc:MGI:3664583]
contactin associated protein-like 5C Gene [Source:MGI Symbol;Acc:MGI:3646013]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa21481 Nonsense Available for shipment Available now
sa45356 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa34635 Nonsense Mutation detected in F1 DNA Not yet available
sa21482 Essential Splice Site Available for shipment Available now
sa31711 Essential Splice Site Available for shipment Available now
sa27395 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa21483 Essential Splice Site Available for shipment Available now
sa41413 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa21481
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112295 Nonsense 242 1306 5 24
ENSDART00000137759 Nonsense 215 1279 4 23

The following transcripts of ENSDARG00000073920 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 24589344)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23745130
GRCz11 9 23555999
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGCGAGGAGATTATATCACTCTGGAGCTTCATCGTGGCAGGCTGGCCT[T/A]GCATCTAAACCTGGGTGAGTTACAGTACTTGGAGAAACCAGCAACTTCCG
Long Flanking Sequence:
TGCGTCTCCTAGCAATGAAGCATACAGCATGTTTCTACGTGAGATTGTTGTGTTCAGAACAGCTTGAAAATGCAATAGCATTTGATTTTCAGCTGTTTTGTGTGCGATGCCTGCTGTTTAAAAGGTTCAGATTGGAAAAGTCATACACTGTAGTGTTACATAAATTACTTTTTTTAAATATCTAAAAACTTTGTTGCTTTGTTGTACACTGTATAGTTATTTTGGTTTAATTTGGATTAAACTGTAAAAAAAAGAAGAAAGAAACATCCAGCAAGTGTTCAATAATAATAAAAACTCTCATGTGTCCACAGGATCGTATGTGGCTGATTTTGATGGCAGAAGCTCTTTGCTTTACCGATTCAACCAGAAGTCTATGAGCACAGTGAAAGATGTTATATCGCTGCGATTTAAGAGTCGACAGGCAGAAGGTGTTTTACTGCATGGAGAAGGCCAGCGAGGAGATTATATCACTCTGGAGCTTCATCGTGGCAGGCTGGCCT[T/A]GCATCTAAACCTGGGTGAGTTACAGTACTTGGAGAAACCAGCAACTTCCGAGGGCTGAGATATTCATATATTTAATCATAGTTGCTTTGTAGTGGATGTTATGCTGTTTTTCCATTGTGGTTATGAATCAAAAATAGCTGTAATGGAATTCATGAGAGGCATTCATAAAGAAAATATTAATGTGCTGCCTTATAAAAGTTTGTTTAAAGTTAATTTTAAATGTCTACATTTCATTAAATTGTTTATTGAGCATTTAATTGAGTAAGTACGTCTTTTAAAGAGATAAAAAAAAAAACATTTTAAGCACCCACTGGTGTAATGCAATTAAAAACAAATATTCAAATTACTGTAATCAAGTAGAATTTCTTAGAAATTGTACTTTATATACTTTTACTTGAGTACAATTTTAGTGCTGTATTGGTACTTTTACTGTGCAATTTTACTTAAAATGTCACTACTTTGTTTATTTTGTATTGCCTACAGGGATTGGCTAAGTAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45356
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112295 Essential Splice Site 308 1306 6 24
ENSDART00000137759 Essential Splice Site 281 1279 5 23

The following transcripts of ENSDARG00000073920 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 24592070)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23747856
GRCz11 9 23558725
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACACTTCAGGACCAAGGGGGACGGAGACTCTCTAGAGGTCGACTATGAG[G/A]TTGGTCTTAAAAAAAAGATAAGCAGTTGATGTGGCAATGTCTGCACCTGT
Long Flanking Sequence:
ACCGGCACAGCTTTACTGGAGCAAGAATAATGTCGACTGAGACTTTCTGTCACTCCCACCAAAAGCTTGAAAAGCAGAATGTCAACATAGGAATATATTGTGTTTCATAATATGTTAAGATAGAAAATTTAAATAGCAGCATTTCTGCTTAATACTAGCCAGACCAGTGTAACCTTGGTAAGCATTAAATACTGTTTGGATATACATTTTAAAATCAAACCAACCCAGAGTTTTGACTGGTAGTGCAAGGTAATGACTTGAAGATCTGCATAATTAATAGCTTACGGCTAATTTGAAATCTCTTGTGATTGTCAGATGACAGCAGGGTGAGATCCAGCAGTGCCCGTATGGTGGTCACTCTGGGCAGTCTTCTGGATGATCTGCACTGGCACTCTGTCCTGATCGAACGCTTTAATAAGCAGGTCAACTTCACTTTGGACAGACACACTCAACACTTCAGGACCAAGGGGGACGGAGACTCTCTAGAGGTCGACTATGAG[G/A]TTGGTCTTAAAAAAAAGATAAGCAGTTGATGTGGCAATGTCTGCACCTGTGGGGTATGTGTGGCTAAAATGGTGTGCAAGAAAGTTTGTCAGATTGAATGATCTGTTAAACTAAATTCATTTGACCTGATAGTGTGCTGATTTTGTTGATTTGGGTCAGATGTGAATTTTTTTTAAAGATTAAAAAAATCATGAATTATACATAGTAATAAATGTGATATGATACTTCAGAAATAATTTTGTTATATGTGTTTAGTGCACAAAAACAATACTGTTAGTGTTAAAAACATTTGTACTGCTTAATGTTTTGAGGAAACTCAAAAGTTTTTTATGAGTCTTTAATGAAAAAAAGTTGTTGTTACATTTATCAAAAAGTAATTGTAATAAAATTCATGAGAGTTACTGTATTAATGAAGAATATATTAATATGTAAAGTTTAATTATAATTGTCAACATTATGAGCAAGCAGTTGAATAAGGATGTCTGAGGCAGTTAATTTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34635
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112295 Nonsense 349 1306 7 24
ENSDART00000137759 Nonsense 322 1279 6 23

The following transcripts of ENSDARG00000073920 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 24602453)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23758239
GRCz11 9 23569108
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGAACCTGTACTACAATGGAGTAAACATCATTGACCTGGCCAAACGA[C/T]GAAAGCCTCAGATCTACAGTGTGGTAAGCACTTGCTTTTGACAGTTTGGT
Long Flanking Sequence:
CTAAATCTATATTACATACAGATTACAAATAAAATGTAGATATAAATATTTGTGATATATAAATAATTTTAACATTGAATGACATTTACTGGGTGTCCTTTATAAACCATGATAATAAAAACTCAGGATAGTCTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTGGTTGGTTGGTTGGTTTGCTGGTTTGTTTTTTGGAAGTAAAACTGTTTTACAATTTTTTTTGTTCTGATGCTGTTTTTGTGGATCCCAATGTGCTCAAATATAAAACAAGTTGTATTTGATTTGTTGTATTCCTTCTCCGTAACAGCTAAGCTTCGGTGGCATCCCACTGCCTGGTAAACCTGGGACTTTTATTCGACGCAATTTTCATGGCTGCATGGAGAACCTGTACTACAATGGAGTAAACATCATTGACCTGGCCAAACGA[C/T]GAAAGCCTCAGATCTACAGTGTGGTAAGCACTTGCTTTTGACAGTTTGGTTAAGACTTAGTGATGCTGCAGTACTCTCATTTACATTTACTTTTATGTGTTTTGCAGACACTTTAATCCAAAGCCACACTGACGATACACTAAAACCACAACCTTGCTATTGCTTTATTATTGGTTTACTATTTGTGCTACTGAAAAAACAGATGTTCACATTATTTGCATGTTCATATTTGGCGGAGGCTGTGGAACATGATTTATTGCATGTTGACAATCTACTGTAAATTTTAACCATAGAATTAAAGGTGATTGTTGCGCTACTGTAATGAAATTCTCTACCAGTAAGCTGCTCAAATCCCACTTACTCCAAATTAATTTAAAATATTAAAAATTAAAGCTTAACAGTGTAGATGCCCCCCTTTCATCATTATTCTTTACTGAAAAAAATAGGATTCAAACACTTTTTTAGGTGAACTGGGGTACAAAAACACATACAGATTTGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21482
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112295 Essential Splice Site 356 1306 7 24
ENSDART00000137759 Essential Splice Site 329 1279 6 23

The following transcripts of ENSDARG00000073920 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 24602478)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23758264
GRCz11 9 23569133
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACATCATTGACCTGGCCAAACGACGAAAGCCTCAGATCTACAGTGTGG[T/C]AAGCACTTGCTTTTGACAGTTTGGTTAAGACTTAGTGATGCTGCAGTACT
Long Flanking Sequence:
CAAATAAAATGTAGATATAAATATTTGTGATATATAAATAATTTTAACATTGAATGACATTTACTGGGTGTCCTTTATAAACCATGATAATAAAAACTCAGGATAGTCTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTGGTTGGTTGGTTGGTTTGCTGGTTTGTTTTTTGGAAGTAAAACTGTTTTACAATTTTTTTTGTTCTGATGCTGTTTTTGTGGATCCCAATGTGCTCAAATATAAAACAAGTTGTATTTGATTTGTTGTATTCCTTCTCCGTAACAGCTAAGCTTCGGTGGCATCCCACTGCCTGGTAAACCTGGGACTTTTATTCGACGCAATTTTCATGGCTGCATGGAGAACCTGTACTACAATGGAGTAAACATCATTGACCTGGCCAAACGACGAAAGCCTCAGATCTACAGTGTGG[T/C]AAGCACTTGCTTTTGACAGTTTGGTTAAGACTTAGTGATGCTGCAGTACTCTCATTTACATTTACTTTTATGTGTTTTGCAGACACTTTAATCCAAAGCCACACTGACGATACACTAAAACCACAACCTTGCTATTGCTTTATTATTGGTTTACTATTTGTGCTACTGAAAAAACAGATGTTCACATTATTTGCATGTTCATATTTGGCGGAGGCTGTGGAACATGATTTATTGCATGTTGACAATCTACTGTAAATTTTAACCATAGAATTAAAGGTGATTGTTGCGCTACTGTAATGAAATTCTCTACCAGTAAGCTGCTCAAATCCCACTTACTCCAAATTAATTTAAAATATTAAAAATTAAAGCTTAACAGTGTAGATGCCCCCCTTTCATCATTATTCTTTACTGAAAAAAATAGGATTCAAACACTTTTTTAGGTGAACTGGGGTACAAAAACACATACAGATTTGCATTTACATTTAGTCATTTTTAGCATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31711
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112295 Essential Splice Site 357 1306 8 24
ENSDART00000137759 Essential Splice Site 330 1279 7 23

The following transcripts of ENSDARG00000073920 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 24608961)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23764747
GRCz11 9 23575616
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCCCTGCATGCATGTAAACTGATGCTTTGACATTCTCTCTTCTCTCAC[A/T]GGGCAACGTGACCTTTTCCTGCTCCGAACCACAGCTGGTGGCCACCACGT
Long Flanking Sequence:
ACCAACTAAAGTTAAAAATATGATATTGTTGTGGGCCACCCATTTAAGACCCGTGAGGACACTAGCTCAGACAACTTTTGATGTTGAAAATATTACCAAAGTTACTTTTATCAAAATGTATTTCGTATATGTATTAACTACTCAAAATGTCAGTCAAAGTCACTTAAAATATGTTAAATAAATCATTATTAAAGATGATGTCCTATAGTTCAATTTAAATGCATGAGTAAGGAAAATAAAATTTTGTACAGTGCAGAAAAACATTAGGAAAGTAATACAATAATATGGAAGAAAGCATTCTGTGTGAACAACCCACTTGCTAATCCTTCATTTGAGATCAGCAGTGTCATTTGAGATCAGAATAAATTCGTTGATTTACCTTGTGTGTGATCAGCTGCAGAAGATTGGCAAGTGGGTCATTTGTACTCAAGACTGCACTGCCATTTGGTCGTTCCCTGCATGCATGTAAACTGATGCTTTGACATTCTCTCTTCTCTCAC[A/T]GGGCAACGTGACCTTTTCCTGCTCCGAACCACAGCTGGTGGCCACCACGTTTCAGAGCTCCAGCAGCAGCTTTCTGTCTCTGCCAGCACCTGCACCAGTCCTGGAGGGACTTTCGGTCCGACTGCAGTTTCGCACCTGGAACCCTGATGGTCTGCTGCTCTCCAGTCCACTGATCTCTGCTCAGGACTCTTGTTACCTGATTTTGAAGATCAGTAGTGGCCGTCTCCATCTCACACACCAGACGTCAGCACTAAAGATGTCAGAAGTGTCAGCTGGTGAGGATGCAGCTCTGTTTGCCCTTATTTTACTTGACTTTAAATGCAAGATCTCCCAAAGTGATGTTTATTTATTAACTAATTTCGAGAGGATCACATGCTTATGACTCCTTGCAGCTGGCCCTTTTTTATCCAATTTATGATTCACCAATCAGATTATTCCTAGCCTCTATAAAATAGTACCATACCAGTGTCATCTTCGTTTTGAAGAATCCCCCCTTCCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27395
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112295 Essential Splice Site 496 1306 9 24
ENSDART00000137759 Essential Splice Site 469 1279 8 23
ENSDART00000112295 Essential Splice Site 496 1306 9 24
ENSDART00000137759 Essential Splice Site 469 1279 8 23

The following transcripts of ENSDARG00000073920 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 24612819)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23768605
GRCz11 9 23579474
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCACCTGAAGAACTATCTGGAAGCCAAAGACAAACAATATTTTGGAGG[T/A]AAGATAATGCATAAATCTTGTTGATGAATGGCTAAGGGCATACACTATGT
Long Flanking Sequence:
AGACTGTAGACACACAGCAGCCACACACAGCTTGGGCGCCCTTCACATGTAATGGCCAGAATTAATTAAATCAAACCTCAAAGAGAATTCATATTTGTGGGGGCAGTGTTGGAGGGGGGTACATTTTTAACAACAAAATTGTTTTTTTGGCACTTTGTATTATATTTGTTTGATAGTGAGTTCTTTGTTCTGACTGAGTTCATGGCTTAGTTGCGTTTAAAAAATTGCGGTTCACTTACAGGTTGTCTTGAATGTCTTTATAGTAGCATGTGTGTTGTTTATTTTGCATCATGCAATTATTATATATGTGGTATAATTACATTAAATGAGTGCGTGTTGTTTTTTTGATCGGCAGGCCAGAGGGTGAATGATGGTTTGTGGCATTCAGTGAGTCTCAGTGCTCGAGGACTGCAGATGACCATGACTCTGGACAATGAGCCCGCATCCAGCATCCACCTGAAGAACTATCTGGAAGCCAAAGACAAACAATATTTTGGAGG[T/A]AAGATAATGCATAAATCTTGTTGATGAATGGCTAAGGGCATACACTATGTACAGTTGCCTTGAACTGTGCCGAAGCACGCTTGTCCACCCTCCCATCTCCCCAATGGCCTGCACTCACATTGCATCTGAGCCTGAGCATGCTTACGTCATTGATGATGCGCTGTTGAGTTTAATAGAAGAGAAGTGCTCTCACTCTGTACAGTGGCGATTGCTTTAGTTATATCATATCAGTCATTTAGGATGCAGTAACAAGCAGTCAAATATTTTGCAGAACAGATCATAAAGTCCTCCTGCTGCAGGTATTAGGAGGTTTGCTGTAACTGCAGCTGACGTGCAGTGAGGGGTTTGCATCTTTAATAAACCTACAGTTTGCATTCACTGAACAGTAAGAATGATTAATTAATCCATATAAAACAGTCCCTTAAAAGTCATGTATTGTCTTCATTTTCGGGCTTCGGCCTTCAGTTTTGTACTCACACTACAAGCCTGAGCCCAAGTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21483
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112295 Essential Splice Site 496 1306 9 24
ENSDART00000137759 Essential Splice Site 469 1279 8 23
ENSDART00000112295 Essential Splice Site 496 1306 9 24
ENSDART00000137759 Essential Splice Site 469 1279 8 23

The following transcripts of ENSDARG00000073920 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 24612819)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23768605
GRCz11 9 23579474
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCACCTGAAGAACTATCTGGAAGCCAAAGACAAACAATATTTTGGAGG[T/A]AAGATAATGCATAAATCTTGTTGATGAATGGCTAAGGGCATACACTATGT
Long Flanking Sequence:
AGACTGTAGACACACAGCAGCCACACACAGCTTGGGCGCCCTTCACATGTAATGGCCAGAATTAATTAAATCAAACCTCAAAGAGAATTCATATTTGTGGGGGCAGTGTTGGAGGGGGGTACATTTTTAACAACAAAATTGTTTTTTTGGCACTTTGTATTATATTTGTTTGATAGTGAGTTCTTTGTTCTGACTGAGTTCATGGCTTAGTTGCGTTTAAAAAATTGCGGTTCACTTACAGGTTGTCTTGAATGTCTTTATAGTAGCATGTGTGTTGTTTATTTTGCATCATGCAATTATTATATATGTGGTATAATTACATTAAATGAGTGCGTGTTGTTTTTTTGATCGGCAGGCCAGAGGGTGAATGATGGTTTGTGGCATTCAGTGAGTCTCAGTGCTCGAGGACTGCAGATGACCATGACTCTGGACAATGAGCCCGCATCCAGCATCCACCTGAAGAACTATCTGGAAGCCAAAGACAAACAATATTTTGGAGG[T/C]AAGATAATGCATAAATCTTGTTGATGAATGGCTAAGGGCATACACTATGTACAGTTGCCTTGAACTGTGCCGAAGCACGCTTGTCCACCCTCCCATCTCCCCAATGGCCTGCACTCACATTGCATCTGAGCCTGAGCATGCTTACGTCATTGATGATGCGCTGTTGAGTTTAATAGAAGAGAAGTGCTCTCACTCTGTACAGTGGCGATTGCTTTAGTTATATCATATCAGTCATTTAGGATGCAGTAACAAGCAGTCAAATATTTTGCAGAACAGATCATAAAGTCCTCCTGCTGCAGGTATTAGGAGGTTTGCTGTAACTGCAGCTGACGTGCAGTGAGGGGTTTGCATCTTTAATAAACCTACAGTTTGCATTCACTGAACAGTAAGAATGATTAATTAATCCATATAAAACAGTCCCTTAAAAGTCATGTATTGTCTTCATTTTCGGGCTTCGGCCTTCAGTTTTGTACTCACACTACAAGCCTGAGCCCAAGTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41413
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
ENSDART00000112295 Nonsense 1067 1306 19 24
ENSDART00000137759 Nonsense 1040 1279 18 23

The following transcripts of ENSDARG00000073920 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 24640576)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23796362
GRCz11 9 23607231
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCAGAGTCCTGCTATGCTCCTCACAGTCAACACTCTCAGCCAGCAGTA[T/A]GTGGCCGTCATCCTTGCTCGAAATGGTGAGATGGCTATGTCATATATCAT
Long Flanking Sequence:
TAATGAATTAACTATTTGCTAACGCTTAATAGATTATTCATAGTGTGTAGTTATTATAAAGTGTTACCAAATAATCTTTTAGTTCCCAATAATGATACAGCAGCTATATTGTGCATTTCTGCTAACAGTTTTTCCACAAGCGACTCCATTGCTTATAGAATCTATTTATATCATAAATGCATGACTTTTAAAGATACTGTTCAAAGTTTAAAGAAAATGTCAAGTGTACACAGGAAATTAAGTGTACTCGGATTAGATTTATAGCCAACGACAAAGTCCATCTGGTCTTTTGTATCCACAGAGGTGTCCATGTCCTTTGAAAGAGGAGCATCGGTCACCTACATTTTTCAGGAGCCGTTCTCTGTGATCCAGAACCGGTCAGCCGCAGTTCTGTCAGTCCCTTCACAATACAGCAAATCCAGAGACAACATGGCACTAAGTTTCCAGACCACTCAGAGTCCTGCTATGCTCCTCACAGTCAACACTCTCAGCCAGCAGTA[T/A]GTGGCCGTCATCCTTGCTCGAAATGGTGAGATGGCTATGTCATATATCATTCTCAATCCTGGGTGTCATTAATGTATGAAAGGTTTATATGTCTATAATAGAGATATTGCAGTGCTAAATGAATTACTCACACCTCTGTTATCTGGATTGCTGTACTGCAAGATTAAATTAAATGAAACATAAAAAGTTATGGTACTTTGTGTTCTACTATAATTAGATGAATTCTGCAGTACTATTGATTAATCATGCTCATTTAGATTTAAACTGTCAGTTTTACAGCTTTATAAATCACTGGAAGGTGTATGAATTGTAAAAAATCACAGTTAAGTAAAACTTTAACGGCCAAACTGGGTTGGATATTGTAACATAACCACCATTGAGAATTACATTCTGTTTTTCAGGCTCACAGTAAAGCATTTAAAGGATACTTCACTCAAAAATTAAAGTTTACGCATACATTCAATTCTATATGATTTTATATGATGCTCTTTCTTTGTAGG
Associated Phenotype:
Not determined